Genitourinary Radiology - Past Meetings
Transcription
Genitourinary Radiology - Past Meetings
Genitourinary Radiology UR001-EB-X A Guide to Penile Duplex Ultrasonography All Day Location: GU/UR Community, Learning Center Participants Bipin Rajendran, MD, Richmond, VA (Presenter) Nothing to Disclose Michael Maldonado, MD, Richmond, VA (Abstract Co-Author) Nothing to Disclose John T. Roseman, MD, Richmond, VA (Abstract Co-Author) Nothing to Disclose Uma R. Prasad, MD, Midlothian, VA (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Penile duplex ultrasonography is a relatively safe, minimally invasive method for evaluation of a number of conditions, including but not limited to Peyronie's disease as well as erectile dysfunction (ED) secondary to atherosclerotic or post-traumatic changes. Our goals are to highlight our experience with this modality by sharing our institution's protocol and to demonstrate a few select cases which highlight both normal sonographic findings as well as unique pathology. TABLE OF CONTENTS/OUTLINE 1) Introduction to penile duplex ultrasonography2) Protocol3) Normal sonographic findings4) Sonographic findings associated with Peyronie's disease5) Sonographic findings associated with erectile dysfunction secondary to atherosclerosis6) Unique sonographic findings in a patient with erectile dysfunction secondary to prior pelvic trauma UR003-EB-X Renal Tumors with Low Signal Intensity on T2-weighted MR Image; Radiologic-pathologic Correlation All Day Location: GU/UR Community, Learning Center Participants Youyeon Kim, MD, Seoul, Korea, Republic Of (Presenter) Nothing to Disclose Deuk Jae Sung, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Na Yeon Han, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Ki Choon Sim, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Beom Jin Park, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Min-Ju Kim, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Sung Bum Cho, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1. To review variable renal tumors which show low signal intensity on T2-weighted image.2. To explain the histopathologic features that create the specific appearance on the MR image.3. To discuss the practicality of the MRI findings for the differential diagnosis of the renal tumors. TABLE OF CONTENTS/OUTLINE Review of variable renal tumors with T2 low signal intensityImage findings of the tumors - AML - RCC Papillary RCC Clear cell RCC other rare tumors TCC Hemangioma Leiomyoma OncocytomaHistopathologic features associated low T2 signal intensity Smooth muscle component Papillary structure High N/C ratio Hemorrhage Use of the MRI finding for the differential diagnosisSummary and discussion UR004-EB-X Imaging of Renal Angiomyolipoma: It's Not All About Fat All Day Location: GU/UR Community, Learning Center Awards Certificate of Merit Participants Haley R. Clark, MD, Dallas, TX (Presenter) Nothing to Disclose Payal Kapur, MD, Dallas, TX (Abstract Co-Author) Nothing to Disclose Ivan Pedrosa, MD, Dallas, TX (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1. Technical considerations for US, CT, and MR when imaging renal angiomyolipoma (AML). 2. Correlation of histopatholgic subtypes of renal AML with imaging characteristics. 3. Diagnostic pitfalls, including other renal malignancies which have overlapping MRI imaging characteristics as renal AML. TABLE OF CONTENTS/OUTLINE Technical aspects: Ultrasound CT Non-contrast Contrast-enhanced Dual source MRI: 2D T1 IP/OP 3D T1 Dixon Spectral fat suppression T2-weighted Contrast enhanced Diffusion-weighted Radiologic-Pathologic Correlation: WHO Classification of AML Classic AML AML without visible fat AML with spontaneous hemorrhage AML status post embolization Enlarging AML Giant exophytic AML Multiple AMLs in Tuberous Sclerosis AML in lymphangioleiomyomatosis AML with epithelial cyst (AMLEC) Epithelioid AML, pre and post treatment with sirolimus Sclerosed epithelioid AML Diagnostic pitfalls: Fat containing clear cell renal cell carcinoma vs AML with minimal but visible fat Papillary renal cell carcinoma vs AML without visible fat Retroperitoneal liposarcoma vs exophytic AML Pseudo-angiomyolipoma after radiofrequency ablation Sclerosing extramedullary hematopoietic tumors UR005-EB-X Retroperitoneal Tumor and Retroperitoneal Fibrosis: CT and MR Characteristics and Pathological Correlative Analysis All Day Location: GU/UR Community, Learning Center Participants Keisuke Miyoshi, Ube, Japan (Presenter) Nothing to Disclose Naofumi Matsunaga, MD, PhD, Ube, Japan (Abstract Co-Author) Nothing to Disclose Masahiro Tanabe, MD, Ube, Japan (Abstract Co-Author) Nothing to Disclose Takaaki Ueda, Ube, Japan (Abstract Co-Author) Nothing to Disclose Sei Nakao, Ube, Japan (Abstract Co-Author) Nothing to Disclose Yuko Harada, MD, Ube, Japan (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The purpose of this exhibit is: 1. To review CT and MR imaging findings of various spectrum of retroperitoneal masses. 2. To highlight key differential diagnostic points of imaging findings with pathologic correlation. TABLE OF CONTENTS/OUTLINE 1. Introduction - anatomy, cellular origin, malignant potential. 2. Clinical features - epidemiology, clinical symptoms and prognosis. 3. Characteristic findings - neoplastic masses (mesodermal origin, neurogenic origin, germ cell origin, lymphoid or hematologic origin) and nonneoplastic masses. 4. Key points for the correlation of radiologic and pathologic features. UR007-EB-X Ultrasonographic Appearance of Testicular Tumors: Ultrasonographic-Pathologic Correlation All Day Location: GU/UR Community, Learning Center FDA Discussions may include off-label uses. Participants Yong-Soo Kim, MD, PhD, Guri City, Korea, Republic Of (Presenter) Nothing to Disclose Sangjoon Lee, MD, Guri, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Sanghyeok Lim, MD, Gyeonggi-do, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1. To understand the ultrasonographic features of testicular tumors on the pathologic basis. 2. To know ultrasonographic findings of characteristic testicular tumors. TABLE OF CONTENTS/OUTLINE I. Germ cell neoplasm1. Seminoma2. Embryonal carcinoma3. Yolk sac tumor (adult, childhood type)4. Teratoma (Mature, Immature, With an overtly malignant component)5. ChoriocarcinomaII. Mixed germ cell tumorsIII. Sex cord-stromal neoplasms1. Leydig cell tumor2. Sertoli cell tumorIV. Mixed germ cell-sex cord-stromal neoplasmsV. Tumors of "passenger" and non-Leydig, interstitial cells1. Lymphoma2. Leukemic infiltrates3. Miscellaneous others, including epidermoid cysts, mesenchymal tumors, and metastatic tumors UR008-EB-X Cystogram "A Forgotten Study" All Day Location: GU/UR Community, Learning Center Awards RSNA Country Presents Travel Award Certificate of Merit Participants Julian Ramirez Arango, MD, Mexico City, Mexico (Presenter) Nothing to Disclose Mary C. Herrera-Zarza, MD, Mexico City, Mexico (Abstract Co-Author) Nothing to Disclose Luis A. Ruiz Elizondo, MD, Mexico City, Mexico (Abstract Co-Author) Nothing to Disclose Alin Marissa Becerril Ayala, MD, Mexico City, Mexico (Abstract Co-Author) Nothing to Disclose Jose L. Criales, MD, Huixquilucan, Mexico (Abstract Co-Author) Nothing to Disclose Kenji Kimura, MD, Mexico City, Mexico (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Even though there are great advances in urologyc imaging, the cystogram continues to be the imaging method of choice for some pathologies, and its the radiologist duty to make a correct diagnostic impression through this method.Cystogram is highly efective, has easy access, low cost and is minimally invasiveThe correct interpretation of the cystogram by the radiologist decrease false positive results and increase our diagnostic ability. TABLE OF CONTENTS/OUTLINE Table of contents /OutlineIntroductionCorrect cystogram techniquesNormal anatomy and its anatomical variantsUses and utilities of cystogramCommon pathologies diagnosed by this method UR100-ED-X Imaging of Gerota's Fascia All Day Location: GU/UR Community, Learning Center Participants Jun Isogai, MD, Asahi, Japan (Presenter) Nothing to Disclose Naoki Harata, Asahi, Japan (Abstract Co-Author) Nothing to Disclose Katsuya Yoshida, MD, Asahi, Japan (Abstract Co-Author) Nothing to Disclose Jun Kaneko, Hasuda, Japan (Abstract Co-Author) Nothing to Disclose Tassei Nakagawa, MD, PhD, Asahi, Japan (Abstract Co-Author) Nothing to Disclose TEACHING POINTS To understand interfascial spread of a wide variety of disorders in retroperitoneal Gerota's fascia. TABLE OF CONTENTS/OUTLINE Anatomy of retroperitoneal interfascial planes. CT or MRI findings of various interfascial disorders in Gerota's fascia. Pneumoretroperitoneum Pancreatic fluid / Bile / Urine collection Retroperitoneal hematoma Retroperitoneal abscess Tumor and inflammatory extension of renal, pancreatic and colon diseases Malignant lymphoma Retroperitoneal dissemination of thoracic tumor Primary retroperitoneal tumor UR101-ED-X Genitourinary Applications of Spectral CT All Day Location: GU/UR Community, Learning Center Participants Nicholas L. Fulton, MD, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Luis A. Landeras, MD, Cleveland, OH (Abstract Co-Author) Institutional Grant support, Koninklijke Philips NV Jason DiPoce, MD, Jerusalem, Israel (Abstract Co-Author) Nothing to Disclose Jacob Sosna, MD, Jerusalem, Israel (Abstract Co-Author) Consultant, ActiViews Ltd Research Grant, Koninklijke Philips NV Prabhakar Rajiah, MD, FRCR, Cleveland, OH (Presenter) Institutional Research Grant, Koninklijke Philips NV TEACHING POINTS Dual energy/spectral CT scanners provide material characterization capabilities which improve diagnostic accuracy, without increasing radiation. There are several techniques of dual energy CT, including a dual layer technology Spectral detector CT enables retrospective generation of spectral images TABLE OF CONTENTS/OUTLINE -Spectral CT- Physics-Techniques of spectral CT-Phantom studies-Advantages and disadvantages of various implementationsGenitourinary applications of spectral CT with illustrations Stone characterization- Uric acid vs non uric acid Renal mass characterization- virtual non contrast, iodine person, effective atomic number based images Adrenal mass characterization Improved lesion detection and characterization Tumor perfusion and response to therapy Urinary stone in iodinated solution Virtual non contrast in multiphasic studies- Radiation dose savings Urothelial tumor detection Artifact reduction Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Prabhakar Rajiah, MD, FRCR - 2014 Honored Educator Jacob Sosna, MD - 2012 Honored Educator Jason DiPoce, MD - 2013 Honored Educator UR102-ED-X Eponyms in Urogenital Radiology: Old Names, But Still Golden Nuggets All Day Location: GU/UR Community, Learning Center Participants Daniel M. Figueira, Niteroi, Brazil (Presenter) Nothing to Disclose Emanuela T. Freitas, MD, Niteroi, Brazil (Abstract Co-Author) Nothing to Disclose Felipe B. Afonso, MD, Niteroi, Brazil (Abstract Co-Author) Nothing to Disclose Joao A. Vianna, Niteroi, Brazil (Abstract Co-Author) Nothing to Disclose Daniel G. Neves, MD, Niteroi, Brazil (Abstract Co-Author) Nothing to Disclose Leonardo K. Bittencourt, MD, PhD, Rio De Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose TEACHING POINTS - Eponyms were historically used in medicine for honorary and educational purposes, but their importance has been questioned in the present, in favor of a more anatomical description of findings and diseases. However, a number of eponyms and 'auntminnies' still constitute useful educational tools and mnemonics in radiology practice.- The urogenital system is rich in eponyms and 'auntminnies', which translate a variable sort of anatomical structures and conditions, such as: Gerota´s fascia, Zuckerckandl´s fascia, Denonvillier´s fascia, Bertin´s column, Malpighi´s pyramid, Weigert-Meyer rule, Bricker surgery, Peyronie disease, etc.- The objective of this work is to review the most well-known and relevant eponyms in urogenital radiology, along with a didatic and illustrative approach, based on mnemonics and pattern recognition. TABLE OF CONTENTS/OUTLINE 1 - What is an eponym? What is an 'auntminnie'?2 - The use of eponyms throughout medical history. Is there any role for them today?3 - Eponyms and 'auntminnies' in the urogenital system: an illustrative and mnemonical approach- Anatomy: Gerota´s fascia, Zuckerckandl´s fascia, Denonvillier´s fascia, Bertin´s column, Malpighi´s pyramid, Retzius´s space.- Malformations: Weigert - Meyer rule.- Diseases: Conn´s disease, Wilms tumor, Peyronie disease.- Syndrome: Zinner´s syndrome, Bourneville syndrome.- Surgery: Bricker Surgery. UR103-ED-X PIRADS v2: A Case-based Review of the New Categorization with Emphasis on Its Impact on MR Guided Biopsy, Its Limitations and Pitfalls All Day Location: GU/UR Community, Learning Center Participants Varaha Tammisetti, MD, Houston, TX (Presenter) Nothing to Disclose Bijan Bijan, MD, Sacramento, CA (Abstract Co-Author) Nothing to Disclose Sadhna Verma, MD, Cincinnati, OH (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1. Review the new version of PIRADS with emphasis on changes from prior version and comparsion to similar other criteria. 2. Illustrate case based examples of each of the PIRADS categories and pitfalls in categorization and interpretation. This will be in a Prostate MR Rad-Path correlation format. 3. Limitations of current PIRADS version. 4. Illustration and review of literature on utilization of PIRADS in each of the clinical settings with emphasis on its role in MR guided (direct or indirect by fusion) targeted biopsy. TABLE OF CONTENTS/OUTLINE 1. Clinical and technical considerations including 'clinically significant cancer', clinical scenarios and technical parameters2. Review of relevant normal anatomy with illustration of each of the lexicon of normal and pathological terms.3. Overview of PIRADS v.2 with review of changes and comparison to other criteria.4. Case based examples of each of PIRADS categories in Peripheral and Transitional zones including benign findings such as prostatitis, asymmetric focal atrophy, periprostatic vessel, calcification, normal central zone. Presented in a quiz format with Rad-Path correlation.5. Limitations of current PIRADS and also pitfalls. Current utility/status of DCE.6. Case based examples on utilization of PIRADS in each of the clinical settings with emphasis on its role in MR guided targeted biopsy. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Sadhna Verma, MD - 2013 Honored Educator UR104-ED-X Prostate Cancer in the Transition Zone and the Anterior Fibromuscular Stroma: Clues to the Diagnosis in Multiparametric MRI with Emphasis on Intraprostatic Patterns of Spread and the Relative Frequency of the Locations All Day Location: GU/UR Community, Learning Center Awards Magna Cum Laude Participants Hiroshi Shinmoto, MD, Tokorozawa, Japan (Presenter) Nothing to Disclose Shigeyoshi Soga, MD, Tokorozawa, Japan (Abstract Co-Author) Nothing to Disclose Chiharu Tamura, Tokorozawa, Japan (Abstract Co-Author) Nothing to Disclose Kentaro Yamada, MD, Tokorozawa, Japan (Abstract Co-Author) Nothing to Disclose Teppei Okamura, MD, Tokyo, Japan (Abstract Co-Author) Nothing to Disclose Hiroko Tomita, Tokorozawa, Japan (Abstract Co-Author) Nothing to Disclose Tatsumi Kaji, MD, Tokorozawa, Japan (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Although the diagnostic performance of multiparametric MRI in peripheral zone (PZ) prostate cancer has been improved up to approximately 80 to 90% sensitivity and specificity, the diagnosis of transition zone (TZ) prostate cancer is still challenging. Thus, the purpose of this exhibit is to present the patterns of intraprostatic spread and the relative frequency of the locations of prostate cancer in the TZ and the anterior fibromuscular stroma (AFMS) based on 155 prostatectomy specimens with multiparametric MRI data, and to provide diagnostic clues as to interpreting multiparametric MRI in TZ and AFMS prostate cancer. TABLE OF CONTENTS/OUTLINE Anatomy of the TZ and AFMS What is anterior prostate cancer (APC)? Clinical importance of APC Morphological features of TZ and AFMS prostate cancer The relative frequency of the locations of TZ and AFMS prostate cancer Atypical locations of TZ prostate cancer The non-cancerous AFMS and BPH mimicking TZ prostate cancer UR106-ED-X Multimodalityimaging Features of Sarcomas of the Abdomen and Pelvis with Radiologic-pathologic Correlation All Day Location: GU/UR Community, Learning Center Participants Kara D. Gaetke-Udager, MD, Ann Arbor, MI (Presenter) Nothing to Disclose Aaron M. Udager, MD, PhD, Ann Arbor, MI (Abstract Co-Author) Nothing to Disclose Katherine E. Maturen, MD, Ann Arbor, MI (Abstract Co-Author) Consultant, GlaxoSmithKline plc; Medical Advisory Board, GlaxoSmithKline plc Corrie M. Yablon, MD, Ann Arbor, MI (Abstract Co-Author) Nothing to Disclose TEACHING POINTS After review of this exhibit, the viewer will be able to: List the types of sarcoma that can occur in the abdomen and pelvis Describe unique and shared imaging features of abdominal and pelvic sarcomas Identify imaging characteristics that aid biopsy planning Explain how the pathologic appearance correlates with the imaging findings Understand the surgical considerations for abdominal and pelvic sarcomas TABLE OF CONTENTS/OUTLINE Background Embryologic origin of soft tissue tumors Nomenclature of soft tissue tumors Surgical considerations Sarcomas of the abdomen and pelvis For each tumor below, we will discuss: Demographics Clinical presentation Pathologic features Multimodality imaging features Treatment options Types of sarcomas Well-differentiated liposarcoma De-differentiated liposarcoma Pleomorphic liposarcoma Myxoid liposarcoma Undifferentiated high-grade pleomorphic sarcoma Leiomyosarcoma Extraskeletal osteosarcoma Chondrosarcoma Ewing sarcoma Synovial sarcoma Alveolar soft part sarcoma Conclusions Challenge of overlapping imaging features Pathologic features can be used to understand imaging and direct clinical management Imaging characteristics guide biopsy decisions Importance of surgical considerations in radiology report Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Katherine E. Maturen, MD - 2014 Honored Educator UR107-ED-X Sonographic Assessment of Tumour Margins at Partial Nephrectomy (PN) - Intraoperative and Ex-Vivo. Review of Technique All Day Location: GU/UR Community, Learning Center Participants Naveed Altaf, MBBS, MRCS, Middlesbrough, United Kingdom (Presenter) Nothing to Disclose Geoffrey P. Naisby, MBBS, Yarm, United Kingdom (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1. To review the technique of ultrasound control of resection margins in Patients undergoing PN - Both Intraoperative and ex-vivo. 2. To discuss the efficacy of this approach and its potential to demonstrate additional findings not seen on the preoperative imaging which can modify surgery. TABLE OF CONTENTS/OUTLINE BackgroundIntraoperative ultrasound is a well-established technique routinely used to facilitate surgical resection during partial nephrectomy.Technique: Ultrasound was performed using a 12MHz probe after mobilisation of kidney and for laparoscopic cases, a laparoscopic USS probe was used. Tumour size and depth was mapped and area of excision marked with diathermy.Following resection, the sample was evaluated in 3 dimensions, recording the closest margin between tumour and outer parenchymal edge. Margins were considered free of tumour when a rim of healthy renal parenchyma was seen completely without a gap or tumour was contained within the pseudocapsule.Discussion:In line with a previous reports of surgical specimen (ex-vivo) ultrasound in assessing margin status for PN, we confirm the safety and efficacy of this approach in our single institution series. Patient characteristics, operative indications, tumour and margin size were comparable to previous series. UR109-ED-X Multimodality Evaluation of Renal Transplant Vascular Complications All Day Location: GU/UR Community, Learning Center FDA Discussions may include off-label uses. Participants Behrad Golshani, MD, Sacramento, CA (Presenter) Nothing to Disclose Wonsuk Kim, MD, Sacramento, CA (Abstract Co-Author) Nothing to Disclose Danny Cheng, MD, Sacramento, CA (Abstract Co-Author) Nothing to Disclose Catherine T. Vu, MD, Denver, CO (Abstract Co-Author) Nothing to Disclose Ghaneh Fananapazir, MD, Sacramento, CA (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The purpose of this exhibit is: To review common and uncommon renal transplant vascular complications across multiple imaging modalities including ultrasound, MRI, CT, and conventional angiography. To discuss pearls and pitfalls related to uncommon renal transplant vascular complications. TABLE OF CONTENTS/OUTLINE Background Renal transplant vascular anatomy Incidence of common and uncommon rental transplant vascular complications Representative ultrasound, CT, MRA and/or digital subtraction angiography images of the following entities will be presented: Tandem renal artery stenosis Renal vein stenosis Pseudo-renal artery stenosis External iliac artery stenosis External iliac vein stenosis Renal artery thrombosis Renal vein thrombosis Extrarenal pseudoaneurysm Intrarenal pseudoaneurysm Arteriovenous fistula Subcapsular hematoma UR110-ED-X Staging of Prostate Cancer: Tips Not to Miss an Extracapsular Extension Reported Posteriorly by the Pathologist All Day Location: GU/UR Community, Learning Center Participants Marta Drake Perez, MD, Santander, Spain (Presenter) Nothing to Disclose Pedro Lastra Garcia-Baron, MD, Santander, Spain (Abstract Co-Author) Nothing to Disclose Alejandro Fernandez Florez, MD, Santander, Spain (Abstract Co-Author) Nothing to Disclose Ainara Azueta Etxebarria, Santander, Spain (Abstract Co-Author) Nothing to Disclose Elena Yllera Contreras, MD, Santander, Spain (Abstract Co-Author) Nothing to Disclose Elena Lopez Uzquiza, Santander, Spain (Abstract Co-Author) Nothing to Disclose Gerardo Lopez Rasines, MD, Santander, Spain (Abstract Co-Author) Nothing to Disclose TEACHING POINTS To summarize the MRI signs of prostate cancer with extracapsular extension, with the histopathologic outcomes as the reference standard. To emphasize the correlation between the imaging findings and the histopathological results. To review the cases where the radiologic pathology correlation failed, giving a second look to the MRI and trying to figure out where the typical mistakes are. TABLE OF CONTENTS/OUTLINE - Importance of an accurate preoperative staging in prostate cancer.- MRI imaging protocol for prostate cancer in 3T magnet without endorectal coil.- MRI criteria to determine extracapsular extension, using radical prostatectomy histopathology as the reference standard. Irregular bulge in the prostatic capsule Broad capsular tumour contact (>12mm) Obliteration of the rectoprostatic angle Obliteration of the vesiculoprostatic angle Asymmetry of the neurovascular bundle Evidence of direct tumor extension- Common mistakes from our daily practice UR111-ED-X Retrograde Urethrogram: Anatomy, Pathology, and Repair All Day Location: GU/UR Community, Learning Center Participants Franco Verde, MD, Baltimore, MD (Presenter) Nothing to Disclose Lynda Mettee, Baltimore, MD (Abstract Co-Author) Nothing to Disclose Edward J. Wright, MD, Baltimore, MD (Abstract Co-Author) Nothing to Disclose Martin Auster, MD, Baltimore, MD (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Knowing anatomy of male urethra is critical for operative repair Know the appearance of stricturesKnow the surgical approach to urethral disease and post-operative appearance on retrograde urethrograms TABLE OF CONTENTS/OUTLINE A. Technique a. Patient prep b. Equipment used c. Positioning and fluoro tipsB. Normal anatomyC. Pathology a. Stricture b. TraumaD. Surgical approachE. Post-operative appearance a. Normal postop retrograde ureterogram b. Leakage c. Followup d. Recurrent stricture UR112-ED-X Magnetic Resonance Imaging Evaluation of Urothelial Cell Carcinoma: Staging and Treatment Planning with Histopathological Correlation All Day Location: GU/UR Community, Learning Center Participants Peter A. Harri, MD, Atlanta, GA (Presenter) Nothing to Disclose Courtney A. Coursey Moreno, MD, Suwanee, GA (Abstract Co-Author) Nothing to Disclose Juan C. Camacho, MD, Atlanta, GA (Abstract Co-Author) Nothing to Disclose Pardeep K. Mittal, MD, Atlanta, GA (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The purpose of this exhibit is: Review basic principles of urothelial cell carcinoma (UCC). Describe the use of magnetic resonance imaging (MRI) to differentiate UCC in the urinary system from other malignant and benign lesions. Demonstrate the use of MRI to adequately stage UCC within the urinary tract and locate distant disease. Discuss the impact of MRI for accurate pre-surgical evaluation and staging on management and treatment options. TABLE OF CONTENTS/OUTLINE Review common presentations of UCC, including key characteristics that define malignancy with histopathological correlations. Review of UCC staging with MRI imaging findings. Discuss the impact of MRI for accurate pre-surgical evaluation and staging on management and treatment options. Important concepts are illustrated with schematic diagrams. Emphasis is placed on practical approaches and image pattern recognition. Conclusions: MRI plays a key role for noninvasive diagnosis of UCC and staging of the tumor, especially for smaller lesions where surgical management can differ depending on the extant of invasion. Adequate knowledge of UCC imaging features on MRI is crucial for appropriate and prompt patient intervention. UR113-ED-X Multiple Renal Masses: A Review of Causes with Emphasis on Differential Diagnosis All Day Location: GU/UR Community, Learning Center Participants Mariano Volpacchio, MD, Buenos Aires, Argentina (Presenter) Nothing to Disclose Christine O. Menias, MD, Scottsdale, AZ (Abstract Co-Author) Nothing to Disclose Mario G. Santamarina, MD, Valparaiso, Chile (Abstract Co-Author) Nothing to Disclose Joaquina Paz Lopez Moras, MD, Buenos Aires, Argentina (Abstract Co-Author) Nothing to Disclose Veronica Rubio, Buenos Aires, Argentina (Abstract Co-Author) Nothing to Disclose Antonio Luna, MD, Jaen, Spain (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The goals of this presentation are: To review causes of multiple renal masses To discuss imaging findings of the different entities To provide imaging-based clues useful to guide to the correct diagnosis TABLE OF CONTENTS/OUTLINE - Introduction- Etiology of multiple renal masses Hereditary Inflammatory and infectious Immunologic Vascular Neoplastic benign, primary malignant, secondary malignant- Imaging findings specific to the kidney and associated findings of each entity - Differential diagnosis cluesSummaryThe presence of multiple renal masses may be an isolated or dominant imaging finding as well as an additional abnormality in the setting of multiorgan involvement.An imaging-based, multimodality approach may be crucial in the differential diagnosis process as well as in patient management.Awareness of the imaging appearance of the various causes in different imaging modalities and integration with other findings may result in a correct diagnosis in most cases as well as in assisting in proper patient work-up and management. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Christine O. Menias, MD - 2013 Honored Educator Christine O. Menias, MD - 2014 Honored Educator Christine O. Menias, MD - 2015 Honored Educator UR115-ED-X Pharmakinetic, Gadolinium and Technical Parameters Affecting Bolus Geometry during Contrast Enhanced Renal MR Angiography: An Overview All Day Location: GU/UR Community, Learning Center Participants Charbel Saade, PhD, Beirut, Lebanon (Presenter) Nothing to Disclose Ghina Al Fout, Beirut, Lebanon (Abstract Co-Author) Nothing to Disclose Batoul Dorkmark, Beirut, Lebanon (Abstract Co-Author) Nothing to Disclose Fadi M. El-Merhi, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Hussain M. Almohiy, PhD, Abha, Saudi Arabia (Abstract Co-Author) Nothing to Disclose Rayan Bou Fakhredin, Beirut, Lebanon (Abstract Co-Author) Nothing to Disclose Bassam El-Achkar, MD, Beirut, Lebanon (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Optimal arterial hyperintensity is essential during MRA Matching scanning parameters such as TR, TE, Flip angle and parallel imaging with with vessel dynamics significantly improves vessel hyperintensity This leads to increased arterial hyperintensity and reduced venous hypointensity This can also lead to a reduced volume of Gadolinium based contrast agents. Reduced gadolinium-based contrast volume can reduce tissue, technique and motion related artefacts This can also lead to reduced specific absorption rate TABLE OF CONTENTS/OUTLINE A. Renal Vascular Anatomy and flow dynamics B. Scanning parameters C. Contrast media parametersD. Linear vs. Macrocyclic GadoliniumE. Parameters affecting bolus geomteryF. Transverse and Longitudinal relaxation ratio and its effect on signal intensityH. Comparison between 1.5T and 3.0T scanning parameters UR116-ED-X What's Going On With My Kidneys? When Diagnosis is Challenging: Multimodality Imaging in Atypical Nephritis All Day Location: GU/UR Community, Learning Center Awards Certificate of Merit Participants Virginia Gomez, San Sebastian, Spain (Presenter) Nothing to Disclose Juan Vega Eraso, San Sebastian, Spain (Abstract Co-Author) Nothing to Disclose Maria Carmen Biurrun Mancisidor, San Sebastian, Spain (Abstract Co-Author) Nothing to Disclose Gorka Arenaza Choperena, San Sebastian, Spain (Abstract Co-Author) Nothing to Disclose Gonzalo Vega-Hazas, San Sebastian, Spain (Abstract Co-Author) Nothing to Disclose Diana Garcia Asensio, Donostia, Spain (Abstract Co-Author) Nothing to Disclose TEACHING POINTS To demonstrate the spectrum of imaging findings of upper urinary tract infections, with emphasis on certain rare entities where little literature has been written about.To discuss the role of the different imaging techniques.To summarize the different risk factors for developing UTI, describing some anatomical conditions mostly involved in recurrent nephritis. TABLE OF CONTENTS/OUTLINE While majority of UTIs are uncomplicated and can be diagnosed and treated based on clinical and laboratory data alone, imaging is required in some clinical scenarios.Different imaging modalities include US, IVU, CT, MRI and we have to be aware of their potential benefits and limitations.We will discuss some diagnostic classic signs and extrarrenal findings in typical scenarios. Thus, we will emphasize and illustrate with cases in which there is no or little literature written about. Such conditions include renal tumors with superimposed infection, atypical infection in kidney´s grafts, anaerobic germ infection associated to urinary stone, atypical form of xantogranulomatous poyelonephritis, subcapsular abscesses...Finally, we will summarize the predisposing factors for developing UTI and recurrent infections with different cases: anomalies on the collecting system and ureter, and anomalies on the position and rotation of the kidney. UR118-ED-X The Added Value of Functional and Molecular Imaging of the Scrotum All Day Location: GU/UR Community, Learning Center Awards Cum Laude Participants Sandra Baleato Gonzalez, MD, PhD, Santiago, Spain (Presenter) Nothing to Disclose Roberto Garcia Figueiras, MD, Santiago de Compostela, Spain (Abstract Co-Author) Nothing to Disclose Joan C. Vilanova, MD, PhD, Girona, Spain (Abstract Co-Author) Nothing to Disclose Gabriel C. Fernandez-Perez, PhD, MD, Avila, Spain (Abstract Co-Author) Nothing to Disclose Nuria Escudero-Garcia, Santiago de Compostela, Spain (Abstract Co-Author) Nothing to Disclose Anxo Martinez De Alegria, MD, Santiago de Compostela, Spain (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The evaluation of scrotum has traditionally been made based on morphologic imaging. Recent developments in imaging techniques have improved the ability to evaluate scrotal entities. Beside this, multiparametric magnetic resonance imaging (MRI) may combine the information from different anatomical, functional and molecular imaging techniques, thus allowing an improved understanding of scrotal pathologies. The aim of this exhibit is: To emphasis the added information of functional and molecular imaging for evaluating the scrotum. To learn about the imaging findings of the scrotum based on different imaging techniques:dynamic contrast-enhanced MRI (DCE-MRI), dynamic contrast-enhanced ultrasound (DCE-US), diffusion-weighted MRI (DWI-MRI), MR spectroscopy imaging (MRSI),CT, PET, and US-elastography. TABLE OF CONTENTS/OUTLINE 1.Clinical setting:1.1. Cryptorchidism1.2. Acute scrotum1.3. Non acute scrotum 1.3.1. Extratesticular lesion 1.3.2. Intratesticular lesions 2. Ultrasound utilities2.1. DCE-ultrasound: evaluate acute scrotum.2.2. Elastography: characterization of lesions 3. MRI utilities3.1. DCE-MRI: characterization of leisons3.2. DWI-W-BODY: staging and monitoring3.3 Spectroscopy: evaluate spermatogenesis UR119-ED-X The Nuts and Bolts of the Acute Scrotum: A Multiple Choice Question Case-Based Review of Acute Scrotal Pathology All Day Location: GU/UR Community, Learning Center Awards Certificate of Merit Participants Christina Ma, MD, Los Angeles, CA (Presenter) Nothing to Disclose Anokh Pahwa, MD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Michael J. Nguyen, MD, Santa Barbara, CA (Abstract Co-Author) Nothing to Disclose Michael L. Douek, MD, MBA, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Steven S. Raman, MD, Santa Monica, CA (Abstract Co-Author) Nothing to Disclose Maitraya K. Patel, MD, Sylmar, CA (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Acute scrotal abnormalities commonly present to the Emergency Department; several conditions require emergent surgical exploration by the urologist. With the help of the clinical history and physical examination, the radiologist can offer a specific diagnosis and guide decision-making particularly regarding surgical intervention. This multiple choice question case-based review will assist the radiologist at all levels of training better identify and diagnose these abnormalities and make appropriate recommendations to the referring clinician. TABLE OF CONTENTS/OUTLINE Comprehensive multimodality imaging review of acute scrotal pathology in a multiple choice question format with pertinent discussion of clinical presentation, management, and differential diagnosis. Cases will include a spectrum of acute scrotal pathology: 1. Ischemia (testicular torsion, torsion of the appendix testis, testicular infarction); 2. Trauma (testicular rupture, intratesticular hematoma, testicular contusion, hematocele); 3. Infection (acute epididymitis including tuberculous epididymitis, abscess, Fournier's gangrene); 4. Testicular and extratesticular neoplasms (germ cell neoplasm, burned out germ cell tumor, lymphoma, metastasis, liposarcoma of the spermatic cord); 5. Enlarged scrotum (scrotal wall edema, hydrocele, spermatic cord hydrocele). UR121-ED-X Evaluation and Follow-up of the Complications of Urinary Tract Surgical Procedures: CT-urographic Patterns All Day Location: GU/UR Community, Learning Center Participants Gianpiero Cardone, MD, Milano, Italy (Presenter) Nothing to Disclose Maurizio Papa, MD, Milan, Italy (Abstract Co-Author) Nothing to Disclose Paola Mangili, PhD, Milano, Italy (Abstract Co-Author) Nothing to Disclose Giuseppe Balconi, Ornago, Italy (Abstract Co-Author) Nothing to Disclose TEACHING POINTS To review the most frequent urinary tract postoperative complications.To illustrate CT-Urographic patterns of urinary tract postoperative complications.To describe the usefulness of CT-Urography in the diagnosis and follow-up of urinary tract postoperative complications. TABLE OF CONTENTS/OUTLINE 1) Most frequent urinary tract postoperative complications: Urinary leaks Uretero-vesical anastomosis dehiscence Ureterocutaneous fistulas Bleeding / hematomas Peritoneal and retroperitoneal fluid collections Urinary tract stenosis 2) Best CT techniques in the evaluation of urinary tract postoperative complications3) Conventional and urographic CT patterns of urinary tract postoperative complications4) CT imaging follow-up of urinary tract postoperative complications CONCLUSIONS1) Ureteral lesions, retroperitoneal hematomas and/or bleeding and fluid collections are the most frequent urinary tract postoperative complications2) Urographic images combined with conventional CT imaging allow an accurate diagnosis and follow-up of urinary tract postoperative complications3) Source axial images and MPR of the urographic acquisition show a better identification of urinary tract lesions4) 3D MIP reconstructions are useful in summarising urographic axial images UR122-ED-X Infiltrative Renal Lesions in Adults - Spectrum of Disease All Day Location: GU/UR Community, Learning Center Awards Certificate of Merit Identified for RadioGraphics Participants Lori M. Gettle, MD, MBA, Hummelstown, PA (Presenter) Nothing to Disclose Uzma A. Rana, MD, MPH, Baltimore, MD (Abstract Co-Author) Nothing to Disclose Nabeel I. Sarwani, MD, Hummelstown, PA (Abstract Co-Author) Nothing to Disclose Cary L. Siegel, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Brent J. Wagner, MD, Reading, PA (Abstract Co-Author) Nothing to Disclose Perry J. Pickhardt, MD, Madison, WI (Abstract Co-Author) Co-founder, VirtuoCTC, LLC; Stockholder, Cellectar Biosciences, Inc; Research Consultant, Bracco Group; Research Consultant, KIT ; Research Grant, Koninklijke Philips NV Thomas M. Dykes, MD, Hershey, PA (Abstract Co-Author) Researcher, Bayer AG TEACHING POINTS Review the differential diagnosis of infiltrative renal lesions in adults. Review imaging modalities and protocols used to evaluate infiltrative renal lesions. Demonstrate the imaging features of benign and malignant infiltrative renal lesions. TABLE OF CONTENTS/OUTLINE Differential diagnosis of benign and malignant infiltrative renal lesions in adults. Imaging modalities and protocols to evaluate infiltrative renal lesions. Ultrasound CT MRI PET-CT Imaging features of infiltrative renal lesions. Benign Pyelonephritis Angiomyolipoma Infarct Contusion Malignant Urothelial carcinoma Lymphoma Less common renal carcinomas Metastases Renal sarcoma Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Perry J. Pickhardt, MD - 2014 Honored Educator UR123-ED-X Imaging Features of Paratesticular Masses All Day Location: GU/UR Community, Learning Center Participants Mustafa Secil, MD, Izmir, Turkey (Presenter) Nothing to Disclose Michele Bertolotto, MD, Trieste, Italy (Abstract Co-Author) Nothing to Disclose Laurence M. Rocher, MD, Kremlin Bicetre, France (Abstract Co-Author) Nothing to Disclose Gokhan Pekindil, MD, Manisa, Turkey (Abstract Co-Author) Nothing to Disclose Jonathan Richenberg, MRCP, FRCR, Brighton, United Kingdom (Abstract Co-Author) Nothing to Disclose Lorenzo E. Derchi, MD, Genova, Italy (Abstract Co-Author) Nothing to Disclose Parvati Ramchandani, MD, Merion Station, PA (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1. To demonstrate the imaging findings of paratesticular masses 2. To illustrate the radiological features in correlation with the pathological findings TABLE OF CONTENTS/OUTLINE Paratesticular masses are relatively rare lesions which include the non-neoplastic lesions, and benign or malignant neoplasms. Nonneoplastic lesions of paratesticular area include the tunical cyst, epididymal cyst, spermatocele, fibrous pseudotumor, spermatic cord cyst, lipomatosis, and polyorchidism. Neoplastic lesions may either be benign or malignant. Benign neoplasms are lipoma, adenomatoid tumor, leiomyoma, angioleiomyoma, angiomyofibroblastoma-like tumor, hemangioma and papillary cystadenoma. Malignant neoplasms are mostly mesenchymal in origin, namely the rhabdomyosarcoma, liposarcoma, leiomyosarcoma, and undifferentiated pleomorphic sarcoma (malignant fibrous histiocytoma). Malignant mesothelioma, metastases due to various primaries, lymphoma/leukemia and plasmocytoma. Imaging findings of these lesions are going to be be presented. UR125-ED-X MRI of the Scrotum : A Complimentary Tool or A Necessary Diagnostic Step? All Day Location: GU/UR Community, Learning Center Participants Ahmed S. Soliman, MBBS, Doha, Qatar (Presenter) Nothing to Disclose Maneesh Khanna, MBBS, Doha, Qatar (Abstract Co-Author) Nothing to Disclose Sushila Ladumor, MBBS, MD, Doha, Qatar (Abstract Co-Author) Nothing to Disclose Ahmed M. Sherif, MBBCh, FRCR, Doha, Qatar (Abstract Co-Author) Nothing to Disclose TEACHING POINTS To understand the: Scrotal anatomy on MRI and its imaging protocol.A review of MRI appearnce of a wide spectrum of scrotal disease . To understand the importance of MRI in problem solving situations such as: -Differentiating stromal from non stromal tumor. -Assessing tunica or epididymal involvement by the neoplastic lesion and evaluating retroperitoneum at the same time Understand the difference of imaging caracteristics between different types of testicular neoplasm in dynamic post contrast studies and diffusion WI. TABLE OF CONTENTS/OUTLINE A. MRI anatomy of the scrotum . B.Technique of MRI of the scrotum : sequences and aim of each. C. Scrotal pathologies : 1. Benign extratesticular lesions : Hematoma, Infection :TB epidydmoorchitis, Adenomatoid tumor, Dilatation of cowper gland etc. 2 .Malignant extratesticular: Sclerosing Liposarcoma of epidydmis . 3. Benign testicular -Chronic infarction,Testicular abscess,Testicular contusion, tubular ectasia of rete testis, Stromal tumours such as Sertoli cell, Leydig cell and granulosa cell tumour . Microlithiasis of the testis. 4. Malignant testicular : Seminomatous and non seminomatous germ cell tumour, lymphoma. D. Role of enhancement characterictics (DCE curves) and DWI in differentiating testicular neoplasms- review of data of a series of more than 10 intratesticular neoplasms . UR126-ED-X Ductal Adenocarcinoma of the Prostate: Imaging and Histopathological Features of this Unusual Suspect All Day Location: GU/UR Community, Learning Center FDA Discussions may include off-label uses. Participants Adam W. Jaster, MD, Dallas, TX (Presenter) Nothing to Disclose Daniel N. Costa, MD, Dallas, TX (Abstract Co-Author) Nothing to Disclose Ronaldo H. Baroni, MD, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose Franto Francis, MD, Dallas, TX (Abstract Co-Author) Nothing to Disclose Neil M. Rofsky, MD, Dallas, TX (Abstract Co-Author) Nothing to Disclose Thais Mussi, MD, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose Ivan Pedrosa, MD, Dallas, TX (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The purpose of this presentation is:1. To review the epidemiology, clinical findings and disease course of the ductal adenocarcinoma of the prostate (DAP) in comparison with the more common acinar adenocarcinoma of the prostate (AAP);2. To compare the unique and overlapping radiological (particularly MR imaging) features of DAP versus AAP with histopathological correlation. TABLE OF CONTENTS/OUTLINE 1. Ductal Adenocarcinoma of the Prostate (DAP) Epidemiology Clinical Features Diagnosis and Staging Clinical Management and Outcomes2. MR Imaging of DAP and Histopathological Correlation Predominantly solid presentation Solid-cystic presentation Predominantly cystic presentation3. Differentiating DAP from AAP and Mixed Tumors Table and illustrations summarizing the imaging and histopathologic features common to both AAP and DAP and the findings favoring one subtype over the other4. Clinical Implications Comparison of staging, clinical management, and outcomes of DAP and AAP (Table)5. Conclusions UR127-ED-X Calling All Kidneys! Sonographic Findings of Renal Pathology Beyond Hydronephrosis with CT and MR Correlation All Day Location: GU/UR Community, Learning Center Participants Dana E. Amiraian, MD, Jacksonville, FL (Presenter) Nothing to Disclose Melanie P. Caserta, MD, Jacksonville, FL (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Ultrasound is an important imaging modality for evaluating the kidneys, and knowledge of sonographic abnormalities can help in identifying and differentiating renal pathology. While not required for most uncomplicated cases of pyelonephritis, ultrasound can help identify complications of renal infection, some of which require emergent intervention. There are various types of renal masses, as well as many mass mimickers, and ultrasound is helpful in detecting and differentiating these entities. Ultrasound is useful for identifying and localizing abnormal echogenic renal structures, which can usually be correlated on CT. TABLE OF CONTENTS/OUTLINE Review of renal ultrasound indications and normal anatomy on ultrasoundSonographic features of renal infection Pyelonephritis Emphysematous pyelonephritis Pyonephrosis Xanthogranulomatous pyelonephritis Tuberculosis HIV nephropathy FungalApproach to renal masses Mimickers Renal cell carcinoma Transitional cell carcinoma Lymphoma AngiomyolipomaEvaluation of echogenic structures Nephrolithiasis Medullary nephrocalcinosis Cortical nephrocalcinosis Papillary necrosisTake-home points UR128-ED-X Retroperitoneal Tumors: MR Imaging Characteristics, Diagnostic Clues, Differential Diagnosis and Histopathological Correlation All Day Location: GU/UR Community, Learning Center Participants Pardeep K. Mittal, MD, Atlanta, GA (Presenter) Nothing to Disclose Peter A. Harri, MD, Atlanta, GA (Abstract Co-Author) Nothing to Disclose Juan C. Camacho, MD, Atlanta, GA (Abstract Co-Author) Nothing to Disclose Lauren F. Alexander, MD, Atlanta, GA (Abstract Co-Author) Spouse, Stockholder, Abbott Laboratories; Spouse, Stockholder, AbbVie Inc; Spouse, Stockholder, General Electric Company William C. Small, MD, PhD, Atlanta, GA (Abstract Co-Author) Nothing to Disclose Courtney A. Coursey Moreno, MD, Atlanta, GA (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1. To describe diagnostic challenges including localization of the retroperitoneal tumors, extent of invasion and characterization of specific pathology such as liposarcoma, leiomyosarcoma.,extragonadal germ cell, paragangliomas and sarcoma etc. 2. To illustrate patterns of spread, tumor components, tumor vascularity helping in narrowing the differential diagnosis. TABLE OF CONTENTS/OUTLINE Presentation will includes MRI characterization of retroperitoneal tumors using a dedicated less than 30 minute protocol of abdominopelvic MRI without and with contrast.Primary retroperitoneal (RP) tumors originating in the retroperitoneum but outside the major RP organs are uncommon. One of the challenges to radiologist is correct localization of the RP lesions, characterization as well extent of the disease, involvement of adjacent structures, identifying the organ of origin.Hence MR imaging is valuable in evaluating RP tumors particularly in staging, assessment of vascular invasion and fat content due its excellent soft tissue contrast. Specific diagnosis might be difficult to achieve due to overlapping features but certain clues will help in narrowing the differential diagnosis such as liposarcoma,leiomysarcoma,solitary fibrous tumor, paraganglioma and lymphoma etc. UR129-ED-X Cysts of the Lower Male Genitourinary Tract, From the Prostate to the Penis All Day Location: GU/UR Community, Learning Center Awards Certificate of Merit Participants Elena Lopez Uzquiza, Santander, Spain (Presenter) Nothing to Disclose Elena Yllera Contreras, MD, Santander, Spain (Abstract Co-Author) Nothing to Disclose Alejandro Fernandez Florez, MD, Santander, Spain (Abstract Co-Author) Nothing to Disclose Pedro Lastra Garcia-Baron, MD, Santander, Spain (Abstract Co-Author) Nothing to Disclose Marta Drake Perez, MD, Santander, Spain (Abstract Co-Author) Nothing to Disclose Gerardo Lopez Rasines, MD, Santander, Spain (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1. To review the embryologic development of the male genital tract (GT).2. To expose the normal anatomy and appearance of the male GT with different imaging techniques.3. To summarize the cystic lesions founded along the male GT, explaining the key findings in order to elaborate an easy differential diagnose. TABLE OF CONTENTS/OUTLINE 1. Embryologic development- Mesonephric (wolffran) ducts.- Paramesonephric (mullerian) ducts.2. Normal appearance- Ultrasound (transrectal, transperineal, testicular, transabdominal)- MRI3. Sample cases and mimics- Intraprostatic cysts (retention cyst, cystic degeneration of BPH and tumours, abscess)- Extraprostatic cysts (seminal vesicle cyst, Cowper duct cyst)- Mimics of prostatic and extraprostatic cysts (urethral diverticulum)- Scrotal and testicular cysts- Mimics of scrotal and testicular cysts (hydrocele, hematocele, pyocele, varicocele)- Perineal cysts (epidermoid cyst of the median raphe)- Penis cysts UR130-ED-X Review of Retroperitoneal Fat-containing Tumors: Etiologies, Radiological Findings and Clinical Management All Day Location: GU/UR Community, Learning Center Awards Certificate of Merit Participants Qiushi Wang, MD, Indianapolis, IN (Presenter) Nothing to Disclose Fatih Akisik, MD, Indianapolis, IN (Abstract Co-Author) Nothing to Disclose Temel Tirkes, MD, Indianapolis, IN (Abstract Co-Author) Nothing to Disclose Mark Tann, MD, Indianapolis, IN (Abstract Co-Author) Nothing to Disclose Kumaresan Sandrasegaran, MD, Carmel, IN (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1) To learn the differential diagnosis of retroperitoneal fat-containing tumors.2) To learn how to differentiate retroperitoneal fatcontaining tumors using radiologic signs.3) To learn clinical management. TABLE OF CONTENTS/OUTLINE 1) Contrast-enhanced CT and MRIs will be reviewed. 2) Brief discussion of how to detect macroscopic and microscopic fat on MR imaging.3) Review the spectrum of retroperitoneal fat-containing tumors.4) The classic and atypical appearances of a spectrum of fat-containing tumors, including myelolipoma, angiomyolipoma, lipoma, liposarcoma, extramedullary hematopoiesis, neurofibromatosis, primary retroperitoneal teratoma, lipoblastomatosis, and hibernoma are discussed. 5) To discuss clinical management of different fat-containing tumors. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Fatih Akisik, MD - 2014 Honored Educator Temel Tirkes, MD - 2013 Honored Educator Temel Tirkes, MD - 2014 Honored Educator Kumaresan Sandrasegaran, MD - 2013 Honored Educator Kumaresan Sandrasegaran, MD - 2014 Honored Educator UR134-ED-X Peripheral Zone Prostate Lesions: Differentiating Lesions with Prostate Magnetic Resonance Imaging Using PI-RADS Version 2 All Day Location: GU/UR Community, Learning Center Participants David C. Gimarc, MD, Aurora, CO (Presenter) Nothing to Disclose Toshimasa J. Clark, MD, Denver, CO (Abstract Co-Author) Nothing to Disclose Jeffrey Meier, MD, Aurora, CO (Abstract Co-Author) Nothing to Disclose Nayana U. Patel, MD, Aurora, CO (Abstract Co-Author) Nothing to Disclose Sajal S. Pokharel, MD, PhD, Aurora, CO (Abstract Co-Author) Nothing to Disclose TEACHING POINTS After viewing the presentation, participants will be able to better understand the differentiation of prostate zonal anatomy, specifically the peripheral zone, and describe the different pathological diagnoses that occur within these zones. They will then be able to explain the utilization and categorization of PI-RADS version 2 with respect to peripheral zone lesions to distinguish benign and malignant etiologies based on findings in various sequences and technical factors. TABLE OF CONTENTS/OUTLINE Prostate Cancer Overview MR and Prostate Imaging: Pictorial Overview Basic Anatomy (Peripheral Zone - PZ) Essential Sequences and Technical Aspects Multiparametric Imaging PI-RADS (version 2) Findings Differentiation of PZ lesions using PI-RADS v. 2 Benign Etiologies Malignant Etiologies Overall assessment (PI-RADS 1-5) Overall Limitations Recurrent Lesions or surveillance Examples/Cases of PZ lesions (benign and malignant) UR135-ED-X Pitfalls and Mimickers on MDCTof the Kidney and Retroperitoneum All Day Location: GU/UR Community, Learning Center Participants Takehiko Gokan, MD, Tokyo, Japan (Presenter) Nothing to Disclose Yoshimitsu Ohgiya, MD, Shinagawa-ku, Japan (Abstract Co-Author) Nothing to Disclose Masanori Hirose, MD, Tokyo, Japan (Abstract Co-Author) Nothing to Disclose Noritaka Seino, Tokyo, Japan (Abstract Co-Author) Nothing to Disclose Nobuyuki Takeyama, MD, Yokohama, Japan (Abstract Co-Author) Nothing to Disclose TEACHING POINTS In diagnosing MDCT of the kidney and the retroperitoneum, there are many pitfalls and mimickers, which may lead to misdiagnosis and erroneous patient management. In this exhibit, we show diagnostic pitfalls on MDCT of the kidney and the retroperitoneum as well as show how to avoid these diagnostic pitfalls and differentiate the mimickers. TABLE OF CONTENTS/OUTLINE The cases will be presented in a quiz format. Key differential diagnostic points, pitfalls, and therapeutic management will be highlighted in the discussion of each case. Diagnostic PitfallsAdrenal pseudotumor due to surrounding normal anatomical structures orextra-adrenal pathological conditionsMissed renal lesion due to evaluation with inappropriate phase after iv contrast.ScanArtifacts: motion artifacts, partial volume artifacts, beam hardening artifacts.Miscellaneous: Diagnostic mimickersPapillary renal cell carcinoma vs. angiomyolipoma with minimal fatRetroperitoneal liposarcoma vs. exophytic growing angiomyolipomaIgG related disease vs. lymphomaTuberculous-like granuloma vs. renal cell carcinomaetc. UR136-ED-X The ABCs of BHD: An In-depth Review of Birt-Hogg-Dubé Syndrome All Day Location: GU/UR Community, Learning Center Participants Shiva Gupta, MD, Houston, TX (Abstract Co-Author) Nothing to Disclose Hyunseon C. Kang, MD, PhD, Houston, TX (Abstract Co-Author) Nothing to Disclose Dhakshina M. Ganeshan, MBBS, FRCR, Houston, TX (Abstract Co-Author) Nothing to Disclose Ajaykumar C. Morani, MD, Houston, TX (Abstract Co-Author) Nothing to Disclose Vikas Kundra, MD, PhD, Houston, TX (Presenter) License agreement, Introgen Therapeutics, Inc TEACHING POINTS Develop an understanding of: Molecular genetics of Birt-Hogg-Dubé Syndrome Histopathology of renal tumors in Birt-Hogg-Dubé Syndrome Pertinent imaging findings and renal tumor subtypes of Birt-Hogg-Dubé Syndrome Treatment options for renal tumors in Birt-Hogg-Dubé Syndrome TABLE OF CONTENTS/OUTLINE I. Introduction to Hereditary Renal Cell Carcinomas (HRCCs) and Birt-Hogg-Dubé SyndromeII. Molecular Genetics of Birt-Hogg-Dubé SyndromeIII. Histopathology of Renal Tumors in Birt-Hogg-Dubé SyndromeIV. Imaging of Birt-Hogg-Dubé Syndrome Renal Tumors: Hybrid Chromophobe Renal Cell Carcinoma (RCC)-Oncocytoma, Chromophobe RCC, Oncocytoma, Clear Cell RCC, Papillary RCC Extrarenal Abdominal Features Pulmonary Features: Pulmonary Cysts, Pneumothoraces Other Findings (e.g. skin lesions)V. Summary Radiologists may be the first to suspect a HRCC syndrome. In-depth knowledge of Birt-Hogg-Dubé syndrome provides a framework for differentiating it from other hereditary RCC syndromes, and understanding the precision therapies for treating RCCs. UR137-ED-X It's Not All About the Prostate! Incidental Extraprostatic Neoplasms and Clinically Significant Findings on Multiparametric Prostate MRI All Day Location: GU/UR Community, Learning Center Participants Ross L. Eppelheimer, MD, Mineola, NY (Presenter) Nothing to Disclose Corinne C. Liu, MD, Mineola, NY (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Multiparametric prostate MRI plays a major role in the assessment and staging of prostate cancer. However, extraprostatic neoplasms and clinically significant incidental findings can be found on MRI. This exhibit will show specific examples of these findings to demonstrate the importance of reviewing the extraprostatic regions of a prostate MRI in order to avoid missing potentially significant findings. TABLE OF CONTENTS/OUTLINE The cases will be presented in an interactive quiz format. Specific cases will be presented to individuals viewing the exhibit. Correct answers will be revealed and the rationale explained. Key differential diagnostic considerations will also be included, if applicable. The list of cases include: Schwannoma arising adjacent to seminal vesicleColon cancer in the setting of ulcerative colitisRight common iliac artery aneurysm with focal dissectionScrotal lipomaHorseshoe kidneyAvascular necrosis of the femoral heads UR138-ED-X The Treated Prostate on 3T Multiparametric Prostate MRI: An Interactive Quiz All Day Location: GU/UR Community, Learning Center Participants Ross L. Eppelheimer, MD, Mineola, NY (Presenter) Nothing to Disclose John Mattimore, Stony Brook, NY (Abstract Co-Author) Nothing to Disclose Corinne C. Liu, MD, Mineola, NY (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Multiparametric prostate MRI plays a major role in evaluating for recurrent disease in patients with biochemical relapse after radical prostatectomy, radiation therapy and cryoablation. Anatomy of the pelvis is distorted after radical prostatectomy while radiation and cryoablation distorts the zonal anatomy. This exhibit will review the postsurgical and post-treatment changes of the prostate after radical prostatectomy, radiation therapy and cryoablation. Participants will understand the pitfalls of the treated prostate that can be mistaken for recurrent disease. We also describe the limitations and strengths of certain sequences of multiparametric prostate MRI in the treated prostate. TABLE OF CONTENTS/OUTLINE The cases will be presented in an interactive quiz format. Specific cases post radical prostatectomy, radiation and cryoablation will be presented to individuals viewing the exhibit. Correct answers will be revealed and the rationale explained.List of cases:Normal periureteral enhancement versus recurrent disease after prostatectomy on prostate MRIImaging characteristics of the prostate and recurrent prostate cancer post cryoablationImaging characteristics of the prostate and recurrent prostate cancer post Brachytherapy and Cyberknife therapy UR139-ED-X Non-invasive Radiological Manifestations of Obstructive Azospermia All Day Location: GU/UR Community, Learning Center Awards Certificate of Merit Participants Wonsuk Kim, MD, Sacramento, CA (Presenter) Nothing to Disclose Arian Nikpour, MD, Sacramento, CA (Abstract Co-Author) Nothing to Disclose Behrad Golshani, MD, Sacramento, CA (Abstract Co-Author) Nothing to Disclose Eugenio O. Gerscovich, MD, Sacramento, CA (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Review the pertinent anatomy and embryogenesis of the male reproductive system with respect to obstructive azospermia. Review various acquired and congenital causes of obstructive azospermia. Review CT, ultrasound, and MR examples related to obstructive azospermia. TABLE OF CONTENTS/OUTLINE Anatomy/Embrogenesis of the male ejaculatory system Clinical relevance Epidemiology Presentation Diagnosis Management Pathophysiology of ejaculatory duct obstruction Acquired Epididymal obstruction Vas deferens obstruction Ejaculatory duct obstruction Congenital Epididymal obstruction Vas deferens obstruction Ejaculatory duct obstruction Review of imaging examples Scrotal ultrasound Transrectal ultrasound CT MRI Summary UR140-ED-X Biochemical Recurrence of Prostate Carcinoma: A Multimodality Approach All Day Location: GU/UR Community, Learning Center Participants Mariano Volpacchio, MD, Buenos Aires, Argentina (Presenter) Nothing to Disclose Antonio Luna, MD, Jaen, Spain (Abstract Co-Author) Nothing to Disclose Diego M. Haberman, MD, Buenos Aires, Argentina (Abstract Co-Author) Nothing to Disclose Victor Llanquipacha, Buenos Aires, Argentina (Abstract Co-Author) Nothing to Disclose Veronica Rubio, Buenos Aires, Argentina (Abstract Co-Author) Nothing to Disclose Mario G. Santamarina, MD, Valparaiso, Chile (Abstract Co-Author) Nothing to Disclose Victoria Franco, Buenos Aires, Argentina (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The goals of this presentation are To review the concept of prostate carcinoma biochemical recurrence To review the diagnostic work-up in patients with biochemical recurrence To discuss the merits and limitations of different imaging modalities in the approach to prostate biochemical recurrence To illustrate typical and atypical findings and patterns of recurrence on different imaging modalities TABLE OF CONTENTS/OUTLINE IntroductionTreatment of prostate cancer and derived imaging findingsBiochemical recurrence concepts and work-upImaging modalities: merits and limitations MDCT MRI Whole Body MRI SPECT PET/CTDiagnostic algorithm and therapeutic options after recurrenceSummaryBiochemical recurrence is a common clinical scenario after both local and systemic treatment.The treating physician is often faced with the challenge represented by a timely and proper diagnosis and localization of the site of recurrence and the ensuing managment.A variety of morphologic, functional and metabolic imaging modalities are currently available and a proper, patient-adjusted and cost-effective approach is crucial in order to achieve adequate management.A rational use of the array of diagnostic tools based on knowledge of their respective strengh and limitations is of paramount importance. UR141-ED-X Dynamic Voiding UrethroMR: A New Diagnostic Approach to Urethral Lesions All Day Location: GU/UR Community, Learning Center Participants Carlos M. Araujo Junior, MD, Rio De Janeiro, Brazil (Presenter) Nothing to Disclose Jose Pedro R. Ravani, MD, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Romulo Varella, MD, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Nara S. Astacio, MD, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Leonardo K. Bittencourt, MD, PhD, Rio De Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose TEACHING POINTS In this article, we describe the protocol and the main findings of dynamic UrethroMR, while reviewing the appearance of urethral strictures secondary to changes related to surgical procedures and STDs, demonstrating its importance in characterizing espongiofibrosis. TABLE OF CONTENTS/OUTLINE MATERIALS AND METHODSImages were acquired in a Siemens Aera 1.5-T Scanner, with multiplanar T1 and T2-weighted sequences, T2 with urographic effect by technical MIP obtained at rest and during voiding effort, SPACE, T1 fat-sat before and after administration of gadolinium.DISCUSSIONMR is a noninvasive imaging method with high spatial resolution, which allows multiplanar evaluation and good tissue characterization. Furthermore, it is highly accurate in the diagnosis of urethral strictures, enabling the identification of lesions that are often underestimated in voiding uretrocistography, and allowing the physician a more accurate surgical plan. MRI also allows complete assessment of the peri-urethral compartments, identifying risk factors and the presence of associated complications.CONCLUSIONUrethroMRI is a new imaging modality that shows potential to identify and quantify urethral strictures, for which surgery remains the best treatment option, and the preoperative evaluation is crucial for success therapy in these patients. UR142-ED-X Magnetic Resonance Imaging of Penile Diseases All Day Location: GU/UR Community, Learning Center Participants Van Lai Nguyen, MD, Rotterdam, Netherlands (Presenter) Nothing to Disclose Mariska Rossius, Rotterdam, Netherlands (Abstract Co-Author) Nothing to Disclose Piotr Wielopolsky, Rotterdam, Netherlands (Abstract Co-Author) Nothing to Disclose Gert Dohle, MD, PhD, Rotterdam, Netherlands (Abstract Co-Author) Nothing to Disclose Gabriel P. Krestin, MD, PhD, Rotterdam, Netherlands (Abstract Co-Author) Consultant, General Electric Company; Research Grant, General Electric Company; Research Grant, Bayer AG; Research Grant, Siemens AG; Speakers Bureau, Siemens AG Roy S. Dwarkasing, MD, Rotterdam, Netherlands (Abstract Co-Author) Nothing to Disclose TEACHING POINTS MRI of the penis is challenging, mainly because of motion issues. In this exhibit we present our experience with dedicated MRI penis, focus on the added value of MRI for penile diseases and conditions and propose recommendations for proper imaging. Teaching points: To describe technical challenges of state of the art MRI of the penis. To presents methods of MRI penis, including application of pelvic phased array and other dedicated external surface receiver coils. To illustrate and describe the added value of MRI for different penile disorders. To propose a practical MRI protocol, including scan parameters, for routine use with a pelvic phased array coil for both 1.5 and 3.0 T MR systems. TABLE OF CONTENTS/OUTLINE 1. Introduction 2. Technical challenges for MRI penis 3. Clinical cases: Added values of MRI penis to clinical assessment and other imaging modalities. 4. Limitations and pitfalls 5. Recommended imaging protocol (1.5 and 3.0T) 6. References. UR143-ED-X A Multimodality Review of Native Renal Vascular Pathology All Day Location: GU/UR Community, Learning Center Participants Sayf A. Al-Katib, MD, Royal Oak, MI (Presenter) Nothing to Disclose Monisha Shetty, MD, Royal Oak, MI (Abstract Co-Author) Nothing to Disclose Marco A. Amendola, MD, Coral Gables, FL (Abstract Co-Author) Nothing to Disclose Beatrice L. Madrazo, MD, Miami, FL (Abstract Co-Author) Nothing to Disclose Syed Zafar H. Jafri, MD, Royal Oak, MI (Abstract Co-Author) Nothing to Disclose Emily Nghiem, Royal Oak, MI (Abstract Co-Author) Nothing to Disclose TEACHING POINTS To review the imaging features of common and uncommon pathology affecting the renal artery, renal vein and intraparenchymal vessels by multiple modalities including CT, US, MRI and angiography. To highlight the presentation and management of this spectrum of native renal vascular pathology. To provide a framework to evaluate the native kidney for vascular pathology. TABLE OF CONTENTS/OUTLINE Renal Artery Pathology Renal artery aneurysm Renal arteriovenous fistula Renal arteriovenous malformation Fibromuscular dysplasia affecting the renal artery Spontaneous isolated renal artery dissection Renal artery stenosis Renal vascular pedicle injury in trauma Renal Vein Pathology Bland renal vein thrombosis Tumor thrombus secondary to renal cell carcinoma and adrenal cortical carcinoma Renal vein leiomyosarcoma Nutcracker phenomenon Renal Parenchymal Vascular Pathology Iatrogenic pseudoaneurysm Subcapsular hematoma after lithotripsy Page kidney Spontaneous parenchymal bleeds Renal cortical necrosis Renal infarction Renal laceration Polyarteritis nodosa UR144-ED-X Computer-Aided Diagnosis of Prostate Cancer on Multi-parametric MRI: How I Do It All Day Location: GU/UR Community, Learning Center Participants Ge Gao, MD, Beijing, China (Presenter) Nothing to Disclose Xiaoying Wang, MD, Beijing, China (Abstract Co-Author) Nothing to Disclose Jue Zhang, Beijing, China (Abstract Co-Author) Nothing to Disclose Chengyan Wang, PhD, Beijing, China (Abstract Co-Author) Nothing to Disclose Juan Hu, Kunming, China (Abstract Co-Author) Nothing to Disclose Xuedong Yang, Beijing, China (Abstract Co-Author) Nothing to Disclose He Wang, MD, Beijing, China (Abstract Co-Author) Research Grant, General Electric Company TEACHING POINTS 1. To review the popular computer-aided diagnosis (CAD) system for identification and classification of prostate cancer(PCa) in clinical work. 2. To explain the workflow of CAD for localization of PCa that combines features derived from multi-parametric MRI (mp-MRI), and evaluate the performance of this system. TABLE OF CONTENTS/OUTLINE 1. Clinical application of CAD for prostate cancer diagnosis2. Clinical promotion of mp-MRI for prostate cancer diagnosis is in a dilemma3. Application and workflow of PCa CAD system for cancer localization Mp-MRI preprocessing Prostate segmentation Sample collection Imaging features extraction Classification: system training and testing Outcome of the CAD system 4. Performance of the lesion localization by CAD system UR145-ED-X Abnormal Descent of the Testes All Day Location: GU/UR Community, Learning Center Participants Pankaj Nepal, MD, Doha, Qatar (Presenter) Nothing to Disclose Devendra Kumar, MBBS, MD, Hamilton, ON (Abstract Co-Author) Nothing to Disclose Subramaniyan Ramanathan, MD, MBBS, Doha, Qatar (Abstract Co-Author) Nothing to Disclose Habeeba Hena, MD, Doha, Qatar (Abstract Co-Author) Nothing to Disclose Mahmoud Al Raheem Heidous, MD, Doha, Qatar (Abstract Co-Author) Nothing to Disclose Atif Wasim Haneef Mohamad, MD, Doha, Qatar (Abstract Co-Author) Nothing to Disclose Maneesh Khanna, MBBS, Doha, Qatar (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1) Undescended testes is the testes that fails to reach bottom of scrotum in expected location. 2) True undescended testes includes intraabdominal testes or canalicular testes found in inguinal canal or superficial ring . 3) However ectopic testes is the one which has wandered from usual path due to abnormal gubernacular insertion and found in uncommon location. 4) Ultrasound is first line of investigation to identify inguinal and superficial undescended testes. 5) MRI is reserved for the intraabdominal and undescended testes not visualized by ultrasound. TABLE OF CONTENTS/OUTLINE 1) Pathway of testes descent in usual as well as unusual locations.2) Brief discussion on complications and clinical features.3) Judicious use of imaging modalities including ultrasound, MRI or laparoscopy for tracing intraabdominal testes and identifiying testicular vessels In imaging.4)Spectrum of demonstration:a) Ultrasound images of testes : in inguinal canal, superficial ring, left iliac fossab) MRI images of testes: in left iliac fossa, superficial to rectus sheath ( ectopic), root of scrotum, inguinal canal, superficial ring and root of penis.c) CT image of testes: Calcified and high mesenteric (ectopic) with germ cell tumor. UR146-ED-X Pathways, Pearls and Pitfalls: An MR Feature-based Algorithm for Renal Mass Characterization All Day Location: GU/UR Community, Learning Center Awards Cum Laude Participants Kristy Lee, MD, Boston , MA (Presenter) Nothing to Disclose Katherine M. Troy, MD, Brookline, MA (Abstract Co-Author) Nothing to Disclose Leo L. Tsai, MD, PhD, Boston, MA (Abstract Co-Author) Co-founder, Agile Devices Inc; Stockholder, Agile Devices Inc; Research Consultant, Agile Devices Inc; Karen S. Lee, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Maryellen R. Sun, MD, Boston, MA (Abstract Co-Author) Research Grant, Glaxo SmithKline plc TEACHING POINTS 1.Incidental renal masses are being discovered with increasing frequency due to the rising number of cross-sectional studies being performed. Although the vast majority of masses are incidental, many are incompletely characterized and indeterminate. MRI allows for accurate characterization which is essential to ensure appropriate medical versus surgical case management 2.Biopsy can play a role in many cases in which diagnosis is in question TABLE OF CONTENTS/OUTLINE Intro: MR imaging protocol; Algorithm: Utilizing characteristic lesion features at each pulse sequence, a stepwise approach to diagnosis of solid and cystic renal masses is presented. The algorithm incorporates factors such as the presence of cystic versus solid components, signal intensity at T2WI and T1WI, microscopic and macroscopic fat, hemorrhage, hemosiderin, restricted diffusion and pattern of enhancement. We demonstrate the utility of this algorithm through a case-based approach and highlight potential pitfalls and pearls. Cases include benign and malignant neoplasms (clear cell, papillary and chromophobe renal cell and urothelial carcinoma, metastases, lymphoma, typical and fat poor angiomyolipoma, oncocytoma, reninoma, and solitary fibrous tumors, and non-neoplastic etiologies such as infectious and inflammatory lesions, infarct, hematoma, and xanthogranulomatous pyelonephritis. UR147-ED-X MR Imaging Spectrum of Penile Prosthesis and Its Complications All Day Location: GU/UR Community, Learning Center Participants Subramaniyan Ramanathan, MD, MBBS, Doha, Qatar (Abstract Co-Author) Nothing to Disclose Pankaj Nepal, MD, Doha, Qatar (Presenter) Nothing to Disclose Devendra Kumar, MBBS, MD, Hamilton, ON (Abstract Co-Author) Nothing to Disclose Maneesh Khanna, MBBS, Doha, Qatar (Abstract Co-Author) Nothing to Disclose Nicola Schieda, MD, Ottawa, ON (Abstract Co-Author) Nothing to Disclose Ahmad Shamsodini, MS, Doha, Qatar (Abstract Co-Author) Nothing to Disclose Mahmoud Al Raheem Heidous, MD, Doha, Qatar (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1) Penile prosthesis is ideal for patients with organic erectile dysfunction which is not responding to medications and non surgical treatments. 2) Types of prosthesis : malleable and inflatable penile prosthesis (IPP). 3) Various complications of prosthesis are persistent pain, bending or deformity, mechanical malfunction, cross over and crural perforations. Complications of the reservoir include rupture, herniation and malfunction. 4) MR evaluation of penile prosthesis is superior due to its high soft tissue contrast.Ultrasound can be used for initial evaluation and reservoir related complications. TABLE OF CONTENTS/OUTLINE 1) Detailed MRI anatomy of normal penis, malleable and inflatable penile prosthesis. 2) Our institutional MRI protocol, common indications. 3) Types of penile implants; malleable or semi rigid and inflatable penile prosthesis. 4) USG and MRI appearance of 3 part IPP including penile cylinders, pump and reservoir. 5)Spectrum of complications for demonstration ( Images for exibits) : - MR images of Buckling or S shaped deformity, displacement of the malleable rod - Cross-over of cylinders, - Reservoir leak, - Reservoir herniation into inguinal canal, - Prosthesis infection and erosion, - Ultrasound images of penile anatomy. UR148-ED-X Multiparametric MR Imaging of the Prostate and Prostatic Bed in the Evaluation of Cancer Recurrence All Day Location: GU/UR Community, Learning Center Participants Dafne D. Melquiades, Rio de Janeiro, Brazil (Presenter) Nothing to Disclose Erick S. Hollanda, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Natalia Sabaneeff, MD, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Bruno R. Falcone, MD, Rio Dejjaneiro, Brazil (Abstract Co-Author) Nothing to Disclose Romulo Varella, MD, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Leonardo K. Bittencourt, MD, PhD, Rio De Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Carolina L. Vaz, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Guilherme M. Cunha, MD, San Diego, CA (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1- Demonstrate that multiparametric pelvic MR imaging is a valuable tool in the diagnosis of the prostate cancer recurrence.2Review the normal findings post-prostatectomy and post-radiation, as well as the findings suspicious for local and distant tumor recurrence.3- Discuss the practical applications and decision algorithms for the management of prostate cancer recurrence, based on the combination of imaging findings and clinical information. TABLE OF CONTENTS/OUTLINE 1- Risk assessment, staging and treatment options for prostate cancer2- Multiparametric MR imaging protocol and postprocessing3- Normal findings after radiotherapy and brachytherapy4- Normal findings after prostatectomy5- What is the available clinical evidence on the performance of multiparametric MR imaging for detection of tumor recurrence?6- MR findings of tumor recurrence:- Post-radiation;- Post-prostatectomy;- Nodal recurrence;- Distant metastases;7- How to use MR imaging information when suspecting of prostate cancer recurrence? UR149-ED-X Staging of Prostate Cancer Using Multiparametric MR Imaging: A Practical Approach All Day Location: GU/UR Community, Learning Center Participants Dafne D. Melquiades, Rio de Janeiro, Brazil (Presenter) Nothing to Disclose Erick S. Hollanda, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Natalia Sabaneeff, MD, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Guilherme M. Cunha, MD, San Diego, CA (Abstract Co-Author) Nothing to Disclose Bruno R. Falcone, MD, Rio Dejjaneiro, Brazil (Abstract Co-Author) Nothing to Disclose Leonardo K. Bittencourt, MD, PhD, Rio De Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Carolina L. Vaz, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Sabrina O. Bernal, MD, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose TEACHING POINTS • Demonstrate through a pictorial essay that multiparametric prostate MR can assist in a relevant way in the preoperative local staging of PCa.• Review the main findings related to the PCa staging. We will briefly discuss the role of PI-RADS criteria in detection and also recent evidence in disease staging.• Discuss about the performance and imaging criteria for the detection of extracapsular extension and seminal vesicle invasion, based on multiparametric MR imaging.• The main clinical signs described for extracapsular extension in T2WI are: nerurovascular bundle asymmetry or tumor involvement, focal bulging or irregularity in prostate contour, obliteration of the rectoprostatic angle, capsular retraction, contact of the tumor with the prostatic capsule and signs of capsule rupture with direct tumor extension to the periprostatic fat. TABLE OF CONTENTS/OUTLINE - Anatomy of the prostate gland and seminal vesicles.- Clinical staging of prostate cancer.- How does staging affect the treatment options?- Multiparametric MR imaging protocol.- Typical MR imaging appearance of prostate cancer.- MR imaging findings for extracapsular extension.- MR imaging findings for seminal vesicle involvement.- MR imaging findings for bladder neck invasion.Imaging pitfalls that may affect staging. UR150-ED-X MRI for the Diagnosis of Prostate Cancer: Basic Knowledge, Optimal Scan Protocols, Interpretations, and New Applications All Day Location: GU/UR Community, Learning Center Participants Ryuji Akita, RT, MS, Hiroshima, Japan (Presenter) Nothing to Disclose Yukiko Honda, MD, Hiroshima, Japan (Abstract Co-Author) Nothing to Disclose Kazushi Yokomachi, RT, Hiroshima, Japan (Abstract Co-Author) Nothing to Disclose Yuji Akiyama, Hiroshima, Japan (Abstract Co-Author) Nothing to Disclose Makoto Iida, Hiroshima, Japan (Abstract Co-Author) Nothing to Disclose Kazuo Awai, MD, Hiroshima, Japan (Abstract Co-Author) Research Grant, Toshiba Corporation; Research Grant, Hitachi, Ltd; Research Grant, Bayer AG; Reseach Grant, DAIICHI SANKYO Group; Medical Advisor, DAIICHI SANKYO Group; Research Grant, Eisai Co, Ltd; Research Grant, Nemoto-Kyourindo; ; ; ; ; TEACHING POINTS We present optimal MR protocols for the diagnosis of prostate cancer.Furtheremore, we demonstrate clinical utility of new applications such as computed diffusion weighted imaging (cDWI) and high resolution 3D TSE T2-weighted imaging.The cDWI may improve sensitivity of prostate cancer and high resolution 3D TSE T2-weighted imaging may improve assessment of local invasion (extracapsular extension and seminal vesicle invasion). TABLE OF CONTENTS/OUTLINE 1. Current diagnostic process 2. Optimal MRI protocol for diagnosing prostate cancer 3. Detectability of prostate cancer by MRI 4. Correlation between MR findings and the clinical T stage or Gleason score 5. Pitfalls of MRI interpretation: Artifacts and changes after biopsy or treatment 6. New applications for MRI 6.1. cDWI 6.2. High resolution 3D TSE T2-weighted imaging UR151-ED-X New Concepts in Kidney Stone Characterization with CT All Day Location: GU/UR Community, Learning Center Participants Blanca Pano Brufau, MD, Barcelona, Spain (Presenter) Nothing to Disclose Rafael Salvador Izquierdo, MD, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose Javier L. Moreno Negrete, MD, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose Carmen Sebastia Cerqueda, MD, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose Laura Bunesch Villalba, MD, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose Carlos Nicolau, MD, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose TEACHING POINTS -To review relevant clinical concepts for radiologists regarding kidney stones, focusing in the fragility and stone burden concepts.To discuss the CT and dual energy CT (DECT) findings to bear in mind when planning treatment .-To analyze current literature regarding CT dose reduction and further classification based on calculi composition. TABLE OF CONTENTS/OUTLINE 1. Introduction: clinical concepts of radiological interest-Composition-Treatment options and how radiological information can help guide the appropriate treatment strategy: expectant attitude, active extraction and medical treatment 2. Contribution of CT in treatment planning2.1. Simple energy MDCT-Detection and localization: the halo and comet tail signs. The HIV PatientCharacterization -Size: Windowing, image magnification and stone burden -Composition (Stone Fragility): homogeneity, shape and density -Limitations in simple energy characterization2.2 DECT-Technique-Parameters for allow differentiation between uric and non-uric acid composition-Post-processing Software3. Future Directions-Further classifications based on stones compositionDecreased radiation dose4. Structured radiological report. Summary of relevant data that CT and DECT can provide to guide the appropriate therapeutic management UR152-ED-X PI-RADS v2: MRI Imaging Features of Prostate Cancer and the Experience of an Active MRI Surveillance Program All Day Location: GU/UR Community, Learning Center Participants Robert M. Marks, MD, San Diego, CA (Presenter) Nothing to Disclose John R. Dryden, MD, SAN DIEGO, CA (Abstract Co-Author) Nothing to Disclose Jonathan Berger, MD, San Diego, CA (Abstract Co-Author) Nothing to Disclose Sean Stroup, MD, San Diego, CA (Abstract Co-Author) Nothing to Disclose Richard S. Montgomery, MD, San Antonio, TX (Abstract Co-Author) Nothing to Disclose TEACHING POINTS This educational exhibit will 1) Discuss the role of MRI in Prostate Cancer 2) Discuss the MRI imaging technique at our institution 3) Review the categories of PI-RADS v2 with pathologically proven MRI cases 4) Discuss the role and clinical experience of an active MRI surveillance program at a tertiary care hospital. TABLE OF CONTENTS/OUTLINE Overview of the indications for Prostate MRI in the diagnosis or surveillance of Prostate Cancer Discuss the imaging technique for Prostate MRI at our institution Include table of MRI parameters Discuss the categories of both T2 and ADC findings of PI-RADS v2 Chart of PI-RADS v2 categories Discuss lesion measurement guidelines for peripheral zone vs. transitional zone Discuss the role of contrast enhancement in PI-RADS v2 Pathologically proven MRI cases for each PI-RADS v2 category Discuss extracapsular extension with representative cases Discuss seminal vesicle invasion with representative cases Discuss the experience of an active MRI surveillance program at a tertiary care medical center Discuss the role of an active MRI surveillance program Benefits of observing a lesion vs. prostatectomy Indication for MRI surveillance Discuss upstaging of tumors based on Prostate MRI after initial biopsy UR153-ED-X Imagenological Review of the Key Findings in Retroperitoneal Fibrosis and its Complications All Day Location: GU/UR Community, Learning Center Participants Karin Daniela Muller Campos, Santiago, Chile (Presenter) Nothing to Disclose Roberto Correa Soto, Salamanca, Spain (Abstract Co-Author) Nothing to Disclose Jorge Ortiz Vega, MD, Santiago, Chile (Abstract Co-Author) Nothing to Disclose Ignacio Maldonado, MD, Santiago, Chile (Abstract Co-Author) Nothing to Disclose Rodrigo Bazaes, MD, PhD, Santiago, Chile (Abstract Co-Author) Nothing to Disclose Cristian Varela, MD, Santiago, Chile (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The purpose of this exhibit is:1. To understand the pathophysiology of retroperitoneal fibrosis and to know the typical clinical manifestation2. To characterize the typical imaging findings of the disease, with an emphasis on differential diagnosis with retroperitoneal malignancies3. To describe the most useful radiologic technique in this disease TABLE OF CONTENTS/OUTLINE - Introduction- Clinical presentation and pathophysiology of retroperitoneal fibrosis.- Imaging techniques and findings:1. Multidetector computed tomography and magnetic resonance2. Applications of Positron emission tomography 3. Radiological findings indicating good prognosis4. Imaging findings of complications and markers of poor prognosis- Common diagnostic pitfalls and differential diagnoses.- Cases to illustrate the radiologic features. UR154-ED-X New Staging and Scoring Systems of Renal Cell Carcinomas: What the Radiologist Needs to Report All Day Location: GU/UR Community, Learning Center Participants Manjiri K. Dighe, MD, Seattle, WA (Presenter) Research Grant, General Electric Company Jean H. Lee, MD, Seattle, WA (Abstract Co-Author) Nothing to Disclose Funda Vakar-Lopez, Seattle, WA (Abstract Co-Author) Nothing to Disclose Ryan O'Malley, MD, Seattle, WA (Abstract Co-Author) Nothing to Disclose Sandeep Vaidya, MD, Seattle, WA (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1. It is important for radiologists to be acquainted not only with the well widespread TNM staging system, but also with the new RCC scoring systems, since their conjoint use is crucial to manage the best treatment approach of renal masses. Since the advent of R.E.N.A.L., 3 more systems appeared and, although they have demonstrated to be reproducible inter-observer, they all have inherent strengths and weaknesses. Because some difficulties have been detected when applying the renal scores, new scoring systems are being developed in order to overcome those problems and to create more practical and simpler scores. 2. The aim of this educational poster is to review the imaging characteristics of various sub-types of renal cell carcinoma and to review the various imaging systems/algorithms used in deciding the appropriate method of treatment of RCC. TABLE OF CONTENTS/OUTLINE 1. To understand the subtypes of renal cell carcinomas (RCCs) and their imaging characteristics 2. To review the new staging and scoring methods available including R.E.N.A.L, P.A.D.U.A, C-index scoring and A.B.L.A.T.E. algorithm. 3. To illustrate various renal tumors using the new scoring systems by means of pictorial examples. 4. To provide reporting macros that can be used for the various staging/scoring systems UR155-ED-X Crystal Clear or Somewhat Murky: A Pictorial Review of Imaging Biomarkers that are Predictive of Cytogenetic Abnormalities in Clear Cell Renal Cell Carcinoma All Day Location: GU/UR Community, Learning Center Participants Jonathan R. Young, MD, Los Angeles, CA (Presenter) Nothing to Disclose Jocelyn A. Young, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Jiaoti Huang, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Steven S. Raman, MD, Santa Monica, CA (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1. Cytogenetics is becoming increasingly important in predicting patient prognosis in RCC because it can more accurately reflect cancer physiology in an individual patient. However, cytogenetic analyses require invasive procedures to obtain tissue samples. 2. Imaging features on multiphasic MDCT may potentially provide a non-invasive means of predicting cytogenetic information and thus influence how cytogenetic information is obtained and utilized to predict patient outcome. 3. For instance, enhancement on 4phase MDCT can help predict the loss of chromosome 8p and the gain of chromosome 20, abnormalities that are associated with a higher tumor grade and greater risk of recurrence. TABLE OF CONTENTS/OUTLINE 1. Epidemiology of Renal Cell Carcinoma2. The Importance and Expanding Role of Cytogenetics in the Management of RCC3. Common Cytogenetic Abnormalities in Clear Cell RCC4. Cytogenetic Abnormalities in Clear Cell RCC with Prognostic Implications5. Multiphasic MDCT Imaging Biomarkers to Predict Cytogenetic Abnormalities with Prognostic Implications UR158-ED-X Multimodality Imaging of Non-Malignant Penile Disorders: A One-Stop Shop for Radiologists All Day Location: GU/UR Community, Learning Center Participants Stephanie A. Lee-Felker, MD, Los Angeles, CA (Presenter) Nothing to Disclose Ely R. Felker, MD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Steven S. Raman, MD, Santa Monica, CA (Abstract Co-Author) Nothing to Disclose Maurice M. Garcia, MD, MS, San Francisco, CA (Abstract Co-Author) Nothing to Disclose Valdair F. Muglia, MD, PhD, Ribeirao Preto, Brazil (Abstract Co-Author) Nothing to Disclose Antonio C. Westphalen, MD, Mill Valley, CA (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The purpose of this exhibit is to:1. Review normal penile anatomy and physiology of erection2. Present the multimodality imaging appearances of an array of common, non-malignant penile disorders on ultrasound, cavernosagram, computed tomography, magnetic resonance imaging, and angiography3. Discuss which penile disorders require urgent urological intervention TABLE OF CONTENTS/OUTLINE 1. Normal penile anatomy: structural, arterial, and venous anatomy2. Normal physiology of erection a. Normal color and spectral Doppler ultrasound of erection3. Multimodality imaging of erectile dysfunction a. Arterial insufficiency b. Venous incompetence, dorsal vein thrombosis c. Priapism i. Low flow priapism ii. High flow priapism: cavernosal artery pseudoaneurysm, cavernosoarterial fistula d. Color and spectral Doppler ultrasound, fluoroscopic cavernosagram, and CT cavernosagram evaluation4. Multimodality imaging of common penile implants and devices, including related complications a. Device malposition b. Infection5. Infectious conditions: abscess6. Inflammatory conditions: Peyronie's disease7. Trauma: penile hematoma, penile fracture UR159-ED-X Beyond Urothelial Bladder Cancers: Uncommon Players All Day Location: GU/UR Community, Learning Center Participants Qiushi Wang, MD, Indianapolis, IN (Presenter) Nothing to Disclose Fatih Akisik, MD, Indianapolis, IN (Abstract Co-Author) Nothing to Disclose Temel Tirkes, MD, Indianapolis, IN (Abstract Co-Author) Nothing to Disclose Mark Tann, MD, Indianapolis, IN (Abstract Co-Author) Nothing to Disclose Kumaresan Sandrasegaran, MD, Carmel, IN (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1. To identify and illustrate the spectrum of primary bladder tumors other than urothelial carcinoma.2. To present typical and atypical radiologic findings of these tumors.3. To correlate radiologic findings with pathology. TABLE OF CONTENTS/OUTLINE 1.The imaging findings on US, CT, MRI and PET of uncommon primary bladder tumors beyond urothelial bladder cancers are presented, with particular attention to what the radiologist may add to diagnosis and help management.2.The tumors discussed include squamous carcinoma, adenocarcinoma, neuroendocrine carcinoma, carcinoid, melanoma, leiomyoma, fibroma, urachal carcinoma, paraganglioma, hemangioma, pheochromocytoma, plasmacytoma, rhabdomyosarcoma, leiomyosarcoma, lymphoma, chloroma, neurofibroma, inflammatory myofibroblastic tumor, nephrogenic adenoma, and solitary fibrous tumor. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Fatih Akisik, MD - 2014 Honored Educator Temel Tirkes, MD - 2013 Honored Educator Temel Tirkes, MD - 2014 Honored Educator Kumaresan Sandrasegaran, MD - 2013 Honored Educator Kumaresan Sandrasegaran, MD - 2014 Honored Educator UR160-ED-X Adrenal Gland Abnormalities Associated with Systemic Conditions: A Pictorial Review of Clinical and Radiological Findings All Day Location: GU/UR Community, Learning Center Participants Qiushi Wang, MD, Indianapolis, IN (Presenter) Nothing to Disclose Fatih Akisik, MD, Indianapolis, IN (Abstract Co-Author) Nothing to Disclose Temel Tirkes, MD, Indianapolis, IN (Abstract Co-Author) Nothing to Disclose Mark Tann, MD, Indianapolis, IN (Abstract Co-Author) Nothing to Disclose Kumaresan Sandrasegaran, MD, Carmel, IN (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1.Learn systemic conditions and associated imaging findings that can involve the adrenal glands.2.Abdominal radiologists need to suspect the systemic conditions that can involve adrenal glands. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Fatih Akisik, MD - 2014 Honored Educator Temel Tirkes, MD - 2013 Honored Educator Temel Tirkes, MD - 2014 Honored Educator Kumaresan Sandrasegaran, MD - 2013 Honored Educator Kumaresan Sandrasegaran, MD - 2014 Honored Educator UR161-ED-X Multiparametric Ultrasonography of Scrotal Pathology: A Pictorial Review All Day Location: GU/UR Community, Learning Center FDA Discussions may include off-label uses. Awards Certificate of Merit Participants Dean Y. Huang, FRCR, London, United Kingdom (Presenter) Nothing to Disclose Eleni Konstantatou, MD, MSc, london, United Kingdom (Abstract Co-Author) Nothing to Disclose Robert J. Eckersley, PhD, London, United Kingdom (Abstract Co-Author) Nothing to Disclose Maria E. Sellars, MD, FRCR, London, United Kingdom (Abstract Co-Author) Nothing to Disclose Paul S. Sidhu, MRCP, FRCR, London, United Kingdom (Abstract Co-Author) Speaker, Bracco Group; Speaker, General Electric Company TEACHING POINTS Innovative ultrasonography techniques, such as contrast-enhanced ultrasonography (CEUS), and strain elastography (SE), have allowed advanced imaging of scrotal pathology. When added to conventional grey-scale US and Doppler US as part of a multiparametric ultrasonography (MP-US) examination, each of these techniques provide information that could be useful when diagnosing disorders within the scrotum. This exhibit aims to increase learners' familiarity with the appearances seen with these techniques, and to illustrate the usefulness of MP-US in imaging intra- and extra- testicular pathology, particularly in the context of confirming benignity, for improved diagnostic confidence. TABLE OF CONTENTS/OUTLINE This exhibit aims to illustrate MP-US appearances of a spectrum of intra- and extra- testicular pathology, including tumors such as seminoma, non-seminomatous germ cell tumors, sex-cord stromal tumors, lymphoma, metastasis, and sarcomas, as well as benign processes such as epidermoid cysts, venous infarction, intra-testicular hematoma, abscesses, segmental infarction, sarcoidosis, post-biopsy scar, testicular cysts, orchitis, adenomatoid lesions, and testicular torsion. The role of the newer techniques such as CEUS and SE in offering the means of better characterizing vascularity and inherent stiffness of lesions is also discussed. UR162-ED-X 'The Ureter...Where Did You Come From? Where Did You Go?' An Interactive Teaching File All Day Location: GU/UR Community, Learning Center Participants Megan T. Elgethun, MD, Pittsburgh, PA (Presenter) Nothing to Disclose Matthew S. Hartman, MD, Pittsburgh, PA (Abstract Co-Author) Nothing to Disclose Paul R. Klepchick, MD, Pittsburgh, PA (Abstract Co-Author) Nothing to Disclose Matthew T. Heller, MD, Pittsburgh, PA (Abstract Co-Author) Consultant, Reed Elsevier; Author, Reedl Elsevier David C. Reisner, MD, Pittsburgh, PA (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The purpose of this exhibit is:1. To review the normal course, embryology and anatomy of the ureter. 2. Discuss the different imaging modalities utilized for evaluation of the ureter.3. Demonstrate and review examples of pathology and surgical procedures affecting the course and appearance of the ureter. 4. To highlight the normal appearance, potential complications and imaging pitfalls of the ureter through the use of an interactive teaching file TABLE OF CONTENTS/OUTLINE This presentation will cover the following sections:1. Normal anatomy, embryology and course of the ureter.2. Review the common imaging modalities used to evaluate the ureter.3. Demonstrate pathologic conditions that affects the normal course and appearance of the ureter.4. Review common surgical procedures, interventions and post operative appearances of the ureter.5. Interactive Teaching File6. Summary UR163-ED-X CT Findings in Long Term Peritoneal Dialysis All Day Location: GU/UR Community, Learning Center Participants Joe Peltz, MD, Montreal, QC (Abstract Co-Author) Nothing to Disclose Shaza Alsharif, MD, Jeddah, Saudi Arabia (Presenter) Nothing to Disclose Catherine Milne, Montreal, QC (Abstract Co-Author) Nothing to Disclose Armen H. Attarian, MD, Mont-Royal, QC (Abstract Co-Author) Nothing to Disclose Benoit D. Mesurolle, MD, Montreal, QC (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The goals of this exhibit are:1. To present and discuss the complications of peritoneal dialysis (PD) catheters encountered in series of 133 patients during CT scan of the abdomen.2. To describe the associated abdominal finings during peritoneal dialysis and after peritoneal dialysis catheter removal. TABLE OF CONTENTS/OUTLINE • Demographics of renal failure and types of dialysis.• Indications of abdominal CT in patients with PD catheters.• Factors contributing to the development of PD related complications.• Review the imaging of complications expected in the long term of peritoneal dialysis catheter, including those that develop after catheter removal based on two institutions experience. UR165-ED-X Role of MRI in Evaluation of Penile Carcinomas: Impact on Staging, Prognosis and Management Decisions All Day Location: GU/UR Community, Learning Center Awards Certificate of Merit Participants Priya Ghosh, MD, MBBS, Kolkata, India (Presenter) Nothing to Disclose Saugata Sen, MBBS, MD, Kolkata, India (Abstract Co-Author) Nothing to Disclose Sumit Mukhopadhyay, MD, Kolkata, India (Abstract Co-Author) Nothing to Disclose Aditi Chandra, Kolkata, India (Abstract Co-Author) Nothing to Disclose Dayananda Lingegowda, MBBS, Kolkata, India (Abstract Co-Author) Nothing to Disclose TEACHING POINTS MRI can accurately delineate the anatomy of penis High contrast of a neoplastic lesion with normal tissue is obtained on T2weighted images (T2WI) and post-gadolinium T1-weighted images (T1WI) Multiplanar imaging with MRI can provide adequate information required for loco-regional staging and prognostication of penile carcinomas as well as diagnose post-operative recurrences TABLE OF CONTENTS/OUTLINE Background: Prognosis and treatment of penile carcinomas depend on local extent and regional nodal staging. Clinical examination can provide preliminary staging of penile neoplasms, but MRI is more accurate in loco-regional staging of penile cancer and has a good correlation with histologic staging Normal imaging anatomy: Corpora cavernosa, crura, corpus spongiosum, urethra, covering layers Technique and sequences Imaging appearance of carcinoma: Hypointense to corpora in T2WI and T1WI, enhances in postgadolinium T1WI, but lesser than corpora Method of staging using MRI: TNM, Jackson staging T1: limited to the subcutaneous tissue T2: involvement of corpora T3: involvement of urethra or prostate T4: invasion of other adjacent structures Nodal assessment: superficial and deep inguinal, pelvic MRI evaluation: Impact on prognosis and management Other penile neoplasms Summary and conclusion UR166-ED-X Array of Imaging Features in Tuberous Sclerosis Renal Disease with Histopathologic Correlation All Day Location: GU/UR Community, Learning Center Participants Jignesh N. Shah, MD, Memphis, TN (Presenter) Nothing to Disclose Harris L. Cohen, MD, Memphis, TN (Abstract Co-Author) Nothing to Disclose John Bissler, Memphis, TN (Abstract Co-Author) Nothing to Disclose Asim F. Choudhri, MD, Memphis, TN (Abstract Co-Author) Nothing to Disclose TEACHING POINTS There are varied renal manifestations of tuberous sclerosis complex (TSC), which can be challenging to diagnose and characterize on imaging. We will review the imaging appearance of different Tuberous Sclerosis renal findings on CT, MRI, angiography, and ultrasound, based upon an imaging database of more than 500 patients with TSC renal disease. Imaging techniques will be reviewed, with an emphasis on MRI, and correlated with histology. The genetic and histologic basis for different imaging features will be reviewed. TABLE OF CONTENTS/OUTLINE 1) Imaging features of various renal menifestations of Tuberous Sclerosis Complex (TSC) which will include:Angiomyolipoma- typical, with macroscopic fat- with microscopic fat but no macroscopic fat- with no microscopic or macroscopic fat- with hemorrhageRenal cystsAutosomal dominant polycystic kidney disease2) Genetic and histologic features reviewed include: Origin of renal angiomyolipoma from renal pericytes; Co-location of autosomal dominant polycystic kidney disease gene with TSC-2 gene UR167-ED-X "Imaging of Urinary Diversions and Postoperative Complications: What the Radiologist Needs to Know" All Day Location: GU/UR Community, Learning Center Participants Arvind Shergill, MBBS, Toronto, ON (Presenter) Nothing to Disclose Seng Thipphavong, MD, Toronto, ON (Abstract Co-Author) Nothing to Disclose Alexandre Zlotta, FRCPC, PhD, Toronto, ON (Abstract Co-Author) Nothing to Disclose Nasir M. Jaffer, MD, Toronto, ON (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Both continent and incontinent diversions are available for urinary reconstruction after radical cystectomy. Ileal conduit is a prototype of incontinent diversions. Continent diversions include cutaneous catheterizable reservoirs and orthotopic neobladder formation. Surgical techniques alter normal anatomy and make imaging interpretation challenging if radiologists are unfamiliar with these procedural details and postoperative imaging appearances. Imaging techniques including CT urogram, fluoroscopic loopogram and pouchography are used for routine follow up and tumor surveillance. Interventional radiological techniques like percutaneous nephrostomy and percutaneous ureteral stent placement are indispensible in the evaluation and treatment of urinary tract related complications. TABLE OF CONTENTS/OUTLINE Learning objectives Description and pictorial review of common surgical techniques Imaging techniques Imaging appearances with focus on understanding complex postoperative anatomy Postoperative complications I. Early (<30 days): Intestinal complications: Ileus, Obstruction, Fistulas, Ischemia Collections: Hematoma, Lymphocele, Abscess Anastomotic leak Urinary Obstruction II. Late (>30 days): Infection Lithiasis Hydronephrosis Herniation Conduit stenosis/stricture Tumoral Recurrence 6. Conclusion UR168-ED-X Adrenal Mass Imaging: A Pictorial Review All Day Location: GU/UR Community, Learning Center Awards Certificate of Merit Participants Masahiro Tanabe, MD, Ube, Japan (Presenter) Nothing to Disclose Takaaki Ueda, Ube, Japan (Abstract Co-Author) Nothing to Disclose Sei Nakao, Ube, Japan (Abstract Co-Author) Nothing to Disclose Keisuke Miyoshi, Ube, Japan (Abstract Co-Author) Nothing to Disclose Naofumi Matsunaga, MD, PhD, Ube, Japan (Abstract Co-Author) Nothing to Disclose TEACHING POINTS It is important that the radiologist be familiar with typical imaging features of adrenal masses and the imaging algorithm for adrenal lesion characterization not only to make the correct diagnosis, but also to avoid unnecessary examinations. The purpose of this exhibit is: 1.To understand an imaging algorithm for adrenal lesion characterization. 2.To review CT and MR imaging findings of adrenal masses. 3.To highlight key differential diagnostic points of imaging findings with pathologic correlation. TABLE OF CONTENTS/OUTLINE 1.Imaging algorithm for incidental adrenal lesion (tumor growth, CT densitometry, CT washouts, MR imaging)2.Characteristic findings• Common lesions (adrenal cortical adenoma, pheochromocytoma, metastasis)• Unusual benign lesions (myelolipoma, ganglioneuroma, schwannoma, hemangioma)• Unusual malignant lesions (adrenal cortical carcinoma, lymphoma, leiomyosarcoma) UR170-ED-X Preoperative Assessment of "Zero Ischemia" Robotic-assisted Partial Nephrectomy Should be Performed with "Kidney Friendly' CT: What Radiologists and Technicians Need to Know about the Low-Energy Low-Contrast Dose Renal CT All Day Location: GU/UR Community, Learning Center Awards Certificate of Merit Participants Satoru Takahashi, MD, Kobe, Japan (Presenter) Nothing to Disclose Yoshiko Ueno, MD, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Utaru Tanaka, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Yuko Suenaga, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Noriyuki Negi, RT, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Kiyosumi Kagawa, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Kazuro Sugimura, MD, PhD, Kobe, Japan (Abstract Co-Author) Research Grant, Toshiba Corporation Research Grant, Koninklijke Philips NV Research Grant, Bayer AG Research Grant, Eisai Co, Ltd Research Grant, DAIICHI SANKYO Group TEACHING POINTS Robotic partial nephrectomy can minimize ischemic damage to the kidney with super-selective renal artery clumping at the distal arterial branches. Low-energy contrast enhanced CT requires less contrast medium for the evaluation of both vessels and tumor. Because both procedures could reduce potential risk to renal function, low energy CT would be desirable for preoperative assessment of robotic-partial nephrectomy.The purpose of this exhibit is:1. To review the procedures of robotic partial nephrectomy and understand vital structures/anatomies for the pre-operative assessment2. To explain CT techniques to demonstrate the required anatomies3. To discuss the usefulness of low-energy CT, particularly 3rd generation dual-source CT, in the preoperative assessment4. To summarize the pros and cons of low-energy CT TABLE OF CONTENTS/OUTLINE Procedures of robotic partial nephrectomy -approach to the kidney -identification of tumor supplying arterial branchCT scanning technique - contrast injection - scan timing - image reconstructionPost processing -3D CTA -vessel tracking of tumor supplying branch -tumor segmentationPros and cons of low-energy CT -amount & rate of contrast injection -concentration of contrast medium -beam-hardening artifact -Iterative reconstruction UR171-ED-X Imaging Characteristics of Central Gland Neoplasms on Multiparametric 3 Tesla MRI of the Prostate All Day Location: GU/UR Community, Learning Center Participants Robert Villani, MD, Manhasset, NY (Presenter) Nothing to Disclose Eran Ben-Levi, MD, Roslyn, NY (Abstract Co-Author) Nothing to Disclose Ardeshir R. Rastinehad, DO, New Hyde Park, NY (Abstract Co-Author) Nothing to Disclose Pnina Herskovits, MD, Manhasset, NY (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1. The central gland of the prostate harbors at least 30% of all prostate gland malignancy. 2. Benign hypertrophic glandular and stromal nodules in the central gland may have many of the same characteristics as neoplasm in the peripheral zone. This results in either overcalling of lesions in the central gland or conversely passing by lesions believing them to be benign. 3. This exhibit will discuss the characteristics of both benign and malignant lesions in the central gland of the prostate with the aim of improving a reader's accurate detection of both. TABLE OF CONTENTS/OUTLINE Anatomy of the prostate gland. Pathophysiology of benign hyperplasia in the central glandReview of the common MRI appearance for benign central nodular hyperplasiaReview of the characteristic MRI appearance of malignant central gland lesions. Artifacts and pitfalls when evaluating 3T multiparimetric MRI prostate imaging of the central gland of the prostate.Management of suspicious findings in the central gland on MRI of the prostate gland UR172-ED-X Study in Contrasts: A Resident's Guide to Contrast Media and Managing Contrast Related Emergencies All Day Location: GU/UR Community, Learning Center Participants Evan Allgood, MD, Torrance, CA (Abstract Co-Author) Nothing to Disclose Jordan M. Anaokar, MD, Torrance, CA (Presenter) Nothing to Disclose TEACHING POINTS Radiology residents field questions related to the safety and appropriate use of intravenous contrast media and are often the first to responders to emergencies in the radiology suite. The aim of this presentation is to help residents identify patients at risk for adverse reactions to intravenous contrast, understand precautions that can be taken to minimize these risks, and prepare them for handling acute contrast reactions. TABLE OF CONTENTS/OUTLINE Risk factors for adverse events related to intravenous contrast media including allergy, renal insufficiency and other miscellaneous conditions Premedication strategies for patients with known contrast allergy Precautions for patients with renal insufficiency, including patients on acute or chronic hemodialysis, to avoid contrast-induced nephrotoxicity and nephrogenic systemic fibrosis Special considerations for women who are pregnant or breast feeding Common myths and misconceptions about intravenous contrast Treatment of mild, moderate and severe contrast allergies and their mimics Self assessment questions UR174-ED-X Imaging of Penile Implant: What Can Go Wrong? All Day Location: GU/UR Community, Learning Center Participants Mariana D. Silva, MD, Sao Paulo, Brazil (Presenter) Nothing to Disclose Aroldo H. Ban, MEd, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose Felipe R. Ferreira, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose Fernando I. Yamauchi, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Ronaldo H. Baroni, MD, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Although other imaging methods are sometimes used for the evaluation of penile prosthesis and other devices, MRI is the modality of choice for investigating malfunctioning or painful penile implants. The purpose of this exhibition is to review all imaging aspects of implants and their different subtypes, including malleable and inflatable models; present a selection of cases to illustrate all major complications such as migration, crossover, fracture, expelling, overlong prostheses and infection; and brief summary of penile implants safety on the MR environment. TABLE OF CONTENTS/OUTLINE . Description of all types of malleable and inflatable penile implants and their aspects on the different imaging modalities, with emphasis on MRI;. Review MRI protocols to investigate painful penile implants and mechanical failures;. Illustrate several cases of complications, including:1.migration;2.extrusion;3.fractures;4.overlong prosthesis;5.buckling;6.crossover;7.infection.8.fibrosis of the corpora cavernosum.. Summary of MRI safety of penile implants UR175-ED-X DWI and the Male Pelvis: What This Technique Can Show Us All Day Location: GU/UR Community, Learning Center Participants Edson D. Barbosa, Nova Iguacu, Brazil (Presenter) Nothing to Disclose Rachel F. Muffareg, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Felipe A. Mattos, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Romulo Varella, MD, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Gabriella M. Borges, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Leonardo K. Bittencourt, MD, PhD, Rio De Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose TEACHING POINTS - MRI is playing an increasingly important role in the avaliation of the diseases that compromise the male pelvis.- A DWI, in addition to being a rapid sequence and not needing the use of intravenous contrast, has become a useful and powerful tool, which has been expanding its borders and gaining new applicabilities, especially in the field of oncology, holding the promise for providing earlier cancer detection and evaluation of treatment response and providing important information in a noninvasive manner.- The objective of this study is to analyze and illustrate some applications that DWI plays in the male pelvis and show the most common pitfalls in the evaluation of the images, recalling also the principles of dwi and how to make the correct interpretation of this images. TABLE OF CONTENTS/OUTLINE - Review the tecniques aspects involving DWI- Demonstrate the increased conspicuity and definition of malignant focal lesions in the male pelvis, especially in the prostate- Predicting aggression, staging and evaluating response or tumor recurrence of cancers of the bladder, prostate, rectum and penile- Assisted in predicting which patients will have biochemical recurrence after radical prostatectomy- Identify pelvic lymph nodes- Evaluation of pelvic collections- New insights- Common pitfalls for DWI imaging in this anatomic region. UR176-ED-X Testicular Adrenal Rests Tumors: Imaging Appearance and Differential Diagnosis All Day Location: GU/UR Community, Learning Center Participants Sandra M. Tochetto, MD, Sao Paulo, Brazil (Presenter) Nothing to Disclose Osmar C. Saito, MD, PhD, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose Raquel A. Moreno, MD, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose Fernando L. Pereira, MD, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose Ronaldo H. Baroni, MD, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose Maria Cristina Chammas, MD, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The purpose of this educational exhibit is to:1-Review the embryological development of the male gonad and the adrenal gland;2Discuss the most common findings at US and MR imaging that can help to establish an accurate diagnosis;3-Report our experience with testicular adrenal rests tumors in patients with congenital adrenal hyperplasia;4-Discuss the differential diagnosis of a bilateral testicular lesion. TABLE OF CONTENTS/OUTLINE The adrenal glands and the gonads share a common embryological origin. During the embryological development, some cells destined to become adrenocortical cells may nestle within the descending gonad.Testicular adrenal rests tumors (TART) are benign lesions that develop due to overstimulation of this ectopic adrenal remnants within the testis. Imaging plays an important role in the detection and surveillance of testicular adrenal rest tumors. US and MR imaging features are characteristic in the context of elevated ACTH serum level (CAH). This exhibit will:1-Review the embryological development of the male gonad and the adrenal gland;2-Discuss the imaging findings (US and MR) of TART;3-Show examples of different presentations of TART with clinical correlation;4-Discuss the implication for male fertility;5-Discuss the most important differential diagnosis. UR177-ED-X MR Imaging of Male-to-Female Sex Reassignment Surgery: A Comprehensive Review of Expected Imaging Findings in the Normal Post Operative and Common Complications All Day Location: GU/UR Community, Learning Center Participants Marina A. Ferreira, Sao Paulo, Brazil (Presenter) Nothing to Disclose Felipe R. Ferreira, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose Aroldo H. Ban, MEd, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose Francisco T. Denes, PhD, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose Berenice B. Mendonca, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose Ronaldo H. Baroni, MD, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The purpose of this exhibition is: 1.Review and summarize the main surgical techniques in male-to-female sex reassignment surgery; 2.Review the role of magnetic ressonance (MR) in the post-operative and the main expected imaging findings; 3. Review and describe the most commons complications after the male-to-female sex reassignment surgery and their presentations on different imaging methods, focusing on magnetic ressonance (MR); 4.Present a sample of cases to illustrate normal expected findings and complications after surgery. TABLE OF CONTENTS/OUTLINE - Definition of transsexualism and its multidisciplinary approach and treatment modalities- The role of sex reassignment surgery for patients in current society- Male-to-female sex reassignment surgery: summarizing the main steps and objectives- Describe the expected imaging findings in the normal post-operative, focusing on MRI imaging (including a description of the suggested protocols)- Describe some of the most common complications after surgery and the imaging findings in those cases- Samples of cases to exemplify normal post-operative MRI findings and common complications UR178-ED-X Eureka! Urachal Abnormalities Made Simpler All Day Location: GU/UR Community, Learning Center Participants Carolina Parada, MD, Buenos Aires, Argentina (Presenter) Nothing to Disclose Sharon Z. Adam, MD, Chicago, IL (Abstract Co-Author) Nothing to Disclose Julie Sanders, MD, Shreveport, LA (Abstract Co-Author) Nothing to Disclose Paul Nikolaidis, MD, Chicago, IL (Abstract Co-Author) Nothing to Disclose Vahid Yaghmai, MD, Chicago, IL (Abstract Co-Author) Nothing to Disclose Frank H. Miller, MD, Chicago, IL (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Understanding the different urachal abnormalities is based on understanding the embryonal development Imaging features of the different abnormalities and the potential complications will be discussed TABLE OF CONTENTS/OUTLINE Embryonal development of the urachus Spectrum of urachal abnormalities including epidemiology Complications of urachal abnormalities Imaging appearance on sonography, CT and MRI of each abnormality - patent urachus, urachal cyst, urachal sinus and urachal diverticulum Imaging appearance on sonography, CT and MRI of associated complications - infection and carcinoma Mimickers of urachal abnormalities Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Frank H. Miller, MD - 2012 Honored Educator Frank H. Miller, MD - 2014 Honored Educator Vahid Yaghmai, MD - 2012 Honored Educator Vahid Yaghmai, MD - 2015 Honored Educator UR179-ED-X Multidetector CT Urography of 2015: Did the Current State of CTU Change? - Current Techniques, Clinical Utility and New Applications All Day Location: GU/UR Community, Learning Center Participants Yukiko Honda, MD, Hiroshima, Japan (Presenter) Nothing to Disclose Toru Higaki, PhD, Hiroshima, Japan (Abstract Co-Author) Nothing to Disclose Yoko Kaichi, Hiroshima, Japan (Abstract Co-Author) Nothing to Disclose Chihiro Tani, MD, Hiroshima, Japan (Abstract Co-Author) Nothing to Disclose Makoto Iida, Hiroshima, Japan (Abstract Co-Author) Nothing to Disclose Kazuo Awai, MD, Hiroshima, Japan (Abstract Co-Author) Research Grant, Toshiba Corporation; Research Grant, Hitachi, Ltd; Research Grant, Bayer AG; Reseach Grant, DAIICHI SANKYO Group; Medical Advisor, DAIICHI SANKYO Group; Research Grant, Eisai Co, Ltd; Research Grant, Nemoto-Kyourindo; ; ; ; ; TEACHING POINTS We focus on matters which have changed for these several years about CTU. First, we describe a current CTU method and various guidelines critically. Second, we show the diagnostic capability of CTU when considering an exposed problem. Third, we introduce urothelial carcinoma(UC) staging criteria and pitfall with indicating several actual cases. We also make a clear when we should perform MR for detecting UC. Finally, we introduce and suggest new CT technologies and future perspective of CTU. TABLE OF CONTENTS/OUTLINE Critically review various multidetector CT urography (CTU) protocols and guidelines The current diagnostic capability of CTU when considering an exposed problem Staging of urothelial carcinoma by using CT and pitfall When should we perform MR? New technologies for CTU and future perspective of CTU UR180-ED-X Radiological Findings of the Normal and Pathologic Perirenal Space All Day Location: GU/UR Community, Learning Center Participants Jose A. Jimenez Lasanta SR, MD, Cerdanyola del Valles, Spain (Presenter) Nothing to Disclose Erika Normantas, Badalona, Spain (Abstract Co-Author) Nothing to Disclose Monse Tenesa, Badalona, Spain (Abstract Co-Author) Nothing to Disclose Eva Barluenga, Badalona, Spain (Abstract Co-Author) Nothing to Disclose Jordi Bechini, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1.-.To describe the normal anatomy of the perirenal space.2.- To present the radiologic features of perirenal space, its main relationships and boundaries.3-. To show the pathological processes that may involve this space4.- To compare the various imaging techniques used in the evaluation of this anatomical region. TABLE OF CONTENTS/OUTLINE A detailed anatomic and pathological review of the perirenal space will be presented. Conditions to be considered are classified as,A. Inflammatory and infectious processes and collections: 1-pyelonephritis - abscess renal, •2. Xanthogranulomatous pyelonephritis, •3. Emphysematous pyelonephritis, •4. Pancreatitis, •5.Post-renal biopsy hematoma, •6. Post-renal trasnplantation hematoma.B. Neoplastic-paraneoplastic conditions: •1.Splenic angiosarcoma splenic, 2.Renal angiomyolipoma, •3. Renal cystic tumor with solid area with enhancement, •4 Retroperitoneal mixoid liposarcoma, •5.Changes after tumor radiofrequency in perirenal space, •6. Lymphoma with renal-perirrenal and mesenteric involvement (with PET-CT), •8. Splenic metastatic adenocarcinoma with perirenal extension, 8. Neuroblastoma with perirenal invasion, •10. Erdhein-Chester disease, •11. Renal Lymphangiectasia UR181-ED-X If It Aint broke, Don't Fix It. 'Utility of Ultrasound in Evaluation of Penile Pathology: A Pictorial Essay and Review of Literature.' All Day Location: GU/UR Community, Learning Center Participants Artur Velcani, MD, Fairfield, CT (Abstract Co-Author) Nothing to Disclose Jonathan R. Weisiger, MD, New Haven, CT (Presenter) Nothing to Disclose TEACHING POINTS 1. Provide basic understanding of the role of US in evaluation of the penis. Review of normal sonographic appearance of the penile soft tissue and vasculature 2. Review non traumatic and traumatic penile pathologies while utilizing ultrasound imaging. 3. Discuss clinical significance and management for each case. TABLE OF CONTENTS/OUTLINE Introduction General anatomy of the penile soft tissue. Review of normal US evaluation of penile vasculature and functional change Most commonly encountered penile pathology: Vascular related abnormalities. Erectile dysfunction a- Normal parameters of penile Dopplerb- Papaverine injection examination with duplex dopplerc- Pre/post injection evaluation of penale blood flow. 2. Priapism aSlow flow and high flow variants.b- Arterial - arterial fistulac- Penile vein thrombosisd- Venous insufficiencye- Venous varixfPseudoaneurysm pre / post embolization Traumaa- Penile/corpus cavernous fracture Infectious a- Cellulitis b- Abscess OtheraPeyronie's disease UR182-ED-X Contrast-enhanced Ultrasound in Urology All Day Location: GU/UR Community, Learning Center Participants Nagaaki Marugami, Kashihara, Japan (Presenter) Nothing to Disclose Toshiko Hirai, MD, Kashihara, Japan (Abstract Co-Author) Nothing to Disclose Junko Takahama, MD, Kashihara, Japan (Abstract Co-Author) Nothing to Disclose Aki Takahashi, MD, Kashihara, Japan (Abstract Co-Author) Nothing to Disclose Kimihiko Kichikawa, MD, Kashihara, Japan (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1) To understand the principle of contrast-enhanced ultrasound (CE-US) compared with contrast-enhanced CT or MRI. 2) To demonstrate the utility of CE-US in diagnosis of urologic disorders compared with multimodality imaging. TABLE OF CONTENTS/OUTLINE 1, Introduction: the development of contrast medica of ultrasound, the principle of CE-US.2, Case presentations 1) Kidney: Renal infarction, Renal cell carcinoma (clear cell RCC, papillary RCC, cystic RCC), Renal oncocytoma, Renal AML, Complicated cysts, etc. 2) Testis: segmental testicular infarction, testicular torsion, testicular abscess, testicular trauma (hemorrhage),3, Discussion4, Summary: contrast-enhanced US can demonstrate high accuracy in the diagnosis of urologic disorders. UR183-ED-X Congenital Abnormalities of Kidney and Ureter: Embryology, Pathophysiology and Imaging with Emphasis on Role of Fetal MRI All Day Location: GU/UR Community, Learning Center Awards Certificate of Merit Participants Jignesh N. Shah, MD, Memphis, TN (Presenter) Nothing to Disclose Saurabh Gupta, MD, Milwaukee, WI (Abstract Co-Author) Nothing to Disclose Harris L. Cohen, MD, Memphis, TN (Abstract Co-Author) Nothing to Disclose TEACHING POINTS • To review embryogenesis of kidneys and ureters and correlate the aberrant embryological pathways with anatomy of congenital renal and ureteric anomalies.• To review imaging findings of a wide spectrum of congenital renal and ureteric abnormalities with emphasis on role of fetal MRI.• To discuss the implications of imaging on management. TABLE OF CONTENTS/OUTLINE Normal embryogenesis of kidneys and ureters; Embryological basis of congenital renal and ureteric abnormalities including renal agenesis, renal ectopia, fusion and rotational abnormalities of kidneys, supernumery kidney, cystic renal disease (ADPKD, ARPKD, MCDK), congenital renal neoplasms (mesoblastic nephroma, wilm's tumor, rhabdoid tumor, clear cell sarcoma), retrocaval ureter, primary megaloureter, duplication of ureter, ectopic ureteric orifice, vesicoureteral reflux; Imaging findings of a wide spectrum of congenital renal and ureteric anomalies with emphasis on role of fetal MRI. Discuss implications of imaging on management. UR184-ED-X Genitourinary and Retroperitoneal Findings in 3 Neurocutaneous Syndromes: Tuberous Sclerosis, Neurofibromatosis, and Von Hippel-Lindau Disease All Day Location: GU/UR Community, Learning Center Participants Katryana M. Hanley-Knutson, MD, Winston Salem, NC (Presenter) Nothing to Disclose George Athanasatos, MD, Winston Salem, NC (Abstract Co-Author) Nothing to Disclose Raymond B. Dyer, MD, Winston Salem, NC (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Identify the common and uncommon genitourinary and retroperitoneal radiographic manifestations of the presented neurocutaneous syndromes. Understand the similarities and differences of the genitourinary and retroperitoneal manifestations of the presented neurocutaneous syndromes. TABLE OF CONTENTS/OUTLINE Tuberous Sclerosis Angiomyolipomas (AML) Renal cysts Renal cell carcinomas (RCC) Retroperitoneal lymphangiomyomatosis (LAM)Neurofibromatosis-1 (NF-1) Retroperitoneal plexiform neurofibromas Renal artery stenosis PheochromocytomasVon HippelLindau Disease Renal cysts Renal cell carcinomas Pheochromocytomas Papillary cystadenomas of the epididymis and broad ligament UR186-ED-X The Good, Bad and Ugly: Cross-Sectional Imaging Spectrum of Fat Containing Genitourinary Lesions and Clinical Implications All Day Location: GU/UR Community, Learning Center Participants Yun S. Xie, MD, San Antonio, TX (Abstract Co-Author) Nothing to Disclose Ameya J. Baxi, MBBS, DMRD, San Antonio, TX (Abstract Co-Author) Nothing to Disclose Amol S. Katkar, MD, San Antonio, CO (Abstract Co-Author) Nothing to Disclose Arpit M. Nagar, MBBS, Columbus, OH (Abstract Co-Author) Nothing to Disclose Vijayanadh Ojili, MD, San Antonio, TX (Presenter) Nothing to Disclose TEACHING POINTS 1. To describe the cross-sectional imaging findings of fat containing genitourinary lesions and discuss the clinical implications of specific imaging findings.2. To discuss the complications encountered with the fat containing lesions, role of imaging in detecting these complications and image-guided interventions in the management of these patients. TABLE OF CONTENTS/OUTLINE 1. Introduction, etiopathogenesis and clinical presentation of fat containing genitourinary lesions.2. Role of cross-sectional imaging modalities (particularly CT).3. Imaging spectrum of fat containing genitourinary lesions (adrenal adenoma, adrenal myelolipoma, renal AML, renal liopma, clear cell RCC, bladder lipoma, ovarian teratoma, uterine lipoleiomyoma, extra-medullary hematopoiesis etc). ED006-SU Genitourinary Sunday Case of the Day Sunday, Nov. 29 8:00AM - 11:59PM Location: Case of Day, Learning Center GU AMA PRA Category 1 Credit ™: .50 Participants Theodora A. Potretzke, MD, Saint Louis, MO (Presenter) Nothing to Disclose Perry J. Pickhardt, MD, Madison, WI (Abstract Co-Author) Co-founder, VirtuoCTC, LLC; Stockholder, Cellectar Biosciences, Inc; Research Consultant, Bracco Group; Research Consultant, KIT ; Research Grant, Koninklijke Philips NV Naoki Takahashi, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Meghan G. Lubner, MD, Madison, WI (Abstract Co-Author) Grant, General Electric Company; Grant, NeuWave Medical, Inc; Grant, Koninklijke Philips NV Anup S. Shetty, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Richard Tsai, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose George A. Carberry, MD, Madison, WI (Abstract Co-Author) Nothing to Disclose Vincent M. Mellnick, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose David U. Kim, MD, Madison, WI (Abstract Co-Author) Nothing to Disclose Yaseen Oweis, MD, MBA, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Zachary J. Viets, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Bernard F. King JR, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1) Recognize imaging findings seen in disorders of the genitourinary systems. 2) Develop differential diagnosis based on the clinical information and imaging findings. 3) Recognize the clinical importance of diagnosis. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Perry J. Pickhardt, MD - 2014 Honored Educator Naoki Takahashi, MD - 2012 Honored Educator Meghan G. Lubner, MD - 2014 Honored Educator Meghan G. Lubner, MD - 2015 Honored Educator SSA09 Genitourinary (New Technologies for Imaging the Genitourinary Tract) Sunday, Nov. 29 10:45AM - 12:15PM Location: E351 GU BQ MR US AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 FDA Discussions may include off-label uses. Participants Julia R. Fielding, MD, Chapel Hill, NC (Moderator) Nothing to Disclose Erick M. Remer, MD, Cleveland, OH (Moderator) Nothing to Disclose Sub-Events SSA09-01 Simultaneous Conventional Dynamic MR Urography and High Temporal Resolution Perfusion MRI of Bladder Tumors Using a Novel Free-Breathing Golden-Angle Radial Compressed-Sensing Sequence Sunday, Nov. 29 10:45AM - 10:55AM Location: E351 Participants Nainesh Parikh, MD, New York, NY (Presenter) Nothing to Disclose Justin M. Ream, MD, Ann Arbor, MI (Abstract Co-Author) Nothing to Disclose Hoi Cheung Zhang, New York, NY (Abstract Co-Author) Nothing to Disclose Kai Tobias Block, PhD, New York, NY (Abstract Co-Author) Royalties, Siemens AG; Hersh Chandarana, MD, New York, NY (Abstract Co-Author) Equipment support, Siemens AG; Software support, Siemens AG; Consultant, Bayer, AG; Andrew B. Rosenkrantz, MD, New York, NY (Abstract Co-Author) Nothing to Disclose PURPOSE To investigate the feasibility of simultaneous conventional dynamic MR urography (MRU) and high temporal resolution perfusion MRI of bladder tumors using a novel free-breathing golden-angle radial acquisition scheme with compressed sensing reconstruction METHOD AND MATERIALS 22 patients with bladder lesions underwent MRU using the GRASP (Golden-angle RAdial Sparse Parallel) technique. Following contrast injection, GRASP was performed of the abdomen and pelvis during free breathing (voxel size 1.4x1.4x3.0 mm, 1,000 radial spokes, acquisition time 3:44 min). Two dynamic data-sets were retrospectively reconstructed from this single acquisition by combining a distinct number of spokes into each dynamic frame: 110 spokes per frame to provide a resolution of approximately 30 seconds, serving as conventional MRU for clinical interpretation, and 8 spokes per frame to provide 2 second resolution images for quantitative perfusion. Using the 2 second resolution images, ROIs were placed within the bladder lesion and normal bladder wall for all patients, an arterial input function was generated from the femoral artery, and the GKM perfusion model was applied. RESULTS Follow-up cystoscopy and biopsy demonstrated 16 bladder tumors (13 stage≥T2, 3 stage≤T1) and 6 benign lesions. All lesions were well visualized using the conventional 25 second clinical dynamic images. Based on the 2 second resolution images, Ktrans was significantly higher in bladder tumors (0.38±0.24) than in either normal bladder wall (0.12±8, p<0.001) or in benign bladder lesions (0.15±0.04, p=0.033). The ratio between Ktrans of the lesion and of normal bladder wall in each patient was nearly double in tumors than in benign lesions (4.3±3.4 vs. 2.2±1.6), and Ktrans was nearly double in stage≥T2 tumors than in stage≤T1 tumors (0.44±0.24 vs. 0.24±0.24), although these did not approach significance (p=0.180-0.209), likely related to small sample size. CONCLUSION GRASP DCE-MRI provides simultaneous conventional dynamic MRU and high temporal resolution perfusion MRI of bladder tumors. Quantitative evaluation of bladder lesions based on the 2 second temporal resolution reconstructions showed associations with pathologic findings in our preliminary cohort. CLINICAL RELEVANCE/APPLICATION The novel GRASP sequence allows quantitative perfusion evaluation of bladder lesions within the context of a clinical MRU examination using a single contrast injection and without additional scan time. SSA09-02 Magnetic Resonance Fingerprinting in Diagnosis of Prostate Cancer: Initial Experience Sunday, Nov. 29 10:55AM - 11:05AM Location: E351 Participants Shivani Pahwa, MD, Clevelnad, OH (Presenter) Nothing to Disclose Chaitra A. Badve, MD, MBBS, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Yun Jiang, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Alice Yu, BS, MS, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Mark D. Schluchter, PhD, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Mark A. Griswold, PhD, Cleveland, OH (Abstract Co-Author) Research support, Siemens AG Royalties, Siemens AG Royalties, General Electric Company Royalties, Bruker Corporation Contract, Siemens AG Lee E. Ponsky, MD, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Vikas Gulani, MD, PhD, Ann Arbor, MI (Abstract Co-Author) Research support, Siemens AG PURPOSE To describe initial experience in detecting prostate cancer (PCa) using quantitative MRI parameters - T1 and T2 relaxation times To describe initial experience in detecting prostate cancer (PCa) using quantitative MRI parameters - T1 and T2 relaxation times derived from magnetic resonance fingerprinting (MRF-FISP), in combination with conventional ADC maps. METHOD AND MATERIALS 63 patients with clinical suspicion of prostate cancer were imaged on 3T Siemens Skyra /Verio scanners. MRF has been shown to measure T1 and T2 relaxation times with high accuracy and precision2. In addition tothe standard multiparametric MRI exam, MRFFISP was acquired (slice thickness: 6 mm, in-plane resolution:1×1 mm2,FOV:400 mm, TR:11-13 ms, flip angle:5-75 deg, duration:50s per slice).b-valuesfor DWI were0, 500, 1000 s/mm2.T1, T2 maps were generated from MRF-FISP dataand regions of interest (ROI)were drawn on T1, T2 and ADC maps in areas suspicious for cancer identified based on PIRADS score, and normal peripheral zone (NPZ). Matched pairs t-tests were used to compare T1, T2, ADC values in biopsy provenPCa and NPZ. Logistic regression model was applied to these parameters in differentiating PCa from NPZ. Receiver operating characteristic (ROC) analysis was performed for the parameters singly and in combination and area under the curve (AUC) was calculated RESULTS 29 patients were diagnosed with cancer on transrectal biopsy. T1, T2, ADC values were significantly lower in cancer compared to NPZ (p<0.0001). Mean T1, T2, ADC for prostate cancer were 1413±60ms, 66±3ms, 745±54 x 10-6mm2/s, respectively. For NPZ, these values were 2058±77ms, 165±8ms, 1736±37 x 10-6mm2/s.The AUC for T1, T2, ADC values in separating PCa from NPZ was 0.978, 0.982, 0.801, respectively. The combination of T2 and ADC produced the most complete separation between cancer and normal tissues, resulting in AUC of 0.995. CONCLUSION MRF-FISP is a novel relaxometry sequence that allows quantitative examination of prostate in a clinical setting. The T1 and T2 relaxation times so obtained, in combination with ADC values show promising results in detecting prostate cancer. CLINICAL RELEVANCE/APPLICATION Quantitative MR parameters can help identify prostate cancer non-invasively. This could have broad applications in diagnosis, guiding biopsy, and following treatment SSA09-03 Contrast-enhanced Ultrasound for Renal Mass Characterization: Comparison of Low MI Timeintensity Curves and Destruction Reperfusion Techniques Sunday, Nov. 29 11:05AM - 11:15AM Location: E351 Participants Wui K. Chong, MD, Chapel Hill, NC (Presenter) Nothing to Disclose Emily Chang, MD, Chapel Hill, NC (Abstract Co-Author) Nothing to Disclose Sandeep Kasoji, Chapel Hill, NC (Abstract Co-Author) Nothing to Disclose Paul Dayton, PhD, Chapel Hill, NC (Abstract Co-Author) Co-founder, SonoVol LLC; Board Member, SonoVol LLC Ersan Altun, MD, Istanbul, Turkey (Abstract Co-Author) Nothing to Disclose Julia R. Fielding, MD, Chapel Hill, NC (Abstract Co-Author) Nothing to Disclose Kevin O. Herman, MD, Raleigh, NC (Abstract Co-Author) Nothing to Disclose W K. Rathmell, Chapel Hill, NC (Abstract Co-Author) Research support, GlaxoSmithKline plc Lee Mullin, PhD, Chapel Hill, NC (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate contrast enhanced US (CEUS) for renal mass characterization in chronic renal insufficiency (CRI), comparing nondestructive (low MI) and destruction-reperfusion techniques. METHOD AND MATERIALS Prospective study comparing 48 subjects: 24 with normal function and renal masses scheduled for excision; 24 with CRI and indeterminate renal lesions on non-contrast US/CT.CEUS was performed on an Acuson Sequoia with CPS software. Perflutren (Definity) 1.3ml was administered IV. Lesions were imaged at a low MI of 0.2. A 3 minute videoclip was recorded. Time Intensity curves (TICs) of the lesion and adjacent parenchyma were generated. After 30 minutes, a 2nd dose of Definity was given and a Destruction Reperfusion (DR) sequence performed on the same lesion. DR was performed under an IND exemption from the FDA. Bubble destruction was performed at an MI of 0.9. Reperfusion images were obtained using Motion Stabilized Persistence software (Siemens). A color-coded parametric map quantifying arrival time was generated in which Green=faster arrival, Red=slower, Black=no contrast. (Arrow=Bosniak IV mass).Reference standard was pathology, contrast CT/MR or absence of change on follow up imaging for benign lesions. Two blinded readers reviewed the low MI images and classified the lesions using Bosniak criteria. RESULTS Lesion size ranged from 1.7-7.6cm (mean 3.5cm). Histopathology of resected masses showed no cavitation or cellular injury from high MI of DR. DR arrival times correlated with low MI TIC parameters. Sensitivity for distinguishing Bosniak I/II/IIF from III and higher was: Reader 1-96%, Reader 2-100%. Specificity was 78% and 63%. Specificity is lower because CEUS detects smaller amounts of contrast than CT/MR, leading to 'overstaging' with standard Bosniak. Reduced time to peak and arrival time (p<0.05) was seen in the parenchyma of CRI subjects compared to parenchyma of those with normal renal function. CONCLUSION CEUS can characterize renal lesions, but Bosniak criteria must be modified because US is more sensitive to slight enhancement. DR does not cause tissue injury, correlates with low MI findings, and takes less time. The parenchyma in CRI showed reduced/ delayed contrast uptake, suggesting CEUS may also be useful for renal functional imaging. CLINICAL RELEVANCE/APPLICATION CEUS can evaluate indeterminate renal lesions and renal function in CRI, a population where CT and MR contrast are contraindicated. SSA09-04 ARFI Evaluation of Small (<4 cm) Renal Masses. A Preliminary Study Sunday, Nov. 29 11:15AM - 11:25AM Location: E351 Participants Costanza Bruno, Verona, Italy (Abstract Co-Author) Nothing to Disclose Alessandra Bucci, MD, Verona, Italy (Presenter) Nothing to Disclose Matteo Brunelli, PhD, Verona, Italy (Abstract Co-Author) Nothing to Disclose Salvatore Minniti, MD, Verona, Italy (Abstract Co-Author) Nothing to Disclose Chiara Dalla Serra, Verona, Italy (Abstract Co-Author) Nothing to Disclose Roberto Pozzi Mucelli, Verona, Italy (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate if ARFI can be a reliable technique in distinguish ccRCCS from other solid and fluid-containing small renal masses. METHOD AND MATERIALS 31 small (<4 cm) renal masses (27 were solid - 17/27 ccRCCs, 3/27 papillary RCCs, 2/27 chromophobe RCCs, 4 oncocytomas and 1 angiomyolipoma - and 4 were cysts) were prospectively evaluated using US and ARFI. Each lesion was assigned an ARFI value obtained from the average of 12 measurements.All the solid masses underwent resection; all the cystic lesions were Bosniak 2, so were evaluated with follow up.The difference existing between the two groups was evaluated by means of Student's t test.A cut off value was determined to distinguish between ccRCCs and other lesions and sensibility, specificity, PPV, NPV and accuracy were determined. RESULTS ccRCCs are characterized by an higher ARFI value and - when compared with all the other lesions - the difference existing between the two groups was statistically significant (p<0.001). Considering a cut off value of 1.95 m/sec sensibility, specificity, PPV, NPV and accuracy were respectively 94.1%, 78.6%, 84.2%, 91.7% and 87.1%. CONCLUSION ccRCC is characterized by an higher ARFI value which can be used to distinguish it from other solid and fluid containing masses. CLINICAL RELEVANCE/APPLICATION ARFI can be an useful tool in the evaluation of small renal masses, helping distinguish cc RCCs from other lesions. SSA09-05 Fusion Imaging of (Contrast-enhanced) Ultrasound with CT or MRI for Kidney Lesions Sunday, Nov. 29 11:25AM - 11:35AM Location: E351 Participants Thomas Auer, Innsbruck, Austria (Abstract Co-Author) Nothing to Disclose Tobias De Zordo, MD, Innsbruck, Austria (Presenter) Nothing to Disclose Daniel Junker, Innsbruck, Austria (Abstract Co-Author) Nothing to Disclose Isabel M. Heidegger, Innsbruck, Austria (Abstract Co-Author) Nothing to Disclose Werner R. Jaschke, MD, PhD, Innsbruck, Austria (Abstract Co-Author) Nothing to Disclose Friedrich H. Aigner, MD, Innsbruck, Austria (Abstract Co-Author) Nothing to Disclose PURPOSE The aim of the study was to evaluate the feasibility of fusion imaging (FI) of (contrast-enhanced) ultrasound (CEUS) with CT/MRI in localization of sonographically challenging kidney lesions and usefulness for assessment of indeterminate kidney lesions METHOD AND MATERIALS From March 2013 to January 2014, 30 consecutive patients were included in this retrospective studyAll patients presented with previously in CT/MRI detected indeterminate kidney lesions that were either not detectable or hard to distinguish in conventional gray-scale ultrasoundIn these patients additional FI was performed by fusion of ultrasound with CT/MRI datasets. In 26 (86.7%) of these patients FI and CEUS was simultaneously conducted RESULTS FI could be performed in all of the 30 patientsFI-indication: In 18 of 30 patients (60%) FI was performed because a lesion of interest could not clearly be allocated due to multiple and directly adjacent similar lesions within one kidney. In 12 of 30 patients (40%) the kidney lesions were solitary or at least isolated but could not be detected with gray-scale US alone.CEUS-indication: Insufficient CT protocol (without NECT) and a not-water-isodens lesion (>20 HU ) in 8 (30.8%) patients borderline CE in CT (10HU20HU) in 11 (42.3%) patients non-conclusive CT/MRI studies in 5 (19.2%) patients CEUS for follow-up in 2 (7.7%) patients.Combined FI-CEUS: FI-CEUS could clearly differentiate between a surgical and non-surgical finding in 24 (80%) of 30 patients In 2 (6.7%) of 30 patients with conducted FI-CEUS lesions remained indeterminateFinal dignosis: Histology revealed a surgical lesion in 6 (20%) patients, while in 18 (60%) patients a non-surgical lesion such as BII/BIIF cysts, abscess formations, cicatricial tissue and a pseudotumor could be found. FI-CEUS didn't determine a final diagnosis in 2 patients (6.7%) In one elderly patient (3.3%) FI was conducted without CEUS because only size control of was demanded In 3 (10%) patients kidney lesions were not confidently detected with FI due to general US limitations CONCLUSION Our data suggest that FI of the kidney is a feasible examination regarding the localization and further assessment of indeterminate kidney lesions. CLINICAL RELEVANCE/APPLICATION The combination of FI with a synchronous CEUS examination can clarify indeterminate renal CT or MRI findings, reduce radiation exposure and is cost effective. SSA09-06 Optimal Energy for Kidney Parenchymal Visualization in Monoenergetic Images Generated from Dual Energy CT Sunday, Nov. 29 11:35AM - 11:45AM Location: E351 Participants Jason DiPoce, MD, Jerusalem, Israel (Presenter) Nothing to Disclose Zimam Romman, Haifa, Israel (Abstract Co-Author) Employee, Koninklijke Philips NV Jacob Sosna, MD, Jerusalem, Israel (Abstract Co-Author) Consultant, ActiViews Ltd Research Grant, Koninklijke Philips NV PURPOSE To evaluate image quality of kidney parenchyma in a spectrum of CT monoenergy levels and to select the optimal Monoenergy levels for visualization. METHOD AND MATERIALS IRB approval was obtained. 30-corticomedullary phase, IV contrast-enhanced CT abdomen scans (18 males, 12 females, mean age of 50 years) were evaluated. In each scan, kidney parenchyma (60 regions) was assessed. The scans were obtained from a 64slice spectral detector CT prototype (Philips Healthcare, Cleveland, OH, USA) at 120 kVp with an average of 150 mAs. For each scan, simultaneous conventional polyenergetic and monoenergetic image datasets at 50, 60, 70, 100, and 140 keV were reconstructed. Two experienced radiologists analyzed subjectively in consensus visualization of the kidney parenchyma and selected the optimal visualization dataset based on the conspicuity of the cortex and medulla and compared to the conventional images. Objective kidney signal-to-noise ratio (SNR) in the optimal monoenergy images was measured and compared to data from the conventional CT images. RESULTS Optimal image quality for kidney visualization was subjectively selected with 60 - 70 keV monoenergy images and was judged to be better than the conventional dataset. The kidney SNR values in optimal monoenergy were highly significantly different (p<0.01) from conventional CT images. Average SNR was 10.9 and 16.3 in the conventional and optimal monoenergy respectively. CONCLUSION Optimal visualization of the kidney parenchyma on dual energy CT images is achieved with monoenergy image reconstruction at 60 70 keV based on both subjective and objective assessments and seems to improve image quality compared to conventional images. CLINICAL RELEVANCE/APPLICATION Optimal image quality in monoenergy images may be supplemental to conventional polyenergetic images and potentially increase the diagnostic yield. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Jason DiPoce, MD - 2013 Honored Educator Jacob Sosna, MD - 2012 Honored Educator SSA09-07 The Use of New Tissue Strain Analytics Measurement in Testicular Lesions Sunday, Nov. 29 11:45AM - 11:55AM Location: E351 Participants Dirk-Andre Clevert, MD, Munich, Germany (Presenter) Speaker, Siemens AG; Speaker, Koninklijke Philips NV; Speaker, Bracco Group; Matthias Trottmann, Munich, Germany (Abstract Co-Author) Nothing to Disclose Julian Marcon, Munich, Germany (Abstract Co-Author) Nothing to Disclose Melvin D'Anastasi, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Alexander Karl, Munich, Germany (Abstract Co-Author) Nothing to Disclose Maximilian F. Reiser, MD, Munich, Germany (Abstract Co-Author) Nothing to Disclose PURPOSE Virtual touch tissue imaging quantification (VTIQ) is a newly developed technique for the sonographic quantification of tissue elasticity. It has been used in the assessment of breast lesions. The purpose of this study was to determine the diagnostic performance of VTIQ in unclear testicular lesions. METHOD AND MATERIALS Twenty patients with known testicular pathology underwent conventional B-mode sonography with additional VTIQ of the testicular lesions using a Siemens Acuson S2000™ and S3000™ (Siemens Medical Solutions, Mountain View, CA, USA) system. Tissue mechanical properties were interpreted and compared in the VTIQ examination. The pathologic diagnosis was established after surgery or in the follow up examination in highly suspicious of benign lesions. RESULTS Over 36 months, 22 focal testicular lesions (median lesion size, 18 mm; range, 4-36 mm in 20 patients (median age, 43 years; range, 22-81 years) were examined. Lesions were hyperechoic (n = 1), hypoechoic (n = 14), isoechoic (n = 1), mixed echogenicity (n = 3) or anechoic (n = 3). Histological examination showed one benign lesion (6.25 %) with a mean size of 7 mm and 15 malignant lesions (93.75 %) with a mean size of 20 mm. The value of the shear wave velocity in normal testis tissue showed a mean shear wave velocity of 1.17 m/s. No value of the shear wave velocity could the measured in cystic lesions. The rest of the benign lesions showed a mean shear wave velocity of 2.37 m/s. The value of the shear wave velocity in germ cell tumours showed a mean shear wave velocity of 1.94 m/s and for seminoma it showed a mean shear wave velocity of 2.42 m/s. CONCLUSION VTIQ is a reliable new method for measuring qualitative and quantitative stiffness of testis lesions and tissue. The qualitative shear- wave elastography features were highly reproducible and showed good diagnostic performance in unclear testicular lesions. The VTIQ technique is a useful in assessing small testicular nodules and pseudo lesions. CLINICAL RELEVANCE/APPLICATION VTIQ is a reliable user independent new method for measuring qualitative and quantitative stiffness of different testis lesions and tissue. The VTIQ technique allows to distinguished different testis lesions and pseudo lesions. SSA09-08 One-stop-shot MRI for Infertility Evaluation: Comparison with US and CT-HSG Sunday, Nov. 29 11:55AM - 12:05PM Location: E351 Participants Javier Vallejos, MD, MBA, Vicente Lopez, Argentina (Abstract Co-Author) Nothing to Disclose Jimena B. Carpio, MD, Buenos Aires, Argentina (Presenter) Nothing to Disclose Ezequiel Salas, MD, Buenos Aires, Argentina (Abstract Co-Author) Nothing to Disclose Carlos Capunay, MD, Buenos Aires, Argentina (Abstract Co-Author) Nothing to Disclose Mariano Baronio, Buenos Aires, Argentina (Abstract Co-Author) Nothing to Disclose Patricia M. Carrascosa, MD, Buenos Aires, Argentina (Abstract Co-Author) Research Consultant, General Electric Company Lorena I. Sarati, Vicente Lopez, Argentina (Abstract Co-Author) Nothing to Disclose PURPOSE Demonstrate the utility of MRI-HSG in the diagnosis of infertility, can through this method show uterine, tubal, ovarian and pelvic causes. METHOD AND MATERIALS 14 patients between 31 and 41 year-old diagnosed with infertility were studied. We performed a transvaginal ultrasound, virtual CTHSG and MRI- HSG at the same day. MRI protocol include high-resolution T2 sequences, fat-suppressed T1, diffusion weighted imaging and contrast dynamic sequence (3D time-resolved imaging of contrast kinetics [TRICKS]). A contrast dilution of saline, iodine and gadolinium was instilled. Antral follicle counts, endometrial cavity findings, uterine wall pathology, tubal patency, and pelvic cavity findings were assessed with modalities. RESULTS In all cases it was observed more ovarian follicles on MRI-HSG than in US. In 65% of patients, Fallopian tubes were visualized completely with MRI-HSG, whereas in the remaining 35% only look at its distal portion. In all cases was demonstrated tubal patency with free peritoneal spillage. In 45% of patients, MRI-HSG showed endoluminal lesions, likes polyps and miomas, that were corroborated with CT-HSG. In 14% of patients, MRI-HSG detected endometrial implants in pelvic cavity that could not be corroborated by the other methods. CONCLUSION MRI-HSG allows a comprehensive evaluation for infertility diagnosis, with visualization and quantification of antral follicles, endometrial cavity, uterine wall and fallopian tubes as well as pelvic cavity findings such as endometrial implants. CLINICAL RELEVANCE/APPLICATION MRI techniques could be combined with HSG procedure in order to enables a one-step-shot imaging for evaluation of female infertility with the advantages of causing less pain and avoidance of exposure to ionizing radiation. SSA09-09 4D Ultrasound Cistoscopy with Fly through in the Evaluation of Urinary Bladder Tumors Preliminary Experience Sunday, Nov. 29 12:05PM - 12:15PM Location: E351 Participants Vito Cantisani, MD, Roma, Italy (Abstract Co-Author) Speaker, Toshiba Corporation; Speaker, Bracco Group; Speaker, Samsung Electronics Co, Ltd; Nicola Di Leo, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Valerio Forte, MD, Rome, Italy (Presenter) Nothing to Disclose Flavio Malpassini, Rome, Italy (Abstract Co-Author) Nothing to Disclose Mauro Ciccariello, Rome, Italy (Abstract Co-Author) Nothing to Disclose Francesco Flammia, Rome, Italy (Abstract Co-Author) Nothing to Disclose Francesco M. Drudi, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Carlo Catalano, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Federica Flammia, Roma, Italy (Abstract Co-Author) Nothing to Disclose Giuseppe Schillizzi, Roma, Italy (Abstract Co-Author) Nothing to Disclose Ferdinando D'Ambrosio, Rome, Italy (Abstract Co-Author) Nothing to Disclose PURPOSE To assess the feasibility and diagnostic efficacy 4D Ultrasound cystoscopy with Fly through as compared with trasditional cystoscopy in evaluating Urinary Bladder tumors. METHOD AND MATERIALS 30 consecutive patients with previous detected urinary bladder lesions at cystoscopy were prospectively evaluated with 2D baseline US, and 4D Ultrasound with fly through (US virtual navigation system) by an expert radiologist blinded to cystoscopy results. The two imaging modalities were compared with cystoscopy and surgical results (N=8 patients) in order to assess the sensitivity and specificity in tumor detection and characterization. The diagnostic performance of 2D features and 4D ultrasound were estimated and compared using ROC curve analysis. RESULTS 24/33 and 31/33 urinary bladder lesions were detected by 2 D US and 4 D Ultrasound respectively. The latter was also able to 24/33 and 31/33 urinary bladder lesions were detected by 2 D US and 4 D Ultrasound respectively. The latter was also able to identify two additional lesions not previously detected at traditional cystoscopy. The US features of the lesions were consistent with the one provided at cystoscopy with not significant differences in term of characterization.Conclusion: Our preliminary results shows that 4 D ultrasound cystoscopy with fly through is more accurate than baseline 2D ultrasound to detect and characterize urinary bladder lesions with results comparable with traditional cystoscopy. CONCLUSION Our preliminary results shows that 4 D ultrasound cystoscopy with fly through is more accurate than baseline 2D ultrasound to detect and characterize urinary bladder lesions with results comparable with traditional cystoscopy. CLINICAL RELEVANCE/APPLICATION New ultrasound software such as 4 D ultrasound cystoscopy with fly through may help us to follow-up patients treated conservatively for urinary bladder lesions. SSA10 Genitourinary (Adrenal and Renal Imaging) Sunday, Nov. 29 10:45AM - 12:15PM Location: E353B CT GU MR AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 FDA Discussions may include off-label uses. Participants Steven C. Eberhardt, MD, Albuquerque, NM (Moderator) Nothing to Disclose Claudia P. Huertas, MD, Medellin, Colombia (Moderator) Nothing to Disclose Seung Hyup Kim, MD, Seoul, Korea, Republic Of (Moderator) Nothing to Disclose Sub-Events SSA10-01 The Role of Peak Enhancement Values in Differentiating Pheochromocytomas from Adrenal Adenomas on CT Sunday, Nov. 29 10:45AM - 10:55AM Location: E353B Participants Mohammed F. Mohammed, MBBS, Vancouver, BC (Presenter) Nothing to Disclose David Ferguson, MBBCh, Vancouver, BC (Abstract Co-Author) Nothing to Disclose Alison C. Harris, MBChB, Vancouver, BC (Abstract Co-Author) Nothing to Disclose William C. Yee, MD,FRCPC, Vancouver, BC (Abstract Co-Author) Nothing to Disclose PURPOSE The purpose of this study is to establish the role of the peak enhancement Hounsfield Unit (HU) value of focal adrenal lesions in differentiating potential pheochromocytomas from adrenal adenomas. METHOD AND MATERIALS The peak enhancement HU values of histologically confirmed pheochromocytomas (n = 24) were retrospectively compared with those of histologically confirmed adrenal adenomas (n = 28) on the 60-second contrast enhanced venous phase and compared utilizing a chi-square test. The studies were performed over a period of 5 years (2009-2014) on multi-detector CT scanners (MDCT). HU values were also measured on unenhanced (n = 34) and 15-minute delayed contrast enhanced (n = 27) phases. Measurements were obtained by drawing a representative region of interest over the target lesion. Peak enhancement values were recorded and absolute washout, relative washout and absolute enhancement (60-second enhanced minus unenhanced) were also calculated when available. Mass size was also recorded. The Student t test was used for comparing absolute enhancement and mass size. RESULTS 83.3% (n = 20) of pheochromocytomas demonstrated a peak enhancement value of 85 HU or greater, compared to 10.7% (n = 3) of adrenal adenomas (p < 0.001, PPV = 86.96%, NPV = 86.2%). Absolute enhancement of pheochromocytomas was also higher than that of adrenal adenomas (mean = 66.2 HU [range, 51-95 HU] vs. 48.1 HU [range, 18-74]; p < 0.005). Of the pheochromocytomas imaged with a triphasic protocol (n = 9), 77.8% (n = 7) met absolute and relative washout criteria for the diagnosis of a lipid-poor adenoma (>= 60% and >=40% respectively). Pheochromocytomas were significantly larger than adrenal adenomas (mean diameter, 4.5 cm [range, 1-8.3 cm] vs. 1 cm [range, 0.8-6.2 cm]; p < 0.0001). CONCLUSION Peak enhancement values of 85 HU or greater in an adrenal lesion on the 60-second post contrast phase strongly suggest a diagnosis of pheochromocytoma rather than adrenal adenoma, regardless of whether or not the lesion demonstrates absolute or relative washout characteristics compatible with a lipid poor adenoma. CLINICAL RELEVANCE/APPLICATION Peak enhancement values on the 60-second post contrast phase should be routinely assessed in the workup of an adrenal lesion to avoid missing a pheochromocytoma. SSA10-02 Proton-Density Fat Fraction: A Viable Tool for Differentiating Adenomas from Nonadenomas in Adrenal Glands, Compared with In-phase and Out-of-phase MR Imaging Sunday, Nov. 29 10:55AM - 11:05AM Location: E353B Participants Meng Xiaoyan, BMedSc, Wuhan, China (Presenter) Nothing to Disclose Hu Daoyu, PhD, Wuhan, China (Abstract Co-Author) Nothing to Disclose Chen Xiao, Wuhan, China (Abstract Co-Author) Nothing to Disclose Zhen Li, MD, PhD, Wuhan, China (Abstract Co-Author) Nothing to Disclose Yanchun Wang, Wuhan, China (Abstract Co-Author) Nothing to Disclose PURPOSE To investigate the application of proton-density fat-fraction (PDFF) measurements for accurately quantifying the fat-content of adrenal nodules, differentiating adenomas from nonadenomas, and compare with in-phase (IP) and out-of-phase (OP) MR imaging. METHOD AND MATERIALS This study was compliant with HIPAA and approved by the Institutional Review Board, with the waivers of informed consent. The consecutive research was performed between Aug 2013 to Aug 2014, 37 patients with 40 adrenal nodules (21 histopathologically proven adenomas, 13 proved pheochromocytomas and 6 clinically proven metastases) who underwent MRI scanning with T1 independent volumetric multi-echo gradient-echo imaging with T2*correction (IDEAL-IQ), following with an axial 3D dual-echo Dixon sequence (LAVA-FLEX) which performed IP and OP images. All MRI examinations were performed on a 3.0-T MR scanner. PDFF, SI index (SII), SI adrenal-to-liver ratio (ALR) and SI adrenal-to-spleen ratio (ASR) were calculated. All statistical analyses were performed by using statistical software SPSS 17.0. RESULTS PDFF of adenomas (21.39±10.09%)was significantly higher than of nonadenomas (2.25±2.73)(p=0.000, <0.05).PDFF was an effective tool for distinguishing adenomas from nonadenomas with an area under the curve (AUC) of 0.982, higher than 3.20 predicted adenomas with a sensitivity of 100% and a specificity of 89.5%.While,the sensitivities and specificities for adenomas were 90.0% and 100%, both for SII, ALR and ASR on IP/OP images, with AUC of 0.942, 0.937, 0.932, respectively. CONCLUSION PDFF measurements provided a more accurate estimation for fat content in adrenal nodules than with IP/OP images, and it could be a precisely parameter for differentiating adenomas from nonadenomas. CLINICAL RELEVANCE/APPLICATION In conclusion, IDEAL-IQ could be a valuable diagnostic tool for discriminating adenomas from nonadenomas with a high sensitivity and a relatively high specificity, avoiding radiation exposure, contrast media side-effect and complicated data calculation. IDEAL-IQ would be a prospective, reliable, and widely used method for diagnosing adrenal gland nodules in clinical study. SSA10-03 Adrenal Calcifications on CT Associated with Familial Cerebral Cavernous Malformation Type I: An Imaging Biomarker for a Hereditary Cerebrovascular Condition Sunday, Nov. 29 11:05AM - 11:15AM Location: E353B Participants Corinne D. Strickland, MD, MS, Boston, MA (Presenter) Shareholder, Thayer Medical Corporation Steven C. Eberhardt, MD, Albuquerque, NM (Abstract Co-Author) Nothing to Disclose Leslie Morrison, MD, Albuquerque, NM (Abstract Co-Author) Nothing to Disclose Li Luo, PhD, Albuquerque, NM (Abstract Co-Author) Nothing to Disclose Blaine L. Hart, MD, Albuquerque, NM (Abstract Co-Author) Nothing to Disclose PURPOSE Cerebral Cavernous Malformation Type I (CCM1) is an autosomal dominant disorder characterized by multiple cavernous malformations in the brain that may cause seizures, cerebral hemorrhage, or focal neurologic deficits. Abdominal manifestations are unproven and poorly described. Individuals of Hispanic descent in the Southwestern US are disproportionately affected by this condition due to a founder mutation in the CCM1/KRIT1 gene. Our aim was to investigate whether adrenal calcifications on CT are associated with CCM1 in carriers of the common Hispanic mutation (CHM). METHOD AND MATERIALS In an IRB-approved, HIPAA-compliant study, abdomen CT scans of 23 CCM1 subjects (10 F, 13 M, mean 48 yrs, range 24-73 yrs) were retrospectively reviewed. All subjects had multiple CCM lesions on brain MRI; 11 had confirmed CHM genotype. As controls, abdomen CTs from 38 unaffected matched subjects (18 F, 20 M, mean 48 yrs, range 23-73 years) and 13 subjects with sporadic (non-familial) CCM (6 F, 7 M, mean 51 yrs, range 26-72 yrs) were reviewed. Size, location, number, laterality of calcifications, and adrenal morphology were recorded. Brain lesion count was recorded for CCM1 subjects. Statistical comparisons between groups were calculated using Fisher exact test and two-sample t test. RESULTS 15 of 23 CCM1 subjects (65%) had small (≤ 5mm), focal calcifications (SFC) in one or both adrenals, compared with 0 in unaffected and sporadic CCM subjects (p<0.001). SFC were either left-sided or bilateral. Glands with SFC had normal adrenal morphology. The presence of SFC correlated positively with number of CCM brain lesions (p=0.048); bilateral SFC correlated positively with patient age (p=0.030). CONCLUSION SFC are found in a majority (65%) of adults with CHM-related CCM1 and may be a clinically silent disease manifestation. SFC in this population are predominantly left-sided, more often bilateral with increasing age, and more common in patients with greater number of brain lesions. These findings add to existing evidence that CCM1 is a multi-system disorder with effects beyond the central nervous system. CCM1 should be considered in the differential diagnosis for focal adrenal calcifications encountered incidentally on CT. CLINICAL RELEVANCE/APPLICATION Incidental adrenal calcifications on CT may detect unrecognized CCM1 and improve diagnostic confidence in equivocal cases. Recognition of this entity is important for management of neurologic manifestations and genetic counseling. SSA10-04 Clinical Value of Dual-Energy Virtual Non-Contrast of Dual-Source CT for Adrenal Adenoma Sunday, Nov. 29 11:15AM - 11:25AM Location: E353B Participants Yang Shitong, Zhengzhou, China (Presenter) Nothing to Disclose PURPOSE To explore the feasibility of using virtual non-contrast (VNC) images in diagnosis of adrenal adenoma in dual-energy scans, and evaluate the sensitivity, specificity, and accuracy of VNC images for the lipid-poor adenoma. METHOD AND MATERIALS The clinical manifestations and CT images for 30 patients with 31 lesions confirmed by pathological results from surgery were reviewed retrospectively. All of the patients were examined by a pre-contrast scan (true non contrast; TNC) and then arterial and venous phase enhanced scan. Then enhanced examinations were performed with dual-energy scan mode (SOMATOM Flash, Siemens Healthcare, Forchheim, Germany). The dedicated post processing application Liver VNC was used to get VNC images at the arterial and venous phase respectively.Mean CT values, signal-to-noise ratio, subjective image quality, and radiation dose were compared between routine TNC and VNC.The correlation between TNC and VNC images of the adrenal adenoma was evaluated. Sensitivity, specificity and accuracy of VNC images for the characterization of lipid-poor adenoma were calculated from chi-square tables of contingency. RESULTS No significant differences were seen for mean CT values in normal adrenal tissue,adrenal adenoma and the muscles of posterior spine between TNC and VNC images (p>0.05),except the abdominal aortic and spleen which the mean CT values in VNC images was higher than TNC image and the differences were statistically significant (p<0.05).SNR of all tissues in VNC images were higher than that in TNC image,and the differences were statistically significant (p<0.05) expect the abdominal aortic(p>0.05).The subjective score of VNC images was lower than that of TNC image, but the difference was no statistically significant(p>0.05).The radiation dose of VNC images was lower than that of TNC(p<0.05).A positive correlation was found for CT values of adrenal adenoma between TNC and VNC images.Sensitivity,specificity,and accuracy from VNC images of arterial phase for the characterization of lipid-poor adenoma were 86.9%,100%,90.3% and from venous phase were 60.9%,87.5%,67.7%. CONCLUSION VNC images calculated from contrast-enhanced dual-energy CT have a potential to replace the TNC images to diagnose the adrenal adenoma and thus reduce the patient's radiation dose. CLINICAL RELEVANCE/APPLICATION Dual-energy VNC have a potential to replace the TNC images to diagnose the adrenal adenoma and thus reduce the patient's radiation dose. SSA10-05 Characterization of Adrenal Lesions Using Rapid Kilovolt-Switching Dual Energy CT: Utility of Contrast-Enhanced Material Suppression Imaging Sunday, Nov. 29 11:25AM - 11:35AM Location: E353B Participants Jason A. Pietryga, MD, Birmingham, AL (Presenter) Nothing to Disclose Mark E. Lockhart, MD, Birmingham, AL (Abstract Co-Author) Nothing to Disclose Therese M. Weber, MD, Birmingham, AL (Abstract Co-Author) Nothing to Disclose Lincoln L. Berland, MD, Birmingham, AL (Abstract Co-Author) Consultant, Nuance Communications, Inc; Stockholder, Nuance Communications, Inc; Bradford Jackson, Birmingham, AL (Abstract Co-Author) Nothing to Disclose Desiree E. Morgan, MD, Birmingham, AL (Abstract Co-Author) Research support, General Electric Company PURPOSE To characterize adrenal lesions as benign or malignant on contrast-enhanced dual energy CT using material suppression imaging (MSI) virtual unenhanced images and pseudo-unenhanced monoenergetic 140keV images. METHOD AND MATERIALS IRB-approved HIPAA-compliant study. A retrospective search identified consecutive adult outpatients who had undergone multiphasic dual energy CT(DECT) with an adrenal lesion (≥1cm) reported. Two patients weighing ≥300 lbs were excluded. A single board-certified radiologist reviewed the CTs and placed ROIs on the adrenal lesions on the noncontrast (NC) series and simultaneously placed matching ROIs on MSI virtual unenhanced and virtual monoenergetic 140 keV images. The lesions were characterized by accepted clinical standards. Spearman rank correlation was performed to evaluate for associations between the virtual unenhanced, pseudo-unenhanced HU and NC HU and t tests to evaluate means. Regression analysis was performed to identify threshold values to characterize adrenal lesions as benign vs malignant. Myelolipomas were excluded from the regression analysis. RESULTS 104 patients (52M,52F, mean age 62, weight 188 lb) with a total of 140 adrenal lesions were identified. 56%(78/140) of the lesions were lipid-rich adenomas, 6%(9/140) lipid-poor adenomas, 20%(28/140) malignancies, 8%(11/140) myelolipomas and 10%(14/140) indeterminate. The mean HUs for adenomas were -6.5 (NC), 11.3 (MSI), 12.5 (140 keV); mean HUs for malignant lesions were 34.2 (NC), 39.1 (MSI) 38.7 (140 keV), all p<0.0001. There were very strong Spearman correlations between NC and MSI HU (.83), NC and 140keV HU (.81) and MSI and 140keV HU (98). Excluding 1 obvious necrotic RCC metastasis, a threshold of 20 HU on MSI and 16 HU on 140keV images correctly characterizes lesions as adenomas with a sensitivity of 68%(59/87) and 53%(46/87), respectively, both with specificity of 100%. CONCLUSION MSI virtual unenhanced and virtual 140keV monoenergetic contrast-enhanced DECT images can be used to characterize adrenal adenomas with a sensitivity of 72% and 59%, respectively, when using new HU threshold values of 20 and 16, respectively. Excluding an obvious necrotic RCC metastasis, both threshold values are 100% specific. CLINICAL RELEVANCE/APPLICATION In this largest DECT series of adrenal lesions, new HU criteria are presented that can characterize lesions on contrast-enhanced DECT, potentially obviating the need for further imaging for most patients. SSA10-07 MASS Criteria as a Predictor of Survival in Sunitinib Treated Metastatic RCC - A Secondary Post-hoc Analysis of a Multi-institutional Prospective Phase III Trial Sunday, Nov. 29 11:45AM - 11:55AM Location: E353B Participants Andrew D. Smith, MD, PhD, Jackson, MS (Presenter) Research Grant, Pfizer Inc; President, Radiostics LLC; President, Liver Nodularity LLC; President, Color Enhanced Detection LLC; Pending patent, Liver Nodularity LLC; Pending patent, Color Enhanced Detection LLC; Frederico F. Souza, MD, Madison, MS (Abstract Co-Author) Nothing to Disclose Manohar Roda, MD, Jackson, MS (Abstract Co-Author) Nothing to Disclose Haowei Zhang, MD, PhD, Jackson, MS (Abstract Co-Author) Nothing to Disclose Xu Zhang, PhD, Jackson, MS (Abstract Co-Author) Nothing to Disclose PURPOSE To validate MASS Criteria as a predictive imaging biomarker in metastatic RCC treated with anti-angiogenic therapy. METHOD AND MATERIALS As part of a published multi-institutional prospective phase III trial, 375 adult patients with metastatic clear cell RCC were treated with sunitinib. In this secondary post-hoc retrospective analysis, initial post-therapy CT images were evaluated by RECIST, Choi Criteria, and MASS Criteria in patients with DICOM format images. Comparison of PFS and OS among MSKCC risk and imaging response groups was evaluated using log-rank test. Inter-observer agreement between 3 readers was assessed in 21 randomly selected cases using intra-class correlation coefficient (ICC). RESULTS Median PFS and OS of the full cohort (N=270) were 1.1 and 2.6 years, respectively. PFS and OS of all MASS Criteria objective response categories were significantly different from one another (p<0.0001 for each). By comparison, PFS of MSKCC low (N=186) and intermediate (N=84) risk groups, PFS of RECIST PR (N=33) and SD (N=228) groups, and OS of Choi Criteria SD (N=36) and PD (N=13) groups were not significantly different (p=0.225, 0.810 and 0.311, respectively). Median PFS for patients with baseline MSKCC Criteria low (N=186) and intermediate (N=84) risk were 1.2 and 0.9 years, respectively. By comparison, median PFS for patients with MASS criteria FR (N=177), IR (N=84), and UR (N=9) were 1.4, 0.5, and 0.1 years, respectively. Inter-observer agreement among 3 readers interpreting 21 randomly selected cases using MASS Criteria was substantial (ICC=0.70). CONCLUSION In patients with metastatic RCC treated with sunitinib, MASS Criteria response on the initial post-therapy CT is predictive of PFS and OS. CLINICAL RELEVANCE/APPLICATION MASS Criteria is currently the only quantitative biomarker for predicting response to anti-angiogenic therapy in metastatic RCC that has been validated in a multi-institutional study and it may potentially be useful in guiding therapy, reducing drug toxicities and costs, and planning adaptive design clinical trials. SSA10-08 Prediction of Survival in Patients with Metastatic Clear Cell Carcinoma Treated with Targeted Antiangiogenic Agent Sunitinib via CT Texture Analysis Sunday, Nov. 29 11:55AM - 12:05PM Location: E353B Participants Masoom A. Haider, MD, Toronto, ON (Presenter) Consultant, Bayer AG Alireza Vosough, MD, MRCP, Aberdeen, United Kingdom (Abstract Co-Author) Nothing to Disclose Farzad Khalvati, PhD,MSc, Toronto, ON (Abstract Co-Author) Nothing to Disclose Alexander Kiss, PhD, Toronto, ON (Abstract Co-Author) Nothing to Disclose Balaji Ganeshan, PhD, London, United Kingdom (Abstract Co-Author) Scientific Director, TexRAD Limited Georg Bjarnason, MD, Toronto, ON (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate the role of CT Texture analysis in prediction of progression free and overall survival and assessment of response to treatment with Sunitinib in patients with metastatic clear renal cell carcinoma (RCC). METHOD AND MATERIALS Contrast enhanced CT texture parameters were assessed in 40 patients with metastatic clear RCC who were treated with Sunitinib. Appropriate measurable lesions were selected based on RECIST criteria before and about two months after treatment with Sunitinib. Texture and histogram analysis of the lesions were performed using TexRad software. Using a Cox regression model, correlation of texture parameters with measured time to progression and overall survival were assessed. RESULTS "Size normalized tumor Entropy" (NE) was found as an independent predictor of time to progression and overall survival and can add to Heng; a well-known prognostic model for metastatic RCC patients. Cox proportional hazards regression analysis (HR) showed that NE was an independent predictor of time to progression. (HR = 0.01 and 0.02; 95% confidence intervals (CI): 0.00 - 0.29 and 0.00 - 0.39; p=0.01 and p=0.01 for NE before and two months after treatment, respectively). NE was also shown to be an independent predictor of overall survival. (HR = 0.01 and 0.01; 95% CI: 0.00 - 0.31 and 0.001 - 0.22; p=0.01 and p=0.003 for NE before and two months after treatment, respectively). CONCLUSION Tumor heterogeneity is a well-known feature of malignancy reflecting areas of increased cellular density, hemorrhage and necrosis. CT texture analysis can quantify heterogeneity by using a range of parameters including size normalized Entropy (NE) as a measure of texture irregularity. Our study showed that NE is an independent predictor of the outcome of treatment with Sunitinib in patients with metastatic RCC and can be used for prediction of time to progression and overall survival in these patients. This can help identify non-responders from the outset with the potential to avoid unnecessary toxicity and to start alternative therapies earlier. CLINICAL RELEVANCE/APPLICATION The ability to identify poor responders early in the course of treatment or before starting the treatment can help patients be spared from toxicity usually associated with these treatments and could potentially receive alternative therapies earlier. Using the costly drugs of treatment only in patients who benefit from them will be a potential for cost-effectiveness improvement. SSA10-09 Arterial Spin Labeling MR Imaging for Detecting Perfusion of Defect of Renal Cell Carcinoma Pseudocapsule and Predicting Renal Capsule Invasion: Initial Experience Sunday, Nov. 29 12:05PM - 12:15PM Location: E353B Participants Hanmei Zhang, Chengdu, China (Presenter) Nothing to Disclose Yinghua Wu, MD,PhD, Chengdu, China (Abstract Co-Author) Nothing to Disclose Panli Zuo, Beijing, China (Abstract Co-Author) Nothing to Disclose Niels Oesingmann, PhD, Erlangen, Germany (Abstract Co-Author) Employee, Siemens AG Bin Song, MD, Chengdu, China (Abstract Co-Author) Nothing to Disclose PURPOSE The defect of pseudo-capsule is tightly correlated with the invasiveness of tumors.This study aimed to prospectively evaluate the performance of combining morphological imaging and functional imaging for detecting the defects of pseudo-capsule in renal tumors,and to predict renal capsule invasion which were confirmed histopathologically. METHOD AND MATERIALS Twelve patients with suspicious renal tumors underwent T2-weighted imaging and contrast-free renal ASL imaging at a 3.0T MR scanner.Renal ASL was performed using a prototype flow-sensitive alternating inversion recovery trueFISP (FAIR-trueFISP) sequence with a TI of 1200 ms for perfusion images and without inversion for M0 images.A modified Look-Locker inversion-recovery (MOLLI) sequence was used for T1 mapping.Renal blood flow (RBF) was quantitatively measured on the perfusion images which were determined on a pixel by pixel basis.For T2-weighted images alone,the discontinuous hypo signal intensity rim was defined as the defect of tumors' pseudo-capsule,for combination of T2-weighted images and ASL,the hypo signals in T2-weighted images as well hyper signals in perfusion images was defined as the defect of tumors' pseudo-capsule.The diagnostic performance was assessed using diagnostic test's index. RESULTS Twelve renal lesions (11 clear cell RCCs and 1 chromophobe RCC) were evaluated in 12 patients.All ccRCCs showed defect of tumors' pseudo-capsule on T2-weighted images.Of the 11 ccRCCs cases,10 cases showed blood flow right on the defect area of tumors' pseudo-capsule on perfusion images and 1 case did not.All the defect areas of tumors' pseudo-capsule seen in the surgery operation had renal capsule invasion.For defecting of tumors' pseudo-capsule,i.e. predicting renal capsule invasion,sensitivity,specificity,positive predictive value and negative predictive value were 100%,33.3%,81.8%,100% for T2weighted images alone and 100%,66.7%,90%,100% for combination of T2-weighted images and ASL images. CONCLUSION The combination of T2-weighted images and ASL images produced promising diagnostic accuracy for predicting renal capsule invasion,which could offer additional imaging information for clinical diagnosis of renal tumors. CLINICAL RELEVANCE/APPLICATION Noninvasively and prospectively evaluated the presence of the defect pseudo-capsule in renal tumors may help predict the invasiveness of tumor and influence clinical therapy strategy. GUS-SUA Genitourinary Sunday Poster Discussions Sunday, Nov. 29 12:30PM - 1:00PM Location: GU/UR Community, Learning Center GU AMA PRA Category 1 Credit ™: .50 Participants Paul Nikolaidis, MD, Chicago, IL (Moderator) Nothing to Disclose Sub-Events GU200-SDSUA1 Obstetrical Ultrasound Sweeps Show Promise for Point-of-Care Diagnosis in Resource-poor Areas Station #1 Participants Matthew D. LeComte, PhD, Burlington, VT (Presenter) Nothing to Disclose Mary Streeter, RT, Burlington, VT (Abstract Co-Author) Nothing to Disclose Sarah Ebert, BS, Burlington, VT (Abstract Co-Author) Nothing to Disclose Betsy L. Sussman, MD, Burlington, VT (Abstract Co-Author) Nothing to Disclose David Jones, MD, Burlington, VT (Abstract Co-Author) Nothing to Disclose Anne Dougherty, MD, Burlington, VT (Abstract Co-Author) Nothing to Disclose Kristen K. DeStigter, MD, Burlington, VT (Abstract Co-Author) Medical Advisory Board, Koninklijke Philips NV; Luminary, McKesson Corporation; Research collaboration, Koninklijke Philips NV; PURPOSE Resource-poor communities lack basic obstetrical (OB) imaging. Imaging the World's program integrates inexpensive ultrasound (US) technology with image compression and Internet data transfer to enable expert obstetrical evaluation. However, effectiveness of this system requires individuals minimally trained as sonographers to acquire images at the point-of-care. This study evaluates whether these providers can acquire quality OB US images for later evaluation by trained readers. METHOD AND MATERIALS Pregnant women were recruited after having a traditional OB US study performed by an expert sonographer (gold standard). Then an individual taught to generate anatomically guided sweeps (scanner) with an ultrasound probe acquired images on consenting subjects. These studies were evaluated by two obstetricians and one radiologist (readers) and compared to the gold standard. The scanner and readers were blinded to the subjects' OB status. The studies were evaluated for visibility of maternal and fetal anatomy, gestational features, placental features and fetal biometry. The readers were asked to rank their confidence level for each feature (confident, probable or uncertain). RESULTS 61 individual studies evaluated by the three readers were included in this preliminary analysis. We found 62% of responses described the fetus as "well visualized" and 36% were "partially visualized" with high confidence. Additionally 97% of reports were rated as confident for intrauterine pregnancy and 98% of reports were rated as confident of fetal position. Placental position was reported in 98% of reads. Features of biometry for dating and fetal cardiac, urinary, abdominal and neuro-anatomy were also appreciated in > 50% of reads. Image quality was also assessed by the readers.A thorough analysis of this data is warranted. We will report on concordance between the sweep and the gold standard diagnostic ultrasound reads as well as inter-observer reliability. CONCLUSION The preliminary data suggests that an individual minimally trained as a sonographer using only anatomical landmarks can generate diagnostic quality OB US images upon which clinical decisions can be made. CLINICAL RELEVANCE/APPLICATION The ability to identify complications early with point-of-care obstetric ultrasound using a pre-prescribed protocol can directly improve perinatal outcomes in resource poor regions. GU201-SDSUA2 Is PIRADs-score more Accurate versus DWI+T2w Based Data at 3T MRI: Analysis According to 189 MR-guided Prostate Biopsies Station #2 Participants Ansgar Malich, MD, Nordhausen, Germany (Presenter) Nothing to Disclose Dino Kovacevic, Nordhausen, Germany (Abstract Co-Author) Nothing to Disclose PURPOSE PIRADS-score was established as the combination of T2w+DWI+contrast uptake analysis suggesting equivalent importance of all features. Due to several contraindications of contrast agent application study aimed to verify, whether DWI+T2w are similar accurate based on MR-guided prostate biopsy results. METHOD AND MATERIALS 213 prostatic lesions were MR-guided biopsied (3T MRI Philips Ingenia) after inconclusive ultrasound guided biopsy and after multiparametric MRI (T2w, dynamic analysis (>5min, single dynamic scan <13s, calculation using DynaCAD+Confirma-CAD) and DWIanalysis (b-value 0-1000). PI-RADs-scheme vs. T2w+DWI were matched to histopathologic outcome. At least 10pt. (DWI+T2w+CE- MRI) or 7pt (DWI+T2w) were accepted as cut off for malignancy. RESULTS 82/213 lesions were PCA and 17/213 ASAP (41/213 cases prostatitis, 35/213 hyperplasia, 32/213 dystrophic prostatic tissue, 6/189 cases paraglandular tissue).Using PIRADS, 3/82 PCA had 9pt and 4 10pt (PIRADS-score 3); 9x11; 14x12; 12x13 (PIRADS-score 4) and 11x14 and 29x15pts (PIRADS-score 5).Using T2w+DWI only, 1 had 5pt; 1 6pt (PIRADS-equivalent 3), 8 7pts; 17 cases 8pts, 16 cases 9pts and 39 10pts. Distribution of ASAP-lesions was: 1x6pt; 4x7pt; 7x8pt; 3x9pt; 2x10pt. Prostatitis was scored according to PIRADS: 2x14/15pt; 23x11-13pts.;15x10pts or less. Using T2w+DWI only, 4 had a sum of 9/10; 25 a score of 7/8 and 11 less. Hyperplastic nodules were scored according to PIRADs 3x14/15pts.; 20x11-13pts; 12xless points. Using DWI+T2w only 6 lesions were scores with 9-10, 21x7/8 points and 8 with less points. Related PPV was: PIRADS: 95/184 (51.6%); DWI/T2w: 96/178 (53.9%); Sensitivity: PIRADS: 95/99 (96.0%); Sens: DWI/T2w: 96/99 (97%). CONCLUSION Especially in case of contraindications for contrast agent application, reliable prostate diagnostic analysis can be obtained without dynamic contrast uptake using PIRADs-scheme without a lowered sensitivity, even for discrimination of prostatitis vs. cancer. Further dynamic parameter such as kep, slope and peak uptake might be of additional use for the diagnostic procedure but not yet embedded in the PIRADS-scheme. CLINICAL RELEVANCE/APPLICATION In case of renal insufficiency reliable prostate MRI at 3T can be performed without contrast application. Point scale of contrast uptake of prostate lesions should be more precise and should include quantitative parameter. GU204-SDSUA5 Utility of CAD Derived Enhancement to Quantify Wash-out Characteristics of Clear Cell Renal Cell Carcinoma Low Grade and High Grade Lesions at Four-Phase MDCT Station #5 Participants Heidi Coy, Los Angeles, CA (Presenter) Nothing to Disclose Michael L. Douek, MD, MBA, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Jonathan R. Young, MD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Pechin Lo, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Matthew S. Brown, PhD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Jonathan G. Goldin, MBChB, PhD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose James Sayre, PhD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Steven S. Raman, MD, Santa Monica, CA (Abstract Co-Author) Nothing to Disclose PURPOSE Although clear cell RCC (ccRCC) are typically detected incidentally by imaging, grading these lesions has only been possible histologically on biopsy or nephrectomy. A robust imaging based method to grade ccRCC correlating with established Furhman Grade (FG) would enable surveillance of low grade lesions and surgical or ablative treatment of high grade lesions.. The purpose of our study was to assess wash-out characteristics of low grade and high grade ccRCC lesions on four-phase CT using a CAD algorithm to quantify lesion enhancement at each phase. METHOD AND MATERIALS With IRB approval for this HIPAA-compliant retrospective study, our pathology and imaging databases were queried to obtain a cohort of ccRCC with preoperative multiphasic multidetector CT imaged with a four-phase renal mass protocol (unenhanced (UN), corticomedullary (CM), nephrographic (NE), and excretory (EX)). A whole lesion 3D contour was obtained in all phases with proprietary software. The CAD algorithm determined a 0.5cm diameter region of peak enhancement <=300HU within the 3D lesion contour. All contours were confirmed by a radiologist. Absolute wash-out was calculated using the adrenal wash-out formula: (CAD lesion enhanced CT (HU) -CAD lesion Delayed CT (HU)/ (CAD lesion Delayed CT (HU)-CAD lesion Unenhanced CT (HU))* 100%). Ttests were used to compare % wash-out between low grade and high grade lesions. P values less than 0.05 were considered to be significant. RESULTS 107 patients (71 (64%) men and 40 (35%) women) with 111 unique ccRCC lesions (80 (72%) low grade (FG I and II) lesions and 31 (28%) high grade (FG III and IV)) lesions were analyzed. Mean lesion size of the low grade lesions was 2.9 cm (range 0.8-6.4). Mean lesion size of the high grade lesions was 5.6 cm (range 1.6-14.4). . High grade lesions had a significantly higher washout percentage (60.2% vs 32.1% p=0.0047) as compared to low grade lesions from the CM to NE phase but similar wash out rates between NE and EX phases (41.9% vs. 44.2%, p=0.6642). CONCLUSION High grade ccRCCs wash out at a significantly faster rate than low grade ccRCCs from the CM to NE phases CLINICAL RELEVANCE/APPLICATION CAD derived ccRCC %wash-out was significantly greater in high grade vs. low grade ccRCC providing a non invasive method of grading at imaging, enabling more aggressive treatment for high grade lesions UR105-EDSUA6 Interactive Experience with Prostate Imaging and Reporting and Data System Version 2 Station #6 Awards Certificate of Merit Identified for RadioGraphics Participants Elmira Hassanzadeh, MD, Boston, MA (Presenter) Nothing to Disclose Erik Velez, BS, San Francisco, CA (Abstract Co-Author) Nothing to Disclose Fiona M. Fennessy, MD, PhD, Boston, MA (Abstract Co-Author) Nothing to Disclose Ruth M. Dunne, MBBCh, Aclare, Ireland (Abstract Co-Author) Nothing to Disclose Mukesh G. Harisinghani, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Clare M. Tempany-Afdhal, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Daniel I. Glazer, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The purpose of this exhibit is:•To describe the experience of using PIRADS v2 in a teaching hospital•To help readers identify various PIRADS v2 scores with an interactive method•To discuss common challenges using PIRADS v2 in the clinical setting TABLE OF CONTENTS/OUTLINE •PIRADS v2 overview•Representative images of various PIRADS v2 scores•Challenges and pitfalls of PIRADS v2 UR157-EDSUA7 Pitfalls of Adrenal and Renal Imaging: A Pictorial Review Station #7 Participants Matthew J. Wu, MD, Halifax, NS (Abstract Co-Author) Nothing to Disclose Seng Thipphavong, MD, Toronto, ON (Abstract Co-Author) Nothing to Disclose Magdi A. Akl, FRCR, Halifax, NS (Abstract Co-Author) Nothing to Disclose Andreu F. Costa, MD,FRCPC, Halifax, NS (Presenter) Nothing to Disclose TEACHING POINTS The learning objectives of this exhibit are: To present a variety of common renal and adrenal lesions with potential pitfalls in diagnosis To review how CT attenuation density, enhancement on CT and MRI, and the presence of fat on MRI, both intra-voxel fat and gross, will influence the diagnosis or differential diagnosis in the kidney and adrenal gland TABLE OF CONTENTS/OUTLINE 1. Title slide2. Disclosures and target audience3. Case-based, image-rich review of common renal and adrenal lesions with potential pitfalls in diagnosis. Cases will include but will not be limited to: Adrenal lesions with gross fat: myelolipoma, extramedullary hematopoiesis, adrenal teratoma, and lipomatous degeneration of adenoma. Adrenal lesions with intra-voxel fat: adenoma, clear-cell RCC and HCC metastases0. Adrenal lesions measuring < 10 HU: adenoma, cyst and myelolipoma without gross fat on CT. Enhancing renal lesions without gross fat: RCC, oncocytomas, lipid-poor angiomyolipomas. Renal lymphoma mimicking lobar pyelonephritis on CT Renal lesions with intra-voxel fat: clear cell RCC, AML, papillary RCC4. Summary5. References6. Author contact GUS-SUB Genitourinary Sunday Poster Discussions Sunday, Nov. 29 1:00PM - 1:30PM Location: GU/UR Community, Learning Center GU AMA PRA Category 1 Credit ™: .50 Participants Paul Nikolaidis, MD, Chicago, IL (Moderator) Nothing to Disclose Sub-Events GU205-SDSUB1 "Surrounding Endometrium Sign" to Differentiate Eccentric Cornual Intra-uterine Pregnancies from Interstitial Ectopic Pregnancy Station #1 Participants Allison L. Grant, MD, MSc, Toronto, ON (Presenter) Nothing to Disclose Ally Murji, Toronto, ON (Abstract Co-Author) Nothing to Disclose Glen Lo, MBBS,BMedSc, Toronto, ON (Abstract Co-Author) Nothing to Disclose Mostafa Atri, MD, Toronto, ON (Abstract Co-Author) Nothing to Disclose PURPOSE The aim of this study was to investigate whether a sign we have observed, "surrounding endometrium sign" (SES), can be used to reliably differentiate eccentric cornual intra-uterine pregnancy (IUP) from interstitial ectopic pregnancy (EP). METHOD AND MATERIALS This was an REB approved retrospective review of all cases in our radiology database with keywords "interstitial" or "cornual" pregnancy from 2007 to 2015. Acquisition of consent was waived. One expert reader reviewed video-clips blindly using the SES sign, defined as extension of the endometrial lining to surround the eccentrically located gestational sac. Cases were called eccentric IUP if SES was present and interstitial EP if SES was absent. Correlation with outcome was made. RESULTS Forty-four evaluable cases were included. Patients were 20 to 42 years old (mean 32.6±5.7). Twenty-four cases were negative for SES sign, supporting a diagnosis of interstitial EP. These cases were managed either with methotrexate (MTX), MTX and surgery, or expectantly because of dropping β-hCG. None of 24 patients had passing of tissue vaginally.Twenty cases were positive for SES. Of those, 11 were prospectively called as eccentric IUPs and therefore appropriately managed. Six had spontaneous abortion, 4 continued to pregnancy > 20 weeks, and one underwent DandC for a desired therapeutic abortion.The remaining 9 cases were called interstitial EP prospectively, and managed as such. Seven patients were treated with MTX, with some evidence in 4 of them of inappropriate management; 2 had f/u imaging which showed definite IUPs that had moved down the uterus, 1 had documentation of passed tissue per vagina (which should not occur with an interstitial ectopic), and one underwent a DandC that showed retained products of conception (which again should not be possible with an interstitial pregnancy). Two patients underwent surgical management where pregnancy tissue was removed transcervically, again questioning the original diagnosis of interstitial pregnancy. CONCLUSION We propose the new 'surrounding endometrial sign' to accurately differentiate between eccentric cornual IUP and interstitial EP. CLINICAL RELEVANCE/APPLICATION 'Surrounding endometrial sign' on US can differentiate between eccentric cornual pregnancy and interstitial pregnancy, thereby potentially salvaging some pregnancies that may otherwise be terminated. GU206-SDSUB2 Utility of Using Abdominal Wall Thickness in Prenatal Ultrasound in Predicting Fetal Outcome for Fetuses at Risk for Intrauterine Growth Restriction Station #2 Participants Lei Wu, MD, Seattle, WA (Presenter) Nothing to Disclose Theodore J. Dubinsky, MD, Seattle, WA (Abstract Co-Author) Stockholder Global Cancer Technology PURPOSE With 2nd or 3rd trimester prenatal ultrasound (US), fetal growth is routinely evaluated by calculating the estimated fetal weight (EFW). An EFW < 10th percentile for gestational age is defined as small for gestational age (SGA), and generally thought to be associated with increased risk of IUGR. However, only a small number of these fetuses (5.2%) are affected by adverse perinatal outcome, and majority are constitutionally small. Besides abnormal UA doppler, other routinely measured biometric parameters do not accurately predict pathologic growth restriction (PGR) (1). Thus, there is a need for better predictors of PGR. Neonates exposed to PGR tend to have lower percent body fat. Thus, we propose the measurement of abdominal wall thickness (AT) as a measure of fetal metabolic reserve and as a possible predictor of PGR. METHOD AND MATERIALS Our study population included singleton live IUP with gestational age (GA) > or = 28w0d based on 1st trimester US with EFW < 90th percentile and no history of maternal diabetes. Fetuses are categorized as normal if the EFW is between 40th and 90th percentiles and no anatomic anomalies are present on US. Those with EFW < 10th percentile are considered SGA. 50 normal and 50 SGA fetuses are included in the study. Adverse perinatal outcome for SGA is evaluated and defined as admission to NICU or neonatal death. AT is measured at its thickest portion in the same slice as the AC measurement. AT of SGA fetuses is compared to that in normal fetuses using a 2-tailed paired T-test. Chi-squared test was used to evaluate the relationship between mean AT in SGA fetuses and adverse outcome. RESULTS The mean GA is 32w0d for normal fetuses and 33w6d for SGA fetuses. The mean AT is 8mm for normal fetuses and 4mm for SGA fetuses (p<0.01). 6 of 50 SGA fetuses were lost to follow up prenatally. Overall, 28 of 44 (63.6%) remaining SGA neonates had adverse outcome, 1 of which (2.2%) resulted in neonatal death. In those with AT > 3mm, 50.0% experienced adverse outcome compared to 100% in fetuses with AT = 3 mm (p<0.01). AT of 3 mm had an OR of 25.0 for adverse outcome. CONCLUSION Using a cutoff value of 3mm, AT is a useful biometric parameter as a predictor of adverse outcome especially if IUGR is questioned. CLINICAL RELEVANCE/APPLICATION Most biometric parameters on prenatal US do not accurately predict pathologic growth restriction. There is a need for better predictors such as our proposed abdominal wall thickness measurement. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Theodore J. Dubinsky, MD - 2012 Honored Educator Theodore J. Dubinsky, MD - 2013 Honored Educator GU207-SDSUB3 Favorable Outcomes and Fertility Perspective in Women Treated by MRgFUS for Uterine Fibroids: Pregnancy Results Station #3 Participants Fabiana Ferrari, MD, L'Aquila, Italy (Presenter) Nothing to Disclose Francesco Arrigoni, Coppito, Italy (Abstract Co-Author) Nothing to Disclose Anna Miccoli, MD, L'Aquila, Italy (Abstract Co-Author) Nothing to Disclose Fernando Smaldone, MD, L'Aquila, Italy (Abstract Co-Author) Nothing to Disclose Giulio Mascaretti, MD, L'Aquila, Italy (Abstract Co-Author) Nothing to Disclose Carlo Masciocchi, MD, L'Aquila, Italy (Abstract Co-Author) Nothing to Disclose PURPOSE The purpose of this study was to discuss about fertility perspective in women treated by MRgFUS and to report pregnancy after this treatment. METHOD AND MATERIALS Fourteen patients, aged between 23 and 42 (mean age 32.5), affected by uterine fibroids, who wanted to get pregnant, were treated in our department with MRgFUS. This study evaluates the findings on 14 patients presenting difficulties to conceive and uterine fibroids smaller than 6 cm. We preliminarily excluded the other causes of infertility with a gynaecological evaluation. All patients had only one treatment. We made a c.e. MRI, in order to control the Non-Perfused-Volume, immediately after treatment, and then after 3, 6 and 12 months from the treatment. After 17-20 months from the treatment, the patients started the course to become spontaneously pregnant. RESULTS After 12 months from treatment, 10 patients had a complete reabsorption of the necrotic areas and 4 had a partial reabsorption. Five months later, the patients started the course to become spontaneously pregnant. Two of them succeeded and 1 has already given birth at term to a healthy infant without any perinatal complications. Another patient with partial reabsorption of the necrotic area gave birth to a baby and another is now in her seventh month of pregnancy. CONCLUSION MRgFUS permits a significant reduction of the symptoms and is a valid alternative method to surgery in fertile women, without any complications in case of uterine implanting. CLINICAL RELEVANCE/APPLICATION MRgFUS is a mini-invasive treatment that permits to save neighbouring healthy structures, and avoid post-surgical complications allowing the uterine implanting. GU208-SDSUB4 Predictive Models for Lymph Node Metastases in Patients with Testicular Germ Cell Tumors Station #4 Participants Vishala Mishra, MBBS, Boston, MA (Presenter) Nothing to Disclose Yun Mao, MD, Chongqing, China (Abstract Co-Author) Nothing to Disclose Sandeep S. Hedgire, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Duangkamon Prapruttam, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Mukesh G. Harisinghani, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose PURPOSE To develop predictive models for lymph node metastasis in testicular germ cell tumors. To develop predictive models for lymph node metastasis in testicular germ cell tumors. METHOD AND MATERIALS 291 patients with testicular germ cell tumors were included, which were divided into seminomatous and nonseminomatous groups. For screening the risk factors for LN metastasis, the tumor-related characteristics (including histopathological information and tumor markers) alpha fetoprotein and the lymph node-related features on CT were compared between metastatic cases and nonmetastatic cases. Two logistic regression models were built for each histological group, one depending on all tumor- and lymph node-related risk factors (Model 1) and another only on tumor-related factors (Model 2). Receivers operating characteristic curves were used to evaluate the predictive abilities of these models. RESULTS 117 positive nodes/regions were identified in 68 patients, including 51 metastases and 17 occult metastases. Based on the selected independent risk factors, the sensitivity, specificity, accuracy, positive predictive value, and negative predictive value of Model 1 and 2 in senimomatous and nonseminomatous groups were (95.5%, 95.3%, 95.3%, 77.8%, and 99.2%), (63.6%, 83.6%, 80.7%, 40.0%, and 93.0%), (93.5%, 94.7%, 94.3%, 89.6%, and 96.8%), and (89.1%, 44.2%, 58.9%, 43.6%, and 89.4%), respectively. CONCLUSION In our study, four models for predicting lymph node metastases in testicular cancer were established based on lymph node- and tumor-related risk factors. In patients without tumor-related factors, regular CT surveillance may be a good choice after orchiectomy, while in patients without lymph node- and tumor-related factors, long interval-time CT follow-up could be considered. CLINICAL RELEVANCE/APPLICATION The predictive abilities of LN-related CT factors (esp. SD) on LN involvement were obviously superior to those of tumor-related factors. In patients without any IRF of Model 2, regular CT surveillance may be enough for predicting LN status, while in the patients without any IRF of Model 1, a long interval-time CT follow-up could be considered. Additionally, right side tumors tend to involve contralateral LNs compared to left side ones, as well as positive inguinal LNs more frequently occur in patients with a history of groin surgery. GU209-SDSUB5 Beyond Virtual Non-Contrast: Dual-Energy CT Fat Fraction for Differentiation Between Benign and Indeterminate Adrenal Nodules Station #5 Participants Gregory A. Bonci, MD, Boston, MA (Presenter) Nothing to Disclose Urvi P. Fulwadhva, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Aaron D. Sodickson, MD, PhD, Wayland, MA (Abstract Co-Author) Research Grant, Siemens AG; Consultant, Bracco Group PURPOSE To evaluate whether dual-energy CT (DECT) can differentiate benign from indeterminate adrenal nodules based on the fat fraction derived from three-material decomposition. METHOD AND MATERIALS The study included 22 patients with adrenal nodules detected on routine Emergency Department portal venous phase DECT scans who also had gold standard non-contrast CT or MRI with chemical shift imaging. Adrenal nodules were categorized as benign if they demonstrated attenuation <= 10 HU on non-contrast CT or loss of signal on chemical shift MR imaging. They otherwise remained indeterminate. DECT scans were performed on a 128x2 slice dual-energy scanner (Siemens FLASH, Forchheim Germany) using tube current modulation (CareDose4D) with reference mAs 400/155 at 80/Sn140 kVp or 201/155 at 100/Sn140 kVp, with the kVp pair selected based on patient size. Source images from each tube were reconstructed as 0.75 x 0.5 mm slices and used for postprocessing on a thin-client server (Syngo via, version VA30). Nodule regions of interest (ROI) were placed to record HU values on the mixed high/low kVp images, and the Liver Virtual Non-Contrast (VNC) application was used to calculate ROI VNC HU values and fat fraction (defined as 0 for a purely soft tissue attenuation lesion and 100% for a purely fat-containing lesion). RESULTS 15 benign and 7 indeterminate adrenal nodules were identified based on gold standard imaging. Contrast-enhanced mixed attenuation values (HU ± STD) could not accurately differentiate between the lesions, with benign nodules measuring 39.9 ± 24.9 and indeterminate nodules 61.6 ± 23.6 (t-test p = 0.07). However, benign and indeterminate lesions demonstrated significantly different fat fraction values (33.5 ± 12.6% versus 6.8 ± 12.0%, p < 0.001) as well as VNC HU attenuation values (7.2 ± 16.2 versus 38.6 ± 14.9, p < 0.001). CONCLUSION DECT fat fraction analysis shows promise in this proof-of-principle cohort for differentiating between benign and indeterminate adrenal nodules. CLINICAL RELEVANCE/APPLICATION Adrenal nodule fat fraction derived from DECT three-material decomposition may provide additional information about nodule tissue composition to aid in differentiating benign from indeterminate lesions. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Aaron D. Sodickson, MD, PhD - 2014 Honored Educator UR108-ED- PIRADS v2: A Case-Based Tutorial SUB6 Station #6 Participants Dennis Toy, New Haven, CT (Presenter) Nothing to Disclose Jay K. Pahade, MD, New Haven, CT (Abstract Co-Author) Nothing to Disclose Mahan Mathur, MD, New Haven, CT (Abstract Co-Author) Nothing to Disclose Mike Spektor, MD, New Haven, CT (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The objectives of the exhibit are to: 1. Familiarize trainees with the newly introduced scoring system that is aimed at standardizing prostate MRI performance and assessment. 2. Offer hands on experience scoring basic and challenging prostate MRI cases, highlight key findings, provide explanations and discuss pitfalls. 3. Provide tables and flow charts to assist in accurate scoring. TABLE OF CONTENTS/OUTLINE Table of contents/Outline:1. Normal prostate anatomy on MRI2. Overview of PIRADS v2 a. Patient preparation b. Technical parameters and requirements c. Scoring d. Reporting3. Quiz format cases followed by labelled answers with explanations and relevant teaching points a. Peripheral zone cases b. Transition zone cases c. Pitfalls d. PIRADS Assessment Category "X"4. Summary tables of scoring system algorithm UR164-EDSUB7 How to Optimize the Adquisition and Analysis of Diffusion-weighted Imaging in the Prostate for Cancer Assessment Station #7 Awards Certificate of Merit Participants Antonio Luna, MD, Jaen, Spain (Abstract Co-Author) Nothing to Disclose Teodoro Martin, MD, Jaen, Spain (Presenter) Nothing to Disclose Lidia Alcala Mata, MD, Jaen, Spain (Abstract Co-Author) Nothing to Disclose Jordi Broncano, MD, Cordoba, Spain (Abstract Co-Author) Nothing to Disclose Javier Sanchez, MD, PhD, Madrid, Spain (Abstract Co-Author) Research Consultant, Koninklijke Philips NV Mariano Volpacchio, MD, Buenos Aires, Argentina (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1. Learn how to improve the sequence design of DWI in the prostate according to the clinical indication2. Analyze the different models of analysis of diffusion signal decay in the prostate and enhance the most useful approach for cancer detection and characterization3. Enhance the current established indications to perform DWI in the prostate and review other new potential ones TABLE OF CONTENTS/OUTLINE 1. Introduction2. DWI sequence design- b values according to analysis method- 1.5 and 3T protocol3. QuantificationMonoexponential model- IVIM- Kurtosis4. Clinical applications- Cancer detection according to PIRADS v2.0 criteria- Nodule characterization (cancer vs chronic prostatitis)- Locoregional staging- Therapy monitoring- Detection of recurrence- Screening of cancer with DWI5. Conclusions VSIO11 Interventional Oncology Series: Percutaneous Management of Renal Tumors: Updates and Ongoing Controversies in 2015 Sunday, Nov. 29 1:30PM - 6:00PM Location: S405AB GU IR OI RO AMA PRA Category 1 Credits ™: 4.25 ARRT Category A+ Credits: 5.00 FDA Discussions may include off-label uses. Participants Debra A. Gervais, MD, Chestnut Hill, MA (Moderator) Nothing to Disclose LEARNING OBJECTIVES 1) To review management options for small renal masses as well as indications for each. 2) To review the data supporting the energy based thermal ablation modalities for ablation of renal masses. 3) To describe the role and limitations of biopsy of renal masses. 4) To review the management of benign solid renal masses. 5) To describe the evidence for ablation of T1b renal masses. Sub-Events VSIO11-01 Updates in the Management of Small (T1a) Renal Masses: Resect, Ablate, or Follow? Participants LEARNING OBJECTIVES View learning objectives under main course title. VSIO11-02 Small Renal Mass (T1a): The Case for Ablation in 2015 Sunday, Nov. 29 1:30PM - 1:50PM Location: S405AB Participants Jeremy C. Durack, MD, New York, NY (Presenter) Scientific Advisory Board, Adient Medical Inc Investor, Adient Medical Inc LEARNING OBJECTIVES View learning objectives under main course title. VSIO11-03 Small Renal Mass (T1a): The Case for Resection in 2015 Sunday, Nov. 29 1:50PM - 2:10PM Location: S405AB Participants Adam S. Feldman, MD, Boston, MA (Presenter) Consultant, Olympus Corporation LEARNING OBJECTIVES View learning objectives under main course title. VSIO11-04 Small Renal Mass (T1a): Both Cases for Intervention are Weak. Active Surveillance Will Do Just as Well Sunday, Nov. 29 2:10PM - 2:30PM Location: S405AB Participants Stuart G. Silverman, MD, Brookline, MA, (sgsilverman@partners.org) (Presenter) Author, Wolters Kluwer nv LEARNING OBJECTIVES View learning objectives under main course title. VSIO11-05 Age Impacts Choice of Partial Nephrectomy vs. Percutaneous Ablation for Stage T1a Renal Cell Carcinoma: a Surveillance, Epidemiology and End Results (SEER)-Medicare Population Study Sunday, Nov. 29 2:30PM - 2:40PM Location: S405AB Participants Minzhi Xing, MD, New Haven, CT (Presenter) Nothing to Disclose Nima Kokabi, MD, Atlanta, GA (Abstract Co-Author) Nothing to Disclose Di Zhang, Pittsburgh, PA (Abstract Co-Author) Nothing to Disclose Hyun S. Kim, MD, Atlanta, GA (Abstract Co-Author) Nothing to Disclose PURPOSE To investigate survival outcomes in patients with stage 1a renal cell carcinoma (RCC) undergoing open or laparoscopic partial nephrectomy (PN) vs. percutaneous cryoablation (CRA) or radiofrequency ablation (RFA) in a large-scale population study. METHOD AND MATERIALS The most recently updated SEER-Medicare linked database was queried for patients with T1aN0M0 RCC (≤4cm, ICD-O-3 C64.9) The most recently updated SEER-Medicare linked database was queried for patients with T1aN0M0 RCC (≤4cm, ICD-O-3 C64.9) diagnosed between 2000 and 2011 and followed to 2012. Patients who underwent therapy were selected from Medicare via CPT carrier claim codes (percutaneous RFA 50592; percutaneous CRA 50593; open PN 50240; laparoscopic PN 50543). Mean overall survival (OS) from therapy was compared between patients who underwent percutaneous ablation vs. partial nephrectomy, with subgroup survival analysis of individual therapies. Kaplan-Meier estimation and Cox proportional hazard models were used for survival analyses and to assess independent prognostic factors for OS. RESULTS A total of 5,983 T1a RCC patients underwent percutaneous ablation or PN within the study period, median age 72.0 yrs, 61.0% male. Of these, 3150 received open PN, 1785 received laparoscopic PN, 419 received CRA and 629 received RFA. Of these, 47.9% of patients undergoing PN were >72 yrs, vs. 67.1% of patients in the ablation group. Mean age of patients receiving ablation was significantly higher than that of the PN group, 80.1 vs. 70.6 yrs, p<0.001. Other factors including gender, ethnicity, mean index tumor size and tumor grade were not significantly different between comparison groups. Patients who underwent PN had significantly higher mean OS compared to the ablation group, 128.7 vs. 75.5 months, p<.001. On Cox regression analysis, younger age was the only independent prognostic factor for survival, HR 0.91 (0.87-0.93, p<0.001). CONCLUSION In T1aN0M0 RCC, patients undergoing ablation were significantly older compared to PN patients. Age was found to be an independent prognostic factor for survival from treatment. CLINICAL RELEVANCE/APPLICATION In T1aN0M0 RCC, age was found to be an independent prognostic factor for survival from treatment and may impact choice of therapy. VSIO11-06 Ablation for Renal Cell Carcinoma: Radiofrequency, Cryoblation, or Microwave? Participants LEARNING OBJECTIVES View learning objectives under main course title. VSIO11-07 Small Renal Mass (T1a): The Case for RFA in 2015 Sunday, Nov. 29 2:40PM - 3:00PM Location: S405AB Participants Debra A. Gervais, MD, Chestnut Hill, MA (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Debra A. Gervais, MD - 2012 Honored Educator VSIO11-08 US-guided Percutaneus Radiofrequency Ablation of Renal Cell Carcinoma: Experience from Treating 120 Renal Masses Over 7 Years Sunday, Nov. 29 3:00PM - 3:10PM Location: S405AB Participants Adriana C. Montealegre Angarita, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose Xavier Serres Creixams, PhD, Barcelona, Spain (Presenter) Nothing to Disclose Enrique Trilla, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose Milton R. Villa III, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose Juan Halaburda Berni, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose Esteban Ramirez Pinto, MD, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose Xavier G. Azogue JR, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose PURPOSE Evaluate the efficacy and safet of ultrasound (US) guided percutaneous radiofrequency ablation (RFA) for small renal masses. Describe the complications of RFA guided by US. Evaluate the technique in their initial ablative capacity and rate of tumor recurrence at one year minimum follow up. Illustrate postablation findings of residual or recurrent renal tumor by using Contrastenhanced US (CEUS) Evaluate the effect of renal function in patients undergoing RFA guided by US METHOD AND MATERIALS Over a 7 year 105 patients with 120 renal masses (tumor size averaged 2.7 cm) were reviewed treated with US-guided percutaneous RFA. Biopsy was performed at the same moment of the procedure from 2009. Cool-tip RFA system was percutaneously inserted under ultrasound guidance. RF was emitted at 100-120 W for 12 minutes to attain temperatures sufficient to ensure tumor kill. The treatment response and technical success were defined by absence of contrast enhancement within the tumor on contrast enhanced CT and CEUS. The patients were followed up with CEUS and computed tomography at 3.6 months and every 6 months thereafter. Multivariate analysis was performed to determine variables associated with procedural outcome. RESULTS Follow-up ranged from 24 months to 84 months.The initial treatment success rate was 95.8%.Five of the remaining tumors were successfully re-treated.Four tumors had recurrence (defined as the occurrence of contrast enhancing tumor 12 months after complete ablation) three of whom required a second ablation and one nephrectomy.The overall technical success rate was 99%. Complications were seven self-limited included hematomas subcapsular or perirenal. In all 104 (99%) patients have preservation of renal function,only one patient developed significant renal function deterioration associated with perirenal hematoma. There were no bowel complications despite the fact that 6 of the tumors were within 1 cm of bowel. Protective strategies progressed from reliance on electrode positioning to hydro dissection. CONCLUSION Our experience to date suggests that US-guided RFA of small renal tumors is a safe and effective, minimally invasive technique in selected patients. CLINICAL RELEVANCE/APPLICATION US-guided RFA of renal tumors can provide benefits compared to other techniques: Intraprocedural monitoring affords visualization of the forming hot ball, helps detect proximity to surrounding structures and does not use ionizing radiation. VSIO11-09 Small Renal Mass (T1a): The Case for Cryoblation Sunday, Nov. 29 3:10PM - 3:30PM Location: S405AB Participants Peter J. Littrup, MD, Providence, RI (Presenter) Founder, CryoMedix, LLC; Research Grant, Galil Medical Ltd; Research Grant, Endo Health Solutions Inc; Consultant, Delphinus Medical Technologies, Inc LEARNING OBJECTIVES View learning objectives under main course title. ABSTRACT Cryoablation of smaller renal cancers (i.e., T1a, or <4 cm) is an out-patient treatment that is safe, effective and flexibility for nearly any renal location. Major cryoablation benefits include its excellent visualization of ablation zone extent, low procedure pain and flexible protection of tumor ablation sites near calyces, bowel and ureter. CT-guidance is the cryoablation guidance modality of choice due to circumferential visualization of low density ice and ready availability. US-guidance can augment renal cryoablation, especially for smaller visible masses and/or placement of interstitial metallic markers during biopsy for selected cases requiring better eventual CT localization. MR-guidance has little clinical benefit or cost-efficacy. For safety, cases will be considered for avoidance of direct calyceal puncture, selection of hydrodissection or balloon interposition for bowel protection, and protection of the uretero-pelvic junction by stent placement. Imaging outcomes of complications and their avoidance will be shown. For optimal efficacy, tumor size in relation to number and size of cryoprobes emphasize the "1-2 Rule" of at least 1 cryoprobe per cm of tumor diameter and no further than 1 cm from tumor margin, as well as cryoprobe spacing of <2cm. Thorough extent of visible cryoablation margins beyond all apparent tumor margins produces very low local recurrence rates for tumors in nearly any renal location, resulting in excellent cost-efficacy by minimizing the need for re-treatments. VSIO11-10 Adjunctive Techniques to Improve Image-Guided Percutaneous Cyroablation of Renal Masses in Difficult Anatomic Locations: Quantifying Procedural Success and Long-term Outcomes Sunday, Nov. 29 3:30PM - 3:40PM Location: S405AB Participants Ahmed Fadl, MD, Mineola, NY (Presenter) Nothing to Disclose Andrew Ho, Bayside, NY (Abstract Co-Author) Nothing to Disclose Samia Sayegh, DO, Mineola, NY (Abstract Co-Author) Nothing to Disclose April Griffith, Mineola, NY (Abstract Co-Author) Nothing to Disclose Siavash Behbahani, MD, Mineola, NY (Abstract Co-Author) Nothing to Disclose Jason C. Hoffmann, MD, Mineola, NY (Abstract Co-Author) Consultant, Merit Medical Systems, Inc; Speakers Bureau, Merit Medical Systems, Inc PURPOSE When performing renal mass cryoablation in difficult anatomic locations, adjunctive techniques such as retrograde pyeloperfusion, hydrodissection, and angioplasty balloon interposition can improve safety and technical success rates. Prior studies have reported the technical success of these techniques, but correlation with longer-term outcomes has not been reported in this specific patient population. This study quantifies the success of these techniques, and correlates with long-term cross-sectional imaging outcomes. METHOD AND MATERIALS Retrospective analysis of percutaneous renal mass cryoablation was performed from September 2011 through October 2014 at a single, tertiary care institution. Cases using adjunctive techniques were analyzed. The diagnostic cross sectional imaging, procedural images and report, and follow-up multi-phasic cross-sectional imaging were reviewed by one radiology resident and one interventional radiology attending. The type of adjunctive technique used, reason for such utilization, and procedural outcome of the technique were recorded. Specifically, in cases of hydrodissection or balloon angioplasty interposition, measurements of the displacement distance were made. Minor and major complications were recorded, per Society of Interventional Radiology criteria. Longer-term outcomes were evaluated by review of follow-up cross-sectional imaging. RESULTS Out of 53 cryoablations during the study period, 9 utilized adjunctive techniques, including hydrodissection (n=8), retrograde pyeloperfusion (n=1), and angioplasty balloon interposition (n=1). Median greatest tumor dimension was 1.9cm (range 1.3-3.5cm). Prior to adjunctive technique, median tumor proximity to closest organ was 0.4cm (range 0.1-1.3cm). After technique was used, median distance to closest organ was 2.8cm (range 0.3-3.3cm). One hydrodissection was unsuccessful, thus angioplasty balloon interposition was then performed. All cases had appropriate ablation zones and protection of adjacent critical structures. No minor or major complications were reported. No patients had evidence of residual or recurrent tumor on follow-up imaging, ranging from 3 to 30 months. CONCLUSION Adjunctive techniques to allow cryoablation of renal masses in difficult anatomic locations have excellent technical success rates and long-term outcomes. CLINICAL RELEVANCE/APPLICATION Improving outcomes of difficult renal mass cryoablations. VSIO11-11 Small Renal Mass (T1a): The Case for Microwave Sunday, Nov. 29 3:40PM - 4:00PM Location: S405AB Participants Fred T. Lee JR, MD, Madison, WI (Presenter) Stockholder, NeuWave Medical, Inc; Patent holder, NeuWave Medical, Inc; Board of Directors, NeuWave Medical, Inc ; Patent holder, Medtronic, Inc; Inventor, Medtronic, Inc; Royalties, Medtronic, Inc LEARNING OBJECTIVES View learning objectives under main course title. VSIO11-12 Long-term Clinical Outcomes Following Radiofrequency and Microwave Ablation of Renal Cell Carcinoma at a Single Large VA Medical Center Sunday, Nov. 29 4:00PM - 4:10PM Location: S405AB Participants Salim E. Abboud, MD, Cleveland, OH (Presenter) Nothing to Disclose Tanay Y. Patel, MD, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Stephanie Soriano, MD, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Nannette Alvarado, MD, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Preet S. Kang, MD, Pepper Pike, OH (Abstract Co-Author) Nothing to Disclose PURPOSE Earlier detection and a desire to preserve renal function and decrease surgical morbidity in the treatment renal cell carcinoma (RCC) has prompted increased use of percutaneous thermal ablation treatments such as radiofrequency ablation (RFA) and more recently microwave ablation (MWA). MWA has the potential to provide more complete ablation compared to RFA in part due to more uniform and higher intra-tumoral temperatures, but only a few small studies have examined the short-and long-term outcomes of MWA for RCC. This retrospective review assesses the experience and technical short- and long-term success rates of using RFA and MWA for RCC at a large VA medical center. METHOD AND MATERIALS Patient and tumor characteristics (tumor size, nearness to collecting system, anterior/posterior location, location relative to polar line, and endophytic/exophytic predominance) were tabulated using descriptive statistics. Group comparisons were performed by using univariate logistic regression analysis to determine factors impacting primary efficacy, secondary efficacy, and technique effectiveness. Kaplan-Meier local tumor progression-free survival following ablation was calculated. RESULTS 71 patients with 78 renal lesions underwent ablation. Mean, primary, and secondary mean follow-up were 35.1, 33.5, and 31.3 months. Total, primary, and secondary technique effectiveness rates were 86%, 82%, and 4%, respectively. Primary efficacy and total technique effectiveness were associated with size, with p values of 0.02 and 0.001. There was no significant difference in survival curves between MWA and RFA treated patients. MWA and RFA groups were not significantly different in terms of age, BMI, or tumor size. Complications occurred in 11.5% of patients, none resulting in death. More than 90% patients were done as outpatients (sent home day of procedure) with moderate sedation. No cases used intubations or general anesthesia. CONCLUSION RFA and MWA both represent effective treatment modalities for RCC. Longer follow-up time and larger tumor size may be associated with the somewhat lower effectiveness rates; the comparable efficacy/complication rates compared to prior ablation studies demonstrate the feasibility of performing ablations on an outpatient basis. CLINICAL RELEVANCE/APPLICATION Image guided percutaneous ablation is an effective and cost-effective treatment modality for RCC in patients that are not surgical candidates. VSIO11-13 To Biopsy or Not Biopsy the Small Renal Mass before Ablation? That Is the Question Participants LEARNING OBJECTIVES View learning objectives under main course title. ABSTRACT Characterization of small renal masses has proven challenging. However, with appropriate CT and MR protocols, the majority of these lesions can now be characterized pre procedurally, enabling a confident diagnosis. In this lecture, we will describe renal mass characterization protocols and describe the common imaging signatures of RCC subtypes and their common mimics including lipid poor AML and oncocytoma. This may eliminate need for preprocedural biopsy. VSIO11-14 Biopsy or No Biopsy Before Ablation? Biopsy Every Renal Mass before Percutaneous Ablation Sunday, Nov. 29 4:30PM - 4:50PM Location: S405AB Participants William W. Mayo-Smith, MD, Boston, MA (Presenter) Author with royalties, Reed Elsevier; Author with royalties, Cambridge University Press LEARNING OBJECTIVES View learning objectives under main course title. VSIO11-15 Biopsy or No Biopsy before Ablation? Don't Trouble Yourself or the Patient with the Renal Mass Biopsy - Imaging Diagnosis Will Do Just as Well in 2015 Sunday, Nov. 29 4:50PM - 5:10PM Location: S405AB Participants Steven S. Raman, MD, Santa Monica, CA (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. VSIO11-16 Thermal Ablation of a Confluent Lesion in the Porcine Kidney with Magnetic Resonance Guided High Intensity Focused Ultrasound (MR-HIFU) Sunday, Nov. 29 5:10PM - 5:20PM Location: S405AB Participants Johanna M. van Breugel, MSc, Utrecht, Netherlands (Presenter) Nothing to Disclose Martijn de Greef, PhD, Utrecht, Netherlands (Abstract Co-Author) Nothing to Disclose Joost W Wijlemans, MD,PhD, Utrecht, Netherlands (Abstract Co-Author) Nothing to Disclose Gerald Schubert, PhD, Vantaa, Finland (Abstract Co-Author) Employee, Koninklijke Philips NV Chrit T. Moonen, PhD, Utrecht, Netherlands (Abstract Co-Author) Nothing to Disclose Maurice V. Bosch, MD, PhD, Utrecht, Netherlands (Abstract Co-Author) Nothing to Disclose Mario G Ries, PhD, Utrecht, Netherlands (Abstract Co-Author) Nothing to Disclose PURPOSE To investigate if MR-HIFU can provide for a reliable confluent volumetric lesion in the renal cortex in a clinically relevant time-frame in a porcine study. METHOD AND MATERIALS Nine anesthetized pigs were placed on a clinical Philips Sonalleve MR-HIFU therapy system integrated with a 1.5T Achieva MRI. Both acoustic energy delivery and MR-thermometry were respiratory gated and active surface cooling was employed to prevent nearfield damage. A honeycomb pattern of at least seven ablation cells (9-25s, 450W acoustic power, 4x4x10 mm3 per cell) were positioned in the cortex of the kidney. The therapeutic endpoint was evaluated by a non-perfused volume (NPV) measurement using DCE-MRI. Subsequently, the animal was euthanized and the extent of induced necrosis was examined using a cellular viability staining (NADH). RESULTS Confluent volumes on NPV-imaging (up ~3 mL) and NADH staining (up to ~4mL) were obtained and temperatures exceeding 60°C were reached in 6 pigs. I.e. heating of the false rib, poor respiratory correction, and a large incidence angle caused poor kidney heating in 3 pigs. CONCLUSION These first results indicate that current clinical MR-HIFU equipment might be suitable for non-invasive therapy of renal masses. Positioning of the sonications and the subject based on anatomical scans is very important, as well as adequate motion compensation. Future work will include a first clinical study on renal cell carcinomas. CLINICAL RELEVANCE/APPLICATION There is an increasing interest in non-invasive kidney sparing therapy for renal cancer, since ~1.6% of men and women will be diagnosed with kidney and renal pelvis cancer during their lifetime, in 25% of all abdominal imaging sessions a renal lesion is found, partial nephrectomy - standard care for tumors <4cm - has a 15% complication rate, and the population is aging and known with comorbidities and poor physical condition. Therefore, several patient studies investigated the feasibility of HIFU for the thermal ablation of renal masses. Mainly a hand-held extracorporeal ultrasound device with US B-mode imaging for guidance or a laparoscopic approach was used. Disadvantages are i.e. the lack of respiratory motion compensation, no real-time visualization of energy deposition, and the complexity of the probe positioning. Alternatively, feasibility of MR-HIFU interventions on the kidney with respect to motion compensated real-time thermometry and acoustic energy delivery was established, recently. VSIO11-17 Outside the Box: Is Ablation Effective for Masses other than T1a RCC Participants LEARNING OBJECTIVES View learning objectives under main course title. VSIO11-18 Percutantous Ablation for T1b Tumors Sunday, Nov. 29 5:20PM - 5:40PM Location: S405AB Participants Thomas D. Atwell, MD, Rochester, MN (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. VSIO11-19 Percutantous Ablation for Angiomyolipomas Sunday, Nov. 29 5:40PM - 6:00PM Location: S405AB Participants Fred T. Lee JR, MD, Madison, WI (Presenter) Stockholder, NeuWave Medical, Inc; Patent holder, NeuWave Medical, Inc; Board of Directors, NeuWave Medical, Inc ; Patent holder, Medtronic, Inc; Inventor, Medtronic, Inc; Royalties, Medtronic, Inc LEARNING OBJECTIVES View learning objectives under main course title. RC107 Renal Cell Carcinoma: How Imaging Can Be Used to Select among Treatment Options and Monitor Response Sunday, Nov. 29 2:00PM - 3:30PM Location: N227 GU AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Erick M. Remer, MD, Cleveland, OH, (remere1@ccf.org) (Coordinator) Nothing to Disclose Steven S. Raman, MD, Santa Monica, CA (Presenter) Nothing to Disclose Raghunandan Vikram, MBBS, FRCR, Houston, TX (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) The attendee will learn how imaging can be used to predict renal tumor subtype and grade. 2) Imaging findings that guide renal tumor management toward percutaneous tumor ablation, partial, and radical nephrectomy will be described. 3) The use of imaging to evaluate patients after tumor ablation and nephrectomy will be reviewed. Assessment methods will be compared and complications will be illustrated. 4) Methods for assessing tumor response after chemotherapy such as RECIST, WHO, Choi / Modified Choi, SACT, and MASS criteria will be discussed with illustrative examples. Imaging appearances of post therapy complications will be reviewed. ABSTRACT Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Raghunandan Vikram, MBBS, FRCR - 2012 Honored Educator RC110 Gynecologic Ultrasound (An Interactive Session) Sunday, Nov. 29 2:00PM - 3:30PM Location: E353B GU OB US AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Sub-Events RC110A Uterus and Endometrium Participants Ruth B. Goldstein, MD, San Francisco, CA (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Be able to state the acceptable standards for endometrial assessment in women with abnormal vaginal bleeding. 2) Be able to recognize a uterine abnormality in a postmenopausal woman that warrants further evaluation including tissue sampling or MRI. 3) Be able to recognize and diagnose adenomyosis. Active Handout:Ruth Beth Goldstein http://abstract.rsna.org/uploads/2015/15001988/RC110A.pdf RC110B Ovarian Masses Participants Phyllis Glanc, MD, Toronto, ON (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Evaluate critical ultrasound features of adnexal masses that permit stratification into benign, indeterminate or suspicious for malignancy. 2) Incorporate the role of guidelines, consensus statements, risk prediction algorithms and serum biomarkers. 3) Consider the role of alternate imaging modalities such as MRI, CT, PET-CT. 4) Utilize appropriate management strategies. ABSTRACT There remains a gap between the state of the knowledge and translation into practice for the diagnosis and management of adnexal masses. Pelvic ultrasound remains the primary imaging modality in the greater majority of cases. Most ovarian masses can be correctly classified on the basis of their ultrasound characteristics, nonetheless many masses that are 'almost certainly benign' or even 'indeterminate' come to prompt surgical exploration, which is not always apprpriate or without its potential risks.. This session will explore further these characteristic findings but also will evaluate the role of serial ultrasound, additional modalities such as MR or CT, serum biomarkers, strategies such as IOTA simple rules and optimization of referral patterns. Active Handout:Phyllis Glanc http://abstract.rsna.org/uploads/2015/15001989/RC110B.pdf RC110C Endometriosis Participants Luciana P. Chamie, MD, PhD, Sao Paulo, Brazil (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Define clinical and epidemiological aspects of endometriosis. 2) Define the importance of imaging mapping for endometriosis before clinical counseling. 3) Apply the most appropriate technique to investigate endometriosis. 4) Define the bowel preparation required for the transvaginal ultrasound to investigate endometriosis. 5) Apply the imaging algorithm to map deeply infiltrative endometriosis. 6) Assess the ultrasonographic findings of deeply infiltrative endometriosis in the most common sites such as bladder, vesicouterine pouch, retrocervical space, vagina, ureters, appendix and rectosigmoid colon. 7) Assess the ultrasonographic findings of ovarian endometriomas and differentiate them from functional cysts. ABSTRACT Endometriosis is a very common gynecological disease affecting millions of women in their reproductive life, often causing pelvic pain and infertility. Clinical history and physical examination may suggest endometriosis, but imaging mapping is necessary to identify the disease and mandatory for clinical couseling and surgical planning. Transvaginal ultrasound after bowel preparation is the best imaging modality as the first-line technique to evaluate patients suspected of endometriosis. The bowel preparation is relatively simple and include the day before and the day of the examination. This method is highly accurate to identify intestinal endometriosis and to determine which layers of the bowel wall are affected. In addition, it provides better assessment of small peritoneal lesions of the retrocervical space, vagina and bladder. Pelvic adhesions can also be evaluated during the exam. URL http://chamie.com.br/download Active Handout:Luciana Pardini Chamie http://abstract.rsna.org/uploads/2015/15001990/Active RC110C.pdf RC113 Pediatric Series: Fetal/Neonatal Sunday, Nov. 29 2:00PM - 3:30PM Location: S102AB GU OB MR PD AMA PRA Category 1 Credits ™: 3.25 ARRT Category A+ Credits: 4.00 Participants Daniela Prayer, MD, Vienna, Austria (Moderator) Nothing to Disclose Amy R. Mehollin-Ray, MD, Houston, TX, (armeholl@texaschildrens.org) (Moderator) Nothing to Disclose Sub-Events RC113-01 Fetal MRI of Genitourinary Tract Abnormalities Sunday, Nov. 29 2:00PM - 2:20PM Location: S102AB Participants Ann M. Johnson, MD, Philadelphia, PA, (johnsona@email.chop.edu) (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Learn basic fetal MRI techniques and relevent embryology. 2) Understand what fetal MRI can add in evaluation of genitourinary (GU) abnormalities. 3) Become familiar with patterns of fetal GU abnormalities with an emphasis on complex lesions affecting multiple organ systems, such as cloacal malformation spectrum and exstrophy. 4) The purpose of the course is to understand the potential role of fetal MRI in the evaluation of fetal genitourinary tract abnormalities. There will be an emphasis on complex lesions affecting multiple organ systems, such as cloacal malformation spectrum and exstrophy. RC113-02 Novel Nanoparticle Gd Contrast Agent Does Not Penetrate the Placental Barrier Sunday, Nov. 29 2:20PM - 2:30PM Location: S102AB Participants Anil N. Shetty, PhD, Houston, TX (Presenter) Nothing to Disclose Ketan B. Ghaghada, PhD, Houston, TX (Abstract Co-Author) Nothing to Disclose Robia Pautler, PhD, Houston, TX (Abstract Co-Author) Nothing to Disclose Wesley Lee, MD, Houston, TX (Abstract Co-Author) Research support, General Electric Company Research support, Koninklijke Philips NV Research support, Siemens AG Research support, Samsung Electronics Co Ltd Haijun Gao, PhD, Houston, TX (Abstract Co-Author) Nothing to Disclose Chandra Yallampalli, DVM,PhD, Houston, TX (Abstract Co-Author) Nothing to Disclose David Rendon, PhD, Houston, TX (Abstract Co-Author) Nothing to Disclose Ananth Annapragada, PhD, Houston, TX (Abstract Co-Author) Stockholder, Marval Pharma Ltd Stockholder, Alzeca Biosciences LLC Stockholder, Sensulin LLC Stockholder, Abbott Laboratories Stockholder, Johnson & Johnson PURPOSE Gd contrast agent usage in placental imaging is generally contraindicated, for concerns related to fetal contrast agent exposure. We therefore developed a A novel liposomal Gd nanoparticle contrast agent for T1-MRI, retaining the Gd on the maternal side, thus shielding the fetus from potential toxicities. In this study, we tested this agent in placental imaging in a mouse model, and measured its transplacental permeability. METHOD AND MATERIALS Female C57BL/6 mice, pregnant at gestational age E16.5±1 days, were imaged by T1-MRI on a 9.4T small animal MRI (Bruker Instruments) using a conventional contrast agent (Multihance, a meglumine salt of Gd-BOPTA chelate) (13 mice) and using the novel nanoparticle Gd agent (9 mice). DCE-MRI was conducted using consecutive 3D-SPGRE sequences at a constant flip angle of 16°, TE/TR=1.93ms/6ms, FOV = 3x3x2.5cm, matrix = 128x128x16. Each image was converted to a T1 map, and the contrast agent concentration on a pixel-by-pixel basis, estimated from the known relaxivity. After imaging, the mice were sacrificed and the Gd content of the placenta and fetus measured using ICP-AES. RESULTS Image and data shown below are representative of each cohort. The placentae are rather small (2mmx3mm) but are still clearly defined, and obviously not invasive into the uterine wall. Signal intensities in the placental and fetal ROI's, indicative of Gd concentration in each compartment, clearly show that the conventional Gd chelate agent penetrates the placental barrier and enters the fetus. The nanoparticle agent however, does not do so, indicated by zero signal in the fetal compartment throughout the duration of this experiment. The ICP-AES study confirmed the imaging study results, with no detectable Gd in the fetal compartment. A separate study in human placentae using an ex vivo perfused placenta preparation, also confirmed these results. CONCLUSION The nanoparticle contrast agent does not penetrate the placental barrier in a mouse model. The data are consistent with separate tests on a perfused human placenta model. CLINICAL RELEVANCE/APPLICATION The incidence of placenta accreta has increased 8-fold in the last 30 years, and improved methods for placental imaging are sorely needed. Nanoparticle Gd contrast agents described in this work could be useful for placental imaging, while maintaining fetal safety. RC113-03 Normal and Abnormal Development of the Cerebellar Vermis - A Quantitative Fetal MRI Study Sunday, Nov. 29 2:30PM - 2:40PM Location: S102AB Participants Gregor Kasprian, MD, Vienna, Austria (Presenter) Nothing to Disclose Gregor Dovjak, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Peter C. Brugger, MD, PhD, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Gerlinde Gruber, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Georg Langs, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Michael Weber, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Ernst Schwartz, MSc, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Dieter Bettelheim, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Daniela Prayer, MD, Vienna, Austria (Abstract Co-Author) Nothing to Disclose PURPOSE Postnatal neurodevelopmental outcome of fetuses with hindbrain malformations is dependent on normal growth and development of the cerebellar vermis. This comparative in vivo and post mortem fetal MRI study aims to quantitatively assess the relative dimensions of respective vermian lobules between 18 to 32 gestational weeks (GW) in normal and pathological conditions. METHOD AND MATERIALS 75 fetuses (18-32 GW, mean 25.7GW) with normal brain development and 20 fetuses with different types of hindbrain malformations were scanned prenatally (1.5T, T2-TSE, voxel size 0.72/0.72/4.4mm - 1.0/1.0/4.4mm) and seven fetuses (16-30GW, mean 21.9GW, 3T, CISS sequence, resolution: 0.33/0.33/0.33mm) scanned within 24 hours postmortem were selected for postprocessing. A T2weighted midline sagittal slice was identified and 2D vermian segmentation was performed using ITK snap (Figure). RESULTS The mean proportional size of 7/9 discriminable vermian lobules did not differ between in vivo and post mortem measurements. The relative size of the following lobules increased during gestation (Pearson, p<0.05): Culmen (r²=.460) and Declive/Folium/Tuber (r²=.453). The proportions of Lingula (r²=-.439), Centrum (r²=-.554), Pyramis (r²=-.303) and Nodulus (r²=-.491) decreased with gestational age. The relative size of the Uvula did not show age specific changes (p=.201). Certain types of hindbrain malformations showed common patterns of cerebellar lobular hypoplasia. CONCLUSION Fetal vermian lobulation can be accurately assessed by MRI between 18 and 32GW in normal and pathological conditions in vivo . Growth of specific vermian lobules is nonuniform during the second and third trimester. Distinct patterns of vermian lobular hypoplasia can be described antenatally. CLINICAL RELEVANCE/APPLICATION Knowledge about the distinct growth patterns of specific vermian lobules is helpful in the prognostic classification of fetal hindbrain malformations. RC113-04 MRI-US Fusion Imaging in Real-Time Virtual Sonography for the Evaluation of Fetal Anomalies: Preliminary Stud Sunday, Nov. 29 2:40PM - 2:50PM Location: S102AB Participants Silvia Bernardo, MD, Rome, Italy (Presenter) Nothing to Disclose Valeria Vinci, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Matteo Saldari, MD, PhD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Antonella Giancotti, Rome, Italy (Abstract Co-Author) Nothing to Disclose Carlo Catalano, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Lucia Manganaro, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Camilla Aliberti, Rome, Italy (Abstract Co-Author) Nothing to Disclose PURPOSE Magnetic resonance imaging (MRI) and ultrasound (US) scanning complement each other in the screening and diagnosis of fetal anomalies. Real-time virtual sonography (RVS) is a new technique that uses magnetic navigation and computer software for the synchronized display of real-time US and multiplanar reconstruction MRI images. The purpose of this study was to evaluate the feasibility and ability of RVS to assess the main pathologies in fetuses with suspected US anomalies. METHOD AND MATERIALS This study was conducted over a two-month period march-april 2015 in 30 patients referred for a morphological fetal US-based evaluation. Patients undergone Fetal MRI at 1.5 T for fetal anomalies were offered fusion imaging (Hitachi HI Vision Ascendus).The MRI image dataset acquired at the time of the examination was loaded into the fusion system and displayed together with the US image on the same monitor. Both sets of images were then manually synchronized and image were registered using multiple planes MR imaging.The ability of this combined image (RVS imaging) to assess the main anatomical sites and fetal anomalies was evaluated and compared with standard B-Mode US and MRI images previously acquired. RESULTS In all cases RVS was technically possible, with a 100% match between MR images and US images. Data registration, matching and fusion imaging were performed in less than 15-20 minutes. On a total of 30 fetuses, 20 were for the encephalic district and 10 for the body (8 thoraco- abdominal; 2 heart). In all cases RVS was technically possible, with a 100% match between MR images and US images. In 10 cases of body abnormalities, fusion imaging helped the diagnosis in 20%. In the 10/20 cases of encephalic pathology, fusion imaging improved the diagnosis; in the other 10 cases MRI was superior to US even using the RVS. CONCLUSION The present work is a preliminary study on the feasibility and practical use of a Fetal MRI-US real-time fusion imaging. Thanks to informations from both US and MRI, fusion imaging allows better identification of the different fetal pathologies and could improve the performance of ultrasound examination. CLINICAL RELEVANCE/APPLICATION Fusion imaging is feasible for the assessment of fetal abnormalities. Because it combines information from both US and MRI techniques, fusion imaging allows better identification of the different fetal pathologies. RC113-05 Predictive Value of the MRI-based Ratio of Fetal Lung Volume to Fetal Body Volume in Congenital Diaphragmatic Hernia in Comparison to the MR Fetal Lung Volume and the Sonographic Lung-to-Head Ratio Sunday, Nov. 29 2:50PM - 3:00PM Location: S102AB Participants Claudia Hagelstein, MD, Mannheim, Germany (Presenter) Nothing to Disclose Silke von Mittelstaedt, Mannheim, Germany (Abstract Co-Author) Nothing to Disclose Meike Weidner, Mannheim, Germany (Abstract Co-Author) Nothing to Disclose Christel Weiss, Mannheim, Germany (Abstract Co-Author) Nothing to Disclose Regine Schaffelder, MD, Mannheim, Germany (Abstract Co-Author) Nothing to Disclose Thomas Schaible, Mannheim, Germany (Abstract Co-Author) Nothing to Disclose Stefan O. Schoenberg, MD, PhD, Mannheim , Germany (Abstract Co-Author) Institutional research agreement, Siemens AG Wolfgang Neff, MD, PhD, Alzey, Germany (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate prognostic accuracy of the MRI-based ratio of fetal lung volume to fetal body volume (MR-FLV/FBV) in fetuses with congenital diaphragmatic hernia (CDH) and to compare it to established prognostic parameters (the observed-to-expected MR fetal lung volume [o/e-MR-FLV] and the US-based observed-to-expected lung-to-head ratio [o/e-LHR]) with regard to survival, extracorporeal membrane oxygenation (ECMO) requirement and development of a chronic lung disease (CLD). METHOD AND MATERIALS Fetal MRI was performed in 132 patients with isolated CDH (mean gestational age 32.8±3.8 weeks) to measure FLV and FLV/FBV. Sonographic assessment of the LHR was performed within three days before or after fetal MRI. To obtain parameters that were independent from gestational age, the o/e-MR-FLV and the o/e-LHR were calculated based on normal controls, whereas calculation of the MR-FLV/FBV is independent from normal controls. RESULTS 91% of the neonates survived, 37% needed ECMO therapy and 45% developed a CLD. All prenatal parameters revealed an excellent correlation with patients´ clinical outcome. MR-FLV/FBV, o/e-MR-FLV and o/e-LHR were significantly higher in survivors (p always <0.0001). Patients with ECMO requirement and patients with CLD showed a significantly lower MR-FLV/FBV, o/e-MR-FLV or o/e-LHR (p always <0.0001). Prognostic accuracy regarding survival was quite similar for the three parameters (AUC MR-FLV/FBV : 0.830, AUC o/e-MR-FLV : 0.868, AUC o/e-LHR : 0.845). Regarding ECMO requirement (AUC MR-FLV/FBV : 0.844, AUC o/e-MR-FLV : 0.843, AUC o/e-LHR : 0.736) and development of CLD (AUC MR-FLV/FBV : 0.778, AUC o/e-MR-FLV : 0.795, AUC o/e-LHR : 0.738) the MRFLV/FBV and o/e-MR-FLV showed a slightly better prognostic accuracy compared to the o/e-LHR. CONCLUSION In CDH, assessment of pulmonary hypoplasia based on the MR-FLV/FBV, the o/e-MR-FLV or the o/e-LHR is quite similar in predicting survival. Regarding ECMO requirement and development of CLD, the o/e MR-FLV and the MR-FLV/FBV showed a slightly better prognostic accuracy compared to the US-based o/e-LHR. Compared to other prognostic parameters, MR-FLV/FBV has the advantage of being independent from the reference to a normal control group. CLINICAL RELEVANCE/APPLICATION In CDH, MRI-based MR-FLV/FBV and o/e-MR-FLV as well as US-based o/e-LHR are excellent and almost equivalent parameters to predict survival, ECMO-requirement and development of CLD. RC113-06 Correlation between Fetal and Postmortem Magnetic Resonance Imaging and Conventional Autopsy in the Detection of Fetal Abnormalities Sunday, Nov. 29 3:00PM - 3:10PM Location: S102AB Participants Matteo Saldari, MD, PhD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Silvia Bernardo, MD, Rome, Italy (Presenter) Nothing to Disclose Carlo Catalano, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Valeria Vinci, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Lucia Manganaro, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose PURPOSE To compare Fetal and postmortem MRI and conventional autoptic findings in cases of major pathological abnormalities. METHOD AND MATERIALS In this prospective study we enrolled 128 fetuses with identified US findings of severe fetal malformations, with local research ethics committee approval. Among these, we performed 94 whole body Fetal MRI on 94 fetuses using a 1.5 T MR scanner and of these, only 89 women undewent termination of pregnancy because of the fetal abnormalities. Of the 89 patients, 80 (90%) consented to postmortem MRI alone; 59 (66%) women consented to both postmortem MRI and conventional autopsy and formed our study group. Following delivery, fetuses were stored in refrigerated compartments prior to MR imaging and autopsy. Also for the post-mortem imaging evaluation we acquired whole body MR imaging using a 1.5 T MR scanner. MR images were reviewed by a team of two radiologists blinded to the autoptic data. Pathologists who performed conventional autopsy were blinded to the MR data; autoptic data were considered the gold standard. RESULTS Final autoptic diagnoses were: polycystic kidney disease (n=15), diaphragmatic hernia (n=10), lissencephaly (n=4), type-2 ArnoldChiari malformation (n=6), Dandy-Walker syndrome (n=13), cloacal malformation (n=1), anencephaly (n=1), holoprosencephaly (n=4), rhombencephalosynapsis (n=2), Walker-Warburg syndrome (n=2), schizencephaly (n=1).MRI-autopsy provided additional information in 10/59 (17%) compared to fetal MRI.In 6 cases (10%) conventional autopsy provided superior diagnostic information compared to MRI-autopsy. On the other hand, in 7 cases (12%) the disruption of the anatomy during autoptic dissection of the fetal body couldn't allow a correct identification of the pathology. CONCLUSION MR autopsy is accepted by nearly all mothers while conventional autopsy is accepted by about two-thirds of mothers, it provides similar information compared to conventional autopsy in case of fetal malformations and it allows the evaluation of the pathology in case of tissue disruption during the autoptic evaluation. CLINICAL RELEVANCE/APPLICATION Fetal MRI can add significant additional information and may be use to guide conventional autopsy RC113-07 Imaging of Ambiguous Genitalia Sunday, Nov. 29 3:10PM - 3:30PM Location: S102AB Participants Jeanne S. Chow, MD, Boston, MA (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) The purpose of this course is to understand the important role of the radiologists in infants with ambiguous genitalia. Imaging techniques as well as important imaging findings will be detailed. ABSTRACT PS12 Sunday Afternoon Plenary Session Sunday, Nov. 29 4:00PM - 5:45PM Location: Arie Crow n Theater CH GI GU MK NR ER AMA PRA Category 1 Credits ™: 1.75 ARRT Category A+ Credits: 1.50 Participants Ronald L. Arenson, MD, San Francisco, CA (Presenter) Nothing to Disclose Sub-Events PS12A Report of the RSNA Research and Education Foundation Participants Burton P. Drayer, MD, New York, NY (Presenter) Advisor, Hologic, Inc Abstract The RandE Foundation - Our Future is Now This year marks the 100th anniversary of the RSNA's founding. As radiology looks toward the future, one wonders what the next 100 years will look like for our specialty and whether the central role of radiologists in healthcare will be sustained. Analogous to our clinical radiology mantra, if we are not at the radiology research table we will be on the menu. As a leading global force in radiology, the RSNA is poised to lead the specialty into the next century and exceed the incredible success of the past 100 years. The RandE Foundation will play a key role in radiology's future by continuing its support of inspiring investigators and those pursuing innovative approaches to education. To meet these research and education needs headon, the Foundation launched Inspire-Innovate-Invest, The Campaign for Funding Radiology's Future® at last year's annual meeting. This bold campaign seeks to raise $17.5 million to fund grants in radiologic research and education, bridging the gaps in funding for promising investigators and educators. To date our campaign has been a success with individuals, private practice and corporate donors generously pushing us to the mid-way point in our goal. There is still a long way to go. The future of our specialty depends on the commitment and generosity of each of us, the members of the imaging community. This year, the Foundation will fund 92 grants totaling $3.6 million. The RandE is funding 25% of our ever increasing number of excellent grant applications. While pleased with these achievements, imagine what the RandE Foundation could fund with additional support from all of us as radiology colleagues? During the meeting week, please take time to visit the RandE Foundation Booth, located on Level 3 of Lakeside Center to learn more about how you can be a part of the campaign and support the RandE Foundation and the future robustness of our specialty. PS12B Image Interpretation Session Participants Jonathan B. Kruskal, MD, PhD, Boston, MA (Presenter) Author, UpToDate, Inc Donald P. Frush, MD, Durham, NC (Presenter) Nothing to Disclose Bruce B. Forster, MD, Vancouver, BC (Presenter) Travel support, Siemens AG; Travel support, Toshiba Corporation; Christine M. Glastonbury, MBBS, San Francisco, CA (Presenter) Author with royalties, Reed Elsevier Michelle M. McNicholas, MD, Dublin, Ireland (Presenter) Nothing to Disclose Melissa L. Rosado De Christenson, MD, Kansas City, MO (Presenter) Author, Thieme Medical Publishers, Inc; Author, Reed Elsevier; Author, American Registry of Pathology; Author, Oxford University Press; ; ; ; Jorge A. Soto, MD, Boston, MA (Presenter) Nothing to Disclose Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Melissa L. Rosado De Christenson, MD - 2012 Honored Educator Jorge A. Soto, MD - 2013 Honored Educator Jorge A. Soto, MD - 2014 Honored Educator Jorge A. Soto, MD - 2015 Honored Educator Jonathan B. Kruskal, MD, PhD - 2012 Honored Educator ED006-MO Genitourinary Monday Case of the Day Monday, Nov. 30 7:00AM - 11:59PM Location: Case of Day, Learning Center GU AMA PRA Category 1 Credit ™: .50 Participants Theodora A. Potretzke, MD, Saint Louis, MO (Presenter) Nothing to Disclose Perry J. Pickhardt, MD, Madison, WI (Abstract Co-Author) Co-founder, VirtuoCTC, LLC; Stockholder, Cellectar Biosciences, Inc; Research Consultant, Bracco Group; Research Consultant, KIT ; Research Grant, Koninklijke Philips NV Naoki Takahashi, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Meghan G. Lubner, MD, Madison, WI (Abstract Co-Author) Grant, General Electric Company; Grant, NeuWave Medical, Inc; Grant, Koninklijke Philips NV Anup S. Shetty, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Richard Tsai, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose George A. Carberry, MD, Madison, WI (Abstract Co-Author) Nothing to Disclose Vincent M. Mellnick, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose David U. Kim, MD, Madison, WI (Abstract Co-Author) Nothing to Disclose Yaseen Oweis, MD, MBA, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Zachary J. Viets, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Bernard F. King JR, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1) Recognize imaging findings seen in disorders of the genitourinary systems. 2) Develop differential diagnosis based on the clinical information and imaging findings. 3) Recognize the clinical importance of diagnosis. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Perry J. Pickhardt, MD - 2014 Honored Educator Naoki Takahashi, MD - 2012 Honored Educator Meghan G. Lubner, MD - 2014 Honored Educator Meghan G. Lubner, MD - 2015 Honored Educator SPSH20 Hot Topic Session: PET/MR and Hyperpolarized MR for GU Imaging Monday, Nov. 30 7:15AM - 8:15AM Location: E450B GU MR NM OI AMA PRA Category 1 Credit ™: 1.00 ARRT Category A+ Credit: 1.00 Participants Zhen J. Wang, MD, Hillsborough, CA, (jane.wang@ucsf.edu) (Moderator) Nothing to Disclose LEARNING OBJECTIVES 1) To become familiar with current PET-MR imaging strategies. 2) To learn the current and future applications of PET-MR in genitourinary oncology including gynecological cancers and prostate cancer. 3) To understand the principles of hyperpolarized carbon-13 MR metabolic imaging 4) To learn the clinical utility of hyperpolarized carbon-13 MR for measuring prostate cancer aggressiveness and response to therapy ABSTRACT URL Sub-Events SPSH20A PET/MRI of Gynecological Malignancies Participants Raj M. Paspulati, MD, Cleveland, OH (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) PET-MRI protocol and workflow for Gynecological cancer. 2) Role of PET-MRI in Gynecological cancer staging, treatment planning and follow up for treatment response. 3) PET-MR Imaging pit falls and limitations. SPSH20B Imaging of Prostate Cancer: Potential of PET/MRI with Tracers beyond FDG Participants Matthias Roethke, MD, Heidelberg, Germany (Presenter) Speaker, Siemens AG LEARNING OBJECTIVES View learning objectives under main course title. Handout:Matthias Roethke http://abstract.rsna.org/uploads/2015/15006404/Roethke Prostate RSNA handout.pdf SPSH20C Hyperpolarized 13C MR Clinical Trials of Prostate Cancer Participants John Kurhanewicz, PhD, San Francisco, CA (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. MSCM21 Case-based Review of Magnetic Resonance (An Interactive Session) Monday, Nov. 30 8:30AM - 10:00AM Location: S100AB GI GU MK MR AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants John R. Leyendecker, MD, Dallas, TX (Director) Nothing to Disclose LEARNING OBJECTIVES 1) Be familiar with the MRI appearance of common musculoskeletal derangements of the hip. 2) Develop a differential diagnosis for musculoskeletal soft tissue tumors based on MRI appearance. 3) Distinguish between common benign and malignant liver neoplasms. 4) Be familiar with the typical MRI appearance of select female pelvic disorders. ABSTRACT This session will help attendees recognize and manage select, commonly encountered musculoskeletal and abdominopelvic abnormalities based on their MRI appearances using a case-based, interactive format. Sub-Events MSCM21A Musculoskeletal MRI of the Hip and Pelvis Participants Mini N. Pathria, MD, San Diego, CA (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. Active Handout:Mini Nutan Pathria http://abstract.rsna.org/uploads/2015/15002720/Active -MSCM21A.pdf MSCM21B MRI of Soft Tissue Masses of the Extremities Participants Kirkland W. Davis, MD, Madison, WI, (kdavis@uwhealth.org) (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Distinguish characteristic extremity soft tissue masses on the basis of signal characteristics, such as high signal on T1-weighted images or low signal on all sequences. ABSTRACT MSCM21C MRI of the Liver Participants Nicole M. Hindman, MD, New York, NY, (Nicole.Hindman@nyumc.org) (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Recognize and analyze benign but unusual liver lesions. 2) Analyze uncommon presentations of liver lesions. 3) Recognize neoplastic mimics of benign lesions in the liver (eg, a colon metastasis mimicking a hemangioma) . ABSTRACT This session will cover common and uncommon presentations of liver lesions on several modalities (ultrasound, CT and MRI). A brief interactive review of common, but atypical presentations of both benign and malignant liver lesions will be presented. Malignant mimics of benign liver lesions will also be shown, with features that should be analyzed in order to better characterize the lesion, and appropriately raise concern (eg, for a metastasis or intrahepatic cholangiocarcinoma instead of a benign hemangioma). Recent advances in liver lesion characterization will be covered. MSCM21D MRI of the Female Pelvic Organs Participants Christine O. Menias, MD, Scottsdale, AZ, (menias.christine@mayo.edu) (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Christine O. Menias, MD - 2013 Honored Educator Christine O. Menias, MD - 2014 Honored Educator Christine O. Menias, MD - 2015 Honored Educator MSRO21 BOOST: Gynecology-Oncology Anatomy - Radiologic Evaluation of Pelvic Malignancies in the Era of Imaging Biomarkers (An Interactive Session) Monday, Nov. 30 8:30AM - 10:00AM Location: S103AB GU BQ RO AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 FDA Discussions may include off-label uses. Participants Saurabh Gupta, MD, Milwaukee, WI (Presenter) Nothing to Disclose Robert S. Hellman, MD, Milwaukee, WI (Presenter) Nothing to Disclose Paul M. Knechtges, MD, Milwaukee, WI (Presenter) Nothing to Disclose Mark D. Hohenwalter, MD, Milwaukee, WI (Presenter) Nothing to Disclose Beth A. Erickson, MD, Milwaukee, WI (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Review uterine/cervical anatomy and current anatomic imaging methods for the evaluation of pelvic malignancy. 2) Review the current role of PET in the imaging of pelvic malignancy. 3) Discuss the growing role of imaging biomarkers ( e.g. diffusion weighted imaging and perfusion imaging) in determining prognosis and treatment response for pelvic malignancies. RC207 Genitourinary Series: Prostate MR 2015: Current Role in Staging and Surveillance and Intervention Monday, Nov. 30 8:30AM - 12:00PM Location: N227 GU MR OI AMA PRA Category 1 Credits ™: 3.50 ARRT Category A+ Credits: 4.00 FDA Discussions may include off-label uses. Participants Peter L. Choyke, MD, Rockville, MD, (pchoyke@nih.gov) (Moderator) Researcher, Koninklijke Philips NV Researcher, General Electric Company Researcher, Siemens AG Researcher, iCAD, Inc Researcher, Aspyrian Therapeutics, Inc Researcher, ImaginAb, Inc Researcher, Aura Biosciences, Inc LEARNING OBJECTIVES 1) To understand why prostate cancer is currently under- and over-diagnosed. 2) To understand the role of multiparametric prostate MRI in guiding biopsy of the prostate. 3) To understand the role in the diagnosis, surveillance and recurrence of cancer. 4) To review current progress in the focal treatment of prostate cancer. ABSTRACT The paradox of prostate cancer is that it is currently being overdiagnosed and underdiagnosed. PSA and blind biopsy has resulted in the overtreatment of men with low risk disease and the undertreatment of men with intermediate high risk tumors that evade blind biopsy. Multiparametric MRI is a major breakthrough in the diagnosis of prostate cancer. Moreover it can be used to monitor patients for active surveillance and guide treatment. New standards for reporting of prostate MRI have been recently development. This course will not only review these important developments but will provide new research results to participants. Sub-Events RC207-01 Intro to Prostate Cancer Monday, Nov. 30 8:30AM - 8:55AM Location: N227 Participants Peter L. Choyke, MD, Rockville, MD, (pchoyke@nih.gov) (Presenter) Researcher, Koninklijke Philips NV Researcher, General Electric Company Researcher, Siemens AG Researcher, iCAD, Inc Researcher, Aspyrian Therapeutics, Inc Researcher, ImaginAb, Inc Researcher, Aura Biosciences, Inc LEARNING OBJECTIVES 1) To understand the limitations of PSA screening and random prostate biopsy. 2) To introduce the concepts of novel screening tests and genomic analysis of prostate biopsies. 3) To review the importance of MRI in improving tumor localization, guiding biopsy, monitoring active surveillance and focally ablating prostate cancer. ABSTRACT See overview abstract ABSTRACT The diagnosis of prostate cancer is evolving quickly. There is increasing recognition that the combination of routine PSA screening and random prostate biopsy overdiagnoses low grade disease and underdiagnoses high grade disease. Autopsy studies show that the normal prostate harbors many low grade and microscopic cancers that never becomes clinically apparent. On the other hand, random biopsies undersample the anterior prostate gland. More accurate screening tests (e.g. PCA-3) are under development for determining which men warrant biopsy. Genomic testing of prostate biopsy samples is also becoming more common and it is thought to improve the prediction of tumor aggressiveness. The increased use of genomics to guide therapy clearly requires that the biopsy sample be representative of the tumor. MR guided biopsies, whether performed in gantry or using MR-US fusion, will improve the quality of the prostate biopsy specimen enabling more accurate genomic testing. Armed with more accurate and reliable tissue diagnosis, more rational decisions regarding active surveillance and/or focal therapy can be made. This course will review advances in MR guided diagnosis, biopsy and therapy of prostate cancer. RC207-02 Detection and Characterization of Prostate Cancer with Multiparametric MRI (mpMRI): Do Learning and Experience Matter for Diagnostic Accuracy? Monday, Nov. 30 8:55AM - 9:05AM Location: N227 Participants Rajan T. Gupta, MD, Durham, NC (Presenter) Consultant, Bayer AG; Speakers Bureau, Bayer AG; Consultant, Invivo Corporation Daniele Marin, MD, Cary, NC (Abstract Co-Author) Nothing to Disclose Bhavik N. Patel, MD,MBA, Durham, NC (Abstract Co-Author) Nothing to Disclose Kirema Garcia-Reyes, MD, Durham, NC (Abstract Co-Author) Nothing to Disclose Kingshuk Choudhury, PhD, Durham, NC (Abstract Co-Author) Nothing to Disclose Lisa M. Ho, MD, Durham, NC (Abstract Co-Author) Nothing to Disclose Tracy A. Jaffe, MD, Durham, NC (Abstract Co-Author) Nothing to Disclose Thomas J. Polascik, MD, Durham, NC (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate effect of dedicated reader education on accuracy/Gleason score estimation of index and anterior prostate cancer (PCa) diagnosis with mpMRI in attending radiologists compared to abdominal imaging fellows. METHOD AND MATERIALS 4 blinded attending abdominal imagers with 2-16 years of experience evaluated 31 prostate mpMRIs in this IRB-approved, HIPAAcompliant, retrospective study for index lesion and anterior PCa detection (including Gleason score estimation). Following dedicated education program, readers reinterpreted cases after a 2-4 month memory extinction period, blinded to initial reads. Reference standard was established combining whole mount histopathology with mpMRI findings by a board-certified radiologist with 5 years of prostate mpMRI experience. Multivariate analysis was performed to assess the effects of learning and reader experience. Results for attending radiologists were then compared with prior reader study results in radiology fellows (using the same set of cases). RESULTS Index cancer detection (attending vs. fellow): pre-education accuracy 64.5% vs. 74.2%; post-education accuracy 71.8% vs. 87.7% (p=0.12 vs. p=0.003). Gleason score estimation (index): pre-education accuracy 46.8% vs. 54.8%; post-education accuracy 57.3% vs. 73.5% (p=0.04 vs. p=0.0005). Anterior PCa detection: pre-education accuracy 46.4% vs. 54.3%; posteducation accuracy 75% vs. 94.3% (p=0.02 vs. p=0.001). Gleason score estimation (anterior): pre-education accuracy 42.9% vs. 45.7%; post-education accuracy 67.9% vs. 80% (p=0.03 vs. p=0.002). These effects were all attributable to learning and not to reader experience based on multivariate analysis. CONCLUSION Accuracy of anterior PCa detection and Gleason score estimation for both index and anterior cancers significantly increased following dedicated reader education for both attendings and fellows. In addition, accuracy for index cancers was statistically significantly improved for fellows post-education. The degree of statistically significant improvement was higher for fellows vs. attendings overall. CLINICAL RELEVANCE/APPLICATION Performance in detection and characterization of PCa on mpMRI can be improved with dedicated reader education, however, it may be that the earlier the educational intervention is done, the more significant the improvement. RC207-04 Abbreviated Prostate MRI (AP-MRI) Monday, Nov. 30 9:15AM - 9:25AM Location: N227 Awards RSNA Country Presents Travel Award Participants Robin Bruhn, Aachen, Germany (Presenter) Nothing to Disclose Simone Schrading, MD, Aachen, Germany (Abstract Co-Author) Nothing to Disclose Christiane K. Kuhl, MD, Bonn, Germany (Abstract Co-Author) Nothing to Disclose PURPOSE It has recently been shown that an Abbreviated MRI Protocol is suitable for breast cancer screening. Aim of this study was to investigate whether an Abbreviated Prostate MRI protocol (AP-MRI), consisting of 2 pulse sequences only (high resolution T2-TSE and DWI in a single plane), acquired without endorectal coil, is sufficient to diagnose prostate cancer (PCa) in men presenting with elevated PSA-levels. METHOD AND MATERIALS Ongoing prospective reader study on 222 men (mean age 53.6 years) with median PSA of 7.1 who underwent multiparametric 3.0TMRI with multi-element surface coil. The AP-MRI took a table time of just under 10 min. The full diagnostic protocol (FDP) took 30 min and included the pulse sequences of the AP-MRI (0.4 mm in-plane axial T2-TSE and DWI with 4 b-values up to 1400 s/mm²), plus additional T2-TSE planes, coronal T1-TSE, and DCE. All MRI studies were read prospectively by two GU-radiologists in consensus according to PIRADS 2.0. Readers first read the AP-MR images and made their diagnoses. Then, they read the FDP. Results of MR-guided biopsy, TRUS/saturation biopsy, and/or final surgical pathology, or MRI and PSA follow up of at least 24 months served as SOR. RESULTS PCa was finally diagnosed in 85/222 men (38.3%), with median size 12 mm, classified as Gleason-6 in 25 patients, Gln-7 in 31, Gln ≥ 8 in 29. Diagnostic indices of the AP-MRI vs. the FDP were: Sensitivity: 93% (79/85) vs. 94% (80/85); Specificity: 89% (122/137) vs. 87% (120/137); PPV: 84% (79/94) vs. 82% (80/97), NPV: 95% (122/128) vs. 96% (120/125). The single cancer that went undetected by AP-MRI was a Gln-6-cancer diagnosed by DCE. A total five additional cancers (Gln-6 in 3, and Gln-7 in 2 patients) went undetected by both, AP-MRI and FDP, and were detected by TRUS biopsy. NPV for biologically relevant prostate cancer (> Gln-6) was 98.8% (95%CI: 95.7%-99.9%) for both, AP-MRI and FDP. CONCLUSION Abbreviated prostate MRI allows diagnosis of biologically relevant PCa in under 10 minutes magnet time, without endorectal coil and without contrast agent, and offers a diagnostic accuracy that is equivalent to that of a full state-of-the-art multi-parametric prostate MRI protocol. CLINICAL RELEVANCE/APPLICATION Abbreviated prostate MRI, if confirmed by further studies, may open the door for systematic MRI screening for prostate cancer. RC207-05 The Natural History of Low-grade Prostate Cancer: Lessons from an Active Surveillance Cohort Monday, Nov. 30 9:25AM - 9:35AM Location: N227 Participants Francesco Giganti, MD, Milan, Italy (Presenter) Nothing to Disclose Neophytos Petrides, London, United Kingdom (Abstract Co-Author) Nothing to Disclose Caroline M. Moore, London, United Kingdom (Abstract Co-Author) Speakers Bureau, Myriad Genetics, Inc; Research Grant, GlaxoSmithKline plc; Consultant, STEBA Biotech NV Mark Emberton, London, United Kingdom (Abstract Co-Author) Consultant, GlaxoSmithKline plc; Consultant, sanofi-aventis Group; Consultant, Glide Pharmaceutical Technologies Limited; Consultant, SonaCare Medical, LLC Clare M. Allen, MBBCh, London, United Kingdom (Abstract Co-Author) Nothing to Disclose Alex P. Kirkham, BMBCh, MD, London, United Kingdom (Abstract Co-Author) Nothing to Disclose PURPOSE To describe the natural history of low-grade prostate cancer by mpMRI changes in patients under active surveillance (AS). METHOD AND MATERIALS This study had an authorization from our institutional ethics review board. From our database on patients with prostate cancer, a total of 86 were enrolled in an AS program and had their first mpMRI in 2012 or before. The two reading radiologists, in consensus, knew tumor location and PSA but were blinded to both patient demographics and date of scan. The scans were reported randomly (reducing any bias assuming an increase in size with time). For each visible lesion we measured volume on the sequence best showing the tumor (the same for all scans), as well as attributing a score based on the European Society of Uroradiology -ESUR2012 guidelines. RESULTS 1. 66/86 patients had Gleason 3+3 and 20/86 Gleason 3+4 tumor. Median maximum cancer core lengths were 1 and 3.5 mm, respectively.2. 38/86 patients did not have a visible lesion on the initial MRI (< 3, ESUR criteria). Of these patients, none had developed at a median of 3.56 years of follow up.3. 40/86 patients had a lesion scoring 3/5 or more (ESUR criteria) on more than 2 scans, enabling an estimation of annual growth rate. 25 had Gleason 3+3, and 15 Gleason 3+4. Median monthly increase in volume was 0.4% for Gleason 3+3 and 1.2% for 3+4 (p=0.049, Mann-Whitney test). No significant difference in the median monthly PSA increase between these groups (0.9 vs 0.6%, p=0.42) was observed.4. In 38/40 patients having 2 scans separated by a median of 1.19 years, 9/38 showed a decrease in lesion size between 5 and 50 %. CONCLUSION In a group of men on AS, we never observed development of a convincing lesion in those negative on the first scan. Conversely, it was possible to measure a growth rate in visible tumors, and it was significantly different for Gleason 3+3 and 3+4. Finally, there is considerable inter-scan variability in volume: this must be taken into account when attrbuting a significant increase to a small lesion. CLINICAL RELEVANCE/APPLICATION The significant difference in rate of increase between small tumors of different grades under AS suggests that it is possible to monitor their size on MRI. RC207-06 Multi-parametric MRI (including PIRADS) Monday, Nov. 30 9:35AM - 10:00AM Location: N227 Participants Clare M. Tempany-Afdhal, MD, Boston, MA (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) The state of the art mpMR protocols/sequences for prostate cancer imaging. 2) How to acquire and interpret high quality images. 3) What ACR-Pi-Rads is and how it can be implemented in clinical practice. 4) Current and future role of Prostate MR and ACR- PiRads. ABSTRACT The current state of the art approaches to prostate cancer Multi-parametric MR(mpMR) Prostate imaging will be presented. MRI techniques at 1.5T and 3.0T and pulse seqeunce optimization for a state of the art mpMRI exam will be reviewed. The roles of each seqeunce will be illustrated with clinical case examples to outline technical aspects and interpretative approaches. As the examinations have become complex and the clinical demands are increasing there isa need for standarization of our techniques and interpretative reporting. Thus in keeping with Bi-Rads and Li-Rads, we are developing Pi-Rads. The current ACR-PiRads will be reviewed - goals, methods and clinical applications will be presented and future vision for the role of prostate MR and ACR-PiRADS will be presented RC207-07 Active Surveillance with MRI Monday, Nov. 30 10:05AM - 10:30AM Location: N227 Participants Sadhna Verma, MD, Cincinnati, OH (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) What is active surveillance and how it is done. 2) Who is a candidate for active surveillance. 3) The role of mpMRI in risk stratification for active surveillance. 4) The relevance of mpMRI in addition to clinical parameters in disease management. ABSTRACT ABSTRACT Active Surveillance with MRI Active surveillance is increasingly acknowledged as a preferred strategy for most men with low-risk disease. This lecture will discuss low risk prostate cancer and how it is managed clinically. Role of mpMRI will be reviewed with clinical case examples to show selection, follow- up or possible removal of patients from active surveillance protocols. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Sadhna Verma, MD - 2013 Honored Educator RC207-08 Longitudinal Follow-up Study of Prebiopsy Multiparametric MRI with Cancer- Negative Findings in Patients with Suspicious Prostate Cancer: A Single Institution Experience Monday, Nov. 30 10:30AM - 10:40AM Location: N227 Participants Jun Gon Kim, Seoul, Korea, Republic Of (Presenter) Nothing to Disclose Chan Kyo Kim, MD, PhD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Jung Jae Park, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Byung Kwan Park, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose PURPOSE Few follow-up studies of prebiopsy prostate multiparametric MRI (mpMRI) with cancer-negative findings have been reported. The aim of this study was to investigate the chance and characteristics of missing cancers on prebiopsy mpMRI with cancer-negative findings based on Prostate Imaging Reporting and Data System (PI-RADS) in patients with suspicious prostate cancer (PCa). METHOD AND MATERIALS 584 consecutive patients (mean, 62.7 years; range, 30-86 years) with suspicious PCa who performed initial (n= 391) or repeated prostate biopsies (n= 193) were enrolled in this retrospective study. All patients underwent prebiopsy 3-T mpMRI including T2weighted, diffusion-weighted and dynamic contrast-enhanced imaging. Random systemic core biopsies and MR-targeted core biopsies in cases of cancer-positive MRI findings were performed, while cases with cancer-negative MRI findings underwent random systemic core biopsies during subsequent follow-up. Biopsy-based definition of clinically significant cancer (CSC) was Gleason ≥ 3 + 4 or Gleason 6 with maximal cancer core length (MCL) ≥ 4 mm. The likelihood of PCa on mpMRI was evaluated based on PI-RADS version 2: score 4 or 5 was considered cancer positive. RESULTS Pathologically the cancers were found in 25% (146/584). The cancer-positive MRI findings were found in 17% (99/584) patients and of these, 85.9% (85/99) had pathologically cancer cores. Of 485 patients with cancer-negative MRI findings, a total of 61 (12.5%) had cancer cores [Gleason 6 (n= 42), 3 + 4 (n= 14), 4 + 3 (n= 2), 8 (n= 2), and 9 (n= 1)]: biopsy-naive patients (n= 38) and patients with negative previous biopsy (n= 23). The mean MCL was 3.4 mm (range, 1-12.6 mm). The CSCs were found in 47.5% (29/61). Accordingly cancer-negative MRI findings missed 6% (29/485) CSCs: 4.1% (20/485) in biopsy-naive patients and 1.9% (9/485) in patients with negative previous biopsy. CONCLUSION Prebiopsy 3-T mpMRI with cancer-negative findings misses approximately 12.5% PCa including 6% CSCs in a cohort of biopsy-naive patients and patients with negative previous biopsy. CLINICAL RELEVANCE/APPLICATION In a cohort of biopsy-naive patients or patients with negative previous biopsy, 3-T multiparametric MRI can improve the detection of clinically significant prostate cancers, which can help to select optimal treatment strategies. RC207-09 Magnetic Resonance/Ultrasound (MR/US) Fusion Biopsy in Clinical Practice: Is Systematic Biopsy still Needed to Detect Clinically Significant Prostate Cancers? Monday, Nov. 30 10:40AM - 10:50AM Location: N227 Participants Andrei S. Purysko, MD, Cleveland, OH (Presenter) Nothing to Disclose Leonardo K. Bittencourt, MD, PhD, Rio De Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Antonio C. Westphalen, MD, Mill Valley, CA (Abstract Co-Author) Nothing to Disclose Andrew J. Stephenson, MD, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Erick M. Remer, MD, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Brian R. Herts, MD, Cleveland, OH (Abstract Co-Author) Research Grant, Siemens AG Erika Schneider, PhD, Cleveland, OH (Abstract Co-Author) Stockholder, General Electric Company Stockholder, Pfizer Inc Stockholder, NitroSci Pharmaceuticals, LLC Jennifer Bullen, MSc, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Cristina Magi-Galluzzi, MD, PhD, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Eric Klein, Cleveland, OH (Abstract Co-Author) Nothing to Disclose PURPOSE To compare the detection rates of clinically significant (CS) prostate cancer (PCa), herein defined as a tumor with Gleason score >= 3 + 4, by MR/US fusion biopsy and systematic extended-sextant TRUS (S-TRUS) biopsy. METHOD AND MATERIALS IIRB-approved, HIPAA compliant retrospective study included 256 men (mean age: 62.3 yrs.) with either suspected PCa (n = 187) or enrolled on active surveillance (n = 69). All patients underwent multiparametric MRI (mpMRI) of the prostate on a 3.0 T magnet without endorectal coil as part of clinical care prior to biopsy, with T2, high B-value diffusion, and dynamic contrast enhancing imaging. Patients with potential tumor by mpMRI (n= 193) underwent MR/US fusion biopsy followed by 12-core systematic biopsy (SB) in the same procedure and performed by the same urologist who was aware of the location of the targets; those with negative mpMRI underwent SB only (n = 63). The results of both biopsy techniques alone and combined were evaluated. RESULTS The overall detection rate of PCa in this population was 51.2% (131/256), and CS PCa was detected in 26.6% (68/256) of the men. The overall detection rate of PCa in this population was 51.2% (131/256), and CS PCa was detected in 26.6% (68/256) of the men. In those with positive mpMRI, there was no significant difference in the number of men with CS PCa detected by either biopsy technique (MR/US fusion biopsy: 46 men [23.8%]; SB: 48 men [24.9%]), and both techniques combined detected more men with CS PCA (66 men [34.2%]). CS PCa was detected exclusively by MR/US fusion biopsy in 18 men (9.3%), and by SB in 20 men (10.4%). In most men with CS PCa exclusively detected by SB, the sextants involved were the same (n = 14) or the immediately adjacent ipsilateral sextant (n = 3) where the MRI target was described; in only 3 men (1.5%) the targets were located in a distant sextant from the site involved by CS PCa. PCa was detected in 28.6% (18/63) of the men with negative mpMRI, but only 2 cases (3.2%) were CS PCa. CONCLUSION More CS PCa was detected when MR/US fusion biopsy was combined with SB, with greater contribution from biopsies of the same or immediately adjacent sextants of the MRI targets. CLINICAL RELEVANCE/APPLICATION In clinical practice, MR/US fusion biopsy should be performed in conjunction with systematic biopsy of the same and immediately adjacent sextants of MRI-targets to ensure the detection of CS PCa detected by mpMRI. RC207-10 MR and MR-US Guided Biopsy Monday, Nov. 30 10:50AM - 11:15AM Location: N227 Participants Daniel J. Margolis, MD, Los Angeles, CA, (daniel.margolis@ucla.edu) (Presenter) Research Grant, Siemens AG LEARNING OBJECTIVES 1) List the indications for in-bore MR-guided and MR/US fusion-guided prostate biopsy. 2) Optimize the protocol and image postprocessing of prostate MRI for lesion detection, selection, and delineation. 3) Understand the differences between in-bore MRguided and MR/US fusion-guided prostate biopsy. 4) Describe the advantages and disadvantages of the different kinds of MR/US fusion-guided prostate biopsy. 5) Communicate with referrers to ensure all information is processed correctly for the biopsy session. ABSTRACT Interest in, and growth of, prostate MRI has been largely driven by increasing use of this technology for lesion detection rather than treatment planning. This shift in focus is accompanied by changes in the MRI protocol, and how this information is used. A growing number of opportunities for targeted biopsy, both in-bore direct MRI-guided and MRI-ultrasound image fusion targeting, is accompanied by nearly as many different approaches. Each has advantages and disadvantages, some obvious, and some surprising. Awareness of these issues and how to master them is crucial for providing optimal patient care. These issues range from the hardware and software necessary to plan and perform the biopsy, to the intricacies of information and data communication, to referral and follow-up. A comprehensive, service-line approach ensures patients are followed appropriately at all stages of this process. ABSTRACT Multiparametric MRI has transformed from a tool primarily used for staging of known cancer into one for detection, localization, and sampling of suspected cancer. This has allowed for streamlining and simplifying the protocol use for imaging the prostate, which presents its own challenges, including managing decreased signal-to-noise ratios and interfacing with image-guided targeted biopsy software and hardware. The various platforms available for image-fusion targeted biopsy include in-bore MRI-directed, "cognitive-" or "mental-fusion" MRI-ultrasound targeted biopsy, software image fusion, articulated arm, and electromagnetic tracking. Attendees will learn how to incorporate image-guided targeted biopsy into their practice, how to interface with clinical collaborators and referrers, and how image-guided targeted biopsy improves confidence in managing men with suspected or known prostate cancer. URL http://1drv.ms/1kzFy7W RC207-11 12 Months Follow-Up Results of MRI-Guided Transurethral Ultrasound Ablation for Treatment of Localized Prostate Cancer Monday, Nov. 30 11:15AM - 11:25AM Location: N227 Participants Maya B. Mueller-Wolf, MD, Heidelberg, Germany (Presenter) Nothing to Disclose Sascha Pahernik, MD, Heidelberg, Germany (Abstract Co-Author) Nothing to Disclose Boris Hadaschik, Heidelberg, Germany (Abstract Co-Author) Nothing to Disclose Timur Kuru, MD, Heidelberg, Germany (Abstract Co-Author) Nothing to Disclose Ionel V. Popeneciu, MD, Heidelberg, Germany (Abstract Co-Author) Nothing to Disclose Gencay Hatiboglu, Heidelberg, Germany (Abstract Co-Author) Nothing to Disclose Joseph Chin, MD, London, ON (Abstract Co-Author) Nothing to Disclose Michele Billia, MD, London, ON (Abstract Co-Author) Nothing to Disclose James D. Relle, MD, West Bloomfield, MI (Abstract Co-Author) Nothing to Disclose Jason M. Hafron, MD, West Bloomfield, MI (Abstract Co-Author) Nothing to Disclose Kiran R. Nandalur, MD, Northville, MI (Abstract Co-Author) Nothing to Disclose Mathieu Burtnyk, DIPLPHYS, Toronto, ON (Abstract Co-Author) Nothing to Disclose Heinz-Peter Schlemmer, MD, Heidelberg, Germany (Abstract Co-Author) Nothing to Disclose Matthias Roethke, MD, Heidelberg, Germany (Abstract Co-Author) Speaker, Siemens AG PURPOSE MRI-guided transurethral ultrasound ablation (MR-TULSA) is a novel minimally-invasive technology to treat organ-confined prostate cancer (PCa), aiming to provide local disease control with a low side-effect profile. Directional plane-wave high-intensity ultrasound generates a continuous volume of thermal coagulation to the prostate using real-time MR-thermometry control. A prospective, multi-institutional Phase I clinical study investigated safety, feasibility, and assessed efficacy of MR-TULSA treatment for PCa. METHOD AND MATERIALS 30 patients with biopsy-proven, low-risk prostate cancer were enrolled: age>=65y, T1c/T2a, PSA<=10ng/ml, Gleason<=3+3 (3+4 in Canada only). Under general anaesthesia, the ultrasound device (TULSA-PRO, Profound Medical Inc., Canada) was positioned in the prostatic urethra with guidance from a 3T MRI (Siemens, Germany). Treatment planning was performed under MRI visualization with therapeutic intent of whole-gland ablation. Treatment was delivered under continuous MRI thermometry feedback control. RESULTS MR-TULSA was well-tolerated by all patients without intraoperative complications. Median (5th-9th percentile) treatment time and prostate volume were 36 (24-54) min and 44 (30-89) ml, respectively. Maximum temperature measured during treatment depicted a continuous region of heating shaped accurately to the prostate to within 0.1 ± 1.3 mm. CE-MRI confirmed the resulting conformal non-perfused volume, and correlated well with the ablative temperatures on MR-thermometry. Successful treatment was further indicated by a median PSA decrease from 5.8 (2.8-8.9) ng/ml to 0.8 (0.1-3.2) ng/ml after one month remaining stable at 0.8 (0.13.7) ng/ml to 12 month. MRI and biopsy findings at 12 month show diminutive prostate volumes, averaging 51% fibrosis (n=29). Positive biopsies (55% of patients) demonstrate 61% reduction in total cancer length. CONCLUSION MRI-guidance enables accurate treatment planning, real-time dosimetry and control of the thermal ablation volume. Primary outcomes show that MR-TULSA is safe and precise for prostate ablation. Phase I data are sufficiently compelling to study MRTULSA in a larger efficacy trial. CLINICAL RELEVANCE/APPLICATION Whole-gland ablation can be safely and accurately achieved using MR-TULSA, which represents a minimally-invasive treatment option for organ-confined prostate cancer. RC207-12 A Pilot Study to Evaluate Outpatient, Transrectal, Magnetic Resonance-guided Laser Focal Therapy for Treatment of Localized Prostate Cancer Monday, Nov. 30 11:25AM - 11:35AM Location: N227 Participants Bernadette M. Greenwood, BS, RT, Indian Wells, CA (Abstract Co-Author) Nothing to Disclose John F. Feller, MD, Indian Wells, CA (Presenter) Consultant, Koninklijke Philips NV Consultant, Visualase, Inc Stuart T. May Sr, MD, Indian Wells, CA (Abstract Co-Author) Nothing to Disclose Roger McNichols, PhD, Houston, TX (Abstract Co-Author) Employee, BioTex, Inc Wes Jones, Indian Wells, CA (Abstract Co-Author) Nothing to Disclose Axel Winkel, DiplEng, Schwerin, Germany (Abstract Co-Author) Employee, Koninklijke Philips NV PURPOSE In the United States alone, new prostate cancer cases for 2014 were estimated at 233,000 and deaths at 29,480. Focal therapies for low risk and intermediate risk localized prostate cancer are increasingly being explored. Our objective is to investigate the safety and feasibility of using outpatient MR- (magnetic resonance) guided laser focal therapy for MR-visible prostate cancer utilizing a transrectal approach for laser applicator placement and therapy delivery. METHOD AND MATERIALS All MR-guided therapy was delivered using a 1.5T Philips Achieva XR system (Philips Healthcare, Best, The Netherlands) for both image acquisition and real-time thermometry. Follow-up multiparametric MRI's (mpMRI) were performed on the same scanner as were all follow-up MR-guided prostate biopsies. DynaCAD and DynaLOC (Invivo, Orlando, FL, USA) software were used for image analysis and interventional planning. Laser therapy was delivered using a Visualase (BioTex, Houston, TX, USA) 15W 980 nm laser applicator introduced transrectally using the DynaTRIM (Invivo, Orlando, FL, USA) RESULTS 34 men were treated. 45 cancer foci were treated. Total procedure time was between 1.5 and 4 hours. MRI volume of coagulation necrosis ranged from 1.2-5.0cc. No serious adverse events or morbidity were reported. 7 treatment regions were positive at 6 month biopsy, consistent with residual/recurrent cancer (23% of subjects, 15% of treated regions). 4 regions were retreated with laser focal therapy. We observed a 35% decrease in mean PSA 1 year post-therapy and no statistically significant change is IPSS and SHIM scores at 6 months post-treatment. 4 patients went on to whole gland therapy: 3 incidence cancer patients (2 Gleason Score 4+4=8, 1 Gleason Score 4+3=7 multi-focal) elected radical prostatectomy (RP). No additional technical difficulty with dissection was reported by the surgeon performing RP. 1 Gleason 3+3=6 elected proton beam therapy (PBT) before undergoing 6 month follow-up and biopsy. Incidence cancer rate was 10%. CONCLUSION Our data indicate that outpatient transrectally delivered MR-guided laser focal therapy for localized prostate cancer is both safe and feasible. CLINICAL RELEVANCE/APPLICATION In the current climate of cost-reduction and emphasis on minimally-invasive treatment of cancer, focal treatment of prostace cancer with a precisely delivered energy source under MRI-guidance may have favorable results for cost control and quality of life. RC207-13 Focal Therapies Monday, Nov. 30 11:35AM - 12:00PM Location: N227 Participants Aytekin Oto, MD, Chicago, IL, (oto@uchicago.edu) (Presenter) Research Grant, Koninklijke Philips NV; ; ; LEARNING OBJECTIVES 1) Emerging paradigm of focal therapy for early stage low risk prostate cancer. 2) Current status of different focal therapy methods including laser ablation, high intensity focused US, electroporation and cryotherapy. 3) Challenges in patient monitoring following focal therapy. 4) Future developments in focal therapy of prostate cancer and the importance of radiologist's involvement. ABSTRACT TITLE: Image guided focal therapy of prostate cancer Focal therapy of low risk early stage prostate cancer is increasingly important as a minimally invasive option for many patients. The rationale, patient selection criteria and challenges for image-guided focal prostate cancer therapy will be discussed. The essential technical details, advantages and disadvantages of clinically available focal therapy methods will be reviewed. Post-therapy patient monitoring options will be presented. Future developments in the area of focal therapy of prostate cancer and opportunities for involvement of radiologists in focal therapy will be explored. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Aytekin Oto, MD - 2013 Honored Educator GUS-MOA Genitourinary Monday Poster Discussions Monday, Nov. 30 12:15PM - 12:45PM Location: GU/UR Community, Learning Center GU AMA PRA Category 1 Credit ™: .50 FDA Discussions may include off-label uses. Participants Zhen J. Wang, MD, Hillsborough, CA (Moderator) Nothing to Disclose Sub-Events GU210-SDMOA1 Got Stones? Utility of Kidney Graft Computed Tomography Prior to Transplantation Station #1 Awards RSNA Country Presents Travel Award Participants Monserrat Reig Sosa, MD, Distrito Federal, Mexico (Presenter) Nothing to Disclose Jorge David Magana, MD, Mexico, Mexico (Abstract Co-Author) Nothing to Disclose Carlos Mendez Probst, MD, Mexico, Mexico (Abstract Co-Author) Nothing to Disclose Jorge Vazquez-Lamadrid, MD, Mexico, Mexico (Abstract Co-Author) Nothing to Disclose PURPOSE To allow a complete evaluation of a cadaveric kidney graft prior to transplant To reduce the morbidity in kidney recipients caused by donor nephrolithiasis To encourage the use of non-enhanced kidney graft CT before transplant, and provide a preventive treatment. METHOD AND MATERIALS Prospective non-enhanced CT Scanners (Siemens Somatom 64, Munich and GE Lightspeed VCT 64, Milwaukee) ex vivo evaluation of cadaveric renal allograft transplants from march 2013 through march 2015 in a reference transplant medical center. The protocols of acquisition included one phase scan with 3 mm thickness cuts and reformatting in 0.6 mm in an overall time of 2 min. After this the scan was reviewed by a board certified radiologist evaluating the following: Presence, location, number, size and density (measured in Hounsfield Units) of the urinary stones. RESULTS 32 cadaveric donors where enrolled in the period of time mentioned (22 males and 8 females), providing a total of 59 kidney grafts. Nine grafts reported stones, multiple stone disease was found in two grafts with 2 and 3 stones respectively, the latest corresponding to one of the donors with bilateral disease The median kidney stone diameter was 2.8 mm (ED 1.03-3.74mm) with an average density of 198.5 HU (ED 51-919 HU) Four of the nine grafts underwent back table retrograde flexible nephroscopy and basket stone removal while under cold ischemia, three out of these were considered successful; In a single unsuccessful case, a 1.2 mm stone could not be located during the intervention, probably because of inadverted flushing The remaining five kidneys were transplanted with a follow up CT performed 12 months after the transplantation in which four of the patients were negative for nephrolithiasis, the fifth patient corresponding to the horseshoe kidney developed new non obstructive stones under 2 mm diameter CONCLUSION This data supports the use of non enhanced MDCT scan kidney graft prior to transplantation to allow an accurate screening for the presence of nephrolithiasis, rendering a helpful diagnostic tool to prevent further complications associated with nephrolithiasis. CLINICAL RELEVANCE/APPLICATION Prevention and oportune tratment in renal ex vivo transplants to improve outcome GU213-SDMOA4 Detection and Characterization of Prostate Cancer with Multiparametric MRI (mpMRI): Do Learning and Experience Matter for Diagnostic Accuracy? Station #4 Participants Rajan T. Gupta, MD, Durham, NC (Presenter) Consultant, Bayer AG; Speakers Bureau, Bayer AG; Consultant, Invivo Corporation Daniele Marin, MD, Cary, NC (Abstract Co-Author) Nothing to Disclose Bhavik N. Patel, MD,MBA, Durham, NC (Abstract Co-Author) Nothing to Disclose Kirema Garcia-Reyes, MD, Durham, NC (Abstract Co-Author) Nothing to Disclose Kingshuk Choudhury, PhD, Durham, NC (Abstract Co-Author) Nothing to Disclose Lisa M. Ho, MD, Durham, NC (Abstract Co-Author) Nothing to Disclose Tracy A. Jaffe, MD, Durham, NC (Abstract Co-Author) Nothing to Disclose Thomas J. Polascik, MD, Durham, NC (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate effect of dedicated reader education on accuracy/Gleason score estimation of index and anterior prostate cancer (PCa) diagnosis with mpMRI in attending radiologists compared to abdominal imaging fellows. METHOD AND MATERIALS 4 blinded attending abdominal imagers with 2-16 years of experience evaluated 31 prostate mpMRIs in this IRB-approved, HIPAAcompliant, retrospective study for index lesion and anterior PCa detection (including Gleason score estimation). Following dedicated education program, readers reinterpreted cases after a 2-4 month memory extinction period, blinded to initial reads. Reference standard was established combining whole mount histopathology with mpMRI findings by a board-certified radiologist with 5 years of prostate mpMRI experience. Multivariate analysis was performed to assess the effects of learning and reader experience. Results for attending radiologists were then compared with prior reader study results in radiology fellows (using the same set of cases). RESULTS Index cancer detection (attending vs. fellow): pre-education accuracy 64.5% vs. 74.2%; post-education accuracy 71.8% vs. 87.7% (p=0.12 vs. p=0.003). Gleason score estimation (index): pre-education accuracy 46.8% vs. 54.8%; post-education accuracy 57.3% vs. 73.5% (p=0.04 vs. p=0.0005). Anterior PCa detection: pre-education accuracy 46.4% vs. 54.3%; posteducation accuracy 75% vs. 94.3% (p=0.02 vs. p=0.001). Gleason score estimation (anterior): pre-education accuracy 42.9% vs. 45.7%; post-education accuracy 67.9% vs. 80% (p=0.03 vs. p=0.002). These effects were all attributable to learning and not to reader experience based on multivariate analysis. CONCLUSION Accuracy of anterior PCa detection and Gleason score estimation for both index and anterior cancers significantly increased following dedicated reader education for both attendings and fellows. In addition, accuracy for index cancers was statistically significantly improved for fellows post-education. The degree of statistically significant improvement was higher for fellows vs. attendings overall. CLINICAL RELEVANCE/APPLICATION Performance in detection and characterization of PCa on mpMRI can be improved with dedicated reader education, however, it may be that the earlier the educational intervention is done, the more significant the improvement. GU214-SDMOA5 Pathologic Correlation between Transperineal in-bore 3-Tesla MR Imaging-Guided Prostate Biopsy and Radical Prostatectomy Station #5 Participants Erik Velez, BS, San Francisco, CA (Presenter) Nothing to Disclose Christopher B. Allard, Boston, MA (Abstract Co-Author) Nothing to Disclose Kemal Tuncali, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Andriy Fedorov, PhD, Boston, MA (Abstract Co-Author) Nothing to Disclose Adam Kibel, Boston, MA (Abstract Co-Author) Nothing to Disclose Clare M. Tempany-Afdhal, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate the accuracy of in-bore transperineal 3-Tesla (T) magnetic resonance (MR) imaging-guided prostate biopsies for predicting final Gleason grades among patients who underwent radical prostatectomy (RP). METHOD AND MATERIALS We reviewed the records of 214 men who underwent transperineal MR imaging-guided biopsy (tpMRGB) from 2010-2015. All patients received a baseline scan using 3-T multiparametric MRI (mpMR) with endorectal coil and were selected for biopsy based on findings of a target to biopsy or having a high degree of clinical suspicion for cancer. The tpMRGB were performed in a 70-cm wide-bore 3-T device. Patients who underwent RP within one year from biopsy were included. Descriptive statistics were performed to assess the concordance between tpMRGB and final pathology among patients with and without previous transrectal ultrasound (TRUS)-guided biopsies. RESULTS A total of 24 men underwent tpMRGB with subsequent RP within one year. At the time of biopsy median age was 65 years (interquartile range [IQR] 11.7) and median PSA was 8.7 ng/mL (IQR 8.9). The median time between biopsy and RP was 85 days (IQR 50.5). Final pathology revealed Gleason 3+4=7 in 12 patients, 4+3=7 in 7 patients, and 4+4=8 in 2 patients. We observed concordance between MR biopsy and RP in 21 cases (87.5%) in terms of summed Gleason scores. Pathologic Gleason upgrading occurred in 3 cases (12.5%), all of which had final pathologic grades of 3+4=7.16 of the 24 patients had previously undergone TRUS biopsies, of which 6 were negative and 10 were positive for Gleason ≤6. tpMRGB revealed Gleason upgrading in 8 of the positive TRUS biopsies, all of which were concordant with RP pathology. Among all patients with negative TRUS biopsies, MR biopsy demonstrated evidence of cancer and was concordant with RP results in 83% of cases. CONCLUSION Gleason scores determined by tpMRGB at 3-T accurately correlate to final RP Gleason score. This may offer a more precise method to diagnose and appropriately treat men with prostate cancer, especially in patients with negative or low-grade TRUS in which clinically significant cancer is suspected. CLINICAL RELEVANCE/APPLICATION Prostate cancer affects 1 in 7 American men. MR-guided prostate biopsies may offer a more accurate means of characterizing prostate pathology than conventional methods. GU215-SDMOA6 Predicting Renal Calculus Composition: Does the Plane of Imaging Matter? Station #6 Participants Ari J. Spiro, MD, Bronx, NY (Presenter) Nothing to Disclose Alla M. Rozenblit, MD, Bronx, NY (Abstract Co-Author) Nothing to Disclose David Hoenig, MD, Bronx, NY (Abstract Co-Author) Nothing to Disclose Victoria Chernyak, MD, Bronx, NY (Abstract Co-Author) Nothing to Disclose PURPOSE To compare accuracy of renal calculus attenuation values measured on axial vs coronal images in classifying stone composition. METHOD AND MATERIALS This retrospective study included patients with nephrolithiasis who had non-contrast CT followed by percutaneous nephrolithotomy (PCNL) and stone composition analysis. By stone composition, patients were divided into Calcium group (with Ca-oxalate monohydrate, Ca-oxalate dehydrate, Ca-apatite calculi), and Urate group ( with urate calculi). Largest size and attenuation of calculi were measured on coronal and axial images. Ability of maximum attenuation value measured on axial (Axial-Max) and coronal (Cor-Max) images to classify stone composition was assessed by receiver-operator curve. RESULTS There were 107 calculi, 16 (14.9%) in Urate group and 91 (85.1%) in Calcium group, with mean patient ages 52.8±14.9 and 57.7±10.5 years (p=0.208), respectively. Median time intervals between CT and PCNL were 48 (IQR 31.5-76.5) and 58 (IQR 30-92) days in Urate and Calcium groups, respectively (p=0.588). Mean calculi sizes were 19.9±9.9mm and 18.2±6.7mm in Urate and Calcium groups, respectively (p=0.536). In Urate group, mean Axial-Max and Cor-Max were 576±162 HU and 621±184 HU (p=0.04), respectively. In Calcium group, mean Axial-Max and Cor-Max were 1,193±317 HU and 1,299±310 HU (p=0.0001), respectively. Areas under the curve were 0.937 (95%CI 0.89-0.99) and 0.941 (95%CI 0.89-0.99) for axial and coronal images, respectively. Axial-Max ≥670 HU has accuracy of 92.5% and LR+ of 7.5 for diagnosing calcium-containing calculi. Cor-Max≥773 HU has accuracy of 94.4% and LR+ of 7.6 for diagnosing calcium-containing calculi. CONCLUSION Maximum renal calculus attenuation values on coronal images are higher than those on axial, but are equally accurate in classifying stone composition. CLINICAL RELEVANCE/APPLICATION We confirm that despite the slight difference in values, coronal images can be used for predicting Ca-containing stones. UR114-EDMOA7 More Than Just a Stone: What Can be Hidden Behind a Renal Colic? Station #7 Participants Elena Inchausti, MBBS, Donostia, Spain (Presenter) Nothing to Disclose Juan Vega Eraso, San Sebastian, Spain (Abstract Co-Author) Nothing to Disclose Carmen Biurrun Mancisidor, MD, Donostia, Spain (Abstract Co-Author) Nothing to Disclose Miren Zubizarreta, Donostia, Spain (Abstract Co-Author) Nothing to Disclose Virginia Gomez, San Sebastian, Spain (Abstract Co-Author) Nothing to Disclose Ane Etxeberria, Donostia, Spain (Abstract Co-Author) Nothing to Disclose TEACHING POINTS - To understand and be concerned of the complications that can turn up from a simple renal colic. - To recognize other situations that because of their physiopathology (identical to nephritic colic) can simulate this entity. TABLE OF CONTENTS/OUTLINE Epidemiology of renal colic. Physiopathology. Diagnostic imaging. We present some cases in which a simple nephritic colic developed different complications: Impaction of the stone along the ureter with hydroureter/hydronephrosis. Spontaneous rupture of renal pelvis(SRRP) with urinoma formation. Recurrent urinary tract infections/pyelonephritis and ureteritis.Other unusual complications exposed are: Spontaneous renal artery dissection with renal infarction. Acute cortical necrosis. Chronic infection: xantogranulomatous pyelonephritis. 5.Other situations mimicking renal colic are: Ureteral TBC. Primary carcinoma of the distal ureter /renal pelvis. Retroperitoneal fibrosis affecting both ureters formig renal abcesses. Peritoneal implant causing hydronephrosis. Blood clot into the ureter, because of a renal AVM. Calcification of suture thread in the ureter (previous renal surgery). UR169-EDMOA8 Rare Sighting: A Review of Uncommon Renal Neoplasms and Mimics with Radiologic-Pathologic Correlation Station #8 Participants Lawrence J. Bahoura, MD, Royal Oak, MI (Presenter) Nothing to Disclose Daniel L. George, MD, Royal Oak, MI (Abstract Co-Author) Nothing to Disclose Monisha Shetty, MD, Royal Oak, MI (Abstract Co-Author) Nothing to Disclose Mitual B. Amin, MD, Royal Oak, MI (Abstract Co-Author) Nothing to Disclose Syed Zafar H. Jafri, MD, Royal Oak, MI (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Renal tumors are commonly encountered on imaging. Although the vast the majority of malignant kidney tumors are clear cell and papillary renal cell carcinomas, there are many, much more rare neoplams, both malignant and benign, as well as mimics of neoplasm that can be difficult to distinguish.This exhibit aims to:1. Present examples of extremely rare, pathologically proven renal neoplasms, mostly malignant, as well as select benign entities and mimics of neoplasm.2. Highlight specific clinical and imaging features, along with pathologic correlation, of the various rare entities to arm the radiologist with knowledge to expedite diagnosis and more effectively guide patient care. TABLE OF CONTENTS/OUTLINE I. ObjectivesII. Rare Renal Neoplasms-Collecting duct carcinoma-Birt-Hogg-Dube Syndrome with chromophobe cell carcinomaSynovial sarcoma of the kidney-Mixed papillary and clear cell carcinoma-Plasmacytoma-Mixed epithelial and stromal tumor-Renal medullary carcinoma-Capsular sarcoma-Capsular leiomyosarcoma-Mixed epithelioid malignant angiomyolipoma-Multilocular cystic nephroma with carcinoma-Metanephric adenoma-Squamous cell carcinoma of the collecting system-Rhabdoid tumorIII. Mimics of neoplasm-Renal sarcoidosis-Hydatid cysts-Renal splenosisIV. DiscussionV. Conclusion GUS-MOB Genitourinary Monday Poster Discussions Monday, Nov. 30 12:45PM - 1:15PM Location: GU/UR Community, Learning Center GU AMA PRA Category 1 Credit ™: .50 FDA Discussions may include off-label uses. Participants Zhen J. Wang, MD, Hillsborough, CA (Moderator) Nothing to Disclose Sub-Events GU216-SDMOB1 Mini-invasive Treatment of Uterine Adenomyosis Using MRgFUS: Success Rate and MRI Imaging Follow-up after 4 Years Station #1 Participants Fabiana Ferrari, MD, L'Aquila, Italy (Presenter) Nothing to Disclose Anna Miccoli, MD, L'Aquila, Italy (Abstract Co-Author) Nothing to Disclose Francesco Arrigoni, Coppito, Italy (Abstract Co-Author) Nothing to Disclose Eva Fascetti, MD, L'Aquila, Italy (Abstract Co-Author) Nothing to Disclose Giulio Mascaretti, MD, L'Aquila, Italy (Abstract Co-Author) Nothing to Disclose Carlo Masciocchi, MD, L'Aquila, Italy (Abstract Co-Author) Nothing to Disclose PURPOSE To demonstrate the efficacy of uterine adenomyosis treatment using Magnetic Resonance imaging-Guided Focused Ultrasounds (MRgFUS) analyzing MRI imaging and success rate after 4 years. METHOD AND MATERIALS A total of 21 patients aged between 28 and 51, affected by uterine adenomyosis (14 focal and 7 diffuse forms) were treated in our department with MRgFUS. We submitted the patients to the same MRI protocol, respectively before treatment and then after 1, 2 and 4 years from the treatment. We analyzed the uterine wall morphology and the possible recurrence of the disease measuring the thickness of the junctional zone. Pre-treatment and post-treatment values were compared. Symptomatology was evaluated through the symptom-severity-score questionnaire comparing the pre-treatment score with the one obtained after 1 and 4 years from the treatment. Patients were submitted to one treatment alone employing the specific therapeutic plan of high-energy-gridsonication. RESULTS After 1 and 4 years from the treatment, 16 patients (76%) with focal adenomyosis did not present recurrence of pathology and a good recovery of the uterine wall morphology was observed. Only 5 (24%) out of 21 patients showed a recurrence of adenomyosis focus after 1 year and were submitted to a second treatment. After 4 years from the treatment, 16/21 patients showed thickness of the junctional zone less then 12 mm; 5/21 had a junctional zone more then 12 mm. After 1 year from the treatment symptomatology presented a reduction of about 80% if compared to the pre-treatment one with a progressive improvement after 4 years. CONCLUSION In cases of focal adenomyosis, MRgFUS permits a good resolution of symptomatology maintaining the integrity of the uterus, without significant recurrence of the pathology. Differently, in the diffuse forms of adenomyosis, which are more difficult to be treated, it is possible to repeat the treatment. MRgFUS allows the control of the pathology which may recur. CLINICAL RELEVANCE/APPLICATION The MRgFUS treatment of adenomyosis permits a significant reduction of the junctional zone thickness and a good resolution of the symptoms especially in the focal forms with the possibility to repeat the treatment in case of recurrences. GU217-SDMOB2 Voxel-Based Whole Lesion Enhancement Parameters: A New Approach to Discriminating Clear Cell Renal Cell Carcinoma from Renal Oncocytoma Station #2 Participants Frank K. Chen, MD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Darryl Hwang, PhD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Mittul Gulati, MD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Steven Cen, PhD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Bhushan Desai, MBBS, MS, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Felix Y. Yap, MD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Megha Nayyar, BA, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Inderbir Gill, MD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Vinay A. Duddalwar, MD, FRCR, Aberdeen, United Kingdom (Presenter) Research Grant, General Electric Company PURPOSE Clear cell renal cell carcinoma (ccRCC) is the most common subtype of renal cell cancer, and renal oncocytoma (RO) is the second most common benign renal neoplasm after angiomyolipoma. Differentiating ccRCC from RO is often a diagnostic challenge given similarities in epidemiology, presentation, and imaging. The purpose of our study is to evaluate the use of voxel-based whole lesion enhancement parameters on contrast enhanced computed tomography to discriminate ccRCC from RO. METHOD AND MATERIALS In this institutional review board-approved study, we retrospectively queried the surgical database for post nephrectomy patients who had pathology proven ccRCC or RO and had preoperative multiphase CECT of the abdomen between June 2009 and August 2013. Preliminary evaluation of 69 patients (46 patients with ccRCC and 23 patients with RO) was performed. Multiphase CT acquisitions were transferred to a Synapse 3D workstation, and tumor regions of interest were manually segmented. Voxel-based contrast enhancement values were collected from the lesion segmentation and displayed as a histogram. Mean and median enhancement, mean and median deenhancement, and histogram distribution parameters skewness, kurtosis, standard deviation, and interquartile range were calculated for each lesion. Comparison between ccRCC and RO was made using each imaging parameter. For enhancement and deenhancement, which had normal distribution, independent t-test was used. For histogram distribution parameters, which did not have normal distribution, Wilcoxon rank sum test was used. RESULTS RO had significantly higher mean and median whole lesion enhancement (p < 0.01) on excretory phase than ccRCC while ccRCC had significantly higher mean (p = 0.01) and median whole lesion deenhancement (p < 0.01). For histogram distribution parameters, ccRCC had significantly higher interquartile range on arterial (p < 0.01) and excretory phases (p = 0.03), significantly higher skewness on excretory phase (p = 0.02), and significantly higher standard deviation on arterial (p = 0.01) and nephrographic phases (p = 0.03) compared to RO. CONCLUSION Preliminary results from our study suggest that voxel-based whole lesion enhancement parameters can be used as a quantitative tool to discriminate ccRCC from RO. CLINICAL RELEVANCE/APPLICATION While enhancement characteristics have been described to differentiate ccRCC from RO, this new method is an additional technique to categorize these lesions. GU218-SDMOB3 Benign Enhancing Solid Components of Mature Ovarian Teratoma : MR Imaging Features and Pathologic Correlation Station #3 Participants Kyeong Ah Kim, MD, Seoul, Korea, Republic Of (Presenter) Nothing to Disclose Hoon Jung Shin, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Chang Hee Lee, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Jae Woong Choi, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Yang Shin Park, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Cheol Min Park, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose PURPOSE Mature teratoma (MT) is one of the most common benign ovarian neoplasm, but the tumor undergoes malignant transformation in 12% of cases. Squamous cell carcinoma is the most commonly associated malignancy. Enhancing portion of MT is known as possibility of malignant transformation on contrast enhanced MR. We recently experienced the cases of benign MT with enhancing solid component on pelvis MR. We have had a question about enhancing solid component within MT of ovary on MR always means malignant transformation. The purpose of this work is to evaluate the benign enhancing solid component within MT of ovary on pelvis MR and to correlate MR findings with pathology. METHOD AND MATERIALS We retrospectively reviewed MR findings and pathologic reports of the 126 patients (n=154 masses) with pathologically confirmed benign and malignant ovarian teratomas who underwent pelvis MR at our institution from January 2004 to January 2015. We identified 22 patients (n=24) who had benign enhancing solid components within MTs. MR images were reviewed for the following characteristics: the largest diameter, appearance, and border of the enhancing solid components and presence of transmural growth, lymphadenopathy, or metastasis. Pathologic analysis were also performed in available cases (n=13). RESULTS The ages of patients ranged from 6 to 68 years (mean; 28.5 years). The enhancing solid components were observed in 24 (18.8%) of 128 MTs. The largest diameter ranged from 5.9 - 42.2 mm (mean, 18 mm). The appearance was variable. 19 (79.2%) of 24 cases had regular borders. No cases showed transmural growth, lymphadenopathy, or metastasis. In pathologic analysis, solid components of MT were confirmed as glial tissue (n=8), thyroid tissue (n=3), and fibrous stroma (n=2). CONCLUSION Enhancing solid component associated with MT of ovary is not infrequent. It does not necessarily indicate malignant transformation. Because of the size and complexity of ovarian MTs, surgical removal is usually recommended; however, excessive surgical intervention can be potentially avoided with an accurate diagnosis. CLINICAL RELEVANCE/APPLICATION Enhancing solid component associated with mature teratoma of ovary on pelvis MR is not infrequent. Excessive surgical intervention can be potentially avoided with an accurate diagnosis. GU219-SDMOB4 Clinical Impact of Prostate Cancer Detection with Extrapolated High b-value DWI Station #4 Participants Sadhna Verma, MD, Cincinnati, OH (Presenter) Nothing to Disclose Jason W. Young, MD, Cincinnati, OH (Abstract Co-Author) Nothing to Disclose Sarad Sarkar, Grass Valley, CA (Abstract Co-Author) Employee, Eigen Rajesh Venkataraman, PhD, Grass Valley, CA (Abstract Co-Author) Employee, Eigen Xu Yang, Grass Valley, CA (Abstract Co-Author) Nothing to Disclose Krishnanath Gaitonde, MD, CIncinnati, OH (Abstract Co-Author) Nothing to Disclose PURPOSE To assess the clinical impact of prostate cancer detection using acquired versus extrapolated high b-value diffusion weighted imaging (DWI) computed using 4 diffusion models. METHOD AND MATERIALS 50 sequential patients from 2013-2015 with pathologically proven prostate cancer (CaP) were chosen for analysis. 3T Multiparametric prostate MRI exams of the patients included one of 2 low b-value DWI protocols (b=100, 600, 1200 or b=15, 250, 800, 1200) and a high b-2000 DWI. Additionally, high b-2000 DWI was extrapolated from the lower b-value images using 4 diffusion models - Monoexponential, IVIM, Stretched exponential and Kurtosis. All images were scored on subjective quality and readability independently by 2 radiologists and 1 resident. Lesions were identified by consensus on all images by the 3 readers and subjectively graded for lesion conspicuity. Lesion-to-background contrast ratios were computed for each lesion on all images. Pathological ground truth was established using MRI-Ultrasound fusion prostate biopsy of the identified lesions. Logistic regression analysis was conducted to compare the CaP predictive capabilities of acquired b-2000 DWI versus computed b-2000 DWI from the 4 models. RESULTS All extrapolated b-2000 series demonstrated unanimously higher ratings for subjective quality and readability then acquired b-2000 except the Kurtosis model (Wilcoxon Rank Test, p<0.0001). All extrapolated DWI (except Kurtosis) also demonstrated better lesion conspicuity in a direct comparison with acquired b-2000 DWI (T-test, p < 0.0001). Mathematical computation demonstrated higher lesion to background contrast ratio (LBCR) for all extrapolated DWI compared to acquired b-2000 DWI (ANOVA, p<0.0001). Logistic regression analysis determined that the LBCR of extrapolated b-2000 DWI was a better predictor of CaP than the LBCR of acquired b-2000 DWI (p-value ~ 0.05). Receiver Operator Curve (ROC) analysis demonstrated higher area under the curve for exponential b2000 DWI (72%) as compared to acquired b-2000 DWI (65%) or PSA (57%) alone CONCLUSION The increased lesion conspicuity of extrapolated DWI vs acquired high b-value DWI may be a major advantage in CaP detection. CLINICAL RELEVANCE/APPLICATION The increased lesion conspicuity of extrapolated DWI vs acquired high b-value DWI may be a major advantage in CaP detection Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Sadhna Verma, MD - 2013 Honored Educator GU220-SDMOB5 Initial Application of T2* Mapping of the Uterine Fibroids in the Screening of MR-HIFU Station #5 Participants Ying Zhu, MD, Bejing, China (Presenter) Nothing to Disclose Queenie Chan, PhD, Hong Kong, China (Abstract Co-Author) Nothing to Disclose Xiaoying Wang, MD, Beijing, China (Abstract Co-Author) Nothing to Disclose PURPOSE In our short-term clinical study, we extracted T2* values from T2* map to investigate that if oxygenation of the fibroids correlated with the efficacy of sonication. METHOD AND MATERIALS Eighteen patients with 25 uterine fibroids who received MR-HIFU treatment were included in our study. T2* mapping were achieved when screening. All data were acquired on a 3T MRI scanner , utilizing a 32-channel phased array coil. Multi echo gradient echo sequence was used. T2* maps of the fibroids were processed by using the post processing software in a proprietary programming environment. The T2* values of the gluteus muscles were also measured to check the stability of the images. Funaki classification was used to classify all fibroids into three types on T2WI as low signal intensity (SI) (type1), intermediate SI (type2), and high SI (type3). Non-perfused volume (NPV) was measured in the contrast-enhanced images immediately after treatment. The volumes of the whole fibroid and residual parts were also measured in the contrast-enhanced images at both post-treatment and three-month follow-up. The residual fibroid was defined as the non-necrotic part. RESULTS Among the 25 treated fibroids, 12 were type1 and 13 were type2. Independent samples t-test revealed that the mean T2* value of type 2 fibroids (31.85±7.40ms) was significantly higher than that of type 1 (25.60±5.08ms, t=-2.28, P=0.032). However there was no significant difference between the two types in the NPV (t=0.54, P=0.60). Spearman correlation analysis showed no significant correlation between the NPV and the T2* value (r=-0.24, P=0.24). We found the volume of residual fibroids was increasing in four of the 25 fibroids, and their mean T2* value (37.40±6.57ms) was significantly higher than the others (27.40±5.89ms, t=-3.05, P=0.006), and the volume change of the residual fibroid had correlation with their T2* value (r=0.499, P=0.011). CONCLUSION Our study showed that the oxygenation might be different in fibroids with different Funaki classification. The four fibroids with growing residual part suggested that T2* mapping may improve the criteria for selecting uterine fibroids amenable to treatment with MR-HIFU. CLINICAL RELEVANCE/APPLICATION The four fibroids with growing residual part suggested that T2* mapping may improve the criteria for selecting uterine fibroids amenable to treatment with MR-HIFU. GU221-SDMOB6 Quantification of Renal Stone Composition in Mixed Stones Using Dual-Energy CT: A Phantom Study Station #6 Participants Shuai Leng, PhD, Rochester, MN (Presenter) Nothing to Disclose Alice Huang, Madison, WI (Abstract Co-Author) Nothing to Disclose Juan Montoya, Rochester, MN (Abstract Co-Author) Nothing to Disclose Xinhui Duan, PhD, Rochester, MN (Abstract Co-Author) Nothing to Disclose James C. Williams, PhD, Indianapolis, IN (Abstract Co-Author) Nothing to Disclose Cynthia H. McCollough, PhD, Rochester, MN (Abstract Co-Author) Research Grant, Siemens AG PURPOSE To demonstrate the feasibility of using dual-energy (DE) CT to accurately quantify the percent composition of uric acid (UA) and non-uric-acid (NUA) components of urinary stones having mixed composition. METHOD AND MATERIALS A total of 24 renal stones were selected and analyzed with microCT to serve as the reference standard for UA and NUA composition. These stones were then placed in 6 water phantoms with lateral widths of 30, 35, 40, 45, 50, and 55 cm to simulate the attenuation from slim to obese adults. The stone-containing phantoms were scanned on a third-generation dual-source CT scanner (Somatom Force, Siemens Healthcare, Germany) using dual-energy modes adaptively selected based on phantom size. The low energy beam was set to 70, 80, 90 or 100 kV, based on patient size, and the high energy beam was consistently set to150 kV plus a 0.6-mm tin filter. Dual energy analysis was performed using an in-house software package, in which the CT number ratio (CTR=low-energy CT number/high-energy CT number) was calculated for each pixel of the stones. Each pixel was then classified as UA or NUA by comparing the CTR with a single preset threshold, which was determined by finding the threshold with the lowest root-mean-square error (RMSE) across all stones compared to the reference standard. Minimal and maximal absolute errors were then calculated. A paired t-test was performed to compare the stone composition determined with DECT with the reference standard of microCT. RESULTS Stone volume ranged from 75.3 to 319.1 mm3. Among these stones, 1 was pure UA, 1 was pure NUA, and the remaining 22 were mixed stones, with the percentage of UA ranging from 12% to 93% and the percentage of NUA ranging from 7% to 88%. The optimal CTR threshold ranged from 1.27 to 1.55, based on phantom size and tube potential. The RMSE was from 9.60% to 12.87% for all phantom sizes. The minimum absolute UA errors ranged from 0.04% to 1.24%, and the maximum absolute UA errors ranged from 22.05% to 35.46%. Paired t-tests showed no significant difference in the UA percentages estimated by DECT and microCT (p values ranged from 0.20 to 0.96). CONCLUSION Accurate quantification of UA and NUA composition in mixed stones is possible using DECT. CLINICAL RELEVANCE/APPLICATION As most urinary stones have mixed compositions, accurate quantification of the composition of mixed stones is essential for clinical application of dual-energy CT for stone composition analysis. UR117-EDMOB7 Renal Papillary and Calyceal Lesions on CT Urography Station #7 Awards Cum Laude Participants Satomi Kawamoto, MD, Baltimore, MD (Presenter) Research Grant, Siemens AG; ; Sheila Sheth, MD, Cockeysville, MD (Abstract Co-Author) Nothing to Disclose Elliot K. Fishman, MD, Owings Mills, MD (Abstract Co-Author) Research support, Siemens AG Advisory Board, Siemens AG Research support, General Electric Company Advisory Board, General Electric Company Co-founder, HipGraphics, Inc TEACHING POINTS Renal papillary and calyceal lesions may cause hematuria, are occasionally encountered on CT urography, but they can be easily overlooked. They are often not seen or subtle on unenhanced or early contrast enhanced CT, and best seen in excretory phase CT urography. Routine use of wide window setting to view excretory phase CT is critical to detect subtle lesions in the renal papillae and calyces. Normal anatomy and CT finding of renal papillae and calyces which should not be mistaken for pathology are also discussed. TABLE OF CONTENTS/OUTLINE 1. Anatomy and normal appearance of renal papillae and calyces on CT urography Simple calyx/compound calyx Anatomy and physiology to explain the mechanism of papillary and calyceal pathology2. Papillary lesions: discuss etiology, typical and atypical appearance on CT urography Papillary necrosis Renal tubular ectasia/medullary sponge kidney Medullary nephrocalcinosis3. Calyceal lesions Calyceal diverticulum Small urothelial neoplasm Pyelitis Forniceal rupture - Physiologic/secondary to infection, fistula formation4. Normal structures which potentially simulate pathology Prominent normal renal papilla which potentially simulates abnormal filling defect Normal papillary blush Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Elliot K. Fishman, MD - 2012 Honored Educator Elliot K. Fishman, MD - 2014 Honored Educator UR173-EDMOB8 Imaging of the Postoperative Genitourinary Tract in Children and Adults Station #8 Participants Daniel Wannemacher, MD, Cincinnati, OH (Abstract Co-Author) Nothing to Disclose Jason W. Young, MD, Cincinnati, OH (Abstract Co-Author) Nothing to Disclose Chandana G. Lall, MD, Orange, CA (Abstract Co-Author) Nothing to Disclose Sadhna Verma, MD, Cincinnati, OH (Abstract Co-Author) Nothing to Disclose Harsha V. Nalluri, MD, Cincinnati, OH (Abstract Co-Author) Nothing to Disclose Nabeel Arastu, MD, Cincinnati, OH (Abstract Co-Author) Nothing to Disclose Kyle M. Lewis, MD, Cincinnati, OR (Abstract Co-Author) Nothing to Disclose Robert E. Hobohm, MD, Cincinnati, OH (Presenter) Nothing to Disclose TEACHING POINTS 1. Understand the normal basic genitourinary tract anatomy. 2. Overview of common and uncommon GU procedures in children and adults and their multimodality imaging findings. 3. Discussion of complications of these procedures and multimodality imaging of complications. TABLE OF CONTENTS/OUTLINE The postoperative imaging of the genitourinary tract in children and adults can be difficult to understand, as the native anatomy often becomes distorted and unrecognizable following these procedures. Common complications of these procedures include hydronephrosis and stricture, which can lead to renal failure and long term morbidity. This exhibit will include a discussion of various common and uncommon non-renal GU procedures in the pediatric and adult population with example cases for illustration. These cases include but are not limited to bladder augmentation surgery, Mitrofanoff appendicovesicostomy, Deflux procedure, cystectomy with urostomy formation, prostatectomy, and interventional recannalization of the distal ureter Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Sadhna Verma, MD - 2013 Honored Educator Chandana G. Lall, MD - 2013 Honored Educator MSMI23 Molecular Imaging Symposium: Oncologic MI Applications Monday, Nov. 30 1:30PM - 3:00PM Location: S405AB GU MI MR OI RO AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 FDA Discussions may include off-label uses. Participants Peter L. Choyke, MD, Rockville, MD, (pchoyke@nih.gov) (Moderator) Researcher, Koninklijke Philips NV Researcher, General Electric Company Researcher, Siemens AG Researcher, iCAD, Inc Researcher, Aspyrian Therapeutics, Inc Researcher, ImaginAb, Inc Researcher, Aura Biosciences, Inc Umar Mahmood, MD, PhD, Charlestown, MA (Moderator) Research Grant, Sabik Medical Inc; Advisory Board, Blue Earth Diagnostics Limited; LEARNING OBJECTIVES 1) To understand the role of molecular imaging in cancer therapy. 2) To understand the impact that new molecular imaging agents could have on drug development. 3) To understand the barriers facing the development of new molecular imaging agents. ABSTRACT Molecular Imaging is expanding in many new directions. Most research is being performed for PET and SPECT agents. However, optical and MRI agents are also being developed. Molecular Imaging can play a role in accelerating the development and approval of new cancer therapeutics by quantifying the impact drugs have in early Phase studies and by selecting the most appropriate patients for trials. Molecular Imaging agents can be useful in determining the utility and mechanism of actions of drugs that are already approved and may provide insights to oncologists regarding the best treatment combinations for individual patients. Molecular Imaging methods have already expanded our knowledge of cancer behavior and this will ultimately lead to new forms of the therapy that will one day cure this dreaded disease. Sub-Events MSMI23A Overview of MI in Oncology Participants Peter L. Choyke, MD, Rockville, MD, (pchoyke@nih.gov) (Presenter) Researcher, Koninklijke Philips NV Researcher, General Electric Company Researcher, Siemens AG Researcher, iCAD, Inc Researcher, Aspyrian Therapeutics, Inc Researcher, ImaginAb, Inc Researcher, Aura Biosciences, Inc LEARNING OBJECTIVES 1) To understand the broad spectrum of activities in molecular imaging including PET, SPECT, optical and MRI. 2) To understand the potential impact of Molecular Imaging on cancer treatment. ABSTRACT Molecular Imaging is expanding at a rapid rate. This overview will provide a panoramic view of the field of Molecular Imaging and major trends that are emerging among the different modalities, PET, SPECT, optical, ultrasound and MRI that constitute molecular imaging. MSMI23B Hyperpolarized MRI of Prostate Cancer Participants Daniel B. Vigneron, PhD, San Francisco, CA (Presenter) Research Grant, General Electric Company LEARNING OBJECTIVES View learning objectives under main course title. MSMI23C Radiogenomics Participants Michael D. Kuo, MD, Los Angeles, CA (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) To discuss the principles behind radgiogenomics and to highlight areas of clinical application and future development. ABSTRACT MSMI23D Somatastatin Receptor Imaging Participants Ronald C. Walker, MD, Nashville, TN, (ronald.walker@vanderbilt.edu) (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Describe the advantages of 68Ga-somatostatin PET/CT over 111In-DTPA-octreotide ]imaging. 2) Detect patients likely to benefit 1) Describe the advantages of 68Ga-somatostatin PET/CT over 111In-DTPA-octreotide ]imaging. 2) Detect patients likely to benefit from peptide receptor radiotherapy (PRRT). ABSTRACT 68Ga-labeled somatostatin analogs (DOTATATE, DOTATOC and DOTANOC) PET/CT imaging provides higher resolution scans than 111In-DTPA-octreotide with less radiation, comparable cost, and imaging completion within 2 hours vs. 2-3 days. 68Gasomatostatin analogs have a higher impact on care than 111In-DTPA-octreotide, including superior ability to identify patients likely to benefit from PRRT. This activity will provide results from the literature and the author's experience to illustrate the advantages of 68Ga-based PET/CT imaging of neuroendocrine tumors. Active Handout:Ronald Clark Walker http://abstract.rsna.org/uploads/2015/15003715/MSMI23D.pdf MSMI23E Multimodal MI in Oncology Participants Umar Mahmood, MD, PhD, Charlestown, MA (Presenter) Research Grant, Sabik Medical Inc; Advisory Board, Blue Earth Diagnostics Limited; LEARNING OBJECTIVES 1) To understand strengths of various imaging modalities for specific target/disease assessment. ABSTRACT Each imaging modality has a set of characteristics that helps define optimal use. These constraints include sensitivity, depth of imaging, integration time for signal, and radiation dose, among other factors. Understanding when each modality can be used and when combining the relative strengths of differerent modalities can be synergistic allows greater molecular information to be acquired. MSRO23 BOOST: Gynecology-Case-based Review (An Interactive Session) Monday, Nov. 30 3:00PM - 4:15PM Location: S103AB GU RO AMA PRA Category 1 Credits ™: 1.25 ARRT Category A+ Credits: 1.50 Participants Kevin V. Albuquerque, MD, MS, Dallas, TX, (kevin.albuquerque@utsouthwestern.edu) (Presenter) Nothing to Disclose April A. Bailey, MD, Dallas, TX (Presenter) Nothing to Disclose Stephen Thomas, MD, Chicago, IL (Presenter) Nothing to Disclose Yasmin Hasan, MD, Chicago, IL (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Present the multimodality management of selected gynecolgic cancers including surgery, radiation and chemotherapy. 2) Highlight the importance of imaging in the diagnosis and followup of gynecologic cancers. 3) Highlight the importance of imaging in the planning and delivery of radiation. ABSTRACT The care of patients with gynecologic cancers requires the collaboration of imaging specialists as well as gynecologic and radiation oncologists. Radiologic imaging is key in defining disease at diagnosis and following patients for detection of recurrence after treatment. In conjunction with computerised planning , sectional imaging allows for sophisticated planning of external beam and brachytherapy and is key in maximizing the benefits of radiation while minimizing the risks. Case examples of the pivotal impact of imaging and its importance in multidisciplinary care will be highlighted in this session SSE10 ISP: Genitourinary (GU Intervention) Monday, Nov. 30 3:00PM - 4:00PM Location: E351 GU CT IR MR AMA PRA Category 1 Credit ™: 1.00 ARRT Category A+ Credit: 1.00 FDA Discussions may include off-label uses. Participants Douglas S. Katz, MD, Mineola, NY (Moderator) Nothing to Disclose Cary L. Siegel, MD, Saint Louis, MO (Moderator) Nothing to Disclose Sub-Events SSE10-01 Genitourinary Keynote Speaker: Renal Tumor Ablation-Current Status and Future Directions Monday, Nov. 30 3:00PM - 3:10PM Location: E351 Participants Ronald J. Zagoria, MD, San Francisco, CA (Presenter) Nothing to Disclose SSE10-02 Real-time MR-guided Renal Cryoablation: Technical Feasibility, Complications and Outcomes Monday, Nov. 30 3:10PM - 3:20PM Location: E351 Participants Georgia Tsoumakidou, MD, Strasbourg, France (Presenter) Nothing to Disclose Herve Lang, Strasbourg, France (Abstract Co-Author) Nothing to Disclose Guillaume Koch, MD,MSc, Strasbourg, France (Abstract Co-Author) Nothing to Disclose Julien Garnon, MD, Strasbourg, France (Abstract Co-Author) Proctor, Galil Medical Ltd Xavier Buy, MD, Bordeaux, France (Abstract Co-Author) Proctor, Galil Medical Ltd Afshin Gangi, MD, PhD, Strasbourg, France (Abstract Co-Author) Nothing to Disclose PURPOSE At present, major improvements in device development, as well as modern special designed MR-suites (with MR-compatible life support and anesthesia equipment) have made the performance of MR-guided percutaneous procedures not only feasible, but also attractive. We retrospectively reviewed our single institution experience with percutaneous MR-guided cryoablation of renal tumours for technical feasibility, complications and outcomes (oncologic, renal function). METHOD AND MATERIALS Between April 2009 and March 2015, 68 patients underwent percutaneous MR-guided renal cryoablation. All procedures were performed in an MR-interventional unit, using a 1.5T large bore, supra-conductive system. Real-time BEAT IRTTT (3-simultaneousplane sequence) and high-resolution T2-Blade/HASTE sequences were used for probe positioning and ice-ball monitoring. RESULTS A total of 79 lesions in 68 patients were treated. Four patients were excluded because of less than 3 month follow-up. Twenty-one patients had a history of renal cancer (15 and 2 treated with total and partial nephrectomy, respectively, 4 with cryoablation). Mean maximal tumour diameter was 22mm (min 5, max 42). Biopsy results were available in 61 patients.Procedure related data (time, number-type of cryoprobes, ice ball size) were collected. Two freeze-thaw cycles were systematically performed. Hydrodissection was used in 37 patients.All procedures were technically successful. Local recurrent tumour was identified in six patients during the first six months of imaging follow-up. The local primary tumour control rate was 92%. One patient developed a late local recurrence at 3 years follow-up. Five out of six early and the late recurrence were treated percutaneously. Peri-operative major complication rate was 4.6% (one active bleeding necessitating embolization, one asymptomatic subcapsular hematoma, and one urothelial damage treated with ureteric catheter insertion). There was no procedural related death. Mean follow-up was 18 (370) months. CONCLUSION Percutaneous renal cryoablation can be performed with high technical and clinical success under MR-guidance. The real-time probe placement, high soft tissue contrast, multi-planar imaging, and the lack of ionizing radiation are some of the advantages of MR vs the CT-guidance. CLINICAL RELEVANCE/APPLICATION Percutaneous cryoablation of T1a renal tumours can be perfromed safely and with high tecnical sucesss under MR-guidance. SSE10-03 Single Institution Review of Percutaneous Cryoablation in the Horseshoe Kidney: An Initial Experience Monday, Nov. 30 3:20PM - 3:30PM Location: E351 Participants Junjian Huang, MD, Rochester, MN (Presenter) Nothing to Disclose Thomas D. Atwell, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Anil N. Kurup, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Stephen Boorjian, Rochester, MN (Abstract Co-Author) Nothing to Disclose Robert Thompson, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Grant D. Schmit, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose PURPOSE To present the initial case series of percutaneous cryoablation of tumors in a horseshoe kidney. METHOD AND MATERIALS This is a single center retrospective review of 5 consecutive patients with a renal mass in a horseshoe kidney treated with percutaneous image-guided cryoablation from June of 2006 to August of 2013. Patient and tumor characteristics were extracted from the electronic medical record. Oncologic outcomes were defined using standardized criteria. RESULTS Average age of patient was 59 years old(4M, 1F), tumor size was 3cm(±1cm), and serum creatinine was 1.1±0.4. Of the 5 patients, 4 patients had biopsy proven clear cell renal cell carcinoma, and 1 patient had biopsy proven carcinoid. Technical success was achieved in all patients. The median follow-up duration is 19 months. There were no major complications. Transient elevation of creatinine, not requiring dialysis, occurred following treatment in one patient which has since normalized to baseline. A single patient had inguinal nerve pain that resolved within 3 months. Mean creatinine at follow-up was 1.1±0.3. All patients remain free of local tumor progression. Two patients expired 46 months and 24 months after ablation due to unrelated disease. CONCLUSION There is a paucity of data with regard to the safety, efficacy, and long term outcome of percutaneous cryoablation in the horseshoe kidney. From our initial series it seems that cryoablation is relatively safe in the treatment of small renal tumors, without impact on renal function. This is the first reported series of cryoablation in the horseshoe kidney and, in select patients, may present an alternative to surgical management. CLINICAL RELEVANCE/APPLICATION Percutaneous cryoablation represents an alternative treatment modality in patients with a small renal mass on a horseshoe kidney. SSE10-04 Placement of Essure Tubal Occlusion Coils by Fluoroscopy; An Option when Hysteroscopic Placement Fails Monday, Nov. 30 3:30PM - 3:40PM Location: E351 Participants Amy S. Thurmond, MD, Portland, OR (Presenter) Nothing to Disclose PURPOSE Nonsurgical tubal occlusion by Essure coils was FDA (Food and Drug Administration) approved in 2002 for hysteroscopic placement by gynecologists. Occasionally hysteroscopic placement of one or both coils is not possible--or the coil perforates or is expelled from the tube. Fluoroscopic fallopian tube catheterization has been used since 1987 as a nonsurgical method for unblocking proximal tubal occlusion in women with infertility. The feasability of fluoroscopic fallopian tube catheterization for placement of Essure coils was explored. METHOD AND MATERIALS Women were referred by their gynecologists because of complications after hysteroscopic placement of the Essure device. No premedication, sedation, or anesthesia was given. Commercially available equipment was used to perform hysterosalpingogram, fallopian tube catheterization, and Essure placement. Equipment consisted of a 9 Fr balloon catheter for use in the cervix and uterus (Cook Medical), a 5 Fr catheter and 0.035 inch diameter hydrophilic guidewire for use in the fallopian tube (Cook Medical), and the Essure device and delivery system (Bayer Pharmaceutical). RESULTS Twelve women had attempt at fluoroscopic Essure placement in 14 tubes. Procedure was successful in 12/14 tubes (86%), including 5 tubes where hysteroscopic placement had failed, 2 tubes where hysteroscopic placement resulted in perforation, 3 tubes in which device was expelled after hysteroscopic placement, and 2 tubes with hydrosalpinx. Fluoroscopic placement failed in 2 tubes, in one because of severe tubal spasm which was also the reason for hysteroscopic failure, and in one tube (in which device had been expelled) because of pain during the procedure attributed to severe endometriosis.There were no complications.Six women have had post-procedure confirmation hysterosalpingograms required by the FDA and all 6 tubes with devices placed fluoroscopically were occluded (100%). CONCLUSION Ten of 12 high risk women (83%) who had failed Essure placement by hysteroscopy on one or both sides had subsequent successful fluosocopic procedures allowing them to rely on the Essure devices for tubal occlusion. Twelve of 14 tubes (86%) were amenable to fluoroscopic placement of the Essure device. CLINICAL RELEVANCE/APPLICATION Ten of 12 women (83%) who would have been considered Essure failures and referred for tubal ligation, were converted to Essure successes by fluoroscopic placement of the device. SSE10-05 Percutaneous Embolization of Varicocele By Steel and Platinum Coils Monday, Nov. 30 3:40PM - 3:50PM Location: E351 Participants Syed Muhammad Faiq, MBBS, Karachi, Pakistan (Presenter) Nothing to Disclose Khair Muhammad, MBBS, Karachi, Pakistan (Abstract Co-Author) Nothing to Disclose Waseem A. Mirza, MBBS, Karachi, Pakistan (Abstract Co-Author) Nothing to Disclose PURPOSE The goal of this study was to present our experience with percutaneous treatment of male varicocele in view of procedural, clinical aspects in adult population. METHOD AND MATERIALS 45 male with clinical moderate to severe varicocele associated with scrotal swelling with "bag of worms" or discomfort in testes, such as heaviness or dull pain after standing all day, referred from urology outpatient department to Radiology Department, where Doppler ultrasound was done which confirms the grade and patient underwent percutaneous varicocele embolization with coil. RESULTS The procedural success rate for spermatic vein occlusion was 93%. Follow-up, achieved of every patient after 6 month in urology outpatient department. Forty two patients (93%) reported disappearance of varicocele and as well as pain relief. In two patients percutaneous embolization procedure failed due to internal jugular vein approach and congenital venous abnormality. None of patients reported a reappearance of their varicocele. No significant complications occurred in 42 patients except pain in two patients and hematoma in two patients at femoral punctured site: none had any 6 months sequelae CONCLUSION Percutaneous embolization of varicocele carried out as outpatient procedure under local anesthesia and is more beneficial to patient in comparison to surgery. It has high procedural success rates, less recurrence rate, when performed by experience interventional radiologist. We believed primary therapy for varicocele treatment should be embolization if we compared various risk factors associated with surgery. CLINICAL RELEVANCE/APPLICATION Procedural and clinical success in elimination of varicocele by steel or platinum coils with low rate of failure and reappearance up to 6 month. High failure rate was seen in our study through internal jugular vein approach for venous access. We believed primary therapy for varicocele treatment should be embolization if we compared various risk factors associated with surgery. SSE10-06 Hysterosalpingo-foam Sonography (HyFoSy): A Prospective Observational Cohort Study of an Innovative, Radiation Free, Safe and Effective, Non(Embryo) Toxic Technique, to Visualize Tubal Patency in an Outpatient / Office Setting Monday, Nov. 30 3:50PM - 4:00PM Location: E351 Participants Anurag Singh, MBBS,MD, Sharjah, United Arab Emirates (Presenter) Nothing to Disclose Tejashree Singh, Dubai, United Arab Emirates (Abstract Co-Author) Nothing to Disclose Kiran C. Patil JR, MD, Jalgaon, India (Abstract Co-Author) Nothing to Disclose PURPOSE This study was conducted to evaluate the efficacy and safety of HyFoSy as a first step routine office procedure for tubal patency testing. METHOD AND MATERIALS A prospective observational cohort study was conducted in a medical center from 26/11/2014 - 4/4/2015. 46 patients with subfertility were examined. The mean age of patients was 31 years. The mean duration of subfertility was 2.2 years. The patients were asked to report for the test, on days 7-9 of their menstrual cycle. All patients were at low risk for tubal disease and had no history of tubal surgery. A non(embryo) toxic foam was created by rigorously mixing 10 ml hydroxymethylcellulose glycerol gel (88.25% water) with 10 ml purified water to give a mixture containing 94.10% water in a 20 ml syringe, and was introduced into the uterine cavity with the help of a disposable 5F single balloon catheter. This foam had low viscosity and was sufficiently stable to show echogenicity for at least 5 minutes. Tubal patency was determined by transvaginal ultrasound demonstration of echogenic dispersion of foam through the Fallopian tubes and the peritoneal spillage. The tubal contour, length and relation of spill with respect to ipsilateral ovary, were also noted. The pain score was calculated. No precautions with regard to pregnancy were advised. RESULTS In 45/46 (98%) patients (except 1 case of cervical stenosis), a successful procedure was performed. In these cases, there was no further need for a hysterosalpingogram (HSG). 42 patients (94%) had bilateral patent tubes and 3 patients (6%) had unilateral patent tubes. Only 1 patient (1/45; 2%) had mild vasovagal discomfort during the procedure that resolved spontaneously. The average pain score was 2.2. All procedures were uneventful and no serious side-effects were observed. Furthermore, in 10 patients (22%) conception occurred within a median of 3 months after the procedure. Review of literature found our results comparable with other similar studies. CONCLUSION Thus, HyFoSy is a successful, less painful and radiatian free technique, easily performed in an office setting as a first step test for tubal patency.Comparison with other tubal patency tests was done as per the literature evaluation and our old experiences. It showed excellent findings in favor of HyFoSy. CLINICAL RELEVANCE/APPLICATION HyFoSy is a radiation free, less painful, non(embryo) toxic, effective alternative to HSG and definitely has a potential to be the new generation patient friendly first step office test for tubal patency. SSE11 Genitourinary (Renal Stone Imaging) Monday, Nov. 30 3:00PM - 4:00PM Location: E353B CT GU MR AMA PRA Category 1 Credit ™: 1.00 ARRT Category A+ Credit: 1.00 FDA Discussions may include off-label uses. Participants Naoki Takahashi, MD, Rochester, MN (Moderator) Nothing to Disclose Sub-Events SSE11-01 In Vitro Imaging of Kidney Stones in Pig Kidneys Using Ultra-short Echo-time (UTE) MRI Monday, Nov. 30 3:00PM - 3:10PM Location: E353B Participants El-Sayed H. Ibrahim, PhD, MSc, Ann Arbor, MI (Presenter) Nothing to Disclose Robert A. Pooley, PhD, Jacksonville, FL (Abstract Co-Author) Nothing to Disclose Joseph G. Cernigliaro, MD, Jacksonville, FL (Abstract Co-Author) Nothing to Disclose Mellena D. Bridges, MD, Jacksonville, FL (Abstract Co-Author) Nothing to Disclose Jamie G. Giesbrandt, MD, Jacksonville, FL (Abstract Co-Author) Nothing to Disclose James C. Williams, PhD, Indianapolis, IN (Abstract Co-Author) Nothing to Disclose William E. Haley, MD, Jacksonville, FL (Abstract Co-Author) Nothing to Disclose PURPOSE Ultra-short echo-time (UTE) MRI provides echo times (TE) in the range of tens of microseconds, which allows for effective imaging of tissues that have rapid signal decay, e.g., kidney stones. In this study, we investigate the imaging performance of UTE MRI for stones embedded within their usual milieu, the kidney, thus mimicking the in vivo situation. METHOD AND MATERIALS 24 kidney stones passed/extracted from patients were obtained. The stones represented 8 different types (confirmed by micro CT): calcium oxalate monohydrate (COM), calcium oxalate dehydrate (COD), brushite, apatite, uric acid (UA), struvite, cystine, and mixed-composition. Each stone type was represented by 3 stones in a range of sizes: small (2-3 mm), medium (4-6 mm), and large (7-10 mm). A total of 8 pig kidneys, purchased from a local meat store, were used in the experiments. Using small cuts, three stones (large, medium, and small) of the same type were inserted into each kidney, each into a different calyx (Fig 1a). The kidneys were arranged in a small plastic container filled with water and covered with a sealed lid (Fig 1b), and then imaged on a Siemens 3T MRI scanner using an 18-channel body surface coil and an optimized 3D UTE pulse sequence. RESULTS All stones were successfully visualized. The resulting images clearly showed the stones' shapes with high resolution (Fig 1c). Although efforts were made to expunge air bubbles throughout the pre-scan process, air gaps still existed inside some of the kidneys, which resulted in some artifacts. Using the body surface coil and large FOV did not adversely affect stone visualization, which is promising for future in vivo imaging. CONCLUSION This study confirms the potential of MRI for in vitro imaging of stones in kidneys using the body surface coil, which is one step closer to in vivo imaging than phantom experiments with head or knee coils. If successful for true in vivo imaging, the UTE technique could serve as an alternative to CT for imaging patients for whom minimization of radiation exposure is desirable. The sequence could be also added to abdominal MRI protocols for comprehensive evaluation of the genitourinary system. CLINICAL RELEVANCE/APPLICATION Although CT is the modality of choice for imaging kidney stones, UTE MRI may provide an effective alternative when there are concerns about radiation exposure. SSE11-02 Low-dose Abdominal Computed Tomography for Urinary Stone Disease - Impact of Additional Spectral Shaping on Image Quality and Dosage Monday, Nov. 30 3:10PM - 3:20PM Location: E353B Participants Patricia Dewes, MD, Frankfurt, Germany (Presenter) Nothing to Disclose Claudia Frellesen, Frankfurt, Germany (Abstract Co-Author) Nothing to Disclose Jan-Erik Scholtz, MD, Frankfurt, Germany (Abstract Co-Author) Nothing to Disclose Sebastian Fischer, MD, Frankfurt, Germany (Abstract Co-Author) Nothing to Disclose Thomas J. Vogl, MD, PhD, Frankfurt, Germany (Abstract Co-Author) Nothing to Disclose Ralf W. Bauer, MD, Frankfurt, Germany (Abstract Co-Author) Research Consultant, Siemens AG Speakers Bureau, Siemens AG Boris Schulz, MD, Frankfurt Am Main, Germany (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate a novel tin filter based abdominal CT technique for urolithiasis in terms of image quality and radiation exposure. METHOD AND MATERIALS 130 consecutive patients with suspected urolithiasis underwent non-enhanced CT in our department with various techniques: 48 patients were examined with a novel tin filtration (150kV Sn) method (group 1) on a third-generation dual-source-CT, 33 patients were examined with automated kV-selection (80-140kV) based on the scout view with the same CT-device (group 2) and 49 patients were examined on a second-generation dual-source-CT (group 3) also with automated kV-selection (80-140kV) based on the scout view. Automated exposure control was active in all groups. Image quality was subjectively evaluated on a 5-point-likertscale by two radiologists and interobserver agreement as well as signal-to-noise-ratio (SNR) was calculated. Dose-Length-Product (DLP) and volume based CT weighted Dose Index (CTDIvol) were used to analyze radiation exposure. RESULTS Image quality was rated in favour for the tin filter protocol with an excellent interobserver agreement (ICC=0.86-0.91). SNR was significantly better in group 1 and 2 compared to second-generation DSCT (p<0.001). On third-generation dual-source CT, there was no significant difference in SNR between the 150 kV Sn and the CAREkV protocol (p=0.5). DLP of group 1 was significantly lower in comparison to group 2 and 3 by 23% and 27% (93 vs. 122 vs. 127mGycm; p<0.002). CTDIvol of group 1 was significant lower compared to group 2 (-36%) and 3 (-32%) (1.95 vs. 3.09 vs. 2.87 mGy; p<0.001). CONCLUSION Additional shaping of a 150kV spectrum by a tin filter substantially lowers patient exposure while improving image quality on abdominal Computed Tomography for urinary stone disease. CLINICAL RELEVANCE/APPLICATION The novel tin filtered technique reduces radiation exposure and improves image quality in comparison to standard low- dose abdominal CT, thus serving to benefit the patient. SSE11-03 Predictive Value of Low Dose and Dual-Energy CT for Successful Stone Disintegration in Shock Wave Lithotripsy: An in-Vitro Study Monday, Nov. 30 3:20PM - 3:30PM Location: E353B Participants Sebastian Winklhofer, MD, San Francisco, CA (Presenter) Nothing to Disclose Largo Remo, Zurich, Switzerland (Abstract Co-Author) Nothing to Disclose Christian Fankhauser, Zurich, Switzerland (Abstract Co-Author) Nothing to Disclose Cedric Poyet, Zurich, Switzerland (Abstract Co-Author) Nothing to Disclose Pirmin Wolfsgruber, Zurich, Switzerland (Abstract Co-Author) Nothing to Disclose Tullio Sulser, MD, Zurich, Switzerland (Abstract Co-Author) Nothing to Disclose Hatem Alkadhi, MD, Zurich, Switzerland (Abstract Co-Author) Nothing to Disclose Paul Stolzmann, MD, Zurich, Switzerland (Abstract Co-Author) Nothing to Disclose PURPOSE Shock wave lithotripsy (SWL) represents the golden treatment for urinary stone disease. Failure of stone disintegration results in repeated treatments or alternative procedures, thereby not only increasing medical costs. The ability to predict successful SWL will improve the selection of patients suitable for SWL. This study investigates single energy computed tomography (SECT) and dualenergy computed tomography (DECT) to predict numbers of shock waves to stone disintegration in an in-vitro setting. METHOD AND MATERIALS A total of 33 human urinary calculi (10 uric acid, 8 hydroxyapatite, 6 calcium oxalate monohydrate, 5 cysteine, 3 struvite, 1 brushite stones, mean size 6±3 mm) were scanned using a 128-slice DECT machine (Somatom Force, Siemens Healthcare, Forchheim, Germany) with single- (120kVp) and dual-energy settings (80/150, 100/150kVp) resulting in 6 different SECT and DECT data sets. Calculi were disintegrated using an electromagnetic Dornier DL50 lithotrypter (Dornier MedTech, Wessling, Germany) over a 2-mm mesh until succesful disintegration. RESULTS All stones were successfully disintegrated by applying a median of 72 shock waves (interquartile range 343). Regarding logistic regression analysis, CT numbers significantly (p<0.01) predicted fewer or more than median shock waves to successful disintegration and differed among data sets (p<0.05), both adjusted for stone composition (p<0.001) and size (p<0.001). Correlation coefficients ranged from rho=0.36 to 0.68 with best correlation for CT numbers and shock waves at 80 kVp (p<0.001). CONCLUSION Lower CT numbers are significantly associated with fewer shockwaves needed which is independent of stone composition and size. Optimal prediction of SWL success may be fascilated on the basis low-dose CT data which is paralleled by a low radiation dose. CLINICAL RELEVANCE/APPLICATION Being able to predict the success of shock wave lithotripsy with low-dose computed tomography would be helpful to determine the optimal management in patients with urinary calculi. SSE11-04 Feasibility of Split-filter Dual-energy CT for in-Vitro Differentiation of Urinary Stones by Using Doseneutral (Compared with Single-energy CT) Protocol Monday, Nov. 30 3:30PM - 3:40PM Location: E353B Participants Anushri Parakh, MBBS,MD, Basel, Switzerland (Presenter) Nothing to Disclose Daniel Boll, Basel, Switzerland (Abstract Co-Author) Nothing to Disclose Andre Euler, MD, Basel, Switzerland (Abstract Co-Author) Nothing to Disclose Caroline Zahringer, Basel, Switzerland (Abstract Co-Author) Nothing to Disclose Fabian Morsbach, Zurich, Switzerland (Abstract Co-Author) Nothing to Disclose Daniel Mueller, Zurich, Switzerland (Abstract Co-Author) Nothing to Disclose Geraldine Stadelmann, Basel, Switzerland (Abstract Co-Author) Nothing to Disclose Sebastian T. Schindera, MD, Basel, Switzerland (Abstract Co-Author) Research Grant, Siemens AG; Research Grant, Ulrich GmbH & Co KG; Research Grant, Bayer AG PURPOSE The study aimed to examine the efficacy of a novel split-filter (using gold and tin filters) single-source dual-energy CT (sf-DECT) in characterizing renal stones as compared to second-generation dual-source dual-energy CT (ds-DECT) in intermediate-sized phantoms using vendor-suggested and dose-neutral (to single-energy CT) protocols. METHOD AND MATERIALS Urinary stones (n=65, size: 2.1-6.4mm) of known chemical composition (15 calcium, 15 struvite, 15 cystine and 20 urate) were embedded in a custom-made kidney model and placed in a 30-cm cylindrical water-containing phantom simulating a medium-sized patient. Scans with vendor-recommended and dose-neutral protocols were performed on ds-DECT (SOMATOM Definition Flash, Siemens; protocol A (vendor-suggested) tube A, 100kVp, 210 reference mAs; tube B, Sn140kVp, 162 reference mAs; protocol B (dose-neutral) tube A, 100kVp, 65 reference mAs; tube B, Sn140kVp, 50 reference mAs) and sf-DECT (SOMATOM Definition Edge, Siemens; protocol C (vendor-suggested) AuSn 120kVp, 640 reference mAs; protocol D (dose-neutral) AuSn 120kVp, 235 reference mAs). Stones were assessed by a dedicated post-processing software. Positive (PPV) and negative (NPV) predictive values were calculated. A comparison of radiation doses between both dual-energy techniques was made using CTDIvol parameter. RESULTS The CTDIvol (in mGy) for protocols A to D measured 13.7, 4.3, 11.2 and 4.4 respectively. Presence of all stones was detected by the four protocols. The PPV of protocols A-D to characterize urate stones were 95.2, 95.2, 94.1 and 58.6 and for non-urate stones were 100, 100, 93.6 and 96.9, respectively. For clinically significant stones (>4 mm), the PPV for characterizing urate or non-urate stones (100 for both) by protocols A and B was not affected. For the same stone size, PPV of protocols C vs. D were 100 vs 76.9 for urate and 96.4 vs. 96.0 for non urate stones. Dose-neutral sf-DECT was particularly inferior to ds-DECT in characterizing urate stones and stones which were less than 4 mm. CONCLUSION While dose-optimization is feasible in differentiation of urate from non-urate stones by ds-DECT for smaller stones, it is accurate for sf-DECT if they are greater than 4 mm in size. CLINICAL RELEVANCE/APPLICATION Sf-DECT is a promising new tool for dual-energy evaluation with a benefit of reduced radiation dose as compared to secondgeneration dual-energy technique. SSE11-05 Virtual Non-enhanced Images Generated from Spectral CT: Determinants of Detection of Urinary Calculi in the Renal Collecting System Monday, Nov. 30 3:40PM - 3:50PM Location: E353B Participants Yan Chen, Zhengzhou, China (Presenter) Nothing to Disclose Peijie Lv, MMed, Zhengzhou, China (Abstract Co-Author) Nothing to Disclose Jianbo Gao, MD, Zhengzhou, China (Abstract Co-Author) Nothing to Disclose PURPOSE To determine which features of urinary calculi are associated with their detection on VNE images generated from Spectral computed tomograpic(CT) urography. METHOD AND MATERIALS This retrospective study was approved by the insititutional ethics committee with waiver of informer consent.A total of53 patients were examined with true nonenhanced (TNE) CT and Spectral CT urography in the excretory phase. Thecontrast medium was virtually removed from excretory-phase images by using material suppressed iodine(MSI),water-based (WB) and calcium-based (CaB) material decomposition (MD) analysis in the spectral imaging viewer.Thesensitivity regarding the detection of calculi on these three groups and the subjective scoring were determined byusing true non-enhanced (TNE) images as the reference standard , and interrater agreement was evaluated byusing the Cohen k test.By using logistic regression, the influences of image noise, attenuation, and stone size, as well as attenuation of the contrast medium, on the stone detection rate were assessed on VNE images. RESULTS 169 stones were detected on the TNE images;149 stones were identified on CaB images (sensitivity,88.2%),145 stoneson WB images(sensitivity, 85.7%),whlie 160 stones on MSI images(sensitivity,94.6%) with significant difference.Compared with the TNE images,the relatively lower subjective scoring of the VNE images (P>0.05) and higher SNR,CNR(P<0.05)were identified. Size (longaxis diameter and short-axis diameter), and attenuation of the calculi,except for the image noise were significantly associated with the detection rate on VNE images (P<0.05). As thresholdvalues on CaB, WB, MSI images, size larger than 2.68 mm , 3.01mm , 2.03mm,maximum attenuation of the calculigreater than 223 HU, 312HU and 203HU respectively were found. CONCLUSION After virtual elimination of contrast medium with material decomposition and MSI, large and high-attenuation calculi can be detected with high reliability. CLINICAL RELEVANCE/APPLICATION VNE images generated at excretory-phase Spectral CT can depict calculi larger than 2.03mm in the presence ofcontrast medium; however, small and hypoattenuating calculi may be missed. SSE11-06 Improved Differentiation between Uric Acid and Non-uric Acid Renal Stones Using DECT Monoenergetic Imaging Monday, Nov. 30 3:50PM - 4:00PM Location: E353B Participants Fabio Lombardo, MD, Verona, Italy (Presenter) Nothing to Disclose Matteo Bonatti, MD, Bolzano, Italy (Abstract Co-Author) Nothing to Disclose Giulia A. Zamboni, MD, Verona, Italy (Abstract Co-Author) Nothing to Disclose Federica Ferro, Bolzano, Italy (Abstract Co-Author) Nothing to Disclose Roberto Pozzi Mucelli, Verona, Italy (Abstract Co-Author) Nothing to Disclose Giampietro Bonatti, Bolzano, Italy (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate monoenergetic attenuation values of renal stones for discriminating between uric acid and non-uric acid stones. METHOD AND MATERIALS IRB-approved retrospective study; need for informed consent was waived. We included in our study 37 patients (23M, 14F; mean age 54y) who underwent CT for symptomatic urolithiasis on our second-generation dual-source scanner. We performed a 120kV single-energy low-dose acquisition of the whole abdomen followed by one or more 100/140kV dual-energy acquisitions limited to the regions in which one or more stones were detected. All patients subsequently underwent stone extraction or they spontaneously expelled the stone within 1 month from the examination; all the obtained stones were analyzed by means of infrared spectroscopy and classified, according to their prevalent composition, as uric acid or non-uric acid stones. When patients had >1 stone, their composition was considered the same for all the stones. Stones largest diameter was noted. One radiologist in training evaluated by means of a round ROI the monoenergetic attenuation values of the stones from 40 to 190 kV. 40/190kV monoenergetic attenuation ratios were calculated. A qualitative analysis on the monoenergetic curves was also performed. RESULTS 75 stones were detected in 37 patients; 36 stones were located in the urinary calices, 13 in the renal pelvis, 25 in the ureters and 1 in the urinary bladder. Mean diameter was 6.1 mm (range 2-28 mm). At spectroscopy, 16/75 stones were prevalently composed by uric acid and 59/75 by cysteine or calcium oxalates/phosphates. Mean 40/190kV monoenergetic attenuation ratios were 0.82 for uric-acid stones (range 0.30-1.34) and 3.82 for non-uric acid stones (range 2.18-7.35)(p<0.0001). All uric-acid stones were correctly characterized using a cut-off of 1.5. Qualitative analysis of monoenergetic curves showed a different and easily recognizable shape both for uric acid and non-uric acid stones. CONCLUSION 40/190 kV attenuation ratios accurately differentiate uric acid from non-uric acid stones. Furthermore, qualitative analysis of monoenergetic curves can be an easy method to rapidly assess stone composition. CLINICAL RELEVANCE/APPLICATION 40/190 kV monoenergetic attenuation ratio accurately predicts renal stone composition, even in small calculi, leading to a more accurate treatment planning. ED006-TU Genitourinary Tuesday Case of the Day Tuesday, Dec. 1 7:00AM - 11:59PM Location: Case of Day, Learning Center GU AMA PRA Category 1 Credit ™: .50 Participants Theodora A. Potretzke, MD, Saint Louis, MO (Presenter) Nothing to Disclose Perry J. Pickhardt, MD, Madison, WI (Abstract Co-Author) Co-founder, VirtuoCTC, LLC; Stockholder, Cellectar Biosciences, Inc; Research Consultant, Bracco Group; Research Consultant, KIT ; Research Grant, Koninklijke Philips NV Naoki Takahashi, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Meghan G. Lubner, MD, Madison, WI (Abstract Co-Author) Grant, General Electric Company; Grant, NeuWave Medical, Inc; Grant, Koninklijke Philips NV Anup S. Shetty, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Richard Tsai, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose George A. Carberry, MD, Madison, WI (Abstract Co-Author) Nothing to Disclose Vincent M. Mellnick, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose David U. Kim, MD, Madison, WI (Abstract Co-Author) Nothing to Disclose Yaseen Oweis, MD, MBA, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Zachary J. Viets, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Bernard F. King JR, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Akira Kawashima, MD, PhD, Phoenix, AZ (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1) Recognize imaging findings seen in disorders of the genitourinary systems. 2) Develop differential diagnosis based on the clinical information and imaging findings. 3) Recognize the clinical importance of diagnosis. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Perry J. Pickhardt, MD - 2014 Honored Educator Naoki Takahashi, MD - 2012 Honored Educator Meghan G. Lubner, MD - 2014 Honored Educator Meghan G. Lubner, MD - 2015 Honored Educator SPSC30 Controversy Session: Gadolinium Contrast Agents and Adverse Effects: Too Much Attention or Too Little? Tuesday, Dec. 1 7:15AM - 8:15AM Location: E451A GU MR SQ AMA PRA Category 1 Credit ™: 1.00 ARRT Category A+ Credit: 1.00 FDA Discussions may include off-label uses. Participants Hero K. Hussain, MD, Ann Arbor, MI (Moderator) Nothing to Disclose Emanuel Kanal, MD, Pittsburgh, PA (Presenter) Consultant, Boston Scientific Corporation; Consultant, Medtronic, Inc; Consultant, St. Jude Medical, Inc; Consultant, Bayer AG; Investigator, Bracco Group; Royalties, Guerbet SA; Martin R. Prince, MD, PhD, New York, NY, (map2008@med.cornell.edu) (Presenter) Patent agreement, General Electric Company; Patent agreement, Hitachi, Ltd; Patent agreement, Siemens AG; Patent agreement, Toshiba Corporation; Patent agreement, Koninklijke Philips NV; Patent agreement, Nemoto Kyorindo Co, Ltd; Patent agreement, Bayer AG; Patent agreement, Lantheus Medical Imaging, Inc; Patent agreement, Bracco Group; Patent agreement, Medtronic, Inc; Patent agreement, Topspins, Inc; Stockholder, Topspins, Inc Richard H. Cohan, MD, Ann Arbor, MI, (rcohan@umich.edu) (Presenter) Consultant, General Electric Company; ; ; Matthew S. Davenport, MD, Cincinnati, OH, (matdaven@med.umich.edu) (Presenter) Book contract, Wolters Kluwer nv; Book contract, Reed Elsevier; LEARNING OBJECTIVES 1) To discuss associations of gadolinium based contrast agents (GBCA) and Nephrogenic Systemic Fibrosis (NSF). 2) To review rates and types of acute adverse reactions in patients receiving GBCA, and to place those in perspective with respect to the risk of NSF. 3) To discuss several other potential safety factors about GBCA, and to compare and contrast incidence of new potential safety factors among the various CNS-approved GBCA. 4) To explain the current thinking regarding imaging patients with renal impairment, and to define renal function thresholds that might be useful for operationalizing imaging in this patient population. ABSTRACT To review associations of gadolinium based contrast agents (GBCA) and Nephrogenic Systemic Fibrosis (NSF), and discuss current practice patterns that led to almost complete elimination of NSF. Speaker: Martin Prince.To review rates and types of acute adverse reactions in patients receiving GBCA, discuss principles of premedication and treatment, and place the acute adverse reaction rate in perspective with respect to the risk of NSF. Speaker: Richard Cohan. To list and integrate several other potential safety factors about GBCA, other than NSF and acute allergic type, into the clinical decision making process about whether or not to administer GBCA, and to compare and contrast incidence of new potential safety factors among the various CNS-approved GBCA available today. Speaker: Emanuel Kanal. To explain the current thinking regarding imaging patients with renal impairment, to highlight the differences that exist between serum creatinine-based and eGFR-based screening, and to define the ranges of renal function thresholds for which caution might be advised to avoid potential harm that might result from the administration of iodinated and gadolinium-based contrast media. Speaker: Matthew Davenport. URL RC307 GU Incidental Findings 2015 - What Is New and Helpful in Managing Them? (An Interactive Session) Tuesday, Dec. 1 8:30AM - 10:00AM Location: E450B GU AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Lincoln L. Berland, MD, Birmingham, AL, (lberland@uabmc.edu) (Coordinator) Consultant, Nuance Communications, Inc; Stockholder, Nuance Communications, Inc; Stuart G. Silverman, MD, Brookline, MA, (sgsilverman@partners.org) (Presenter) Author, Wolters Kluwer nv Elaine M. Caoili, MD, MS, Ann Arbor, MI (Presenter) Nothing to Disclose Susan M. Ascher, MD, Washington, DC (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Appreciate the need for and value of recommendations for managing incidental findings. The participants should also be able to choose from a variety of methods to bring these recommendations to the point of interpretation. 2) Identify incidental adnexal cystic lesions that require further evaluation to include the type and timing of follow up examinations. 3) Apply appropriate imaging criteria and thresholds to better distinguish benign adrenal adenomas from more clinically important lesions. 4) Manage incidental renal masses, even when they are incompletely characterized, such as when they are too small to characterize or detected on an examination that is not designed to evaluate them fully. Please bring your charged mobile wireless device (phone, tablet or laptop) to participate. RC310 First Trimester Ultrasound (An Interactive Session) Tuesday, Dec. 1 8:30AM - 10:00AM Location: S402AB GU OB US AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Active Handout:Carol Beer Benson http://abstract.rsna.org/uploads/2015/15001996/Active RC310.pdf Sub-Events RC310A Ectopic Pregnancy Participants Anne M. Kennedy, MD, Salt Lake City, UT (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Diagnose tubal ectopic. 2) Differentiate Cesarean scar implantation from a normal, low-lying pregnancy. 3) Recognize the more unusual sites of ectopic pregnancy (cervical, interstitial, abdominal). 4) Understand the indications for expectant vs. medical vs. surgical management . ABSTRACT Ectopic pregnancy can be a life-threatening condition for young, healthy women. The availability of senstive urine pregnancy tests means that we are seeing patients at a time when It may be very difficult to see any sonographic findings of pregnancy. The session will review and illustrate examples of the recommended descriptive terms 'pregnancy of unknown location',' probable ectopic' and 'definite ectopic' both of which refer to tubal ectopics.We will also review the appearance of heterotopic pregnancy and non-tubal ectopics including Cesarean scar implantation, interstitial and cervical implantation, and abdominal and ovarian ectopic with demonstration of the role of color Doppler, 3D ultrasound and other imaging modalities.Modern management of ectopic pregnacy has become much less aggressive, in part because the diagnosis is made so much earlier. The indications for the various treatment options will be outlined with illustrative case of local injection as well as intraoperative photos during laparoscopy. Active Handout:Anne M. Kennedy http://abstract.rsna.org/uploads/2015/15001997/RC310A.pdf RC310B Diagnosis of Miscarriage Participants Peter M. Doubilet, MD, PhD, Boston, MA, (pdoubilet@partners.org) (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Know the sonographic criteria for definite miscarriage and probable miscarriage in the early first trimester. 2) Understand that any saclike intrauterine structure (rounded edges, no yolk sac or embryo) in a woman with a positive pregnancy test is highly likely to be a gestational sac. 3) Understand that nonvisualization of an intrauterine gestational sac in a woman with hCG above the 'discriminatory' level (2000 mIU/ml) does not exclude the possibility of a normal pregnancy. ABSTRACT This lecture will cover the diagnosis of early first trimester miscarriage in two settings: (i) ultrasound demonstrates no intrauterine gestational sac ('pregnancy of unknown location'); (ii) ultrasound demonstrates an intrauterine gestational sac but no embryo or heartbeat. In the first of these settings, the role of the quantitative hCG level will be discussed, including whether a single measurement can be used to rule out a normal intrauterine pregnancy. In the second setting, the currently accepted criteria for definite miscarriage and for probable miscarriage will be presented. The lecture will also address findings that indicate a high likelihood of impending pregnancy failure when an embryo with heartbeat is seen on ultrasound. Active Handout:Peter Michael Doubilet http://abstract.rsna.org/uploads/2015/15001998/RC310B Early1stTriMiscarriage--RSNA2015.pdf RC310C Mid-late First Trimester Participants Carol B. Benson, MD, Boston, MA (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Recognize the importance of evaluating the developing fetal head during the late first trimester for early detection of large neural tube defects. 2) Incorporate measurement of the nuchal translucency into their assessment of the fetuses of gestational age 1114 weeks. 3) Recognize sonographic abnormalities of the ventral wall to distinguish normal physiologic bowel herniation from defects including omphalocele and gastroschisis. ABSTRACT This lecture will discuss the sonographic appearance of fetal anatomy in the latter part of the third trimester in order to help participants recognize abnormalities of the fetus at this early gestational age. While many anomalies cannot be detected until later in pregnancy, the discussion will focus on those anomalies that can be detected in the first trimester. Specific topics covered will be central nervous system anomalies, including anencephaly, encephalocele and holoprosencephaly, ventral wall defects including omphalocele and gastroschisis, bladder outlet obstruction, and skeletal anomalies including skeletal dysplasias. Detection of anomalies early in gestation, before the second trimester, permits time to assess the fetus for other anomalies, syndromes, and aneuploidy. RC329 Characterization of Complex and Sonographically Indeterminate Adnexal Masses (An Interactive Session) Tuesday, Dec. 1 8:30AM - 10:00AM Location: E353B GU MR US AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Sub-Events RC329A Overview of the Clinical Indications for Using MRI Participants Andrea G. Rockall, MRCP, FRCR, London, United Kingdom (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) To be familiar with the typical clinical presentation of adnexal masses. 2) To understand the role role of ultrasound in the initial evaluation and diagnosis of adnexal masses. 3) To know the current indications for MRI in the characterisation of adnexal masses. ABSTRACT Clinical presentation of adnexal masses can be due to symptoms (such as acute or chronic pelvic pain or sepsis) or may be incidental. Ultrasound is the initial investigation in almost every case, although CT may be used initially in patients presenting with an acute abdomen. Ultrasound features that can differentiate benign from malignant adnexal masses are well defined and over 80% of cases can be confidently characterised on the basis of ultrasound findings. However, when the nature of a mass is indeterminate on ultrasound, MRI can be useful in further characterisation of the mass. This can be particularly useful in cases where fertility preservation is of paramount importance or where the risks of surgery are high due to other co-morbidities. This lecture will include a full discussion of the current indications for MRI in characterisation of adnexal masses. RC329B Review of Scoring System for Complex and Sonographically Indeterminate Adnexal Masses (The RULES) Participants Isabelle Thomassin-Naggara, MD, Paris, France (Presenter) Speakers Bureau, General Electric Company; Research Consultant, Olea Medical LEARNING OBJECTIVES 1) To learn how to optimise the MRI protocol and how to improve the characterisation of indeterminate complex adnexal masses. 2) To understand the added value of functional sequences (DCE MRI and DWI) in diagnosing adnexal masses. 3) To present a novel diagnostic score named ADNEX MR score for classified adnexal masses using MR imaging according to their positive predictive value. ABSTRACT For complex adnexal masses, MR imaging add to conventional criteria of malignancy common to all imaging modalities (bilaterality, tumor diameter larger than 4 cm, predominantly solid mass, cystic tumor with vegetations, and secondary malignant features, such as ascites, peritoneal involvement, and enlarged lymph nodes) specific features based on the characterization of the solid tissue (including vegetation, thickened irregular septa and solid portion) of the adnexal tumor. Using ADNEX MR-SCORING system for adnexal masses, areas under the curve for diagnosis of malignancy is high both for experienced and junior reader (AUCR1/R2=0.980/0.961). A score is 4 or greater is associated with malignancy with a sensitivity of 93.5% (58/62) and specificity of 96.6% (258/267), the risk of malignancy is high, and the patient should be referred to a cancer center. When the diagnostic score is 3 or less, the association with malignancy is minimal and the patient may benefit from more imaging follow-up or conservative treatment. Finally, if the diagnostic score is 2, the mass has a very low risk to be malignant (<2%). This new MR diagnosis classification will be detailed with interactive clinical cases during this session RC329C Interactive Cases Participants Elizabeth A. Sadowski, MD, Madison, WI (Presenter) Nothing to Disclose Isabelle Thomassin-Naggara, MD, Paris, France (Presenter) Speakers Bureau, General Electric Company; Research Consultant, Olea Medical LEARNING OBJECTIVES 1) Develop a method for classifying adnexal masses on MRI by assessing their signal characteristics and enhancement patterns. 2) Assess the risk of ovarian cancer based on the MRI appearance of an adnexal lesion and clinical information. 3) Emphasize the role of MRI in the evaluation of adnexal lesions. ABSTRACT ABSTRACT There is a spectrum of ovarian neoplasms ranging from benign to malignant. Identifying the MR imaging features suggestive of benign versus worrisome lesions can help appropriately triage adnexal lesions into follow up versus surgical consultation. The purpose of the interactive session is to review the imaging features of benign and worrisome adnexal lesions on MRI and to discuss the appropriate follow up in each case. RC351 Pelvic MRI in Oncology: Pearls for Practice Tuesday, Dec. 1 8:30AM - 10:00AM Location: E350 GU MR OI RO AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Sub-Events RC351A Practical Approach to Understanding Gene Mutations with Interpretation of Imaging in Gynecologic Malignancy Participants Priya R. Bhosale, MD, Houston, TX (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) To learn the gentic mutations present in Endomtrial and Ovarian Cancer. 2) Pathogenesis of Ovarian Cancer. 3) Implications on image interpretation. ABSTRACT Endometrial cancer is teh most common female gynecologic malignancy.Epithelial ovarian cancer is the most common cause of gynecological cancer death in the United States. More recently epithelial ovarian tumors have been broadly classified into two distinct groups. The type I tumors have low grade serous, clear cell, endometrioid, and mucinous histological features. Typically, these tumors are slow growing and confined to the ovary, and are less sensitive to standard chemotherapy. BRAF and KRAS somatic mutations are relatively common in these tumors, which may have important therapeutic implications. Type II tumors are high grade serous cancers of the ovary, peritoneum, and fallopian tube. These tumors are clinically aggressive and are often widely metastatic at the time of presentation. We will discuss the gene mutations associated with different endometrial and epithelial ovarian cancer, pathogenesis, implications on therapy and imaging. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Priya R. Bhosale, MD - 2012 Honored Educator RC351B Pearls and Pitfalls in Prostate MRI Participants Aradhana M. Venkatesan, MD, Houston, TX, (avenkatesan@mdanderson.org) (Presenter) Institutional research agreement, Koninklijke Philips NV LEARNING OBJECTIVES 1) List the elements of common prostate MRI acquisition protocols, defining the roles for each pulse sequence in prostate cancer detection. 2) List imaging findings critical to accurate prostate cancer detection and staging. 3) Identify imaging pitfalls in the detection and staging of prostate cancer. 4) Describe common MRI findings of treated prostate cancer. 4) List the elements of the Prostate Imaging-Reporting and Data System (PI-RADS) structured reporting scheme. 5) List the updated changes reflected in the most recent PI-RADSv2 structured reporting scheme. ABSTRACT Prostate cancer is one of the most frequently diagnosed cancers in the male population. It is the second most common type of cancer detected in American men and their second leading cause of cancer death. The proposed refresher course will provide an overview of MRI for prostate cancer imaging, including a discussion of salient imaging findings on multi-parametric MRI, pitfalls in imaging interpretation, and an overview of existing standardized reporting templates for prostate MR interpretation. RC351C How to Perform and Interpret MRI of the Bladder and Urethra: Anatomy, Technique, and Applications Participants Mukesh G. Harisinghani, MD, Boston, MA (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) MR techniques to image the bladder and urethra will be discussed. 2) Pointers for optimal MR evaluation will be discussed. 3) Pointers for accurate diagnosis on MRI will be discussed. ABSTRACT The propsed course will be provide an overview of applying MR for imaging the bladder and uretheral region RC352 Carotid and Renal Doppler (Hands-on) Tuesday, Dec. 1 8:30AM - 10:00AM Location: E264 GU VA US AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 FDA Discussions may include off-label uses. Participants Gowthaman Gunabushanam, MD, New Haven, CT, (gowthaman.gunabushanam@yale.edu) (Moderator) Editor, WebMD Health Corp ; Gowthaman Gunabushanam, MD, New Haven, CT, (gowthaman.gunabushanam@yale.edu) (Presenter) Editor, WebMD Health Corp ; Mark E. Lockhart, MD, Birmingham, AL, (mlockhart@uabmc.edu ) (Presenter) Nothing to Disclose Shweta Bhatt, MD, MBBS, Rochester, NY (Presenter) Nothing to Disclose Wui K. Chong, MD, Chapel Hill, NC, (wk_chong@med.unc.edu) (Presenter) Nothing to Disclose Corinne Deurdulian, MD, Los Angeles, CA (Presenter) Nothing to Disclose Vikram S. Dogra, MD, Rochester, NY (Presenter) Editor, Reed Elsevier Edward G. Grant, MD, Los Angeles, CA (Presenter) Research Grant, General Electric Company ; Medical Advisory Board, Nuance Communications, Inc Ulrike M. Hamper, MD, MBA, Baltimore, MD (Presenter) Nothing to Disclose Felix A. Hester, Helena, AL (Presenter) Nothing to Disclose Michelle L. Robbin, MD, Birmingham, AL, (mrobbin@uabmc.edu) (Presenter) Consultant, Koninklijke Philips NV; Leslie M. Scoutt, MD, New Haven, CT (Presenter) Consultant, Koninklijke Philips NV Ravinder Sidhu, MD, Rochester, NY, (ravinder_sidhu@urmc.rochester.edu) (Presenter) Nothing to Disclose Sadhna Verma, MD, Cincinnati, OH (Presenter) Nothing to Disclose Margarita V. Revzin, MD, Wilton, CT, (margarita.revzin@yale.edu) (Presenter) Nothing to Disclose Davida Jones-Manns, Hampstead, MD (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Describe the technique and optimally perform carotid Doppler ultrasound. 2) Describe the technique and optimally perform renal Doppler ultrasound. 3) Review qualitative and quantitative criteria for diagnosing abnormalities in carotid and renal ultrasound Doppler examinations. ABSTRACT This hands-on course will provide participants with a combination of didactic lectures and an extended 'live' scanning opportunity on normal human volunteers, as follows: Didactic lectures (30 minutes): 1. Carotid Doppler Ultrasound: scanning technique, diagnostic criteria and interesting teaching cases. 2. Renal Doppler Ultrasound: scanning technique, diagnostic criteria and interesting teaching cases. Mentored scanning (60 minutes): Following the didactic lectures, the participants will proceed to a scanning area with normal human volunteers and ultrasound machines from different manufacturers. Participants will be able to perform live scanning with direct assistance (if needed) by faculty. Faculty will be able to offer feedback, help participants improve their scanning technique as well as answer any questions. Faculty will also be available to answer general questions relating to all aspects of vascular Doppler, not limited to carotid and renal Doppler studies. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Leslie M. Scoutt, MD - 2014 Honored Educator Sadhna Verma, MD - 2013 Honored Educator SSG06 ISP: Genitourinary (Imaging Gynecological Malignancy) Tuesday, Dec. 1 10:30AM - 12:00PM Location: N229 GU MR OI BQ AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Susanna I. Lee, MD, PhD, Boston, MA (Moderator) Nothing to Disclose Andrea G. Rockall, MRCP, FRCR, London, United Kingdom (Moderator) Nothing to Disclose Sub-Events SSG06-01 Genitourinary Keynote Speaker: Gynecologic Cancer Imaging-Present and Future Tuesday, Dec. 1 10:30AM - 10:40AM Location: N229 Participants Susanna I. Lee, MD, PhD, Boston, MA (Presenter) Nothing to Disclose ABSTRACT The past decade has seen the development of MRI and FDG PET-CT, both of which now play central and complementary roles in treatment planning and followup of women with uterine, ovarian and vulvar cancer. Ongoing investigations of novel techniques such as diffusion and perfusion imaging, and of PET tracers capable of targeting hypoxia and hormone receptors, will push cancer radiology firmly into the realm of the molecular, quantitative and predictive in the coming decade. PET-MRI, capable of concurrent multi-modality functional imaging, will likely prove to be a mainstay in personalized gynecologic cancer care. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Susanna I. Lee, MD, PhD - 2013 Honored Educator SSG06-02 High Grade Serous Ovarian Cancer: BRCA Mutation Status and CT Imaging Phenotypes Tuesday, Dec. 1 10:40AM - 10:50AM Location: N229 Participants Stephanie Nougaret, MD, New York, NY (Presenter) Nothing to Disclose Yuliya Lakhman, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Hebert Alberto Vargas, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Maura Micco, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Melvin D'Anastasi, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Sarah A. Johnson, MD, Toronto, ON (Abstract Co-Author) Nothing to Disclose Ramon E. Sosa, BA, New York, NY (Abstract Co-Author) Nothing to Disclose Krishna Juluru, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Noah Kauff, New York, NY (Abstract Co-Author) Nothing to Disclose Hedvig Hricak, MD, PhD, New York, NY (Abstract Co-Author) Nothing to Disclose Evis Sala, MD, PhD, New York, NY (Abstract Co-Author) Nothing to Disclose PURPOSE To investigate the associations between BRCA mutation status and preoperative CT imaging phenotypes in women with high-grade serous ovarian cancer (HGSOC). METHOD AND MATERIALS 115 patients with HGSOC (76 BRCA mutation-positive and 39 BRCA mutation-negative) and CT scans prior to the primary cytoreductive surgery were included in this retrospective HIPAA-compliant study. Two radiologists (R1 and R2) independently reviewed all CT scans and R1 determined total measurable peritoneal tumor volume (TPTV) for each patient. Associations between BRCA mutation status, CT imaging features, and TPTV were analyzed using Fisher exact test and Mann Whitney test. Inter-reader agreement was assessed with the Cohen's kappa. Kaplan-Meier and Cox proportional hazards regression survival analyses were performed. RESULTS BRCA mutation-positive HGSOC had less frequent peritoneal disease, mesenteric infiltration, and lymphadenopathy at CT (p = 0.0002, < 0.0001-0.03, 0.03 for both readers, respectively). Furthermore, the pattern of peritoneal implants was correlated with the BRCA mutation status: nodular pattern was more common in BRCA-associated tumors whereas infiltrative pattern was more frequent in sporadic tumors (p = 0.0009 and p = 0.0005 for R1 and R2, respectively). BRCA mutation-positive HGSOC had higher mean TPTV (125 cm3 ± 171) than sporadic tumors (56 cm3 ± 95) (p<0.001). Irrespective of BRCA mutation status, mesenteric involvement by tumor was associated with shorter progression-free survival (p <0.0001 for both readers) and overall survival (p<0.0002 and p<0.0001 for R1 and R2, respectively). CONCLUSION BRCA mutation status in HGSOC was linked to the distinct CT imaging phenotypes. Mesenteric disease at CT was an independent predictor of reduced survival in both BRCA mutation-positive and sporadic tumors. CLINICAL RELEVANCE/APPLICATION BRCA-associated HGSOC have characteristic prognostically significant morphology on CT. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Stephanie Nougaret, MD - 2013 Honored Educator Evis Sala, MD, PhD - 2013 Honored Educator SSG06-03 Advanced Cervical Cancer: Quantitative Assessment of Early Response to Neoadjuvant Chemotherapy with Intravoxel Incoherent Motion Diffusion-weighted Magnetic Resonance Imaging Tuesday, Dec. 1 10:50AM - 11:00AM Location: N229 Participants Yanchun Wang, Wuhan, China (Presenter) Nothing to Disclose Dao Y. Hu, MD, PhD, Wuhan, China (Abstract Co-Author) Nothing to Disclose PURPOSE To investigate the utility of intravoxel incoherent motion (IVIM) diffusion-weighted magnetic resonance imaging (MRI) for predicting and monitoring the response of cervical cancer to neoadjuvant chemotherapy (NACT). METHOD AND MATERIALS This prospective study was approved by an institutional review board, and informed consent was obtained from all patients. A total of 42 patients with primary cervical cancer were recruited into this study. IVIM diffusion-weighted MRI was performed on all patients at three time points (prior to NACT, 3 weeks after the first NACT, and 3 weeks after the second NACT).The response to treatment was determined according to the Responded Evaluation Criteria in Solid Tumors (RECIST) three weeks after the second NACT treatment, and the subjects were categorized into responders and non-responders. The standard ADC, true diffusion coefficient (D), perfusion-related pseudo-diffusion coefficient (D*), and perfusion fraction (f) values were determined. RESULTS Patients were divided into responders (n=24) and non-responders (n=18) according to the RECIST guidelines. Before treatment, the D and standard ADC values were significantly higher in responders than in non-responders (both p<0.01). No significant differences were observed in D* and f . Analysis of the receiver operating characteristic (ROC) curves indicated that the threshold of D<0.93×10-3mm2/s and the standard ADC<1.11×10-3mm2/s could be used to differentiate responders from non-responders, yielding area under curve (AUC) values of 0.804 and 0.768, respectively. Three weeks after both the first and second NACT treatments, the D and standard ADC values in the responders were still significantly higher than those in the non-responders.D* and f values still showed no significant differences.The ROC curve analysis indicated that the AUC values for D and standard ADC were 0.823 and 0.763 for the second time point and 0.787 and 0.794 for the last time point. CONCLUSION IVIM may be useful for predicting and monitoring the efficacy of NACT in cervical cancer. D and standard ADC values could represent reliable early predictors of the NACT response prior to treatment. Furthermore, these parameters can be used to monitor NACT responses during and after therapy. CLINICAL RELEVANCE/APPLICATION These results should be useful for both patients and clinical doctors. Patients who are unsuitable for NACT could be given radiation or surgical treatment in a more timely manner. SSG06-04 Prognostic Value of Diffusion-weighted MRI and PET/CT During Concurrent Chemoradiotherapy in Uterine Cervical Cancer Tuesday, Dec. 1 11:00AM - 11:10AM Location: N229 Participants Jung Jae Park, MD, Seoul, Korea, Republic Of (Presenter) Nothing to Disclose Chan Kyo Kim, MD, PhD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Byung Kwan Park, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate the prognostic value of diffusion-weighted MRI (DWI) and PET/CT during concurrent chemoradiotherapy (CCRT) of cervical cancer for predicting disease progression. METHOD AND MATERIALS This retrospective study included 67 consecutive patients (median age, 55 years; range, 28-78 years) who received CCRT for locally advanced cervical cancer. All patients underwent both 3T-DWI and PET/CT before and during (at 4 weeks) treatment. The mean apparent diffusion coefficient (ADC) and maximum standardized uptake value (SUVmax) were measured on the tumors and the percentage changes of each parameter between the two time points (ΔADC and ΔSUVmax) were calculated. In the prediction of disease progression, the diagnostic performance of tumor ΔADC and ΔSUVmax was evaluated using the time-dependent receiver operating characteristics (ROC) curve analysis. The relationship between disease progression and clinical and imaging parameters was investigated using univariate and multivariate Cox regression analyses. RESULTS During a mean follow-up of 2.7 years, disease progression was identified in 16 patients (23.9%): local recurrence (n= 7), distant metastasis (n= 8) and both local recurrence and distance metastasis (n= 1). During treatment, the mean ADC and SUVmax significantly increased and decreased, respectively (both P < 0.001). The mean ΔADC and ΔSUVmax were 42.6 ± 17% and 67.6 ± 16.5%, respectively. In the prediction of disease progression, the integrated area under the curve of ΔADC (0.791) and ΔSUVmax (0.781) were not significantly different ( P = 0.88) and the optimal cut-offs of ΔADC and ΔSUVmax were 35.1% and 60.7%, respectively. On multivariate Cox regression analysis, the ΔADC (< 35.1%) and ΔSUVmax (< 60.7%) were the only independent predictors of disease progression after treatment (hazard ratio, 4.1 and 4.5; P , 0.04 and 0.03, respectively). CONCLUSION The percentage changes of DWI and PET/CT parameters during CCRT offer similar prognostic value for the prediction of posttreatment disease progression in patients with cervical cancer. CLINICAL RELEVANCE/APPLICATION DWI, as a noninvasive tool, can be used in the prediction of therapeutic outcomes following concurrent chemoradiotherapy in patients with cervical cancer, instead of PET/CT with the risk of ionizing radiation exposure. SSG06-05 Application of Non-Gaussian Water Diffusional Kurtosis Imaging in the Assessment of Uterine Tumors: A Preliminary Study Tuesday, Dec. 1 11:10AM - 11:20AM Location: N229 Participants Aliou A. Dia, MD, Suita, Japan (Presenter) Nothing to Disclose Masatoshi Hori, MD, Suita, Japan (Abstract Co-Author) Nothing to Disclose Hiromitsu Onishi, MD, Suita, Japan (Abstract Co-Author) Nothing to Disclose Makoto Sakane, MD, Suita, Japan (Abstract Co-Author) Nothing to Disclose Takahiro Tsuboyama, MD, Suita, Japan (Abstract Co-Author) Nothing to Disclose Noriyuki Tomiyama, MD, PhD, Suita, Japan (Abstract Co-Author) Nothing to Disclose Mitsuaki Tatsumi, MD, PhD, Suita, Japan (Abstract Co-Author) Nothing to Disclose Tomoyuki Okuaki, RT, Chuo-Ku, Japan (Abstract Co-Author) Employee, Koninklijke Philips NV PURPOSE To retrospectively evaluate the feasibility and the value of diffusional kurtosis imaging (DKI) in the assessment of uterine tumors compared with that of conventional diffusion weighted imaging (DWI) and with pathological findings as gold-standard. METHOD AND MATERIALS Sixty-one women (mean age: 54.85 years ±14.09, range 26-89 years) with histopathologically proven uterine cancers (51 cervical cancers and 10 corpus cancers) underwent 3-T MR imaging using DKI with high b values (b=700, 1000, 1700 and 2500 s/mm2) and DWI (b=0 s/mm2, b=700 s/mm2). Thirteen of the 61 patients (21.3 %) had coexisting leiomyomas.ROI-based measurements of diffusivity (D), kurtosis (K) and ADC of the uterine cancers, leiomyomas, healthy myometrium and endometrium were performed.The areas under the ROC curve (AUC) in differentiating malignant from benign lesions were also compared. RESULTS Mean D of uterine cancers (0.879 mm/s2 ± 0.30) was significantly lower than that of the leiomyomas (1.174 mm/s2±0.43) (P=0.006), the healthy myometrium (1.178 mm/s2± 0.27) (P=0.000) and the healthy endometrium (1.308 mm/s2±0.5) (P=0.013). Mean K of uterine cancers (0.754 mm/s2± 0.22) was moderately higher than that of leiomyomas (0.686 mm/s2± 0.24), the healthy myometrium (0.708 mm/s2± 0.19) and the healthy endometrium (0.568mm/s2± 0.25).No significant difference was found between the mean K of the uterine cancers, the leiomyomas, the healthy myometrium and endometrium (P=0.33, 0.27 and 0.23).There was no significant difference in AUC between D and ADC. CONCLUSION D is not superior or inferior to the conventional ADC in the differentiation between benign and malignant uterine lesions. The K that is related to the microstructural complexity was higher in uterine cancers than that of leiomyomas but without any significant difference, opposite to K values in white matter tissue of the brain, in breast or prostate cancers where the mean K of malignant lesions was significantly higher than of the benign lesions. CLINICAL RELEVANCE/APPLICATION The D, in non-Gaussian DKI, is equal to the conventional ADC in differentiating benign from malignant uterine lesions. The K of uterine malignant tumors was not significantly higher than that of the benign lesions, unlike in breast or prostate cancers. SSG06-06 Clinical Value of Proton (1H-) Magnetic Resonance Spectroscopy (MRS) Using Body-phased Array Coil at 3.0 T in Pretreatment Assessment for Cervical Cancer Patients Tuesday, Dec. 1 11:20AM - 11:30AM Location: N229 Participants Gigin Lin, MD, Guishan, Taiwan (Presenter) Nothing to Disclose Yu-Ting Huang, Guishan, Taiwan (Abstract Co-Author) Nothing to Disclose Koon-Kwan Ng, Guishan, Taiwan (Abstract Co-Author) Nothing to Disclose Yu-Chun Lin, MSC, Taoyuan, Taiwan (Abstract Co-Author) Nothing to Disclose Tzu-Chen Yen, MD, PHD, Taoyuan, Taiwan (Abstract Co-Author) Nothing to Disclose Hung-Hsueh Chou, MD, Taoyuan, Taiwan (Abstract Co-Author) Nothing to Disclose Angel Chao, MD, Taoyuan, Taiwan (Abstract Co-Author) Nothing to Disclose Chiun-Chieh Wang, Guishan, Taiwan (Abstract Co-Author) Nothing to Disclose Chyong-Huey Lai, Guishan, Taiwan (Abstract Co-Author) Nothing to Disclose Pen-An Liao, MD, Taipei City, Taiwan (Abstract Co-Author) Nothing to Disclose PURPOSE To determine the clinical value of proton (1H-) magnetic resonance spectroscopy (MRS) using body-phased array coil at 3.0 T, in To determine the clinical value of proton (1H-) magnetic resonance spectroscopy (MRS) using body-phased array coil at 3.0 T, in pretreatment assessment for cervical cancer patients. METHOD AND MATERIALS We prospectively enrolled 52 histology proven cervical cancer patients (age 27-80 years) and 30 age-matched surgical candidates for benign uterine myoma without evidence of cervical cancer. Pretreatment MR study plus MRS and diffusion weighted imaging (DWI) sequences were carried out at a 3.0 T system using body-phased array coil for the pelvis. PRESS localized 1H-MRS was applied to cervical tumor or normal tissue, with resonances analyzed by using the LC-Model algorithm. Cramer-Rao lower bound (CRLB) threshold of 20% was used as quality control. We compared resonances based on: (1) tumor vs normal cervical tissue, (2) histopathology type (squamous vs adenocarcinoma) (3) T stage = IIb (4) nodal metastasis (5) distant metastasis using MannWhitney test. RESULTS Cervical tumor showed a lower 1.3-ppm lipid level (0.30 vs 1.01μM, P < .05), as compared with normal cervical tissue. Squamous cell carcinoma demonstrated lower levels in 1.3-ppm lipid (0.17μM vs 0.59μM, P < .05) and 0.9-ppm lipid (0.04μM vs 0.16μM, P < .05), as compared with adenocarcinoma. Tumor with T stage >= IIb had lower levels in 1.3-ppm lipid (0.15μM vs 0.53μM, P < .05), 0.9-ppm lipid (0.04μM vs 0.15μM, P < .05) and total choline (0.04μM vs 0.16μM, P < .05). Tumors with nodal metastasis contained lower levels of 1.3-ppm lipid (0.16μM vs 0.44μM, P < .05) and glutamine (0.01μM vs 0.02μM, P < .005), whereas tumors with distant metastasis contained a lower level of 1.3-ppm lipid (0.12μM vs 0.50μM, P < .05). However, resonances from cervical tumor were independent to maximal tumor size or ADC value on MRI. CONCLUSION 1H-MRS using body-phased array coil at 3.0 T in cervical cancer patients is useful in differentiating tumor, histopathology type, T stage >= IIb, nodal or distant metastasis, and is independent to maximal tumor size or ADC value on MRI. CLINICAL RELEVANCE/APPLICATION 1H-MRS using body-phased array coil at 3.0 T added additional dimensions for pretreatment assessment in cervical cancer patients. SSG06-07 Impact of Multiparametric MRI (mMRI) on the Therapeutic Management of Suspicious Adnexal Masses Detected by Transvaginal Ultrasound (TVUS) Tuesday, Dec. 1 11:30AM - 11:40AM Location: N229 Participants Simone Schrading, MD, Aachen, Germany (Presenter) Nothing to Disclose Sabine M. Detering, Aachen, Germany (Abstract Co-Author) Nothing to Disclose Dirk Bauerschlag, Aachen, Germany (Abstract Co-Author) Nothing to Disclose Christiane K. Kuhl, MD, Bonn, Germany (Abstract Co-Author) Nothing to Disclose PURPOSE Incidental adnexal masses at TVUS are common and diagnostically challenging. The primary goal of imaging is accurate tissue characterization to guide further management, i.e. the choice between plain follow-up vs laparoscopic surgery vs. open surgery. Aim of this study was to evaluate the diagnostic utility of mMRI for further management stratification in patients with such adnexal masses METHOD AND MATERIALS Prospective IRB-approved trial on 126 women (mean age 54.6 years) with inconclusive adnexal masses at TVUS. All women underwent conventional work up, including pelvic examination, TVUS, and CA-125 levels. In addition, all women underwent mMRI at 3T with high resolution T2-TSE in three planes, DWI (max. b-800) and DCE. Likelihood of malignancy and appropriate management (i.e. follow-up vs. laparoscopic vs. open surgery) was first determined based on results of conventional methods, and then, independently, based on mMRI. Then, all methods were reviewed in synopsis. Final surgical pathology served as standard-ofreference or clinical and imaging follow-up of at least 24 months RESULTS In 65% (82/126) of patients the adnexal mass finally classified as benign, in 29% (36/126) as malignant and in 6% (8/126) as borderline. The diagnostic indices for TVUS+CA-125 alone vs. MRI alone vs. all methods combined were as follows: Sensitivity: 86% (31/36) vs. 97% (35/36) vs. 100% (36/36); Specificity: 32% (29/90) vs. 83% (75/90) vs. 80% (68/90); PPV: 34% (31/91) vs. 70% (35/50) vs. 74% (40/54), NPV: 65% (29/44) vs. 98% (75/76) vs. 100% (72/72). After mMRI, the therapeutic management was changed in 41/126 (34%) of patients. In 30 patients in whom surgery had been recommended based on conventional assessment, mMRI correctly diagnosed typical benign findings; these patients underwent follow-up instead of surgery. None of these women developed malignancy during follow-up. In another 11 patients, mMRI results correctly suggested malignancy such that open surgery was performed instead of laparoscopic surgery CONCLUSION Compared with conventional assessment (pelvic exam, TVUS, CA-125), mMRI correctly changed the management in one-third of women with incidental adnexal masses. It helps avoid unnecessary surgery, or unnecessary surgical steps (conversion from laparoscopic to open surgery) CLINICAL RELEVANCE/APPLICATION Pelvic mMRI helps to significantly improve clinical management of asymptomatic women with incidental adnexal masses identified on TVUS SSG06-08 Preoperative Tumor Texture Analysis from MRI Predicts Deep Myometrial Invasion and High Risk Histology in Endometrial Carcinomas Tuesday, Dec. 1 11:40AM - 11:50AM Location: N229 Participants Sigmund Ytre-Hauge, MD, Bergen, Norway (Presenter) Nothing to Disclose Erik Hanson, PhD, Bergen, Norway (Abstract Co-Author) Nothing to Disclose Arvid Lundervold, MD, PhD, Bergen, Norway (Abstract Co-Author) Nothing to Disclose Jone Trovik, MD, Bergen, Norway (Abstract Co-Author) Nothing to Disclose Helga Salvesen, MD, PhD, Bergen, Norway (Abstract Co-Author) Nothing to Disclose Ingfrid S. Haldorsen, MD, PhD, Bergen, Norway (Abstract Co-Author) Nothing to Disclose PURPOSE Tumor heterogeneity is a key feature of malignant disease. Heterogeneity in MR images can be quantified by texture analysis. We aimed to explore whether high risk histological features are reflected in texture parameters derived from preoperative MRI in endometrial carcinomas. METHOD AND MATERIALS Preoperative pelvic contrast-enhanced MRI (1.5T) including diffusion-weighted imaging (DWI) was prospectively performed in 99 patients with histologically confirmed endometrial carcinomas. Tumor region of interest (ROI) was manually drawn encircling the uterine tumor on axial T1-weighted contrast-enhanced (CE) series on the slice displaying the largest cross-section tumor area. Histogram based texture features (standard deviation, skewness and kurtosis) were calculated from these tumor ROIs. Texture parameters were analyzed in relation to established histological subtype and grade, surgicopathological staging parameters (deep myometrial and cervical stroma invasion and lymph node metastases) and MRI based tumor volume and tumor apparent diffusion coefficient (ADC) value using Mann-Whitney U test, Jonckheere-Terpsta trend test and Pearson's bivariate correlation test. RESULTS Large standard deviation (SD) in the tumor ROIs was significantly associated with presence of deep myometrial invasion (p=0.009). Lower values for skewness were observed in the tumor ROIs from endometrioid high grade tumors (p=0.012) and from nonendometrioid tumors (by definition always high grade lesions, p=0.020). Kurtosis was positively correlated to tumor volume (r= 0.27; p=0.006) and negatively correlated to tumor ADC value (r=-0.28; p=0.006). CONCLUSION MRI derived tumor texture features reflecting tumor heterogeneity are significantly related to high risk histology and predict deep myometrial invasion in endometrial carcinomas. Thus, tumor texture features based on MRI represent promising biomarkers to aid preoperative tumor characterization for risk stratified surgical treatment. CLINICAL RELEVANCE/APPLICATION Tumor texture features derived from MRI reflect high risk endometrial carcinoma and may aid preoperative risk classification for stratified surgery. SSG06-09 Endometrial Cancer MR Staging Accuracy in a Large Multi-site UK Cancer Network Over Three Years: Can the Reported Single Centre Staging Accuracies be Met in Clinical Practice? Tuesday, Dec. 1 11:50AM - 12:00PM Location: N229 Participants Neil Soneji, BSC, MBBS, London, United Kingdom (Abstract Co-Author) Nothing to Disclose Annarita Ferri, MD, Chieti, Italy (Presenter) Nothing to Disclose Victoria Stewart, London, United Kingdom (Abstract Co-Author) Nothing to Disclose Roberto Dina, MD, London, United Kingdom (Abstract Co-Author) Nothing to Disclose Nishat Bharwani, MBBS, FRCR, London, United Kingdom (Abstract Co-Author) Nothing to Disclose Andrea G. Rockall, MRCP, FRCR, London, United Kingdom (Abstract Co-Author) Nothing to Disclose PURPOSE To determine the radiological staging accuracy of endometrial cancer (EC) from images acquired from multiple MR scanners across a 10 centre UK cancer network over three years. METHOD AND MATERIALS Retrospective study of 382 consecutive patients with EC imaged in 9 external hospitals and 3 internal hospital sites discussed at our tertiary gyne-oncology centre between October 2011-October 2014. All patients with tertiary centre reports for both final histology and MRI were included (n=270). The radiological stage provided at MDT discussion was compared to the 'gold standard' histological report. Parameters assessed included depth of myometrial invasion, cervical and nodal stage. The use of DWI or DCE and the site for incorrect staging were recorded. MedCalc statistical software version 15.2.2 was used. RESULTS 242 of 270 MRI reports (90%) included a final FIGO stage; of these 147 scans were performed internally and 95 at an external hospital. Accuracy of the reported depth of invasion was 72.7% for all cases (72.8% for internal and 72.6% for external scans). Sensitivity, specificity, positive and negative predictive values & accuracy with DWI (n=204) were 67%, 77%, 64%, 79%, 73% and without DWI (n=38) were 75%, 69%, 53%, 86%, 71% (p>.05). Accuracy with DCE (n=109) was 72% and without (n=130) was 73%. For cervical stromal invasion, sensitivity, specificity, PPV, NPV and accuracy for all scans were 59%, 94%, 64%, 93% and 89%. As a percentage of all causes of staging error, depth of invasion accounted for 41-52%, cervix stromal invasion 20-32% and nodal stage 8-16% depending on whether the patient was scanned internally or externally, or whether DWI or DCE were included (p>.05). CONCLUSION Staging accuracy in a large multi-site cancer network over three years does not meet the reported staging accuracies in metaanalyses of smaller single centre published research (pooled sensitivity/specificity of 86-90%). DWI and DCE did not affect staging accuracy, although only a small number of cases did not have these. The underlying causes for the reduction in sensitivity and specificity need to be evaluated in order to translate the highest achievable MR staging accuracy to long term routine practice. CLINICAL RELEVANCE/APPLICATION Accuracy of MR staging of endometrial cancer in a multi-site cancer network over three years does not reach single centre study results. The causes for staging inaccuracies need to be understood. SSG09 Molecular Imaging (Gynecologic Oncology) Tuesday, Dec. 1 10:30AM - 12:00PM Location: S504CD BR GU MI MR RO AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 FDA Discussions may include off-label uses. Participants Kathryn A. Morton, MD, Salt Lake City, UT (Moderator) Nothing to Disclose Zaver M. Bhujwalla, PhD, Baltimore, MD (Moderator) Nothing to Disclose Sub-Events SSG09-01 First Clinical Trial on Ultrasound Molecular Imaging Using KDR-Targeted Microbubbles in Patients with Breast and Ovarian Lesions Tuesday, Dec. 1 10:30AM - 10:40AM Location: S504CD Participants Juergen K. Willmann, MD, Stanford, CA (Presenter) Research Consultant, Bracco Group; Research Consultant, Triple Ring Technologies, Inc; Research Grant, Siemens AG; Research Grant, Bracco Group; Research Grant, Koninklijke Philips NV; Research Grant, General Electric Company Lorenzo Bonomo, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Antonia Testa, Rome, Italy (Abstract Co-Author) Nothing to Disclose Pierluigi Rinaldi, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Guido Rindi, Rome, Italy (Abstract Co-Author) Nothing to Disclose Sanjiv S. Gambhir, MD, PhD, Stanford, CA (Abstract Co-Author) Board Member, Enlight Biosciences; Board Member, ImaginAb, Inc; Board Member, FUJIFILM Holdings Corporation; Board Member, ClickDiagnostics, Inc; Consultant, FUJIFILM Holdings Corporation; Consultant, Gamma Medica, Inc; Speaker, ImaginAb, Inc; Stock, Enlight Biosciences; Stock options, Enlight Biosciences; Travel support, Gamma Medica, Inc PURPOSE To assess if clinical ultrasound molecular imaging (USMI) using a novel clinical grade human kinase domain receptor (KDR)-targeted microbubble (BR55, Bracco) is safe and allows assessment of KDR expression in patients with breast and ovarian lesions, using immunohistochemistry (IHC) as gold standard. METHOD AND MATERIALS 21 women (34-66 yrs) with focal breast lesions and 24 women (48-79 yrs) with focal ovarian lesions were injected IV with BR55 (0.03-0.08 mL/kg bw) and 2D USMI of the target lesions was performed dynamically every 2 min starting 5 min after injection up to 29 min, using the linear 15L8 probe (Siemens) or the endocavitary 1123 probe (Esaote). Normal breast tissues surrounding the lesion or the contralateral presumed normal ovary served as intra-patient controls. Blood pressure, EKG, oxygen levels, heart rate, CBC, and metabolic panel were obtained before, and 30 min, 1h, 24h after BR55 administration. Persistent focal BR55 binding on USMI was visually assessed in consensus by 2 blinded offsite radiologists as none, possibly or definitely. Patients underwent surgical resection of the target lesions and tissues were stained for CD31 and KDR. A pathologist assessed vascular KDR expression using a 4-point scale (none, weak, intermediate, high). Adjudication was performed in consensus (offsite radiologists and pathologist) to match clinically. RESULTS USMI with BR55 was well tolerated by all patients at all doses, without safety concerns. Among the 40 patients included in the analysis, KDR expression was higher in malignant breast and ovarian lesions (score 2.40±0.63 and 2.08±0.64, respectively) compared to benign breast and ovarian lesions (2.08±0.64 and 1.33±0.50). KDR expression matched well with presence of focal BR55 binding on USMI in malignant breast (13/15; 86.7%) and ovarian (11/13; 84.6%) lesions, as well as benign breast (2/3; 66.7%) and ovarian (8/9; 88.9%) lesions. Focal USMI signal could be detected up to 29 min after injection. CONCLUSION Use of BR55 in USMI of breast and ovarian lesions is safe and effective and preliminary data indicate that KDR-targeted USMI signal matches well with vascular KDR expression on IHC. CLINICAL RELEVANCE/APPLICATION This study provides proof of principle on feasibility and safety of KDR-targeted USMI in patients with breast and ovarian lesions and lays the foundation for further clinical trials. SSG09-02 Imaged EGFR Expression Level Reflects Inhibited Growth-Pathway Node in Model of Triple-Negative Breast Cancer Tuesday, Dec. 1 10:40AM - 10:50AM Location: S504CD Participants Eric Wehrenberg-Klee, MD, Boston, MA (Presenter) Nothing to Disclose Nafize S. Turker, PhD, Boston, MA (Abstract Co-Author) Nothing to Disclose Pedram Heidari, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Mauri Scaltriti, PhD, New York, NY (Abstract Co-Author) Nothing to Disclose Umar Mahmood, MD, PhD, Charlestown, MA (Abstract Co-Author) Research Grant, Sabik Medical Inc; Advisory Board, Blue Earth Diagnostics Limited; PURPOSE Triple-negative breast cancer (TNBC) is an aggressive breast cancer subtype for which targeted inhibitors of the RTK/PI3K/AKT/mTOR growth pathway have demonstrated early treatment success. The surface receptor EGFR is one of the dominant RTKs mediating downstream growth signals along this pathway and changes in EGFR expression may be predictive of therapeutic inhibition. We sought to demonstrate that the changes in EGFR expression predictive of treatment response could be non-invasively assessed. METHOD AND MATERIALS 64Cu-DOTA-cetuximab F(ab´)2 was prepared from cetuximab monoclonal antibody and probe affinity for EGFR assessed. A panel of TNBC cell lines (MDMBA468, MDMBA231, HCC70) was treated with the AKT inhibitor GDC-0068 or the PI3K inhibitor GDC-0941 for one day at a range of concentrations. Following treatment, we assessed in vitro EGFR probe uptake. In vitro uptake study results were compared to protein quantification as assessed by Western blot. After treatment of HCC70 mouse xenografts with control, GDC-0068, or GDC-0941 for two days, PET-CT imaging of HCC-70 tumors with 64Cu-DOTA-EGFR F(ab´)2 was performed. RESULTS In vitro treatment with GDC-0068 resulted in increased EGFR Probe uptake of 25%, 139%, and 16% for MDAMB468, MDMBA231, and HCC70, respectively. In vitro treatment with GDC-0941 resulted in increased EGFR uptake of 6%, 87%, and 88%, for the same panel of cell lines. In vitro uptake studies demonstrate close correlation with changes in EGFR expression as assessed by Western blot. In vivo imaging of HCC70 mouse xenografts with EGFR PET Probe after treatment with control, GDC-0068, or GDC-0941 demonstrate SUVmean of 0.32 (±0.03), 0.50 (±0.01), 0.62 (±0.01), with all comparisons significant (p<0.01). CONCLUSION We demonstrate in a murine model of triple-negative breast cancer that changes in EGFR expression induced by targeted therapeutics can be non-invasively assessed using a 64Cu-DOTA-EGFR F(ab´)2 PET imaging probe. We demonstrate that changes in the level of EGFR expression, potentially indicative of therapeutic response, differ depending on the growth-pathway inhibited. CLINICAL RELEVANCE/APPLICATION Noninvasive assessment of changes in EGFR expression could be a valuable clinical tool for rapid assessment of therapeutic efficacy of targeted growth pathway inhibitors in TNBC, allowing for dynamic clinical decision making in response to imaged resistance profiles. SSG09-03 FACBC PET/CT Before and After Neoadjuvant Therapy in Locally Advanced Breast Cancer: A Prospective Pilot Clinical Trial Tuesday, Dec. 1 10:50AM - 11:00AM Location: S504CD Participants Gary A. Ulaner, MD, PhD, New York, NY (Presenter) Research support, General Electric Company; Research support, F. Hoffmann-La Roche Ltd Serge Lyashchenko, New York, NY (Abstract Co-Author) Nothing to Disclose Hanh Pham, New York, NY (Abstract Co-Author) Nothing to Disclose Jason S. Lewis, PhD, New York, NY (Abstract Co-Author) Nothing to Disclose PURPOSE Genes for amino acid transport proteins are highly upregulated in both invasive ductal carcinoma (IDC) and ILC, as compared to normal breast epithelium. This molecular phenotype may allow for the development of imaging agents based on amino acid metabolism. We evaluated whether Fluorine-18 labeled 1-amino-3-fluorocyclobutane-1-carboxylic acid (FACBC), an amino acid analog labelled with fluorine-18, could be used as an imaging agent for local staging of locally advanced breast cancer before and after neoadjuvant therapy. METHOD AND MATERIALS This prospective clinical trial is being performed under IRB approval. In this trial, newly diagnosed breast cancer patients that are planned for neoadjuvant systemic therapy followed by surgical resection undergo FACBC PET/CT prior to systemic therapy and then again following completion of systemic therapy. Maximum Standardized Uptake Values (SUVmax) and other quantitative measures of FACBC-avidity are measured for the primary breast tumor and nodal metastases before and after systemic therapy. Following surgery, FACBC results are correlated with postoperative histopathologic results. RESULTS Of 28 planned patients, we have currently accrued 23. All 23 accrued patients have undergone the pre-neoadjuvant therapy FACBC PET/CT. All 23 primary breast lesions were FACBC avid with SUVmax values of 2.3 to 17.5. 18 of 23 patients (78%) had FACBC avid axillary nodes with SUVmax values of 1.2 to 14.6. In 2 of 23 patients (9%), an unsuspected extra-axillary local nodal metastasis was detected on the pre neoadjuvant therapy FACBC PET/CT. SUVmax of these nodes was 2.1 and 2.2, and both were pathologically proven to be metastases. 15 of 23 patients (65%) have completed both pre- and post-neoadjuvant PET/CT scans and histological analysis following surgical resection. In 13 of these 15 patients (87%), a reduction of SUVmax in the primary breast cancer of greater than 90% could accurately identify the presence or absence of complete response/near complete response as defined by post surgical histologic analysis. CONCLUSION This pilot trial of FACBC PET/CT in locally advanced breast cancer demonstrates potential uses of FACBC PET/CT before and after neoadjuvant therapy. CLINICAL RELEVANCE/APPLICATION Further work on FACBC as a radiotracer in locally advanced breast cancer is warranted. SSG09-04 Operation-naive Invasive Ductal Carcinoma of the Breast. Comparison of Staging Performed with Whole Body DWI, PET, PET-CT, and PET-MR Tuesday, Dec. 1 11:00AM - 11:10AM Location: S504CD Participants Onofrio A. Catalano, MD, Napoli, Italy (Presenter) Nothing to Disclose Bruce R. Rosen, MD, PhD, Charlestown, MA (Abstract Co-Author) Research Consultant, Siemens AG Angelo Luongo, Napoli, Italy (Abstract Co-Author) Nothing to Disclose Mark Vangel, PhD, Charlestown, MA (Abstract Co-Author) Nothing to Disclose Marco Catalano, Napoli, Italy (Abstract Co-Author) Nothing to Disclose Umar Mahmood, MD, PhD, Charlestown, MA (Abstract Co-Author) Research Grant, Sabik Medical Inc; Advisory Board, Blue Earth Diagnostics Limited; Emanuele Nicolai, Napoli, Italy (Abstract Co-Author) Nothing to Disclose Andrea Soricelli, MD, Napoli, Italy (Abstract Co-Author) Nothing to Disclose Marco Salvatore, MD, Napoli, Italy (Abstract Co-Author) Nothing to Disclose PURPOSE To compare the performance of whole body (WB) DW, WB-PET, WB-PETCT, and WB-PETMR in patients with newly diagnosed invasive ductal breast cancer, before undergoing treatment. METHOD AND MATERIALS 49 consecutive women with newly diagnosed invasive ductal carcinoma of the breast underwent WB-DWI, WB-PET, WB-contrast enhanced (CE) PETCT and WB-CE-PETMR before treatment. A radiologist and a nuclear medicine physician evaluated in consensus the studies and searched for occurrence, number, and location of metastases. Final staging and number of lesions, according to each technique, were compared. Pathology and imaging follow up were used as the ground truth reference. RESULTS All the techniques correctly staged 32/49 patients: stage2b in 8, 2c in 7, 3c in 4, 4 in 13. They provided discordant stages in 17/49 patients: 1 (stage 2a): staged-4 by WB-PET; 4 (stage 2b): 3/4 staged-2a by WB-PET and WB-PETCT, 1/4 staged-4 by WB-DWI;3 (stage 3a): 2/3 staged-2b by WB-PET and WB-PETCT, 1/3 staged-4 by WB-DWI;3(stage 3c): 2/3 staged-2a by WB-PET and WBPETCT, 1/3 staged-4 by WB-PET and WB-PETCT;6 (stage 4): 1/6 staged-3a by WB-PET, WB-DWI, and WB-PETCT, 1/6 staged-2b by WB-PET and WB-PETCT, 1/6 staged-2b by WB-PET, WB-DWI, and WB-PETCT, 1/6 staged-3a by WB-DWI, 1/6 staged-3c by WB-DWI, and 1/6 staged-3a by WB-PET, WB-PETCT and 3c by WB-DWI. Staging performance of WB-PETMR (49 correctly staged) was significantly better than WB-PETCT (38 correctly staged) (P=0.001, chi square-test).The best performing modality for malignant lymph-node detection was WB-PETMR (47 of 49 patients), followed by WB-DWI (37/49), followed by WB-PET and WBPETCT (15 patients each). Significantly more malignant nodes were detected by WB-PETMR (P<0.0001, paired t-tests). At least as many true-positive lesions were detected by WB-PETMR than by any of the other three modalities for 46 patients. The corresponding number of patients for WB-PET, WB-PETCT, and WB-DWI were 40, 39 and 34, respectively. CONCLUSION PETMR allows a better accuracy in initial staging of surgical-naive ductal invasive breast cancer. The higher performance is likely related to the additive information of PET, DWI, as well as of the other sequences (STIR, T1-weighted Dixon, HASTE, ADC maps, and CE-T1-weighed images) of WB-PETMR CLINICAL RELEVANCE/APPLICATION When available WB-PETMR should be considered for proper staging of naive ductal invasive breast cancer. SSG09-05 Multiparametric 18F-FMISO PET/MRI for Assessment of Treatment Response to Chemo-radiation and Hypoxia Monitoring in Cervix Cancer Patients: A Feasibility Study Tuesday, Dec. 1 11:10AM - 11:20AM Location: S504CD Participants Petra Georg, MD,PhD, Wiener Neustadt, Austria (Abstract Co-Author) Nothing to Disclose Piotr Andrzejewski, MA, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Pascal A. Baltzer, MD, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Stephan H. Polanec, MD, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Wolfgang Wadsak, Vienna, Austria (Abstract Co-Author) Speaker, General Electric Company; Consultant, THP Medical; Research Grant, ABX GmbH; Research Grant, Rotem GmbH Alina Sturdza, MD, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Georgios Karanikas, MD, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Stephan Polterauer, MD, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Richard Poetter, MD, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Thomas H. Helbich, MD, Vienna, Austria (Abstract Co-Author) Research Grant, Medicor, Inc; Research Grant, Siemens AG; Research Grant, C. R. Bard, Inc Dietmar Georg, PhD, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Katja Pinker, MD, New York, NY (Presenter) Nothing to Disclose PURPOSE To demonstrate feasibility of combined multiparametric positron emission tomography/magnetic resonance imaging at 3T (3T MP PET/MRI) and to assess treatment response and hypoxia monitoring in cervix cancer patients undergoing chemo-radiation therapy. METHOD AND MATERIALS In this IRB-approved prospective study 7 patients underwent sequential 3T MP 18F-FMISO PET/MRI at baseline; 2 and 5 weeks (w) after start and 3 months (FU) after treatment. MRI protocol consisted of a high-resolution isotropic T2-w SPACE, a DWI EPI (b=50/850 sec/mm²) and a high-resolution contrast-enhanced (CE) T1-w VIBE sequence. Patients were injected with 330 MBq 18F-FMISO and scanning was started 240 min after injection. CT data was used for attenuation correction. PET and MR image registrations were performed using Mirada RTx (Mirada Medical, Oxford, UK , ver. 1.4.0.23) software. Gross tumour volume (GTV) was contoured by an experienced radiation oncologist on PET/MRI data sets. The volume of GTV was assessed for tumor size, CEkinetics, restricted diffusivity and 18F-FMISO-avidity using SUVmax and SUV (SUVnorm ) normalized to gluteal muscle uptake. At follow up, cervix was contoured, since all patients showed clinically complete remission. RESULTS 3T MP 18F-FMISO PET/MRI was successfully performed in all patients at every time-point. Median GTV volume was 43.9cc at baseline, 22.4cc after 2w (20-25Gy) and 7.7cc after 5w (40-45Gy). Mean ADC values were 1.02x10-3mm2/sec increasing to 1.18x10-3mm2/sec after 2w and to 1.27x10-3mm2/sec after 5w and to 1.37x10-3mm2/sec at FU. All GTVs showed mean initialenhancement (IE) followed by a plateau with an increasing IE at 2w and 5w and wash-out at 5w. At FU, there was a persistent enhancement. The mean 18F-FMISO SUVnorm was 3.1 at baseline and decreased to 2.3 at 2w and 2.0 at 5w and follow-up. In all patients there was never the whole tumor 18F-FMISO-avid, but 18F-FMISO-avid spots within the tumor indicative of hypoxia could be identified before and during the course of therapy. CONCLUSION MP 18F-FMISO PET/MRI in cervix cancer patients at 3T is feasible and enables non-invasive monitoring of morphological and functional changes during treatment. CLINICAL RELEVANCE/APPLICATION 3T MP 18F-FMISO PET/MRI can depict areas of tumor hypoxia during therapy and thus identify patients at risk who need an aggressive treatment approach. SSG09-06 Correlation of PET-MR Biomarkers with Breast Cancer Molecular Subtypes, Grading and Presence of Distant Metastases at Time of Presentation Tuesday, Dec. 1 11:20AM - 11:30AM Location: S504CD Participants Onofrio A. Catalano, MD, Napoli, Italy (Presenter) Nothing to Disclose Bruce R. Rosen, MD, PhD, Charlestown, MA (Abstract Co-Author) Research Consultant, Siemens AG Carlo Iannace, MD, San Leucio del Sannio, Italy (Abstract Co-Author) Nothing to Disclose Angelo Luongo, Napoli, Italy (Abstract Co-Author) Nothing to Disclose Marco Catalano, Napoli, Italy (Abstract Co-Author) Nothing to Disclose Mark Vangel, PhD, Charlestown, MA (Abstract Co-Author) Nothing to Disclose Umar Mahmood, MD, PhD, Charlestown, MA (Abstract Co-Author) Research Grant, Sabik Medical Inc; Advisory Board, Blue Earth Diagnostics Limited; Maria Lepore, MD, Avellino, Italy (Abstract Co-Author) Nothing to Disclose Bethany L. Niell, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Emanuele Nicolai, Napoli, Italy (Abstract Co-Author) Nothing to Disclose Andrea Soricelli, MD, Napoli, Italy (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate if PET-MR biomarkers correlate with molecular genetic subtypes, grading, and presence of distant metastases at time of presentation in naïve ductal invasive breast cancers. METHOD AND MATERIALS 21 consecutive patients with naïve ductal invasive breast cancer and genetic molecular subtype profiling underwent whole-body contrast enhanced FDG-PET-MR (Biograph mMR, Siemens). Two readers, using commercially available software, measured the following PET-MR biomarkers: ADC, Ktrans, Ve, Kep, IAUC, SUVmax, SUVmean, and MTV. They were correlated with genetic molecular subtypes, grading and occurrence of distant metastases. RESULTS Genetic molecular subtypes were as follows: ER-7, ER+14; PR-8, PR+13; HER2-11, HER2+10; Ki67-low (<=35%), Ki67 medium/high (>35%). Grading was G2 in 14 and G3 in 7. Six patients had distant metastases. The following biomarkers were higher in the ERand PR- compared to ER+ and PR+ patients: Kep (9234±1320 versus 6492 ±2358, p0.01), SUVmax (14.19±7.17 versus 6.17±4.24, p0.004), and SUVmean (8.44±4.01, p0.004). ADC directly correlated with the degree of Ki67 expression (1019±256 for Ki67<=35%, 1338±105 forKi67>35%, p0.002). The following biomarkers were lower in HER2- patients compared to HER2+ cases: ADC (1050±280 versus 1306±122, p0.009), Kep (6726±2240 versus 8599±2122, p0.028), SUVmax (6.29±4 versus 11.8±7.65, p0.046), and SUVmean (3.72±2.28 versus 7.03±4.43, p0.04).G2 patients experienced lower Kep (6638±2391 versus 8944±1764, p0.04) and lower SUVmax (6.83±4.73 versus 12.89±8.07, p 0.04) than G3 patients.No biomarkers correlated with presence of distant metastases. CONCLUSION In naïve ductal invasive breast cancers, PET-MR biomarkers correlate with molecular genetic subtypes and with grading, but not with the presence of distant metastases. CLINICAL RELEVANCE/APPLICATION PET-MR biomarkers might have prognostic and therapeutic implications on patients' management. SSG09-07 Impact of Estrogen Receptor Gene Mutations on [18F]-Fluoroestradiol Uptake in Breast Cancer Tuesday, Dec. 1 11:30AM - 11:40AM Location: S504CD Participants Manoj Kumar, MS, Madison, WI (Abstract Co-Author) Nothing to Disclose Ginny L. Powers, PhD, Madison, WI (Abstract Co-Author) Nothing to Disclose Justin Jeffery, Madison, WI (Abstract Co-Author) Nothing to Disclose Yongjun Yan, PhD, Madison, WI (Abstract Co-Author) Nothing to Disclose Amy M. Fowler, MD, PhD, Saint Louis, MO (Presenter) Nothing to Disclose PURPOSE Accurately predicting therapeutic responsiveness in women with breast cancer remains challenging. Positron emission tomography (PET) imaging using [18F]-16alpha-17beta-fluoroestradiol (FES) provides a way to non-invasively and longitudinally examine the subset of tumors expressing estrogen receptor alpha (ERα) which comprise approximately 70% of all breast cancers. However, the effect of mutations in the gene encoding ERα, recently identified in patients with endocrine-resistant, metastatic breast cancer, on FES uptake is unknown. We developed a model system to test how mutations in ERα influence the uptake of FES. METHOD AND MATERIALS Stable cell lines expressing either wild-type ERα (231-ER) or a point mutation in the ligand-binding pocket, G521R (231-G521R), were created in the ERα-negative human breast cancer cell line MDA-MB-231. ERα-positive MCF7 human breast cancer cells were used as a positive control and parental MDA-MB-231 cells were used as a negative control. Cell uptake of FES was measured in vitro with microPET/CT imaging and gamma counting. In addition, in vivo FES uptake was measured in MCF7 and 231-ER tumors grown as xenografts in athymic nude mice. RESULTS FES uptake was observed both in vitro and in vivo in the MCF7 and 231-ER cells/tumors. However, there was no significant FES uptake in the 231-G521R cells or parental MDA-MB-231 cells. The 231-ER cells had a similar dose response curve to MCF7 in competition assays using increasing doses of cold estradiol, and as consistent with the uptake data, 231-G521R binding was not altered by cold competition. CONCLUSION These data support the use of stable cell lines expressing variant forms of ERα as models for demonstrating the effects of ERα gene mutations on FES uptake. Ongoing studies are focusing on the effects of recently identified clinically-relevant ERα mutations on FES uptake and on the prediction of response to ER-targeted therapies. CLINICAL RELEVANCE/APPLICATION FES-PET imaging provides a non-invasive way to probe ERα function and may prove useful in identifying the development of ERα gene mutations and thus predicting endocrine resistance in ERα-positive breast cancer patients. SSG09-08 Imaging Patients with Breast and Prostate Cancers Using Combined 18F NaF/18F FDG and TOF simultaneous PET/ MRI Tuesday, Dec. 1 11:40AM - 11:50AM Location: S504CD Participants Ryogo Minamimoto, MD, PhD, Stanford, CA (Presenter) Nothing to Disclose Andreas M. Loening, MD, PhD, San Francisco, CA (Abstract Co-Author) Nothing to Disclose Valentina Taviani, PhD, Stanford, CA (Abstract Co-Author) Nothing to Disclose Sanjiv S. Gambhir, MD, PhD, Stanford, CA (Abstract Co-Author) Board Member, Enlight Biosciences; Board Member, ImaginAb, Inc; Board Member, FUJIFILM Holdings Corporation; Board Member, ClickDiagnostics, Inc; Consultant, FUJIFILM Holdings Corporation; Consultant, Gamma Medica, Inc; Speaker, ImaginAb, Inc; Stock, Enlight Biosciences; Stock options, Enlight Biosciences; Travel support, Gamma Medica, Inc Shreyas S. Vasanawala, MD, PhD, Palo Alto, CA (Abstract Co-Author) Research collaboration, General Electric Company; Consultant, Arterys; Research Grant, Bayer AG; Andrei Iagaru, MD, Stanford, CA (Abstract Co-Author) Research Grant, General Electric Company; Research Grant, Bayer AG PURPOSE We previously reported the pilot evaluation of a simultaneous PET/MRI scanner with TOF capability, as well as the use of combined 18F NaF/18F FDG PET/CT in cancer patients. Here we prospectively compared the combined 18F NaF/18F FDG PET/ MRI against 99mTc-MDP in patients with breast and prostate cancers for the detection of metastatic disease. METHOD AND MATERIALS Fifteen patients referred for 99mTc-MDP bone scans were prospectively enrolled from Oct 14 - Mar 15. The cohort included 7 men with prostate cancer and 8 women with breast cancer, 41 - 85 year-old (average 61 ± 13). 18F NaF (0.7-2.2 mCi, mean: 1.2 mCi) and 18F FDG (3.8-5.2 mCi, mean: 4.2 mCi) were subsequently injected from separate syringes. The PET/MRI was done 6-30 days (average 9.3 ± 3.2) after bone scan. The whole body MRI protocol consisted of T2-weighted, DWI, and contrast-enhanced T1weighted imaging. Lesions detected with each test were tabulated and the results were compared. RESULTS All patients tolerated the PET/MRI exam, and PET image quality was diagnostic despite the marked reduction in the administered dosage of radiopharmaceuticals (80% less for 18F NaF and 67% less for 18F FDG compared to standard protocols). Five patients had no bone metastases identified on either scans. Bone scintigraphy and PET/MRI showed osseous metastases in 9 patients, but more numerous bone findings were noted on PET/MRI than on bone scintigraphy in 3 patients. One patient had negative bone scan, but bone metastases were seen on PET/MRI. Lesions outside the skeleton were identified by PET/MRI in 3 patients. CONCLUSION The combined 18F NaF/18F FDG PET/MRI is superior to 99mTc-MDP scintigraphy for evaluation of skeletal disease extent. Further, it detected extra-skeletal disease that may change the management of these patients, while allowing a significant reduction in radiation exposure from lower dosages of PET radiopharmaceuticals administered. A combination of 18F NaF/18F FDG PET/MRI may provide the most accurate staging of patients with breast and prostate cancers prior to the start of treatment. CLINICAL RELEVANCE/APPLICATION The combined 18F NaF/18F FDG PET/MRI is superior to 99mTc-MDP scintigraphy for evaluation of skeletal disease extent. SSG09-09 In Vivo Assessment of Ovarian Tumor Response to Tyrosine Kinase Inhibitor Pazopanib using Hyperpolarized 13C-Pyruvate MRS and 18F-FDG PET/CT Imaging in a Mouse Model Tuesday, Dec. 1 11:50AM - 12:00PM Location: S504CD Participants Murali Ravoori, Houston, TX (Abstract Co-Author) Nothing to Disclose Sheela Singh, Houston, TX (Abstract Co-Author) Nothing to Disclose Jaehyuk Lee, Houston, TX (Abstract Co-Author) Nothing to Disclose James Bankson, PhD, Houston, TX (Abstract Co-Author) Nothing to Disclose Vikas Kundra, MD, PhD, Houston, TX (Presenter) License agreement, Introgen Therapeutics, Inc PURPOSE Early response measures for ovarian cancer are needed to common targets such as tyrosine kinases. Via effects on signaling within tumor cells or via effects on angiogenesis, such inhibitory drugs have the potential to alter tumor metabolism. 18Fluorodeoxyglucose (18F-FDG) mimics glucose and can be used to evaluate early glycolysis. Hyperpolarization magnetic resonance spectroscopy (MRS) imaging can be used to study pyruvate, which can be produced by glycolysis and other pathways and sits at a decision point for aerobic versus anaerobic metabolism. Our purpose was to assess whether either early or late components of metabolism can serve as indicators of response of ovarian cancer to tyrosine kinase inhibitor (including angiogenesis inhibitor via VEGF receptor inhibition) Pazopanib. METHOD AND MATERIALS Seventeen days after injection of 2 x 106 human ovarian SKOV3 tumors cells into female nude mice, treatment with vehicle or Pazopanib (2.5 mg/mouse po) was initiated. Longitudinal T2-weighted MR, hyperpolarized pyruvate MRS, and 18F-FDG PET/CT imaging were performed pre-treatment as well as 2 days and 2 weeks after treatment. RESULTS Pazopanib was effective in inhibiting ovarian tumor growth compared to control (p<0.05). Significantly higher pyruvate to lactate conversion (lactate/pyruvate+lactate ratio) was found 2 days after treatment with pazopanib compared to pre-therapy (p<0.005, n=8). This was not seen with control or with 18F-FDG PET/CT imaging. CONCLUSION Findings suggest that later metabolic events (pyruvate to lactate conversion) may serve as as an early indicator of response of ovarian cancer to tyrosine kinase (angiogenesis) inhibitor pazopanib in mouse models, even when early glycolytic events do not. CLINICAL RELEVANCE/APPLICATION Hyperpolarized 13C-Pyruvate MRS may serve as an early indicator of response to tyrosine kinase (angiogenesis) inhibitors such as pazopanib in ovarian cancer even when 18F-FDG PET/CT does not. GUS-TUA Genitourinary Tuesday Poster Discussions Tuesday, Dec. 1 12:15PM - 12:45PM Location: GU/UR Community, Learning Center GU AMA PRA Category 1 Credit ™: .50 FDA Discussions may include off-label uses. Participants Antonio C. Westphalen, MD, Mill Valley, CA (Moderator) Nothing to Disclose Sub-Events GU223-SDTUA2 NSsaFe study: An Observational Study on the Incidence of Nephrogenic Systemic Fibrosis in Renal Impaired Patients Following Gadoterate Meglumine Administration Station #2 Participants Jennifer V. Frabizzio, MD, Abington, PA (Presenter) Consultant, Guerbet SA PURPOSE : To determine the incidence of nephrogenic systemic fibrosis (NSF) in patients with renal impairment after administration of gadoterate meglumine (DOTAREM®) and to collect data on the safety profile of gadoterate meglumine in a post-marketing observational study. METHOD AND MATERIALS : Safety data are being collected worldwide for hundreds of patients with moderate to severe renal impairment undergoing contrast-enhanced magnetic resonance with gadoterate meglumine. At inclusion, clinical history, indication for MR imaging and renal function are recorded, and patients are followed up for over 2 years with 3 visits separated by at least 3 months. During follow-up visits, adverse events (AEs) are recorded with particular focus on any symptoms related to NSF. If NSF is suspected then biopsy is performed for confirmation. RESULTS As of February 10, 2015, the safety data of 512 patients (mean age: 69.5 years (range: 21-95); male: 59.8%) were available for review. The mean eGFR was 37.3 ±15.9 ml/min/1.73m2 (range: 4.0-74.2) including 68.4% of moderate, 16.2% of severe, 12.7% of end-stage renal insufficiency and 2.7% of kidney transplanted patients. To date, 288 patients attended the first follow-up visit (between 3 and 12 months after MRI), 176 patients attended the second follow-up visit (between 13 and 21 months after MRI) and 114 patients the third follow-up visit (between 22 and 27 months after MRI). No AEs related to DOTAREM® were reported. Seven patients (1.4%) had serious adverse events due to underlying disease that were not related to gadoterate meglumine. Not a single case of NSF has been observed. CONCLUSION : This interim analysis of the NSsaFe study records no cases of NSF in patients with moderate to severe renal impairment after the administration of gadoterate meglumine. CLINICAL RELEVANCE/APPLICATION A gadolinium agent with no incidence of NSF could allow for patients with renal impairment to obtain constast could provide more accurate diagnosis and potentially eliminate the need to obtaining GFR laboratory values pre MRI. GU224-SDTUA3 Quantitative Enhancement Analysis in Small Renal Mass: Differentiation of Clear Cell Carcinoma from Other Subtypes and Angiomyolipoma with Minimal Fat at Three-phase Multi-detector CT Station #3 Participants See Hyung Kim, Daegu, Korea, Republic Of (Presenter) Nothing to Disclose Jung Hee Hong, Daegu, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose PURPOSE To quantitatively assess whether enhancement characteristics at three-phase MDCT can help differentiate clear cell RCCs from papillary, chromophobe RCCs and AMLs with minimal fat. METHOD AND MATERIALS IRB approved this retrospective study. A total of 409 clear cell, 62 papillary, 41 chromophobe RCCs and 51 AMLs with minimal fat were included. Mean attenuations between clear cell RCC and the other three groups in each phase were compared using t-test. Enhancement values, such as percentage enhancement ratio (PER), enhancement change (EC) and absolute washout ratio (AWR), were calculated and compared using cutoff analysis with optimal threshold level among four groups. RESULTS Mean attenuation of clear cell RCCs was significantly greater than papillary and chromophobe RCCs in corticomedullary and early nephrographic phases, and AMLs with minimal fat in corticomedullary phase. AMLs with minimal fat were significantly great in nonenhanced phase. There were significant differences in PER, EC and AWR of clear cell RCC, compared with those of papillary (148.8 vs. 262.5, P=0.002, 0.581 vs. 1.285, P=0.001, and 37.1 vs. -70.5, P=0.001), chromophobe RCCs (148.8 vs. 169.8, P=0.02, 0.581 vs. 0.751, P=0.02, and 37.1 vs. 28.8, P=0.03) and AMLs with minimal fat (148.8 vs. 194.2, P=0.01, 0.581 vs. 0.981, P=0.02, and 37.1 vs. 13.4, P=0.008). Diagnostic performances to differentiate clear cell RCCs from papillary, chromophobe RCCs and AMLs with minimal fat had accuracies, ranging 80.9% (399/471) to 88.5% (417/471), 70.2% (321/457) to 74.1% (339/457) and 80.6% (371/460) to 85.0% (391/460). CONCLUSION Enhancement values may help differentiate clear cell RCCs from papillary RCCs, chromophobe RCCs and AMLs with minimal fat. CLINICAL RELEVANCE/APPLICATION Enhancement characteristics of three phase MDCT are helpful for differentiating clear cell RCCs from other subtypes and AMLs with minimal fat. GU225-SDTUA4 Clinical Value of Proton (1H-) Magnetic Resonance Spectroscopy (MRS) using Body-phased Array Coil at 3.0 T in Pretreatment Assessment for Cervical Cancer Patients Station #4 Participants Gigin Lin, MD, Guishan, Taiwan (Presenter) Nothing to Disclose Yu-Ting Huang, Guishan, Taiwan (Abstract Co-Author) Nothing to Disclose Koon-Kwan Ng, Guishan, Taiwan (Abstract Co-Author) Nothing to Disclose Yu-Chun Lin, MSC, Taoyuan, Taiwan (Abstract Co-Author) Nothing to Disclose Tzu-Chen Yen, MD, PHD, Taoyuan, Taiwan (Abstract Co-Author) Nothing to Disclose Hung-Hsueh Chou, MD, Taoyuan, Taiwan (Abstract Co-Author) Nothing to Disclose Angel Chao, MD, Taoyuan, Taiwan (Abstract Co-Author) Nothing to Disclose Chiun-Chieh Wang, Guishan, Taiwan (Abstract Co-Author) Nothing to Disclose Chyong-Huey Lai, Guishan, Taiwan (Abstract Co-Author) Nothing to Disclose PURPOSE To determine the clinical value of proton (1H-) magnetic resonance spectroscopy (MRS) using body-phased array coil at 3.0 T, in pretreatment assessment for cervical cancer patients. METHOD AND MATERIALS We prospectively enrolled 52 histology proven cervical cancer patients (age 27-80 years) and 30 age-matched surgical candidates for benign uterine myoma without evidence of cervical cancer. Pretreatment MR study plus MRS and diffusion weighted imaging (DWI) sequences were carried out at a 3.0 T system using body-phased array coil for the pelvis. PRESS localized 1H-MRS was applied to cervical tumor or normal tissue, with resonances analyzed by using the LC-Model algorithm. Cramer-Rao lower bound (CRLB) threshold of 20% was used as quality control. We compared resonances based on: (1) tumor vs normal cervical tissue, (2) histopathology type (squamous vs adenocarcinoma) (3) T stage = IIb (4) nodal metastasis (5) distant metastasis using MannWhitney test. RESULTS Cervical tumor showed a lower 1.3-ppm lipid level (0.30 vs 1.01μM, P < .05), as compared with normal cervical tissue. Squamous cell carcinoma demonstrated lower levels in 1.3-ppm lipid (0.17μM vs 0.59μM, P < .05) and 0.9-ppm lipid (0.04μM vs 0.16μM, P < .05), as compared with adenocarcinoma. Tumor with T stage >= IIb had lower levels in 1.3-ppm lipid (0.15μM vs 0.53μM, P < .05), 0.9-ppm lipid (0.04μM vs 0.15μM, P < .05) and total choline (0.04μM vs 0.16μM, P < .05). Tumors with nodal metastasis contained lower levels of 1.3-ppm lipid (0.16μM vs 0.44μM, P < .05) and glutamine (0.01μM vs 0.02μM, P < .005), whereas tumors with distant metastasis contained a lower level of 1.3-ppm lipid (0.12μM vs 0.50μM, P < .05). However, resonances from cervical tumor were independent to maximal tumor size or ADC value on MRI. CONCLUSION 1H-MRS using body-phased array coil at 3.0 T in cervical cancer patients is useful in differentiating tumor, histopathology type, T stage >= IIb, nodal or distant metastasis, and is independent to maximal tumor size or ADC value on MRI. CLINICAL RELEVANCE/APPLICATION 1H-MRS using body-phased array coil at 3.0 T added additional dimensions for pretreatment assessment in cervical cancer patients. GU226-SDTUA5 Post Ablation MRI Evaluation of the Prostate and Predictors of Local Tumour Recurrence Station #5 Participants Tristan Barrett, MBBS, BSc, Guildford, United Kingdom (Presenter) Nothing to Disclose Masoom A. Haider, MD, Toronto, ON (Abstract Co-Author) Consultant, Bayer AG John Trachtenberg, MD, Toronto, ON (Abstract Co-Author) Nothing to Disclose Sangeet Ghai, MD, Toronto, ON (Abstract Co-Author) Nothing to Disclose PURPOSE To determine the morphologic changes in the prostate gland after focal laser ablation therapy for prostate cancer and to assess the value of different MRI sequences for the detection of recurrent/residual disease METHOD AND MATERIALS Nineteen patients undergoing focal ablation therapy for prostate cancer were followed up clinically and with MRI at 3-7 months post therapy, with findings correlated to subsequent biopsy. The overall gland volume was compared to baseline size and morphological features were assessed on anatomical T2 imaging including signal intensity, atrophy, capsular retraction, and loss of zonal anatomy. Diffusion-weighted imaging was quantitatively assessed using apparent diffusion co-efficient (ADC) maps and dynamic-contrastenhanced (DCE) MRI uptake curves were calculated for treatment regions. RESULTS At follow-up biopsy, 8 patients (42.1%) had no evidence of prostate cancer in the region of the gland treated, and 11 (57.9%) demonstrated recurrent/residual disease. Prostate gland volume reduced in 17/19, with a median decrease of 11.6% and a statistically significant correlation between the size of ablation zone decrease in volume. There was no significant difference in ADC values, nor in any of the T2-weighted imaging signs assessed between the groups. 7/8 patients with no disease demonstrated type I enhancement curves on DCE-MRI, and none had a type III curve. 4/11 patients with recurrent/residual disease demonstrated a type III enhancement curve; 3 of these patients had Gleason 3+4 disease on biopsy and there was a significant correlation between the type of enhancement curve and post-treatment Gleason score. CONCLUSION The prostate gland undergoes expected atrophy following focal ablation therapy. Diffusion-weighted imaging and T2-weighted imaging do not accurately distinguish residual disease. DCE-MRI enhancement curves show promise for differentiating residual disease from fibrosis, making it the optimal sequence for follow-up assessment in this patient cohort. CLINICAL RELEVANCE/APPLICATION Multi-parametric MRI of the prostate and DCE in particular are helpful in evaluating presence of residual disease post focal ablation for PCa and may be used for follow up of pateints to detect recurrence of significant disease, rather than subjecting the patients to repeated biopsies. GU227-SDTUA6 Incidental Ovarian Lesions on CT in Post-menopausal Women with a History of Non-ovarian Malignancy: Can We Tell Benign from Malignant? Station #6 Participants Akshay D. Baheti, MBBS, Seattle, WA (Presenter) Nothing to Disclose Kiran Gangadhar, MD, Seattle, WA (Abstract Co-Author) Nothing to Disclose Daniel S. Hippe, MS, Seattle, WA (Abstract Co-Author) Research Grant, Koninklijke Philips NV; Research Grant, General Electric Company Ryan O'Malley, MD, Seattle, WA (Abstract Co-Author) Nothing to Disclose Carolyn L. Wang, MD, Seattle, WA (Abstract Co-Author) Nothing to Disclose PURPOSE Determine whether the ACR white paper on managing incidental adnexal lesions seen on CT (based on SRU guidelines)can be used in a high-risk population of late postmenopausal women (>55 years)with known non-ovarian cancer and whether CT morphology of the lesions can be used to discriminate benign from malignant METHOD AND MATERIALS IRB and HIPAA compliant retrospective review was performed of 140 patients with 158 adnexal lesions,classified as simple cystic,complex cystic,solid-cystic and solid based on CT morphology and features described in the ACR paper. Lesions were categorized as benign,indeterminate or malignant based on pathology,imaging stability(median f/u 34 months)or response to therapy.Intergroup comparison was done based on patient and lesion features with Fisher's exact test and permutation tests to account for dependence between bilateral lesions in same patient. RESULTS 20/158(13%) malignant, 44/158(28%) indeterminate and 94/158(59%) benign lesions were noted.19/20 malignant lesions were metastases while 1 was indeterminate for colorectal metastasis vs ovarian primary. 0/105 simple cysts,2/27 complex cysts,15/21 solid-cystic and 3/5 solid lesions were malignant.Cysts classified complex due to high HU(>20) without septations or calcifications(16/27) were all benign.Compared to benign lesions, malignant ones were more likely to have a solid component (M:18/20 vs B:4/94,OR=202,p<0.001) rather than purely cystic features.Enhancing components and septae were more common in malignant lesions(p<0.001). Overall, 61/140(44%)patients had metastases.Presence of peritoneal metastases significantly correlated with ovarian involvement by malignancy(OR=30.9,p<0.001). Malignancy in adnexal lesions was significantly associated with primary tumor type(p=0.02),with breast and colorectal cancers most common to metastasize to ovaries(5 each). CONCLUSION Our study supports the ACR recommendations on incidental adnexal lesions even in patients with known non-ovarian neoplasm.Simple adnexal cysts are highly unlikely to be malignant,while lesions that are not simple cystic should be viewed with suspicion.Peritoneal metastases have a significant correlation with ovarian involvement. CLINICAL RELEVANCE/APPLICATION The current ACR white paper on managing incidental adnexal lesions on CT extrapolates US-based criteria.We endorse the same using a high-risk cohort.We also evaluate them further based on CT morphology,primary tumor and metastatic pattern. UR120-EDTUA7 Decoding MR Defecography: A Case-Based Approach Station #7 Participants Guangzu Gao, MD, New Haven, CT (Presenter) Nothing to Disclose Samira Rathnayake, MD, New Haven, CT (Abstract Co-Author) Nothing to Disclose Mike Spektor, MD, New Haven, CT (Abstract Co-Author) Nothing to Disclose Steffen Huber, MD, New Haven, CT (Abstract Co-Author) Nothing to Disclose Jay K. Pahade, MD, New Haven, CT (Abstract Co-Author) Nothing to Disclose Mahan Mathur, MD, New Haven, CT (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Magnestic resonance (MR) defecography can pose a challenge to the uninitiated for a variety of reasons, often related to unfamiliarity with the relevant pelvic anatomy, confusion regarding the parameters used to measure organ descent and/or limited knowledge of the pathologic entities themselves. The purpose of this exhibit is to help the viewer master these concepts, providing the relevant information in a simple, yet comprehensive, quiz-based approach. TABLE OF CONTENTS/OUTLINE Cases will be presented in a quiz format followed by a brief explanation of the answer, highlighting the relevant concepts. We will present a summary slide at the end of all the cases which will provide the relevant information in a tabulated form. The following are the list of cases that will be presented/discussed: Normal anatomy Example of normal images at different phases rest, squeeze, evacuation). Normal parameters (PCL line, H line, M line, anorectal angle) will also be showcased Abnormal entities: Anterior compartment (cystocele, urethral hypermobility)- Middle compartment (uretrovaginal prolapse, enterocele, sigmoidocele, peritoneocele) Posterior comparemtent (anterior and posterior rectocele, rectal intussusceptions, rectal prolapse) Descending perineal syndrome Spastic pelvic floor syndrome (dyssynergic defecation) Summary tables UR185-EDTUA8 Neoplastic and Non-neoplastic Proliferative Diseases of the Perinephric Space Station #8 Participants Morooj Al Subhi, MD, Montreal, QC (Presenter) Nothing to Disclose Maria Tsatoumas, MD, Outremont, QC (Abstract Co-Author) Nothing to Disclose Vipul Bist, Montreal, QC (Abstract Co-Author) Nothing to Disclose Amer Alaref, MD, Montreal, QC (Abstract Co-Author) Nothing to Disclose Benoit P. Gallix, MD, PhD, Montpellier, France (Abstract Co-Author) Nothing to Disclose Caroline Reinhold, MD, MSc, Montreal, QC (Abstract Co-Author) Consultant, GlaxoSmithKline plc TEACHING POINTS 1. To review the cross-sectional anatomy of the perirenal space. 2. To describe the interlacing network through which various pathologic processes infiltrate and spread within the perirenal space.3. To illustrate the specific imaging findings of neoplastic and non-neoplastic processes of the perirenal space. TABLE OF CONTENTS/OUTLINE OUTLINE• Cross-sectional anatomy of perirenal space Anatomic borders Pathways of spread via interlacing network• Neoplastic conditionso Lymphomao Plasma-cell neoplasmo Metastaseso Primary renal cell carcinomao Retroperitoneal malignancies• Nonneoplastic conditionso Fluid (hematoma, urinoma, abcess, cysts, lymphangioma)o Inflammatory (pancreatitis, xanthogranulomatous pyelonephritis)o Proliferative (retroperitoneal fibrosis, amyloid, extramedullary hematopoisis, rosai-dorfman and erdheim-chester disease)CONCLUSION1. Cross-sectional imaging is crucial in diagnosing pathologic processes of the perirenal space. 2. Although considerable overlap of the imaging findings exist, specific imaging features in combination with clinical history, can help suggest the correct diagnosis. 3. Imaging-guided percutaneous biopsy can be performed to establish the diagnosis in indeterminate cases allowing for accurate patient management. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Caroline Reinhold, MD, MSc - 2013 Honored Educator Caroline Reinhold, MD, MSc - 2014 Honored Educator GUS-TUB Genitourinary Tuesday Poster Discussions Tuesday, Dec. 1 12:45PM - 1:15PM Location: GU/UR Community, Learning Center GU AMA PRA Category 1 Credit ™: .50 FDA Discussions may include off-label uses. Participants Antonio C. Westphalen, MD, Mill Valley, CA (Moderator) Nothing to Disclose Sub-Events GU228-SDTUB1 Incidence of Contrast-Induced Nephropathy, Dialysis, and Renal Graft Loss after Transplant Renal Angiography Station #1 Participants Ghaneh Fananapazir, MD, Sacramento, CA (Presenter) Nothing to Disclose Behrad Golshani, MD, Sacramento, CA (Abstract Co-Author) Nothing to Disclose Michael T. Corwin, MD, Sacramento, CA (Abstract Co-Author) Nothing to Disclose Sima Naderi, MD, Sacramento, CA (Abstract Co-Author) Nothing to Disclose Chris Bent, MD, SACRAMENTO, CA (Abstract Co-Author) Nothing to Disclose Ramit Lamba, MD, Sacramento, CA (Abstract Co-Author) Nothing to Disclose PURPOSE To report the incidence of contrast-induced nephropathy (CIN), dialysis, and renal graft loss attributable to direct intraarterial injection of the transplanted renal artery in renal allograft recipients. METHOD AND MATERIALS Our institutional review board approved this retrospective health insurance portability and accountability act complaint study. Onehundred patients underwent conventional transplant renal arteriography. Serum creatinine levels were recorded at baseline, prior to the arteriogram, and within the 24-72 hours after the angiogram. CIN was assessed on those patients who had a serum creatinine within the 24-72 hour window. CIN was defined as an increase in serum creatinine of > 0.5 mg/dL and/or 1.5 times the prearteriogram creatinine. In those patients with CIN, as well as those who did not meet the criteria for assessing the creatinine in the 24-72 hour window, clinical outcomes of need for dialysis and renal allograft loss 30 days after angiography were evaluated. RESULTS Thirty-seven patients met the criteria for assessing for CIN, of which three patients (8%) demonstrated CIN after arteriogram. None of the patients with CIN or those who did not meet the criteria to assess for CIN required dialysis or had graft failure at 30 days. CONCLUSION Even in patients with a single renal allograft, the risk of CIN appears to be low, with no subsequent need for dialysis or graft loss. CLINICAL RELEVANCE/APPLICATION Caution regarding administration of iodinated contrast to renal transplant recipients may have been previously overstated and administration may be performed safely. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Ramit Lamba, MD - 2014 Honored Educator GU252-SDTUB3 70 kV renal CT Angiography with 3rd Generation Dual-source CT for the Preoperative Assessment of Robotic-assisted Laparoscopic Partial Nephrectomy: Preliminary Study Station #3 Participants Satoru Takahashi, MD, Kobe, Japan (Presenter) Nothing to Disclose Yoshiko Ueno, MD, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Yuko Suenaga, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Utaru Tanaka, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Noriyuki Negi, RT, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Kiyosumi Kagawa, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Kazuro Sugimura, MD, PhD, Kobe, Japan (Abstract Co-Author) Research Grant, Toshiba Corporation Research Grant, Koninklijke Philips NV Research Grant, Bayer AG Research Grant, Eisai Co, Ltd Research Grant, DAIICHI SANKYO Group PURPOSE Robotic partial nephrectomy can minimalize the volume of ischemia during procedure with super-selective renal artery clumping at Robotic partial nephrectomy can minimalize the volume of ischemia during procedure with super-selective renal artery clumping at the distal arterial branches. Although meticulous evaluations of intra-renal arterial are warranted, the evaluation is challenging on current renal CT angiography (CTA) because of limited contrast between the intra-renal arterial branches and the renal cortex. Since low-energy CT radically improve contrast enhancement in CTA, we evaluated the ability of 70 kV renal CTA with 3rd generation dual-source CT for depicting intra-renal arterial branches. METHOD AND MATERIALS We retrospectively evaluated 23 patients who underwent renal CTA for suspicious renal neoplasm on 192-slice 3rd generation dualsource CT scanner at 70 kV. All patients were given 510 mgI/Kg of contrast media (CM) with an injection rate of 5 mL/s and CTA was acquired using bolus-tracking technique. CT values of the abdominal aorta, the main trunk of the renal artery, and the renal cortex were measured. The most distal artery detected on 0.6 mm slice images was recorded for each patient. The images were evaluated using semi-automatic vessel tracking between the main trunk of the renal artery and the proximal interlobar artery. Success rate of vessel tracking was recorded for each patient. These results were compared with historical control scanned in conventional multi-slice CT at 120 kV. RESULTS CT values of the abdominal aorta, renal artery, and the renal cortex at 70 kV (793, 737, 326 HU respectively) were statistically greater than those at 120 kV (330, 321, 154 HU; p<.0001). Although CT value differences between the artery and the renal cortex were greater at 70 kV protocol, CT value ratio were not significantly different. 70 kV protocol could demonstrate the distal interlobar artery in most of cases (86%), while the proximal part of interlobar artery were barely depicted at 120 kV. Consequently, success rates of semi-automatic vessel tracking at 70 kV were greater than those at 120 kV (89 % vs. 30 %). CONCLUSION 70 kV renal CTA with 3rd generation dual-source CT could successfully demonstrate the intra-renal branches of the renal artery, leading to easy and reliable assessment of the tumor-supplying arterial branches. CLINICAL RELEVANCE/APPLICATION 70 kV renal CTA with 3rd generation dual-source CT is of great use for the preoperative assessment of robotic-assisted partial nephrectomy by demonstrating the tumor supplying arteries. GU231-SDTUB4 Diagnostic Accuracy of MRI and Diffusion-weighted Magnetic Resonance Imaging in Predicting Response to Neo-adjuvant Chemo-radiotherapy (nCRT) in Patients with Locally Advanced Cervical Carcinoma (LACC): Correlation with Pathological Response Station #4 Participants Ersilia Devicienti, Rome, Italy (Presenter) Nothing to Disclose Anna Lia Valentini, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Benedetta Gui, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Elena Rodolfino, Rome, Italy (Abstract Co-Author) Nothing to Disclose Maura Micco, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Lorenzo Bonomo, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose PURPOSE To assess diagnostic accuracy of MRI and diffusion-weighted magnetic resonance imaging (DWI) in predicting response to neoadjuvant chemo-radiotherapy (nCRT) in patients with locally advanced cervical carcinoma (LACC) and subsequently treated with radical hysterectomy, in correlation with pathological response METHOD AND MATERIALS 70 women (mean age: 52.6 years) with histologically proven cervical cancer and stage FIGO>IB bulky underwent 1.5 T conventional MRI and DWI, before (pre-nCRT MRI) and at the end of nCRT (post-nCRT MRI). Tumor volume and mADCs (calculated at b=0 and 800 s/mm2) were measured at each assessment in order to assess imaging-response to treatment. Radical hysterectomy was performed 4 weeks after post-nCRT MRI. Treatment response was classified, according to histopathological results, as complete response (CR), microscopical residual disease (microRD<3mm) and macroscopical residual disease (macroRD>3mm). Sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of MRI were calculated at first grouping histopathology microRD as CR and also grouping histopathology microRD as macroRD RESULTS According to histopathology, 33/70 patients showed CR, 21/70 had microRD and 16/70 showed macroRD. At MRI 46 patients showed complete response and 24 patients showed partial response to nCRT. Diagnostic accuracy, sensitivity, specificity, PPV and NPV of MRI were respectively 82,86%, 87,50 %, 81,48%, 58,33 % and 95,65% when grouping histopathology microRD with CR and 70,00%, 54,05%, 87,88%, 83,33% and 63,04% when grouping histopathology microRD with macroRD CONCLUSION MRI and DWI imaging showed high diagnostic accuracy and in particular high VPN in evaluation of tumor response to nCRT in patients with LACC. However its diagnostic accuracy is limited in patients with histopathological microRD (< 3mm) because of intrinsic limit of MRI in spatial resolution CLINICAL RELEVANCE/APPLICATION In this study, in which we enrolled a large number of patients with LACC proven by pathological results, MRI shows high diagnostic accuracy in the evaluation of tumor response to nCRT and it is a reliable tool for surgery modulation GU232-SDTUB5 Diagnostic Accuracy of PI-RADS v2: Validation with Targeted In-Bore MRI-Guided Prostate Biopsy Station #5 Participants Ely R. Felker, MD, Los Angeles, CA (Presenter) Nothing to Disclose Stephanie A. Lee-Felker, MD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Daniel J. Margolis, MD, Los Angeles, CA (Abstract Co-Author) Research Grant, Siemens AG David S. Lu, MD, Los Angeles, CA (Abstract Co-Author) Consultant, Medtronic, Inc Speaker, Medtronic, Inc Consultant, Johnson & Johnson Research Grant, Johnson & Johnson Consultant, Bayer AG Research Grant, Bayer AG Speaker, Bayer AG Robert A. Princenthal, MD, Thousand Oaks, CA (Abstract Co-Author) Employee, Koninklijke Philips Electronics NV John F. Feller, MD, Indian Wells, CA (Abstract Co-Author) Consultant, Koninklijke Philips NV Consultant, Visualase, Inc Martin I. Cohen, MD, Thousand Oaks, CA (Abstract Co-Author) Nothing to Disclose Bernadette M. Greenwood, BS, RT, Indian Wells, CA (Abstract Co-Author) Nothing to Disclose Hyung J. Kim, PhD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Steven S. Raman, MD, Santa Monica, CA (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate the diagnostic performance of the recently proposed PI-RADS v2 scoring system, using in-bore magnetic resonance (MR) guided biopsy (MRGB), and to determine the correlation between PI-RADS v2 score and biopsy Gleason score (GS). METHOD AND MATERIALS IRB-approved, HIPAA-compliant, retrospective study of 153 consecutive patients (102 men with elevated PSA and suspected PCa, and 51 men on active surveillance; mean age 65.6 +/- 8.5 years, median PSA 7.8 ng/mL) with 191 lesions referred for mpMRI (T2WI, DWI, DCE) at 3T followed by MRGB.Targets were originally selected by one of four experienced genitourinary radiologists and then re-scored using PI-RADS v2 criteria by a fifth radiologist who was blinded to clinical information and biopsy histology. Test characteristics, including sensitivity and specificity, were calculated. Clinically significant disease (CSD) was defined as GS 7 or higher. PI-RADS v2 scores were compared among CSD, clinically insignificant PCa, and benign targets. Spearman Rank test was used to assess correlation between PI-RADS v2 score and biopsy GS. RESULTS Biopsies were clinically significant PCa, insignificant PCa and benign in 63 (33%), 37 (19%) and 91 (48%) patients, respectively. CSD had significantly higher mean PI-RADS v2 score (4.49 +/- 0.56) than insignificant PCa (3.97 +/- 0.79) and benign targets (2.96 +/- 0.73) (p < 0.0001). There was a positive correlation between PI-RADS v2 score and GS (r = 0.64, p < 0.0001). Sensitivity, specificity, accuracy, PPV, and NPV of PI-RADS 5 for CSD were: 52%, 93%, 80%, 79%, and 80%; of PI-RADS 4 or higher for PCa were: 90%, 75%, 83%, 80%, and 87%. The NPVs of PI-RADS < 4 for PCa and CSD were 88% and 97%, respectively. CONCLUSION PI-RADS v2 performs well as a predictor of MRGB outcome and has moderate to good correlation with biopsy GS. CLINICAL RELEVANCE/APPLICATION MRGB is high-yield for detection of CSD in patients with PI-RADS v2 4 and 5 targets.The high NPV of PI-RADS v2 < 4 for CSD suggests that monitoring of these lesions, rather than immediate targeted biopsy, may be a consideration for management. GU233-SDTUB6 Evaluation for Reliability and Validity of Newly Developed MRI-based Radiological Scoring System for Invasive Placenta Previa Station #6 Participants Yoshiko Ueno, MD, Kobe, Japan (Presenter) Nothing to Disclose Tetsuo Maeda, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Kazuhiro Kitajima, MD, Nishinomiya, Japan (Abstract Co-Author) Nothing to Disclose Satoru Takahashi, MD, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Utaru Tanaka, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Yuko Suenaga, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Kazuro Sugimura, MD, PhD, Kobe, Japan (Abstract Co-Author) Research Grant, Toshiba Corporation Research Grant, Koninklijke Philips NV Research Grant, Bayer AG Research Grant, Eisai Co, Ltd Research Grant, DAIICHI SANKYO Group PURPOSE To examine the reliability and validity for a newly developed MRI-based radiological scoring system for invasive placenta previa METHOD AND MATERIALS This study was based on the retrospective review of prenatal MR images of 70 patients (median age: 35 years) who underwent MR examination at 1.5 T for the screening of invasive placenta previa. Eighteen out of 70 patients were pathologically diagnosed with invasive placenta previa. MR imaging included axial, coronal and sagittal T2-weighted half-Fourier single-shot turbo spin echo sequence and sagittal T1-weighted gradient echo sequence. Cumulative radiological score (CRS) was defined as a sum of Likert 5point agree/disagree scale for six MR features: T2 dark band, intraplacental abnormal vascularity, uterine bulging, heterogeneous placenta, myometrial thinning and placental protrusion sign. Two expert radiologists (reader A and B) and two inexperienced residents (reader C and D) who were blinded to the patient's outcome independently calculated their CRS (range 5-30). The interrater reliability of the CRS was assessed by intraclass correlation coefficient (ICC) measurement. The correlation between the CRS and invasive placenta previa was assessed by logistic regression analysis. For evaluation of the diagnostic performance of the CRS for invasive placenta previa, the receiver operating characteristic (ROC) analysis was performed. RESULTS The inter-rater reliability was excellent for the expert radiologists (ICC: 0.85), fair-to-good among all four readers (ICC: 0.72) and the inexperienced residents (ICC: 0.66). In logistic regression analysis, there was a significant correlation between the CRS and invasive placenta previa for all readers (R2, A: 0.57, B: 0.61, C: 0.45, D: 0.55, p<0.05). ROC analysis showed the cut off value was 17 (Sensitivity: 88.9%, Specificity: 92.3%, Accuracy: 91.4%; for reader A, Sensitivity: 83.3%, Specificity: 92.3%, Accuracy: 90.0%; for reader B, Sensitivity: 83.3%, Specificity: 92.3%, Accuracy: 90.0%; for reader C, Sensitivity: 50.0%, Specificity: 98.0%, Accuracy: 85.7%; for reader D). CONCLUSION We have developed a new MRI-based radiological scoring system that demonstrates excellent or fair-to-good inter-rater reliability, significant association, and high diagnostic performance with invasive placenta previa. CLINICAL RELEVANCE/APPLICATION This new MRI-based radiological scoring system is suitable for the diagnosis of invasive placenta previa. UR124-EDTUB7 Hypovascular Focal Lesions of the Kidney: Imaging Spectrum with CT, CEUS, MR and Pathology Correlation Station #7 Participants Javier L. Moreno Negrete, MD, Barcelona, Spain (Presenter) Nothing to Disclose Blanca Pano Brufau, MD, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose Laura Herrero, MD, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose Rafael Salvador Izquierdo, MD, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose Carmen Sebastia Cerqueda, MD, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose Carlos Nicolau, MD, Barcelona, Spain (Abstract Co-Author) Nothing to Disclose TEACHING POINTS -Recognize the multiple differentials of a hypovascular renal focal lesion, point out the imaging features of the most frequent etiologies and review the diagnostic keys of the least frequent causes.-Review the Bosniak classification (with particular emphasis in CEUS and CT), the management of renal cysts and the correlation between the different imaging techniques.-Propose a diagnostic approach for hypovascular renal lesions. TABLE OF CONTENTS/OUTLINE Introduction Introduction. CT, MR and CEUS protocols and technical issues. Avascular (Cystic) lesions. Review of Bosniak's Classification by CT. Evaluation of CEUS and MR for Cyst Classification. Benign (Bosniak I-II) Indeterminate (Bosniak IIF) Malignant (Bosniak III-IV) Hypovascular lesions. Benign. Infections, vascular causes, fatty AMLs, granulomatous diseases (Sarcoid) Malignant UR002-EBTUB Top Ten Pearls and Pitfalls of Magnetic Resonance Urography (MRU) Hardcopy Backboard Participants Marc Dilauro, MD, MSc, Ottawa, ON (Abstract Co-Author) Nothing to Disclose Nicola Schieda, MD, Ottawa, ON (Presenter) Nothing to Disclose Najla Fasih, MBBS, Ottawa, ON (Abstract Co-Author) Nothing to Disclose Krishna Prasad Shanbhogue, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Trevor A. Flood, MD, FRCPC, Ottawa, ON (Abstract Co-Author) Nothing to Disclose Evan S. Siegelman, MD, Philadelphia, PA (Abstract Co-Author) Consultant, BioClinica, Inc; Consultant, ICON plc; Consultant, ACR Image Metrix TEACHING POINTS 1. Understand how to design and implement a comprehensive MRU protocol 2. Appreciate common technical pitfalls and how to detect and avoid them 3. Develop an approach to the diagnosis of urothelial pathologies with MRU and understand common interpretive pitfalls TABLE OF CONTENTS/OUTLINE Technical Pitfalls/Pearls1. Insufficient distention mimics/obscures pathology; Saline/Furosemide improves distention 2. Peristalsis mimics strictures; Thick-slab heavily T2W TSE dynamic sequences capture peristalsis 3. TSE flow artifact mimics filling defects; Acquire orthogonal TSE and balanced SSFP 4. T2* effects overwhelm T1 shortening; Dilute gadolinium concentration or use Gadoxetic acid Interpretive Pitfalls/Pearls1. Hemorrhage may demonstrate restricted diffusion; Do not rely solely on DWI for diagnosis2. Not all hilar masses are urothelial cell carcinoma (UCC); Hilar RCC mimics UCC 3. Infiltrative lesions are not always UCC; Other malignancies (e.g. lymphoma) and benign (e.g. pyelonephritis, contusion) causes should be considered4. Not all bladder wall thickening is malignant; Benign etiologies preserve the bladder wall layers5. Not all venous tumor thrombus is from RCC; UCC rarely causes venous thrombosis6. Satisfaction of search is critical in MRU; UCC often demonstrates multifocality Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Evan S. Siegelman, MD - 2013 Honored Educator Krishna Prasad Shanbhogue, MD - 2012 Honored Educator Krishna Prasad Shanbhogue, MD - 2013 Honored Educator MSCC33 Case-based Review of Nuclear Medicine: PET/CT Workshop-Cancers of the Abdomen and Pelvis (In Conjunction with SNMMI) (An Interactive Session) Tuesday, Dec. 1 1:30PM - 3:00PM Location: S406A GI GU CT NM AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Janis P. O'Malley, MD, Birmingham, AL (Director) Nothing to Disclose Ciaran J. Johnston, MD, Dublin, Ireland (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Identify the utility of PET CT in staging a wide variety of primary and recurrent GI, GU and gynecological cancers. 2) Differentiate patterns of physiological FDG uptake from pathologic processes. 3) Expalin the importance of CT correlation for selected cancer subgroups. 4) Describe the role of PET CT in assessing patient response to radiation therapy and chemotherapy, including early assessment and PET influenced treatment strategies. SSJ10 Genitourinary (Prostate Intervention) Tuesday, Dec. 1 3:00PM - 4:00PM Location: E353C GU IR MR US AMA PRA Category 1 Credit ™: 1.00 ARRT Category A+ Credit: 1.00 FDA Discussions may include off-label uses. Participants Aytekin Oto, MD, Chicago, IL (Moderator) Research Grant, Koninklijke Philips NV; ; ; Temel Tirkes, MD, Indianapolis, IN (Moderator) Nothing to Disclose Sub-Events SSJ10-01 MR-guided In-bore versus MRI/Ultrasound Fusion Plus TRUS-guided Prostate Biopsy: A Prospective Randomized Trial in Patients with Prior Negative Biopsies Tuesday, Dec. 1 3:00PM - 3:10PM Location: E353C Awards Trainee Research Prize - Resident Participants Lars Schimmoeller, MD, Duesseldorf, Germany (Presenter) Nothing to Disclose Michael Quentin, MD, Dusseldorf, Germany (Abstract Co-Author) Nothing to Disclose Christian Arsov, MD, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose Dirk Blondin, MD, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose Robert Rabenalt, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose Gerald Antoch, MD, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose Andreas Hiester, Dusseldorf, Germany (Abstract Co-Author) Nothing to Disclose Erhard Godehardt, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose Helmut Erich Gabbert, D-40225 Dusseldorf, Germany (Abstract Co-Author) Nothing to Disclose Peter Albers, MD, PhD, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose PURPOSE This study prospectively compares the PCa detection rate (PCa-DR) of MR-guided in-bore biopsy (IB-GB) alone and MRI/ultrasound fusion-guided biopsy combined with a systematic TRUS-GB (FUS+TRUS-GB) in patients with at least one negative TRUS-GB and PSA level ≥4ng/ml. METHOD AND MATERIALS 253 patients were included in this study. After multiparametric prostate MRI (T2WI, DWI, DCE-MRI) at 3T patients with any PIRADS sum score ≥10 were prospectively randomized to IB-GB or FUS+TRUS-GB. Analysis of detection rates for PCa and significant PCa (Gleason score ≥7), highest Gleason score, number of biopsy cores to detect one (significant) PCa, positivity rate of biopsy cores, and tumor involvement per biopsy core were performed. RESULTS 210 patients met all study requirements and were prospectively randomized, 106 patients receiving IB-GB and 104 patients FUS+TRUS-GB (age 65.3±7.1 vs. 66.7±6.8 years; median PSA 10.0 vs. 10.8 ng/ml, IQR 7.8-14.9 vs. 7.4-15.5 ng/ml). Mean number of cores was 5.61±0.80 vs. 17.38±1.17; p<0.001. PCa-DR for IB-GB was 36.8% (29.2% for significant PCa) and for FUS+TRUS-GB 39.4% (31.7%); p=0.776 and p=0.765. Mean highest Gleason score of 7.24±0.96 vs. 7.46±1.01; p=0.233. Positivity rate per biopsy core was 20.7% (123/595) vs. 11.6% (210/1,808); p<0.001. Number of biopsy cores needed to detect one PCa or one significant PCa was 15.3 vs. 44.1 and 19.2 vs. 54.8. CONCLUSION The combined biopsy approach did not significantly improve the overall PCa-DR compared to targeted IB-GB alone, but required significantly more cores. A prospective comparison of MR-targeted biopsy alone to systematic TRUS-GB is justified. CLINICAL RELEVANCE/APPLICATION We did not observe a difference between IB-GB and FUS+TRUS-GB to detect PCa. SSJ10-02 Accuracy of Targeted Prostate Biopsy Using MR-ultrasound Fusion to Guide Biopsies Directed to Focal Lesions Suspicious for Malignancy: A Retrospective Study of 286 Patients Tuesday, Dec. 1 3:10PM - 3:20PM Location: E353C Participants Guilherme C. Mariotti, MD, Jundiai, Brazil (Presenter) Nothing to Disclose Tatiana Martins, MD, Belo Horizonte, Brazil (Abstract Co-Author) Nothing to Disclose Marcos R. Queiroz, MD, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose Thais Mussi, MD, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose Rodrigo Gobbo, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose Ronaldo H. Baroni, MD, Sao Paulo, Brazil (Abstract Co-Author) Nothing to Disclose PURPOSE Demonstrate an increase in the accuracy of targeted prostate biopsy using MR-ultrasound fusion to guide biopsies directed to focal Demonstrate an increase in the accuracy of targeted prostate biopsy using MR-ultrasound fusion to guide biopsies directed to focal lesions suspicious for malignancy in a retrospective study of 286 patients. METHOD AND MATERIALS A single-institutional, IRB approved retrospective analysis of 286 patients in our database, which underwent targeted prostate biopsies using MR-ultrasound fusion from August 2013 to January 2015.We included all patients with suspected prostatic cancer based on clinical or laboratory findings (positive digital rectal examination or high PSA) submitted to multiparametric MRI and US-MRI fusion prostate biopsy.We excluded 7 patients with MRI-biopsy interval >= 6 months, 17 patients that underwent biopsy for staging of known cancer or active surveillance and 1 patient for whom clinical data was unavailable. RESULTS A total of 261 patients were included. Of these, 45 patients (17%) underwent previous negative transrectal US-guided biopsies. Table 1 summarizes demographic data of our casuistic.Pre-procedure MRI followed a Likert scale for suspition: Likert 1: 1 patient (0,4%); Likert 2: 18 patients (6,9%); Likert 3: 100 patients (38,3%); Likert 4: 75 patients (28,7%); Likert 5: 67 patients (25,7%).Overall positivity of the biopsies for tumors was 59% (154 cases), with 79% (123 cases) significant cancer (Gleason>=7), 19% (30 cases) non-significant cancer (Gleason 6) and 1 case of STUMP. Analyzing only the Likert 4 and 5 cases, in a total of 142 cases, the overall positivity was 76% (108 cases), with 90% (96 cases) significant cancer (Gleason>=7), 10% (11 cases) nonsignificant cancer (Gleason 6) and 1 leiomyoma. In our institution, the positivity of US-guided random biopsies, in a large sample of other patients in the same period (331 patients), was around 52%. CONCLUSION Our study demonstrates a significant improvement in the performance of prostate biopsy with US- MRI fusion compared to random US-guided biopsies, with potential clinical impact. CLINICAL RELEVANCE/APPLICATION Random prostate biopsies performed on a sextant-basis have a high incidence of false-negative results, and often diagnose microfocal lesions with low clinical significance. Targeted prostate biopsies using MR-ultrasound fusion have shown to detect clinically significant lesions and increase the accuracy of the procedure, with better clinical outcomes. SSJ10-03 Targeted MR-guided Prostate Biopsy: Are Two Biopsy Cores per MRI Lesion Required? Tuesday, Dec. 1 3:20PM - 3:30PM Location: E353C Participants Lars Schimmoeller, MD, Duesseldorf, Germany (Presenter) Nothing to Disclose Michael Quentin, MD, Dusseldorf, Germany (Abstract Co-Author) Nothing to Disclose Christian Arsov, MD, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose Frederic Dietzel, Dusseldorf, Germany (Abstract Co-Author) Nothing to Disclose Dirk Blondin, MD, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose Gerald Antoch, MD, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose Andreas Hiester, Dusseldorf, Germany (Abstract Co-Author) Nothing to Disclose Robert Rabenalt, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose Peter Albers, MD, PhD, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose PURPOSE This study evaluates the efficiency and potential benefit of taking two biopsy cores per MRI lesion when performing targeted MRguided prostate biopsy. METHOD AND MATERIALS 1545 biopsy cores of 774 intraprostatic lesions (two cores per lesion) in 290 patients (66.2±7.8 years; median PSA 8.2 ng/ml; IQR 6.0-12.0 ng/ml) were retrospectively evaluated regarding PCa detection, Gleason score, and tumor infiltration of the first (FBC) compared to the second biopsy core (SBC). All patients received previously a multiparametric (mp)-MRI (T2WI, DWI, DCE) of the prostate at 3T and all lesions were histologically verified by MR-guided in-bore biopsy. RESULTS 491 biopsy cores were prostate cancer (PCa) positive, 239 of 774 (30.9%) FBC and 252 of 771 (32.7%) SBC (p=0.446). 61 FBC vs. 78 SBC detected significant PCa with a Gleason score ≥4+3=7 (25.5% vs. 31.0%; p=0.125). 687 SBC (89.1%) showed no histologic difference to the FBC. 74 SBC resulted in a higher tumor involvement per core when detecting the same Gleason sore (38.1%). In total 29.9% of the PCa lesions were Gleason-upgraded by SBC. 40 SBC detected PCA by negative FBC (5.2%). 43 SBC resulted in a Gleason upgrade (5.6%). 20 SBC showed a Gleason upgrade from a Gleason score 3+3=6 to ≥3+4=7 (2.6%) and 4 SBC to a Gleason score ≥4+3=7 (0.5%). 14 SBC showed a Gleason upgrade from 3+4=7 to ≥4+3=7 (1.8%). CONCLUSION The benefit of a second targeted biopsy core per suspicious MRI lesion is likely minor, especially regarding a significant Gleason upgrade. Therefore a further reduction of biopsy cores is feasible when performing a targeted MR-guided in-bore prostate biopsy. CLINICAL RELEVANCE/APPLICATION Provided a correct biopsy position was documented a second biopsy core per MRI lesion may be omitted for targeted MR-guided inbore biopsy. SSJ10-04 Prostate Cancer Aggressiveness: Correlation Between Multiparametric MRI and Molecular Stagging Using the CCP Score (Prolaris™ test) Tuesday, Dec. 1 3:30PM - 3:40PM Location: E353C Participants Raphaele M. Renard-Penna, Paris, France (Presenter) Nothing to Disclose Geraldine Cancel-Tassin, Paris, France (Abstract Co-Author) Nothing to Disclose Eva M. Comperat, MD, Paris, France (Abstract Co-Author) Nothing to Disclose Justine Varinot, Paris, France (Abstract Co-Author) Nothing to Disclose Pierre Mozer, MD, PhD, Paris, France (Abstract Co-Author) Nothing to Disclose Morgan Roupret, Paris, France (Abstract Co-Author) Nothing to Disclose Marc O. Bitker, Paris, France (Abstract Co-Author) Nothing to Disclose Olivier Lucidarme, MD, Paris, France (Abstract Co-Author) Consultant, Bracco Group Consultant, F. Hoffmann-La Roche Ltd Consultant, Boehringer Ingelheim GmbH Olivier Cussenot, Paris, France (Abstract Co-Author) Nothing to Disclose PURPOSE To correlate the ESUR-PI-RADS components as prognostic imaging biomarkers in localized prostate cancer to the Gleason score and the molecular CCP score (Prolaris™) . METHOD AND MATERIALS 107 patients who had a multiparametric (mp) MRI before (RP) were selected. The largest lesion (index lesion) was measured on T2MRI (Fig 1A) and ADC map and was classified with the ESUR-PI-RADS scoring system. A region of interest (ROI) was drown in the center of each target, on the ADC map . A single ADC ROI was correlated to histologically index proven lesion. The index lesions pointed out by mp MRI were matched on RP specimens and were run in Myriad's Research Laboratory in accordance with the Prolaris™ protocol in order to perform CCP score RESULTS For each index lesion the Pearson's correlations between, pretherapeutic CAPRA score, compoments of the ESUR-PIRADS score, including the maximal diameter (Tmax) and the topography of the index tumor were compared with the histo-pathological observations on the RP specimen.ESUR-PI RADS score and its components were tested with logistic regression model in oreder to assess their predictive value for Gleason's grade 4, CCP score value on the index lesion.On one hand, significant negative correlation was found between mean ADCs and diameter of the index lesion with Gleason's grade 4 ( p=0.0078). The logistic regression model including Tmax (over 10mm) and ADC (under 800) predict with confidence Gleason'grade 4 in the index lesion (Fig 3). On the other hand, The Tmax or ADC size of the index lesion, remains unable to point out the aggressiveness of 7 tumours defined by CCP score. Among those, six were Gleason 6 (3+3) with a median Tmax of 8mm, and one of 8 mm was Gleason 7(3+4) CONCLUSION By mapping image features to gene expression data we were able to show that diffusion imaging and tumor size offer a potential for in vivo non invasive assessment of prognostic cancer aggressiveness.However CCP score related to high risk of lethal cancer did not, completely match with the mpMRI tumour map and Gleason score in 7% of patients. These results previosuly suggested by large scale genomic analysis suggest that the further management of early stages PCa could strongly beneficed of targeted biopsy with moelcular analysis CLINICAL RELEVANCE/APPLICATION This radio genomic correlation suggest that management of PCa could strongly benefit from both MRI targeted biopsy and subsequent molecular analysis. SSJ10-05 Multi-parametric MRI (MpMRI) Findings after Focal Laser Ablation for Prostate Cancer (Pca) Tuesday, Dec. 1 3:40PM - 3:50PM Location: E353C Participants Aytekin Oto, MD, Chicago, IL (Presenter) Research Grant, Koninklijke Philips NV; ; ; Shiyang Wang, PhD, Chicago, IL (Abstract Co-Author) Nothing to Disclose Xiaobing Fan, PhD, Chicago, IL (Abstract Co-Author) Nothing to Disclose Stephen Thomas, MD, Chicago, IL (Abstract Co-Author) Nothing to Disclose Ambereen Yousuf, MBBS, Chicago, IL (Abstract Co-Author) Nothing to Disclose Gregory S. Karczmar, PhD, Chicago, IL (Abstract Co-Author) Nothing to Disclose Tatjana Antic, Chicago, IL (Abstract Co-Author) Nothing to Disclose Scott Eggener, Chicago, IL (Abstract Co-Author) Research Grant, Visualase, Inc Speakers Bureau, Johnson & Johnson PURPOSE To describe the quantitative and qualitative MpMRI findings following focal laser ablation of Pca METHOD AND MATERIALS 27 patients with 36 cancer foci on baseline MRI, underwent MRI guided focal laser ablation were prospectively followed with, immediate (36/36 sites), 3-month (36/36 sites) and 12-month (24/36 sites) post-procedure 3T MpMRI and TRUS guided biopsy at 12 months. Qualitative and quantitative MpMRI findings including size and appearance of ablation defect, ADC, K(trans) and Ve were recorded and compared between the follow-up studies and between patients with and without residual disease. RESULTS 36 cancer foci were ablated in 27 patients. Ablation defect was clearly visible on 36/36, 11/36 and 0/24 sites on the immediate, 3month and 12-month post-contrast DCE-MR images respectively, with a gradual decrease in size on 3 month MRI even in visible cases. Focal atrophy/scarring was noted at the site of ablation in 10/36 and 20/24 sites on 3-month and 12-month MRI. Mean K(trans) values were significantly lower on post-procedure MRI`s compared to baseline values (p<0.05). Mean ADC values on 3month MRI were significantly higher than the baseline ADC values (p<0.05). There was not significant change in Ve (p>0.05). In 2/4 cases with residual cancer, focal early enhancement was noted on 12-month DCE-MR Images. Other than 1 case with residual cancer, no focal lesion (other than diffuse and ill-defined changes secondary to ablation) was noted at the ablation site on 12month T2 and ADC images. CONCLUSION Immediate post-contrast MR images are helpful for identification of the ablation defect. Quantitative MR parameters such as ADC and K (trans) change significantly following ablation. Early focal enhancement on DCE-MR Images at the ablation zone at 12-month MRI is a suspicious finding for residual tumor. CLINICAL RELEVANCE/APPLICATION Follow-up MR images can be obtained at 12 months after laser ablation and early focal enhancement at the ablation zone can be considered suspicious for residual cancer. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Aytekin Oto, MD - 2013 Honored Educator SSJ10-06 Primary and Secondary Prostate Biopsy Settings: Differences When Performing Targeted MR-guided Biopsies Tuesday, Dec. 1 3:50PM - 4:00PM Location: E353C Participants Frederic Dietzel, Dusseldorf, Germany (Presenter) Nothing to Disclose Lars Schimmoeller, MD, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose Michael Quentin, MD, Dusseldorf, Germany (Abstract Co-Author) Nothing to Disclose Dirk Blondin, MD, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose Christian Arsov, MD, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose Gerald Antoch, MD, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose Andreas Hiester, Dusseldorf, Germany (Abstract Co-Author) Nothing to Disclose Robert Rabenalt, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose Erhard Godehardt, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose Peter Albers, MD, PhD, Duesseldorf, Germany (Abstract Co-Author) Nothing to Disclose PURPOSE This study evaluates the MR-guided in-bore biopsy (IB-GB) in patients, who were either biopsy naive (primary biopsy) or who had undergone at least one previous negative trans-rectal ultrasound-guided biopsy (secondary biopsy) with regard to cancer detection rate, tumor localization and lesion size. METHOD AND MATERIALS In total, 1,602 biopsy cores from 297 patients (66.1±7.8y; median PSA 8.2ng/ml; prostate volume 58±30ml) in primary (n=160) and secondary (n=137) prostate biopsies settings were evaluated in this retrospective study. All patients received diagnostic prostate MRI (T2WI, DWI, DCE) at 3T. All lesions described on MRI were biopsied with IB-GB and examined histologically. RESULTS In 148 patients 511 cores were positive for prostate cancer (PCa). Clinically significant PCa was found in 82.4% (any Gleason pattern ≥4). PCa detection rate for patients with primary biopsies was 55.6% and 43.1% for secondary biopsies. In patients with primary vs. secondary biopsies, PCa was located peripherally in 62.5% vs. 49.5% (p=0.04), in the transition zone in 27.3% vs. 27.5% (p=0.53), and in the anterior stroma in 10.2% vs. 22.9% (p<0.01). Higher grade PCa (Gleason score ≥4+3=7) occurred apically in 38.5% (p=0.01). PCa detection rates for patients with smaller prostate volumes (<30ml vs. 30-50ml vs. >50ml; p<0.01) or larger lesion sizes (>0.5cm3 vs. 0.5-0.25cm3 vs. <0.25cm3; p<0.01) were significantly higher. CONCLUSION In primary and secondary prostate biopsies PCa detection rates were significantly higher for larger lesions and smaller prostate glands. In secondary biopsies, PCa was anteriorly located at a significantly more frequent rate. Higher grade PCa was detected in both settings in an apical location more often. CLINICAL RELEVANCE/APPLICATION MRI-guided in-bore biopsy led to high detection rates, especially of clinically significant PCa, in primary and secondary prostate biopsies. SSJ11 Genitourinary (Multimodality Imaging of Pregnancy and Pelvic Floor) Tuesday, Dec. 1 3:00PM - 4:00PM Location: E353B GU MR US AMA PRA Category 1 Credit ™: 1.00 ARRT Category A+ Credit: 1.00 Participants Elizabeth A. Sadowski, MD, Madison, WI (Moderator) Nothing to Disclose Mary C. Frates, MD, Sharon, MA (Moderator) Nothing to Disclose Sub-Events SSJ11-01 Dynamic Contrast-enhanced MRI Combined with Diffusion Weighted Imaging in Differential Diagnosis of Malignant Gestational Trophoblastic Neoplasia and Postpartum Retained Placental Tuesday, Dec. 1 3:00PM - 3:10PM Location: E353B Participants Kangkang Xue, Zhengzhou, China (Presenter) Nothing to Disclose Jingliang Cheng, MD, Zhengzhou, China (Abstract Co-Author) Nothing to Disclose Yong Zhang, DO, Zhengzhou, China (Abstract Co-Author) Nothing to Disclose Tianxia Bei, Zhengzhou, China (Abstract Co-Author) Nothing to Disclose PURPOSE To explore the application value of dynamic contrast-enhanced MRI (DCE-MRI) combined with diffusion weighted(DW-MRI) in the differential diagnosis of malignant gestational trophoblastic neoplasia(MGTN) and postpartum retained placental tissue(RPT). METHOD AND MATERIALS The institutional review board approved this retrospective stuty and waived the requirement for informed consent. 74 cases(median age, 30.6 years; age range, 20-48 years) of MGTN and RPT confirmed clinically were retrospectively analyzed, all patients underwent DCE-MRI and DW-MRI(500 and 1000 mm²/s) at 3.0T. Types of time signal-intensity curves(TIC) and quantitative analysis of time to peak(TTP), maximum contrast enhancement ratio(MCER) and ADC values of each case were performed. Differences in TTP, MCER, and ADC values between MGTN and RPT were evaluated using the independent samples t-test respectively.The sensitivity, specificity and accuracy of dynamic contrast-MRI, DW-MRI and combination of the two methods in diagnosing MGTN and RPT were calculated. RESULTS There were 39 MGTN, of which 13 lesions were invasive mole and 26 lesions were choriocarcinoma. There were 35 RPT, of which 14 lesions were normal retained placenta, 6 lesions were adherent placenta and 15 lesions were implanted placenta. The mean ADC value and TTP of MGTN(1.38±0.11×10-3mm²/s, 37.84±3.73 s) were significantly different( p<0.01 ) from that of RPT(2.03±0.56×10-3mm²/s, 102.11±9.14 s).The MECR of MGNT(248.58±19.28%) was not significantly different (P>0.05) from that of RPT(236.45±16.77%) statistically. The sensitivity, specificity and accuracy in diagnosing MGTN and RPT was 84.62%, 85.71%, 85.13% for DCE-MRI; 89.74%, 88.57%, 89.19% for DW-MRI; 94.87%, 94.29%, 94.59% for combination of the two methods. CONCLUSION MGTN and RPT has different features in DCE-MRI and DW-MRI respectively, and the combination of the two methods can provide high application value for the differential diagnosis of MGTN and RPT. CLINICAL RELEVANCE/APPLICATION The clinical issues and standard imaging features of malignant gestational trophoblastic neoplasia and postpartum retained placental tissue are similar, and the combination of DWI and dynamic-enhanced MRI can help clinician distinguish them, so as to decide treatment plans. SSJ11-02 Variable Sonographic Features and Imaging Underdiagnosis of Partial Molar Pregnancy Tuesday, Dec. 1 3:10PM - 3:20PM Location: E353B Participants Julia Savage, MD, Ann Arbor, MI (Presenter) Nothing to Disclose Katherine E. Maturen, MD, Ann Arbor, MI (Abstract Co-Author) Consultant, GlaxoSmithKline plc; Medical Advisory Board, GlaxoSmithKline plc Erika Mowers, MD, Ann Arbor, MI (Abstract Co-Author) Nothing to Disclose Katherine Pasque, MD, Ann Arbor, MI (Abstract Co-Author) Nothing to Disclose Ashish P. Wasnik, MD, Ann Arbor, MI (Abstract Co-Author) Nothing to Disclose Vanessa Dalton, MD, Ann Arbor, MI (Abstract Co-Author) Nothing to Disclose Jason Bell, MD, Ann Arbor, MI (Abstract Co-Author) Nothing to Disclose PURPOSE The goal of this study is to describe the ultrasound findings in histopathologically proven molar pregnancies and to correlate these findings with clinical parameters including serum beta-hCG levels and partial vs. complete molar pregnancy. METHOD AND MATERIALS Retrospective chart review revealed 72 women with failed pregnancy or elective termination with histopathologic diagnosis of molar pregnancy and available ultrasound images between January 1, 2001 to December 31, 2011. Clinical data, ultrasound images and reports were reviewed. RESULTS Mean age of women was 30.45 ± 6.97 years of age (range: 16-49), with 1.25 ± 1.49 prior pregnancies (range: 1-11). Mean gestational age (GA) by last menstrual period was 74.45 ± 19.07 days (range: 39-138) and median serum beta-hCG was 64,400 (range: 447-662,000), with expected positive correlations between mean sac diameter (MSD) vs. beta-hCG (r=0.45, p=0.004) and MSD vs. GA (r=0.54, p<.0001). Pathologic results showed 49 partial and 23 complete moles. By imaging, partial moles were more commonly described as having a discrete gestational sac (85.7 vs 21.7%, p<.0001), yolk sac (48.9 vs. 4.6%, p=0.0003), or fetal pole (57.1 vs. 0%, p<.0001), while complete moles were more likely to show clearly abnormal tissue in the uterus (82.6 vs. 20.8%, p<.0001) and to be prospectively diagnosed as molar pregnancy by the dictating radiologist (86.9 vs. 40.82%, p=0.0002). CONCLUSION Partial molar pregnancy is associated with a highly variable sonographic appearance and frequent detection of recognizable products of conception, which may contribute to its underdiagnosis by imaging. Complete molar pregnancy is more strikingly abnormal and thus recognizable by imaging, and commonly diagnosed prospectively. CLINICAL RELEVANCE/APPLICATION Suspicion of hydatidiform mole in failed pregnancy has impacts on clinical management including: need for uterine evacuation, submission of products of conception to pathology, and serum b-hCG surveillance; failure to prospectively suggest or diagnose molar pregnancy may negatively impact patient care. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Katherine E. Maturen, MD - 2014 Honored Educator SSJ11-03 Performance of Translabial Ultrasound versus Pelvic Floor MRI in the Detection of Transvaginal Mesh Implant Complications Tuesday, Dec. 1 3:20PM - 3:30PM Location: E353B Participants Karoly Viragh, MD, Los Angeles, CA (Presenter) Nothing to Disclose Seth A. Cohen, MD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Shlomo Raz, MD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Steven S. Raman, MD, Santa Monica, CA (Abstract Co-Author) Nothing to Disclose PURPOSE The goal of the study was to determine the efficacy of 2D and 3D dynamic translabial ultrasound versus pelvic floor MRI in the detection of transvaginal mesh implant complications. METHOD AND MATERIALS With IRB approval and HIPAA compliance, a retrospective observational study was performed to correlate the intraoperative findings of transvaginal mesh implant complications (perforation, extrusion, fluid collections) with the standard pre-operative translabial ultrasound and pelvic floor MRI evaluations in women who were treated with suburethral transvaginal mesh implant for stress urinary incontinence or pelvic organ prolapse. The pre-operative translabial ultrasound and MRI examinations were reviewed with attention to technical details. The sensitivity of ultrasound in identifying complications was calculated. The location of the transvaginal mesh with respect to the bladder and urethra was also evaluated (extraluminal, intramural, intraluminal). Factors for technical improvement were identified. RESULTS The study cohort included 200 women (mean age 55 years) with transvaginal mesh implants for who underwent 2D and 3D dynamic translabial ultrasound, pelvic floor MRI and mesh excision at our institution between 2007 and 2013. Descriptive statistics were provided. 17 patients were found to have perforation into the urethra and/or bladder during surgery. None were found to have extrusion or significant fluid collections. Translabial ultrasound had a sensitivity of (12/17) 70.5%, whereas detection of mesh fragments by MRI was challenging even in retrospect. Limitations were due to suboptimal visualization of the mesh fragments, which could be improved with pre-procedural hydration for bladder distention and the use of vaginal gel to better image the suburethral space. CONCLUSION 2D and 3D dynamic translabial ultrasound is a powerful real-time method for transvaginal mesh localization and for visualizing complications, most importantly perforation into the urethra and/or bladder, which allows for better surgical planning and preoperative patient counseling. CLINICAL RELEVANCE/APPLICATION Translabial ultrasonography is a powerful real-time diagnostic technique for the evaluation of female pelvic floor dysfunction and is more sensitive than MR in detecting transvaginal mesh perforation. SSJ11-04 To Determine the Ultrasound Predictors of Successful Treatment of Ectopic Pregnancy Using a Single Dose Methotrexate Protocol: Preliminary Results Tuesday, Dec. 1 3:30PM - 3:40PM Location: E353B Participants Margarita V. Revzin, MD, Wilton, CT (Presenter) Nothing to Disclose Dennis Toy, New Haven, CT (Abstract Co-Author) Nothing to Disclose Regina J. Hooley, MD, New Haven, CT (Abstract Co-Author) Nothing to Disclose Leslie M. Scoutt, MD, New Haven, CT (Abstract Co-Author) Consultant, Koninklijke Philips NV PURPOSE Uncomplicated ectopic pregnancy (EP) usually is managed with methotrexate (MTX) and other non-surgical interventions. There is limited data on the expected US findings of MTX treated EPs. The aim of the present study is to identify US predictors of successful treatment with MTX. METHOD AND MATERIALS This is a retrospective IRB approved and HIPAA compliant cohort study, exempt from informed consent. The medical records of 121 women (mean age of 29 + 5.3 years) who were diagnosed with an EP and underwent a single dose treatment with MTX were reviewed. Only those subjects who had a visible EP without heart activity on US prior to treatment and who had a follow up US after treatment were included in the study (n=52). Post treatment EP were evaluated with respect to the change in size, shape, echogenicity of the EP, presence of a gestational and yolk sac, fetal heart rate, vascularity, and hemoperitoneum after treatment. Results were correlated with patient b-hCG levels, clinical symptoms and necessity for surgical intervention. Qualitative and quantitative parameters were analyzed using parametric and nonparametric tests. RESULTS Separate assessment of the US findings with respect to their sensitivity(Ss), specificity (Sp), NPV and PPV respectively are as follows: EP change in size 53%, 57%, 45%, 55%, shape 89%, 75%, 85%, 78%, echogenicity 87%, 78%, 85%, 90%, avascularity 79%, 90%, 85%, 88%; and absent or small hemoperitoneum 90%, 86%, 87%, 78% ; A combination of at least three of these findings was most accurate with Ss 95%, Sp 96%, PPV 95%, NPV 90%.Presence of fetal heart activity, increased size of yolk sac and gestational sac, large amount of hemoperitoneum were strong US predictors of failure of MTX treatment with Ss 100%, Sp 100%, PPV 100%, NPV 99% CONCLUSION A combination of at least three US findings including stable shape and echogenicity, avascularity and absence or small amount of hemoperitoneum are best US predictors of successful MTX treatment of EPs. Detection of fetal heart activity, large hemoperitoneum, and increase in size of gestational and yolk sac are strong US predictors of a failure of MTX treatment. Change in size of the EP after MTX treatment is not a reliable predictor of either treatment success or failure. CLINICAL RELEVANCE/APPLICATION US findings aid in prediction of successful treatment of ectopic pregnancy using a single dose methotrexate protocol Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Leslie M. Scoutt, MD - 2014 Honored Educator SSJ11-05 Accuracy of MRI in the Prenatal Diagnosis of the Abnormally Adherent Placenta: Comparison with Findings at the Time of Delivery Tuesday, Dec. 1 3:40PM - 3:50PM Location: E353B Participants Sherelle L. Laifer-Narin, MD, Englewood, NJ (Presenter) Nothing to Disclose Sidney Z. Brejt, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Sarah Goodman, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Jason Wright, New York, NY (Abstract Co-Author) Nothing to Disclose Jeffrey H. Newhouse, MD, Bronxville, NY (Abstract Co-Author) Research Consultant, PAREXEL International Corporation PURPOSE To evaluate the accuracy of magnetic resonance imaging in diagnosing invasive placentation. METHOD AND MATERIALS A retrospective review of all patients referred for MRI of the placenta from December 2004 to December 2014 was performed. Indications for MRI included abnormal appearance of the placenta on ultrasound, history of prior cesarean delivery, and history of prior uterine surgery. MRI reports were reviewed for placental location, presence or absence of abnormal placentation according to established MRI findings, and suspicion for parametrial involvement. Criteria included the presence of dark intraplacental bands, heterogeneous signal intensity, abnormal vascularization and thickened nodular contour along the urinary bladder surface, uterine bulging into the bladder, and loss of the myometrial margin. MRI was considered positive even if only one of these criteria were present. Comparison was made with findings at either delivery or operation, and pathology reports. RESULTS 256 MRI exams were reviewed. 144 exams were negative both on MRI and delivery/pathology. 8 exams interpreted as normal on MRI underwent hysterectomy with pathology demonstrating placenta accreta. 80 exams were interpreted as positive for abnormal placentation, and were diagnosed as accreta, increta, or percreta on delivery/pathology. 24 cases interpreted as positive on MRI had normal placental delivery and pathology. MR diagnosis of abnormal placentation had a sensitivity of 91%, specificity of 86%, PPV of 77%, NPV of 95%, and an accuracy of 87.5%. CONCLUSION Placental adhesive disorder is a significant cause of maternal morbidity and mortality. Prenatal MRI is accurate in evaluating invasive placentation in patients at high risk for this condition. CLINICAL RELEVANCE/APPLICATION MRI can provide topographic information specifically in cases with lateral extension into the parametrical regions. Identification of abnormal placentation assists the clinician in planning the mode of delivery, extent and location of surgical incision, and determining the need for multidisciplinary involvement and assistance. SSJ11-06 3T Pelvic MRI Thresholds for Pelvic Organ Prolapse before and after First Childbirth Tuesday, Dec. 1 3:50PM - 4:00PM Location: E353B Participants Mark E. Lockhart, MD, Birmingham, AL (Presenter) Nothing to Disclose Holly Richter, MD, Birmingham, AL (Abstract Co-Author) Research Grant, Pelvalon, Inc; Consultant, Pelvalon, Inc; Consultant, Kimberly-Clark Corporation; Royalties, UpToDate, Inc Gordon W. Bates, MD, Birmingham, AL (Abstract Co-Author) Nothing to Disclose Timothy M. Beasley, PhD, Birmingham, AL (Abstract Co-Author) Nothing to Disclose Desiree E. Morgan, MD, Birmingham, AL (Abstract Co-Author) Research support, General Electric Company PURPOSE To evaluate the usefulness of published 3T MRI parameters suggesting pelvic organ prolapse before and after first childbirth METHOD AND MATERIALS In this IRB-approved HIPAA-compliant prospective cohort study, patients presenting for reproductive assistance were recruited to complete validated questionnaires, clinical pelvic exams, baseline dynamic 3T MRI, and repeat MRI 6 months after delivery. Subjects were nulliparous women, at least 19 years age, and asymptomatic by Pelvic Floor Distress Inventory-20. Predetermined published thresholds or 2 SD beyond means in the literature for pelvic prolapse on MRI were evaluated. Also, a 10% change from baseline to postpartum was considered a significant change. Using 120 cc rectal gel and pelvic phased array coil over the pelvis, static 3mm axial and coronal T2 FSE sequences were followed by 10 mm thick dynamic sagittal HASTE at rest and during strain. The 10 mm sagittal sequence then evaluated pelvic floor mobility during evacuation of the rectal gel. MRI parameters were measured by a fellowship-trained radiologist, blinded to clinical data. RESULTS 19 subjects (mean age 31 years) completed baseline clinical and MRI studies, and 10 (mean age 30.5 years) of them completed postpartum clinical and MRI studies. None developed significant pelvic floor symptoms by the PFDI-7 and PISQ-12 questionnaires after childbirth. None had levator tears at baseline; two subjects developed tears postpartum. Mean pelvic floor mobility was increased in patients after childbirth and 17 pelvic soft tissue parameters increased by greater than 10% postpartum. At baseline 7/133 (5.3%), 8/209 (3.8%), and 79/209 (37.8%) of pelvic soft tissue measurements exceeded published thresholds (indicating prolapse) at rest, strain, and evacuation, respectively, majority in the anterior compartment. After pregnancy and childbirth, 4/70 (5.7%), 6/110 (5.5%), and 51/110 (46.4%) exceeded thresholds at rest, strain, and evacuation, respectively, in this asymptomatic population. Osseous parameters remained unchanged. CONCLUSION Although published soft tissue parameters work well for rest and strain MR imaging, their values in evacuatory series are frequently exceeded, even in asymptomatic nulliparous and primiparous women. CLINICAL RELEVANCE/APPLICATION In nulliparous and primiparous women, the evacuatory phase will commonly exceed published MRI thresholds for pelvic organ prolapse and therefore results should be used with caution. SSJ14 Molecular Imaging (Prostate/Neuroendocrine Tumors) Tuesday, Dec. 1 3:00PM - 4:00PM Location: S504CD GU BQ MI MR AMA PRA Category 1 Credit ™: 1.00 ARRT Category A+ Credit: 1.00 FDA Discussions may include off-label uses. Participants Peter L. Choyke, MD, Rockville, MD (Moderator) Researcher, Koninklijke Philips NV Researcher, General Electric Company Researcher, Siemens AG Researcher, iCAD, Inc Researcher, Aspyrian Therapeutics, Inc Researcher, ImaginAb, Inc Researcher, Aura Biosciences, Inc Vikas Kundra, MD, PhD, Houston, TX (Moderator) License agreement, Introgen Therapeutics, Inc Sub-Events SSJ14-01 Promising Role of Ga-68 PSMA PET/CT over Conventional Imaging in Staging and Restaging of Carcinoma Prostate Tuesday, Dec. 1 3:00PM - 3:10PM Location: S504CD Participants Venkatesh Rangarajan, MBBS, Mumbai, India (Presenter) Nothing to Disclose Archi Agrawal, MBBS, Mumbai, India (Abstract Co-Author) Nothing to Disclose Rasika Kabnurkar, MBBS, Mumbai, India (Abstract Co-Author) Nothing to Disclose Nilendu C. Purandare, DMRD, Mumbai, India (Abstract Co-Author) Nothing to Disclose Sneha A. Shah, Mumbai, India (Abstract Co-Author) Nothing to Disclose PURPOSE 1) To study the utility of Ga-68 Prostate Specific Membrane Antigen (PSMA) Positron Emission Tomography/Computed Tomography (PET/CT) for staging and restaging of Carcinoma Prostate (CaP).2) To compare the efficacy of Ga-68 PSMA PET/CT with Contrast Enhanced Computed Tomography (CECT) and F18 Sodium Fluoride (NaF) PET/CT for lesion detection METHOD AND MATERIALS Retrospective audit of prospectively maintained data of 25 patients of CaP (3 for staging and 22 with biochemical failure for restaging) who underwent Ga-68 PSMA PET/CT, CECT and F18 NaF PET/CT scan. The imaging findings were analyzed on lesionlesion and patient-patient basis for concordance and discordance. RESULTS All the 3 cases imaged for staging evaluation demonstrated Ga-68 PSMA uptake at the site of primary while CECT demonstrated lesion in only 1 patient. In cases with suspected biochemical failure, local recurrence was detected in 59% (13/22) patients on Ga68 PSMA PET/CT as against 9 % (2/22) detected on CECT. In 25 patients studied, Ga-68 PSMA PET/CT detected 43 metastatic nodes compared to 29 detected on CECT. Ga-68 PSMA detected additional metastases in sub cm sized nodes in 24% (6/25) patients. Ga-68 PSMA had incremental value in detecting occult extranodal metastases involving urinary bladder, pararectal nodule and peritoneal deposit in 8% (2/25) patients .In 25 patients, 109 skeletal lesions were detected on Ga-68 PSMA while F18 NaF PET/CT demonsrated147 lesions. Concordance in imaging findings of Ga-68 PSMA PET/CT and F 18 Fluoride PET/CT was noted in 68% (17/25) patients. Ga-68 PSMA PET/CT had an incremental value in staging of 1 patient where it detected lytic and marrow metastases. In restaging group, 7 patients showed additional lesions on F18 NaF PET/CT. CONCLUSION Ga-68 PSMA PET/CT is superior in detection of primary, nodal and soft tissue metastases as compared to conventional imaging techniques. However, F18 NaF PET/CT appears to detect more skeletal lesions in patients with biochemical failure in our study and further prospective trials are warranted to confirm these findings. CLINICAL RELEVANCE/APPLICATION Ga-68 PSMA PET/CT has an incremental value as a one stop shop in staging and restaging of carcinoma prostate SSJ14-02 18F-fluoro-4-thia-palmitate (18F-FTP) PET Imaging for Evaluation of Exogenous Fatty Acid Metabolism in Prostate Cancer: Implications for Treatment Optimization Tuesday, Dec. 1 3:10PM - 3:20PM Location: S504CD Participants Pedram Heidari, MD, Boston, MA (Presenter) Nothing to Disclose Shadi A. Esfahani, MD, MPH, Boston, MA (Abstract Co-Author) Nothing to Disclose Giorgia Zadra, PhD, Boston, MA (Abstract Co-Author) Nothing to Disclose Michael S. Placzek, PhD, Charlestown, MA (Abstract Co-Author) Nothing to Disclose Benjamin Larimer, PhD, Charlestown, MA (Abstract Co-Author) Nothing to Disclose Jacob M. Hooker, PhD, Charlestown, MA (Abstract Co-Author) Nothing to Disclose Massimo Loda, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Umar Mahmood, MD, PhD, Charlestown, MA (Abstract Co-Author) Research Grant, Sabik Medical Inc; Advisory Board, Blue Earth Diagnostics Limited; PURPOSE Upregulation of de novo lipogenesis is a major metabolic change in PCa development, and correlates with tumor progression and Upregulation of de novo lipogenesis is a major metabolic change in PCa development, and correlates with tumor progression and poor prognosis. Differentiation of diet-derived versus de novo fatty acid (FA) utilization in PCa is essential in designing anti-lipogenic therapeutics. We aim to evaluate the use of 18F-fluoro-4-thia-palmitate (18F-FTP) PET for assessment of exogenous FA utilization by PCa. METHOD AND MATERIALS 14C incorporation into lipids of LNCaP cells by a glucose donor (marker of de novo lipogenesis) was measured by a beta-counter after treatment with vehicle, IPI-9119, or C75. Growth inhibition rescue of LNCaP cells was performed using Cell Titer Glo assay after incubation with IPI-9119 alone or in the presence of BSA or of BSA-conjugated palmitate. For in-vitro 18F-FTP uptake study LNCaP cells were incubated with IPI-9119, C75, Etomoxir, SSO, DMSO, and combination of IPI-9119 with Etomoxir or C75 for 24 hours. The cells were then incubated with 18F-FTP and harvested to measure retained activity corrected for cell count. IACUC approval was obtained. Mice with subcutaneous LNCaP xenografts were fasted. PET data was acquired in list mode after injection of 18F-FTP. The SUVmean and tracer influx constant were measured. RESULTS 14C incorporation in lipids decreased to approximately 25% of control using both IPI-9119 and C75 indicating FASN inhibition. LNCaP growth inhibition was aborted by BSA-conjugated palmitate. 18F-FTP uptake significantly increased with IPI-9119 treatment, while C75, etomoxir, SSO treatment reduced 18F-FTP uptake. 18F-FTP PET demonstrated significantly decreased uptake in LNCaP tumors following treatment with C75 and etomoxir compared to control (SUVmean=0.20±0.01, 0.25±0.2, and 0.40±0.02, respectively). CONCLUSION We demonstrated that metabolic imaging using 18F-FTP can be used to assess the exogenous FA utilization by PCa. As expected, IPI-9119 (selective FASN inhibitor) increased the exogenous FA (18F-FTP) uptake while C75, which induces a host of metabolic modulations other than FASN inhibition paradoxically reduces 18F-FTP uptake. Etomoxir (FAO inhibitor) and SSO (FA transporter inhibitor) reduce 18F-FTP uptake as expected. CLINICAL RELEVANCE/APPLICATION Understanding the effect of exogenous lipid availability on therapeutic potential of targeting de novo lipogenesis is critical in prostate cancer treatment. This could lead to treatment strategies that result in maximal efficacy. SSJ14-03 Feasibility of Hyperpolarized 13C-Pyruvate Magnetic Resonance Spectroscopy for Pancreatic Cancer Diagnostic Imaging Tuesday, Dec. 1 3:20PM - 3:30PM Location: S504CD Participants Stephanie K. Carlson, MD, Rochester, MN (Presenter) Royalties, Medspira, LLC Alan Penheiter, PhD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Prasanna K. Mishra, PhD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Fergus J. Couch, PhD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Slobodan I. Macura, PhD, Rochester, MN (Abstract Co-Author) Nothing to Disclose John D. Port, MD, PhD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Malgorzata Marjanska, PhD, Minneapolis, MN (Abstract Co-Author) Nothing to Disclose Claire E. Bender, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose PURPOSE Hyperpolarized (HP) 13C magnetic resonance spectroscopic imaging (MRSI) is a recently developed technique that allows the detection of injected 13C-labeled agents and their metabolites in real-time. The purpose of this study was to identify and explore potential metabolic pathways in pancreatic ductal adenocarcinoma (PDAC) that could be targeted with HP-13C MRSI to increase the diagnostic accuracy of pancreatic cancer imaging. METHOD AND MATERIALS We performed gene expression profiling using laser capture microdissection and RNAseq on histologically-confirmed primary PDAC tumors and normal pancreas tissue from 21 patients. A promising, highly upregulated and imageable metabolic pathway (the conversion of pyruvate to lactate) was identified. To further explore this pathway in vivo, mice bearing genetically-engineered PDAC tumors were injected with 200 microliters of 80 mM [1-13C]-pyruvate. Tumors were quench-frozen and excised 30 s postinjection. Spectroscopic data on tumor lysates was obtained using 1H and 13C nuclear magnetic resonance. Studies were approved by our IRB and IACUC. RESULTS Gene expression studies showed that transcripts encoding transporters and enzymes responsible for cellular import of pyruvate, export of lactate, and conversion of pyruvate to lactate are almost universally upregulated in PDAC compared to normal pancreas, while competing pathways of mitochondrial pyruvate metabolism and cytoplasmic pyruvate to alanine conversion are consistently low. NMR analysis of PDAC tumors showed a tumor metabolic signature consistent with a very high lactate concentration and high lactate-to-alanine ratio. Quantitative analysis after injection of [1-13C]-pyruvate showed a 4.8-fold enrichment of intratumoral [113C]-lactate over natural abundance, indicating that ~5% of the total lactate in the tumor at 30 s post-injection was derived from the injected [1-13C]-pyruvate. CONCLUSION PDAC tumors have a pyruvate-lactate metabolic signature that can be quantitated with 13C-pyruvate NMR. Further exploration of HP-13C-pyruvate MRSI for PDAC is warranted. CLINICAL RELEVANCE/APPLICATION A new molecular imaging strategy for PDAC used in conjunction with existing morphological imaging could transform patient management in clinically-challenging scenarios. SSJ14-04 Evaluation of Fast Non-enhanced PET/MR Examination Protocols in a Fully Integrated PET/MR System for Patients with Neuroendocrine Tumours: Direct Comparison to Multiphase Contrastenhanced PET/CT Tuesday, Dec. 1 3:30PM - 3:40PM Location: S504CD Participants Ferdinand F. Seith, BSC, Tuebingen, Germany (Presenter) Nothing to Disclose Christian la Fougere, Munich, Germany (Abstract Co-Author) Nothing to Disclose Christina Pfannenberg, MD, Tuebingen, Germany (Abstract Co-Author) Nothing to Disclose Konstantin Nikolaou, MD, Tuebingen, Germany (Abstract Co-Author) Speakers Bureau, Siemens AG Speakers Bureau, Bracco Group Speakers Bureau, Bayer AG Nina Schwenzer, MD, Tuebingen, Germany (Abstract Co-Author) Nothing to Disclose Cornelia Brendle, MD, Tubingen, Germany (Abstract Co-Author) Nothing to Disclose Christina Schraml, MD, Tuebingen, Germany (Abstract Co-Author) Nothing to Disclose PURPOSE In patients with neuroendocrine tumours (NET), kidney failure is a common complication of radionuclide therapy. It is known that multiphase contrast-enhanced PET/CT is superior to non-enhanced PET/CT in diagnosing metastases with low or no tracer uptake as well as small lesions especially in the liver. However, due to the superior soft tissue contrast of MRI it is possible that nonenhanced PET/MR offers the same information as contrast-enhanced PET/CT. The aim of the study was therefore to evaluate a fast protocol in PET/MR without contrast agent in direct comparison to multiphase contrast-enhanced PET/CT as gold standard. METHOD AND MATERIALS 39 Patients (22 female, 58±13 years) were examined in multiphase contrast-enhanced 68Ga-DOMITATE-PET/CT in a clinical setup and in PET/MR subsequently. 2 blinded readers investigated PET/MR examinations of the abdomen with 3 different setups: T2HASTE+PET (30min), T2HASTE+TSET2+PET (35min) and T2HASTE+TSET2+DWI+PET (35min). The T2HASTE was acquired under free breathing with continuous table move. DWI was acquired with two b-values (0, 800 s/mm2). Metastatic lesions were defined as functional and/or morphological suspicious lesions or lymph nodes. The results were compared with the contrast-enhanced PET/CT, follow-up examinations and histopathology, if available. RESULTS T2HASTE sequences were of diagnostic quality in all patients. DWI suffered from artefacts especially in the upper regions of the liver. Compared with contrast-enhanced PET/CT high agreement was found with T2HASTE+TSET2+DWI+PET. CONCLUSION A protocol for PET/MR including T2HASTE, TSET2, DWI and PET seems to provide comparable results compared with multiphase contrast-enhanced PET/CT. With an estimated time of 35 min for a whole body examination, this might serve as a legitimate alternative to contrast-enhanced PET/CT for patients with kidney failure in the future. CLINICAL RELEVANCE/APPLICATION In patients with neuroendocrine tumours (NET) and kidney failure, fast non-enhanced PET/MR protocols can serve as a legitimate alternative to multiphase contrast-enhanced PET/CT examinations. SSJ14-05 Qualitative and Quantitative Comparison of 68Ga-DOTATATE PET/CT and PET/ MRI in Neuroendocrine Tumours Tuesday, Dec. 1 3:40PM - 3:50PM Location: S504CD Participants Francesco Fraioli, MD, London, United Kingdom (Presenter) Nothing to Disclose Alshaima Alshammari, London, United Kingdom (Abstract Co-Author) Nothing to Disclose Evangelia Skoura, Athens, Greece (Abstract Co-Author) Nothing to Disclose Rizwan Syed, MBBS, FRCR, London, United Kingdom (Abstract Co-Author) Nothing to Disclose Sofia Michopoulou, London, United Kingdom (Abstract Co-Author) Nothing to Disclose Jamshed Bomanji, London, United Kingdom (Abstract Co-Author) Nothing to Disclose Ashley M. Groves, MBBS, Hitchin, United Kingdom (Abstract Co-Author) Investigator, GlaxoSmithKline plc; Investigator, General Electric Company; Investigator, Siemens AG; ; ; PURPOSE Many Neuroendocrine tumours (NET) show high somatostatin receptor avidity. The aim of this study is to compare 68Ga-DOTATATE PET/CT with 68Ga-DOTATATE PET/MRI imaging in patients with known NET, and assess the confidence in anatomic lesion detection and localization. Furthermore, the value of each sequence of MRI was separately evaluated. METHOD AND MATERIALS We analysed the data of 38 NET patients. Cross over of both 68Ga-DOTATE PET/CT and PET/MRI scans were performed. MR protocol was as follow: T1 MPR, pre and post gadolinium injection, T2 haste, DW1 (b0, 500, 1000). Two observers for 68GaDOTATATE PET/MRI and one observer for 68Ga-DOTATATE PET/CT, independently, reviewed the images and inter observer and inter modality correlation was assessed by using interclass correlation. RESULTS Our initial data showed good inter modality correlation between 68Ga-PET/CT and PET/MRI. All lesions considered as malignant in PET/CT were equally depicted in PET/MRI in the compared regions. Both modalities, revealed liver metastases in the same number of patients (18 patients), and bone metastases in 7 patients. However, counting the number of liver lesions in each patient, 68GaDOTATATE PET/MRI was able to recognize more lesions in 3 patients. On the other hand, more lung lesions were detected in the lung in the CT component compared to MRI component (7 lesions versus 4). The contrast and DWI sequence of PET/MRI did not have a significant effect on final outcome, but in a selected number of cases these images confirmed and helped to further characterize and detect more lesions. Inter observer reliability was equally very good in both modalities. CONCLUSION This study demonstrates the potential of 68Ga-DOTATOC PET/MRI in patients with NET, with special advantages in the characterization of liver lesions. CLINICAL RELEVANCE/APPLICATION 68Ga-DOTATOC PET/MRI can help in diagnosis and staging of patients with NET, with special advantages in the characterization of liver lesions. SSJ14-06 68Ga-DOTATOC Uptake in Somatostatin Expressing Tumors is Directly Related to Specific Activity: Implications for Receptor Quantitation Imaging Tuesday, Dec. 1 3:50PM - 4:00PM Location: S504CD Participants Pedram Heidari, MD, Boston, MA (Presenter) Nothing to Disclose Dominik Berzaczy, MD, Vienna, Austria (Abstract Co-Author) Nothing to Disclose Alicia Leece, Boston, MA (Abstract Co-Author) Nothing to Disclose Shadi A. Esfahani, MD, MPH, Boston, MA (Abstract Co-Author) Nothing to Disclose Umar Mahmood, MD, PhD, Charlestown, MA (Abstract Co-Author) Research Grant, Sabik Medical Inc; Advisory Board, Blue Earth Diagnostics Limited; PURPOSE The importance of specific activity (SA) has been previously shown in functional PET imaging studies. We hypothesized that tracer uptake, measured using semiquantitative (SUV) or quantitative (Patlak plot) parameters, would vary considerably according to SA in cancer receptor imaging. This study aims to evaluate the effect of SA on PET parameters used for quantitation of 68Ga-DOTATOC uptake in somatostatin receptor (SSTR) tumor models. METHOD AND MATERIALS In-vitro, SSTR2 expression level was assessed using Western blot across multiple cancer lines including IMR32, Capan1, A549 and AR42J, and was normalized for Β-actin expression. The SSTR2/Β-actin ratio was correlated to in-vitro 68Ga-DOTATOC uptake normalized for cell counts. AR42J and IMR32 normalized 68Ga-DOTATOC uptake was plotted against 68Ga-DOTATOC SA ranging from 0.2 to 20 Ci/g and correlation was assessed. The in-vitro studies were performed in triplicate. For in-vivo studies Institutional Animal Care and Use Committees approval was obtained. Subcutaneous AR42J xenografts were implanted in Nu/Nu mice. Dynamic PET scans in list mode were acquired following injection of 68Ga-DOTATOC with a wide range of SAs (0.3 - 50 Ci/g). Net tracer influx (Ki), SUVmax and SUVmean were plotted against the SA to establish the correlation between quantitative parameters and SA. Patlak-plot was used to calculate the tracer influx constant for the tumor ((Ki= (k1 × k3 / k2 + k3)). RESULTS We observed a consistent ratio between 68Ga-DOTATOC uptake per cell and SSTR2/Β-actin level across the cell lines (R2=0.95, p<0.024). In-vitro we demonstrated a linear correlation between SA and 68Ga-DOTATOC uptake per cell in IMR32 (R2=0.98, P<0.015) and AR42J (R2=0.99, P<0.005). We found that Ki, SUVmax, and SUVmean decreased in a linear fashion with reduction in SA. Quantitative 68Ga-DOTATOC PET parameters had a direct linear correlation with SA (R2=0.89, p<0001 for Ki, R2=0.66, p<0.0001 for SUVmax and R2=0.82 and p<0.0001 for SUVmean). CONCLUSION 68Ga-DOTATOC uptake is strongly correlated to SSTR2 expression for each given SA. However, 68Ga-DOTATOC uptake in SSTRexpressing tumors increases in a linear fashion with increase in SA, over the range studied. CLINICAL RELEVANCE/APPLICATION 68Ga-DOTATOC uptake by tumors can vary widely with change in specific activity. Quantitation for radiotherapy dosimetry and response assessment is improved with correction for specific activity. RC407 Quality and Safety in GU Radiology: Update on Best Practices, Contrast Material, and Radiation Dose Tuesday, Dec. 1 4:30PM - 6:00PM Location: E350 GU SQ AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Giles W. Boland, MD, Boston, MA (Coordinator) Principal, Radiology Consulting Group; Royalties, Reed Elsevier Richard H. Cohan, MD, Ann Arbor, MI, (rcohan@umich.edu) (Presenter) Consultant, General Electric Company; ; ; James A. Brink, MD, Boston, MA (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Understand the background and current status of best practice clinical and workflow management and its imperitive for improving patient outcomes. 2) To review indications for premedication prior to contrast material administration. To summarize the current understanding of iodinated contrast media nephrotoxicity. To describe common errors made in treating contrast reactions. 3) To understand the requirement to match radiation dose according to the individual patient, clinical question and modality used. To outline meaningful radiation metrics including organ dosages and the overall radiation absorbed to estimate patient risk. ABSTRACT BEST PRACTICES: Increasingly medicine is being defined and evaluated based on patient outcomes rather than procedural events. While best practices are evolving and sometimes incomplete, many do exist, yet there is marked departmental variation from one organization to another. This session will outline why and how best practice implementation, particularly as it relates to IV contrast use and radiation dose, is essential to achieve better patient outcomes. This will require evaluation of current practices and comparison to nationally driven guidelines, with subsequent compliance to guidelines where they exist. CONTRAST SAFETY: Some patients have contrast reactions despite premedication. Patients who have repeated reactions in this setting tend to have reactions of similar severity. Studies performed with control groups suggest that there is minimal to no increased risk of contrastinduced renal failure in patients who receive iodinated contrast material; however, the control groups likely included patients at increased risk of acute kidney injury. Some errors treating contrast reactions relate to failure to administer epinephrine or using the wrong dose / wrong route. The act of administering this drug can also be problematic. RADIATION DOSE: In all radiological examinations that utilize x-rays, there are always three important issues that must be taken into consideration. The first relates to the appropriate amount of radiation to be used, which must always explicitly take into account the imaging task at hand as well as the physical characteristics of the patient undergoing the CT examination. The second issue is how to transform the radiation incident on the patient into the organ doses received which are essential to understanding (any) patient risks. The final consideration is to understand the radiological significance of the radiation absorbed by the patient, and to estimate (any) radiological risks, as well as the corresponding uncertainties. RC410 Ultrasound Elastography Tuesday, Dec. 1 4:30PM - 6:00PM Location: S406B GI GU HN NR US AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Sub-Events RC410A Thyroid Elastography Participants Richard G. Barr, MD, PhD, Campbell, OH (Presenter) Consultant, Siemens AG; Consultant, Koninklijke Philips NV; Research Grant, Siemens AG; Research Grant, SuperSonic Imagine; Speakers Bureau, Koninklijke Philips NV; Research Grant, Bracco Group; Speakers Bureau, Siemens AG; Consultant, Toshiba Corporation; Research Grant, Esaote SpA LEARNING OBJECTIVES 1) Explain the difference between strain and shear wave elastography. 2) Understand the techniques to be able to perform thyroid ultrasound elastography. 3) Apply ultrasound elastography into routine clinical practice of thyroid nodules. ABSTRACT Thyroid nodules are very common and work-up of these nodules remains challenging. Fine needle aspiration has been the method of choice for diagnosing suspicious lesions with a sensitivity of 54%-90% and specificity of 60-96% for detection of malignant lesions. Malignant thyroid lesions are statistically stiffer than benign lesions. Ultrasound elastography can assess the stiffness of thyroid lesions. Several studies have been performed evaluating strain and shear wave elastography to characterize thyroid nodules. Strain elastography is qualitative while shear wave elastography is quantitative. These studies suggest that ultrasound elastography may improve sensitivity and specificity of characterizing thyroid lesions over B-mode imaging alone. There is a learning curve for performing adequate thyroid ultrasound elastography. Both cystic lesions and calcified lesions are difficult to evaluate with elastography. There is some overlap of stiffness values between benign and malignant thyroid nodules and elastography should not eliminate biopsy of suspicious lesions based on B-mode imaging. Stiff lesions on elastography should increase the suspicion for malignancy. This presentation will discuss the differences between strain and shear wave elastography, discuss technique and pitfalls in performing the examination, review the literature, and discuss published guidelines. RC410B Renal Elastography: Where Are We? Participants Nicolas Grenier, MD, Bordeaux CEDEX, France, (nicolas.grenier@chu-bordeaux.fr) (Presenter) Advisory Board, Supersonic Imagine; Travel support, Guerbet SA LEARNING OBJECTIVES 1) To become familiar with the advantages and limits of the different elastography technologies applied to kidney. 2) To understand the factors affecting reliability and reproducibility of elasticity measurement within the kidney. 3) To learn about the intrarenal changes responsible for elasticity changes. 4) To learn about the clinical impact of elasticity measurement in renal parenchymal diseases. 5) To learn about the clinical impact of elasticity measurement in renal tumors. ABSTRACT Ultrasound elastography is a new imaging technique under development that provides information about renal stiffness. Kidney elasticity quantification with ultrasound should be better performed with a quantitative technique, based on shear wave velocity measurements (ARFI or SSI methods). Kidney stiffness changes can be affected by mechanical factors such as external pressure induced by the probe and intrarenal characteristics such as tissue anisotropy, which is high in renal medulla, vascularization, which is high within the cortex, and hydronephrosis. Chronic kidney disease (CKD) incidence and prevalence are increasing in Western countries, due particularly to diabetes mellitus and hypertension-related nephropathies. During progression of such renal parenchymal diseases, cellular density may increase, mainly during acute inflammatory phases, and the interstitial matrix may be invaded by fibrosis. All components of these tissue changes may induce an increase of renal elasticity which is not specifically related to fibrosis. Tubular, glomerular, interstitial and vascular changes may also be responsible for an increase of stiffness. This is why, further studies are now necessary before to understand the real impact of elastography measurement in clinical nephrology. Considering characterization of renal tumors with elastography, clinical experience is still limited. Preliminary results show that benign tumors seem to have lower values of elasticity than malignant ones, but, here too, more experience is also necessary. RC410C Liver Elastography Participants Paul S. Sidhu, MRCP, FRCR, London, United Kingdom, (paulsidhu@nhs.net) (Presenter) Speaker, Bracco Group; Speaker, General Electric Company LEARNING OBJECTIVES 1) To understand the concept of liver fibrosis grading and the implications for healthcare management. 2) To review the basis for the assessment of liver fibrosis using elastography, with emphasis on the different techniques. 3) To understand the differences in the techniques and the variability in measurement assessment. 4) To achieve an overview of the need and position of this technique in clinical care. ABSTRACT Liver fibrosis and cirrhosis from many causes is an important cause of long term morbidity and mortlaity. Most cases are a consequence of chronic viral disease (Hepatitis B and C) with alcoholic lever disease an important ethiological factor. The degree of liver fibrosis, and the presence of established cirrhosis confer differnet mamangement stratergies, with imaging playing an important role in the non-invasive assessment of patents with chronic liver disease. Fibrosis grading traditionally performed using the Metavir or Ishak scoring system is essentially a hiistological grading system. Ultimately the possibility to avoid a liver biopsy is the aim, if a non-invasive technique can stage the grade of fibrosis, establishing correct patient management. Liver ultrasound elastography is a developing technique that offers this possibility, with varying methods of aassessment ranging form strain methods and shear wave methods. These techniques will be explained, the status of the current standing of the techniques will be summarised, and the level of technology offered by differnet machines will be reviewed. An overall summary of the current status and the implications for clinical practice will be discussed. ED006-W E Genitourinary Wednesday Case of the Day W ednesday, Dec. 2 7:00AM - 11:59PM Location: Case of Day, Learning Center GU AMA PRA Category 1 Credit ™: .50 Participants Theodora A. Potretzke, MD, Saint Louis, MO (Presenter) Nothing to Disclose Perry J. Pickhardt, MD, Madison, WI (Abstract Co-Author) Co-founder, VirtuoCTC, LLC; Stockholder, Cellectar Biosciences, Inc; Research Consultant, Bracco Group; Research Consultant, KIT ; Research Grant, Koninklijke Philips NV Naoki Takahashi, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Meghan G. Lubner, MD, Madison, WI (Abstract Co-Author) Grant, General Electric Company; Grant, NeuWave Medical, Inc; Grant, Koninklijke Philips NV Anup S. Shetty, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Richard Tsai, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose George A. Carberry, MD, Madison, WI (Abstract Co-Author) Nothing to Disclose Vincent M. Mellnick, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose David U. Kim, MD, Madison, WI (Abstract Co-Author) Nothing to Disclose Yaseen Oweis, MD, MBA, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Zachary J. Viets, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Bernard F. King JR, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1) Recognize imaging findings seen in disorders of the genitourinary systems. 2) Develop differential diagnosis based on the clinical information and imaging findings. 3) Recognize the clinical importance of diagnosis. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Perry J. Pickhardt, MD - 2014 Honored Educator Naoki Takahashi, MD - 2012 Honored Educator Meghan G. Lubner, MD - 2014 Honored Educator Meghan G. Lubner, MD - 2015 Honored Educator SPSH40 Hot Topic Session: Molecular Imaging and Radionuclide Therapy for Prostate Cancer W ednesday, Dec. 2 7:15AM - 8:15AM Location: E451A GU MI OI RO AMA PRA Category 1 Credit ™: 1.00 ARRT Category A+ Credit: 1.00 FDA Discussions may include off-label uses. Participants Uwe Haberkorn, MD, Heidelberg, Germany, (uwe.haberkorn@med.uni-heidelberg.de) (Moderator) Nothing to Disclose Eric M. Rohren, MD, PhD, Houston, TX (Moderator) Nothing to Disclose Alexander Drzezga, MD, Cologne, Germany (Moderator) Research Grant, Eli Lilly and Company; Speakers Bureau, Siemens AG; Speakers Bureau, General Electric Company; Speakers Bureau, Piramal Enterprises Limited; Research Consultant, Eli Lilly and Company; Research Consultant, Piramal Enterprises Limited; ; ; ; ; ; ABSTRACT Radium-223 is a recently approved therapy for treatment of bone metastases in patients with metastatic prostate carcinoma. As an alpha-emitting radioisotope, radium has the potential to be a powerful therapy for treatment of a variety of skeletal malignancies. In this presentation, the use of radium-223 in the treatment of prostate cancer will be reviewed through a case-based format. Future directions in radium-223 therapy will be discussed. URL Sub-Events SPSH40A Ra-223 Therapy for Skeletal Metastases from Prostate Cancer Participants Eric M. Rohren, MD, PhD, Houston, TX (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Review the chemical and physical features of radium-223 dichloride. 2) Discuss the clinical utility of radium-223 therapy. 3) Understand the technique for radium-223 administration. 4) Review the anticipated outcomes of radium-223 therapy through casebased review. ABSTRACT Radium-223 is a recently approved therapy for treatment of bone metastases in patients with metastatic prostate carcinoma. As an alpha-emitting radioisotope, radium has the potential to be a powerful therapy for treatment of a variety of skeletal malignancies. URL Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Eric M. Rohren, MD, PhD - 2015 Honored Educator SPSH40B Comparison of Ga-68 and F-18 Labeled Small Molecule PSMA Tracers for Prostate Cancer Imaging Participants Carsten Kobe, Cologne, Germany (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Understand the concept of PSMA PET-imaging in the diagnosis of prostate cancer in general and in comparison to conventional methods. 2) Learn about the currently available alternatives for radiolableling of PSMA-tracers, e.g. 68-Gallium and 18F-Fluoride and their characteristics. 3) Gain insights from first comparative studies about the clinical value of the availble tracers with regard to their sensitivity, specificity and practicability. SPSH40C PSMA Ligands for Imaging and Therapy of Prostate Cancer Participants Uwe Haberkorn, MD, Heidelberg, Germany (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Understand the background and pharmacokinetics of PSMA ligands for PET/CT. 2) Estimate the value of PSMA-based imaging in comparison to choline-based imaging. 3) Assess the value of PSMA-targeting for diagnosis and therapy. 4) Estimate the effects and side effects of endoradiotherapy with PSMA ligands ABSTRACT The prostate-specific membrane antigen (PSMA) is frequently over-expressed in prostate cancer (PCa) which led to the The prostate-specific membrane antigen (PSMA) is frequently over-expressed in prostate cancer (PCa) which led to the development of several PSMA-targeting molecules are for the detection and therapy of metastatic castration resistant prostate cancer (mCRPC).In a first diagnostic study 82.8% of 319 patients investigated with 68Ga-PSMAHBED-PET/CT at least one lesion indicative for PCa was detected. Amongst lesions investigated by histology, 30 were false-negative in 68Ga-PSMAHBED-PET/CT, all other lesions (n=416) were diagnosed true-positive or -negative. Fifty of 116 patients available for follow-up received a local treatment after 68Ga-PSMAHBED-PET/CT. A comparison of the 68Ga-PSMA-ligand with 18F-fluoromethylcholine PET/CT revealed 78 PC-suspicious lesions in 32 patients using 68Ga-PSMA-PET/CT and 56 lesions in 26 patients using Choline-PET/CT (significant with p=0.04). All lesions detected by 18F-fluoromethylcholine-PET/CT were also seen by 68Ga-PSMA-PET/CT. Since the ligand bound to PSMA is internalized, the target may also be used for endoradiotherapy. We used a small molecule inhibitor of PSMA MIP-1095 for therapy in 25 men with final stage mCRPC. PSA values decreased by >50% in 60.7% of the men treated. 84.6 % of men with bone pain showed complete or moderate reduction in pain. Hematological toxicities were mild. 25% of men treated had a transient slight to moderate dry mouth. No adverse effects on renal function were observed.In order to increase the therapeutic flexibilty a theranostic PSMA ligand coupled to DOTA was synthesized which allows coupling to Ga-68 for diagnostic use or to Lu-177 or Ac225 for therapy. Initial experience in 30 patients shows promising results concerning antitumor activity with mild side effects. URL MSCP41 Case-based Review of Pediatric Radiology (An Interactive Session) W ednesday, Dec. 2 8:30AM - 10:00AM Location: S406A CH GI GU OB PD AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Sudha A. Anupindi, MD, Philadelphia, PA (Director) Nothing to Disclose LEARNING OBJECTIVES 1) To apply a systematic approach in the evaluation of pediatric diseases. 2) To identify essential imaging features of various pediatric congenital, musculoskeletal, abdominal and neurological diseases using a multimodality approach. 3) To understand and develop best imaging practice for various pediatric diseases. ABSTRACT To apply a systematic approach in the evaluation of pediatric diseases To identify essential imaging features of various pediatric congenital, musculoskeletal, abdominal and neurological diseases using a multimodality approach To understand and develop best imaging practice for various pediatric diseases Sub-Events MSCP41A Fetal Thoracic and Abdominal Anomalies Participants Christopher I. Cassady, MD, Houston, TX (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. MSCP41B Pediatric Abdominopelvic Tumors Participants M. Beth McCarville, MD, Memphis, TN (Presenter) Support, General Electric Company LEARNING OBJECTIVES View learning objectives under main course title. MSCP41C Congenital Disorders of the Genitourinary Tract Participants Tracy N. Kilborn, MBChB, Cape Town, South Africa (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. MSES41 Essentials of Genitourinary Imaging W ednesday, Dec. 2 8:30AM - 10:00AM Location: S100AB GU MR US AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Sub-Events MSES41A Catching Ovarian Cancer Participants Elizabeth A. Sadowski, MD, Madison, WI (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Review the types of ovarian epithelial neoplasm seen on imaging. 2) Assess the risk of ovarian cancer based on imaging appearance of an adnexal lesion and clinical information. 3) Emphasize the role of MRI in further evaluation of adnexal lesions. ABSTRACT There is a spectrum of ovarian epithelial neoplasms ranging from benign to malignant. Current theories regarding the precursor lesions are debated; however, the pathway from benign epithelial neoplasm to low grade carcinoma follows an indolent course and is distinctly different from the aggressive evolution of high grade carcinoma. An understanding of the pathogenesis of low grade versus high grade ovarian epithelial neoplasms can be helpful to radiologists, when they are faced with an adnexal lesion. Identifying the imaging features suggestive of benign, intermediate and worrisome lesions can triage adnexal lesions into follow up versus treatment. The purpose of this presentation is to review the imaging features of benign, indeterminate and worrisome adnexal lesions and to discuss the appropriate follow up in each case. MSES41B US and MRI: Imaging of Chronic Pelvic Pain in Women Participants Mostafa Atri, MD, Toronto, ON (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) To review MRI and US features of adenomyosis and their correlation with pathology. 2) To discuss staging and US and MRI features of endometriosis and their role in the management of this condition. 3) To familiarize imagers with US features of diverticulosis/diverticulitis and how to differentiate it from colitis. ABSTRACT Chronic pelvic pain constitutes 10-40% of gynecology visits at a total cost of 39 billion dollars/year in USA. The most common etiologies are gynecological with GI, urology and MSK conditions being the other causes. During this presentation, imaging features of adenomyosis, endometriosis, pelvic congestion, and US features of diverticulosis/diverticulitis are reviewed. Both adenomyosis and endometriosis are common conditions affecting women. They are frequently seen as an incidental finding that can be accurately evaluated by MRI and US in symptomatic patients. There is close correlation between pathology and imaging features of adenomyosis. The main role of imaging in the evaluation of endometriosis is in the staging of the disease to plan for surgery. US features of uncomplicated diverticulitis are discussed. Transvaginal US can accurately diagnose diverticulosis/diverticulitis that should be sought for in women undergoing US to evaluate for chronic pelvic pain. Handout:Mostafa Atri http://abstract.rsna.org/uploads/2015/15001868/IMAGING CHRONIC PELVIC PAIN FINAL RSNA 2015 FINAL.pdf MSES41C Imaging of the Bladder and Ureters Participants Manjiri K. Dighe, MD, Seattle, WA (Presenter) Research Grant, General Electric Company LEARNING OBJECTIVES 1) Review embryology and discuss congenital anomalies of the bladder and ureter. 2) Classify and discuss imaging appearance of ureteric and bladder disease. 3) To discuss the protocols and imaging appearance of bladder and ureteric pathology on various modalities. 4) Review the staging of bladder and ureteric malignancies. 5) Discuss the imaging appearance of various stages of bladder and ureteric cancer. 6) Illustrate the newer techniques for imaging of bladder and ureter. ABSTRACT The ureter is an extra-peritoneal structure surrounded by fat.; The ureter is divided into three portions: the proximal ureter (upper) is the segment that extends from the ureteropelvic junction to the area where the ureter crosses the sacroiliac joint, the middle ureter courses over the bony pelvis and iliac vessels, and the pelvic or distal ureter (lower) extends from the iliac vessels to the bladder. It is a dynamic organ and not a simple conduit through which urine flows. Benign and malignant lesions can affect the ureter and these maybe due to contiguous involvement from the kidney or bladder. The ureter can be imaged by a variety of modalities including computed tomography (CT), magnetic resonance imaging (MR), direct pyelography (DP) both antegrade (AP) and retrograde (RP), nuclear medicine diuretic scan and voiding cystourethrography (VCUG). Benign lesions like endometriosis, Ureteritis, Ureteritis cystica can affect the ureter as well. Transitional cell carcinoma in the ureter is usually diagnosed on imaging. Bladder carcinoma is the fourth most common cancer in men and women. Knowledge of imaging options and appearance is necessary for both radiologists and urologists. Transitional cell carcinoma (TCC) is the most common bladder neoplasm with squamous cell and adenocarcinoma found in less than 10% of cases.; Benign lesions are uncommon but some can be suggested by their imaging appearance. Cystoscopy allows tissue diagnosis and treatment of superficial lesions. Although magnetic resonance imaging (MRI) and computed tomography (CT) both have limitations in detailing depth of muscle invasion, both have a prominent role helping to define the lesion and in staging. This presentation illustrates the role of MR and CT in evaluating bladder and ureter with a discussion of the newer techniques of MR Diffusion Weighted Imaging (DWI) and virtual cystoscopy by CT or MR. MSRO41 BOOST: Genitourinary-Oncology Anatomy (An Interactive Session) W ednesday, Dec. 2 8:30AM - 10:00AM Location: S103CD GU RO AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 FDA Discussions may include off-label uses. Participants Jelle O. Barentsz, MD, PhD, Nijmegen, Netherlands (Presenter) Nothing to Disclose Albert J. Chang, MD, PhD, San Francisco, CA (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Introduce imaging anatomy relevant to prostate cancer and review imaging issues for contouring primary tumors, nodal regions, and adjacent critical structures. 2) Review how the integration of different imaging modalities can affect tumor delineation. 3) How to choose appropriate imaging methods for specific purposes and to discuss the significance of certain imaging findings. RC507 Bladder, the Forgotten Organ: Role of CT, MRI, and PET in Diagnosis, Staging, and Surveillance of Cancer W ednesday, Dec. 2 8:30AM - 10:00AM Location: N229 GU CT MR NM AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Stuart G. Silverman, MD, Brookline, MA, (sgsilverman@partners.org) (Coordinator) Author, Wolters Kluwer nv Andrew B. Rosenkrantz, MD, New York, NY (Presenter) Nothing to Disclose Homer A. Macapinlac, MD, Houston, TX (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Learn the latest developments on the role of CT, MRI, and PET/CT in the detection, diagnosis, staging, and surveillance of patients with bladder cancer. 2) Learn currently recommended CT, MRI, and PET/CT techniques and protocols and how to implement them in clinical practice. 3) Learn how to interpret CT, MRI, and PET/CT scans of the bladder with an emphasis on case review and diagnostic pitfalls. ABSTRACT The urinary bladder is the most common site of malignancy of the urinary tract and is imaged by radiologists on many abdominal imaging exams. However, historically the bladder has been a 'forgotten' organ and thought to be largely the purview of the urologist due to the central role that cystoscopy has played in both the diagnosis and local staging of bladder cancer. Recent advances in CT, MRI, and PET have emerged that now allow radiologists to play an important role in the detection, diagnosis, staging, and surveillance of patients with or suspected of having bladder cancer. This course will detail these advances and explain how, when, and why radiologists should be using these three modalities in clinical practice today. Using illustrative case examples, advances in knowledge such as how CT urography can be used to detect bladder cancer, how MR urography can be used to distinguish muscleinvasive from superficial tumors and evaluate the upper tracts, and how PET/CT (and the newly introduced PET/MRI) can be used to stage and follow patients. With additional advances in low dose CT, emerging MRI techniques, and novel PET agents, radiology will play an increasingly vital role in the care of patients with bladder cancer in the future. RC510 Second and Third Trimester Obstetrical Ultrasound (An Interactive Session) W ednesday, Dec. 2 8:30AM - 10:00AM Location: E450B GU OB US AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants LEARNING OBJECTIVES Please bring your charged mobile wireless device (phone, tablet or laptop) to participate. Sub-Events RC510A 3D Ultrasound in Obstetrics Participants Beryl R. Benacerraf, MD, Brookline, MA (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) To learn the principles of 3D sonography and the applications for fetal scanning. To evaluate clinical situations where 3D scanning is helpful and where it is not useful beyond the 2D examination. 2) To see examples of fetal malformations scanned in 3D using surface rendering and multiplanar reconstruction. 3) To learn how to use volume scanning to dramatically reduce scan time and improve you scanning efficiency by rescanning stored volumes of complete fetal anatomy. ABSTRACT Three-dimensional (3D) ultrasound allows us to acquire a volume and display any plane of section within that volume regardless of the scanning orientation. The ability to display a 3D image of any type or plane has been one of the most powerful recent advances in sonography, particularly in the field of obstetrics and gynecology. In imaging of the fetus, 3D ultrasound is advantageous in demonstrating many types of fetal defects and dysmorphologic facial features using surface rendering. The fetal brain is also one of the areas where 3D ultrasound has been most helpful, since the reconstruction of the third non-scanning plane is crucial in demonstrating planes of section not previously visible sonographically. The corpus callosum is an example of one area not readily imaginable in standard imaging planes. The fetal sutures are also easy to image with 3D, which is particularly helpful in fetuses with suspected craniosynostosis. 3D ultrasound is key for imaging fetal skeletal abnormalities, providing additional information on affected fetuses as compared to 2D. Evaluation of the spine using 3D has been helpful to determine the level of spina bifida, thus providing crucial information regarding prognosis. Evaluation of the fetal heart is an intense area of research interest, and the heart can be imaged in realtime 3D (4D) using a method called STIC. This method provides the ability to obtain a full volume of the beating heart to evaluate in detail off line with or without color Doppler and while it is beating.Volume imaging is also key in improving efficiency of the ultrasound department. The entire fetus can be imaged easily by acquiring and archiving a few volumes. This way, the patient can spend far less time in the ultrasound room and the entire scan can be done remotely and virtually using the stored volumes. This techniques reduces operator dependency usually associated with 2D ultrasound. RC510B Fetal Genitourinary Anomalies Participants Roya Sohaey, MD, Portland, OR (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Apply the Urinary Tract Dilation classification system to fetal imaging practice. 2) Develop an anatomic approach for differential diagnosis of urinary tract obstruction. 3) Develop an understanding of which cases would benefit from fetal MR. ABSTRACT By the conclusion of this course, the participant will be able to apply the prenatal UrinaryTract Dilation (UTD) classification system for diagnosis and follow-up planning. The learner will develop an anatomic approach towards differential diagnosis for obstructive causes of UTD, renal cystic dysplasia and complex genitourinary anomalies. In addition, a fetal sex-based approach for analysis of complex lower tract anomalies will be discussed. The course will demonstrate how fetal MR is useful as a problem solving tool in certain complex cases. The lecture is didactic and case-based in format. RC510C Placenta Participants Sara M. Durfee, MD, Boston, MA (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Identify the cause of vaginal bleeding in patients with placental abnormalities that include placenta previa and placental abruption. 2) Describe the sonographic features of placenta accreta. 3) Define trophotropism and describe how this process leads to both normal and abnormal placentation. ABSTRACT After this presentation, the participant will understand how the normal placenta develops and how factors such as trophotropism lead to placental abnormalities. Specific abnormalities such as placenta previa, placental abruption and placenta accreta will be addressed in detail. In addition, first trimester abnormalities such as the chorionic bump and subchorionic hematomas will be discussed. The presenter will describe the sonographic appearance of succenturiate lobe, circumvallate placenta and sonolucencies within the placenta and will comment on placental masses. RC550 Fallopian Tube Catheterization (Hands-on) W ednesday, Dec. 2 8:30AM - 10:00AM Location: E260 GU OB AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Amy S. Thurmond, MD, Portland, OR (Moderator) Nothing to Disclose Ronald J. Zagoria, MD, San Francisco, CA, (ron.zagoria@ucsf.edu) (Presenter) Nothing to Disclose Lindsay S. Machan, MD, Vancouver, BC (Presenter) Nothing to Disclose A. Van Moore JR, MD, Charlotte, NC (Presenter) Nothing to Disclose Anne C. Roberts, MD, La Jolla, CA (Presenter) Nothing to Disclose David M. Hovsepian, MD, Stanford, CA (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Obtain hands-on experience with fallopian tube catheterization using uterine models and commercially available catheters and guidewires. 2) Review the evolution of interventions in the fallopian tubes. 3) Learn safe techniques for fallopian tube recanalization for promoting fertility, and fallopian tube occlusion for preventing pregnancy. 4) Discuss the outcomes regarding pregnancy rate and complications. 5) Appreciate ways to improve referrals from the fertility specialists and expand your practice. ABSTRACT Fallopian tube catheterization using fluoroscopic guidance is a relatively easy, inexpensive technique within the capabilities of residency trained radiologists. Fallopian tube cathterization can be used to dislodge debris from the tube in women with infertility,or to place FDA-approved tubal occlusion devices in women who do not desire fertility. The fallopian tube is the 1 mm gateway between the egg and the sperm. Noninvasive access to this structure for promoting, and preventing, pregnancy has been sought for over 160 years. This hands-on course allows participants use commercially available catheters and devices in plastic models for fallopian tube catheterization, and to speak directly to world experts about this exciting procedure. MSRO42 BOOST: Genitourinary-Integrated Science and Practice (ISP) Session W ednesday, Dec. 2 10:30AM - 12:00PM Location: S103CD GU OI RO AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 FDA Discussions may include off-label uses. Participants Stanley L. Liauw, MD, Chicago, IL (Moderator) Nothing to Disclose George B. Rodrigues, MD, London, ON (Moderator) Nothing to Disclose Sub-Events MSRO42-01 Invited Speaker: W ednesday, Dec. 2 10:30AM - 10:40AM Location: S103CD Participants Rodney J. Ellis, MD, Pepper Pike, OH (Presenter) Nothing to Disclose MSRO42-02 A Phase I Dose Escalation Study of Hypofractionated Radiation Therapy for Favorable Risk Prostate Cancer: Acute Toxicity and Early Efficacy W ednesday, Dec. 2 10:40AM - 10:50AM Location: S103CD Participants Nicholas J. Sanfilippo, MD, New York, NY (Presenter) Nothing to Disclose William C. Huang, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Herbert Lepor, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Silvia C. Formenti, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Benjamin Cooper, New York, NY (Abstract Co-Author) Nothing to Disclose Smith Beverly, New York, NY (Abstract Co-Author) Nothing to Disclose Barry Rosenstein, New York, NY (Abstract Co-Author) Nothing to Disclose Samir S. Taneja, MD, New York, NY (Abstract Co-Author) Consultant, Eigen Consultant, GTx, Inc Consultant, Bayer AG Consultant, Healthtronics, Inc Speaker, Johnson & Johnson Investigator, STEBA Biotech NV Royalties, Reed Elsevier ABSTRACT Purpose/Objective(s): The optimal radiation schedule for the curative treatment of prostate cancer remains unknown. Prostate cancer patients receiving definitive external beam radiation therapy (EBRT) are typically treated 5 days per week for 7-9 weeks. This prolongation of treatment time increases healthcare costs and is less convenient for patients. There is data supporting the notion that the a/ß ratio for prostate cancer cells is between 1 and 3, suggesting a clinical benefit to hypofractionation. We therefore conducted a Phase I dose escalation trial in men with low to low-intermediate risk prostate adenocarcinoma.Materials/Methods: All men with clinical T1-2c, Gleason Score (GS) 6, prostate cancer with a prostatic specific antigen (PSA) less than 10 ng/dL were eligible for this trial. Men with clinical T1-2c, GS 7 prostate cancer and/or PSA 10 - 20 ng/dL were included provided the biopsy demonstrated low volume disease (Results: From June, 2012 to December, 2014, 9 patients were accrued to the three dose cohorts with a median follow-up of 11 months (range: 2 – 30). Patients had a median age of 63, pre-treatment PSA of 4.9 ng/dL, and pre-treatment AUA score of 10. Four patients had a GS of 7. The maximum tolerated dose (MTD) was 57.6 Gy with all patients completing treatment with less than or equal to grade 2 maximum gastrointestinal, genitourinary, dermatologic or fatigue related toxicity (Table 1). Six patients have at least 1 PSA post-treatment (3 months after completion) with a median PSA decrease of 65%. One patient of the six with > 11 month follow-up had grade 2 rectal telangiectasia requiring minor endoscopic cautery. The remaining 5 patients had no grade 2 toxicity thus far.Conclusion: All three dose levels were well tolerated with no MTD identified. Further follow-up is warranted for long term toxicity and efficacy.Table 1: Acute toxicity in patients undergoing hypofractionated radiation.Grade of ToxicityCTCAE v. 4.0Dose Level 154 Gy/ 18 Fxn = 3Dose Level 255.8 Gy/ 18 Fxn = 3Dose Level 357.6 Gy/ 18 Fxn = 3Gastrointestinal023011032000Genitourinary000212312100Dermatitis0333Fatigue03111022 MSRO42-03 Robotic Stereotactic Body Radiation Therapy for Organ Confined Prostate Cancer W ednesday, Dec. 2 10:50AM - 11:00AM Location: S103CD Participants Jonathan A. Haas, MD, Mineola, NY (Presenter) Speaker, Accuray Incorporated Aaron E. Katz, MD, Garden City, NY (Abstract Co-Author) Nothing to Disclose Seth Blacksburg, MD, MBA, New York, NY (Abstract Co-Author) Speakers Bureau, Bayer AG; Owen Clancey, PhD, Mineola, NY (Abstract Co-Author) Nothing to Disclose Michael Santoro, MD, East Meadow, NY (Abstract Co-Author) Nothing to Disclose Richard Ashley, MD, Garden City, NY (Abstract Co-Author) Nothing to Disclose Dimitri Kessaris, MD, Manhasset, NY (Abstract Co-Author) Nothing to Disclose Robert Mucciolo, MD, Massapequa, NY (Abstract Co-Author) Nothing to Disclose Astrid Sanchez, Mineola, NY (Abstract Co-Author) Nothing to Disclose Diane Accordino, RN, Mineola, NY (Abstract Co-Author) Nothing to Disclose Susan Lowery, BA, Mineola, NY (Abstract Co-Author) Nothing to Disclose William Macmelville, Mineola, NY (Abstract Co-Author) Nothing to Disclose Christopher Mendez, BA, Mineola, NY (Abstract Co-Author) Nothing to Disclose Matthew R. Witten, PhD, Mineola, NY (Abstract Co-Author) Nothing to Disclose ABSTRACT Purpose/Objective(s): The unique radiobiology of prostate cancer supports a hypofractionated as opposed to a conventionally fractionated dose regimen with a potential for improved outcomes and reduced toxicities. We report on our continued experience using a robotic linear accelerator to deliver stereotactic body radiation therapy for localized prostate cancer.Materials/Methods: From April 2006 through December 2014, a total of 1207 patients with localized carcinoma of the prostate were treated with robotic stereotactic body radiation therapy at a single institution. All patients had T1c to T2b disease. 493 patients had low risk disease. 548 patients had intermediate risk disease. 166 patients had high risk disease. Pretreatment PSAs ranged from .77 to 205. 126 patients received hormonal therapy prior to treatment at the discretion of their urologist. Treatment planning was done with CT scans fused with an MRI scan except in 31 cases where an MRI scan could not be done for medical reasons such as a pacemaker. Dose was prescribed to the 83% to 87% line, 5 mm beyond the capsule except posteriorly 3 mm. 1037 patients with low and intermediate risk disease received CyberKnife only to a dose of 3500 to 3625 cGy over 5 fractions. All patients received 1500 mg of amifostine intrarectally 50 minutes prior to each treatment fraction.Results: The median initial PSA was 6.2. The median follow-up was 33 months. The median post treatment PSA is 0.35. At the time of last follow-up, 12 patients have had a PSA failure by Phoenix biochemical definition. 1 patient with low risk disease failed. 7 patients with intermediate risk disease failed and 4 patients with high risk disease failed. There were 136 patients with a minimum follow up of at least 36 months and 56 patients with a minimum follow up of at least 48 months. There are 26 patients with a minimum follow up of 60 months. 272 patients achieved a PSA below 0.2 and 413 patients reached a PSA below 0.4. The median treatment PSA at 12 months is 0.90. The median PSA at 24 months is 0.45. The median PSA at 36 months is 0.40. the median PSA at 48 months is 0.25. The median treatment PSA at 60 months is 0.20. With a median follow up of 33 months, the biochemical disease free survival for low risk, intermediate risk, and high risk was 99.7%, 98.7%, and 97.5% respectively. 2 patients had symptomatic hematuria which resolved with hyperbaric oxygen. 2 patients required green light laser for urinary retention. 1 patient has required catheterization. 3 patients had rectal bleeding which resolved with rowasa enemas and hyperbaric oxygen.Conclusion: Stereotactic body radiation therapy using a robotic linear accelerator continues to be extremely well tolerated and efficacious in the management of localized prostate cancer. High rates of local control can be achieved while also achieving low rates of bladder and rectal toxicity. This study confirms prior reported series with a larger number of patients. MSRO42-04 The Effect of Radiation Timing on PSA Reduction in High Risk Prostate Cancer Patients Treated with Definitive Radiation Therapy W ednesday, Dec. 2 11:00AM - 11:10AM Location: S103CD Participants Apar Gupta, Boston, MA (Presenter) Nothing to Disclose Steven Vernali, Boston, MA (Abstract Co-Author) Nothing to Disclose Ankit Agarwal, BS, Boston, MA (Abstract Co-Author) Nothing to Disclose Muhammad M. Qureshi, MBBS,MPH, Boston, MA (Abstract Co-Author) Nothing to Disclose Alexander E. Rand, BA, Boston, MA (Abstract Co-Author) Nothing to Disclose Ariel E. Hirsch, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose ABSTRACT Purpose/Objective(s): We previously found that neither time to treatment (TTT) nor elapsed time of treatment (ETT) had any effect on PSA velocity in patients with low- and intermediate-risk prostate cancer. In this analysis, we sought to examine the effects of TTT and ETT on PSA change in patients with high-risk prostate cancer.Materials/Methods: We performed a retrospective review of 1,584 patients who were diagnosed with prostate cancer at our institution between January 2005 and December 2013, and found 412 patients with non-metastatic disease who completed treatment with definitive external beam radiation therapy (EBRT). A total of 146 patients who also received concurrent androgen-deprivation therapy (ADT) were included in the analysis. TTT was calculated as days between positive prostate biopsy and EBRT start date, and ETT was calculated as days between EBRT start and stop date. Demographic data on race/ethnicity, primary language spoken, insurance status, marital status, and age were also collected. Analysis of variance was performed to analyze the relationship of these factors with absolute and percentage change in pre- and post-EBRT PSA levels. Data were analyzed using a 0.05 level of significance.Results: Median age at diagnosis was 67 years (range 50-85 years); 11% had a Gleason score (GS) of 6, 49% GS 7, and 40% GS 8-10. Median TTT was 134 days and median ETT was 62 days. No demographic variable was found to be significantly related to absolute or percentage change in PSA. No optimal threshold of days from diagnosis to treatment (TTT) was identified to predict change in PSA level. ETT was significantly related to PSA change, after adjusting for demographic variables. Those who fell in the upper quartile of ETT (>64 days) were found to have a 94.2% decline in PSA, compared to 98.0% for those who fell in the lower three quartiles (p=0.03).Conclusion: A delay in treatment prior to starting EBRT did not have an effect on post-EBRT PSA level, relative to initial PSA level. However, a delay during EBRT was related to a lesser reduction in PSA decline. Further research is warranted in this area to elucidate the clinical significance of differences in PSA reduction. MSRO42-05 Patient Inversion Therapy for Bowel (PITB) to Achieve Maximum Displacement in Radiotherapy for Prostate Cancer W ednesday, Dec. 2 11:10AM - 11:20AM Location: S103CD Participants Gordon L. Grado, MD,PhD, Scottsdale, AZ (Abstract Co-Author) Nothing to Disclose David Constantinescu, Charleston, IL (Presenter) Nothing to Disclose Scott Thompson, CMD, Scottsdale, AZ (Abstract Co-Author) Nothing to Disclose Carrie S. Petrone, RN, Scottsdale, AZ (Abstract Co-Author) Nothing to Disclose Mary M. Grado, BSN,MS, Scottsdale, AZ (Abstract Co-Author) Nothing to Disclose Michael C. Grado, BA, Scottsdale, AZ (Abstract Co-Author) Nothing to Disclose Thayne Larson, MD, Scottsdale, AZ (Abstract Co-Author) Research Consultant, NxThera, Inc PURPOSE The purpose of this study was to evaluate a new and novel approach to the valuation and reduction of small bowel volume from the irradiated fields in the treatment of prostate cancer. This technique utilizes inversion therapy to either completely displace small or large bowel from the irradiated field or to significantly reduce the volume of bowel irradiated in the PTV. This procedure has potential application in multiple areas of abdominal and pelvic radiation therapy. METHOD AND MATERIALS Between January 2014 and March 2015, 14 consecutive patients were identified where small or large bowel was directly within the irradiated PTV. Patients were evaluated with bladder distention, patient positioning, and inversion therapy to displace bowel from the irradiated PTV. Inversion therapy had the greatest effect in displacing and maintaining displacement of bowel from the irradiated volume. Several inversion tables were evaluated prior to the procedure and the two safest devices with the most clinical experience for inversion therapy were selected for this trial. Dose volume histograms were compared with and without inversion. RESULTS Patients were identified with loops of bowel directly within the radiated field due to previous surgery or anatomy. Standard techniques for bowel displacement (patient positioning, bladder distention, belly-board), were ineffective at displacing sufficient bowel from the irradiated volume to affect greater radiation dose delivery. Inversion therapy was selected for bowel displacement which when combined with bladder distention maintained the displacement during the course of radiation therapy. 13/14 patients were found to have sufficient bowel displacement to allow greater radiation dose delivery to the PTV without compromising field size or prescribed dose. 1/14 patients did not benefit from this technique. CONCLUSION Patient inversion therapy for bowel (PITB) achieved excellent bowel displacement for radiation therapy to the pelvis. In these patients, neither the radiation therapy field nor the prescribed dose had to be compromised. Patients also had fewer bowel and bladder symptoms during the pelvic radiation therapy. This technique is determined to be useful, easily applicable, and well tolerated by patients. CLINICAL RELEVANCE/APPLICATION This procedure permits higher radiation therapy dose delivery to the PTV with fewer side effects and morbidity due to less small/large bowel volume irradiated. MSRO42-06 Institutional Experience of Long-term (10-15 Years) Results with High Dose Rate (HDR) Salvage Therapy for Recurrent Prostate Cancer W ednesday, Dec. 2 11:20AM - 11:30AM Location: S103CD Participants Nevine M. Hanna, MD, Sandy, UT (Presenter) Nothing to Disclose ABSTRACT Purpose/Objective(s): Limited treatments are available for recurrent prostate cancer patients. Modality selection can be challenging for both the patient and their physicians. HDR brachytherapy has been used extensively as a boost after external beam radiation therapy, but is increasingly being tested as salvage treated for locally recurrent prostate cancer. We report our long-term results for HDR salvage brachytherapy in patients with initially low, intermediate, and high risk prostate cancer.Materials/Methods: Patients (n=27) with a median age of 71 (57-84) years at recurrence with low- (n=10), intermediate- (n=8), and high-risk prostate cancer (n=9) treated at the California Endocurietherapy (CET now at UCLA) between 1991 and 2009 were analyzed. Median HDR brachytherapy dose prescription was 36 (22-46) Gy in 6 (3-8) fractions. Five patients did receive additional external beam radiation therapy (EBRT) after HDR brachytherapy to an EBRT dose of 36 (36-50) Gy. Presenting disease characteristics were median recurrent PSA 8.1 (1.4-86.7) ng/mL, Gleason Score 7 (5-10), median prostate volume 23.2 (0-80) cc. Androgen deprivation therapy (ADT) was administered in 68% for a median of 6 (3-96) months. Risk groups were defined according to the NCCN guidelines. Sustained PSA nadir+2 was used to define biochemical relapse. Statistical analyses being performed are to include Kaplan-Meier analyses and univariate and multivariate Cox proportional analyses.Results: Preliminary analysis shows that the median overall follow-up time was 6.90 (0.30-15.92) years. The 5, 10 and 15 year overall survival (OS) rates were 86%, 36% and 11%, respectively. The 5, 10 and 15 year distant metastases-free survival (DMFS) rates were 68%, 29% and 11%, respectively. Biochemical progression free survival (BPFS) for the initially presenting low, intermediate and high grade patients is 122, 59, and 41 months, respectively. On univariate analyses, BPFS after salvage HDR was most significantly impacted by PSA at recurrent diagnosis (p=0.007) but not significantly affected by risk group at initial diagnosis (P>0.05). Univariate Cox analyses and multivariate analyses are currently underway to determine the impact of ADT on these parameters.Conclusion: Our long-term data validates HDR salvage brachytherapy in recurrent prostate cancer patients as a standard treatment option which offers excellent rates of disease control. MSRO42-07 Designing and Implementing an Innovative Phantom-Based Simulator Training Program for Prostate Brachytherapy Using Advanced Magnetic Resonance Imaging W ednesday, Dec. 2 11:30AM - 11:40AM Location: S103CD Awards Trainee Research Prize - Resident Participants Nikhil G. Thaker, MD, Houston, TX (Presenter) Nothing to Disclose Tze Yee Lim, Houston, TX (Abstract Co-Author) Nothing to Disclose Rajat Kudchadker, Houston, TX (Abstract Co-Author) Nothing to Disclose Tharakeswara K. Bathala, MD, Houston, TX (Abstract Co-Author) Nothing to Disclose Thomas Pugh, Houston, TX (Abstract Co-Author) Nothing to Disclose Usama Mahmood, Houston, TX (Abstract Co-Author) Nothing to Disclose Deborah A. Kuban, MD, Houston, TX (Abstract Co-Author) Nothing to Disclose Teresa Bruno, Houston, TX (Abstract Co-Author) Nothing to Disclose Jihong Wang, PhD, Houston, TX (Abstract Co-Author) Nothing to Disclose R. Jason Stafford, PhD, Houston, TX (Abstract Co-Author) Nothing to Disclose Thomas A. Buchholz, MD, Houston, TX (Abstract Co-Author) Nothing to Disclose S J. Frank, MD, Houston, TX (Abstract Co-Author) Board Member, C4 Imaging LLC; Stockholder, C4 Imaging LLC; Advisory Board, Elekta AB PURPOSE Prostate brachytherapy (PB) is a well-established treatment for localized prostate cancer and has the potential to deliver excellent outcomes at low cost. However, high-quality PB requires hands-on training and expertise in image-guidance, which is minimally emphasized in current radiation oncology training. Additionally, MRI holds promise of improving target delineation over CT imaging. Our objective was to design and implement a unique pilot training program that utilizes advanced MRI and a phantom simulator approach to improve the quality of PB education. METHOD AND MATERIALS Our existing PB phantom simulator program was adapted to introduce MRI treatment planning and post-implant evaluation. The simulator program emphasized six core areas: patient selection, simulation, treatment planning, implantation, treatment evaluation, and outcome assessment. Trainees in the simulator program were residents, fellows, or physicists. The program utilized the Iodine125 pre-operative planning technique and a transrectal ultrasound device to implant prostate phantoms. MRI markers were substituted for spacers to allow for visualization. RESULTS Forty one trainees have completed the phantom simulator program to date. Ten implants were successfully conducted during the MRI-phantom simulator pilot program. MRI 3DT2 CUBE sequence could adequately delineate the prostate, seminal vesicles, rectum and bladder in the CIRS 053MM phantom. Dummy seeds could be well-visualized with post-implant CT scans. However, seed identification on MRI required a learning curve due to the need to identify MRI markers, which flanked each dummy seed (Figure). The MRI markers facilitated detection of up to 97% of seeds in implanted phantoms by identifying the signal voids between MRI markers. CONCLUSION This proof-of-principle educational curriculum successfully adapted a phantom simulator training program to implement advanced MRI simulation, treatment planning, and post-implant dosimetry. Analysis of implants showed that most organs could be adequately visualized with MRI and that most seeds could be identified with the aid of MRI markers. Phantom-based simulator training programs can provide a valuable educational opportunity to learn the PB process and to learn how to implement advanced image-guidance. CLINICAL RELEVANCE/APPLICATION Phantom-based simulator training can enhance practical expertise with advanced imaging technology and image-guide therapies. MSRO42-09 Stereotactic Body Radiation Therapy for Primary Lesion of Renal Cell Carcinoma W ednesday, Dec. 2 11:50AM - 12:00PM Location: S103CD Participants Hotaka Nonaka, Chuo, Yamanashi, Japan (Presenter) Nothing to Disclose ABSTRACT Purpose/Objective(s): We assessed the efficacy and toxicity of stereotactic body radiation therapy (SBRT) for primary lesion of renal cell carcinoma (RCC).Materials/Methods: We retrospectively reviewed 9 patients (7 male and 2 female) with stage I RCC treated with SBRT between 2007 and 2014. The diagnosis of RCC was judged according to imaging. The median age was 73 years old (range, 59-79). Three patients had high serum creatinine level before SBRT. Four patients had history of prior contralateral nephrectomy. The median diameter of tumor was 18 mm (range, 9-26). A total dose of 60-70 Gy in 10 fractions was administered at the 95% of planning target volume or internal target volume. Median biologically effective dose was 119 Gy (range 96-119), using an a/ß value of 10 Gy. Overall survival (OS) and local progression-free survival (LPFS) were based on Kaplan Meier estimates. Toxicity was scored according to NCI-CTCAE, version 4.0. Renal disorder was graded by referring to pretreatment renal function.Results: The median follow-up duration after SBRT was 28 months (range, 11-89). Clinical response was partial response (PR) in 5 tumors, stable disease (SD) in 4 tumors. Five tumors with PR has decreased gradually in size for 11-56 months (median, 42) after SBRT. Three patients developed distant metastases. The 2- and 3- year OS rate were 85.7% and 64.3%, respectively (median survival time, 44 months). The 3- year LPFS rate was 100%. In a case of a patient with SD tumor, autopsy was performed at 29 months after SBRT, and it showed almost complete necrosis of tumor tissues with a small amount of viable renal carcinoma cells. Three patients developed Grade 3 chronic kidney disease (CKD), 1 had Grade 2 CKD. All patients with Grade 3 CKD had high serum creatinine level before SBRT, and 2 of these patients had prior contralateral nephrectomy before SBRT. Severe toxicity for other organs at risk was not observed.Conclusion: SBRT for primary lesion of RCC resulted in acceptable LPFS and toxicity. Because of slow tumor response, we need long-term follow up to observe the effect of SBRT for RCC. Multicenter prospective study is mandatory to evaluate true local effect and toxicity and to compare SBRT versus other local treatment modalities for RCC. SSK08 Genitourinary (Functional Imaging of the Kidneys) W ednesday, Dec. 2 10:30AM - 12:00PM Location: E450B GU MR US AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Harriet C. Thoeny, MD, Bern, Switzerland (Moderator) Nothing to Disclose Zhen J. Wang, MD, Hillsborough, CA (Moderator) Nothing to Disclose Sub-Events SSK08-01 Assessing the Role of Quantification of Shear Wave Velocity and Tissue Elasticity in the Detection of Interstitial Fibrosis within the Transplant Kidney W ednesday, Dec. 2 10:30AM - 10:40AM Location: E450B Participants David Ferguson, MBBCh, Vancouver, BC (Presenter) Nothing to Disclose Amdad M. Ahmed, MBChB, FRCR, Birmingham, United Kingdom (Abstract Co-Author) Nothing to Disclose Mohammed F. Mohammed, MBBS, Vancouver, BC (Abstract Co-Author) Nothing to Disclose Caitlin Schneider, Vancouver, BC (Abstract Co-Author) Nothing to Disclose Christopher Nguan, Vancouver, BC (Abstract Co-Author) Nothing to Disclose Alison C. Harris, MBChB, Vancouver, BC (Abstract Co-Author) Nothing to Disclose PURPOSE Novel ultrasound techniques allow for the assessment of tissue fibrosis. One such technique ('Virtual Touch IQ') allows for both qualitative and quantitative measurement of shear wave velocity to assess tissue strain and detect underlying fibrosis. Using this technique, in the setting of renal allograft failure, we aim to compare the gold standard of renal biopsy and histological grade with that of shear wave velocity measurement to evaluate for potential underlying interstitial fibrosis. METHOD AND MATERIALS Patients undergoing renal biopsy for renal graft dysfunction within the ultrasound department were enrolled prospectively over an eight-month period. In addition to routine routine renal ultrasound with Doppler imaging, shear wave velocity measurements using 'Virtual Touch IQ' were obtained from the target area for renal cortical biopsy. Sufficient magnitude of the shear wave was confirmed on quality display. Biopsies were performed and reviewed by a nephropathologist, blinded to the imaging results, with histological categorization according to the Banff classification.Shear wave velocities and histological grade were compared to determine significance. Statistical analysis was performed using the Mann Whitney test and Spearman-correlation-coefficient (rho). RESULTS Fourteen patients were identified and subcategorized according to the Banff category with respect to interstitial fibrosis as normal (n=4), grade 1(n=4), grade 2 (n=3) and grade 3(n=3). Median shear wave velocity was demonstrated to be significantly higher in renal transplants with biopsy proven interstitial fibrosis (median=2.512m/s) than those without interstitial fibrosis (median=1.925m/s) (Mann Whitney U=4, n1=4, n2=10, p<0.05). Positive correlation was also identified between the mean shear wave velocity and Banff categories (rho= 0.731, p=0.003). CONCLUSION Preliminary data indicates that shear wave velocity within cortex of the transplant kidney correlates significantly with interstitial fibrosis in the context of renal allograft failure. CLINICAL RELEVANCE/APPLICATION Shear wave velocity analysis is a potentially valuable non-invasive tool to assess for renal allograft interstitial fibrosis. SSK08-02 Improved Temporal Resolution and Image Contrast for Kidney DCE-MRI by 3D Spoiled Gradientrecalled Echo Sequence with Compressed Sensing W ednesday, Dec. 2 10:40AM - 10:50AM Location: E450B Participants Kai Zhao, PhD, Beijing, China (Presenter) Nothing to Disclose Bin Chen, Beijing, China (Abstract Co-Author) Nothing to Disclose Jue Zhang, Beijing, China (Abstract Co-Author) Nothing to Disclose Xiaoying Wang, MD, Beijing, China (Abstract Co-Author) Nothing to Disclose PURPOSE To verify the feasibility of combine Compressed Sensing (CS) technique in dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) of kidney METHOD AND MATERIALS Nine healthy New Zealand rabbits underwent kidney DCE-MRI studies on a clinical 3.0T MR scanner. 3D spoiled gradient-recalled echo sequence modified with CS scheme was scanned before and after the administration of 0.05 mmol/kg of Gd-DTPA with the following parameters: TR = 3.3ms, TE = 1.3ms, FA = 15°, slice thickness = 3 mm, matrix =128×128, FOV = 180mm and 16 slices were acquired. Four accelerations (2-x, 3-x, 4-x, 8-x) were scanned as well as the fully sampling every other day for each animal in DCE MR imaging. The contrast-to-noise ratio (CNR) and signal-to-noise ratio (SNR) of the reconstructed images of the kidney were analyzed and compared to that of the fully sampled images separately. RESULTS The images with 2-X, 3-X, 4-X, 8-X CS acceleration and fully sampled results were shown from row 1 to row 5. The 8-X accelerated images appeared blurring which may due to the loss of a mass of high frequency information (Figure 1).Signal intensity curves of cortex and medulla were represented in Figure 2. The reconstructions of 8-X were also blurring.Superior CNR performance between cortex and tissue CNR_ct, and medulla and tissue CNR_mt were found for all the time points after contrast administration. CNR_ct of CS reconstructed images were significantly larger than that of the conventional fully sampled images at all accelerations throughout the enhancement (p<.01 for 2-X; p<.001 for 3-X and 4-X). CNR_mt of CS reconstructed images were also significantly larger than that of the fully sampled images (p<.01 for 2-X; p<.001 for 3-X and 4-X). CNR_cm measured from cortical and medullary regions were larger in CS reconstructed images, especially at the initial time of enhancement: 44.00 10.0 for 2-X, 43.30 8.0 for 3-X and 49.78 14.9 for 4-X vs. 15.28 6.7 for 1-X (p<.001 for all) (Table 1).In SNR analysis, SNR-cortex (SNR_c) and SNR-medulla (SNR_m) of CS reconstructed images were all found statistically different from conventional fully sampled images (p<.001) (Table 2). CONCLUSION Compressed sensing is a feasible and promising acceleration method to improve temporal resolution and image contrast in renal DCE-MRI. CLINICAL RELEVANCE/APPLICATION CS is a promising imaging method with both improved temporal resolution and image contrast, which will be widely used in the future. SSK08-03 Noninvasive Evaluation of Stable Renal Allograft Function Using Shear-Wave Elastography W ednesday, Dec. 2 10:50AM - 11:00AM Location: E450B Participants Jung Jae Park, MD, Seoul, Korea, Republic Of (Presenter) Nothing to Disclose Chan Kyo Kim, MD, PhD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Beom Jun Kim, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Byung Kwan Park, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose PURPOSE Protocol renal allograft biopsies improve outcomes via early detection and treatment of subclinical rejection (SCR). Shear-wave elastography (SWE) assesses quantitatively the tissue elasticity. The aim of our study was to investigate the feasibility of SWE in evaluating patients with stable renal allograft function who underwent protocol biopsies. METHOD AND MATERIALS 95 patients (mean age, 48.3 years; range, 21-73 years) with stable renal allograft function who underwent ultrasound (US)-guided protocol biopsies at 10 days or 1 year after transplantation were enrolled in this retrospective study. All US and elasticity examinations of renal allograft were performed by a commercial scanner using a convex transducer (C5-1 ElastoPQ, Philips iU 22). SWE was performed immediately before protocol biopsies. Tissue elasticity (kPa) in the cortex was measured for all renal allografts. Clinical and US variables were compared between patients with SCR and without SCR using the Student t -test. The correlation between estimated glomerular filtration rate (eGFR) and tissue elasticity was evaluated in all patients by Pearson correlation. Diagnostic performance of tissue elasticity to distinguish between patients with SCR and without SCR was analyzed using a receiver operating characteristics (ROC) curve analysis. RESULTS Acute rejection (AR) was pathologically confirmed in 34 patients. The mean tissue elasticity of ARs (31.0 ± 12.8 kPa) was statistically greater than that no ARs (24.5 ± 12.2 kPa) ( P < 0.001), while the resistive index values did not show statistical difference between ARs and no ARs ( P = 0.112). Clinical variables including age, kidney size, creatinine and eGFR revealed statistical differences between ARs and no ARs ( P < 0.05). Tissue elasticity demonstrated a moderate negative correlation with eGFR (correlation coefficient= -0.604, P < 0.001). At ROC curve analysis, the area under the curve (AUC) of tissue elasticity was 0.651 and followed eGFR (AUC= 0.728). CONCLUSION SWE, as a noninvasive tool, may be feasible in distinguishing between allograft with SCR and without SCR in patients with stable renal function. Moreover, it may demonstrate functional state of renal allografts. CLINICAL RELEVANCE/APPLICATION As a feasible technique, shear-wave elastography may help to noninvasively assess functional state of patients with stable renal allograft function. SSK08-04 Assessment of Renal Allograft Function Early after Transplantation Using Renal IVIM with Healthy as Control W ednesday, Dec. 2 11:00AM - 11:10AM Location: E450B Participants Lihua Chen, Tianjin, China (Presenter) Nothing to Disclose Tao Ren, Tianjin, China (Abstract Co-Author) Nothing to Disclose Wen Shen, Tianjin, China (Abstract Co-Author) Nothing to Disclose Panli Zuo, Beijing, China (Abstract Co-Author) Nothing to Disclose PURPOSE Graft dysfunction is a common complication following transplantation,which is associated with allograft survial. Intravoxel incoherent Graft dysfunction is a common complication following transplantation,which is associated with allograft survial. Intravoxel incoherent motion (IVIM) has potential to assess renal function in patients with renal and allograft dysfunction. The purpose of the current study in renal allografts early after transplantation was to investigate relationship between estimated glomerular filtration rate (eGFR) and diffusion and perfusion parameters calculated using IVIM imaging, compared with healthy kidney, and to gain the sensitive IVIM parameters for monitoring allograft function. METHOD AND MATERIALS A total of 71 subjects were performed on a 3.0T MRI scanner (MAGNETOM Trio, a Tim system, Siemens AG, Erlangen, Germany) using IVIM sequence with 11 b values( 0, 10, 20, 40, 60, 100, 150, 200, 300, 500, and 700 s/mm2 ). Subjects were divided into 3 groups: group 1, healthy volunteers (n=19); group 2, allografts with good allograft function(eGFR≥60mL/min/1.73m2, n=33); group 3, allografts with impaired allograft function(eGFR<60mL/min/1.73m2, n=19).To separate the perfusion and diffusion, a biexponential fit was used to calculate the diffusion coefficient of slow (ADCslow); the diffusion coefficient of fast (ADCfast) and perfusion fraction (FP). Differences in IVIM parameters between the cortex and medulla in each group were compared using paired samples t test. Differences of IVIM parameters between three groups were compared using LSD test.Relationships between eGFR and IVIM parameters were assessed using spearman correlation coefficient. RESULTS The ADC, ADCslow, Fp values of renal cortex were significantly higher in group 1 and group 2 compared to group 3(all p<0.01). The ADC, ADCslow values of renal medulla were significantly higher in group 1 and group 2 compared to group 3(all p<0.01). For allografts, significant differences in ADC, ADCslow, FP values of renal cortex and ADC, ADCslow values of renal medulla were observed between group 2 and group 3. In renal allografts, there was a significant positive correlation between eGFR and ADC, ADCslow , Fp value of cortex, ADC, ADCslow value of medulla(all p<0.05). CONCLUSION The ADC, ADCslow, FP values of renal cortex and ADC, ADCslow values of renal medulla may be useful for detect renal allograft dysfunction. IVIM technique is a reliable imaging for evaluating and monitoring allograft function. CLINICAL RELEVANCE/APPLICATION IVIM technique can be used to evaluate and monitor allograft function SSK08-05 Renal Hemodynamics and Oxygenation Evaluated by ASL, BOLD and Oxygen Extraction Fraction (OEF) Imaging in Animal Model of Diabetic Nephropathy W ednesday, Dec. 2 11:10AM - 11:20AM Location: E450B Awards Trainee Research Prize - Medical Student Participants Rui Wang, PhD, Beijing, China (Presenter) Nothing to Disclose Xiaoying Wang, MD, Beijing, China (Abstract Co-Author) Nothing to Disclose Xuedong Yang, Beijing, China (Abstract Co-Author) Nothing to Disclose Kai Zhao, PhD, Beijing, China (Abstract Co-Author) Nothing to Disclose Xueqing Sui, Beijing, China (Abstract Co-Author) Nothing to Disclose Zhiyong Lin, Beijing, China (Abstract Co-Author) Nothing to Disclose PURPOSE To investigate the feasibility of evaluating renal hemodynamics and oxygenation changes by arterial spin labeling (ASL), blood oxygen level dependent (BOLD) and oxygen extraction fraction (OEF) imaging in diabetic nephropathy (DN) rabbits. METHOD AND MATERIALS Seventeen New Zealand rabbits were divided into 2 groups: DN group, 12 rabbits with intravenously injection of alloxan at 100 mg/kg; and control group, 5 rabbits with injection of same dosage of 0.9% saline. At 72hr after the injection, blood glucose level was tested for all. Rabbits with blood glucose level higher than 16.0 mmol/L were considered as successfully established of diabetes mellitus (DM) model. MR examination was performed at 3T MR scanner (GE) with an 8-channel knee coil. For each rabbit, 2 times of MR exam were performed: baseline (before injection) and 72hr after model established successfully. ASL imaging was conducted with the labeling strategy of flow-sensitive alternating inversion recovery (FAIR) and BOLD was conducted with multiple gradient echo (mGRE) sequence. The measurement of renal OEF was derived from Yoblonsky's model with multi-echo gradient and spin echo (MEGSE) sequence. Then the rabbits were sacrificed for pathological study of the kidney. Quantitative RBF, R2* and OEF values were obtained within manually drawn ROIs, including cortex (CO) and outer medulla (OM). One-way ANOVA and paired-sample T test was performed to test the differences of RBF, R2* and OEF for inter- and inner-group. RESULTS Ten of 12 rabbits in DN group were successfully established DM model and renal pathological damages can be observed in these rabbits. There was no statistically significant difference of RBF, R2* or OEF between two groups at baseline (p>0.05). Compared with baseline, R2* and OEF in OM at 72 hr was significantly increased in DN group (p=0.018 and 0.048, respectively), while the control group was not (p>0.05). In CO, R2* also elevated significantly at 72 hr compared with baseline (p=0.04). For control group, there was no significant difference in CO or OM between baseline and 72 hr (p>0.05). CONCLUSION The combination of ASL, BOLD and OEF MRI may enable a comprehensive assessment of the functional status of early DN pathophysiological changes. CLINICAL RELEVANCE/APPLICATION It would be valuable for clinicians to early detect renal pathophysiological changes for diabetes without symptoms. SSK08-06 Diffusion Weighted Imaging and Diffusion Tensor Imaging for Detection of Acute Kidney Injury in Patients Following Lung Transplantation W ednesday, Dec. 2 11:20AM - 11:30AM Location: E450B Participants Susanne Tewes, MD, Hannover, Germany (Presenter) Nothing to Disclose Gregor Warnecke, Hannover, Germany (Abstract Co-Author) Nothing to Disclose Mi-Sun Jang, Hannover, Germany (Abstract Co-Author) Nothing to Disclose Dagmar Hartung, MD, Hannover, Germany (Abstract Co-Author) Nothing to Disclose Matti Peperhove, MD, Hannover, Germany (Abstract Co-Author) Nothing to Disclose Marcel Gutberlet, Dipl Phys, Hannover, Germany (Abstract Co-Author) Nothing to Disclose Christine Fegbeutel, Hannover, Germany (Abstract Co-Author) Nothing to Disclose Bjoern Juettner, Hannover, Germany (Abstract Co-Author) Nothing to Disclose Axel Haverich, Hannover, Germany (Abstract Co-Author) Nothing to Disclose Frank K. Wacker, MD, Hannover, Germany (Abstract Co-Author) Research Grant, Siemens AG Research Grant, Pro Medicus Limited Faikah Gueler, MD, Hannover, Germany (Abstract Co-Author) Nothing to Disclose Katja Hueper, Hannover, Germany (Abstract Co-Author) Nothing to Disclose PURPOSE Loss of renal function is a frequent complication after lung transplantation (lutx) and is associated with higher morbidity. Thus, imaging biomarkers to noninvasively monitor renal damage and to guide treatment strategies to preserve renal function are of clinical relevance. The purpose was to evaluate diffusion weighted imaging (DWI) and diffusion tensor imaging (DTI) for detection of renal impairment in lutx-patients. METHOD AND MATERIALS 54 patients 14±2 days after lutx and 12 healthy volunteers underwent MRI on a 1.5T scanner. Respiratory-triggered DWI (10 bvalues, 0-1000 s/mm²) and DTI sequences (20 diffusion direction, b=0,600 s/mm²) were acquired. Maps of apparent diffusion coefficient (ADC) and fractional anisotropy (FA) were calculated. Renal function was monitored daily and acute kidney injury (AKI) was defined according to AKIN-criteria within 48h after surgery. Factors contributing to AKI such as duration of surgery, immunosuppressive drugs and blood product infusion were documented. Statistical analysis comprised ANOVA and correlation analysis. Values are given as mean±SEM. RESULTS 59% (32/54) of lutx-patients developed AKI. ADC of renal medulla was significantly lower in patients with AKI compared to patients without AKI (2.07±0.03 vs 2.17±0.04*10-³ mm²/s, p<0.05) and to healthy volunteers (2.07±0.03 vs 2.21±0.03*10-³ mm²/s, p<0.01). FA-values of renal medulla were significantly reduced compared to healthy volunteers in both groups (AKI: 0.27±0.01, no AKI: 0.28±0.01, healthy: 0.33±0.02, p<0.001), and did not differ between patients with and without AKI. ADC and FA negatively correlated with the amount of blood product infusion (r=-0.41 and r=-0.42, p<0.01) and ADC was correlated with eGFR at the day of MRI (r=-0.52, p<0.001). No correlations with duration of surgery and tacrolimus levels at the day of the MRI were observed. CONCLUSION Diffusion imaging showed significant renal changes in lutx-patients compared to healthy volunteers irrespective of whether AKI was diagnosed according to standard criteria. ADC reduction was stronger in patients with AKI. Amount of blood product infusion correlated with MRI parameters and may be a contributing factor to renal damage following major surgery. CLINICAL RELEVANCE/APPLICATION Diffusion imaging detects renal damage following major surgery and may help to improve patient management to prevent further renal damage. SSK08-07 Evaluation of Ultra-fast, Single Breath-Hold Renal ASL Perfusion-Preliminary Results of Healthy Volunteers W ednesday, Dec. 2 11:30AM - 11:40AM Location: E450B Participants Melissa Ong, MD, Mannheim, Germany (Presenter) Nothing to Disclose Thorsten Honroth, Bremen, Germany (Abstract Co-Author) Research funded, Siemens AG Guenther Matthias, Bremen, Germany (Abstract Co-Author) Research funded, Siemens AG Bernd Kuehn, PhD, Erlangen, Germany (Abstract Co-Author) Nothing to Disclose Stefan O. Schoenberg, MD, PhD, Mannheim , Germany (Abstract Co-Author) Institutional research agreement, Siemens AG Daniel Hausmann, MD, Mannheim, Germany (Abstract Co-Author) Nothing to Disclose PURPOSE Evaluation of 3D ultra-fast, single breath-hold arterial spin labeling magnetic resonance imaging (ASL MRI) for the measurement of renal perfusion. METHOD AND MATERIALS We included 7 (5 male, mean age 29) healthy volunteers who did not suffer from any medical condition. A single-shot pulsed ASL (PASL) prototype sequence with a 3D GRASE readout using background suppression was implemented on a 3.0 Tesla Magnetom Skyra MRI scanner (Siemens Healthcare, Erlangen, Germany). 24 slices with a resolution of 4.7mm x 4.7mm x 4mm were acquired for 4 different inflow times (TI = 750ms, 1000ms, 1250ms, 1500ms) within a single breath-hold of 23s, including an integrated calibration scan (M0). The prototype sequence allowed a multi-slice measurement of the whole kidney in one exam. The exam was performed using a standard 18-channel body matrix coil. No contrast agent was applied. Subjective image quality was rated by two radiologists according to a 5-point Likert-scale (5=excellent; 1=non-diagnostic). Mean renal cortical and medullary blood flow was measured in the upper and lower pole of the kidney. RESULTS All images were rated as diagnostic. Overall image quality was rated as good (4; 25-75% quartile 3-4). Mean cortical perfusion values were 224±28 mL/100mL/min for the upper and 224±37 mL/100mL/min for the lower pole, mean medullary perfusion value ranged between 107±16 mL/100mL/min and 101±14 mL/100mL/min for the upper and lower pole, respectively. CONCLUSION Ultra-fast, single breath-hold renal ASL perfusion in healthy volunteers shows promising results regarding image quality and feasibility. CLINICAL RELEVANCE/APPLICATION Ultra-fast, single breath-hold ASL perfusion facilitates contrast-free creation of parametric perfusion maps, which can be repeated arbitrarily and hence potentially serve to monitor therapy. SSK08-08 Diffusion-weighted Magnetic Resonance Imaging of Kidneys in Patients with Chronic Kidney Disease W ednesday, Dec. 2 11:40AM - 11:50AM Location: E450B Participants Katarzyna M. Sukowska, MD, Warsaw, Poland (Presenter) Nothing to Disclose Piotr Palczewski, MD, Warsaw, Poland (Abstract Co-Author) Nothing to Disclose Agnieszka Furmanczyk-Zawiska, Warsaw, Poland (Abstract Co-Author) Nothing to Disclose Wojciech Szeszkowski, Warsaw, Poland (Abstract Co-Author) Nothing to Disclose Dorota Piotrowska-Kownacka, Warsaw, Poland (Abstract Co-Author) Nothing to Disclose Magdalena Durlik, Warsaw, Poland (Abstract Co-Author) Nothing to Disclose Marek Golebiowski, Warsaw, Poland (Abstract Co-Author) Nothing to Disclose PURPOSE To assess the apparent diffusion coefficient (ADC) values of renal parenchyma in patients in different stages of chronic kidney disease (CKD). To correlate ADC measurements with creatinine blood level, estimated glomerular filtration rate (eGFR), and ADC values obtained from healthy subjects. METHOD AND MATERIALS 20 healthy volunteers and 34 patients in different stages of CKD were examined on a 1.5 unit (Ingenia, Philips, The Netherlands). The inclusion criteria for patients with CKD were: biopsy proven CKD and no hydronephrosis or renal artery stenosis. Blood samples to assess the serum creatinine level were taken immediately before examination. The MR examination included two diffusion weighted sequences: one with 16 b values uniformly distributed from 0 to 750; the other one with 10 b values including 6 low (0150) and 4 high (300-900) b values. ADC values were measured with whole-kidney manually placed region of interest. Statistical analysis was performed using the Statistica software (version 10.0; Statsoft, Inc., US). Unpaired Student's t-test were used to evaluate the differences in ADC. ROC curves were drawn to find out area under the curve for differentiation of CKD groups and cutoff ADC values were calculated so as to achieve the highest average sensitivity and specificity. To investigate the relationship between ADC values and serum creatinine / eGFR, Pearson's correlation coefficient was calculated by bivariate correlation. All P values <0.05 were taken as statistically significant. RESULTS A significant positive correlation between ADC and eGFR and a negative correlation between ADC and creatinine blood level was observed. There were statistical differences between ADC values in healthy individuals and patients in moderate and severe stage of CKD. Based on ADC measurements cut-off values were established allowing for identification of patients with eGFR higher than 60 ml/min/1.73m2 and lower then 30ml/min/1.73m2. CONCLUSION The DWI has a potential role in assessing renal function as ADC values correlate with eGFR and the level of renal damage in severe stages of CKD. CLINICAL RELEVANCE/APPLICATION The ability of DWI to noninvasively assess eGFR may provide an additional tool for monitoring the course of disease and for stratifying the risk of contrast medium administration in patients with CKD. SSK08-09 Intravoxel Incoherent Motion MRI for Differentiating Renal Hypoperfusion from Increased Cellularity after Ischemia-Reperfusion W ednesday, Dec. 2 11:50AM - 12:00PM Location: E450B Participants Mike Notohamiprodjo, Munich, Germany (Presenter) Nothing to Disclose Katharina Stella Winter, Munich, Germany (Abstract Co-Author) Nothing to Disclose Michael Staehler, MD, Munich, Germany (Abstract Co-Author) Nothing to Disclose Andreas D. Helck, MD, Munich, Germany (Abstract Co-Author) Nothing to Disclose Olaf Dietrich, PhD, Munich, Germany (Abstract Co-Author) Nothing to Disclose Moritz Schneider, Munich, Germany (Abstract Co-Author) Nothing to Disclose PURPOSE To differentiate hypoperfusion from inflammatory hypercellularity after renal ischemia-reperfusion due to partial nephrectomy using Intravoxel Incoherent Motion MRI. METHOD AND MATERIALS This IRB approved prospective study was performed according to the declaration Helsinki. 15 patients with renal tumors underwent MR at 3T (Magnetom Verio, Siemens Healthcare) directly before and one week after partial nephrectomy. Diffusion weighted imaging was acquired with an EPI-sequence (10 b-values 0-800 s/mm2, 3 averages, 6 directions). IVIM-analysis was performed with homebuilt software (PMI 0.4, IDL) by biexponential fitting of the tissue Dslow (mm2/s*10-3) and the pseudo-diffusion Dfast (mm2/s*103) as well as the perfusion component f (%). Apparent diffusion coefficient (ADC; mm2/s*10-3) was derived from monoexponential analysis. To compare parameters between baseline and follow-up the paired Wilcoxon signed-rank test and to compare nonnephrectomized and partially nephrectomized kidneys the non-paired Mann-Whitney U test was used. RESULTS In the baseline examination prior to partial nephrectomy there were no significant differences between tumor bearing and contralateral kidney, whereas the follow-up measurement showed significant differences for ADC (p<0.001), Dfast (p=0.02) and most pronounced for f (p<0.001). Partially nephrectomized kidneys showed a significant decrease of ADC (2.5±0.3 vs. 2.3±0.2, p<0.01), Dfast (8.6±1.8 vs. 7.3±1.7, p = 0.02) and again most pronounced for f (19.2±3.0 vs. 13.7±4.4 p < 0.01). There were no significant differences for Dslow (operated kidney 2.0±0.2 vs. 2.0±0.2; contralateral kidney 2.1±0.2 vs. 2.0±0.1) Nonnephrectomized contralateral kidneys expressed a significant increase of ADC (2.5±0.2 vs. 2.7±0.3, p < 0.01), and f (19.3±2.6 vs. 21.5±4.0, p = 0.03). There was no significant correlation of the alteration of each parameter to clamping time. CONCLUSION IVIM detects significant changes, particularly of the perfusion fraction in the operated and contralateral kidney after partial nephrectomy suggesting that ischemia-reperfusion associated diffusion restriction is correlated to hypoperfusion rather than increasing inflammatory cellularity. CLINICAL RELEVANCE/APPLICATION IVIM MRI suggest that renal ischemia-reperfusion associated diffusion restriction is correlated to hypoperfusion rather than increasing inflammatory cellularity. SSK09 Genitourinary (Prostate Imaging and Staging) W ednesday, Dec. 2 10:30AM - 12:00PM Location: N228 GU MR OI AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Andrew B. Rosenkrantz, MD, New York, NY (Moderator) Nothing to Disclose Antonio C. Westphalen, MD, Mill Valley, CA (Moderator) Nothing to Disclose Ronaldo H. Baroni, MD, Sao Paulo, Brazil (Moderator) Nothing to Disclose Sub-Events SSK09-01 Computed Very High B-Value Diffusion-Weighted Imaging of the Prostate: How High Should We Go? W ednesday, Dec. 2 10:30AM - 10:40AM Location: N228 Participants Nainesh Parikh, MD, New York, NY (Presenter) Nothing to Disclose Justin M. Ream, MD, Ann Arbor, MI (Abstract Co-Author) Nothing to Disclose Andrea S. Kierans, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Max X. Kong, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Samir S. Taneja, MD, New York, NY (Abstract Co-Author) Consultant, Eigen Consultant, GTx, Inc Consultant, Bayer AG Consultant, Healthtronics, Inc Speaker, Johnson & Johnson Investigator, STEBA Biotech NV Royalties, Reed Elsevier Andrew B. Rosenkrantz, MD, New York, NY (Abstract Co-Author) Nothing to Disclose PURPOSE To assess the impact of a broad range of computed b-values (1,500-5,000 s/mm2) on prostate cancer detection. METHOD AND MATERIALS 49 patients undergoing 3T prostate MRI before radical prostatectomy were included. Exams included DWI with a maximal acquired b-value of 1,000 s/mm2, from which six computed DWI image sets (b-values ranging from 1,500-5,000 s/mm2) were generated. Two radiologists [R1 (attending), R2 (fellow)] independently evaluated the ADC map as well as each DW image set, blinded to the b-value, to assess dominant lesion location. Pathologic findings from radical prostatectomy served as the reference standard. RESULTS Sensitivity for tumor: R1-82% (ADC), 80% (b1000), 86% (b1500), 88% (b2000), 86% (b2500), 84% (b3000), 76% (b4000), 65% (b5000); R2-71% (ADC), 63% (b1000), 76% (b1500), 71% (b2000), 70% (b2500), 65% (b3000), 57% (b4000), 37% (b5000). Sensitivity for Gleason score≥7 tumor: R1-83% (ADC), 80% (b1000), 93% (b1500), 93% (b2000), 90% (b2500), 90% (b3000), 80% (b4000), 65% (b5000); R2-75% (ADC), 68% (b1000), 80% (b1500), 78% (b2000), 78% (b2500), 70% (b3000), 60% (b4000), 38% (b5000). PPV for tumor: R1-95% (ADC), 95% (b1000), 93% (b1500), 96% (b2000), 98% (b2500), 93% (b3000), 95% (b4000), 87% (b5000); R2-85% (ADC), 82% (b1000), 93% (b1500), 88% (b2000), 92% (b2500), 94% (b3000), 93% (b4000), 75% (b5000). Dominant lesion visual conspicuity (1-5 scale): R1-3.4±1.5 (ADC), 2.5±1.2 (b1000), 3.3±1.4 (b1500), 3.2±1.3 (b2000), 3.2±1.4 (b2500), 3.1±1.4 (b3000), 2.8±1.4 (b4000), 2.7±1.5 (b5000); R2-3.2±1.6 (ADC), 2.1±1.1 (b1000), 3.2±1.5 (b1500), 3.1±1.6 (b2000), 3.0±1.6 (b2500), 2.5± 1.5 (b3000), 1.8±1.0 (b4000), 1.3±0.6 (b5000). Reader confidence (1-5 scale): R1-3.2±1.5 (ADC), 2.6±1.3 (b1000), 3.1±1.4 (b1500), 3.1±1.4 (b2000), 3.1±1.5 (b2500), 3.1±1.5 (b3000), 3.0±1.6 (b4000), 2.8±1.7 (b5000); R23.3±1.7 (ADC), 2.2±1.2 (b1000), 3.2±1.6 (b1500), 3.4±1.7 (b2000), 3.4±1.8 (b2500), 3.1± 1.8 (b3000), 2.6±1.6 (b4000), 1.9±1.3 (b5000). CONCLUSION Computed b-values in the range of 1,500-2,500 s/mm2 were optimal for prostate cancer detection, comparing favorably with the ADC map. b-values of 1,000 or 3,000-5,000 exhibited lower performance. CLINICAL RELEVANCE/APPLICATION Computed b-values of 1,500-2,500 s/mm2 (but not higher) help optimize prostate DWI, thereby facilitating targeted prostate biopsy and tailored treatments based on imaging guidance. SSK09-02 Utility of Apparent Diffusion Coefficient (ADC) in Intermediate Grade (Gleason score 3+4=7) Prostate Cancer Diagnosed at Non-targeted TRUS-guided Needle Biopsy W ednesday, Dec. 2 10:40AM - 10:50AM Location: N228 Participants Radu Rozenberg, MD, Ottawa, ON (Abstract Co-Author) Nothing to Disclose Nicola Schieda, MD, Ottawa, ON (Abstract Co-Author) Nothing to Disclose Shaheed Hakim, Ottawa, ON (Abstract Co-Author) Nothing to Disclose Trevor A. Flood, MD, FRCPC, Ottawa, ON (Abstract Co-Author) Nothing to Disclose Rebecca Thornhill, PhD, Ottawa, ON (Abstract Co-Author) Nothing to Disclose Christopher Lim, MD, Ottawa, ON (Presenter) Nothing to Disclose PURPOSE To determine the ability of ADC analysis to predict Gleason score (GS) upgrading of tumor and extra-prostatic extension (EPE) after radical prostatectomy (RP) in 3+4=7 prostate cancer (PCa). METHOD AND MATERIALS With REB approval, 54 men with GS 3+4=7 PCa at non-targeted TRUS-guided biopsy underwent 3-Tesla MRI and RP between 20122013. Outcomes at RP included: A) upgrading to GS 4+3=7 and B) organ confined disease (OCD). >0.5 mL tumors were contoured by a blinded GU radiologist by correlating ADC to RP histopathology map. Mean ADC, ADC ratio (normalized to peripheral zone), histogram analysis (10th, 25th and 50th centile ADC) and texture analysis features were compared between groups using multivariate analysis, regression modeling and ROC analysis. RESULTS 25.9% (14/54) patients were upgraded to GS 4+3=7 and 51.9% (28/54) patients had EPE after RP. There was no difference in age (p=0.38, 0.85), PSA (p=0.96, 0.95) or % of core biopsies with Gleason pattern 4 (p=0.56, 0.89) between groups. Mean ADC (mm2/sec), ADC ratio, 10th, 25th and 50th centile ADC were similar between GS 3+4=7 (0.94 ± 0.24, 0.58 ± 0.15, 0.77 ± 0.31, 0.94 ± 0.28 and 1.15 ± 0.24) and GS 4+3=7 tumors (0.96 ± 0.20, 0.55 ± 0.11, 0.71 ± 0.26, 0.89 ± 0.19 and 1.11 ± 0.16), p>0.05. 10th centile ADC was lower in tumors with EPE (0.69 ± 0.31 versus 0.82 ± 0.28), p=0.02; with no difference comparing all other conventional ADC parameters, p>0.05. Regression models combining texture features improved prediction of GS upgrade: A) Kurtosis+Entropy+Skewness (AUC 0.76 [SE=0.07], p<0.001; sensitivity 71%, specificity 73%) and B) Kurtosis+Heterogeneity+Entropy+Skewness (AUC 0.77 [SE=0.07], p<0.001); sensitivity 71%, specificity 78%). CONCLUSION Amongst Gleason score 3+4=7 prostate cancers diagnosed at TRUS-guided biopsy, mean ADC and ADC histogram analysis is not predictive of upgrading after RP, while ADC texture-analysis improves accuracy. 10th centile ADC is predictive of EPE. CLINICAL RELEVANCE/APPLICATION Conventional ADC analysis cannot predict upgrading of Gleason score 3+4=7 prostate cancer diagnosed at TRUS-guided biopsy; however, ADC texture-analysis improves accuracy and 10th centile ADC can predict organ confined disease. SSK09-03 High Resolution 3-Tesla Endorectal Prostate MR Imaging: A Multireader Study of Radiologist Preference and Perceived Interpretive Quality of 2D and 3D T2-weighted FSE MR Images W ednesday, Dec. 2 10:50AM - 11:00AM Location: N228 Participants Antonio C. Westphalen, MD, Mill Valley, CA (Presenter) Nothing to Disclose Susan M. Noworolski, PhD, San Francisco, CA (Abstract Co-Author) Nothing to Disclose Saunak Sen, San Francisco, CA (Abstract Co-Author) Nothing to Disclose Mukesh G. Harisinghani, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Kartik S. Jhaveri, MD, Toronto, ON (Abstract Co-Author) Speaker, Bayer AG Steven S. Raman, MD, Santa Monica, CA (Abstract Co-Author) Nothing to Disclose Andrew B. Rosenkrantz, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Zhen J. Wang, MD, Hillsborough, CA (Abstract Co-Author) Nothing to Disclose Ronald J. Zagoria, MD, San Francisco, CA (Abstract Co-Author) Nothing to Disclose John Kurhanewicz, PhD, San Francisco, CA (Abstract Co-Author) Nothing to Disclose PURPOSE The goal of this study was to compare the perceived quality of 3-Tesla axial T2-weighted high-resolution 2D and high-resolution 3D FSE endorectal MR images of the prostate. METHOD AND MATERIALS We studied 85 men (median age=65 years, 46 to 83) with proven or suspected prostate cancer who had endorectal MR imaging with 2D and 3D T2-weighted FSE MR images. Six radiologists from various institutions independently reviewed axial T2 weighted MR images shown individually and paired. Readers identified their preferred images and scored using a 5-point scale their confidence in identifying tumor. They also scored the delineation of the zonal anatomy and capsule, tumor conspicuity, and image quality (artifacts, distortion, and sharpness) using a 3-point scale. We used a meta-analysis routine to calculate pooled estimates based on a random-effects model. A formal analysis of heterogeneity was also done. The presence of heterogeneity is consistent with differences in the readers' scores. We used a mixed effect logistic regression, taking into account the clustering effect, to determine if prior treatment and number of years of reader's experience were predictors of the option for 2D or 3D images. RESULTS Each reader had a strong preference for a given T2-weighted MR sequence, favoring one of the two techniques in at least approximately 70% of cases; but the choices were evenly distributed between the two sequence options. The pooled estimate shows that the 3D image is preferred in about 47% of the times (95% CI=20% to 74%). The choice for one or other techniques was not associated with prior treatment or readers' years of experience. There was no significant difference in confidence in tumor identification (p=0.16 to 1.00). There was no difference in delineation of the zonal anatomy (p=0.19), prostatic capsule (p=0.14), and tumor conspicuity (p=0.89). Similarly, no difference was found when assessing motion artifact (p=0.48) and distortion (p=0.41). 2D FSE images were significantly sharper than 3D FSE (p<0.001), but also more likely to exhibit artifacts not related to motion (p=0.002). CONCLUSION There are strong individual preferences for the 2D or 3D FSE MR images, but a wide variability among radiologists. There were differences in image quality, but not in the sequences' ability to delineate the glandular anatomy and depict cancer. CLINICAL RELEVANCE/APPLICATION 2D and 3D FSE techniques appear to be equally adequate fro clinical use. SSK09-04 Multi-Parametric MRI Performance in Prostate Cancer Detection: Stratified by Gleason Scores and Tumor Size on Whole Mount Histopathology W ednesday, Dec. 2 11:00AM - 11:10AM Location: N228 Participants Pooria Khoshnoodi, MD, Los Angeles, CA (Presenter) Nothing to Disclose Daniel J. Margolis, MD, Los Angeles, CA (Abstract Co-Author) Research Grant, Siemens AG Hector E. Alcala, MPH, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Nelly Tan, MD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Wei-Chan Lin, MD, Taipei, Taiwan (Abstract Co-Author) Nothing to Disclose David Y. Lu, MD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Jiaoti Huang, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Robert E. Reiter, MD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose David S. Lu, MD, Los Angeles, CA (Abstract Co-Author) Consultant, Medtronic, Inc Speaker, Medtronic, Inc Consultant, Johnson & Johnson Research Grant, Johnson & Johnson Consultant, Bayer AG Research Grant, Bayer AG Speaker, Bayer AG Steven S. Raman, MD, Santa Monica, CA (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate the prostate cancer (CaP) detection rate by multi-parametric MR imaging (MP-MRI) confirmed by whole mount histopathology (WMHP) stratified by Gleason Scores (GS) and tumor size. METHOD AND MATERIALS A HIPPA-compliant, IRB-approved study of 290 consecutive men who underwent prostate MP-MRI before radical prostatectomy (RP) from October 2010 to January 2015 was performed. Clinical, MP-MRI (T2W, DWI and DCE) and pathologic features (WMHP slides, GS, maximal diameter) were obtained. The index tumor was defined as the pathological lesion with the highest GS or largest tumor when multiple foci had identical GS. A genitourinary (GU) radiologist and a GU pathologist reviewed each case. Each tumor focus on WMHP which matched with concordant target on MP-MRI was considered detected tumor. Chi-squared tests were used to test difference in MRI tumor detection rates by tumor grade (GS=3+3 defined as low grade vs. GS>6 as high grade) and tumor size (<1 cm defined as small vs. ≥ 1cm as large tumor). Logistic regression was used to test a tumor grade by tumor size in MRI detection. Statistical analyses were conducted using Stata 12.1. P-values below .05 were considered significant. RESULTS 290 patients had 639 unique CaP foci on WMHP. Of 639 total tumors foci on pathology, 310 (48.5%) and of 290 total index lesions, 224 (77.2%) were detected on MP-MRI. MRI detected 86/326 (26.4%) of low grade tumors vs. 223/313 (71.2%) of high grade tumors, and 56/257 (21.8%) of small vs. 253/382 (66.2%) large tumors. MRI detected 44/212 (20.8%) of low grade small tumors vs. 12/45 (26.7%) of high grade small tumors, and 42/114 (36.8%) low grade large tumors vs. 211/268 (78.7%) of high grade large tumors. (p<.05) CONCLUSION We found that MP-MRI missed 51.6% of all CaP. However, when CaP stratified by size and GS, larger tumors were associated with increased detection rate for both high and low grade tumors. There was also a significant size by grade interaction, such that the difference in detection rates by grade was much larger among tumors 1cm or larger. These findings suggest that the MP-MRI tends to detect larger with higher grade CaP lesions. In our study, MP-MRI detected 78.7% of all high grade large CaP foci. CLINICAL RELEVANCE/APPLICATION MP-MRI which combines anatomic with functional and physiologic assessment of prostate cancer has substantially improved diagnostic capabilities of detecting clinically significant prostate tumors. SSK09-05 Distortion in Diffusion-Weighted Prostate MRI: Readout-Segmented EPI DWI vs. Single-Shot EPI DWI W ednesday, Dec. 2 11:10AM - 11:20AM Location: N228 Participants Ivan Platzek, MD, Dresden, Germany (Presenter) Nothing to Disclose Angelika Borkowetz, MD, Dresden, Germany (Abstract Co-Author) Nothing to Disclose Marieta Toma, MD, Dresden, Germany (Abstract Co-Author) Nothing to Disclose Thomas Brauer, MD, Dresden, Germany (Abstract Co-Author) Nothing to Disclose Hagen H. Kitzler, Dresden, Germany (Abstract Co-Author) Nothing to Disclose Verena Plodeck, MD, Dresden, Germany (Abstract Co-Author) Nothing to Disclose Manfred Wirth, Dresden, Germany (Abstract Co-Author) Nothing to Disclose Michael Laniado, MD, Dresden, Germany (Abstract Co-Author) Reviewer, Johnson & Johnson PURPOSE The aim of this study was to evaluate the utility of segmented-readout echo planar diffusion-weighted imaging (SR EPI DWI) for prostate imaging in comparison to conventional single shot EPI DWI (SS EPI DWI), with an emphasis on distortion artifacts. METHOD AND MATERIALS Sixty-eight patients with suspected prostate cancer were included in this prospective study. Patient age varied between 46 and 77 y (65 y on average). All patients underwent multiparametric prostate MRI (mpMRI) at 3T, which included T2-weighted images, dynamic contrast-enhanced (DCE) images, and both SR EPI DWI and SS EPI DWI. Apparent diffusion coefficient maps (ADC) maps were generated for both SR EPI DWI and SS EPI DWI. Overall lesion classification was based on the PI-RADS scoring system proposed by the European society of Urogenital Radiology (ESUR). Distortion on ADC maps was classified on a five point scale. Furthermore, the maximum distortion in the anteroposterior direction was measured in each patient for both SR EPI DWI and SS EPI DWI. RESULTS ADC maps based on SR EPI DWI showed no evidence of distortion in 58/68 patients (85%), while ADC maps based on SS EPI DWI showed no distortion in 42/68 patients (61.7%). Distortion scores were higher (indicating stronger distortion) for SS EPI DWI as compared to SR EPI DWI in 19/68 patients (27.9%) and lower in only one patient (1.5%). Visual evaluation showed significantly less distortion for SR EPI DWI in comparison to EPI DWI (p = 0.0001). Average maximum distortion (1.5 ± 2.6 mm) was significantly lower in SR EPI DWI in comparison to SS EPI DWI (4.9 ± 9.7 mm) (p < 0.0001). Ninety-six prostate lesions were detected with mpMRI in total. PI-RADS scores did not differ significantly between mpMRI including SR EPI DWI and mpMRI including SS EPI DWI (p = 0.464). Mean ADC values based on SS EPI DWI (0.93 ± 0.21) were slightly lower than those based on SR EPI DWI (0.96 ± 0.22)(p = 0.047). CONCLUSION SR EPI DWI of the prostate has significantly less pronounced distortion artifacts compared to SS EPI DWI. As prostate lesion detection and lesion classification based on PI-RADS scores do not change significantly when SR EPI DWI is used instead of SS EPI DWI, SR EPI DWI is a promising alternative to conventional diffusion-weighted sequences. CLINICAL RELEVANCE/APPLICATION The use of SR EPI DWI instead of conventional SS EPI DWI in prostate MRI reduces distortion and can help improve correlation between DWI and T2-weighted images. SSK09-06 Accuracy and Inter-Observer Variability of Prostate Imaging-Report and Data System (PI-RADS) Version 2.0 for Characterization of Lesions Identified on Multiparametric Magnetic Resonance Imaging of the Prostate W ednesday, Dec. 2 11:20AM - 11:30AM Location: N228 Participants Andrei S. Purysko, MD, Cleveland, OH (Presenter) Nothing to Disclose Leonardo K. Bittencourt, MD, PhD, Rio De Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Brian R. Herts, MD, Cleveland, OH (Abstract Co-Author) Research Grant, Siemens AG Antonio C. Westphalen, MD, Mill Valley, CA (Abstract Co-Author) Nothing to Disclose Erick M. Remer, MD, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Andrew J. Stephenson, MD, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Jennifer Bullen, MSc, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Cristina Magi-Galluzzi, MD, PhD, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Eric Klein, Cleveland, OH (Abstract Co-Author) Nothing to Disclose PURPOSE To measure the accuracy and inter-observe variability of PI-RADS version 2.0 for the characterization of prostate lesions identified on mpMRI. METHOD AND MATERIALS IRB-approved, HIPAA compliant retrospective study including 171 men (mean age: 61.5 yrs.) either being investigated for prostate cancer (n = 128) or enrolled in active surveillance (n =43), who were examined on a 3.0 T magnet without endorectal coil, and were found to have potential targets for biopsy. Two readers with 8 yrs. of experience in abdominal imaging independently reviewed and assigned a PI-RADS V.2 assessment category to the dominant MRI targets. The reference standard was the combined results from the MR/US fusion biopsy and transrectal ultrasound guided 12-core systematic biopsy (SB) performed in all the patients and in the same procedure. Clinically significant (CS) PCa was defined as tumors with Gleason score >= 3 + 4. Receiver operating characteristic (ROC) analysis was performed. RESULTS PCa was detected in 49.1% (84/171) and CS PCa was detected in 32.3% (55/171) of the men. Using PI-RADS category > 3 to discriminate any PCa from non-cancerous lesions, the sensitivity (Sen), specificity (Sp) and area under the ROC curve (AUC) were 77.4%, 84.9% and 85.7% for reader 1 and 69.1%, 87.2%, and 77.9% for reader 2. Using PI-RADS category > 3 to discriminate only clinically significant PCa from clinically insignificant prostate cancer and benign lesions, the Sen, Sp, and AUC were 98.2%, 79.1%, and 91.1% for reader 1 and 92.7%, 84.4%, and 90.4% for reader 2. The inter-observer agreement coefficient was 0.68 (95% CI: 0.61- 0.75). CONCLUSION PI-RADS V.2 had high sensitivity, specificity and accuracy for the discrimination of clinically significant PCa from other pathology, with good inter-observer agreement. CLINICAL RELEVANCE/APPLICATION Lesions with a PI-RADS V.2 assessment category > 3 should be considered for targeted biopsy, while avoiding the biopsy of lesions with a category < 3 reduces the number of negative biopsies and/or detection of clinically insignificant lesions. SSK09-07 Predicting Organ-confined Prostate Cancer in the Era of Multiparametric MRI: Comparing the Accuracy of the Partin Tables and mpMRI W ednesday, Dec. 2 11:30AM - 11:40AM Location: N228 Participants Alison F. Brown, BA, Durham, NC (Presenter) Nothing to Disclose Thomas J. Polascik, MD, Durham, NC (Abstract Co-Author) Nothing to Disclose Rachel K. Silverman, MS, Chapel Hill, NC (Abstract Co-Author) Nothing to Disclose Kae Jack Tay, MBBS,MMed, Durham, NC (Abstract Co-Author) Nothing to Disclose Rajan T. Gupta, MD, Durham, NC (Abstract Co-Author) Consultant, Bayer AG; Speakers Bureau, Bayer AG; Consultant, Invivo Corporation PURPOSE To investigate the accuracy of the Partin tables and multiparametric magnetic resonance imaging (mpMRI) in predicting organconfined (OC) prostate cancer (PCa) after radical prostatectomy (RP), and to determine if radiologic staging information from mpMRI versus digital rectal exam (DRE) to augment the Partin tables increases the predictive accuracy of this widely used nomogram. METHOD AND MATERIALS In this retrospective, HIPAA-compliant, IRB-approved study, 157 patients underwent 3T mpMRI with endorectal coil before RP. MpMRI was used to assess clinical stage and an updated version of the Partin tables was used to calculate the probability of each patient to harbor OC disease. Logistic regression models predicting OC disease were created using mpMRI staging alone and with PSA as a covariate. Two sets of probabilities were obtained from the Partin tables, using clinical staging from either DRE or mpMRI. The area under curve (AUC) was used to calculate the predictive accuracy of each of these four predictive methods. RESULTS The predictive accuracy of mpMRI alone in predicting OC disease on pathological analysis is greater (AUC=0.86) than the Partin tables (AUC=0.70), and is further improved when combined with PSA values (AUC=0.88). The accuracy of the Partin nomogram in predicting OC disease decreases (AUC=0.59) when clinical stage is based on mpMRI versus DRE. CONCLUSION The superior predictive accuracy of mpMRI compared to Partin tables in predicting OC disease on pathological analysis validates results of smaller previously published studies, including one from our group. Partin table probabilities are calculated using clinical stage based on DRE result, a less sensitive test than mpMRI; therefore, this frequently leads to disease understaging. Consequently, although mpMRI has been shown to more accurately predict clinical stage than DRE, using mpMRI stage in the Partin nomogram does not improve its accuracy. In conclusion, mpMRI staging information is valuable as a stand-alone test when available based on its AUC value, but should not be applied to the Partin nomogram in its existing form. CLINICAL RELEVANCE/APPLICATION As more accurate clinical staging information is becoming available due to mpMRI, nomograms that incorporate mpMRI stage are needed to better predict OC PCa and assist in surgical planning prior to RP. SSK09-08 Diagnostic Differentiation of Prostate Cancer from Prostatic Hyperplasia: What Diffusion Kurtosis Imaging Can Help Us? W ednesday, Dec. 2 11:40AM - 11:50AM Location: N228 Participants Chen Lihua, Dalian, China (Presenter) Nothing to Disclose Ailian Liu, MD, Dalian, China (Abstract Co-Author) Nothing to Disclose Qingwei Song, MD, Dalian, China (Abstract Co-Author) Nothing to Disclose Ma Chunmei, MD, Dalian, China (Abstract Co-Author) Nothing to Disclose Meiyu Sun, Dalian, China (Abstract Co-Author) Nothing to Disclose Zibin Tong, Dalian, China (Abstract Co-Author) Nothing to Disclose Ye Li, Dalian, China (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate the feasibility of the typical parameters of DKI in diagnositic differentiation of prostate carcinoma from prostatic hyperplasia. METHOD AND MATERIALS One hundred and thirteen patients with the suspicion of prostate disease were recruited in the study. All the patients, with written informed consent obtained, were performed MRI exams on a 3.0T scanner in a protocol containing the routine T1WI, T2WI, contrast-enhanced MRI, DWI and DKI. From the following histopathological examination, it was confirmed that prostate carcinoma was in 30 and prostatic hyperplasia in 29. MR images were reviewed and analyzed by author and one experienced radiologist who has five years experience in prostate diagnosis, using a dedicated software in Functool on GE ADW4.4 workstation. For each focus, the mean value of the parameters of DKI (MK, Ka, Kr, FA, MD, Da, Dr) and DWI(ADC) was measured: in PCa group, the area where shows low signal on T2WI image, high signal on MK image and histopathological positive was the focus, regions of interest (ROIs) drew three times in the tumor, the size of the ROI was chosen to cover the 2/3 of the tumor(fig 1) , then the average value was used in statistics. In BPH group, three identical ROIs (70mm2)were drew in the central zone, the average value was used in statistics. The type of time-signal intensity curve(TIC) was observed by two observers collectively. ICC test was used to examine the consistency of the measurements, Pearson test was used to examine the relevance between MD and ADC value,and student's t-test was executed to compare the obtained parametric values with p> 0.05 concerned statistical significant. The ROC curve of all the parameters were drew and analyzed. RESULTS The ICC value of the DKI parameters and DWI parameter in the PCa group and BPH group were respectively, 0.963,0.935,0.959,0.905,0.970,0.909,0.967,0.977and 0.804,0.899,0.913,0.901,0.923,0.902,0.911,0.931, exhibiting an amenable consistency. The mean MK, Ka, Kr of PCa were significantly higher (p < 0.01) than the BPH, while the mean MD, Da, Dr of cancerous tissue was found to be significantly lower (p < 0.01) than the hyperplasia tissue. No statistically significant difference was observed between FA values of two groups (p >0.05). The area under the ROC curve of all parameters were higher than 0.9. CONCLUSION DKI demonstrated can supply many meritorious parameters, with most useful in diagnostic differentiation of prostate cancer from prostatic hyperplasia. Combining with the routine prostate MRI, DKI may help in increasing the sensitivity and specificity of cancer detection. CLINICAL RELEVANCE/APPLICATION Combining with the routine prostate MRI, DKI may help in increasing the sensitivity and specificity of cancer detection. SSK09-09 Incidental Bone Lesions on Staging MRI for Prostate Cancer: Prevalence and Clinical Importance W ednesday, Dec. 2 11:50AM - 12:00PM Location: N228 Participants Rachel Schor-Bardach, MD, New York, NY (Presenter) Nothing to Disclose Niamh M. Long, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Jane D. Cunningham, FFRRCSI, New York, NY (Abstract Co-Author) Nothing to Disclose Anna Kirzner, MD, Brooklyn, NY (Abstract Co-Author) Nothing to Disclose Ramon E. Sosa, BA, New York, NY (Abstract Co-Author) Nothing to Disclose Debra A. Goldman, MS, New York, NY (Abstract Co-Author) Nothing to Disclose Chaya Moskowitz, New York, NY (Abstract Co-Author) Nothing to Disclose Hedvig Hricak, MD, PhD, New York, NY (Abstract Co-Author) Nothing to Disclose David M. Panicek, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Hebert Alberto Vargas, MD, New York, NY (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate the prevalence of bone lesions identified on prostate MRI and determine the associations between their imaging features, clinical/pathologic characteristics and the presence of prostate cancer (PCa) bone metastases. METHOD AND MATERIALS In this IRB approved, retrospective study, the medical records of 3765 patients undergoing staging prostate MRI for newlydiagnosed (PCa) between 2000-2014 were reviewed. Amongst these, the MRI exams of all patients with bone metastases and a random selection of patients without bone metastases (matched with a 3:1 ratio to patients with bone metastases) were reviewed by 2 independent readers (R1 and R2) for presence, size and signal characteristics of bone lesions on T1-weighted sequences along with their subjective level of suspicion (1-5 Likert scale) for the likelihood of bone metastases on MRI. Prostate-specific antigen levels, biopsy Gleason Score, clinical stage and National Comprehensive Cancer Network (NCCN) risk categories were recorded. The reference standard was bone biopsy and/or at least 1-year follow-up after MRI. Associations between MRI and clinical/pathologic findings were tested using Fisher's exact and Wilcoxon Rank Sum tests. Inter-reader agreement and diagnostic accuracy for bone metastases detection were assessed using Cohen's simple Kappa statistic and areas under the receiving operating characteristics curve (AUC). RESULTS 57 out of 3765 patients (1.5%) had bone metastases. None of the patients with low-risk PCa according to the NCCN criteria had bone metastases. Inter-reader agreement on MRI was fair to substantial (k=0.26-0.70). There was at least 1 bone lesion present on MRI in 72% (95% CI: 0.66-0.78) and 70% (95% CI: 0.64-0.76) of patients according to R1 and R2. The AUC for detecting bone metastases on MRI was 0.97 (95% CI: 0.94-1.00) and 0.90 (95% CI: 0.84-0.95) for R1 and R2. Larger lesion diameter (p<0.0001 for both) and absence of intratumoral fat (p=0.0013-0.0020) were significantly associated with bone metastases for both readers. CONCLUSION Bone lesions in prostate MRI are present in the majority of patients undergoing initial staging for PCa, and infrequently represent metastatic disease. CLINICAL RELEVANCE/APPLICATION MRI findings should be interpreted in the context of clinical features which increase the likelihood of metastatic disease. GUS-W EA Genitourinary Wednesday Poster Discussions W ednesday, Dec. 2 12:15PM - 12:45PM Location: GU/UR Community, Learning Center GU AMA PRA Category 1 Credit ™: .50 Participants Susanna I. Lee, MD, PhD, Boston, MA (Moderator) Nothing to Disclose Sub-Events GU234-SDWEA1 Dose 70 kV CT Imaging with 3rd Generation Dual-source CT Simply Increase Pseudo-enhancement of Renal cyst? Importance of Considering Reduced Requirement of Contrast Dosage: A Phantom Study Station #1 Participants Satoru Takahashi, MD, Kobe, Japan (Presenter) Nothing to Disclose Noriyuki Negi, RT, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Kiyosumi Kagawa, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Erina Suehiro, RT, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Wakiko Tani, RT, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Toshinori Sekitani, MS, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Hideaki Kawamitsu, MD, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Kazuro Sugimura, MD, PhD, Kobe, Japan (Abstract Co-Author) Research Grant, Toshiba Corporation Research Grant, Koninklijke Philips NV Research Grant, Bayer AG Research Grant, Eisai Co, Ltd Research Grant, DAIICHI SANKYO Group PURPOSE Thanks to improved iodine absorption of lower kV, attenuation of iodine contrast medium (CM) at 70 kV is 2.0-time greater than those at 120 kV with 3rd generation dual-source CT scanner. Although identical HU values could be theoretically achieved with half dose of CM at 70 kV comparing to 120 kV, diagnostic ability would be impaired with increased beam hardening effect at lower kV imaging. The purpose of this phantom study is to compare the degree of pseudo-enhancement under identical surrounding attenuation at different energy CT scan, assuming contrast enhanced CT protocols of 70 kV CT with half dose CM and 120 kV CT with full dose. METHOD AND MATERIALS Circular phantom (26 cm in diameter) filled with different concentration of diluted CM (240 HU or 116 HU at 120 kV) and equipped with 7 cylindrical inserts of water and various concentration of CM (0.4, 4.5, 10.7, 24.8, 63.6, 127.6 HU at 120 kV, respectively) was scanned at 70 kV or 120 kV with identical radiation dose (CTDIvol of 7.6 mGy) using 3rd generation dual-source CT scanner. HU values of inserted water, representing pseudo-enhancement due to beam-hardening artifacts, as well as those of diluted CM in cylindrical inserts, indicating slightly enhancing lesions, were measured. Pseudo-enhancement and contrast to noise ratio (CNR) of the phantoms with surrounding 116 HU CM scanned at 70 kV were compared to those of 240 HU at 120 kV to simulate contrast enhanced CT protocols of 70 kV with half dose CM and 120 kV with full dose CM. RESULTS Diluted CM of 116 HU at 120 kV demonstrated HU value of 234±18 at 70 kV, while 240 HU CM showed 501±29 HU at 70 kV. Pseudoenhancement of water insert with 240 HU phantom at 120 kV scan (23.9±0.3 HU) were significantly greater than those with 116 HU at 70 kV scan (12.4±0.7 HU, p<.0001). At 120 kV scan with surrounding 240 HU diluted CM, CNR of 24.8 HU or greater phantom showed significant difference from water, while 4.5 HU or greater phantom showed significantly different CNR from water at 70 kV scan with 116 HU diluted CM. CONCLUSION To consider double HU values of iodine CM at 70 kV compared to 120 kV scans, a half contrast dose CT at 70 kV causes less pseudo-enhancement and better CNR for subtle enhancement. CLINICAL RELEVANCE/APPLICATION Considering pseudo-enhancement of renal cyst, contrast enhanced CT protocol of 70 kV with half dose CM would be more desirable than 120 kV with full dose CM. GU251-SDWEA2 Multiphasic MDCT Imaging Features Can Help Discriminate Sarcomatoid RCC and Collecting Duct Carcinoma from Clear Cell RCC Station #2 Participants Jonathan R. Young, MD, Los Angeles, CA (Presenter) Nothing to Disclose Jocelyn A. Young, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Daniel J. Margolis, MD, Los Angeles, CA (Abstract Co-Author) Research Grant, Siemens AG Michael L. Douek, MD, MBA, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Steven Sauk, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Margaret Hsu, MD, Sacramento, CA (Abstract Co-Author) Nothing to Disclose Steven S. Raman, MD, Santa Monica, CA (Abstract Co-Author) Nothing to Disclose PURPOSE To investigate whether imaging features on multiphasic MDCT can discriminate sarcomatoid RCC (sRCC) and collecting duct carcinoma (CDC) from clear cell RCC (ccRCC). sRCC and CDC are rare, aggressive variants of RCC. In the setting of metastasis, upfront cytoreductive nephrectomy has survival benefit in ccRCC. However, for sRCC and CDC, upfront cytoreductive nephrectomy has little or no survival benefit, as it delays the administration of systemic therapy. METHOD AND MATERIALS With IRB approval for this HIPAA-compliant retrospective study, we derived a cohort of 166 ccRCCs, 7 sRCCs, and 4 CDCs with preoperative multiphasic MDCT with up to four phases (unenhanced, corticomedullary, nephrographic, and excretory). Each lesion was reviewed by two fellowship-trained GU radiologists with 7 and 12 years experience for contour, spread pattern, pattern of enhancement, neovascularity, and calcification until a consensus was reached. RESULTS sRCCs were more likely than ccRCCs to have an irregular contour (57% v 2%, p<0.001) and an infiltrative spread pattern, defined as infiltration into adjacent renal parenchyma, collecting system, or neighboring structures, (71% v 10%, p<0.001). CDCs were also more likely than ccRCCs to have an irregular contour (75% v 2%, p<0.001) and an infiltrative spread pattern (100% v 10%, p<0.001). An infiltrative spread pattern has a specificity of 90% and sensitivity of 71% in discriminating sRCC from ccRCC and a specificity of 90% and sensitivity of 100% in discriminating CDC from ccRCC. An irregular contour has a specificity of 98% and sensitivity of 57% in discriminating sRCC from ccRCC and a specificity of 98% and sensitivity of 75% in discriminating CDC from ccRCC. CONCLUSION Solid renal lesions with an irregular contour or an infiltrative spread pattern are suspicious for sRCC or CDC. Lesions with these imaging features should be biopsied first rather than taken directly to nephrectomy, as upfront cytoreductive nephrectomy has little or no survival benefit and delays the administration of systemic therapy. CLINICAL RELEVANCE/APPLICATION An infiltrative spread pattern and irregular contour have a relatively high specificity and sensitivity in discriminating sRCC and CDC from ccRCC. Lesions with these imaging features should be biopsied first rather than taken directly to nephrectomy, as upfront cytoreductive nephrectomy has little or no survival benefit and delays the administration of systemic therapy. GU236-SDWEA3 CT Findings of Advanced Papillary Renal Cell Carcinoma Type-2: Comparison with Advanced Clear Cell Renal Cell Carcinoma Station #3 Participants Nagaaki Marugami, Kashihara, Japan (Presenter) Nothing to Disclose Toshiko Hirai, MD, Kashihara, Japan (Abstract Co-Author) Nothing to Disclose Junko Takahama, MD, Kashihara, Japan (Abstract Co-Author) Nothing to Disclose Aki Takahashi, MD, Kashihara, Japan (Abstract Co-Author) Nothing to Disclose Kimihiko Kichikawa, MD, Kashihara, Japan (Abstract Co-Author) Nothing to Disclose PURPOSE Papillary renal cell carcinoma (papRCC) type-2 is categorized as a subtype with worse prognosis. Advanced papRCC type-2 is likely to show heterogeneous and ill marginated mass mimicking advanced clear cell renal cell carcinoma (ccRCC). The purpose of this study is to clarify the features of the CT findings of papRCC type-2 and to compare between advanced papRCC type-2 (over T3a) and advanced ccRCC. METHOD AND MATERIALS The materials ware 19 papRCC and 44 ccRCC (over T3a) histologically proven in 256 consecutive patients with RCC undergoing preoperative CT and nephrectomy. Before and after injection of contrast media, CT images were obtained at plain, corticomedullary, and nephrogenic phases. For visual assessment, the tumor size, heterogeneity, tumor margin, calcification, renal vein invasion, lymph node/ distant metastasis and degrees of enhancement at corticomedullary phase (type A: same or less than renal medulla enhancement, type B: less than renal cortex enhancement, type C: same as renal cortex enhancement). For quantitative assessment, CT values at each phase were measured. We compared between papRCC and ccRCC for these factors. RESULTS Among all papRCC, 11 advanced papRCC (T3a over) were evaluated: the mean tumor size (7.3cm), heterogeneity (8/11), ill margin (8/11), calcification (2/11), renal vein invasion (7/11), metastases (3/11), enhancement type (type A; 4, type B; 5, type C; 2). The mean CT values were 34.0, 64.7 and 60.2 HU at plain, corticomedullary, and nephrogenic phases, respectively. Compared with advanced ccRCC, there were significant difference only in CT values at corticomedullary phase (papRCC vs.cc RCC:64.7 vs. 104.7 HU) and degrees of enhancement (type A; 4, B; 5, C; 2 vs. type A; 0 ,B; 8,C; 36). CONCLUSION Although advanced papRCC type-2was morphologically similar to advanced ccRCC, the degree of enhancement of papRCC type-2 at corticomedullary phase was significantly less than that of advanced ccRCC. CLINICAL RELEVANCE/APPLICATION For the patient with unresectable advanced RCC, contrast-enhanced CT findings may help us to determine whether it is conventional ccRCC or papRCC type-2 and to select the appropriate drug for molecular targeting therapy as part of a personalized treatment plan. GU237-SDWEA4 Is it Possible to Indicated Renal Function by Virtue of Iodine Concentration Derived from DECT Renal Imaging? Station #4 Participants Min Li, Shenyang, China (Abstract Co-Author) Nothing to Disclose Ke Ren, MD, ShenYang, China (Abstract Co-Author) Nothing to Disclose Yangyang Kan, Shenyang, China (Abstract Co-Author) Nothing to Disclose Yu Zhao, Shenyang, China (Abstract Co-Author) Nothing to Disclose Ke Xu, MD, Shenyang, China (Abstract Co-Author) Nothing to Disclose Long Cui, MD, PhD, Shenyang, China (Presenter) Nothing to Disclose PURPOSE This study aims at assess the feasibility of using quantified iodine concentration derived from DECT renal imaging to reflect renal function. METHOD AND MATERIALS 78 patients who underwent enhanced DECT abdominal scanning in our hospital were enrolled in this study. According to the renal function results, they were divided into healthy group and abnormal group given serum creatinine, blood urea and cysteine-c level separately. Enhanced renal images were derived at arterial phase, nephrographic phase and late phase respectively, and the Iodine concentration was determined by virtue of the dual energy material decomposition algorithm. However, to avoid the across differences, the iodine enhancement level were normalized by divide the iodine concentration in renal cortex with the iodine concentration in the aorta at arterial phase. The normalized iodine concentration (NIC) level between normal and abnormal renal function group were compared to analysis the difference. RESULTS Out of the 78 patients (Age: 59.6±10.4, Male: 53), there were 3, 15 and 42 patients whose blood urea, cys-c and serum creatinine level were out of the healthy range. NIC difference analysis based on serum creatinine was neglect due to limited abnormality cases. NIC in the abnormal blood urea group were 0.59±0.12, 1.22±0.23 and 1.17±0.16 for arterial, nephrographic and late phase respectively; while in the normal blood urea group were 0.60±0.21, 1.40±0.34 and 1.30±0.25. The difference between these two groups was significant at late phase (t=-1.992, P=0.05). NIC in the normal cys-c group were 0.56±0.12, 0.66±0.15, 0.61±0.08 respectively, while in the abnormal cys-c group they were 0.64±0.26, 0.71±0.18, 0.68±0.14. The difference between two groups is also significant at late phase (t=-2.688, P<0.01). CONCLUSION It is feasible to indicate serum creatinine abnormality and cys-c abnormality given the late phase NIC derived from dual energy. CLINICAL RELEVANCE/APPLICATION Dual energy scanning is able to not only provide the anatomical details but also reflect the functionality of the kidney. GU239-SDWEA6 Single-phase Split-bolus Dual-energy CT Urography after Furosemide Intravenous Injection for Evaluating Urinary Stones and Bladder Tumors Station #6 Participants Jun Gon Kim, Seoul, Korea, Republic Of (Presenter) Nothing to Disclose Chan Kyo Kim, MD, PhD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Sohee Song, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Jung Jae Park, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Byung Kwan Park, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose PURPOSE To investigate the feasibility of single-phase split-bolus dual-energy CT (DECT) after furosemide intravenous injection for evaluating urinary stones and bladder tumors, and to measure the potential radiation dose reduction. METHOD AND MATERIALS A total of 218 consecutive patients (mean age, 53 years; range, 28-77 years) who underwent split-bolus DECT urography after furosemide intravenous injection were enrolled in this retrospective study. The protocol included true noncontrast (TNC) and singlephase (combined nephrographic-excretory) postcontrast DECT scans. Virtual noncontrast (VNC), linearly blended and iodine overlay (IO) images were reconstructed from postcontrast DECT scans. The number and size of urinary stones were assessed on TNC and VNC images. Image quality of VNC and TNC was qualitatively evaluated using a 5-point scale. The CT numbers of bladder tumors were also analyzed on TNC and reconstructed image. The potential dose reduction of a single-phase from dual-phase protocol was measured. RESULTS 169 urinary stones (mean size, 7.58 mm; range, 2-32.2 mm) in 56 patients and 19 bladder tumors (mean size, 12.7 mm; range, 4-56 mm) in 10 patients were analyzed. On VNC images, 98.2% (149/169) stones were detected and the remaining 11.8% (20/169) stones were missed. The mean size of the missed stones on VNC image was 2.33 mm (range, 1.6-3.4 mm), but all stones ≥ 3.5 mm were detected. For bladder tumors, the CT numbers on TNC and VNC images were 34.0 HU and 32.9 HU, respectively ( P = 0.754); the enhancement values of linearly blended and IO images were 68.2 HU and 78.2 HU, respectively ( P = 0.023); and accordingly, all tumors were characterized on IO images. The overall imaging quality of the VNC was significantly inferior to the TNC images (P= 0.012), but the quality scales of the VNC were fair or more. The mean dose of single-phase DECT acquisition was 4.23 mSv comparing with 7.08 mSv of the dual-phase study, resulting in about 40% reduction of radiation exposure by omitting TNC. CONCLUSION Single-phase split-bolus DECT urography using furosemide intravenous injection appears to be feasible for evaluating clinically significant stones and bladder tumors, with potentially reduced radiation exposure. CLINICAL RELEVANCE/APPLICATION Single-phase split-bolus DECT urography after furosemide intravenous injection can be used to evaluate clinically significant stones and bladder tumors. UR131-EDWEA7 Optimizing Renal Transplant Ultrasound Parameters Station #7 Participants Rajiv Rao, MD, Sacramento, CA (Presenter) Nothing to Disclose Ghaneh Fananapazir, MD, Sacramento, CA (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Teaching Points for this Exhibit:1. Optimization: To discuss the technical principles that contribute to optimal ultrasound imaging of renal transplants.2. Artifacts: To review the major imaging artifacts that the radiologist commonly encounters when interpreting a post-operative renal transplant ultrasound. TABLE OF CONTENTS/OUTLINE 1. Probe selection: use of high frequency probes2. Pressure artifact and its effect on resistive indices3. Gain settings on grayscale, color and spectral Doppler images4. Wall filter settings: masking true arcuate artery resistive indices5. Velocity scale settings: color and spectral Doppler6. Angle of Insonation Optimization to eliminate false spectral broadening Optimization to eliminate directional ambiguity Optimization to obtain accurate velocity measurements 7- Aliasing Physical principles behind the phenomenon Artifacts created on color and spectral Doppler settings Clinical use of the artifact to demonstrate stenosis Fixing aliasing artifact8- Spectral broadening9- Color Doppler findings in nonvascular structures GUS-W EB Genitourinary Wednesday Poster Discussions W ednesday, Dec. 2 12:45PM - 1:15PM Location: GU/UR Community, Learning Center GU AMA PRA Category 1 Credit ™: .50 Participants Susanna I. Lee, MD, PhD, Boston, MA (Moderator) Nothing to Disclose Sub-Events GU240-SDWEB1 Diffusion Kurtosis Imaging of Uterine Endometrial Cancer: Preliminary Study Station #1 Participants Shigeaki Umeoka, MD, Osaka City, Japan (Presenter) Nothing to Disclose Akira Yamamoto, MD, PhD, Kyoto, Japan (Abstract Co-Author) Nothing to Disclose Koji Sakai, Kyoto, Japan (Abstract Co-Author) Nothing to Disclose Aki Kido, MD, Kyoto, Japan (Abstract Co-Author) Nothing to Disclose Thorsten Feiweier, DIPLPHYS, PhD, Erlangen, Germany (Abstract Co-Author) Employee, Siemens AG Stockholder, Siemens AG Patent holder, Siemens AG Kaori Togashi, MD, PhD, Kyoto, Japan (Abstract Co-Author) Research Grant, Bayer AG Research Grant, DAIICHI SANKYO Group Research Grant, Eisai Co, Ltd Research Grant, FUJIFILM Holdings Corporation Research Grant, Nihon Medi-Physics Co, Ltd Research Grant, Shimadzu Corporation Research Grant, Toshiba Corporation Research Grant, Covidien AG PURPOSE 1.To investigate the feasibility and utility of DKI for the assessment of uterine endometrial cancer2.To correlate ADC, D and K values with histologic subtypes of endometrial lesion METHOD AND MATERIALS A total of twenty-nine patients (age 28-86) with clinically suspected endometrial lesions prospectively underwent MR imaging at 3T, including DKI ( b-factors 0, 100, 500, 1000, 1500, 2000, 2500s/mm², Three orthogonal MPG directions with monopolar scheme (prototype sequence)). D (diffusion coefficient) and K (Kurtosis; the deviation of tissue diffusion from a Gaussian pattern) map images were generated on a voxel-by-voxel basis with in-house software. ADC map images were also calculated based on diffusionweighted images with b-factors of 0, 500 and 1000 s/mm². Obtained ADC, D, and K values of the endometrial lesions were correlated with histological findings, subdivided into three categories (1. No malignant endometrial lesion, 2. Low-grade (grade 1) endometrial cancer, 3. High-grade (grade 2 or 3) endometrial cancer) using student t-test. RESULTS Histologically, 17 patients had endometrial carcinoma (11 low grade, 6 high grade) and 12 patients had benign conditions. 26 of 29 endometrial lesions (89.7%) could be successfully visualized as lower signal intensity areas compared to the myometrium on ADC, D, and K map images. Of these 26 cases, the D, ADC (10-3mm2/s) and K values were 1.65±0.72, 1.52±0.50 and 0.64±0.11 for nonmalignant endometrial lesion, 0.79±0.13, 0.67±0.11 and 0.87±0.08 for low-grade endometrial cancer, 0.81±0.16, 0.73±0.11 and 1.10±0.08 for high-grade endometrial cancer, respectively. All K-, D- and ADC-values of the tumor show significant differences between non-malignant and malignant lesion. Although no significant differences of D- and ADC-values between low- and highgrade cancer are observed, the K-value tends to be significantly higher in high-grade cancer than in low-grade cancer.. CONCLUSION DKI seems an effective, non-invasive method for the assessment of endometrial lesions. ALL D-, K-, and ADC-values are helpful for the differentiation between benign and malignant endometrial lesion. Only the K-value shows an excellent correlation with histological subtypes of uterine endometrial cancer, and may serve as a new, useful prognostic biomarker. CLINICAL RELEVANCE/APPLICATION Diffusion kurtosis imaging is well related to histological characteristics, including tumor cellularity and architectural distortion. GU241-SDWEB2 Prediction of Disease Progression after Concurrent Chemoradiotherapy in Uterine Cervical Cancer: Value of Diffusion-weighted Imaging Station #2 Participants Jung Jae Park, MD, Seoul, Korea, Republic Of (Presenter) Nothing to Disclose Chan Kyo Kim, MD, PhD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Byung Kwan Park, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose PURPOSE To investigate the value of diffusion-weighted imaging (DWI) as a predictor of disease progression after concurrent chemoradiotherapy (CCRT) in uterine cervical cancer. METHOD AND MATERIALS Our retrospective study included 100 consecutive patients (median age, 55 years) who received CCRT for locally advanced cervical cancer. All enrolled patients underwent 3T-MRI including T2-weighted imaging (T2WI) and DWI at 1 month after completion of CCRT. The presence or absence of residual tumor on T2WI and DWI was determined using a 5-point probability scale. For predicting disease progression after completion of CCRT, the diagnostic performance of the presence of residual tumor on T2WI and DWI was evaluated using the time-dependent receiver operating characteristics (ROC) curve analysis. The relationship between MR (presence of residual tumor on T2WI and DWI, and tumor size) and clinical variables (age, FIGO stage and histologic type) and disease progression was investigated using the Cox regression analysis. RESULTS After a mean follow-up of 2.6 years, disease progression developed in 24 patients (24.0%): local recurrence (n= 10), distant metastasis (n= 11) and both local recurrence and distance metastasis (n= 3). At ROC curve analysis, the integrated area under the curve was significantly greater on DWI (0.751) than on T2WI (0.659) for predicting disease progression ( P = 0.009). For predicting disease progression, the positive predictive values of DWI versus T2WI were 54.4% versus 32.7% at the first, 73.0% versus 37.2% at the second, and 72.7% versus 39.3% at the third year after CCRT, respectively, which were statistically different (all P -values< 0.03). On univariate analysis, the presence of residual tumor on T2WI or DWI, and non-squamous cell carcinoma were significantly associated with disease progression ( P < 0.01). However, the presence of residual tumor on DWI was the only independent predictor of disease progression (hazard ratio, 6.34; P < 0.0001) on multivariate analysis. CONCLUSION The presence of residual tumor on DWI at 1 month after completion of CCRT appears to be the only independent predictor for disease progression in patients with locally advanced cervical cancer. CLINICAL RELEVANCE/APPLICATION As an imaging marker, the presence of residual cervical cancer on DWI at 1 month after completion of CCRT may help to predict therapeutic outcomes, which may play a crucial role in developing a personalized treatment. GU242-SDWEB3 Percutaneous and Laparoscopic Cryoablation (CA) of Renal Carcinomas: Mid-term CT and MR Imaging Follow-up Station #3 Participants Gianpiero Cardone, MD, Milano, Italy (Presenter) Nothing to Disclose Maurizio Papa, MD, Milan, Italy (Abstract Co-Author) Nothing to Disclose Andrea Losa, MD, Milano, Italy (Abstract Co-Author) Nothing to Disclose Tommaso Maga, MD, Milan, Italy (Abstract Co-Author) Nothing to Disclose Paola Mangili, PhD, Milano, Italy (Abstract Co-Author) Nothing to Disclose Giuseppe Balconi, Ornago, Italy (Abstract Co-Author) Nothing to Disclose PURPOSE This study aims to determine the safety and efficacy of CA in the management of small renal carcinomas and to assess its medium term outcome. METHOD AND MATERIALS We report the mid-term CT/MR imaging follow-up in 115 pts who gained at least 5 years follow-up after CA of 96 renal carcinomas. Treatment was administered under laparoscopic US guidance in 101 pts and using percutaneous CT guidance in 14 pts. Pts were followed up clinically, biochemically and by imaging 24 hours after surgery, and subsequently every 6 months. Imaging follow-up was obtained using a 1,5T MR system in 104 cases and using CT in 11 pts with contraindications to MR. RESULTS 24 hours after treatment all cryolesions were more than 1 cm larger than the original masses; cryolesions decreased in size by an average of 38% at 1 month, 64% at 6 months, 80% at 12 months and 93% at 84 months following LC. Early postprocedural MR and CT ce- images showed complete ischemia of cryolesions. Follow-up revealed no evidence of local recurrence in 111/115 pts (96%). 4 pts showed local recurrence at 12, 24 and 96 months. 12/115 pts (9%) demonstrated metachronous nodules in the same or in the contralateral kidney at 12, 24 and 48 months. 2 pts showed a pancreatic metastatic nodule at 12 and 24 months. 11/115 pts died for metastasis of a previous malignancy. 1 pt showed ureteral fistula and 1 pt showed proximal ureteral stenosis. No significant rise in creatinine level was noted postprocedurally. After surgery 11% of the cases showed small perilesional haematomas. CONCLUSION Our experience suggests that CA is a safe, well tolerated and minimally invasive therapy for small renal carcinomas. MR is an effective tool in the imaging follow-up of renal lesions treated with CA, and the high contrast resolution of MR allows a better evaluation of vascularization of treated areas on subtracted ce images compared to CT. CT can be used as an alternative choice to MR, but lower contrast resolution of CT to MR makes it difficult to differentiate the cryolesion from the surrounding perilesional collections. CLINICAL RELEVANCE/APPLICATION CA is a safe, well tolerated and minimally invasive therapy for small renal carcinomas. MR and CT are effective imaging techniques in the follow-up of renal lesions treated with CA. GU243-SDWEB4 Correlation of Renal IVIM Diffusion Parameters to DCE-MRI Perfusion Parameters from a ThreeCompartment Model Station #4 Participants Octavia Bane, PhD, New York, NY (Presenter) Nothing to Disclose Mathilde Wagner, MD,PhD, Paris, France (Abstract Co-Author) Nothing to Disclose Hadrien Dyvorne, PhD, New York, NY (Abstract Co-Author) Nothing to Disclose Henry Rusinek, PhD, New York, NY (Abstract Co-Author) Nothing to Disclose Jeff L. Zhang, PhD, Salt Lake Cty, UT (Abstract Co-Author) Consultant, Bristol-Myers Squibb Company Bachir Taouli, MD, New York, NY (Abstract Co-Author) Consultant, Guerbet SA PURPOSE To correlate cortical and medullary intravoxel-incoherent motion diffusion-weighted imaging (IVIM-DWI) parameters to DCE-MRI parameters using a validated three-compartment model. METHOD AND MATERIALS IVIM-DWI and DCE-MRI data were analyzed in 20 patients (M/F 14/6, age 58±7 y; serum eGFR=85± 26 ml/min) with liver disease who underwent abdominal MRI at 1.5T. A bipolar diffusion sequence with single-shot EPI readout and spectral fat saturation was acquired in 17 interleaved slices in the coronal plane with respiratory triggering and 16 b-values. 64 coronal 3D FLASH DCE-MRI volumes were acquired over repeat breath-holds with a mean temporal resolution of 2.7 sec, during injection of 0.05 mmol/kg of GdBOPTA at 3 ml/sec.ROIs were placed on the motion-corrected IVIM images (FireVoxel) in the renal cortex and medulla, avoiding major vessels, lesions and fat. Mean ROI signal was fitted to the IVIM model.The cortex and medulla in each kidney, as well as the aorta at the level of the renal arteries, were semi-automatically segmented from the DCE-MRI volumes using validated software (Perf4DSegm).GFR, whole kidney, cortical and medullary renal plasma flow (RPF), as well as mean transit times (MTT) for the compartments and the whole kidney, were calculated. RESULTS Renal IVIM parameters obtained were in accordance with previous studies; cortical ADC and perfusion fraction (PF) were significantly higher compared to medulla (p=0.0005 and p=0.0007, respectively). DCE-MRI parameters obtained in 18/20 patients (due to truncated arterial input function in 2 patients) were in agreement with previous studies using the three-compartment model. DCE-MRI eGFR was significantly correlated with serum eGFR (Spearman r=0.595, p=0.011), but under-estimated serum eGFR (slope = 0.47, p = 0.005; intercept = 14.12, p = 0.279). RPF values were significantly higher in the cortex than in the medulla (p<10^-6). Significant correlation was observed for pooled cortical and medullary PF and ADC with RPF (Fig.1; PF r=0.327, p=0.005, ADC r=0.387, p=0.001). Cortical RPF correlated with ADC (r=0.49, p=0.003), but not with PF. No other DCE-MRI and IVIM parameters were correlated. CONCLUSION Cortical and medullary ADC and PF were moderately correlated with RPF in this initial ongoing study. CLINICAL RELEVANCE/APPLICATION IVIM diffusion cannot be substituted for DCE-MRI in the evaluation of renal plasma and tubular flow. The techniques provide complementary information on renal function. GU244-SDWEB5 Texture Analysis on T2-weighted MRI to Evaluate for Biochemical Recurrence in Prostate Cancer Patients Station #5 Participants Anna M. Brown, BEng, Bethesda, MD (Presenter) Nothing to Disclose Sandeep Sankineni, MD, Bethesda, MD (Abstract Co-Author) Nothing to Disclose Joanna Shih, Bethesda, MD (Abstract Co-Author) Nothing to Disclose Richard Ho, Bethesda, MD (Abstract Co-Author) Nothing to Disclose Maria Merino, MD, Bethesda, MD (Abstract Co-Author) Nothing to Disclose Peter Pinto, Bethesda, MD (Abstract Co-Author) Nothing to Disclose Peter L. Choyke, MD, Rockville, MD (Abstract Co-Author) Researcher, Koninklijke Philips NV Researcher, General Electric Company Researcher, Siemens AG Researcher, iCAD, Inc Researcher, Aspyrian Therapeutics, Inc Researcher, ImaginAb, Inc Researcher, Aura Biosciences, Inc Baris Turkbey, MD, Ankara, Turkey (Abstract Co-Author) Nothing to Disclose PURPOSE To assess whether texture analysis can evaluate whole-prostate T2-weighted MRI scans for biochemical recurrence (BCR) in postprostatectomy patients. METHOD AND MATERIALS Initially 337 patients who underwent prostate multi-parametric MRI (mpMRI) followed by radical prostatectomy between 5/2007 3/2014 were included in this study, all with ≥1 year follow-up. In this cohort, 21 patients were determined to have BCR based on the American Urologic Association definition. One patient was excluded for having brachytherapy seeds present on his baseline mpMRI. A matched cohort analysis was performed on the basis of age, pre-treatment prostate specific antigen (PSA), and race, and 18/20 patients were able to be matched with controls (recurrence-free prostate cancer patients). Ultimately, 36 patients were included in the study (n=18 BCR, n=18 matched controls).Pre-treatment T2-weighted turbo-spin echo MRI scans were acquired at 3T using an endorectal coil and a 16-channel surface/cardiac coil. Whole-prostate contour voxels of interest (VOIs) were assessed using the texture analysis program MaZda (Technical University of Lodz, Poland). Feature reduction was performed using the Mutual Information method in MaZda, resulting in seven texture features that were incorporated into a linear discriminant analysis (LDA) model. Receiver-operator characteristic (ROC) curve analysis was then used to evaluate the LDA model. RESULTS For the BCR patients, mean age and PSA were 59 yrs (range 41-73) and 19.2 ng/mL (range 4.5-51.1), respectively. The mean age and PSA for the matched control patients were 60 yrs (range 51-76) and 19.1 ng/mL (range 2.62-55.7), respectively. ROC analysis of the LDA model of the seven texture features resulted in an area under the curve (AUC) of 0.87 and p=0.00017 in distinguishing BCR from matched control whole-prostate VOIs. Using a cutoff MDF1 of 3.01, the sensitivity was 89% and specificity was 78%, and 30/36 (83%) patients were classified correctly. CONCLUSION The LDA model separates BCR from matched control patients with reasonably high accuracy. Our approach can potentially be used to predict BCR candidates at the pre-treatment phase. Further work is now needed to prospectively test this model. CLINICAL RELEVANCE/APPLICATION Texture analysis shows potential to distinguish prostate cancer patients with biochemical recurrence from a matched cohort of recurrence-free patients based on baseline T2-weighted MRI features. GU245-SDWEB6 Single Phase Enhanced CT for the Detection of Urolithiasis: Can It be an Alternative to Nonenhanced CT or Muliphase Protocols? Station #6 Participants Christelle Chedrawy, MD, Chicago, IL (Presenter) Nothing to Disclose Girish Kumar, MD, Stickney, IL (Abstract Co-Author) Nothing to Disclose Nancy Wilkins, Glenview, IL (Abstract Co-Author) Nothing to Disclose Anita H. Kelekar, MD, Palatine, IL (Abstract Co-Author) Nothing to Disclose Dheeraj Reddy Gopireddy, MD, MPH, Chicago, IL (Abstract Co-Author) Nothing to Disclose Rita Agarwala, MD, Oak Brook, IL (Abstract Co-Author) Nothing to Disclose PURPOSE To determine the usefulness of enhanced CT for detection of renal and ureteral calculi. To determine the usefulness of enhanced CT in identifying alternate diagnosis if not suspected. METHOD AND MATERIALS Between January 2014 and December 2014, 70 CT scans performed in the outpatient center for renal stone detection, hematuria or flank pain were randomly reviewed. 69 were performed with at least 2 phases, including a noncontrast examination. One study was performed with contrast only. 27 studies positive for renal calculi were reviewed independently by two radiology residents. The number of stones seen on enhanced examinations was then compared to the number detected on the nonenhaned studies. RESULTS Stones were not seen in 7 studies (26 %) and 9 (33%) studies by observer 1 and 2 respectively. At least 66 % of the missed stones were less than 3 mm in size. Nearly all of the stones were calyceal. None of the stones that were not detected on the enhanced study were associated with hydronephrosis, hydroureter, perinephric stranding or other secondary signs. The studies negative for urolithiasis demonstrated on the enhanced examination significant pathology such as prostatomegaly and bladder cancer, accounting for patient's presenting symptoms. CONCLUSION Enhanced CT can be used in the detection of urolithiasis. Missed stones on enhanced CT were not associated with significant obstructive changes and may be questionably clinically significant. CLINICAL RELEVANCE/APPLICATION Although nonenhanced CT has been proven to be the most accurate diagnostic study with a high sensitivity (95-96%) and specificity (98%) , enhanced CT performed in the nephrographic phase may present an alternative to detection of urolithiasis. Additionally, it increases a physician diagnostic certianty by identifying alternate significant pathology not initially suspected. UR132-EDWEB7 PI-RADS v2.0 - An Atlas and Illustrated Manual Station #7 Participants Erick S. Hollanda, Rio de Janeiro, Brazil (Presenter) Nothing to Disclose Dafne D. Melquiades, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Fernanda Miraldi, MD, Rio de Janeiro/Niteroi, Brazil (Abstract Co-Author) Nothing to Disclose Andrei S. Purysko, MD, Cleveland, OH (Abstract Co-Author) Nothing to Disclose Natalia Sabaneeff, MD, Rio de Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose Leonardo K. Bittencourt, MD, PhD, Rio De Janeiro, Brazil (Abstract Co-Author) Nothing to Disclose TEACHING POINTS The joint initiative for standardization of the interpretation and communication of multiparametric prostate MR findings has culminated on the development of the second version of PI-RADS. In this presentation, we demonstrate the typical imaging findings in each assessment category, underscoring the main changes over the previous PI-RADS version. Of note, we highlight the adoption of a 'dominant' parameter for each zonal compartment of the prostate, corresponding to DWI for the peripheral zone and T2WI for the transition zone. DCE is now only applied to differentiate between scores 3 and 4 in the peripheral zone. The notion of lesion size was now incorporated to DWI and T2WI criteria, using a threshold of 1.5 cm to differentiate between scores 4 and 5 for highly-suspicious lesions. TABLE OF CONTENTS/OUTLINE Why and when to use Multiparametric prostate magnetic ressonace imaging (mpMRI).PI-RADS v2 vs. PIRADS v1. Brief history and evolution. Rationale for the imaging criteria.mpMRI protocols and functinal sequences.The 'dominant' sequence based on zonal anatomy, a recent implementation from PI-RADS v2.Sample cases, with assessment categories and troubleshooting.How to use mpMRI with PI-RADS in routine clinical practice. Decision making and risk stratification.Besides detection, is PI-RADS any good for tumor staging? MSSR43 RSNA/ESR Emergency Symposium: Abdominal Emergencies (An Interactive Session) W ednesday, Dec. 2 1:30PM - 3:00PM Location: S402AB GI CT ER AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Ronald J. Zagoria, MD, San Francisco, CA, (ron.zagoria@ucsf.edu) (Moderator) Nothing to Disclose Andras Palko, MD, PhD, Szeged, Hungary (Moderator) Medical Advisory Board, Affidea Group; Sub-Events MSSR43A Abdominal Injuries Participants Andras Palko, MD, PhD, Szeged, Hungary, (palko.andras@med.u-szeged.hu) (Presenter) Medical Advisory Board, Affidea Group; LEARNING OBJECTIVES 1) To explain the significance of injury mechanism and its role in the formation of consequent abdominal lesions and their complications. 2) To outline the role of proper imaging technique and diagnostic algorithm in the sufficiently fast diagnosis of abdominal injuries. 3) To learn more about the typical and unusual findings of various abdominal traumatic conditions. ABSTRACT Abdominal injuries require a timely and reliable diagnosis in order to prevent the potentially lethal outcome. The armory of clinical tools (physical examination, lab tests) does not fulfill these criteria, since they are either not fast, or not reliable. Imaging diagnostic modalities help the clinician to acquire the necessary amount of information to initiate focused and effective treatment. However, the selection of the appropriate imaging algorithm, modality and technique, as well as the precise detection and interpretation of essential imaging findings are frequently challenging, especially because the circumstances, under which these examinations are performed (open wounds, bandages, non-removable life-supporting equipment, lack of patient cooperation, etc.), are frequently less than optimal. Knowledge of critical imaging signs, symptoms and the role they play in the evaluation of the patient's condition, but also fast decision-making and ability to closely cooperate with the clinicians are skills of key importance for radiologist members of the trauma team. MSSR43B The Enemy Within, Non-Traumatic Abdominal Emergencies Participants Ronald J. Zagoria, MD, San Francisco, CA, (ron.zagoria@ucsf.edu) (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Attendees will be able to better analyze CT scans for non-traumatic causes of abdominal pain. 2) Attendees will learn the CT signs and causes of bowel ischemia. 3) Attendees will learn the CT findings of common causes of an "acute" abdomen. 4) Attendees will learn the imaging findings of acute, nontraumatic urinary tract and GI tract emergencies. ABSTRACT This segment of the course will go over the optimal imaging approach for patients presenting with acute abdominal pain. CT findings will be emphasized. Key imaging findings of nontraumatic causes of acute abdominal pain including gastrointestinal tract and urinary tract pathology will be explained. A systematic approach for the imaging evaluation of patients wih abdominal emergencies will be illustrated and explained including proper scan protocols and analysis of imaging findings. Imaging diagnosis of urinary tract obstruction, infection, bowel obstruction, and ischemia will be emphasized. MSSR43C Interactive Case Discussion Participants Andras Palko, MD, PhD, Szeged, Hungary (Presenter) Medical Advisory Board, Affidea Group; Ronald J. Zagoria, MD, San Francisco, CA, (ron.zagoria@ucsf.edu) (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Attendees will be able to better analyze CT scans for traumatic and non-traumatic causes of abdominal pain. 2) Attendees will learn the CT signs and causes of bowel ischemia and injuries. 3) Attendees will learn the CT findings of common causes of a traumatic and non-traumatic 'acute' abdomen. 4) Attendees will learn the imaging findings of acute, traumatic and nontraumatic urinary tract and GI tract emergencies. ABSTRACT Using cases and an audience response system, this segment of the course will go over the optimal imaging approach for patients presenting with acute abdominal pain and abdominalk injuries. CT findings will be emphasized. Key imaging findings of traumatic and nontraumatic causes of acute abdominal pain including gastrointestinal tract and urinary tract pathology will be explained. A systematic approach for the imaging evaluation of patients wih abdominal emergencies will be illustrated and explained including proper scan protocols and analysis of imaging findings. Imaging diagnosis of blunt an penetrating abdominal injuries, urinary tract obstruction, infection, bowel obstruction, and ischemia will be emphasized. MSRO43 BOOST: Genitourinary-Case-based Review (An Interactive Session) W ednesday, Dec. 2 3:00PM - 4:15PM Location: S103CD GU RO AMA PRA Category 1 Credits ™: 1.25 ARRT Category A+ Credits: 1.50 Participants Spencer C. Behr, MD, Burlingame, CA (Moderator) Research Grant, General Electric Company; Consultant, General Electric Company Paul Nguyen, Boston, MA (Moderator) Consultant, Medivation, Inc; Consultant, GenomeDx Biosciences Inc Daniel J. Margolis, MD, Los Angeles, CA, (daniel.margolis@ucla.edu) (Presenter) Research Grant, Siemens AG George B. Rodrigues, MD, London, ON (Presenter) Nothing to Disclose Todd Morgan, MD, Ann Arbor, MI (Presenter) Research funded, Myriad Genetics, Inc; Research funded, MDxHealth SA Russell Szmulewitz, MD, Chicago, IL (Presenter) Advisory Board, Pfizer Inc; Advisory Board, Bayer AG LEARNING OBJECTIVES 1) To apply oncologic decision making in prostate cancer. 2) To recognize critical clinical manifestations of prostate cancer. 3) To discern clinically significant from insignificant signs and findings in prostate cancer. SSM11 ISP: Genitourinary (Intravenous Contrast Issues and CT Dose Reduction) W ednesday, Dec. 2 3:00PM - 4:00PM Location: E352 CT GU SQ AMA PRA Category 1 Credit ™: 1.00 ARRT Category A+ Credit: 1.00 Participants Matthew S. Davenport, MD, Cincinnati, OH (Moderator) Book contract, Wolters Kluwer nv; Book contract, Reed Elsevier; Dean A. Nakamoto, MD, Beachwood, OH (Moderator) Research Grant, Galil Medical Ltd; Research agreement, Toshiba Corporation Sub-Events SSM11-01 Genitourinary Keynote Speaker: Safety and Efficacy of Corticosteroid Prophylaxis W ednesday, Dec. 2 3:00PM - 3:10PM Location: E352 Participants Matthew S. Davenport, MD, Cincinnati, OH (Presenter) Book contract, Wolters Kluwer nv; Book contract, Reed Elsevier; SSM11-02 The Effect of IV Contrast on Renal Function in Patients on Metformin W ednesday, Dec. 2 3:10PM - 3:20PM Location: E352 Participants Cody W. McHargue, BA, San Francisco, CA (Presenter) Nothing to Disclose Arti D. Shah, MD, San Francisco, CA (Abstract Co-Author) Nothing to Disclose Judy Yee, MD, Clayton, CA (Abstract Co-Author) Research Grant, EchoPixel, Inc Priyanka Jha, MBBS, Sacramento, CA (Abstract Co-Author) Nothing to Disclose Isabel Allen, San Francisco, CA (Abstract Co-Author) Nothing to Disclose Donald Chau, BA, San Francisco, CA (Abstract Co-Author) Nothing to Disclose Robert Rushakoff, MD, San Francisco, CA (Abstract Co-Author) Nothing to Disclose PURPOSE Due to concerns of acute kidney injury and the theoretical risk of lactic acidosis with metformin, the Food and Drug Administration mandates that metformin be held for two days after intravenous (IV) contrast until renal function is checked and in an acceptable range. However, there is minimal evidence to support this practice. Further investigation is warranted. METHOD AND MATERIALS We conducted a retrospective cohort study of 130 adult outpatients at the San Francisco Veterans Affairs Medical Center to determine if there was a change in renal function in diabetic patients on metformin who underwent computed tomography (CT) scans with IV contrast between 2007-2014. Patients were excluded if immediately hospitalized after the CT scan. The generalized estimating equations method was used to determine whether IV contrast and pre-contrast creatinine (Cr; or pre-contrast estimated glomerular filtration rate [eGFR]) were associated with a change in Cr (or eGFR). Covariates included: age, gender, BMI, diabetes (DM) duration and HbA1c. RESULTS In our cohort, mean age was 67±10 years, 119 (91%) were male, 71 (55%) were Caucasian, and 63 (49%) were higher risk (precontrast eGFR <60 ml/min/1.73m2). Mean DM duration was 6.5±6.0 years and mean HbA1c was 7.1±1.3%. Mean pre- and postcontrast Cr were 1.13±0.25 mg/dL and 1.09±0.26 mg/dL; p=0.02 (overall t-test). Mean pre- and post-contrast eGFR were 72±24 ml/min/1.73m2 and 75±26 ml/min/1.73m2; p=0.006 (overall t-test). In fully-adjusted models, there was a significant decrease in Cr post-contrast: β-coefficient -0.24 (95% confidence interval [CI] -0.35 to -0.12), p<0.001. There was no significant change in eGFR post-contrast: β-coefficient -0.06 (95% CI -0.16 to 0.03), p=0.19. A subgroup analysis of patients with pre-contrast eGFR < 60 ml/min/1.73m2 showed similar results. CONCLUSION There is no evidence of deterioration in renal function in outpatients on metformin who receive IV contrast, even in a cohort with a large proportion of higher risk patients. Therefore, our results suggest that the current practice of holding metformin after IV contrast should be re-evaluated. CLINICAL RELEVANCE/APPLICATION The practice of holding metformin and checking Cr two days after IV contrast should be re-evaluated as there was no evidence to suggest a decline in renal function in a cohort with high risk patients. SSM11-03 The Presence of a Solitary Kidney is not an Independent Risk Factor for Acute Kidney Injury Following Contrast-enhanced CT W ednesday, Dec. 2 3:20PM - 3:30PM Location: E352 Participants Jennifer S. McDonald, PhD, Rochester, MN (Abstract Co-Author) Research Grant, General Electric Company Richard W. Katzberg, MD, Sacramento, CA (Abstract Co-Author) Research Grant, Siemens AG Research Grant, Bayer AG Investigator, Siemens AG Investigator, Bayer AG Robert J. McDonald, MD, PhD, Rochester, MN (Presenter) Nothing to Disclose Eric E. Williamson, MD, Rochester, MN (Abstract Co-Author) Research Grant, General Electric Company David F. Kallmes, MD, Rochester, MN (Abstract Co-Author) Research support, Terumo Corporation Research support, Medtronic, Inc Research support, Sequent Medical, Inc Research support, Benvenue Medical, Inc Consultant, General Electric Company Consultant, Medtronic, Inc Consultant, Johnson & Johnson PURPOSE To determine whether patients with a solitary kidney are at higher risk for contrast-induced acute kidney injury (AKI) than matched control bilateral kidney patients. METHOD AND MATERIALS This retrospective study was HIPAA compliant and approved by our Institutional Review Board. Adult patients with bilateral kidneys or a solitary kidney from unilateral nephrectomy who received a contrast-enhanced computerized tomography (CT) scan at our institution from January 2004 to August 2013 were identified. The effects of contrast exposure on the rate of AKI (defined as a rise in maximal observed serum creatinine (SCr) of either 1) > 0.5 mg/dL or 2) > 0.3 mg/dL or 50% over baseline within 24-72 hours of exposure), and 30-day post-scan emergent dialysis and death were determined following propensity score-based 1:3 matching of solitary and control bilateral kidney patients. RESULTS Propensity score matching yielded a cohort of 247 solitary kidney patients and 691 bilateral kidney patients. The rate of AKI was similar between the solitary and bilateral kidney groups [SCr > 0.5 mg/dL AKI definition odds ratio (OR) = 1.11 (95% confidence interval (CI) 0.65 - 1.86); p = 0.70; SCr > 0.3 mg/dL or 50% AKI definition OR = 0.96 (95% CI 0.41 - 2.07). p = 0.99]. The rate of emergent dialysis was rare and also similar between cohorts (OR = 1.87 (0.16-16.4), p=.61). Though the rate of mortality was higher in the solitary kidney group (OR = 1.70 (1.06-2.71), p=.0202), chart review found that no death was attributable to AKI. CONCLUSION This study did not detect any significant differences in the rate of AKI, dialysis, or death attributable to contrast-enhanced CT in patients with solitary versus bilateral kidneys. CLINICAL RELEVANCE/APPLICATION Contrast-enhanced CT protocols can be guided by image optimization, rather than contrast-induced nephropathy risk in solitary kidney patients. SSM11-04 New Insights in the MRI Excretory Phase: The Use of Gd-EOB-DTPA for the Evaluation of the Excretory System W ednesday, Dec. 2 3:30PM - 3:40PM Location: E352 Participants Caterina Colantoni, MD, Milan, Italy (Presenter) Nothing to Disclose Antonio Esposito, MD, Milan, Italy (Abstract Co-Author) Nothing to Disclose Anna Palmisano, MD, Milan, Italy (Abstract Co-Author) Nothing to Disclose Francesco A. De Cobelli, MD, Milan, Italy (Abstract Co-Author) Nothing to Disclose Alessandro Del Maschio, MD, Milan, Italy (Abstract Co-Author) Nothing to Disclose PURPOSE Excretory MR urography is a useful complementary technique in many MR imaging studies of the abdomen to assess kidney excretion and the urinary collecting system. However, after the injection of a standard dose gadolinium-based contrast media, frequently, the collecting system is unassessable for T2* effect due to very high concentration of Gd in the urine. Aim of the present study was to compare the enhancement of the urinary collecting system after the injection of a single standard dose of Gd-based contrast media known for different renal excretion rates: Gadobutrol, Gadobenate dimeglumine, and Gd-EOB-DTPA. METHOD AND MATERIALS In 60 patients (pts) with normal creatinine clearance and without urinary tract dilatation, mean signal intensities (pixel values) of the renal pelvis and of the paravertebral muscles for the calculation of renal pelvis/skeletal muscle ratio, were evaluated on 3D fast T1-weighted gradient-echo sequences with fat suppression obtained during excretory phase after intravenous injection of 0.1 mmol/kg contrast media: 20pts were studied with Gadobutrol, 20pts with Gadobenate dimeglumine, and 20pts with Gd-EOB-DTPA, respectively. Urinary collecting system was considered assessable/not-assessable according to the presence of T2* effect. RESULTS The mean signal intensities of renal pelvis were 1954±1368.5 (pixel values) for Gadobutrol, 2488±843.8 for Gadobenate dimeglumine, and 3605±1025.3 for Gd-EOB-DTPA, respectively. The mean signal intensity ratio was 2.2±1.59 for Gadobutrol, 2.7±0.88 for Gadobenate dimeglumine, and 3.8±1.46 for Gd-EOB-DTPA. No significant differences were found between the mean signal intensity ratio of Gadobutrol and that of Gadobenate dimeglumine (p>0.05); significant differences were found between the mean signal intensity ratio of Gadobutrol and of Gd-EOB-DTPA (p<0.005), and that of Gadobenate dimeglumine and of Gd-EOB-DTPA (p<0.001). Urinary collecting system was considered not-assessable in 8/20pts for Gadobutrol, in 1/20pt for Gadobenate dimeglumine, and in 0/20pts for Gd-EOB-DTPA. CONCLUSION The urinary collecting system was considered assessable in all pts studied after injection of a standard dose of Gd-EOB-DTPA, and this could be due to the low urine excretion rate. CLINICAL RELEVANCE/APPLICATION The use of Gd-EOB-DTPA in the excretory MR urography can improve the assessability of the excretory system, with no evidence of T2* shortening effects. SSM11-05 Feasibility and Image Quality of Reduced Dose CT Intravenous Pyelogram Using Model-Based Iterative Reconstruction in Patients with Hematuria W ednesday, Dec. 2 3:40PM - 3:50PM Location: E352 Participants Isabelle Boulay-Coletta, MD, Paris, France (Abstract Co-Author) Nothing to Disclose Linda N. Morimoto, MD, Stanford, CA (Presenter) Nothing to Disclose Dominik Fleischmann, MD, Palo Alto, CA (Abstract Co-Author) Research support, Siemens AG; Lior Molvin, Stanford, CA (Abstract Co-Author) Speakers Bureau, General Electric Company Lu Tian, Stanford, CA (Abstract Co-Author) Nothing to Disclose Juergen K. Willmann, MD, Stanford, CA (Abstract Co-Author) Research Consultant, Bracco Group; Research Consultant, Triple Ring Technologies, Inc; Research Grant, Siemens AG; Research Grant, Bracco Group; Research Grant, Koninklijke Philips NV; Research Grant, General Electric Company PURPOSE To evaluate the feasibility and image quality of Reduced Dose (RD) CT Intravenous Pyelogram (IVP) using Model-Based Iterative Reconstruction (MBIR) compared to Standard Dose (SD) CT IVP using Adaptive Statistical Iterative Reconstruction (ASIR) in patients referred for work-up of hematuria. METHOD AND MATERIALS In this IRB approved and HIPAA compliant study, 66 consecutive patients (44 males and 22 women; mean age, 62 years; mean BMI, 27 kg/m²) referred for a dual phase CT IVP (non-contrast and combined split-bolus nephrographic-excretory phase) were prospectively included and either imaged with SD CT IVP with 40% ASIR technique (n=34) or RD CT IVP with MBIR technique (n=32) on a 64-slice CT scanner (GE Discovery 750 HD). Quantitative measurements of image noise on both non-contrast and postcontrast imaging in addition to radiation dose and patients' BMI were recorded by one reader. Two independent, blinded readers assessed subjective image quality, including image noise, sharpness of the renal cortex and collecting system (calyces, renal pelvis, ureters, and bladder), presence of artifacts, and overall image quality impression on non-contrast and post-contrast images utilizing 4 or 5-point grading scales. RESULTS Both patient groups were not significantly different (26.8 +/- 7.8 kg/m² versus 27.5 +/- 4.8 kg/m²) in regards to BMI. Radiation dose was reduced by an average of 49% (p<0.01) on RD CT IVP (CTDI vol = 7.7 +/- 2.8 mGy) compared to SD CT IVP (CTDI vol =15.1 +/- 4.8 mGy) on post-contrast imaging. Overall dose reduction averaged 36% with non-contrast and contrast-enhanced imaging (RD CT IVP CTDIvol =15.31 +/- 2.8 mGy versus SD CT IVP CTDI vol = 23.91 +/- 5.3 mGy). Overall image quality impression of the collecting system, artifacts, and image sharpness were not significantly different (p>0.05) between RD CT IVP and SD CT IVP. Subjective image noise was significantly lower (p<0.01) in RD CT IVP, which was also reflected by a quantitative reduction of image noise by an average of 44% (p<0.01) on non-contrast imaging and 37% (p<0.01) on post-contrast imaging. CONCLUSION RD CT IVP is feasible and allows for a substantial dose reduction compared to SD CT IVP protocol without compromising image quality. CLINICAL RELEVANCE/APPLICATION Introduction of iterative reconstruction algorithms which can be implemented with routine clinical CT IVP protocols to reduce radiation exposure while yielding diagnostic quality images. SSM11-06 Reduced Radiation Dose with Iterative Reconstruction in 100 kVp CT Urography: With different Iodine Dosage W ednesday, Dec. 2 3:50PM - 4:00PM Location: E352 Participants Huihui Wang, MD, Beijing, China (Presenter) Nothing to Disclose Juan Hu, Kunming, China (Abstract Co-Author) Nothing to Disclose Xuedong Yang, Beijing, China (Abstract Co-Author) Nothing to Disclose Xiaoying Wang, MD, Beijing, China (Abstract Co-Author) Nothing to Disclose He Wang, MD, Beijing, China (Abstract Co-Author) Research Grant, General Electric Company Jian Jiang, MD, Beijing, China (Abstract Co-Author) Research Grant, General Electric Company PURPOSE To evaluate the image quality and radiation dose in CT urography at 100kVp with iterative reconstruction, combining a different iodine dosage. METHOD AND MATERIALS This study was approved by the institutional review board. From March to June 2012, 45 consecutive patients who underwent CTU for hematuria were divided into 3 groups: group A, 100kVp and 0.9mL/kg contrast material (CM) (9 men, 6 female; mean age 49.4 years; mean BMI 22.6kg/m2); group B, 100kVp and 1.1mL/kg CM (8 men,7 female; mean age 50.1years; mean BMI 22.6kg/m2); group C, 120kVp and 1.1mL/kg CM (13men, 2 female; mean age 58.5 years, mean BMI 23.5kg/m2). Automatic tube current was used in all groups. The 100kVp images (group A and B) were reconstructed with 80% adaptive statistical iterative reconstruction (ASiR), while filter back projection (FBP) for 120kVp images (group C). Urinary tract was divided into 11 segments, and mean CT values and contrast-to-noise ratio (CNR) of each segment in the excretory phase were measured respectively in 3 groups. The radiation dose in excretory phase was compared (volume computed tomography dose index, CTDIvol; size-specific dose estimate, SSDE and estimated effective dose, ED). RESULTS There were no significant differences among group A, B and C for age, BMI and transverse circumstance (all P>0.05). All examinations were considered to be of acceptable image quality and inter-observer agreement was good (K=0.717, P<0.001). There were no significant differences in mean attenuations of all urinary segments among 3 groups (P>0.05). Image noise was much less in group A and B (both P<0.001) than that of group C, but there was no significant difference between group A and B (P=0.934). CNRs in most segments were higher in group B than group C(P=0.001~0.062) and similar between group A and C(P=0.024~0.896), but there were no notable differences in CNRs between group A and B (P>0.05). Mean CTDIvol, SSDE and ED in excretory phase in group A and B were significantly lower than those of group C(P<0.05). Iodine dosage was reduced by 18.2% in group A than group B and C. CONCLUSION Given subjective and objective image quality, CTU at 100 kVp with 80% ASiR resulted in reduction of radiation dose, and 0.9mL/kg CM (320mgI/ml) iodine dosage was workable. CLINICAL RELEVANCE/APPLICATION High radiation exposure and Contrast-Induced Nephropathy for CTU have drawn much attention and anxiety, 100kVp with 80% ASiR and 0.9mL/kg CM may offer a means of resolution. SSM24 ISP: Vascular/Interventional (Gentiourinary Interventions-Treating Conditions of the Prostate and Uterus) W ednesday, Dec. 2 3:00PM - 4:00PM Location: E450B GU IR AMA PRA Category 1 Credit ™: 1.00 ARRT Category A+ Credit: 1.00 FDA Discussions may include off-label uses. Participants Sandeep Bagla, MD, Woodbridge, VA (Moderator) Consultant, Hansen Medical Inc; Consultant, NeuWave Medical, Inc; Consultant, CeloNova BioSciences, Inc; Consultant, Medtronic, Inc; Consultant, DFINE, Inc'; Consultant, Boston Scientific Charles T. Burke, MD, Chapel Hill, NC (Moderator) Nothing to Disclose Sub-Events SSM24-01 Evaluation of Changes in Quality of Life Related to Uterine Fibroid Embolization (UFE): Preliminary Results of the French SFICV EFUZEN Study W ednesday, Dec. 2 3:00PM - 3:10PM Location: E450B Participants Helene Kovacsik, MD, PhD, Montpellier, France (Abstract Co-Author) Nothing to Disclose Sebastien Bommart, MD, Montpellier, France (Abstract Co-Author) Nothing to Disclose Marc R. Sapoval, MD, PhD, Paris CEDEX 15, France (Abstract Co-Author) Nothing to Disclose Denis Herbreteau, MD, Tours, France (Presenter) Nothing to Disclose Jean-Paul Beregi, MD, Nimes, France (Abstract Co-Author) Nothing to Disclose Jean-Michel Bartoli, MD, Marseille, France (Abstract Co-Author) Nothing to Disclose PURPOSE Main goal:- To evaluate quality of life before and one year after UFESecondary goals:- To determine impact of imaging findings (MRI data) before and 3-6months after UFE on changes in quality of life METHOD AND MATERIALS Study design: prospective, multicenter (25 centers) French observational studyPatients: 264 consecutive symptomatic women referred in the center for UFE using EmbozeneÒ (Celonova) particles. Methods:Clinical data: the quality of life score was calculated using the previously validated UFS-QOL by Spies, before and one year after UFE.Imaging data: MRI were performed before and 3-6 months after UFE. Data recorded were uterine and main fibroid volume, percentage of fibroid enhancement after injection of gadolinium. Impact of imaging data before and after UFE on QOL scores was searched. RESULTS 189 patients (85.9%) showed monorrhagia at baseline. This was reduced to 39 patients (18%) at 1 year of follow up. 171 patients (78.1%) had pelvic pressure symptoms at baseline. This was reduced to 42 patients (19.4%) after 1 year of follow up.Complete QOL study was obtained in 192 women. Improvement of QOL score at one year after UFE a was found 183/203 (90.2%) for HRQL, 163/192 (84.9%) for Symptoms Severity. The probability of presenting a profuse bleeding was significantly reduced (by 62%) among patients with high reduction of fibroid volume (>=30%), as compared to patients with low fibroid volume reduction (<30%) (OR=0.38; 95%CI: [0.18;0.80]) (p = 0.011) The Impact of percentage of uterine volume or main fibroid reduction and decrease of fibroid enhancement on change in post embolization global UFS-QOL score was not established. CONCLUSION At one year post embolization, UFE improves significantly quality of life CLINICAL RELEVANCE/APPLICATION UFE is not only an effective technique but is also considered highly satisfactory by women SSM24-02 Vascular/Interventional Keynote Speaker: Current Status of Prostate Artery Embolization as a Treatment for BPH W ednesday, Dec. 2 3:10PM - 3:20PM Location: E450B Participants Sandeep Bagla, MD, Woodbridge, VA (Presenter) Consultant, Hansen Medical Inc; Consultant, NeuWave Medical, Inc; Consultant, CeloNova BioSciences, Inc; Consultant, Medtronic, Inc; Consultant, DFINE, Inc'; Consultant, Boston Scientific SSM24-03 Percutaneous Ablation of Oligometastatic Prostate Cancer: Oncologic Outcomes and Safety W ednesday, Dec. 2 3:20PM - 3:30PM Location: E450B Participants Andrew Erie, MD, Rochester, MN (Presenter) Nothing to Disclose Jonathan M. Morris, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Brian T. Welch, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Anil N. Kurup, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Adam J. Weisbrod, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Thomas D. Atwell, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Grant D. Schmit, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Eugene D. Kwon, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Matthew R. Callstrom, MD, PhD, Rochester, MN (Abstract Co-Author) Research Grant, Thermedical, Inc Research Grant, General Electric Company Research Grant, Siemens AG Research Grant, Galil Medical Ltd PURPOSE To determine the oncologic outcomes and safety of percutaneous ablation in the treatment of oligometastatic prostate cancer. METHOD AND MATERIALS This is a retrospective, single-institution review of 31 patients with oligometastatic prostate cancer who underwent 43 percutaneous ablations of their limited (≤5) metastatic sites. Eight patients (26%) were antigen deprivation therapy-naïve (ADTnaïve) and received ablation with the purpose of delaying ADT. Twenty-three patients (74%) underwent ablation either because of resistance to systemic therapies or a more aggressive multimodal treatment approach was preferred. Study endpoints included procedural complications, local control, progression free survival (PFS), and androgen deprivation therapy-free survival (ADT-FS). ADT-FS was defined as the time between percutaneous ablation and the initiation of ADT. RESULTS Local control was achieved in 35 (81.4%) of 43 tumors with a median follow-up of 8 months (range, 3-60 mo) after ablation. Tumor recurrence was found in 8 (18.6%) of 43 tumors at a median follow-up of 6 months (range, 2-38 mo). Median prostate-specific antigen (PSA) measurements were significantly lower approximately 2 months after ablation compared to before ablation (0.27 ng/dl [range <0.01 to 7.7] and 1.5 ng/dl [range <0.01 to 72.0], respectively (p=0.02)). Estimated PFS rates for all patients at 6 and 12 months after ablation were 65% (95% CI, 44-80) and 45% (95% CI, 24-64), respectively. Of the 8 ADT-naïve patients who underwent ablation with purpose to delay ADT, all (100%) achieved local control and the ADT-FS at 12 months was approximately 70%. None of the ablations were associated with major complications. CONCLUSION Percutaneous ablation of oligometastatic prostate cancer appears safe, achieves acceptable local control rates, and can delay disease progression when used in combination with other therapies. Percutaneous ablation may be particularly valuable in ADTnaïve patients who do not tolerate or prefer to delay ADT. CLINICAL RELEVANCE/APPLICATION Percutaneous ablation can be used as part of a multimodal treatment approach for oligometastatic prostate cancer and can delay hormone therapy in ADT-naïve patients. SSM24-04 Frequency of Penile and Rectal Collateral Flow from Prostatic Arteries during Prostatic Artery Embolization W ednesday, Dec. 2 3:30PM - 3:40PM Location: E450B Participants Ari J. Isaacson, MD, Chapel Hill, NC (Abstract Co-Author) Advisory Board, BTG International Ltd Charles T. Burke, MD, Chapel Hill, NC (Presenter) Nothing to Disclose PURPOSE The most common mechanism of complication during prostatic artery embolization (PAE) is non-target embolization. Avoidance of branches supplying the bladder is commonly described. Less commonly discussed are intra-prostatic collaterals supplying the penis and rectum, although they are frequently seen during PAE. Because of the risks associated with non-target embolization as a result of these shunts, it would be beneficial to have an understanding of their incidence, as well as from what prostatic artery branches they arise. The purpose of this study was to retrospectively determine the frequency of rectal and penile collateral flow from each prostatic artery branch as seen during PAE. METHOD AND MATERIALS DSA images from PAEs performed between April 2013 and March 2015 were evaluated by two interventional radiologists experienced in performing PAE. A consensus determination was made about which arteries were catheterized (the anterolateral prostatic artery (ALPA), the posterolateral prostatic artery (PLPA) or a common trunk (CT) of the two) and about the presence of collateral flow to the arteries supplying the penis and/or the rectum from each catheterized artery. The overall incidence of such collaterals was calculated as well as the frequency in which they arose from each prostatic artery branch. RESULTS During 26 PAEs, 58 prostatic arteries were catheterized (36 ALPAs, 10 PLPAs and 12 CTs). Collateral flow to arteries supplying the penis or rectum was identified in 18/26 PAEs (69%). Flow to the penile arteries was seen in 13/36 (36%) ALPA catheterizations and in 5/12 (42%) CT catheterizations. Flow to rectal branches was seen in 8/10 (80%) PLPA catheterizations and in 4/12 (33%) CT catheterizations. No flow to penile branches was observed from a PLPA, nor was there flow to a rectal branch seen from an ALPA. CONCLUSION Shunting to the penis and/or rectum was present during the majority of PAEs. Collateral flow to the rectum from the PLPA or from a CT was seen quite frequently and collateral flow to the penis from an ALPA or CT was seen with moderate frequency during prostatic artery catheterization. CLINICAL RELEVANCE/APPLICATION Understanding the incidence of rectal and penile collateral pathways from the specific branches of the prostatic arteries will allow for greater detection of these findings during PAE in order to avoid complications. SSM24-05 Prostate Cancer Treatment with Irreversible Electroporation (IRE): Experience, Safety and Efficacy after 4.5 Years in 222 Patients W ednesday, Dec. 2 3:40PM - 3:50PM Location: E450B Participants Michael K. Stehling, MD, PhD, Offenbach, Germany (Presenter) Nothing to Disclose Enric Guenther, Dipl Phys, Frankfurt, Germany (Abstract Co-Author) Nothing to Disclose Nina Klein, MSc, Offenbach am Main, Germany (Abstract Co-Author) Nothing to Disclose Stephan Zapf, Frankfurt, Germany (Abstract Co-Author) Nothing to Disclose Ducksoo Kim, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Boris Rubinsky, PhD, Berkeley, CA (Abstract Co-Author) Nothing to Disclose PURPOSE Irreversible Electroporation (IRE) is a novel tissue ablation method. It selectively destroys cells whilst preserving tissue infrastructure and is hence an ideal method for focal prostate cancer (PCa) therapy. It preserves (or allows regeneration of) vital surrounding structures such as neurovascular bundle, inferior sphincter and rectum, thus minimizing the side-effects of PCa therapy, mainly being impotence and incontinence. METHOD AND MATERIALS We have employed IRE for the treatment of 222 patients with primary (stages T1-T4) and recurrent PCa after surgery (18/222), radiation therapy (4/222) and HIFU (3/222). All patients underwent mp-MRI prior to and after IRE (T2, diffusion, perfusion, in selected cases 1H spectroscopy). 44% of patients underwent additional 3D-transperineal biopsy before IRE. Treatment was carried out by rectal US-guided transperineal IRE-electrode insertion under general anesthesia and deep muscle relaxation. 161 patients had focal and 61 whole gland ablations. All patients had follow-ups with PSA and mp-MRI for documentation of local tumor control. RESULTS Initial tumor control was achieved in all patients. Within the follow-up period of up to 4y, the recurrence rates were 0/45 (Gleason <7), 4/103 (Gleason 7) and 5/54 (Gleason >7). There were no IRE-related complications and toxicity was extremely low: 16 patients reported a transient reduction of erectile function (EF) (recurred after 6-8m), 5 a permanent reduction and 2 a permanent loss of EF. There were no cases of IRE-related incontinence, even when the lower urinary sphincter was included in the treatment field; a partially included rectum also remained intact. Treatment was completed within 24h in all patients with a single overnight stay in the clinic. Patients had no wound pain. CONCLUSION IRE treatment of PCa is safe. In the short-term follow-up with MRI and PSA (maximum 4.5y) it is effective. Toxicity is significantly lower compared to other PCa treatments. Based on our data incontinence can be avoided altogether. MRI and 3D-biopsy are suitable for pre-treatment work-up and MRI for post-treatment follow-up. IRE has the potential to become an important tool for PCa therapy. CLINICAL RELEVANCE/APPLICATION IRE treatment is an alternative to the current treatment options for PCa, with much lower invasiveness and toxicity. It is effective in all stages of PCa and offers treatment options in advanced and recurrent PCa not amenable to other therapies. SSM24-06 Phase II Clinical Trial for Evaluation of MRI-guided Laser Induced Interstitial Thermal Therapy (LITT) for Low-to-intermediate Risk Prostate Cancer W ednesday, Dec. 2 3:50PM - 4:00PM Location: E450B Participants Aytekin Oto, MD, Chicago, IL (Presenter) Research Grant, Koninklijke Philips NV; ; ; Shiyang Wang, PhD, Chicago, IL (Abstract Co-Author) Nothing to Disclose Ambereen Yousuf, MBBS, Chicago, IL (Abstract Co-Author) Nothing to Disclose Sydeaka Watson, PhD, Chicago, IL (Abstract Co-Author) Nothing to Disclose Tatjana Antic, Chicago, IL (Abstract Co-Author) Nothing to Disclose Scott Eggener, Chicago, IL (Abstract Co-Author) Research Grant, Visualase, Inc Speakers Bureau, Johnson & Johnson PURPOSE To assess the oncologic efficacy and safety of MRI-guided laser-induced interstitial thermal therapy of biopsy confirmed and MRvisible prostate cancer. METHOD AND MATERIALS 27 patients with biopsy proven low-to-intermediate risk prostate cancer underwent MRI-guided laser ablation of the cancer using Visualase laser ablation device. All patients had a pre-procedure endorectal MRI which showed suspicious foci concomitant with the positive sextant on TRUS-guided biopsy. The area of interest was targeted transperineally using 1.5 T Philips MRI scanner and Visualase ablation device. Ablation was monitored by real time MR thermometry using Visualase MRI thermometry software. Perioperative, early and late complications and adverse events were recorded. Follow-up was performed with 3-month MRI and MRguided biopsy, 12-month MRI and TRUS guided biopsy and validated quality of life questionnaires to assess urinary and sexual function. RESULTS MRI-guided laser ablation of prostate cancer was successfully performed in all 27 patients without significant peri-procedural complications. All patients were discharged home the same day. Average duration of the procedure was 3 hours 17 minutes and average duration of a single laser ablation was 1 minute 22 seconds. Total number of ablations per patient ranged from 2-8, with a median of 4. The treatment created an identifiable hypovascular defect in all cases. Post procedure complications were minor and included urinary symptoms, perineal bruising and erectile dysfunction, all of which self- resolved. Validated quality of life urinary and sexual questionnaires obtained before and 12 months after the procedure did not reveal any significant differences (p≥0.05). 1/27 and 3/17 patients had residual cancer in the ablation zone at 3 months and 12 months respectively. CONCLUSION Short-term follow-up results of MRI-guided focal laser ablation for treatment of clinically localized, low-to-intermediate risk prostate cancer appear promising. It may offer a minimally invasive procedure for select patients that does not appreciably alter sexual or urinary function. CLINICAL RELEVANCE/APPLICATION Short-term results of our phase II trial show that MRI-guided focal laser ablation can be a safe and feasible option for treatment of low-to-intermediate risk prostate cancer. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Aytekin Oto, MD - 2013 Honored Educator MSCU42 Case-based Review of US (An Interactive Session) W ednesday, Dec. 2 3:30PM - 5:00PM Location: S406A GI GU US AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Deborah J. Rubens, MD, Rochester, NY (Moderator) Nothing to Disclose LEARNING OBJECTIVES 1) Recognize the diverse applications of ultrasound throughout the body and when it provides the optimal diagnostic imaging choice. 2) Understand the fundamental interpretive parameters of ultrasound contrast enhancement and its applications in the abdomen. 3) Know the important factors to consider when choosing ultrasound vs CT for image guided procedures and how to optimize ultrasound for technical success. ABSTRACT Ultrasound is a rapidly evolving imaging modality which has achieved widespread application throughout the body. In this course we will address the major anatomic areas of ultrasound use, including the abdominal and pelvic organs, superficial structures and the vascular system. Challenging imaging and clinical scenarios will be emphasized to include the participant in the decision-making process. Advanced cases and evolving technology will be highlighted, including the use of ultrasound contrast media as a problem solving tool, and the appropriate selection of procedures for US-guided intervention. Active Handout:Deborah J. Rubens http://abstract.rsna.org/uploads/2015/15002752/Active MSCU42.pdf Sub-Events MSCU42A Challenging Abdominal Cases Participants Oksana H. Baltarowich, MD, Philadelphia, PA (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. ABSTRACT View abstract under main course title. MSCU42B Acute Pelvic Pain Participants Leslie M. Scoutt, MD, New Haven, CT, (leslie.scoutt@yale.edu) (Presenter) Consultant, Koninklijke Philips NV LEARNING OBJECTIVES View learning objectives under main course title. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Leslie M. Scoutt, MD - 2014 Honored Educator MSCU42C Superficial Ultrasound Imaging: Head to Toe Participants Deborah J. Rubens, MD, Rochester, NY (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. MSRT46 ASRT@RSNA 2015: Prostate Cancer and MR Imaging: What Do We Want to See and How to Get It W ednesday, Dec. 2 3:40PM - 4:40PM Location: N230 GU MR OI AMA PRA Category 1 Credit ™: 1.00 ARRT Category A+ Credit: 1.00 Participants James Stirling, DCR, DMS, Middlesex, United Kingdom, (james.stirling@kcl.ac.uk ) (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) To learn the anatomy and comon pathology of the prostate gland. 2) To learn the factors and how to optimise prostate sequences eg. T1, T2 and STIR whole pelvis sequences, small field of view T2 axial, sagital and coronal sequences, diffusion weighted imaging, contrast enhanced T1 and T2* dynamic sequences. 3) To learn how different sequences are used with primary, secondary and metastatic prostate cancer. 4) To give a taste of hybid PET/MR 18F Choline imaging. ABSTRACT Over the last couple of years MRI of prostate cancer has moved from just T1 and T2 imaging to multi-parametric, multi-modality imaging. To produce high quality imaging, sequence parameter factors have to be optimized, balancing clinical requirements with patient comfort, total on-table time, scanner capabilities and limitations. The lecture will include prostatic anatomy and how different sequences can characterize benign and malignant disease. The talk will show the sequences that are needed and how to optimize them. This will include T2 small field of views, diffusion weighted imaging, T1 and T2* dynamic contrast enhanced sequences and intrinsic susceptibility weighted imaging. As prostate cancer develops and is treated the imaging protocols change. The protocols include surveillance and staging and then progress to recurrence and metastatic whole body imaging. MRI is now being complemented with PET in hybrid machines combining the strengths of both modalities. This lecture will show how MR imaging of malignant prostate disease changes as the disease progresses. SPSC44 Controversy Session: Prostate Imaging: Just What MR Technique is Best? W ednesday, Dec. 2 4:30PM - 6:00PM Location: E450A GU MR AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Rajan T. Gupta, MD, Durham, NC (Moderator) Consultant, Bayer AG; Speakers Bureau, Bayer AG; Consultant, Invivo Corporation LEARNING OBJECTIVES 1) The goal of this session is to explore the different techniques that comprise high quality multiparametric MRI of the prostate. More specifically, we will deal with some of the key protocol questions that one must tackle in order to set up mpMRI in their own practice. Examples of the topics to be discussed include 1.5T vs. 3T imaging; endorectal coil vs. phased array body coil use; the optimal diffusion weighted metrics to be used to assess lesion aggressiveness, etc.; the changing role of dynamic contrast enhanced MRI in prostate imaging, especially in light of the recent release of PI-RADS version 2; and finally, the optimal techniques to evaluate for disease recurrence after therapy. The format of the session will be both didactic and interactive with audience participation. Sub-Events SPSC44A Introduction to Session and Overview of Multiparametric Prostate MRI Participants Rajan T. Gupta, MD, Durham, NC (Presenter) Consultant, Bayer AG; Speakers Bureau, Bayer AG; Consultant, Invivo Corporation LEARNING OBJECTIVES View learning objectives under main course title. SPSC44B 1.5T vs 3T Imaging: Pros and Cons Participants Rajan T. Gupta, MD, Durham, NC (Presenter) Consultant, Bayer AG; Speakers Bureau, Bayer AG; Consultant, Invivo Corporation Francois Cornud, MD, Paris, France (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. SPSC44C Diffusion Weighted Imaging Participants Andrew B. Rosenkrantz, MD, New York, NY (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. SPSC44D Dynamic Contrast Enhanced Imaging Participants Sadhna Verma, MD, Cincinnati, OH (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Sadhna Verma, MD - 2013 Honored Educator SPSC44E Imaging of Recurrence in Prostate Cancer Participants Adam Froemming, MD, Rochester, MN (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. SPSC46 Controversy Session: Ultrasound versus CT for Suspected Renal Colic: Which Modality Rocks in the ER? W ednesday, Dec. 2 4:30PM - 6:00PM Location: S404CD GU CT US ER AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Judy Yee, MD, San Francisco, CA (Moderator) Research Grant, EchoPixel, Inc Mitchell E. Tublin, MD, Pittsburgh, PA (Presenter) Nothing to Disclose Aaron D. Sodickson, MD, PhD, Wayland, MA, (asodickson@bwh.harvard.edu) (Presenter) Research Grant, Siemens AG; Consultant, Bracco Group D. Mark Courtney, MD, MSc, Chicago, IL (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Describe the advantages of ultrasound and present a cost effective, rational algorithm for its use in the evaluation of ER patients with potential renal colic. 2) Understand the benefits of CT over ultrasound in ER imaging of suspected renal colic. 3) Understand the perspective and preferences of the ER physician for the workup of renal colic and the effect on clinical workflow. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Aaron D. Sodickson, MD, PhD - 2014 Honored Educator ED006-TH Genitourinary Thursday Case of the Day Thursday, Dec. 3 7:00AM - 11:59PM Location: Case of Day, Learning Center GU AMA PRA Category 1 Credit ™: .50 Participants Theodora A. Potretzke, MD, Saint Louis, MO (Presenter) Nothing to Disclose Perry J. Pickhardt, MD, Madison, WI (Abstract Co-Author) Co-founder, VirtuoCTC, LLC; Stockholder, Cellectar Biosciences, Inc; Research Consultant, Bracco Group; Research Consultant, KIT ; Research Grant, Koninklijke Philips NV Naoki Takahashi, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose Meghan G. Lubner, MD, Madison, WI (Abstract Co-Author) Grant, General Electric Company; Grant, NeuWave Medical, Inc; Grant, Koninklijke Philips NV Anup S. Shetty, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Richard Tsai, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose George A. Carberry, MD, Madison, WI (Abstract Co-Author) Nothing to Disclose Vincent M. Mellnick, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose David U. Kim, MD, Madison, WI (Abstract Co-Author) Nothing to Disclose Yaseen Oweis, MD, MBA, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Zachary J. Viets, MD, Saint Louis, MO (Abstract Co-Author) Nothing to Disclose Bernard F. King JR, MD, Rochester, MN (Abstract Co-Author) Nothing to Disclose TEACHING POINTS 1) Recognize imaging findings seen in disorders of the genitourinary systems. 2) Develop differential diagnosis based on the clinical information and imaging findings. 3) Recognize the clinical importance of diagnosis. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Perry J. Pickhardt, MD - 2014 Honored Educator Naoki Takahashi, MD - 2012 Honored Educator Meghan G. Lubner, MD - 2014 Honored Educator Meghan G. Lubner, MD - 2015 Honored Educator SPSH50 Hot Topic Session: Dual-energy CT for GU Imaging Thursday, Dec. 3 7:15AM - 8:15AM Location: E350 GU CT AMA PRA Category 1 Credit ™: 1.00 ARRT Category A+ Credit: 1.00 Participants Hersh Chandarana, MD, New York, NY (Moderator) Equipment support, Siemens AG; Software support, Siemens AG; Consultant, Bayer, AG; LEARNING OBJECTIVES 1) This course will cover the basics and application of Dual Energy CT in GU Radiology. ABSTRACT Sub-Events SPSH50A Principles of DECT Participants Daniel T. Boll, MD, Durham, NC (Presenter) Research Grant, Siemens AG; Research Grant, Koninklijke Philips NV; Research Grant, Bracco Group SPSH50B DECT of GU Masses-2015 Update Participants Terri J. Vrtiska, MD, Rochester, MN (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Discuss DECT advantages for renal mass evaluation. 2) Describe useful DECT applications for renal mass characterization. 3) Summarize recent literature and future opportunities of DECT of renal masses. ABSTRACT Application of DECT to renal mass evaluation and improved characterization. URL SPSH50C Establishing DECT in Your Practice: Nuts and Bolts Participants Avinash R. Kambadakone, MD, Boston, MA (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Describe the basic principles, technique and clinical applications of DECT. 2) Identify and appraise the different technologies, workflow implications and challenges of DECT in day-to-day practice. 3) Apply and incorporate the most appropriate DECT protocols into routine practice. ABSTRACT URL RC607 A Case-based Audience Participation Session (Genitourinary) (An Interactive Session) Thursday, Dec. 3 8:30AM - 10:00AM Location: E352 GU AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Paul J. Chang, MD, Chicago, IL, (pchang@radiology.bsd.uchicago.edu) (Coordinator) Co-founder, Stentor/Koninklijke Philips NV; Researcher, Koninklijke Philips NV; Medical Advisory Board, lifeIMAGE Inc; Medical Advisory Board, Merge Healthcare Incorporated William W. Mayo-Smith, MD, Boston, MA (Presenter) Author with royalties, Reed Elsevier; Author with royalties, Cambridge University Press Andrea G. Rockall, MRCP, FRCR, London, United Kingdom (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) The participant will be introduced to a series of Genitourinary case studies via an interactive team game approach designed to encourage "active" consumption of educational content. 2) The participant will be able to use their mobile wireless device (tablet, phone, laptop) to electronically respond to various Genitourinary case challenges; participants will be able to monitor their individual and team performance in real time. 3) The attendee will receive a personalized self-assessment report via email that will review the case material presented during the session, along with individual and team performance. Please bring your charged mobile wireless device (phone, tablet or laptop) to participate. ABSTRACT The extremely popular audience participation educational experience is back! :GU Diagnosis Live is an expert-moderated session featuring a series of interactive Genitourinary case studies that will challenge radiologists' diagnostic skills and knowledge. Building on last year's successful Diagnosis Live premiere, GU Diagnosis Live is a lively, fast-paced game format: participants will be automatically assigned to teams who will then use their personal mobile devices to test their knowledge of GU radiology in a fastpaced session that will be both educational and entertaining. After the session, attendees will receive a personalized selfassessment report via email that will revview the case material presented durinig the session, along with individual and team performance. : RC610 Ultrasound Contrast (An Interactive Session) Thursday, Dec. 3 8:30AM - 10:00AM Location: S402AB GI GU US AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 FDA Discussions may include off-label uses. Participants Sub-Events RC610A Renal Masses Participants Edward G. Grant, MD, Los Angeles, CA (Presenter) Research Grant, General Electric Company ; Medical Advisory Board, Nuance Communications, Inc LEARNING OBJECTIVES 1) Understand the indications for the use of contrast enhanced ultrasound in renal masses. 2) Be familiar with the advantages and disadvantages of contrast enhanced ultrasound in comparison to other forms of cross sectional imaging with regard to its application to renal masses. 3) Be able to analyze contrast enhanced ultrasound images of the kidney. 4) Understand the basics of quantitative contrast imaging of renal masses. ABSTRACT Contrast enhanced ultrasound (CEUS) has numerous applications in the imaging of renal masses. It has the particular advantage in this population of being able to be used in patients with renal failure which is not the case with either CT or MRI. Obviously CEUS does not use ionizing radiation and is less expensive than other techniques. A further advantage is the fact that ultrasound is a real time technique and vascular characteristics of lesions can be evaluated throughout the examination. Applications of CEUS in the kidney include imaging of complex cysts (flow in wall, septae etc.) and evaluation of pseudolesions (column of Bertin, infarct, scars). It can also be used to further characterize indeterminate masses on CT/MR and may be able to classify some lesions as benign versus malignant, or suggest their actual histology. The diagnostic capability of CEUS is facilitated by its ability to provide quantitative information. Given the lack of ionizing radiation and absence of nephrotoxicity CEUS is ideal for patients undergoing active surveillance of a renal mass or post resection/RFA.The evaluation of complex renal cysts is one of the most common indications for CEUS. Observed features at CEUS are typically similar to those of the Bosniak classification and this has now been adapted for use with ultrasound contrast. In solid renal masses CEUS may provide information that can help determine the nature of the mass and its anatomy as well as the number of individual lesions. This is particularly valuable in patients in whom other contrast agents are contraindicated. One notable example is the characteristic enhancement pattern of papillary versus clear cell renal cell carcinoma. The former typically enhances less than the surrounding parenchyma throughout the examination while the latter dramatically hyperenhances in the arterial phase. Again, quantitative imaging can further add to the confidence of the diagnosis in such cases. RC610B Contrast Ultrasound of the Liver and Gallbladder Participants Hans-Peter Weskott, MD, Hannover, Germany, (weskotthp@t-online.de) (Presenter) Luminary, General Electric Company; Speaker, Bracco Group LEARNING OBJECTIVES 1) Understanding the indications of contrast enhanced ultrasound (CEUS) in focal liver and gallbladder diseases. 2) Learning about the importance of the three contrast phases and how CEUS performes in detecting and characterizing focal liver lesions and to characterize inflammatory and tumorous changes of the gallbladder wall. 3) Learning about the potential value as well as the limitations of CEUS in liver an gallbladder diseases. 4) Learning how CEUS performs when compared to B-mode and Color Doppler ultrasound, CT and MRI imaging. ABSTRACT Liver: In patients with favorable scanning conditions CEUS is at least as sensitive as contrast enhanced CT (CECT) in detecting malignant liver lesions. Due to its high temporal resolution, even a hyper-enhancement of a few seconds can reliably be detected, thus improving the characterization of focal liver lesions. A majority of malignant lesions can therefore be characterized as hypo-, iso- or hyper-enhancing. During the arterial phase the tumor`s vessel architecture and direction of contrast filling is important for characterizing a lesions character. Due to a high spatial resolution, novel contrast imaging techniques allow detection of washed out lesions down to 3mm in size. CEUS characterizes focal liver lesions with a much higher diagnostic confidence than conventional US and is comparable to CT and MRI. CEUS also improves intraoperative tumor detection and characterization. Using time intensity analysis a change in contrast enhancement and kinetics helps in estimating tumor response to chemotherapy. CEUS is also used to monitor local ablation therapy and is a useful imaging tool to detect early tumor recurrence. Gallbladder: CEUS can be used to better visualize ulceration, perforation, and tumors of its wall. It thus helps in optimizing clinical management, including timing for surgery. CEUS does not affect renal or thyroid function and is therefore helpful in older patients and the preferred imaging technique in young patients and those with impaired renal function. RC610C Participants Contrast Ultrasound of Bowel Stephanie R. Wilson, MD, Calgary, AB (Presenter) Research Grant, Lantheus Medical Imaging, Inc; Equipment support, Siemens AG; Equipment support, Koninklijke Philips NV LEARNING OBJECTIVES 1) Attendees will recognize the association of hypervascularity with inflammatory processes in the bowel on the basis of neoangiogenesis. 2) They will appreciate the value of CEUS of the bowel, with provision of both subjective and objective blood flow determinations, useful in determining disease activity and in assessing response to therapy. . 3) They will apply the common interpretations of time itensity curves to obtain peak enhancement and area under the curve information, recognizing their direct relationship to inflammatory disease with increasing parameters. ABSTRACT RC629 Prostate MRI Using PI-RADS (Prostate Imaging Reporting and Data System) (An Interactive Session) Thursday, Dec. 3 8:30AM - 10:00AM Location: E450B GU MR AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants LEARNING OBJECTIVES 1) Describe the clinical indications for prostate MRI and MRI-targeted interventions. 2) Assess technical considerations for performance of multi-parametric prostate MRI, including pulse sequences, coils, contrast administration, magnetic field strength. 3) Integrate information from T2, DCE, and DWI to analyze and report prostate MRI exams using new ACR-PIRADS methodology. Please bring your charged mobile wireless device (phone, tablet or laptop) to participate. Sub-Events RC629A Introduction to PI-RADS Participants Jeffrey C. Weinreb, MD, New Haven, CT (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. RC629B Technical Considerations Participants Clare M. Tempany-Afdhal, MD, Boston, MA (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. RC629C How to Use PI-RADS Participants Jelle O. Barentsz, MD, PhD, Nijmegen, Netherlands (Presenter) Nothing to Disclose LEARNING OBJECTIVES View learning objectives under main course title. Active Handout:Jelle O. Barentsz http://abstract.rsna.org/uploads/2015/14000510/Active RC629C.pdf RC629D Interactive Clinical Case Review Participants LEARNING OBJECTIVES View learning objectives under main course title. SSQ09 ISP: Genitourinary (Renal Mass Evaluation) Thursday, Dec. 3 10:30AM - 12:00PM Location: E353B GU CT MR AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Raghunandan Vikram, MBBS, FRCR, Houston, TX (Moderator) Nothing to Disclose Daniele Marin, MD, Cary, NC (Moderator) Nothing to Disclose Sub-Events SSQ09-01 Genitourinary Keynote Speaker: Contemporary Challenges of Imaging Renal Masses Thursday, Dec. 3 10:30AM - 10:40AM Location: E353B Participants John R. Leyendecker, MD, Dallas, TX (Presenter) Nothing to Disclose SSQ09-02 Do Incidental Hyperechoic Renal Lesions Measuring ≤ 1cm Warrant Further Imaging? Outcomes of 161 Lesions Thursday, Dec. 3 10:40AM - 10:50AM Location: E353B Participants Abimbola Ayoola, MD, New York, NY (Presenter) Nothing to Disclose Andrew B. Rosenkrantz, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Ankur Doshi, MD, New York, NY (Abstract Co-Author) Nothing to Disclose PURPOSE Although follow-up CT or MRI has been advised for further evaluation of incidental hyperechoic renal lesions on ultrasound (US), this approach is variably followed in clinical practice given the lack of robust data to guide optimal follow-up recommendations. Thus, the purpose of our study was to determine the outcomes of incidental hyperechoic renal lesions measuring ≤ 1cm based on a large single-center cohort in order to better inform management strategies for such lesions. METHOD AND MATERIALS We retrospectively identified 161 hyperechoic renal lesions on US measuring ≤ 1cm (mean size 0.7 ± 0.2 cm) that had either (a) a follow-up CT or MRI or (b) at least 2 year follow-up by US. Mean patient age was 63 ±13 years (range 30-88 years). The initial US and follow-up imaging were reviewed to assess for a change in size or definitive lesion characterization. RESULTS Follow-up imaging consisted of US in 23.0% (37/161), CT in 45.3% (73/161) and MRI in 31.7% (51/161). 57.1% (92/161) of lesions were confirmed as angiomyolipomas on CT or MRI. 19.9% (32/161) showed less than 4mm growth on long-term US follow-up (mean 62±26 months, range 24-110 months). 11.8% (19/161) had no correlate on CT or MRI. 6.2% (10/161) were too small to definitively characterize on CT. 3.1% (5/161) were not visualized on follow-up US. CT characterized one lesion (0.6%) as a stone and one lesion (0.6%) as a hyperdense cyst. One lesion (0.6%) on CT was an enhancing solid mass without macroscopic fat, presumed to represent an RCC, although was lost to follow-up. This lesion was not as hyperechoic as the renal sinus fat on the initial US. CONCLUSION The overwhelming majority of hyperechoic renal lesions ≤ 1cm with the classic US appearance of an angiomyolipoma were benign or stable on follow-up imaging. Thus, these lesions may not warrant any further imaging evaluation. CLINICAL RELEVANCE/APPLICATION To our knowledge, we have provided the largest study to date to assess outcomes of small hyperechoic renal lesions on follow-up imaging that support the benignity of this US finding. SSQ09-03 Post-operative Outcomes of Cystic Renal Cell Carcinomas Defined on Pre-operative Computed Tomography: A Retrospective Study in 1315 Patients Thursday, Dec. 3 10:50AM - 11:00AM Location: E353B Participants Jung Jae Park, MD, Seoul, Korea, Republic Of (Presenter) Nothing to Disclose Chan Kyo Kim, MD, PhD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Byung Kwan Park, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Byong Chang Jeong, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Seong Il Seo, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose PURPOSE Post-operative outcomes of cystic renal cell carcinomas (RCCs) defined on preoperative imaging were not widely investigated and the cut-off of cystic proportion is arbitrary. We aimed to evaluate the post-operative outcomes of cystic RCCs defined on preoperative computed tomography (CT) and to identify the optimal cut-off of cystic proportion in association with patients' prognosis. METHOD AND MATERIALS Our retrospective study included 1315 consecutive patients who received surgery for single sporadic RCC and had adequate preoperative CT for analysis. The cystic proportion of RCC was calculated on pre-operative CT by a radiologist. The optimal cut-off of cystic proportion in RCC was explored by locating the minimum P value on log rank test regarding cancer-specific survival. The RCCs were categorized as cystic and non-cystic groups according to (1) conventional cut-off (i.e. proportion of cystic component≥ 75%) and (2) the optimal cut-off, and then cancer-specific and recurrence-free survival rates were compared between the two groups. The clinical, pathologic, and imaging variables were analyzed using the Cox regression analysis to determine the independent predictor of cancer-specific survival. RESULTS Of the 1315 RCCs, 107 (8.1%) were identified as cystic RCCs using the conventional cut-off. During a median follow-up of 4.9 years, patients with cystic RCC revealed neither metastasis nor recurrence after surgery. The cancer-specific and recurrence-free survival rates of cystic RCCs were significantly better than those of non-cystic RCCs (both P < 0·001). In association with cancerspecific survival rate, the optimal cut-off of cystic proportion in RCC was 45%, and 197 (15.0%) patients were defined as cystic RCCs accordingly. On multivariate Cox regression analysis, cystic RCC defined by the optimal cut-off (45%) was one of the independent predictors of cancer-specific survival (hazard ratio, 0.34; P = 0.03). CONCLUSION Cystic RCCs defined on pre-operative CT are associated with low metastatic potential and favorable outcomes after surgery. Furthermore, the optimal cut-off of cystic proportion in association with cancer-specific survival is 45%. CLINICAL RELEVANCE/APPLICATION Cystic renal cell carcinomas (RCCs) defined by preoperative CT may be managed differently from non-cystic RCCs for selecting optimal treatment methods. SSQ09-04 The Radiogenomic Risk Score: Construction of a Prognostic Quantitative, Noninvasive Image-based Molecular Assay for Renal Cell Carcinoma Thursday, Dec. 3 11:00AM - 11:10AM Location: E353B Participants Neema Jamshidi, MD, PhD, Los Angeles, CA (Presenter) Nothing to Disclose Eric Jonasch, MD, Houston, TX (Abstract Co-Author) Consultant, Pfizer Inc Consultant, Novartis AG Consultant, GlaxoSmithKline plc Consultant, AstraZeneca PLC Research funded, Pfizer Inc Research funded, GlaxoSmithKline plc Research funded, Bristol-Myers Squibb Company Research funded, Novartis AG Research funded, Exelixis, Inc Research funded, Onyx Pharmaceuticals, Inc Matthew A. Zapala, MD,PhD, Boston, MA (Abstract Co-Author) Nothing to Disclose Ronald L. Korn, MD, PhD, Scottsdale, AZ (Abstract Co-Author) Chief Medical Officer, Imaging Endpoints; Founder, Imaging Endpoints; Shareholder, Imaging Endpoints Lejla Aganovic, MD, La Jolla, CA (Abstract Co-Author) Nothing to Disclose Hongjuan Zhao, Stanford, CA (Abstract Co-Author) Nothing to Disclose T S. Raviprakash, Umea, Sweden (Abstract Co-Author) Nothing to Disclose Robert Tibshirani, Stanford, CA (Abstract Co-Author) Nothing to Disclose Sudeep Banerjee, BA, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose James Brooks, Stanford, CA (Abstract Co-Author) Nothing to Disclose Borje Ljungberg, MD, San Diego, CA (Abstract Co-Author) Nothing to Disclose Michael D. Kuo, MD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose PURPOSE Quantitative multi-gene assays are effective clinical decision making tools in oncology, however cost, risks associated with tissue procurement, and difficulty in framing subcellular information within a larger physiological context limits their overall utility. We evaluated the feasibility of reconstructing quantitative non-invasive molecular assays (NIMA) in clear cell renal cell cancer (ccRCC) using data extracted from a single computed tomography (CT) scan. METHOD AND MATERIALS In this IRB approved study, gene expression profile data and contrast enhanced CT scans from 70 ccRCC patients in a training set were initially analyzed. A NIMA for a previously validated ccRCC-specific SPC prognostic gene signature was constructed termed the Radiogenomic Risk Score (RRS), using the microarray data and a 28 trait image array to evaluate each CT scan using multiple regression of gene expression analysis. The predictive power of the RRS NIMA was then prospectively validated in an independent dataset (n=77) to confirm its relationship to the SPC gene signature and to quantify individual risk. RESULTS Our quantitative NIMA faithfully represents the tissue-based molecular assay it models. The RRS scaled with the SPC gene signature (R=0.57, p=6.2e-4, classification accuracy 70.1%, p<0.001) and predicted disease-specific survival (log rank p<0.001). Independent validation confirmed the relationship between the RRS and the SPC gene signature (R=0.45, p=1.3e-4, classification accuracy 68.6%, p<0.001) and disease-specific survival (log-rank p<0.001) and that it was independent of stage, grade and performance status (multivariate Cox model p<0.05, log-rank p<0.001). CONCLUSION A NIMA for the ccRCC-specific SPC prognostic gene signature that is predictive of disease-specific survival and independent of stage was constructed and validated confirming that quantitative NIMA construction is feasible. CLINICAL RELEVANCE/APPLICATION Non-invasive molecular assays can be constructed that efficiently capture both pre-specified quantitative molecular phenotypes as well as systems-level phenotypes not accessible by genomic-based tests alone, with a range of potential clinical applications including prognostication and patient stratification in human clinical trials. SSQ09-05 CAD Derived Absolute Attenuation Discriminates Clear Cell Renal Cell Carcinoma from Benign Mimics and RCC Subtypes at Four-Phase MDCT Thursday, Dec. 3 11:10AM - 11:20AM Location: E353B Participants Heidi Coy, Los Angeles, CA (Presenter) Nothing to Disclose Jonathan R. Young, MD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Michael L. Douek, MD, MBA, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Moe Moe Ko, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose War War Ko, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Pechin Lo, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Matthew S. Brown, PhD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose James Sayre, PhD, Los Angeles, CA (Abstract Co-Author) Nothing to Disclose Steven S. Raman, MD, Santa Monica, CA (Abstract Co-Author) Nothing to Disclose PURPOSE Currently, all solid enhancing non-fatty renal neoplasms are presumed to be malignant. Up to 30% of these lesions are benign, most commonly oncocytoma. Renal Cell Carcinoma (RCC) subtypes are a heterogeneous group treated by surgery, ablation or active surveillance with a prognosis based on histology. The purpose of our study is to determine if peak enhancement derived from volumetric 3D lesion contour and a Computer Aided Diagnostic (CAD) algorithm can discriminate clear cell RCC (ccRCC) from benign RCC mimics and RCC subtypes. METHOD AND MATERIALS With IRB approval for this HIPAA-compliant retrospective study, our pathology and imaging databases were queried to obtain a cohort of RCC, oncocytoma, and lipid-poor angiomyolipoma (AML) with preoperative multiphasic multidetector CT imaged with a four-phase renal mass protocol (unenhanced, corticomedullary (C), nephrographic (N), and excretory (E)). A whole lesion 3D contour was obtained in all phases with proprietary software. The CAD algorithm determined a 0.5cm diameter region of peak enhancement ≤300HU within the 3D lesion contour. All contours were confirmed by a radiologist. T-tests were used to compare peak multiphasic enhancement. P values <0.05 were considered significant. RESULTS 206 patients (65% men, 35% women) with 223 unique renal masses (105 (47%) ccRCC, 41(18%) oncocytoma (O), 18 (8%) chromophobe RCC (chRCC), 45 (20%) papillary RCC (pRCC), 14 (6%) lipid-poor AML) were analyzed. In the C phase, CAD absolute peak attenuation of the ccRCC (174 HU) was greater than that of O (167 HU, p=0.333), chRCC (136 HU, p=0.007), pRCC (85 HU, p<0.0001), and lipid-poor AML (144 HU, p=0.004). In the N phase, CAD absolute peak attenuation of the ccRCC (144 HU) was greater than that of O (132 HU, p=0.015), chRCC (106 HU, p<0.0001), pRCC (103 HU, p<0.0001), and lipid-poor AML (115 HU, p<0.0001). In the E phase, CAD absolute peak attenuation of the ccRCC (118 HU) was greater than that of O (104 HU, p=0.001), chRCC (86 HU, p<0.0001), pRCC (86 HU, p<0.0001), and lipid-poor AML (98 HU, p=0.001). CONCLUSION CAD derived absolute attenuation discriminates ccRCC from indolent RCC subtypes and benign RCC mimics at four-phase MDCT CLINICAL RELEVANCE/APPLICATION CAD enhancement is a robust method to discriminate clear cell RCC from RCC subtypes and benign mimics, enabling clinicians to stratify patients to active surveillance, preoperative biopsy or surgical therapy. SSQ09-06 Prognostic Value of Newly Proposed Response Criteria in Assessing Tumor Response in Advanced Renal Cell Carcinoma Thursday, Dec. 3 11:20AM - 11:30AM Location: E353B Participants Hyunseon C. Kang, MD, PhD, Houston, TX (Presenter) Nothing to Disclose Shiva Gupta, MD, Houston, TX (Abstract Co-Author) Nothing to Disclose Wei Wei, Houston, TX (Abstract Co-Author) Nothing to Disclose Lina Lu, MS, Houston, TX (Abstract Co-Author) Nothing to Disclose Marc Matrana, MD, New Orleans, LA (Abstract Co-Author) Nothing to Disclose Nizar M. Tannir, MD, Houston, TX (Abstract Co-Author) Consultant, Onyx Pharmaceuticals, Inc; Consultant, Bayer AG; Consultant, Pfizer Inc; Speakers Bureau, Bayer AG; Speakers Bureau, Onyx Pharmaceuticals, Inc; Speakers Bureau, Pfizer Inc; Research funded, Pfizer Inc; Research funded, Eli Lilly and Company; Research funded, F. Hoffmann-La Roche Ltd; Spouse, Stockholder, Merck & Co, Inc Haesun Choi, MD, Houston, TX (Abstract Co-Author) Nothing to Disclose PURPOSE Several new solid tumor response criteria have been proposed to overcome the limitations of traditional size based criteria. This study examines the prognostic value of these criteria, and the additive value of clinical risk factors, in patients with advanced renal cell carcinoma (RCC) treated with pazopanib. METHOD AND MATERIALS Fifty-seven patients with metastatic RCC, who were treated with pazopanib after progression with other targeted therapies, were studied retrospectively. Two sets of CTs (pre- and 1-3.5 months post-treatment) were reviewed by 2 abdominal radiologists. Tumor response on the post-therapy scan was evaluated with RECIST, Choi, modified Choi, MASS, the 10% threshold criteria, as well as a consensus subjective reader assessment, simulating radiologists' clinical interpretation. In addition to these criteria, combined criteria incorporating MSKCC risk factors + imaging criteria were used to define response groups. Response evaluations were correlated with overall survival (OS) and progression-free survival (PFS) using the log-rank test. Only patients with partial response (PR) or stable disease (SD) were included in the analysis of PFS. RESULTS The 6 patients with progressive disease (PD) by RECIST, and the 22 patients with PD by the subjective reader assessment, had significantly worse OS compared to patients with SD or PR. There was no significant difference in OS between responders and nonresponders by Choi, modified Choi, or MASS criteria. When MSKCC risk factors were combined with imaging criteria, the combined criteria defined groups of patients with significantly worse OS. Patients with PR by modified Choi criteria showed significantly longer PFS compared to those with SD (p=0.033). PR and SD groups defined by other criteria did not show a significant difference in PFS. The MSKCC risk factors did not improve the prognostic ability of imaging-based criteria to predict patients with longer PFS. CONCLUSION Patients with PD by either RECIST or the subjective reader assessment had significantly worse survival compared to SD or PR groups. The addition of MSKCC risk factors significantly increased the predictive value of all criteria for OS. This effect was dominated by the MSKCC criteria, which were strongly correlated with survival. CLINICAL RELEVANCE/APPLICATION In the salvage therapy setting, the addition of clinical risk factors improves the predictive value of imaging-based tumor response criteria. SSQ09-07 Diagnostic Accuracy of Unenhanced MRI for Suspicious Malignant Renal Lesions Inend Stage Renal Failure Patients with Acquired Cystic Disease Thursday, Dec. 3 11:30AM - 11:40AM Location: E353B Participants Rafel Tappouni, MBBCh, FRCPC, Winston-Salem, NC (Presenter) Nothing to Disclose David D. Childs, MD, Clemmons, NC (Abstract Co-Author) Research Grant, Endocare, Inc Shadi Qasem, Winston-Salem, NC (Abstract Co-Author) Nothing to Disclose Keyanoosh Hosseinzadeh, MD, Winston-Salem, NC (Abstract Co-Author) Consultant, Bayer AG PURPOSE To determine sensitivity, specificity and accuracy of unenhanced MRI in detecting malignant lesions in end stage renal failure patients with acquired renal cystic disease (ARCD). To assess added value of diffusion weighted imaging (DWI) in characterizing lesions. To identify MRI features associated with malignant lesions. METHOD AND MATERIALS Unenhanced renal MRIs of 55 patients with ARCD were retrospectively reviewed in consensus by two blinded radiologists. Lesions less than 1 cm were excluded. Lesions were scored based on size, T1 and T2 signal, homogeneity, hemosiderin, and DWI on a 5 point scale: 1 as definitely benign, 2 as probably benign, 3 as indeterminate, 4 as probably malignant and 5 as definitely malignant. Preliminary scoring was performed without DWI and repeated with DWI. Scores 1-2 were grouped as benign and 3-5 as malignant.Sensitivity, specificity and accuracy of diagnosis was calculated by comparing to nephrectomy samples performed within 6 months of the MRI in 40 patients and five year imaging and clinical follow up in 15 patients. Stability over a 5 year period was deemed benign. Chi square test assessed the imaging features. Scores were renumbered to a 3-level confidence score: 0, indeterminate; 1, probably benign and malignant; 2, definitely benign and malignant, and a paired t-test was performed to compare confidense levels. RESULTS There were 26 cysts (8 nephrectomy, 18 imaging follow up) and 34 solid lesions including 1 urothelial carcinoma, 2 oncocytomas and 31 renal cell carcinomas. Lesion size ranged from 1-17cm.MRI features suggestive of malignancy included T1 iso or hyperintensity (p=0.0003), T1 heterogeneity (p=0.0037), T2 heterogeneity (p=0.0092), and presence of hemosiderin (p=0.0034). The sensitively, specificity and accuracy for preliminary diagnosis versus final diagnosis using DWI were 82, 69, 77 and 82, 73, 78 respectively. The area under the receiver operator curve for the diagnosis with DWI was 0.8512. The addition of DWI resulted in an increase of the confidence score (p=0.001). CONCLUSION Unenhanced renal MRI is an accurate modality in characterizing lesions in ARCD. DWI can increase the confidence for the diagnosis of malignant renal lesions. T1 iso and hyperintensity, T1 and T2 signal heterogeneity and the presence of hemosiderin are associated with malignant lesions. CLINICAL RELEVANCE/APPLICATION Unenhanced renal MRI is accurate in the detection of malignant lesions in ARCD. SSQ09-08 Impact of Imaging and Histological Findings on the Prognosis of xp-11 Translocation Renal Cell Cancer Thursday, Dec. 3 11:40AM - 11:50AM Location: E353B Participants Pauley T. Gasparis, MD, Indianapolis, IN (Presenter) Nothing to Disclose Kumaresan Sandrasegaran, MD, Carmel, IN (Abstract Co-Author) Nothing to Disclose Kevin A. Parikh, Indianapolis, IN (Abstract Co-Author) Nothing to Disclose Kunal B. Gala, MBBS, MD, Mumbai, India (Abstract Co-Author) Nothing to Disclose Clinton D. Bahler, MD, Indianapolis, IN (Abstract Co-Author) Nothing to Disclose Chandru P. Sundaram, Indianapolis, IN (Abstract Co-Author) Nothing to Disclose PURPOSE Xp11 translocation renal cell cancer (Xp11RCC) is an uncommon RCC (<1%) in the general population but accounts for 30% of RCC presenting under the age of 18 years. We wanted to identify imaging features at presentation and histological findings of the resected tumor that predicted overall survival (OS), progression-free survival (PFS), and the occurrence of local and distant metastases. METHOD AND MATERIALS Retrospective review of pathology database from Jan 2001 to Mar 2015 revealed 22 cases with Xp11RCC. Imaging findings at presentation were available in 18 of these cases. Detailed analysis of imaging findings for tumor size, calyceal invasion, necrosis, hemorrhage, exophytic growth, presence of local or distant metastases at presentation were recorded. Pathological findings including T-staging, margin positivity, Fuhrman grade and immunostain positivity were recorded. Clinical and imaging databases were used to determine OS, and PFS. Multivariate regression analysis and Kaplan-Meier survival statistics were performed. RESULTS Mean age at surgery was 40.2 (range 10-83) years. 15 of 22 patients were over 18 years. 1-, 2- and 3-year survivals were 88%, 79%, and 73% respectively. On CT / MRI, the majority of tumors enhanced to a lesser degree than adjacent cortex (13/18), were heterogeneous (11/18) and exophytic (14/18). Necrosis was seen in 5 tumors and correlated with larger tumor size (p<0.01), while calyceal invasion (seen in 6 tumors) did not (p=0.07). On multivariate logistic regression analysis, PFS correlated only with Fuhrman grade (p=0.04) and calyceal invasion (p=0.05) and recurrence of metastatic disease correlated only with initial tumor size (p=0.05). Age and gender at presentation, tumor heterogeneity, and necrosis did not correlate with prognosis. On analysis of overall survival, tumors > 5 cm had a substantially worse outcome than those < 5 cm (log rank test, Chi Square 6.73, p<0.01). CONCLUSION For staging scans of Xp11RCC, radiologists should assess tumor size and calyceal invasion as these have the most impact on survival. Unlike previous studies, we did not find younger patients to have better clinical outcomes. CLINICAL RELEVANCE/APPLICATION Calyceal invasion by tumor and tumor size > 5cm predict adverse outcome in Xp11 RCC. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Kumaresan Sandrasegaran, MD - 2013 Honored Educator Kumaresan Sandrasegaran, MD - 2014 Honored Educator SSQ09-09 How Does the Surrounding Background Fat Affect Enhancement of Exophytic Renal Lesions? A Phantom Study Thursday, Dec. 3 11:50AM - 12:00PM Location: E353B Participants Adeel R. Seyal, MD, Chicago, IL (Presenter) Grant, Siemens AG Atilla Arslanoglu, MD, Chicago, IL (Abstract Co-Author) Grant, Siemens AG Faezeh Sodagari, MD, Chicago, IL (Abstract Co-Author) Grant, Siemens AG Yuri Velichko, PhD, Chicago, IL (Abstract Co-Author) Nothing to Disclose Paul Nikolaidis, MD, Chicago, IL (Abstract Co-Author) Nothing to Disclose Vahid Yaghmai, MD, Chicago, IL (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate the effect of surrounding tissue composition on renal lesion enhancement at multidetector computed tomography. METHOD AND MATERIALS Two phantoms (A and B) simulating renal lesions were constructed with 15 test tubes (1.5 cm in diameter) each. For phantom A, the tubes were embedded in fat (-90 HU); and for phantom B, the tubes were embedded in agar gel (neutral medium; 7.3HU). The tubes were filled with a serial dilution of iodinated contrast [iohexol (300mg/mL)]. Both phantoms were scanned twice using a 64slice scanner at 120kVp and constant 150mAs. Attenuation was calculated by a centrally placed region-of-interest within each test tube and the surrounding medium and averaged over five slices for each acquisition. Mean of measurements from both acquisitions were used for analysis. The amount of contrast needed to attain an enhancement of 10HU and 20HU were determined. Regression, paired t and Wilcoxon signed rank tests were used for analysis. RESULTS Iodine concentration of 0.285 and 0.675 mg/mL resulted in enhancement of 10 HU and 20 HU, respectively, for a lesion surrounded by fat and 7.3 HU and 16.62 HU when lesion surrounded by neutral medium. At any given iodine concentration, the contrast enhancement was significantly greater for a lesion surrounded by fat when compared with the lesion surrounded by neurtal medium (P<0.0001). CONCLUSION A renal mass surrounded by fat tends to show greater enhancement compared with one surrounded by a neutral medium. CLINICAL RELEVANCE/APPLICATION Thresholds for enhancement may be different for renal lesions surrounded by fat when compared to intraparenchymal or partially exophytic lesions. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Vahid Yaghmai, MD - 2012 Honored Educator Vahid Yaghmai, MD - 2015 Honored Educator SSQ10 Genitourinary (Benign and Malignant Gynecological Diseases) Thursday, Dec. 3 10:30AM - 12:00PM Location: E450B GU MR AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Harris L. Cohen, MD, Memphis, TN (Moderator) Nothing to Disclose Mindy M. Horrow, MD, Philadelphia, PA (Moderator) Spouse, Director, Merck & Co, Inc Sub-Events SSQ10-01 Fractal Analysis of the Leiomyoma before Uterine Artery Embolization Using Contrast-Enhanced MRI and Its Effect on the Outcome Thursday, Dec. 3 10:30AM - 10:40AM Location: E450B Participants Nagy N. Naguib, MD, MSc, Frankfurt Am Main, Germany (Presenter) Nothing to Disclose Nour-Eldin A. Nour-Eldin, MD,PhD, Frankfurt Am Main, Germany (Abstract Co-Author) Nothing to Disclose Tatjana Gruber-Rouh, Frankfurt Am Main, Germany (Abstract Co-Author) Nothing to Disclose Thomas Lehnert, MD, Frankfurt Am Main, Germany (Abstract Co-Author) Nothing to Disclose Renate M. Hammerstingl, MD, Frankfurt Am Main, Germany (Abstract Co-Author) Nothing to Disclose Stefan Zangos, MD, Frankfurt Am Main, Germany (Abstract Co-Author) Nothing to Disclose Thomas J. Vogl, MD, PhD, Frankfurt, Germany (Abstract Co-Author) Nothing to Disclose PURPOSE To test whether fractal analysis of the leiomyoma using contrast-enhanced MRI correlates with the leiomyoma volume before and after uterine artery embolization (UAE) and with the percentage change at 3 month follow-up enabling its usage as a prognostic factor for treatment success. METHOD AND MATERIALS The study was retrospectively performed on 33 females (Mean Age: 44.85 +/- 3.95) with 64 leiomyomas. For fractal analysis; MRI images were exported and converted into 8-Bit greyscale images. The greyscale images were then loaded into the computer program ImageJ and analysis was performed using the FracLac plugin. The analysis was performed using the differential-boxcounting method at 12 different grid positions. The Mean Fractal dimension for each leiomyoma was calculated by drawing a ROI around each leiomyoma. On the other hand the volume of each leiomyoma was calculated before and 3 months after UAE using contrast-enhanced MRI. The correlation between the mean Fractal dimension of each leiomyoma and its volume before and after UAE as well as the percentage change in leiomyoma volume was tested for statistical significance using Spearman-Rank Correlation test. RESULTS The mean Fractal Dimension of all leiomyomas was 1.0622 +/- 0.1472 (Range: 0.74 - 1.31). The mean leiomyoma volume before UAE was 97.38 ml +/- 160.86 (Range: 1.65 - 987.34). At follow-up the mean leiomyoma volume was 68.08 ml +/- 138.3 (Range: 0.15 - 875.05). The mean percentage volume change at follow-up was 52.54% [reduction] +/- 26.99 (Range: 40.05%[increase] 96.57%[reduction]). A statistically significant strong positive correlation between the mean fractal dimension of each leiomyoma and its volume before and after UAE was observed (rho = 0.77, p<0.0001 and rho = 0.78, p<0.0001 respectively). A statistically significant strong negative correlation between the mean fractal dimension of each leiomyoma and its percentage volume change at 3 month follow-up was noted (rho = -0.68, p<0.0001). CONCLUSION The smaller the mean fractal dimension of a leiomyoma before UAE the higher will be the percentage volume reduction at 3 month follow-up after UAE. CLINICAL RELEVANCE/APPLICATION Leiomyomas with low mean fractal dimension tend to have a significantly better response at 3 month follow-up following UAE. Hence fractal dimension can be used as a prognostic factor for patient selection. SSQ10-02 Color Doppler Evaluation Of Utero-Ovarian Circulation In Polycystic Ovarian Syndrome and Its Correlation With Hormonal and Biochemical Parameters Thursday, Dec. 3 10:40AM - 10:50AM Location: E450B Participants Shivi Jain, MD, Varanasi, India (Presenter) Nothing to Disclose Akanksha Singh, MD, Varanasi, India (Abstract Co-Author) Nothing to Disclose Madhu Jain, MD, Varanasi, India (Abstract Co-Author) Nothing to Disclose Ram C. Shukla, MD, MBBS, Varansi, India (Abstract Co-Author) Nothing to Disclose Ashish Verma, MBBS,MD, Varanasi, India (Abstract Co-Author) Nothing to Disclose Arvind Srivastava, Varanasi, India (Abstract Co-Author) Nothing to Disclose PURPOSE To find out the variations in utero-ovarian circulation and their association with various endocrinal and biochemical parameters in women with Polycystic Ovarian Syndrome (PCOS). METHOD AND MATERIALS 65 patients of reproductive age group who had clinical and biochemical findings suggestive of PCOS by Rotterdam criteria (2003) were selected for TVS with Color Doppler study in early follicular phase (3rd-5th day of menstrual cycle). 58 age-matched women with normal clinical and biochemical parameters were taken as controls. The RI (Resistance Index), PI (Pulsatility Index) and PSV (Peak Systolic Velocity) of ovarian stromal and uterine arteries were assessed after the estimation of LH, LH: FSH ratio, free testosterone level, fasting Insulin level and fasting glucose:insulin ratio. RESULTS The mean value of LH, LH: FSH, free testosterone and fasting glucose:insulin ratio was significantly higher (p<0.001) in PCOS patients in comparison to control (LH 7.95 ± 1.34 vs 5.60 ± 0.51; LH: FSH=1.93 ± 0.17 vs 1.16 ± 0.22; free testosterone 3.63 ± 0.40 vs 1.71 ± 0.31; fasting glucose:insulin ratio 4.0 ± 0.60 vs 7.51 ± 0.49). The mean ovarian stromal RI, PI and PSV in PCOS was significantly lower (p<0.001) as compared to control (0.43 ± 0.08, 0.58 ± 0.10, 11.41 ± 2.53 vs 0.79 ± 0.21, 0.86 ± 0.03, 9.40 ± 0.73 respectively). Similarly, uterine artery PI was significantly higher (p<0.001) in PCOS when compared to control (3.05 ± 0.45 vs 2.43 ± 0.31). There was significantly negative correlation of ovarian stromal RI with serum LH: FSH ratio(r=0.617.p< 0.01). The Uterine artery PI positively correlated with LH: FSH ratio(r=0.548, p<0.01), free testosterone (r=0.532, p< 0.01), fasting Insulin(r=0.414, p< 0.01), fasting glucose:insulin ratio (r=0.484, p<0.01) and inversely with ovarian stromal RI (r=0.410, p<0.01). CONCLUSION Hormonal dysfunction is responsible for hemodynamic changes in utero-ovarian circulation in patients with PCOS. Ultrasonography along with color Doppler plays a significant role in the diagnosis and monitoring of Polycystic Ovarian Syndrome. CLINICAL RELEVANCE/APPLICATION The decreased PSV and increased PI and RI of uterine artery may explain recurrent early abortions in PCOS. Significant negative correlation between ovarian stromal RI and LH: FSH ratio confirms hormonal dysfunction. SSQ10-03 Contrast Enhanced 3D STIR T2-Weighted SPACE in Evaluating Sacral Nerve Plexus in Pelvic Endometriosis: Compared with Conventional 2D Sequence Thursday, Dec. 3 10:50AM - 11:00AM Location: E450B Participants Xiaoling Zhang, Guangzhou, China (Presenter) Nothing to Disclose Meizhi Li, Guangzhou, China (Abstract Co-Author) Nothing to Disclose Jian Guan, MD, Guangzhou, China (Abstract Co-Author) Nothing to Disclose Mingjuan Liu, MMEd, Guangzhou, China (Abstract Co-Author) Nothing to Disclose Shurong Li, GuangZhou, China (Abstract Co-Author) Nothing to Disclose Yan Guo, MD, Guangzhou, China (Abstract Co-Author) Nothing to Disclose Huanjun Wang, MD, GuangZhou, China (Abstract Co-Author) Nothing to Disclose PURPOSE To prospectively evaluate microstructural abnormalities in sacral nerve plexus in women with pelvic endometriosis at 3.0T MRI. METHOD AND MATERIALS Twenty women with clinically diagnosed pelvic endometriosis and 20 age-matched healthy women were enrolled in this study. In addition to conventional coronal 2D T2WI TSE imaging, contrast enhanced coronal 3D STIR T2-weighted SPACE was obtained to produce multiplanar (MPR) images. All examinations were assessed independently by two radiologists for the infiltration of the sacral plexus by endometriotic lesions and the abnormal anatomical features of the sacral plexus. Agreement between 2D- and 3Dsequences and inter-observer-agreement was evaluated using kappa-statistics. RESULTS The sacral nerve roots in healthy subjects and patients were clearly visualized on both sequences. The diameter of the sacral nerve roots in patients was larger than in the control group. Most of the patients with endometriosis displayed local thickening or indistinction in the fibers of sacral plexus. There were no significant difference between the results of the 2 radiologists (F=2.563, P=0.086). Contrast enhanced 3D STIR T2-weighted SPACE was preferable in evaluating sacral nerve plexus in pelvic endometriosis than regular 2D sequences. CONCLUSION Changes of the microarchitecture of the sacral nerve plexus were revealled in the patients with pelvic endometriosis on MRI. Contrast enhanced 3D STIR T2-weighted SPACE can display the infiltration of scaral nerve fibers by endometriotic lesions and the abnormal anatomical features of scaral nerve plexus. CLINICAL RELEVANCE/APPLICATION Contrast enhanced 3D STIR T2-weighted SPACE was applied as a method of magnetic resonance neurography to reveal the correlation between the changes of scracal plexus and chronic pelvic pain in patients with pelvic endometriosis . SSQ10-04 MRI-US Fusion Imaging in Real-Time Virtual Sonography for the Evaluation of Pelvic Endometriosis: Preliminary Study Thursday, Dec. 3 11:00AM - 11:10AM Location: E450B Participants Valeria Vinci, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Lucia Manganaro, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Silvia Bernardo, MD, Rome, Italy (Presenter) Nothing to Disclose Matteo Saldari, MD, PhD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Maria Eleonora Sergi, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Carlo Catalano, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose Federica Capozza, Rome, Italy (Abstract Co-Author) Nothing to Disclose PURPOSE Real-time virtual sonography (RVS) is a new technique that uses magnetic navigation and computer software for the synchronized display of real-time US and multiplanar reconstruction MRI images. The purpose of this study was to evaluate the feasibility and ability of RVS to detect pelvic endometriosis. METHOD AND MATERIALS This study was conducted over a two-month period in march-april 2015 on 25 patients referred for a Clinical and US suspect of endometriosis. Patients underwent pelvic MRI at 3 T and fusion imaging was offered (Hitachi HI Vision Ascendus) . The MRI image dataset acquired at the time of the examination was loaded into the fusion system and displayed together with the US image on the same monitor. Both sets of images were then manually synchronized and image were registered using multiple planes MR imaging. RESULTS 2patients had endometriosis of the vescico-uterine pouch, with urinary symptoms associated.7patients had endometriosis of the middle compartment mainly shown as ovarian endometriomas in 6 cases and adenomyosis in 3 cases.19had signs of endometriotic implants in the posterior compartment shown as fibrotic plaque over the serosal surface of the uterus and rectum in 12 cases. In 1 case there was a deep infiltrating intestinal endometriosis over the rectum. A retroflexed uterus was associated in 6 cases. 6 cases showed fibrotic strands between the uterus and the rectum with thickening of the uterosacral ligaments.Regarding endometriosis of the medial compartment, there was an overlap of data of 100% between MRI and RVS, both appearing superior to a standard US evaluation.Endometriosis of the vescico-uterine pouch was better visualized in MRI.Fibrotic strand were displayed in both methods with an overlap of 100%; on the contrary, relying on RVS it was more difficult to differentiate between active plaque and predominantly fibrotic plaque because of the difficulty in visualizing the hemorrhagic foci. However the infiltration of the bowel wall was better undressed in RVS. CONCLUSION Thanks to information from both US and MRI, fusion imaging allows better identification of the pelvic implants, superior to the standard US evaluation. CLINICAL RELEVANCE/APPLICATION Thanks to information from both US and MRI, fusion imaging allows better identification of the pelvic implants, superior to the standard US evaluation. SSQ10-05 Diagnostic Value of MR Imaging to Diagnose Adnexal Torsion Thursday, Dec. 3 11:10AM - 11:20AM Location: E450B Participants Sophie Beranger-Gibert, Paris, France (Abstract Co-Author) Nothing to Disclose Hajer Sakly, Paris, France (Abstract Co-Author) Nothing to Disclose Marcos Ballester, MD, Paris, France (Abstract Co-Author) Nothing to Disclose Marie Bornes, Paris, France (Abstract Co-Author) Nothing to Disclose Marc J. Bazot, MD, Paris, France (Abstract Co-Author) Nothing to Disclose Emile Darai, Paris, France (Abstract Co-Author) Nothing to Disclose Isabelle Thomassin-Naggara, MD, Paris, France (Presenter) Speakers Bureau, General Electric Company; Research Consultant, Olea Medical PURPOSE To retrospectively evaluate the diagnostic performance of MR imaging for the diagnosis of adnexal torsion (AT) in a series of patients with an equivocal adnexal mass at ultrasonography in a context of acute or sub acute pelvic pain. METHOD AND MATERIALS Our institutional ethics committee approved the study and granted a waiver of informed consent. All patients with acute or subacute pelvic pain undergoing MR exam for the exploration of an equivocal adnexal mass (January 2007 to December 2012) with surgical exploration or clinical and radiological follow up at least of 3 months were retrospectively included (n=58). Three radiologists blinded to the clinical, ultrasonographic and surgical data retrospectively and independently reviewed MR images. Features associated with AT were identified using univariate and recursive partitioning multivariate analysis. RESULTS Twenty-two patients (38%) had a diagnosis of AT. The accuracy of MR image interpretation by each reader was 83.8% (26/31), 90.3% (28/31), 83.8% (26/31) in a context of acute pelvic pain and 92.5% (25/27), 88,8% (24/27), 81.5% (22/27) in a context of sub acute pelvic pain for reader 1, 2 and 3 respectively. On multivariate analysis, whirlpool sign (OR=6.5 [1.36-31], p=0.01) and a thickened tube (OR=8.2 [1.2-56.8], p=0.03) were associated with adnexal torsion, with substantial inter-reader agreement (kappa 0.71-0.84, and 0.82-0.86, respectively). The presence of adnexal hemorrhagic content helps to predict ovarian viability (p=0.009) CONCLUSION MR imaging is an accurate technique for the diagnosis of adnexal torsion in the setting of patients with adnexal mass having acute or sub acute pelvic pain. CLINICAL RELEVANCE/APPLICATION MR imaging is an accurate second line technique to diagnose adnexal torsion without any pelvic irradiation with the ability to predict ovarian viability without any gadolinium injection. SSQ10-06 Can Diffusion-weighted MR Imaging Differentiate Uterine Sarcomas from Leiomyomas? Thursday, Dec. 3 11:20AM - 11:30AM Location: E450B Participants Jun Gon Kim, Seoul, Korea, Republic Of (Presenter) Nothing to Disclose Chan Kyo Kim, MD, PhD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Jung Jae Park, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Byung Kwan Park, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose PURPOSE Differentiation uterine sarcoma from leiomyoma is a major challenge. The aim of this study was to investigate the utility of diffusionweighted imaging (DWI) in differentiating uterine sarcomas from leiomyomas. METHOD AND MATERIALS Between January 2010 and August 2014, 188 patients with surgically confirmed 38 uterine sarcomas (16 leiomyosarcomas, 12 malignant mixed Mullerian tumors, 9 endometrial stromal sarcomas, and 1 undifferentiated pleomorphic sarcoma) and 150 leiomyomas were enrolled in this retrospective study. All patients underwent preoperative routine pelvic MR imaging at 3T, including DWI. DWI was obtained using a STIR single-shot echo-planar imaging technique with background suppression (b= 0 and 1000 s/mm2). The apparent diffusion coefficient (ADC) and signal intensity on T2-weighted imaging (T2SI) were calculated in the tumors, normal myometrium and gluteus muscle. In the differentiation of sarcomas from leiomyomas, various parameters (ADC, diffusion restriction, tumor-myometrium or gluteus muscle contrast ratio [TCRm or TCRg] on T2-weighted imaging, necrosis, hemorrhage, and size) were evaluated. RESULTS The mean ADC values of sarcomas (0.939 ± 0.253) were statistically lower than those of leiomyomas (1.347 ± 0.327 × 10-3mm2) ( p < 0.001). For differentiating sarcomas from leiomyomas, the parameters including diffusion restriction, T2SI, TCRm, TCRg, necrosis and hemorrhage were statistically significant (all p -values < 0.001). At receiver operating characteristics curve analysis, the area under the curves of diffusion restriction and ADC in differentiating sarcomas from leiomyomas were 0.902 and 0.860, respectively and were statistically greater than other parameters (TCRm, TCRg, necrosis, hemorrhage and size) ( p < 0.05): with a cutoff ADC value of 1.111 × 10-3mm2, the sensitivity and specificity were 79% and 80%, respectively. For the degree of diffusion restriction, sarcomas showed moderate or strong in 97% (37/38), while leiomyomas revealed absent or mild in 69% (104/150). CONCLUSION DWI at 3T may be a useful technique for the differentiation of uterine sarcomas from leiomyomas. CLINICAL RELEVANCE/APPLICATION As a noninvasive technique, preoperative DWI at 3T can be used to predict sarcomas in patients with uterine myometrial masses, which may give potential for planning treatment strategies. SSQ10-07 Variations in Reporting Recommendations for Son Graphically Evaluated Endometrial Stripe in Post Menopausal Bleeding in a Subspeciality Practice Thursday, Dec. 3 11:30AM - 11:40AM Location: E450B Participants Aoife Kilcoyne, MBBCh, Boston, MA (Presenter) Nothing to Disclose Avinash R. Kambadakone, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Colin J. McCarthy, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Giles W. Boland, MD, Boston, MA (Abstract Co-Author) Principal, Radiology Consulting Group; Royalties, Reed Elsevier Susanna I. Lee, MD, PhD, Boston, MA (Abstract Co-Author) Nothing to Disclose Debra A. Gervais, MD, Chestnut Hill, MA (Abstract Co-Author) Nothing to Disclose PURPOSE Endometrial cancer is the most common gynecologic cancer in the United States. Early diagnosis and intervention is imperative to improve prognosis and survival. In the setting of postmenopausal vaginal bleeding (PMB), sonographically determined endometrial stripe thickness is an established criteria for predicting risk of cancer and thereby serving as a guide to trigger endometrial sampling. Current guidelines recommend tissue sampling for endometrial stripe measuring >5mm, however, there is limited data on adherence to these guidelines. The purpose of this study was to evaluate the variability in reporting recommendations for sonographically determined endometrial stripe thickness measuring 5mm in patients with PMB at a subspecialty practice in an academic teaching institution. METHOD AND MATERIALS In this ongoing study, we performed a review of the 'RENDER' radiology database to identify pelvic ultrasound exams performed on women aged 18-80years between January 1st 2009 and December 31st 2014 for evaluation of PMB. Using natural language processing, the radiology reports of these exams were then analysed for endometrial stripe thickness, reporting patterns in the body, impression of radiology report and the recommendations, if any. The search terms used for the focused search included 'endometrial stripe', '5mm', 'postmenopausal'. The variations in the reporting recommendations based on the endometrial stripe thickness were then evaluated. RESULTS Of the 253 reports reviewed, 58 (24.6%) were not relevant - the search identified patients with an endometrial stripe of greater or less than 5mm. In 74 reports (29.2%), no recommendation was made. In 73 reports (28.8%), endometrial biopsy was recommended. Other recommendations included: biopsy or imaging 14 (6%), no intervention 11 (4%), further imaging 8 (3%), gynaecology review 4 (2%), gynaecology review and biopsy 4 (2%), follow-up imaging 2 (1%). CONCLUSION In a subspecialty abdominal imaging practice at an academic institution, considerable variation exists on the reporting recommendation for evaluation of PMB with endometrial stripe thickness measuring 5mm with only 30% of reports adhering to established guidelines. CLINICAL RELEVANCE/APPLICATION The findings of this study highlight the need for development of standardised approaches/tools to bring about clarity in terms of management options/further investigation of abnormal endometrial thickening in the setting of postmenopausal bleeding. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Debra A. Gervais, MD - 2012 Honored Educator Susanna I. Lee, MD, PhD - 2013 Honored Educator SSQ10-08 Cystic Adnexal Lesions Analyzed by International Ovarian Tumor Analysis (IOTA) Criteria in Routine Clinical Practice Thursday, Dec. 3 11:40AM - 11:50AM Location: E450B Participants Claire E. Beaumont, MD, Madison, WI (Abstract Co-Author) Nothing to Disclose Jessica B. Robbins, MD, Madison, WI (Abstract Co-Author) Nothing to Disclose Elizabeth A. Sadowski, MD, Madison, WI (Presenter) Nothing to Disclose Mark A. Kliewer, MD, Madison, WI (Abstract Co-Author) Nothing to Disclose Lisa Barroilhet, MD, Madison, WI (Abstract Co-Author) Nothing to Disclose Laura Huffman, MD, Madison, WI (Abstract Co-Author) Nothing to Disclose Katherine E. Maturen, MD, Ann Arbor, MI (Abstract Co-Author) Consultant, GlaxoSmithKline plc; Medical Advisory Board, GlaxoSmithKline plc PURPOSE The simple rules developed by the IOTA group direct management of adnexal cysts based on sonographic imaging features. The diagnostic performance of these criteria in routine practice has not been formally evaluated since the original study was published in 2010. The goal of our research is to determine how well the IOTA simple rules criteria perform in stratifying cystic lesions and detecting ovarian cancer in routine radiology practice. METHOD AND MATERIALS Patient consent was waived for this IRB approved retrospective review of transvaginal US studies on non-pregnant post-menarchal women performed between January-March 2011. Adnexal cysts larger than 3 cm were evaluated according to the IOTA rules. The incidence of benign adnexal lesions, borderline tumors and ovarian carcinoma was calculated. Surgical pathology, resolution on follow-up imaging and/or normal gynecological pelvic examination at 2 years were the accepted end points. RESULTS 108 lesions in 104 women met inclusion criteria. Mean age=41±14 years; range=13-84. 3 lesions (2.8%) met simple rule 1 (malignant): 30% (1/3) were cystadenomas and 30% (1/3) carcinoma, with no borderline tumors. 95 lesions (88%) met simple rule 2 (benign): 10.5% (10/95) were benign ovarian neoplasms (dermoids=2; cystadenomas=8), with no borderline tumors or carcinomas. 10 lesions (9.2%) met simple rule 3 (indeterminate): 20% (2/10) were benign ovarian neoplasms, 20% (2/10) borderline tumors, and 10% (1/10) carcinoma. Thus, the IOTA rules gave a definitive (non-indeterminate) result in 98/108 (90.7%) of cases and correctly triaged 100% of borderline and malignant neoplasms either to further imaging evaluation or surgery. CONCLUSION The results of this pilot study indicate that the IOTA rules successfully detect borderline and malignant neoplasms. However, the vast majority of lesions in routine practice are benign in both sonographic appearance and clinical behavior. Full and nuanced evaluation of diagnostic performance in routine clinical practice will require a larger number of cancers, to be evaluated in our ongoing research. CLINICAL RELEVANCE/APPLICATION The IOTA simple rules were able to detect borderline and malignant ovarian neoplasms in our clinical practice and aided in directing women with such lesions to oncologic specialists. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Katherine E. Maturen, MD - 2014 Honored Educator SSQ10-09 MR Imaging and Semi-automated Texture analysis for Differentiating Atypical Appearing Uterine Leiomyomas from Leiomyosarcomas Thursday, Dec. 3 11:50AM - 12:00PM Location: E450B Participants Yuliya Lakhman, MD, New York, NY (Presenter) Nothing to Disclose Joshua L. Chaim, DO, New York, NY (Abstract Co-Author) Nothing to Disclose Harini Veeraraghavan, New York, NY (Abstract Co-Author) Nothing to Disclose Diana S. Feier, MD, Cluj-Napoca, Romania (Abstract Co-Author) Nothing to Disclose Hebert Alberto Vargas, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Ramon E. Sosa, BA, New York, NY (Abstract Co-Author) Nothing to Disclose Debra A. Goldman, MS, New York, NY (Abstract Co-Author) Nothing to Disclose Chaya Moskowitz, New York, NY (Abstract Co-Author) Nothing to Disclose Robert Soslow, New York, NY (Abstract Co-Author) Nothing to Disclose Nadeem Abu-Rustum, New York, NY (Abstract Co-Author) Nothing to Disclose Hedvig Hricak, MD, PhD, New York, NY (Abstract Co-Author) Nothing to Disclose Evis Sala, MD, PhD, New York, NY (Abstract Co-Author) Nothing to Disclose PURPOSE To investigate whether qualitative magnetic resonance (MR) imaging features and texture analysis (TA) can distinguish between atypical appearing uterine leiomyomas (ALM) and leiomyosarcomas (LMS) METHOD AND MATERIALS Forty-one women with ALM (n=22) or LMS (n=19) at histopathology and MRI between January 1, 2007 and December 31, 2013 were included in this retrospective study. Two readers (R1 and R2), blinded to histopathologic diagnoses, independently evaluated all cases. R2 manually segmented each tumor on axial T2-weighted image. Intensity based gray scale correlation matrix (GLCM) textures and Gabor edge based GLCM textures were computed for each segmented tumor. Relationships between clinical characteristics, imaging features, and histopathology were tested with Fisher's exact test. Each tumor was assigned a score of 0 to 4 based on the total number of most statistically significant features present. Diagnostic accuracy with exact 95% confidence intervals was calculated for each feature and score. Texture features were analyzed with a random forest (RF) classifier to automatically distinguish ALM from LMS. RF classifier was optimized by varying the number of decision trees and its performance was tested with five-fold cross validation. RESULTS Nodular borders, hemorrhagic foci, "T2 dark" areas, and central (±peripheral) unenhanced area(s) were significant predictors of LMS (p<0.0001 for each feature and reader). Sensitivity and specificity of each feature for LMS were 0.84/0.74 and 0.91/0.86 for nodular borders, 0.95/1.0 and 0.82/0.95 for hemorrhagic foci, 0.84/0.79 and 0.86/0.86 for "T2 dark" areas, and 0.95/1.0 and 0.73/0.68 for central (±peripheral) unenhanced area(s) for R1/R2, respectively. When any 3 of these features were detected in a lesion, the sensitivities and specificities were 1.0/0.95 and 0.95/1.0 for R1/R2, respectively. The best classification accuracy of computer-generated image features was achieved with 25 decision trees (AUC=0.86, sensitivity=0.95, specificity=0.69). The Gabor edge-based texture features were more relevant than the intensity based texture features for the classification. CONCLUSION Presence of certain qualitative MRI features can reliably distinguish ALM from LMS. Texture analysis as a semi-automated adjunct may add certainty to the diagnosis of LMS. CLINICAL RELEVANCE/APPLICATION MR imaging and semi-automated texture analysis are useful in distinguishing atypical appearing leiomyomas from leiomyosarcoma. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Evis Sala, MD, PhD - 2013 Honored Educator MSRT54 ASRT@RSNA 2015: Renal and Urographic CT Imaging Thursday, Dec. 3 11:45AM - 12:45PM Location: N230 GU CT AMA PRA Category 1 Credit ™: 1.00 ARRT Category A+ Credit: 1.00 Participants Robert C. Chatelain, RT, Ottawa, ON (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) To identify normal anatomy and its variants demonstrated by CT of the urinary system. 2) To explain the value of having specific dedicated protocols for the renal and urographic imaging. 3) To differentiate renal and urographic pathologies by origin (congenital, neoplastic, vascular etc.) ABSTRACT The urinary system is subject to a wide variety of pathological processes and anatomical variants. Fortunately, it lends itself well to being imaged by a range of modalities. This presentation will focus on the imaging of the urinary system using Computed Tomography (CT). Due to high spatial resolution, CT is an excellent tool to evaluate stones, masses, traumatic injuries and infections. Non contrast CT is the procedure of choice to evaluate kidney stones. CT is also used to differentiate malignant from nonmalignant renal masses, to evaluate the local spread of a renal malignancy and CT angiography (CTA) is an excellent tool to define the anatomy of the renal arteries and veins. GUS-THA Genitourinary Thursday Poster Discussions Thursday, Dec. 3 12:15PM - 12:45PM Location: GU/UR Community, Learning Center GU AMA PRA Category 1 Credit ™: .50 Participants Dean A. Nakamoto, MD, Beachwood, OH (Moderator) Research Grant, Galil Medical Ltd; Research agreement, Toshiba Corporation Sub-Events GU246-SDTHA1 Volumetric Stone Burden Measurement by 3D Reconstruction on NCCT is not a more Accurate Predictor of Stone Free Status after PCNL than 2D Stone Burden Measurements Station #1 Participants Brandon Nadeau, MD, London, ON (Presenter) Nothing to Disclose Thomas Tailly, London, ON (Abstract Co-Author) Nothing to Disclose Philippe Violette, London, ON (Abstract Co-Author) Nothing to Disclose Yige Bao, London, ON (Abstract Co-Author) Nothing to Disclose Justin Amann, MD, London, ON (Abstract Co-Author) Nothing to Disclose Hassan Razvi, London, ON (Abstract Co-Author) Research Consultant, Olympus Corporation; Research Consultant, HistoSonics, Inc ; Royalties, Cook Group Incorporated ; ; ; John D. Denstedt, MD, London, ON (Abstract Co-Author) Royalties, Cook Group Incorporated PURPOSE Stone burden has been reported as an independent predictor of post-operative outcomes for percutaneous nephrolithotomy (PCNL). We aimed to identify the optimal method for imaging quantification of stone burden to predict residual stone at 3 months post percutaneous nephrolithotomy (PCNL). METHOD AND MATERIALS We identified 246 patients from a prospective database of PCNL procedures performed at a single tertiary center between January 2006 and December 2013. Pre-operative stone burden was assessed by three different methods on reformatted coronal CT images: 1) estimated elliptical surface area (SA) calculated as longest perpendicular diameter * π /4; 2) manual surface area measurement with digital calipers; 3) 3D volume rendering using automated CT software. SA's were reported in increments of 500mm². Logistic regression, receiver operative characteristics (ROC) curve analysis and area under the curve (AUC) were used to evaluate the predictive value of each method. Primary outcome was stone-free status (SFS) at discharge. Secondary outcomes included SFS at 3 months post-procedure, and operative time. RESULTS Our cohort had a mean age of 55.7 years, was 40.9% female and had an 19.2% incidence of residual stone. All measurement methods accurately predicted stone-free status at discharge; OR1: 1.47, CI 1.16-1.86; OR2: 1.51, CI 1.12-2.05, OR3: 1.20, CI: 1.04-1.38 respectively. Areas under the curve of ROC analysis were 0.661, 0.658 and 0.662 respectively, demonstrating almost equivalent predictive value of each measurement method. Similar results were seen for predicting stone-free rate at 3 months postprocedure. CONCLUSION Our results indicate that the use of complex techniques to measure pre-operative stone burden on CT including manually-derived surface area or 3D volumetric reformations provide no added value in predicting post-operative outcomes for PCNL when compared to traditional 2D measurements based on maximum diameter. CLINICAL RELEVANCE/APPLICATION Volumetric measurement of renal stone burden on CT by automated 3D rendering provides no added value in predicting operative outcomes for percutaneous nephrolithotomy compared to traditional 2D measurements. GU248-SDTHA3 Detecting the Main Composition of Urinary Stones with Dual-source Dual-energy Computed Tomography in Vivo Station #3 Participants Gu Mu Yang Zhang, MD, Beijing, China (Presenter) Nothing to Disclose Hao Sun, MD, Beijing, China (Abstract Co-Author) Nothing to Disclose Huadan Xue, MD, Beijing, China (Abstract Co-Author) Nothing to Disclose Zheng Yu Jin, MD, Beijing, China (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate the accuracy of dual-source dual-energy computed tomography (DSDECT) in predicting the main composition of urinary calculi in vivo METHOD AND MATERIALS Patients with suspected urolithiasis from March of 2014 to Februrary of 2015 underwent DSDECT for urinary stone composition analysis before percutaneous nephrolithotomy or ureterorenoscopy. All patients were scanned by DSDECT using the dual-energy renal stone protocol. Material-specific chromatic images were made using dedicated post-processing software. Two radiologists interpreted the images and analyzed the composition of stones independently. The final determination of the composition of stones was made by fourier transform infrared spectrometry postoperatively. The accuracy of DSDECT in evaluating stone composition was analyzed. RESULTS A total of 81 urinary calculi from 67 patients(50 male, 17 female, mean age: 50 years) were included in this study. There are 43 stones with single composition (uric acid n=5, cystine n=2, hydroxylapatite n=5, calcium oxalate n=31) and 38 stones with mixed composition(uric acid/calcium oxalate n=4, cystine/hydroxylapatite n=1, calcium oxalate/hydroxylapatite n=33). The accuracy for detecting uric acid, cystine, hydroxylapatite and calcium oxalate were 77.8%(7/9), 100%(3/3), 97.4%(38/39) and 98.5%(67/68). As for detecting the main composition of stones, DSECT correctly identified 7 of the 9 calculi mainly composed of uric acid and all the rest of 64 calculi mainly composed of calcium oxalate, 3 calculi mainly composed of cystine and 5 calculi mainly composed of hydroxylapatite. The overall accuracy of DSDECT in predicting the main composition of stones was 97.5%(79/81). CONCLUSION DSDECT could accurately distinguish the four stone composition and accurately predict the main composition of urinary calculi. CLINICAL RELEVANCE/APPLICATION DSDECT could facilitate the optimization of clinical management of urolithiasis by accuratley predicting the main composition of stones in vivo GU235-SDTHA6 Prostate Imaging Reporting and Data System Version 2 Improves Diagnostic Performance of Multiparametric MR Imaging of the Prostate for Experienced and Unexperienced Reader Station #6 Participants Moritz Kasel-Seibert, Jena, Germany (Presenter) Nothing to Disclose Rene Aschenbach, MD, Jena, Germany (Abstract Co-Author) Nothing to Disclose Marcus Horstmann, Jena, Germany (Abstract Co-Author) Nothing to Disclose Marc-Oliver Grimm, Jena, Germany (Abstract Co-Author) Nothing to Disclose Ulf K. Teichgraeber, MD, Jena, Germany (Abstract Co-Author) Research Consultant, W. L. Gore & Associates, Inc; Research Consultant, Siemens AG; Research Consultant, CeloNova BioSciences, Inc ; Research Consultant, General Electric Company; Tobias Franiel, Jena, Germany (Abstract Co-Author) Nothing to Disclose PURPOSE This study evaluates the diagnostic performance of the multiparametric magnetic resonance imaging (mpMRI) based Prostate Imaging Reporting and Data System (PI-RADS) version 2, in comparison to version 1. METHOD AND MATERIALS 138 lesions in 82 consecutive patients with elevated PSA and at least one negative transrectal ultrasound guided systematic biopsy were retrospectively evaluated and scored according to PI-RADS V1 and V2 by an experienced and unexperienced blinded reader. All patients underwent endorectal mpMRI (T2-weighted imaging + diffusion weighted imaging + dynamic contrast enhanced MRI) at 1.5T. Results of targeted in-bore MRI guided biopsy were used as reference standard. Diagnostic parameters were calculated on a per lesion basis. RESULTS For the experienced reader scoring with PI-RADS V2 and a threshold of ≥ 4 increased specificity (0.81 vs. 0.67), positive predictive value (0.63 vs. 0.48) and negative predictive value (0.90 vs. 0.88) while maintaining sensitivity of 0.77 in comparison to PI-RADS V1. For the unexperienced reader all diagnostic parameters improved respectively as follows: sensitivity 0.79 vs. 0.67, specificity 0.78 vs 0.68, positive predictive value 0.60 vs. 0.46, negative predictive value 0.90 vs. 0.84. The use of PI-RADS V2 with a threshold of ≥ 3 resulted in 39 more lesions for the experienced and 9 more lesions for the unexperienced reader which would have been correctly classified as benign. Inter-reader agreement improved for PI-RADS V2 (κ=0.51) compared to V1 (κ=0.25). CONCLUSION PI-RADS V2 compared to PI-RADS V1 led to an improvement of diagnostic parameters. Inter-reader agreement between experienced and unexperienced reader increased from fair to moderate. CLINICAL RELEVANCE/APPLICATION PI-RADS V2 compared to V1 improves diagnostic accuracy for the detection of prostate cancer while higher inter-reader reliability suggests a more replicable and understandable reporting system. UR133-EDTHA7 Scrotal Ultrasound versus MRI: The Ball is in your Court Station #7 Awards Certificate of Merit Participants Ian Mills, MD, New Haven, CT (Presenter) Nothing to Disclose Mike Spektor, MD, New Haven, CT (Abstract Co-Author) Nothing to Disclose Steffen Huber, MD, New Haven, CT (Abstract Co-Author) Nothing to Disclose Jay K. Pahade, MD, New Haven, CT (Abstract Co-Author) Nothing to Disclose Mahan Mathur, MD, New Haven, CT (Abstract Co-Author) Nothing to Disclose TEACHING POINTS Magnetic resonance (MR) interpretation of scrotal pathology can present a unique challenge for the unintiated, particularly since ultrasound (US) is often the first, and many times the only, imaging study that is required. Nevertheless, MR imaging is useful in this setting, potentially serving as a problem solving tool for indeterminate lesions seen on US. The purpose of this exhibit is to showcase the MR imaging appearance of a variety of neoplastic and non-neoplastic conditions of the scrotum. Specific imaging features which facilitate differentiation of these conditions will be discussed and MR/US imaging correlatation will be emphasized. TABLE OF CONTENTS/OUTLINE MRI technique and indications Normal anatomy Non-neoplastic conditions Epididymo-orchitis (including TB) Testicular hematoma Tubular ectasia of the rete testis Polyorchidism Cryptorchidism Hydrocele, hematocele/pyocele Epididymal cyst, spermatocele Focal testicular infarct Adrenal rests Testicular prosthesis Extra-testicular lipoma Inguinal hernia Neoplastic conditions Seminoma Mixed germ cell tumor Lymphoma Adenomatoid tumor of the epididymis Spermatic cord sarcoma Summary/Conclusion GUS-THB Genitourinary Thursday Poster Discussions Thursday, Dec. 3 12:45PM - 1:15PM Location: GU/UR Community, Learning Center GU AMA PRA Category 1 Credit ™: .50 FDA Discussions may include off-label uses. Participants Dean A. Nakamoto, MD, Beachwood, OH (Moderator) Research Grant, Galil Medical Ltd; Research agreement, Toshiba Corporation Sub-Events GU230-SDTHB1 Innovative Single Acquisition Split Bolus Dual Energy CT (SBDECT) Protocol for Comprehensive Evaluation of Renal Masses: Preliminary Results of Prospective Randomized Trial Station #1 Awards Trainee Research Prize - Resident Participants Dinesh Manoharan, MBBS, New Delhi, India (Presenter) Nothing to Disclose Sanjay Sharma, MD, FRCR, New Delhi, India (Abstract Co-Author) Nothing to Disclose Chandan J. Das, MD, MBBS, New Delhi, India (Abstract Co-Author) Nothing to Disclose Rajeev Kumar, MD,MChir, New Delhi, India (Abstract Co-Author) Nothing to Disclose Geetika Singh, MBBS, MD, New Delhi, India (Abstract Co-Author) Nothing to Disclose Pratik Kumar, MSc, PhD, New Delhi, India (Abstract Co-Author) Nothing to Disclose Arun K. Gupta, MBBS, MD, New Delhi, India (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate the diagnostic accuracy of single acquisition SBDECT compared to standard triple phase MDCT in evaluation of suspected renal masses. METHOD AND MATERIALS The study was approved by institutional review board. Eighty consenting adults (>18y, 52M,28F) from April 2014 to March 2015, with suspected renal mass(es) on ultrasound requiring further evaluation by CT were randomly assigned into two groups: single acquisition SBDECT (n=41, Gp A) or standard triple phase MDCT (n=39, Gp B). Patients were scanned in Siemens Somaton Definition Flash 2x128 slice scanner. Gp A protocol consisted of 40 ml iodinated IV contrast hand injected at 0s, 45ml @ 4ml/s at 820s and 60ml @ 3.5ml/s at 852s with single dual energy CT image acquisition after the end of third bolus. Gp A scan parameters tube potential/ref mAs were 100kVp/230mAs and Sn140kVp/178mAs). In Gp B protocol, single energy CT images were acquired in non contrast (0s), corticomedullary (28s), nephrographic (80s) and delayed (15min) phase. Histopathology /FU were used as the reference standard. Two readers in consensus qualitatively rated vascular, parenchymal enhancement and urinary tract opacification. Effective radiation dose was calculated. RESULTS Overall 169 masses (36 malignant, 133 benign) were analyzed in Gp A. All 36 malignant and 130/133 of benign masses (sens 100%, spec 97.74%, PPV 92.31% , NPV 100%, Acc 98.22%) were correctly diagnosed. Three were false positive. In Gp B, total 93 masses (28 malignant, 65 benign) were analyzed. It diagnosed correctly 26/28 malignant and 64/65 benign masses (sens 92.86%, spec 98.46%, PPV 96.29% and NPV 96.96%, Acc 96.72%). Two were false negative and one was false positive. Arterial and venous enhancement was excellent in 88% and 86% respectively. Renal parenchymal enhancement was excellent in 69%. Intrarenal collecting system and upper ureter showed complete opacification in 72%. Mean effective dose was 8.7 mSv and 23.9 mSv in Gp A and Gp B respectively (p<0.05). CONCLUSION The accuracy of single acquisition SBDECT is comparable to the standard triple phase MDCT in characterizing renal masses. It is a dose efficient protocol providing adequate image quality of renal parenchyma, vascular anatomy and pelvicalyceal system. CLINICAL RELEVANCE/APPLICATION Proposed CT protocol can be effectively used for routine evaluation of renal masses with much lower radiation dose to a patient. GU254-SDTHB3 Prostate Cancer: Correlation of Intravoxel Incoherent Motion MR Parameters with Gleason Score Station #3 Participants Dal Mo Yang, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Hyun Cheol Kim, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Sang Won Kim, MD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Geon-Ho Jahng, PhD, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Ye Na Son, Seoul, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Woo Jin Yang, Seoul, Korea, Republic Of (Presenter) Nothing to Disclose PURPOSE To evaluate the potential of IVIM imaging to predict histologic prognostic parameters by investigating whether IVIM parameters correlate with Gleason score. METHOD AND MATERIALS A total of 41 patients with histologically-proven prostate cancer who underwent prostate MR imaging using a 3T MRI machine were included in this study. For the eight DWI b-values (0, 10, 20, 50, 100, 200, 500, and 800 sec/mm2), the spin-echo echo-planar imaging (EPI) sequence was performed. The D, f, D*, and ADCfit values were compared between three different groups of prostate cancer: Gleason score 6 (n = 9), Gleason score 7 (n = 16), and Gleason score 8 or higher (n = 16). Receiver operating characteristic (ROC) curves were generated for D, f, D*, and ADCfit to assess the ability of each parameter to distinguish cancers with low Gleason scores from cancers with intermediate or high Gleason scores. RESULTS Pearson's coefficient analysis revealed significant negative correlations between the Gleason score and ADCfit (r = -0.490, P = 0.001) and the Gleason score and D values (r = -0.514, P = 0.001). On the other hand, the Gleason score was poorly correlated with the f (r = 0.168, P = 0.292) and D* values (r = -0.108, P = 0.500). The ADCfit and D values of prostate cancers with Gleason scores of 7 or ³ 8 were significantly lower than those of prostate cancers with a Gleason score of 6 (P < 0.05). ROC curves were constructed to assess the ability of the IVIM parameters to discriminate prostate cancers with a Gleason score of 6 from those with Gleason scores of 7 or ³ 8. The areas under the curve (AUCs) ranged from 0.671 to 0.974. ADCfit and D yielded the highest Az value (0.960-0.956), whereas f yielded the lowest Az value (0.633). CONCLUSION The pure molecular diffusion parameter, D, was the best IVIM parameter for discriminating prostate cancers with low Gleason scores from prostate cancers with intermediate or high Gleason scores. CLINICAL RELEVANCE/APPLICATION The accurate assessment of prostate cancer aggressiveness is important for deciding the most appropriate initial treatment strategy. We believe Intravoxel incoherent motion (IVIM) imaging may provide information about tumor aggressiveness without prostate biopsy determination. GU255-SDTHB4 Characterization of Renal Masses in MR Reporting: Pathologic Correlation as Part of a Performance Quality Review at an Academic Center Station #4 Participants Helen S. Xu, BA, Boston, MA (Presenter) Nothing to Disclose Leo L. Tsai, MD, PhD, Boston, MA (Abstract Co-Author) Co-founder, Agile Devices Inc; Stockholder, Agile Devices Inc; Research Consultant, Agile Devices Inc; Eric U. Yee, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Maryellen R. Sun, MD, Boston, MA (Abstract Co-Author) Research Grant, Glaxo SmithKline plc PURPOSE To evaluate the accuracy of MR diagnosis of renal masses through retrospective review of MRI reports from an academic medical center with pathologic correlation as gold standard. METHOD AND MATERIALS A retrospective review of MRI reports from MR renal mass examinations performed at a single site was correlated with pathological diagnosis. 100 renal masses were assessed with dedicated contrast-enhanced renal mass protocol MR examinations prior to biopsy/surgical resection from August 2013-November 2014. All imaging was performed on-site and reported by abdominal imaging radiologists with fellowship training in body MRI. Pathologic diagnoses included clear-cell renal cell carcinoma (ccRCC) (n=62), papillary RCC (n=11), chromophobe RCC (n=6), RCC with papillary and oncocytic features (n=1), unclassified RCC (n=1), oncocytoma (n=13), oncocytic neoplasm with papillary features (n=1), AML (n=4) and AML with papillary adenoma (n=1). The leading diagnosis, differential diagnoses, and descriptors (such as T2 signal intensity and enhancement pattern) from the MR reports were compared to the pathological diagnosis of each lesion. RESULTS The sensitivity and specificity of a primary MRI diagnosis of ccRCC was 83% and 58%, for papillary RCC 91% and 98%, and for angiomyolipoma 75% and 99%, respectively. Only 8% of oncocytomas were primarily diagnosed on MRI, with the remainder prospectively reported as likely ccRCC. No chromophobe RCC was the primary diagnosis on MRI, with only 1 (17%) included in the differential. 50% of ccRCCs and 77% of oncocytomas were described as T2-hyperintense with 65% and 69% respectively having enhancement similar-to or greater-than the renal cortex. 73% of papillary RCCs were described as T2-hypointense, and 73% were hypoenhancing. CONCLUSION Papillary RCCs were diagnosed with the greatest accuracy, likely due to its unique MR characteristics. Lower specificity for ccRCC is due in part to overlap of MR characteristics with other lesions, posing a particular diagnostic challenge for less-common lesions such as oncocytomas and chromophobe RCC. CLINICAL RELEVANCE/APPLICATION While MRI can accurately diagnose many renal masses to aid treatment planning, challenges remain in differentiating lesions that have similar MR features as ccRCC, in particular oncocytic neoplasms. GU256-SDTHB5 Imaging Features of Abdominal Wall Endometriosis Station #5 Participants Gail Yarmish, MD, New York, NY (Presenter) Nothing to Disclose Evis Sala, MD, PhD, New York, NY (Abstract Co-Author) Nothing to Disclose Hedvig Hricak, MD, PhD, New York, NY (Abstract Co-Author) Nothing to Disclose Robert Soslow, New York, NY (Abstract Co-Author) Nothing to Disclose Yuliya Lakhman, MD, New York, NY (Abstract Co-Author) Nothing to Disclose Debra A. Goldman, MS, New York, NY (Abstract Co-Author) Nothing to Disclose Chaya Moskowitz, New York, NY (Abstract Co-Author) Nothing to Disclose Hebert Alberto Vargas, MD, New York, NY (Abstract Co-Author) Nothing to Disclose PURPOSE To assess the utility of various morphologic and quantitative CT features in differentiating abdominal wall endometriosis from other masses of the abdominal wall. METHOD AND MATERIALS Institutional review board approval and waiver of informed consent were obtained for this HIPAA compliant study. CT studies of 105 female patients with histologically evaluated abdominal wall masses were reviewed (median age of 41 years with range: 21 - 55 years); 24.8% (26/105) had histologically proven endometriosis. The other most common diagnoses included desmoid (13.3%; 14/105), leiomyosarcoma (7.6%; 8/105), adenocarcinoma (5.7%; 6/105), clear cell adenocarcinoma (4.8%; 5/105), serous cystadenocarcinoma (3.8%; 4/105) and fibromatosis (2.9%; 3/105). Two radiologists blinded to the final histopathologic diagnosis independently evaluated all cases and recorded their CT imaging features: size, number, location, density, enhancement, heterogeneity, presence of calcifications, associated scars, intraperitoneal disease, and the newly described "comet-tail" sign. Histopathologic specimens served as a gold standard. Associations between CT features and endometriosis were tested using the Fisher exact and the Wilcoxon Rank Sum tests. P-values were adjusted for multiple testing using the false discovery rate approach. Inter-reader concordance was also calculated. RESULTS The CT features significantly associated with endometriosis were location below the umbilicus (p=0.0264), homogeneity (p=0.0264), and "comet tail" sign (p<0.0001). Inter-reader agreement ranged from slight for mass enhancement (k=0.20) to almost perfect on calcifications (k=0.85), comet tail sign (k=0.97), cystic density (k=0.85), position above or below umbilicus (k=0.97), intraperitoneal disease (k=0.97), multiple abdominal wall masses (k=0.94), association with scar (k=0.88), mass heterogeneity (k=0.90), and mass location (k=0.90). CONCLUSION CT features are helpful in distinguishing abdominal wall endometriosis from other abdominal wall soft tissue masses. CLINICAL RELEVANCE/APPLICATION Abdominal wall endometriosis is often misinterpreted when encountered on CT, however there are discriminating imaging features which can assist the radiologist in making this diagnosis. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Evis Sala, MD, PhD - 2013 Honored Educator GU257-SDTHB6 Virtual Non-contrast Imaging for CT Urography with Third-generation Dual-source Dual-energy CT Scanner Station #6 Participants Satoru Takahashi, MD, Kobe, Japan (Presenter) Nothing to Disclose Yoshiko Ueno, MD, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Kiyosumi Kagawa, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Yuko Suenaga, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Kazuhiro Kitajima, MD, Nishinomiya, Japan (Abstract Co-Author) Nothing to Disclose Noriyuki Negi, RT, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Utaru Tanaka, Kobe, Japan (Abstract Co-Author) Nothing to Disclose Kazuro Sugimura, MD, PhD, Kobe, Japan (Abstract Co-Author) Research Grant, Toshiba Corporation Research Grant, Koninklijke Philips NV Research Grant, Bayer AG Research Grant, Eisai Co, Ltd Research Grant, DAIICHI SANKYO Group PURPOSE Virtual non-contrast (VNC) imaging with dual energy CT has been expected to replace true non-contrast imaging. In the excretory phase of CT urography (CTU), however, VNC images are of suboptimal quality because of the densely opacified urine in the collecting system, even with 2nd generation dual source CT (DSCT) scanner. The purpose of this study is to investigate the ability of VNC imaging in CTU with 3rd generation DSCT compared with those with 2nd generation scanner. METHOD AND MATERIALS We retrospectively compared 33 consecutive patients who underwent CTU with 192-slice 3rd generation DSCT scanner using a dual-energy combination of 100 & 150Sn kV, with 19 historical controls with 128-slice 2nd generation DSCT scanner using a 100 & 140Sn kV. CT values of the renal pelvis and the urinary bladder were measured on both mixed images and VNC images of excretory phase CTU. On mixed images, CT values of the area with suboptimal iodine suppression (any pixel that showed >40 HU on VNC images) were compared between 2nd and 3rd generation DSCT. Subjective assessment of the ability of iodine suppression on VNC was scored on a 5-point scale. The ability of detecting urinary stones was also compared. Radiation dose (CTDIvol) was recorded in each case. RESULTS There were no statistically significant differences in CT values of the renal pelvis and the urinary bladder between 2nd and 3rd generation DSCTU on mixed images (renal pelvis, 528 HU vs. 756 HU; urinary bladder, 282 HU vs. 273 HU), as well as VNC images (renal pelvis, 44 HU vs. 42 HU; urinary bladder, 20 HU vs. 8.8 HU). However, mean CT values of the area with suboptimal iodine suppression were lower with 2nd generation (457±177 HU) than 3rd generation DSCT (686±161 HU; p<.0001). No statistically significant differences were found between subjective assessments of VNC with 2nd and 3rd generation DSCT. Renal stones greater than 2-mm in diameter were detected on VNC with both 2nd and 3rd generation DSCT. CTDIvol of the excretory phase CTU was significantly greater with 2nd generation DSCT than 3rd generation (2nd, 10.4±2.0 mGy; 3rd, 7.7± 1.7 mGy; p<.0001). CONCLUSION 3rd generation DSCT could provide more optimal iodine suppression on VNC for the excretory phase CT urography. CLINICAL RELEVANCE/APPLICATION VNC imaging with 3rd generation DSCT is effective for suppressing iodine attenuation of densely opacified urinary tract in CT urography. UR156-EDTHB7 Male Factor Infertility: Role of Imaging Station #7 Awards Identified for RadioGraphics Participants Pardeep K. Mittal, MD, Atlanta, GA (Presenter) Nothing to Disclose Peter A. Harri, MD, Atlanta, GA (Abstract Co-Author) Nothing to Disclose Juan C. Camacho, MD, Atlanta, GA (Abstract Co-Author) Nothing to Disclose Nima Kokabi, MD, Atlanta, GA (Abstract Co-Author) Nothing to Disclose Matthew S. Hartman, MD, Pittsburgh, PA (Abstract Co-Author) Nothing to Disclose Courtney A. Coursey Moreno, MD, Suwanee, GA (Abstract Co-Author) Nothing to Disclose TEACHING POINTS -Demonstrate role of imaging to identify correctable causes of male infertility.-Describe imaging is critically important in diagnosis of pre-testicular, testicular and post-testicular conditions causing infertility in males as well as assessment of obstructive causes of azoospermia.-Demonstrate basic concepts in male reproduction, differential diagnosis and clinical evaluation. TABLE OF CONTENTS/OUTLINE Infertility failure to conceive after regular unprotected sexual intercourse in the absence of known reproductive pathology over a period of 1-2 years. According to WHO 20% causes of infertility are due to male factors where as 27% abnormalities are found in both partners thus male factors are almost in 50% of casesMale factors:Pretesticular: hypogonadism, pituitary failure, estrogen excess, cortisol excess/ deficiency. Testicular: varicocele, rete testis, cryptorchidism, tumors, granulomatous disease etc.Posttesticular: congenital absence of vas deferens, utricular / Müllerian duct cyst, ejaculatory duct obstruction etc.Abnormalities causing testicular failure and impaired spermatogensis cannot be corrected whereas obstructive processes are potentially correctableSummary: Radiologists should be familiar with evaluation of infertility and common radiological findings and disease processes associated with male factor infertility MSCA51 Case-based Review of the Abdomen (An Interactive Session) Thursday, Dec. 3 1:30PM - 3:00PM Location: S406A GI GU OB ER AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Douglas S. Katz, MD, Mineola, NY, (dkatz@winthrop.org) (Director) Nothing to Disclose LEARNING OBJECTIVES 1) To review a series of clinically relevant, abdominal imaging cases, with audience participation. 2) To review important concepts and potential pitfalls of: the liver on sonography; the acute abdomen on US, CT, and MR; liver transplants on multi-modality imaging; genitourinary imaging; and trauma imaging 3) To provide take home points for the audience based on specific actual case material which was instructional or problematic for the presenters. ABSTRACT Sub-Events MSCA51A Hepatic Tumor Imaging Participants Puneet Bhargava, MD, Shoreline, WA (Presenter) Editor, Reed Elsevier LEARNING OBJECTIVES 1) Review imaging appearances of common hepatic tumors. 2) Review key imaging findings that aid in differential diagnosis. ABSTRACT Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Puneet Bhargava, MD - 2015 Honored Educator MSCA51B Abdominal Trauma Imaging Participants Savvas Nicolaou, MD, Vancouver, BC (Presenter) Institutional research agreement, Siemens AG LEARNING OBJECTIVES 1) Review the technique and protocols, with an emphasis on MDCT, for imaging of blunt and penetrating abdominal and pelvic trauma. 2) Demonstrate examples of the spectrum of injuries and the accompanying management associated with abdominal trauma, including hepatic and hepatobiliary (gallbladder) injuries, bowel and mesenteric injuries, and pelvic injuries including bladder and vascular injuries. 3) Demonstrate significance of arterial and portal venous phase imaging in the setting blunt abdominal and pelvic trauma, and the utility of whole body imaging. 4) Review new imaging applications and techniques such as iterative reconstruction and dual-energy CT, which can help better image abdominal and pelvic injuries post-trauma. ABSTRACT MSCA51C Acute Abdomen Imaging Participants Stephan W. Anderson, MD, Boston, MA (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) The participant will be exposed to the current literature related to imaging of acute abdominal pain using CT. 2) The participant will be able to apply an evidence-based approach to CT protocol development in the imaging of acute abdominal pain. 3) The participant will be able to independently evaluate the published literature in this area in a critical fashion and continue to apply recent developments to their own practice. RC707 GU Ultrasound 2015: The Expert's Update on Kidney, Gynecologic and Testicular US Thursday, Dec. 3 4:30PM - 6:00PM Location: N227 GU OB US AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants John J. Cronan, MD, Providence, RI (Coordinator) Nothing to Disclose Mindy M. Horrow, MD, Philadelphia, PA, (horrowm@einstein.edu) (Presenter) Spouse, Director, Merck & Co, Inc Paula J. Woodward, MD, Salt Lake City, UT (Presenter) Vice President, Reed Elsevier LEARNING OBJECTIVES 1) The learner will be made aware of the importance of acute kidney injury (AKI) and associated ultrasound findings. 2) Ultrasound criteria of cystic adnexal masses will be reviewed. 3) Testicular and scrotal pathology and the importance of ultrasound will be explained. ABSTRACT Ultrasound has taken on new importance in the evaluation of the kidney, female pelvis and the scrotum/ testicles. We will explain the ultrasound findings of acute kidney injury (AKI), the evaluation of pelvic masses and the necessary follow-up. Finally, a review of the testicle and ultrasound findings will complete the course. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Mindy M. Horrow, MD - 2013 Honored Educator RC807 GYN and Pelvic Floor 2015: Latest Imaging Guidelines and Angles Simplified! Friday, Dec. 4 8:30AM - 10:00AM Location: N227 GU CT MR US AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Mark E. Lockhart, MD, Birmingham, AL, (mlockhart@uabmc.edu) (Coordinator) Nothing to Disclose Reena C. Jha, MD, Washington, DC (Presenter) Nothing to Disclose Maitray D. Patel, MD, Phoenix, AZ (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Describe current best practice recommendations for management of adnexal asymptomatic, incidental, and/or potentially physiologic findings on pelvic US, CT, and MR based on lesion characteristics and patient clinical factors. 2) Understand the reference lines and angles in pelvic MRI that are used in the evaluation of pelvic floor disorders. 3) Understand the typical imaging characteristics of the endometrium and myometrium according to patient age and stage of the reproductive cycle, and review associated benign pathology. ABSTRACT This session will present on topics related to pelvic imaging. At the conclusion of the three presentations, the participants should have an improved understanding of imaging characteristics of the ovaries and uterus, including endometrium. Also, the imaging parameters used in evaluation of pelvic floor abnormalities such as organ prolapse and structural abnormalities related to incontinence will be reviewed. In each lecture, the imaging characteristics of a variety of disease processes will be covered. Active Handout:Maitray D. Patel http://abstract.rsna.org/uploads/2015/14000842/RC807.pdf RC808 Emergency Ultrasound Pitfalls (An Interactive Session) Friday, Dec. 4 8:30AM - 10:00AM Location: E353C GI GU OB US ER AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Sub-Events RC808A Pitfalls in Right Upper Quadrant Ultrasound Participants Mindy M. Horrow, MD, Philadelphia, PA, (horrowm@einstein.edu) (Presenter) Spouse, Director, Merck & Co, Inc LEARNING OBJECTIVES 1) Describe technical factors that may improve visualization of cholelithiasis including appropriate frequency transducer and identification of gallbladder neck. 2) Identify non biliary causes of gallbladder wall thickening. 3) Recognize causes for nonvisualization of a fluid filled gallbladder and how to differentiate the gallbladder from other fluid filled structures in the right upper quadrant. 4) Describe situations in which color Doppler is essential to detect renal causes of right upper quadrant pain. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Mindy M. Horrow, MD - 2013 Honored Educator RC808B Pediatric Abdominal Ultrasound Pitfalls Participants Susan D. John, MD, Houston, TX (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Use optimal protocols for performing abdominal US in infants and children. 2) Avoid diagnostic errors in pediatric gastrointestinal US caused by common artifacts and variables in exam performance. 3) Recognize variations in pathology and important secondary findings that are helpful for the diagnosis of acute or emergent conditions in the pediatric abdomen. ABSTRACT RC808C Non-obstetrical Gynecologic Ultrasound Pitfalls Participants Ana P. Lourenco, MD, Providence, RI, (alourenco@lifespan.org) (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Recognize commonly encountered gynecological ultrasound pitfalls. 2) Describe strategies to avoid these pitfalls. ABSTRACT This session will review common pitfalls encountered in gynecologic ultrasound and highlight strategies for avoiding such pitfalls. Case-based presentations will illustrate the varied presentations of ovarian torsion, non-gynecologic etiologies for acute pelvic pain including ureteral calculi and acute appendicitis, and a variety of uterine, ovarian and adnexal abnormalities. The benefits and limitations of transabdominal and transvaginal imaging, as well as color Doppler, will be highlighted with examples to demonstrate the utility of each technique. Active Handout:Ana P. Lourenco http://abstract.rsna.org/uploads/2015/15003351/Active RC808C.pdf RC808D First Trimester Ultrasound Pitfalls Participants Mariam Moshiri, MD, Seattle, WA (Presenter) Consultant, Reed Elsevier; Author, Reed Elsevier LEARNING OBJECTIVES 1) To review the relatively recent report of the Society of Radiologists in Ultrasound, on new ultrasound criteria for evaluation of first trimester pregnancy. 2) To demonstrate potential pitfalls of sonographic performance and interpretation in the first trimester of pregnancy, and to discuss how to avoid them. 3) To review other relevant, very recent literature on first trimester pregnancy ultrasound performance and interpretation. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Mariam Moshiri, MD - 2013 Honored Educator Mariam Moshiri, MD - 2015 Honored Educator RC818 Global Cancer Imaging-Insights from Overseas Friday, Dec. 4 8:30AM - 10:00AM Location: E261 GU MI MR OI AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 FDA Discussions may include off-label uses. Participants Sub-Events RC818A Functional and Molecular Imaging at Oxford University Participants Fergus V. Gleeson, MBBS, Oxford, United Kingdom (Presenter) Consultant, Alliance Medical Limited; Consultant, Blue Earth Diagnostics Limited; Consultant, Polarean, Inc; LEARNING OBJECTIVES 1) To learn about the functional and molecular imaging research being conducted within the Radiology Department of Oxford University Hospitals NHS Trust. ABSTRACT There is increasing functional and molecular imaging being performed in medicine. The Radiology department at the Churchill Hospital in Oxford is conducting a number of trials in these areas, and has designed these trials around interventions to measure the effect of these new techniques. It has also taken the opportunity to raise the profile of Radiology within the University, to promote greater collaboration with basic scientists, attracting increased funding, and opportunities for scientists and physicians. RC818B Lessons Learned from the National Irish Breast Screening Program: The First 12 years-One Million Mammograms On Participants Michelle M. McNicholas, MD, Dublin, Ireland (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) To review the results of the Irish National Breast Screening Program following 12 years of screening with over 1,000,000 mammograms performed. 2) To understand the essential components of setting up and maintaining a national breast screening program in Ireland. This includes the rationale for the decisions made at the outset, such as age range, frequency of screens, centralisation of service and responsibility of the screening process to the end of primary surgery. 3) To understand the need for and the mechanism of developing a national registry of eligible women in the absence of a national unique identifier. 4) To understand the need for a client charter which sets out client guarantees, objectives and goals around issues of consent, timeliness of screening results and recall to assessment, biopsy results and admission for surgery and further treatment where indicated. 5) To understand the necessity of national guidelines, annual reports and external accreditation. 6) To demonstrate the essential need for ongoing review of key performance indicators (recall rate, biopsy rate, cancer detection rate, DCIS rate, open biopsy rate, false negative rate, interval cancer rate) as surrogates of program success. 7) To understand the importance of communication and feedback to clients, units, practitioners and media in maintaining uptake. 8) To understand the reporting structure and the composition of various roles within the multidisciplinary medical and surgical teams. 9) To understand the requirements for ongoing training and education of all staff - physicians, technologists, nurses, physicists, administrative staff. 10) To understand the factors affecting radiation dose to the screened population and the over-riding responsibility of the ALARA principle, such as: role of physics team, mammographic technique, equipment choice, technologist expertise and training, quality assessment. 11) To understand the operational issues of different screening units, double reading, discrepancy cases, dealing with interval cancers, dealing with outliers in key performance parameters. 12) To understand the positive spinoff s from the program including increased awareness, improving national standards in the screening and the symptomatic population and the contribution to improved diagnostic and treatment options. 13) To understand how the program achieved, maintained, and monitored performance and how it adapted to changes in practice as issues or controversies arose. 14) To discuss whether this population screening program has been a successful and cost effective health care initiative for Ireland. 15) Ultimately, to understand whether the Irish National Breast Screening Program has led to improved survival in women with breast cancer in Ireland. RC818C MRI of Pelvic Malignancy-The View from Down Under Participants Nicholas J. Ferris, MBBS, Clayton, Australia, (nicholas.ferris@monashhealth.org) (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) To learn about the local availability and funding of MRI in investigating pelvic malignancy that is unique to Australia.2) To understand the current usage of Pelvic MRI in investigating pelvic malignancy in the Australian population.3) To review some typical examples of Pelvic MRI in Oncology that illustrate the advantages of MRI in the assessment of pelvic malignancies and impact MRI has on patient management in the multidisciplinary setting. ABSTRACT Most medical imaging tests in Australia are heavily subsidized by the Federal government as part of the 'Medicare' national health insurance system.Prostate cancer is a common problem in Australian men, and MRI appears to be a very useful tool in its assessment and management, however it remains unfunded in the Medicare system. To remedy this, a group of clinicians has made application to the Medicare Services Advisory Committee (MSAC) for inclusion of the test on the Medicare Benefits Schedule. Steps in the recently revised MSAC procedure will be reviewed, with reference to the current application for prostate MRI.The impact of its current unfunded status on the uptake of prostate MRI will be briefly reviewed.Despite the lack of government support, there has been considerable experience with the technique 'Down Under', leading to some important publications in the international literature about the role of MRI in selection of patients for biopsy, and the choice of biopsy target. RC818D Imaging of HCC-A Korean Perspective Participants Byung Ihn Choi, MD, PhD, Seoul, Korea, Republic Of (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) To learn recent imaging techniques for the qualitative and quantitative diagnosis, selection of treatment methods, and evaluation of monitoring after treatment for HCC. 2) To understand the imaging findings of hepatocarcinogenesis from regenerate nodule going through low and high grade dysplastic nodule, early HCC and finally to advanced HCC. 3) To review current clinical practice guidelines including role of imaging for the diagnosis and treatment for HCC with focus on recent change of guidelines by rapid progression of imaging biomarkers. ABSTRACT RC829 Body MRI: Clinical Challenges (An Interactive Session) Friday, Dec. 4 8:30AM - 10:00AM Location: E450A GI GU MR OI AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Sub-Events RC829A Imaging Perianal Fistulae Participants Damian J. Tolan, MBBCh, FRCR, Leeds, United Kingdom, (damian.tolan@nhs.net) (Presenter) Speaker, Bracco Group; Speaker, Merck & Co, Inc LEARNING OBJECTIVES 1) To understand how to describe the different types of fistula. 2) To learn how to perform, interpret and report MRI for the initial assessment of fistula in ano. 3) To learn the implications of MR findings in planning surgical treatment. RC829B Pelvic Endometriosis Participants Evan S. Siegelman, MD, Philadelphia, PA (Presenter) Consultant, BioClinica, Inc; Consultant, ICON plc; Consultant, ACR Image Metrix LEARNING OBJECTIVES 1) Review the theories concerning the pathogenesis of endometriosis. 2) Discuss the clincial indications that may indicate the use of pelvis imaging to diagnose endometriosis. 3) Assess the current MR techniques used in the detection and characterization of endometriosis. 4) Describe the imaging features of endometriomas and deeply infiltrative endometriosis. ABSTRACT Endometriosis is defined as the presence of ectopic endometrial glands and stroma outside the uterus. Endometriosis is a common cause of pelvic pain and infertility, affecting as many as 10% of premenopausal women. Radiologists should be familiar with the various imaging manifestations of endometriosis, especially those that allow its differentiation from other pelvic lesions. The MR 'pearls' offered here apply to the detection and characterization of pelvic endometriosis. The inclusion of T1-weighted fatsuppressed sequences is recommended for all MR examinations of the female pelvis because such sequences facilitate the detection of small endometriomas and aid in their differentiation from mature cystic teratomas. Benign endometriomas can exhibit restricted diffusion and should not be confused with ovarian cancer. Although women with endometriosis are at risk for developing clear cell and endometrioid epithelial ovarian cancers (ie, endometriosis-associated ovarian cancers), imaging findings such as enhancing mural nodules should be confirmed before a diagnosis of ovarian malignancy is suggested. The presence of a dilated fallopian tube, especially one containing hemorrhagic content, is often associated with pelvic endometriosis. Deep (solid infiltrating) endometriosis can involve the pelvic ligaments, anterior rectosigmoid colon, bladder, uterus, and cul-de-sac, as well as surgical scars; the lesions often have poorly defined margins and T2 signal hypointensity as a result of fibrosis. The presence of subcentimeter foci with T2 hyperintensity representing ectopic endometrial glands within these infiltrating fibrotic masses may help establish the diagnosis. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Evan S. Siegelman, MD - 2013 Honored Educator RC829C Cholangiocarcinoma Diagnosis and Staging: What the Surgeon Needs to Know Participants Eduard E. De Lange, MD, Charlottesville, VA, (delange@virginia.edu) (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) To learn about staging cholangiocarcinoma. 2) To understand how the tumor is classified surgically. 3) To get insight into the various surgical procedures for tumor resection. 4) To understand the importance of vascular involvement for determining tumor resectability. ABSTRACT Active Handout:Eduard E. De Lange http://abstract.rsna.org/uploads/2015/15002799/RC829C.pdf Handout:Eduard E. De Lange http://abstract.rsna.org/uploads/2015/15002799/Course RC829C- de Lange EE - Cholangiocarcinoma - What the surgeon needs to know.xps RC851 Imaging in Practice: DWI in the Abdomen and Pelvis Friday, Dec. 4 8:30AM - 10:00AM Location: S406A GI GU MR AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 Participants Sub-Events RC851A How to Perform DWI - Principles and Protocol Participants Shreyas S. Vasanawala, MD, PhD, Palo Alto, CA (Presenter) Research collaboration, General Electric Company; Consultant, Arterys; Research Grant, Bayer AG; LEARNING OBJECTIVES 1) Understand basic principles of contrast formation in diffusion weighted MRI. 2) Understand sources of artifacts in diffusion weighted MRI. 3) Know techniques to reduce artifacts to produce diagnostic quality diffusion weighted images. ABSTRACT Diffusion-weighted imaging is being used with increasing frequency in body MRI. The basic mechanism of contrast generation is the use of large motion-sensitizing gradients such that water molecules undergoing random motion are dephased, resulting in signal loss. Tissues and lesions with high cellularity have reduced diffusive motion of water, which results in relatively high signal. However, a number of issues make diffusion-weighted imaging in the body challenging relative to neurological applications. First, the vast majority of clinical DWI is performed with an echo-planar technique, which suffers from image distortions due to field inhomogeneity. These become problematic particularly where there are gas-tissue interfaces, such as at the dome of the liver and near gas-filled bowel. The presentation will discuss methods to minimize these distortions. Second, the T2 relaxation rates of abdominal tissues are less than that of pelvic viscera and much less than that of the brain, whereas normal water diffusivity is higher; as the choice of diffusion sensitivity (b value) heavily influences the echo time, lower b values must be used. Third, motion from cardiac pulsations, respiration, and peristalsis produce artifacts, some of which are easily recognizable, and others which can subtly hide pathology. Techniques to minimize these pitfalls will be presented. Finally, issues of reproducibility that affect the practical clinical use of DWI for lesion characterization in body MRI will be discussed, along with approaches to improve reliability. RC851B Interpretation of DWI - How to Create and Use ADC Maps in Your Practice Participants Thomas A. Hope, MD, San Francisco, CA, (thomas.hope@ucsf.edu) (Presenter) Advisory Committee, Guerbet SA; Research Grant, General Electric Company LEARNING OBJECTIVES 1) Understand the principles of calculating ADC. 2) Understand the effect of b-value selection and weighting on diffusion calculations. 3) Explore the value of IVIM and other parameters. ABSTRACT In order to incorporate diffusion weighted imaging into clinical practices, it is important to understand how diffusion data is evaluated. Qualitatively, one can simply say that lesions are "bright" on diffusion, but intensity on high b-value imaging is not always equal to a lesion that has reduced diffusion. The understanding and implementation of quantitative analysis is therefore critical for both research and everyday clinical practice. The first step is the calculation of the apparent diffusion coefficient (ADC) map, which is used to help tease out the differences in intrinsic T2 hyperintensity and diffusivity. The calculation of the ADC map is greatly affected by the methodology used as well as the selection of b-values acquired. The ADC of a tissue describes how quickly signal decreases as the b-value is increased. Those lesions with high diffusivity will have high ADC values, while those lesions with reduced diffusion will have lower ADC values. In addition to ADC, other parameters have been describe that affect the measured diffusivity. The most commonly discussed is intravoxel incoherent motion (IVIM) that is thought to represent the random movement of blood within the capillary system, often called pseudodiffusion. This parameter has its greatest effect on diffusion weighted images at low b-values. URL RC851C Applications of DWI in Clinical Practice - When It Does and Doesn't Help Participants Frank H. Miller, MD, Chicago, IL (Presenter) Nothing to Disclose LEARNING OBJECTIVES 1) Demonstrate the utility of diffusion weighted imaging in the abdomen. 2) Show advantages and limitations of diffusion weighted imaging in the abdomen. ABSTRACT Diffusion weighted imaging (DWI) has been used in neuroimaging for many years. It has only more recently become feasible in the abdomen. The objective of this talk is to emphasize the important role that diffusion-weighted imaging can have in your practice and that it can be used routinely without difficulty in the abdomen and pelvis. DWI potentially can detect additional lesions and direct the radiologist to lesions that are not as well seen on conventional imaging. DWI helps in characterization of lesions but does have limitations in specificity which will be discussed. Qualitative and quantitative evaluation can be performed and the applications of these techniques clinically will be described. The strengths and limitations of DWI in multiple organs including the liver, pancreas, adrenal gland, kidney, and evaluation for metastases and infections will be discussed. DWI is especially helpful for identify lymph node and peritoneal metastases. Emerging techniques include the use of diffusion weighted imaging to assess response to therapy following liver-directed therapy will also be discussed. In summary, DWI should be used routinely if not being used at your institution. This talk will show benefits and limitations of DWI in a number of organs in the body. Honored Educators Presenters or authors on this event have been recognized as RSNA Honored Educators for participating in multiple qualifying educational activities. Honored Educators are invested in furthering the profession of radiology by delivering high-quality educational content in their field of study. Learn how you can become an honored educator by visiting the website at: https://www.rsna.org/Honored-Educator-Award/ Frank H. Miller, MD - 2012 Honored Educator Frank H. Miller, MD - 2014 Honored Educator SST07 Genitourinary (MR and CT of the Urothelium) Friday, Dec. 4 10:30AM - 12:00PM Location: E351 GU CT MR AMA PRA Category 1 Credits ™: 1.50 ARRT Category A+ Credits: 1.50 FDA Discussions may include off-label uses. Participants David D. Childs, MD, Clemmons, NC (Moderator) Research Grant, Endocare, Inc Paul Nikolaidis, MD, Chicago, IL (Moderator) Nothing to Disclose Sub-Events SST07-01 Quantitative Assessment of Voxel-wise Apparent Diffusion Coefficient using K-means Clustering to Predict and Assess Chemotherapeutic Response in Bladder Cancer Friday, Dec. 4 10:30AM - 10:40AM Location: E351 Participants Huyen T. Nguyen, PhD, Columbus, OH (Abstract Co-Author) Nothing to Disclose Amir Mortazavi, MD, Columbus, OH (Abstract Co-Author) Nothing to Disclose Kamal S. Pohar, MD, Columbus, OH (Abstract Co-Author) Nothing to Disclose Zarine K. Shah, MD, Columbus, OH (Abstract Co-Author) Nothing to Disclose Guang Jia, PhD, Baton Rouge, LA (Abstract Co-Author) Nothing to Disclose Michael V. Knopp, MD, PhD, Columbus, OH (Abstract Co-Author) Nothing to Disclose Debra Zynger, MD, Columbus, OH (Abstract Co-Author) Nothing to Disclose Hendrik Von Tengg-Kobligk, MD, Bern, Switzerland (Presenter) Research Grant, W. L. Gore & Associates, Inc PURPOSE To evaluate the value of k-means clustering of voxel-wise Apparent Diffusion Coefficient (ADC) in the assessment of chemotherapeutic response in bladder cancer. METHOD AND MATERIALS 10 bladder cancer patients who received neoadjuvant chemotherapy were included in this initial study. Patients were scanned on a 3T multi-transmit system (Achieva, Philips Healthcare) using a 32-channel phased-array surface coil. Each patient had a baseline (before chemotherapy) MRI and a post-chemotherapy MRI, followed by radical cystectomy. High resolution T2W imaging was performed prior to DWI. DWI data were processed on in-house software written in IDL (Exelis, VIS) to acquire voxel-wise ADC for each tumor. The k-means clustering was implemented to segment each tumor in three clusters (labeled as clusters 1, 2, 3 with low, intermediate, high ADC). The volume fractions (VFs) of three clusters in a tumor at baseline and post-chemotherapy were correlated with the tumor response. P<0.05 was considered to be statistically significant. Color cluster maps were overlaid on ADC maps to visualize the cluster distribution. RESULTS Using pathological findings and radiologic volume estimation of bladder tumors, 6 patients were defined as responders and 4 as nonresponders. At baseline, responders showed a significantly higher VF of cluster 1 and lower VF of cluster 2 (all P<0.04) than nonresponders (Figure 1). In contrast with resistant cases, responsive tumors showed a decrease in VF of cluster 1 and an increase in that of cluster 3 after chemotherapy. These differences in the post-chemotherapy changes of cluster VFs were found to be statistically significant (all P<0.04) between responders and non-responders. CONCLUSION As ADC characterizes the micro-cellularity in body tissues, the heterogeneity of tumor micro-cellularity can be quantified using kmeans clustering of voxel-wise ADC to enable the early assessment and predication of chemotherapeutic response in bladder cancer. CLINICAL RELEVANCE/APPLICATION k-means clustering of voxel-wise ADC can be useful in predicting chemotherapeutic response at baseline and assessing chemotherapy-induced changes of micro-cellularity in bladder cancer. SST07-02 MDCT Urography Using a 320-detector Row Scanner: Comparison of the Wide Volume (W-V) Scan Mode and Conventional Helical Scan Mode in Terms of Radiation Dose and Image Quality Friday, Dec. 4 10:40AM - 10:50AM Location: E351 Participants Catherine Roy, MD, Strasbourg, France (Presenter) Nothing to Disclose Raphael Quin, Strasbourg, France (Abstract Co-Author) Nothing to Disclose Mickael Ohana, MD, MSc, Strasbourg, France (Abstract Co-Author) Nothing to Disclose Guillaume Alemann, MD, MS, Strasbourg, France (Abstract Co-Author) Nothing to Disclose Aissam Labani, MD, Strasbourg, France (Abstract Co-Author) Nothing to Disclose Pierre G. Leyendecker, MD, Strasbourg, France (Abstract Co-Author) Nothing to Disclose PURPOSE To prospectively compare the conventional helical scan mode and W-V scan mode in CT Urography examinations using a 320- detector row scanner in terms of image quality, radiation dose and accuracy of the automatic stitching for alignment of ureteral segments in the W-V scan mode. METHOD AND MATERIALS A cohort of 70 patients underwent a multiphasic CT Urography examination using a 320-detector CT scanner (Aquilion ONE, Toshiba Medical Systems) including a medullary phase using the helical scan mode(collimation:80x0.5mm, rotation:0.5s,1mm/0.8mm, acquisition time:4-6s) and an excretory phase using the W-V scan mode (collimation:200x0.5mm, rotation:0.5s,1mm without overlapping and 4 to 5 volumes to cover the entire urinary tract, acquisition time:6-7s). Adaptative blending was used to stitch the wide volumes. Both scans modes were performed at 120kVp with the same FOV, length of coverage and iterative reconstruction (AIDR 3D). The Body Mass Index (BMI) of each patient and the dose-length product (DLP) was also recorded.For the quantitative analysis, the signal to noise ratio (SNR) was calculated in the iliopsoas muscle. For qualitative analysis, two independent experienced readers were asked to subjectively assess the presence of motion artefacts as well as the quality of the volumes matching by analysis the continuity of the ureter on the excretory phase, using a four-point scale. RESULTS The mean DLP was significantly lower for the W-V acquisition than for the helical acquisition (136.8+/-28mGy·cm vs 232.8+/41mGy·cm,respectively) equal to 42.53% (p<0.05), regardless of the patient's BMI. The SNR was quite similar with W-V and helical scan mode (15.3+/-1.9 vs 17.3+/-2.5, respectively). No significant difference was noted for the presence of motion artifacts between both modes.In 85% of cases, there was no disruption of the continuity of the ureter with the W-V scan mode after stitching of the volumes. In 12% of cases, there was minimal discontinuity of one segment and in 3% of cases there was an inadequate matching of the volumes. CONCLUSION Wide Volume scanning using a 320-MDCT allows a significant radiation dose reduction (42%) while preserving image quality in comparison to helical scanning. The lack of overranging with minimal overbeaming explain those results. CLINICAL RELEVANCE/APPLICATION Wide volume scanning allows a significant reduction of radiation dose with a perfect continuity of the ureter and an excellent image quality . SST07-03 Comparison between Conventional Cystourethrography and MRI with Voiding MRcystourethrography in the Evaluation of Male Urethral Strictures Friday, Dec. 4 10:50AM - 11:00AM Location: E351 Participants Marco Di Girolamo, MD, Rome, Italy (Presenter) Nothing to Disclose Ines Casazza, Rome, Italy (Abstract Co-Author) Nothing to Disclose Simone Mariani, Rome, Italy (Abstract Co-Author) Nothing to Disclose Francesco Carbonetti, MD, Rome-Roma, Italy (Abstract Co-Author) Nothing to Disclose Giulia Francione, Rome, Italy (Abstract Co-Author) Nothing to Disclose Vincenzo David, MD, Rome, Italy (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate the accuracy of conventional retrograde and voiding cystourethrography and MRI together with voiding MRcystourethrography in the evaluation of male urethral strictures. METHOD AND MATERIALS We evaluated 39 male patients with urethral strictures diagnosed with urine flow velocity recording and conventional retrograde and voiding cystourethrography. All these patients underwent MRI and voiding MR-cystourethrography using a 1.5T superconductive magnet. The patients had urine-filled bladders and high-resolution sagittal TSE T2-weighted scans were performed (TR:6250ms; TE:90ms;sl.thick.:3mm; acq.time:3'38"). Voiding MR-cystourethrography was performed with T1-weighted spoiled 3D gradient-echo acquisitions on sagittal plane (TR:12ms; TE:2,7ms; flip-angle:40°; sl.thickness: 2mm; acq.time:12s) after the filling of bladder lumen with contrast-material-enhanced urine obtainded by the i.v administration 20 mg of furosemide followed by ¾ of the normal dose of a paramagnetic contrast agent (Magnevist, Bayer Pharma, Germany). After micturition high-resolution coronal TSE T2weighted scans were performed at the level of the stenosis. Two radiologists in consensus evaluated the morphology and length of the urethral stenosis with the two modalities and with MRI the entity and the site of spongio-fibrosis was assessed. RESULTS 3 patients were not able to perform voiding MR-cystourethrography. In 36 patients evaluated with two imaging modalities 32 single and 4 double urethral strictures were detected. The measurement of the stenosis length was equal or superior with voiding MR cystourethrography and the analysis of 3D sagittal scans allowed a better evaluation of the morphology of the urethral strictures in comparison with conventional cystourethrography. Spongio-fibrosis was found in 30 patients (83%). The site of spongio-fibrosis was always assessed with MRI (dorsal, ventral, dorsal and ventral and circular fibrosis). CONCLUSION MRI with voiding MR-cystourethrography shows the morphology and the length of the urethral strictures better than conventional cystourethrography and allows the detection and site of spongio-fibrosis, avoiding radiation exposure to the gonads and urinary catheterization. CLINICAL RELEVANCE/APPLICATION MRI could be proposed as all-in-one technique for the evaluation of urethral stenosis, allowing their detection and length assessment and determining the presence and site of spongiofibrosis. SST07-04 Efficiency of Diffusion-weighted (DW) MRI to Evaluate the Excreto Urinary Wall Lesions: A Prospective Study of 95 Patients Friday, Dec. 4 11:00AM - 11:10AM Location: E351 Participants Catherine Roy, MD, Strasbourg, France (Presenter) Nothing to Disclose Aissam Labani, MD, Strasbourg, France (Abstract Co-Author) Nothing to Disclose Mickael Ohana, MD, MSc, Strasbourg, France (Abstract Co-Author) Nothing to Disclose Guillaume Alemann, MD, MS, Strasbourg, France (Abstract Co-Author) Nothing to Disclose Guillaume Bierry, MD, PhD, Strasbourg, France (Abstract Co-Author) Nothing to Disclose Herve Lang SR, MD, Strasbourg, France (Abstract Co-Author) Nothing to Disclose PURPOSE The purpose was to investigate the reliability of DW-MRI in differentiating malignant from benign thickening or masses of the entire urinary excretory wall. METHOD AND MATERIALS We prospectively evaluated 95 patients referred for 52 upper urinary tract (UUT) and 43 bladder (Bl) lesions during a period of 5 years (from january 2010 to january 2015) . MR examinations were performed on a 3T unit (Achieva, Philips Medical System) including to our conventional protocol using T2 and T1 sequence before and after contrast media injection an axial DWI (TR/TE : 7000/55, FOV : 250-300, ETL : 53, slice thickness : 4 mm, acquisition time : 4 min, Sense factor : 2, b =0 and 1000 mm2/sec) under free breathing with a respiratoy compensatory device (navigator echo) for UUT. The final diagnosis and standard of reference was the pathological analysis performed after MR examination, obtained either after surgery (74 cases) or by selective cytology and endoscopic biopsy (21 cases) with a follow up imaging (at least one year) for 11 of them. Mann-Whitney test and Student -t test were used to determine the efficiency of the mean ADC value. RESULTS Maximal axial diameter was 34±24mm for malignant (39 UUT; 33 Bl) and 15±5mm for benign lesions (13 UUT; 10 Bl), respectively. For UUT, the mean ADC value in the malignant lesions was significantly lower than that in the benign lesions: 0.99+0.27 x103mm2/s against 1.54+0.43 x10-3mm2/s, respectively (p=0.0005). Thirty-three malignant lesions had an ADC value inferior to 1 x103mm2/s and only one benign lesion. There was a significant difference among the mean ADC values of different grades of malignant tumors, corresponding to 0.84 ± 0.12 x10-3mm2/s-1 and 1.0 ± 0.20 x10-3mm2s-1 (p<0.01) in high-grade and low-grade excretory epithelioma, respectively For bladder, the mean ADC value in the malignant lesions was not significantly inferior to that of benign lesions (1.22 ± 0.3 x10-3mm2/s against 1.32± 0.2x10-3mm2/s, p=0.41) CONCLUSION DW-MRI is efficient in the differentiation between benign from malignant lesion located on the upper urinary tract. It does not seem according those data reliable for bladder tumors. DW sequence must be included in MR protocols for exploration of upper urinary tract. CLINICAL RELEVANCE/APPLICATION DW must be included in MR protocols for exploration of upper urinary tract. DW-MRI is efficient in the differentiation between benign from malignant lesion only in the upper urinary tract. SST07-05 ADC as a Novel Biomarker to Predict the Local Stage and Tumor Grade of Bladder Cancer Friday, Dec. 4 11:10AM - 11:20AM Location: E351 Participants Chandan J. Das, MD, MBBS, New Delhi, India (Presenter) Nothing to Disclose T. Razik, New Delhi, India (Abstract Co-Author) Nothing to Disclose Sanjay Sharma, MD, FRCR, New Delhi, India (Abstract Co-Author) Nothing to Disclose Deepnarayan Srivastava, Delhi, India (Abstract Co-Author) Nothing to Disclose Amlesh Seth, MBBS, MCHIR, New Delhi, India (Abstract Co-Author) Nothing to Disclose Arun K. Gupta, MBBS, MD, New Delhi, India (Abstract Co-Author) Nothing to Disclose PURPOSE To evaluate the role of ADC as a novel biomarker to predict the local stage and tumor grade of bladder cancer using histopathology (of post TURBT/cystectomy specimen) as the gold standard. METHOD AND MATERIALS The study was approved by the local institutional ethics committee. MRI of 25 patients were performed in a 3 Tesla imaging system (Achieva, Philips). Routine T1W and T2W images were obtained, followed by Diffusion Weighted Imaging in four b values (b0, 500, 1000, and 1500). All the patients had their surgery done within 1 month of performing MRI. Tumour staging was assessed with the criteria used byTakeuchi et al,( 2009). For the tumour grade, freehand ROI values were obtained from the ADC map and their mean calculated. Images were reviewed by two experienced radiologists in consensus, both blinded to the histopathology report. Subsequently, the sensitivity, specificity, positive and negative predictive values were assessed using standard statistical tests. Results were compared with the histopathology. RESULTS DWI had a sensitivity of 76.9% in detecting muscle invasion with a high specificity of 91.7%. The positive and negative predictive values were 90.9 and 78.6% respectively. The ADC values were (0.786 + 0.045) x 10-3 for high grade lesions and (1.049 + 0.113) x 10-3 for low grade lesions, with a significant difference between the two (p< 0.05). We could not found any additive value of T2 weighted imaging when combined with DWI. DWI images acquired in coronal and sagiital plane were better for evaluation of bladder dome lesion whereas axial plane DWI were best for rest of the lesions. CONCLUSION DWI showed a high specificity and positive predictive value in identifying muscle invasion. ADC values showed significant correlation with the tumor grade and can be used as novel imaging biomarker for predicting redict the local stage and tumor grade of bladder cancer.. CLINICAL RELEVANCE/APPLICATION ADC can be used as a noninvasive tool to evaluate bladder tumor and may avoid repeated cystoscopy or biopsy during follow up of low grade lesions following TURBT. DWI at 3T is superior to T2WI for evaluating the T stage of bladder cancer, particularly in differentiating T1 tumors from those T2 or higher, and in detecting stalks of papillary bladder tumors. SST07-06 Detection of Urothelial Carcinomas: Comparison of Reduced-dose Based Iterative Reconstruction with Standard-Dose Filtered Back Projection Friday, Dec. 4 11:20AM - 11:30AM Location: E351 Participants See Hyung Kim, Daegu, Korea, Republic Of (Abstract Co-Author) Nothing to Disclose Jung Hee Hong, Daegu, Korea, Republic Of (Presenter) Nothing to Disclose PURPOSE To retrospectively assess radiation dose, image quality and diagnostic performance of CT urography detecting urothelial carcinomas for performing reduced-dose with iterative reconstruction (IR) in comparison to standard-dose with filtered back projection (FBP). METHOD AND MATERIALS Institutional review board approved this study. 2163 patients (age range, 28-81years; 1452 male) at high-risk for urothelial carcinomas randomly underwent standard-dose scanning with FBP (120kVp for >80kg, 100kVp for 50-80kg) or reduced-dose scanning with IR (100kVp for >80kg, 80kVp for 50-80kg) according to the body weight. Objective and subjective image quality between the two groups with same weight scope was compared, using two-way analysis. The predictive accuracy detecting urothelial carcinomas were also calculated by using as standard reference. RESULTS Mean effective dose was 26% (15.5mSv vs. 11.1mSv) and 30% (7.91mSv vs. 5.01mSv) lower with the reduced-dose scanning. Objective image noise had no significant difference, except for 120kVp with FBP and 80kVp with IR (ranging from 7.2 to 7.9 vs. 9.4 to 9.9, P <.0102). SNR and CNR had no significant difference. Subjective image quality had no significant difference in visual image noise, artifacts, ureter depiction and overall image quality, except for artifacts in 100kVp with FBP and 80kVp with IR (5 [4-5] vs. 4 [3-4]) (P >.05). Diagnostic accuracies on lesion level were 89.6% (89/98, 120kVp with FBP), 91.3% (105/115, 100kVp with FBP), 92.9% (79/85, 100kVp with IR) and 88.8% (111/125, 80kVp with IR), respectively. CONCLUSION Reduced-dose images with IR showed radiation dose reduction and equivalent image quality with ensuring diagnosis detecting urothelial carcinomas as compared with standard-dose images with FBP, thus these robust capabilities may use in clinical practice. CLINICAL RELEVANCE/APPLICATION Reduced-dose images with IR could be of help to reduce radiation dose with equivalent image quality for detecting urothelial carcinomas as compared with standard-dose images with FBP. SST07-07 Recurrence Patterns in Transitional Cell Carcinoma of the Upper Urinary Tract Friday, Dec. 4 11:30AM - 11:40AM Location: E351 Participants Betsa Parsa, Boston, MA (Presenter) Nothing to Disclose Vishala Mishra, MBBS, Boston, MA (Abstract Co-Author) Nothing to Disclose Sandeep S. Hedgire, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Yun Mao, MD, Chongqing, China (Abstract Co-Author) Nothing to Disclose Duangkamon Prapruttam, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose Mukesh G. Harisinghani, MD, Boston, MA (Abstract Co-Author) Nothing to Disclose PURPOSE This study included patients diagnosed with UT-TCC who underwent nephroureterectomy between 2003-2008. Tumor location, morphology, TNM staging and histologic grade were recorded based on radiological examinations . The pattern and timing of recurrence was evaluated at 3, 6, 12, 24, 36 and 60 months in a five-year imaging and clinical follow up period (2008-2013). METHOD AND MATERIALS This included patients diagnosed with UT-TCC who underwent nephroureterectomy between 2003-2008. Tumor location, morphology, TNM staging and histologic grade were recorded based on radiological examinations and clinical notes. The pattern and timing of recurrence was evaluated at 3, 6, 12, 24, 36 and 60 months in a five year follow up period (2008-2013). RESULTS 68 patients with an average age of 77.5 yrs were included in this study. At initial work-up, renal, ureteric and renal plus ureteric lesions were present in 34, 25 and 9 patients respectively. Of 59 patients for whom tumor morphology was available, 34 had massforming lesions and 25 were seen as filling defects. The majority of patients had a T-stage of Ta (n=28) or T3 (n=23), while nodal involvement was mostly absent. Tumors were grade 3 in 44.1% and grade 2 in 33.8%.Most recurrences were noted at 3 and 24 months. Patients with bilateral tumors had a higher recurrence rate at 3, 12, and 24-month follow-ups while for unilateral tumors the chance was higher at 36-month follow-up. Recurrence rate was also higher in patients with T2, N1 and pathologic grade 3 and in patients with T2, N1 and N2 at 3- and 12-month follow-ups, respectively. Pathological grade 1 tumors showed late recurrence at 5-yr follow up. Overall, recurrence occurred in 20 cases during the 5-yr follow-up, which was commonly located in lymph nodes, bladder. Multivariate analysis showed T-stage and location of primary tumor were independent predictors of tumor-free survival (p=0.021, 0.038 respectively). Average tumor-free survival time was 56.5 months. CONCLUSION Nodal, bladder, hepatic and bone metastasis are common in UT-TCC with most of them occurring at 3 and 24 months. T-stage and location are independent predictors of tumor-free survival. Tumors confined to either kidney or ureter, lower T, N stage and histologic grade were associated with longer survivals. CLINICAL RELEVANCE/APPLICATION Information on the pattern of recurrence in UT-TCC patients can lead to more effective planning of imaging surveillance strategy. SST07-08 The Incremental Value of Diffusion-Weighted MR Images in the Tumor Detection and the Staging of Preoperative T Categorization in Renal Pelvic Carcinoma: Effect of Reader Experience Friday, Dec. 4 11:40AM - 11:50AM Location: E351 Participants Rika Yoshida, MD, Izumo, Japan (Presenter) Nothing to Disclose Takeshi Yoshizako, MD, Izumo, Japan (Abstract Co-Author) Nothing to Disclose Hiroshi Mori, Izumo, Japan (Abstract Co-Author) Nothing to Disclose Minako Maruyama, Izumo, Japan (Abstract Co-Author) Nothing to Disclose Takashi Katsube, Izumo City, Japan (Abstract Co-Author) Nothing to Disclose Shinji Andou, MD, Izumo, Japan (Abstract Co-Author) Nothing to Disclose Tomonori Nakamura, Izumo, Japan (Abstract Co-Author) Nothing to Disclose Nobuko Yamamoto, MD, Izumo, Japan (Abstract Co-Author) Nothing to Disclose Megumi Nakamura, Izumo, Japan (Abstract Co-Author) Nothing to Disclose Hajime Kitagaki, MD, Izumo, Japan (Abstract Co-Author) Nothing to Disclose PURPOSE The purpose of this study is to retrospectively assess the incremental value of diffusion-weighted MRI (DWI) to T2-weighted image (T2WI) in the tumor detection and the staging of preoperative T categorization in renal pelvic carcinoma by readers of different experience levels. METHOD AND MATERIALS Thirty-two urothelial carcinoma in 32 patients underwent preoperative MRI examination, including T2WI and DWI (b=0, 800 s/mm) and contrast-enhanced imaging (CEI). All patients had total nephrectomy within 1 month of MRI. Two radiologists (reader 1 had 5 years and reader 2 had 18 years of experience) independently reviewed three image sets (T2WI alone, T2WI plus DWI, and T2WI plus CEI) regarding tumor detection and the discrimination of locally advanced tumors. RESULTS The pathologic T category was T1 in 5 (15.6%), T2 in 6 (18.8%), T3a in 9 (28.1%), T3b in 11 (34.4%), and T4 in 1 (3.1%).T2WI plus DWI enabled a high detection rate (97%, 31/32) without significant differences.In reader 1, for the diagnosis of T3 or higher categories, the accuracies were relatively low in all three image sets (75.0% each for T2WI alone and T2WI plus CEI and 71.9% for T2WI plus DWI). For discriminating tumors with macroscopic renal invasion from those with microscopic renal invasion or less, T2WI plus DWI (90.6%) was significantly more accurate than T2WI alone (68.8%) (p < 0.05), with with areas under receiver operating characteristic curves (AUC) of 0.82 and 0.73, respectively.In reader 2, for the diagnosis of T3 or higher categories, the accuracies were relatively low in all three image sets (each sets were 71.9%). For discriminating tumors with macroscopic renal invasion from those with microscopic renal invasion or less, the accuracies were relatively high in all three image sets (84.3% for T2WI alone, 94.8% for T2WI plus CEI and 90.6% for T2WI plus DWI), with AUC of 0.88, 0.95, and 0.93, respectively.For the diagnosis of T categorization, T2WI added DWI improved interobserver agreement from fair (κ = 0.21, 0.32) to substantial (κ = 0.60, 0.73). CONCLUSION DWI improved the tumor detection rate and the diagnostic performance for T categorization of renal pelvic cancer without contrast material, especially for the relatively inexperienced reader. CLINICAL RELEVANCE/APPLICATION DWI improved the tumor detection rate and the diagnostic performance for T categorization of renal pelvic cancer without contrast material. SST07-09 Organ Confined Urinary Bladder Carcinoma: A Comparative Analysis for "Submucosa Linear Enhancement" Sign on Early Phase of DCE-MRI and the "Inchworm" Sign on DWI Friday, Dec. 4 11:50AM - 12:00PM Location: E351 Participants Huanjun Wang, MD, GuangZhou, China (Presenter) Nothing to Disclose Jian Guan, MD, Guangzhou, China (Abstract Co-Author) Nothing to Disclose Yan Guo, MD, Guangzhou, China (Abstract Co-Author) Nothing to Disclose PURPOSE To investigate the pathogenetic mechanism of "submucosa linear enhancement" and to further evaluate its application value in preoperative staging of organ confined bladder carcinoma. METHOD AND MATERIALS The examination protocol was approved by the institutional medical ethics committee and informed consent was obtained from all patients. 59 patients with suspected or confirmed urothelial bladder cancer and no renal function impairment were enrolled in the study. All patients underwent MRI within 2-weeks before surgery. Two image sets of T2WIandDW-MRI and T2WIandDCE-MRI were independently interpreted by two readers at 2-week intervals by analyzing whether there were "inchworm" sign on DWI and "submucosa linear enhancement" sign on early phase of DCE-MRI, which were further comparatively analyzed with pathology. Tumor size was also compared. RESULTS 92 carcinomas (79 T1, 13 T2) were analyzed. 58 presented "submucosa linear enhancement" on early phase of DCE-MRI which manifested three types as follow: continuous linear enhanced submucosa gathering toward into the center of tumor (39), continuous straight and no gathering linear enhanced submucosa(14) and interrupted linear enhanced submucosa(5) respectively, and the remaining 34 lesions presented no significant linear enhanced submucosa. 42 carcinomas (38 T1, 4 T2) presented "inchworm" sign on DWI, with the remaining 50 lesions (41 T1, 9 T2) shown not. Statistical significance were found for tumor size between carcinomas presented "inchworm" sign and those without, which had a median of 21.5mm for the former, and 13.0mm for the latter. CONCLUSION Presentation of "submucosa linear enhancement" under the tumor base on DCE-MRI is a significant imaging sign which can be applied in preoperative staging of organ confined bladder carcinoma. Presentation of either straight or gathered continuous "enhanced submucosa line" often suggests bladder muscle wall have not been involved. CLINICAL RELEVANCE/APPLICATION DCE-MRI and DWI can supply us an optimal imaging tool for preoperative staging of organ confined bladder carcionoma and is highly recommended.