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Augmented reality assisted MRI/US fusion for non-rectal fully trans-perineal prostate biopsy 增强现实辅助MRI/US融合非直肠完全经会阴前列腺活检
IF 0.4
Urology Case Reports Pub Date : 2025-08-06 DOI: 10.1016/j.eucr.2025.103159
Braden Millan , Nikhil Pramod , Jaskirat Saini , Ruben Blachman-Braun , Baris Turkbey , Sheng Xu , Ming Li , Michael Evans , Gabreille Stefy , Sandeep Gurram , Bradford Wood , Peter A. Pinto
{"title":"Augmented reality assisted MRI/US fusion for non-rectal fully trans-perineal prostate biopsy","authors":"Braden Millan ,&nbsp;Nikhil Pramod ,&nbsp;Jaskirat Saini ,&nbsp;Ruben Blachman-Braun ,&nbsp;Baris Turkbey ,&nbsp;Sheng Xu ,&nbsp;Ming Li ,&nbsp;Michael Evans ,&nbsp;Gabreille Stefy ,&nbsp;Sandeep Gurram ,&nbsp;Bradford Wood ,&nbsp;Peter A. Pinto","doi":"10.1016/j.eucr.2025.103159","DOIUrl":"10.1016/j.eucr.2025.103159","url":null,"abstract":"<div><div>Augmented reality (AR) technologies enable the superimposition of imaging upon a patient in real time with three dimensional instrument tracking during procedures. We sought to demonstrate the feasibility of using an AR system (XR90, MediView XR Inc., Cleveland, OH) to fuse a pelvic multi-parametric magnetic resonance image segmentation with ultrasound to perform a non-rectal, fully trans-perineal (FTP), AR-assisted prostate biopsy. AR-assisted biopsy results were congruent with standard fusion biopsy results, showing benign prostate tissue. No adverse events occurred. Limitations include the current workflow and reliance on a non-specialized ultrasound probe.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"Article 103159"},"PeriodicalIF":0.4,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144829022","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Synchronous giant bilateral renal tumors as initial presentation of Von Hippel-Lindau disease: Sequential surgical management and transition to renal replacement therapy 同步巨大双侧肾肿瘤作为Von Hippel-Lindau病的初始表现：序贯手术治疗和过渡到肾脏替代治疗
IF 0.4
Urology Case Reports Pub Date : 2025-08-06 DOI: 10.1016/j.eucr.2025.103150
Alberto E. Fuentes , Renato A. Ramírez , Gabriela P. Vera , Felipe A. Del Valle , Alfonzo E. Bruzzone , Francisco A. Rojas , José P. Arenas , Diego P. Barrera
{"title":"Synchronous giant bilateral renal tumors as initial presentation of Von Hippel-Lindau disease: Sequential surgical management and transition to renal replacement therapy","authors":"Alberto E. Fuentes ,&nbsp;Renato A. Ramírez ,&nbsp;Gabriela P. Vera ,&nbsp;Felipe A. Del Valle ,&nbsp;Alfonzo E. Bruzzone ,&nbsp;Francisco A. Rojas ,&nbsp;José P. Arenas ,&nbsp;Diego P. Barrera","doi":"10.1016/j.eucr.2025.103150","DOIUrl":"10.1016/j.eucr.2025.103150","url":null,"abstract":"<div><div>Synchronous bilateral renal cell carcinoma (RCC) is rare and often linked to hereditary syndromes such as Von Hippel-Lindau (VHL) disease. We present a 27-year-old male with acute appendicitis, whose CT incidentally revealed bilateral renal tumors and pancreatic cysts. Further evaluation identified cerebellar and retinal hemangioblastomas, confirming VHL. Due to tumor complexity, sequential laparoscopic radical nephrectomies were performed, followed by hemodialysis initiation and transplant planning. Pathology showed multifocal clear cell RCC, ISUP grades 2–3. This case illustrates an atypical VHL presentation, where early syndromic suspicion and multidisciplinary coordination enabled timely and effective management.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"Article 103150"},"PeriodicalIF":0.4,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144829021","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Bilateral synchronous percutaneous nephrolithotomy in single session: A case from a district hospital. 地区医院双侧同步经皮肾镜取石术一例。
IF 0.4
Urology Case Reports Pub Date : 2025-08-06 eCollection Date: 2025-09-01 DOI: 10.1016/j.eucr.2025.103152
Mohamad Rheza Firmansyah, Andhika Hernawan Novianda, Widi Atmoko, Octoveryal Aslim
{"title":"Bilateral synchronous percutaneous nephrolithotomy in single session: A case from a district hospital.","authors":"Mohamad Rheza Firmansyah, Andhika Hernawan Novianda, Widi Atmoko, Octoveryal Aslim","doi":"10.1016/j.eucr.2025.103152","DOIUrl":"10.1016/j.eucr.2025.103152","url":null,"abstract":"<p><p>Kidney stones are the most common urological condition worldwide, with rising prevalence. Bilateral cases present challenges such as longer surgery, anesthesia risks, and extended hospitalization. We report a case of a 59-year-old female with bilateral hydronephrosis and multiple stones, successfully treated with bilateral synchronous percutaneous nephrolithotomy (PCNL) at a district-level hospital in Surakarta, Indonesia. Using existing nephrostomy access and meticulous planning, the procedure minimized operative time and blood loss. Full stone clearance was achieved without complications, and renal function remained stable. Bilateral synchronous PCNL is a cost-effective, efficient option in selected patients, requiring advanced surgical expertise and well-coordinated care.</p>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"103152"},"PeriodicalIF":0.4,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12356340/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144875732","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A rare case of spontaneous kidney rupture from xanthogranulomatous pyelonephritis presenting with neurological symptoms and septic peritonitis. 一例罕见的黄色肉芽肿性肾盂肾炎自发性肾破裂，表现为神经系统症状和脓毒性腹膜炎。
IF 0.4
Urology Case Reports Pub Date : 2025-08-06 eCollection Date: 2025-09-01 DOI: 10.1016/j.eucr.2025.103155
Hoi-Lung Wong, Henry Hong-Yin Lie, Ting-Fung Wong, Wilson Pui-Long Hung, Rong Na, Chiu-Fung Tsang, Terence Chun-Ting Lai, Brian Sze-Ho Ho, Ada Tsui-Lin Ng
{"title":"A rare case of spontaneous kidney rupture from xanthogranulomatous pyelonephritis presenting with neurological symptoms and septic peritonitis.","authors":"Hoi-Lung Wong, Henry Hong-Yin Lie, Ting-Fung Wong, Wilson Pui-Long Hung, Rong Na, Chiu-Fung Tsang, Terence Chun-Ting Lai, Brian Sze-Ho Ho, Ada Tsui-Lin Ng","doi":"10.1016/j.eucr.2025.103155","DOIUrl":"10.1016/j.eucr.2025.103155","url":null,"abstract":"<p><p>Xanthogranulomatous pyelonephritis (XGP) is a rare, chronic inflammatory kidney disorder. It typically arises in patients with a history of nephrolithiasis, urinary tract obstruction, or recurrent infections. Additional risk factors include diabetes and immunocompromised states. We present an unusual instance of XGP in a patient without known risk factors, who developed spontaneous kidney rupture complicated by life-threatening sepsis. This case underscores the importance of maintaining XGP in the differential diagnosis even for atypical presentations, particularly when sepsis is the dominant clinical feature. Given the risk of serious complications, prompt diagnosis and intervention are crucial. Nephrectomy is the mainstay treatment of XGP.</p>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"103155"},"PeriodicalIF":0.4,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12356320/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144875731","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pull-through vaginoplasty with anterior sagittal transrectal approach in high confluence urogenital sinus and 46XX, DSD: A case report and literature review. 经直肠前矢状入路高汇合度泌尿生殖窦及46XX， DSD阴道成形术1例并文献复习。
IF 0.4
Urology Case Reports Pub Date : 2025-08-06 eCollection Date: 2025-09-01 DOI: 10.1016/j.eucr.2025.103146
Angger Satria Pamungkas, Gerhard Reinaldi Situmorang, Muhammad Ridha, Irfan Wahyudi
{"title":"Pull-through vaginoplasty with anterior sagittal transrectal approach in high confluence urogenital sinus and 46XX, DSD: A case report and literature review.","authors":"Angger Satria Pamungkas, Gerhard Reinaldi Situmorang, Muhammad Ridha, Irfan Wahyudi","doi":"10.1016/j.eucr.2025.103146","DOIUrl":"10.1016/j.eucr.2025.103146","url":null,"abstract":"<p><p>We report our experience of pull-through vagina with anterior sagittal approach of high. UGS in 46,XX disorder of sex development (DSD). Rare case of 4-year-old girl presented with UGS and 46,XX DSD with the chief complaint of purulent urination since 2 years ago. Patient underwent pull-through vaginoplasty with anterior sagittal approach. Surgical wound was in good condition, there was no leakage and urine production on both urethral catheter and cystostomy was good. Pull-through vagina with anterior sagittal approach is feasible procedure, which provides excellent exposure and easy identification of the vaginal confluence for UGS patient.</p>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"103146"},"PeriodicalIF":0.4,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12357241/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144875739","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
RIRS using a flexible and navigable suction ureteral access sheath and thulium fiber laser in a patient taking anticoagulants with multiple large kidney stones. Clinical case. RIRS采用灵活可导航的输尿管吸入鞘和铥纤维激光治疗多发性大肾结石服用抗凝剂患者。临床病例。
IF 0.4
Urology Case Reports Pub Date : 2025-08-06 eCollection Date: 2025-09-01 DOI: 10.1016/j.eucr.2025.103153
Dmitriy Sytnik, Sergey Popov, Yury Mikheev
{"title":"RIRS using a flexible and navigable suction ureteral access sheath and thulium fiber laser in a patient taking anticoagulants with multiple large kidney stones. Clinical case.","authors":"Dmitriy Sytnik, Sergey Popov, Yury Mikheev","doi":"10.1016/j.eucr.2025.103153","DOIUrl":"10.1016/j.eucr.2025.103153","url":null,"abstract":"<p><p>Percutaneous nephrolithotomy is one of the modern methods for treating kidney stones larger 2 cm. When anticoagulation therapy cannot be stopped, retrograde intrarenal surgery (RIRS) is recommended. We report a case of RIRS using flexible and navigable suction ureteral access sheath (FANS-UAS) and Thulium fiber laser (TFL) in a patient with multiple large kidney stones who could not be stopped on anticoagulant therapy. The surgery was successful and without complications. RIRS using FANS-UAS and TFL in this group of patients has high efficacy and safety.</p>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"103153"},"PeriodicalIF":0.4,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12356322/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144875740","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Penile epidermoid inclusion cyst after circumcision: A case report. 包皮环切术后阴茎表皮样包涵囊肿1例。
IF 0.4
Urology Case Reports Pub Date : 2025-08-06 eCollection Date: 2025-09-01 DOI: 10.1016/j.eucr.2025.103151
Mohammed E Azoz, Ahmed K Osman, Mohammed A Idris, Mohammed A Musa, Moataz M Alhasan, Sakina S Baloul, Mohammed Y Bakhiet
{"title":"Penile epidermoid inclusion cyst after circumcision: A case report.","authors":"Mohammed E Azoz, Ahmed K Osman, Mohammed A Idris, Mohammed A Musa, Moataz M Alhasan, Sakina S Baloul, Mohammed Y Bakhiet","doi":"10.1016/j.eucr.2025.103151","DOIUrl":"10.1016/j.eucr.2025.103151","url":null,"abstract":"<p><p>Epidermoid inclusion cysts are benign lesions resulting from implantation and proliferation of epidermal elements within the dermis, often following trauma and surgery. They are rare in penile region, especially in pediatric patients. This report describes a four-year-old boy who experienced a painless swelling of the penile foreskin two years after undergoing traditional circumcision. Clinical examination revealed a mobile mass on the ventral aspect of the foreskin. Surgical excision, as well as circumcision, were performed under general anesthesia, and histopathology confirmed the diagnosis. The patient recovered after surgery, with no recurrence.</p>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"103151"},"PeriodicalIF":0.4,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12355407/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144875738","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Immediate repair in complete anterior urethral injury caused by blunt trauma: a case report and literature review. 钝性创伤致完全性前尿道损伤立即修复一例报告并文献复习。
IF 0.4
Urology Case Reports Pub Date : 2025-08-06 eCollection Date: 2025-09-01 DOI: 10.1016/j.eucr.2025.103157
Nurcholis, Rinto Hariwibowo, Adhitama Alam Soeroto
{"title":"Immediate repair in complete anterior urethral injury caused by blunt trauma: a case report and literature review.","authors":"Nurcholis, Rinto Hariwibowo, Adhitama Alam Soeroto","doi":"10.1016/j.eucr.2025.103157","DOIUrl":"10.1016/j.eucr.2025.103157","url":null,"abstract":"<p><p>Injury of the urethra is a rare but significant medical condition, often caused by blunt trauma. In Indonesia, incidence is underreported. A 48-year-old male with blunt perineal trauma presented with open penile-scrotal wound and inability to void. Suspecting anterior urethral rupture, urinary diversion was performed. Due to unavailable urethrography and open wound, surgical exploration was necessary and confirmed complete rupture, managed by primary anastomosis. Complete urethral ruptures are uncommon, and initial management requires urinary diversion, with delayed urethroplasty based on severity. This case highlights diagnostic and treatment challenges in complete anterior urethral rupture.</p>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"103157"},"PeriodicalIF":0.4,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12355405/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144875736","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dual paraneoplastic syndrome with prostate cancer: A case of syndrome of inappropriate secretion of antidiuretic hormone (SIADH) and humoral hypercalcemia of malignancy (HHM). 双副肿瘤综合征伴前列腺癌：抗利尿激素分泌不当伴恶性肿瘤体液性高钙血症综合征1例。
IF 0.4
Urology Case Reports Pub Date : 2025-08-06 eCollection Date: 2025-09-01 DOI: 10.1016/j.eucr.2025.103148
Junya Abe, Takashi Muranaka, Yasuharu Kunishima
{"title":"Dual paraneoplastic syndrome with prostate cancer: A case of syndrome of inappropriate secretion of antidiuretic hormone (SIADH) and humoral hypercalcemia of malignancy (HHM).","authors":"Junya Abe, Takashi Muranaka, Yasuharu Kunishima","doi":"10.1016/j.eucr.2025.103148","DOIUrl":"10.1016/j.eucr.2025.103148","url":null,"abstract":"<p><p>We report the case of an 85-year-old man diagnosed with metastatic prostate cancer three years earlier. While on combined androgen blockade, he developed hematuria, hematochezia, and fatigue. These symptoms were attributed to local progression of prostate cancer and syndrome of inappropriate antidiuretic hormone secretion (SIADH). Water restriction, palliative radiation, and tolvaptan alleviated the symptoms. Four months later, he experienced appetite loss and fatigue due to hypercalcemia, ultimately leading to a diagnosis of humoral hypercalcemia of malignancy (HHM).</p>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"103148"},"PeriodicalIF":0.4,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12356318/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144875734","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ectopic adrenal tissue in an inguinal hernia sac: A case report 腹股沟疝囊内肾上腺组织异位1例
IF 0.4
Urology Case Reports Pub Date : 2025-08-05 DOI: 10.1016/j.eucr.2025.103145
Nandini Sateesh Desai, Aditi Dalvi, Sanjay Oak, Paras Kothari, Abhaya Gupta, Shahaji Deshmukh
{"title":"Ectopic adrenal tissue in an inguinal hernia sac: A case report","authors":"Nandini Sateesh Desai,&nbsp;Aditi Dalvi,&nbsp;Sanjay Oak,&nbsp;Paras Kothari,&nbsp;Abhaya Gupta,&nbsp;Shahaji Deshmukh","doi":"10.1016/j.eucr.2025.103145","DOIUrl":"10.1016/j.eucr.2025.103145","url":null,"abstract":"<div><div>Adrenal ectopy is the rare occurrence of adrenal tissue at abnormal locations with hernia sac being particularly infrequent. 2-year-old male child with swelling in right inguinal region was diagnosed as reducible inguinal hernia. Intraoperatively during hernia repair, the sac was identified with a thick yellow nodule adherent to it. Separation of sac from cord structures along with high ligation of sac was done. The histopathological analysis of abnormal tissue was consistent with ectopic adrenal cortical tissue. We conclude that abnormal tissue found incidentally at inguinoscrotal surgeries should be removed, since ectopic adrenal tissue can potentially cause morbidity in the future.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"Article 103145"},"PeriodicalIF":0.4,"publicationDate":"2025-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144773174","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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