发布求助
文献互助 智能选刊 最新文献

Urology Case Reports最新文献

筛选
英文 中文
Utility of blue-light cystoscopy and tumor-informed ctDNA for management of recurrent high-risk NMIBC with prostatic urethral involvement: A case report 蓝光膀胱镜检查和肿瘤知情ctDNA治疗复发性高风险NMIBC伴前列腺尿道累及1例报告
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-01-27 DOI: 10.1016/j.eucr.2026.103362
Mahdi Hemmati Ghavshough, Melinda Z. Fu, Jennifer Sykes, Disha Patel, Saum Ghodoussipour, Vignesh T. Packiam
{"title":"Utility of blue-light cystoscopy and tumor-informed ctDNA for management of recurrent high-risk NMIBC with prostatic urethral involvement: A case report","authors":"Mahdi Hemmati Ghavshough,&nbsp;Melinda Z. Fu,&nbsp;Jennifer Sykes,&nbsp;Disha Patel,&nbsp;Saum Ghodoussipour,&nbsp;Vignesh T. Packiam","doi":"10.1016/j.eucr.2026.103362","DOIUrl":"10.1016/j.eucr.2026.103362","url":null,"abstract":"<div><div>Non–muscle-invasive bladder cancer (NMIBC) with prostatic urethral involvement (PUI) is rare and difficult to manage, especially after intravesical therapy or pelvic radiation. We report a 78-year-old man with recurrent high-risk NMIBC and PUI after bacillus Calmette–Guérin and mitomycin C. Blue-light cystoscopy (BLC) during restaging identified additional carcinoma in situ and high-grade T1 disease not seen with white light. Histopathology showed no stromal invasion, and tumor-informed circulating tumor DNA (ctDNA) testing was negative, indicating no molecular residual disease. Despite favorable findings, the patient elected radical cystectomy, which revealed no residual tumor. This case highlights the complementary roles of BLC and ctDNA.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103362"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146078538","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
Congenital hypospadias complicated with pelvic cystic lesions and accessory urethra:A case report 先天性尿道下裂合并盆腔囊性病变及副尿道1例
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-01-28 DOI: 10.1016/j.eucr.2026.103357
Aersi Madanyeti , Zhangjie Zheng , Feng Tang , Jianping Peng
{"title":"Congenital hypospadias complicated with pelvic cystic lesions and accessory urethra:A case report","authors":"Aersi Madanyeti ,&nbsp;Zhangjie Zheng ,&nbsp;Feng Tang ,&nbsp;Jianping Peng","doi":"10.1016/j.eucr.2026.103357","DOIUrl":"10.1016/j.eucr.2026.103357","url":null,"abstract":"<div><div>This study reports a sporadic case of a 44-year-old male with congenital hypospadias complicated by a seminal vesicle cyst and accessory urethra. The patient presented with recurrent dysuria, and after undergoing laparoscopic seminal vesiculectomy combined with targeted anti-infective therapy, his symptoms were significantly relieved with favorable recovery. This case suggests that comprehensive imaging evaluation, individualized surgical planning, and long-term standardized follow-up are of great value in the diagnosis and treatment of such complex urinary system malformations.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103357"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146078543","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
Idiopathic neonatal priapism in a 5-day-Old Somali neonate from a low-resource setting: A case report 来自低资源环境的5天大的索马里新生儿特发性新生儿阴茎异常勃起：1例报告
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-01-21 DOI: 10.1016/j.eucr.2026.103355
Abdihamid Hassan Hilowle , Abdisalam Ismail Hassan , Nuradin Mohamed Nur , Abdikarin Ahmed Mohamed , Abdikarim Hussein Mohamed
{"title":"Idiopathic neonatal priapism in a 5-day-Old Somali neonate from a low-resource setting: A case report","authors":"Abdihamid Hassan Hilowle ,&nbsp;Abdisalam Ismail Hassan ,&nbsp;Nuradin Mohamed Nur ,&nbsp;Abdikarin Ahmed Mohamed ,&nbsp;Abdikarim Hussein Mohamed","doi":"10.1016/j.eucr.2026.103355","DOIUrl":"10.1016/j.eucr.2026.103355","url":null,"abstract":"<div><div>Neonatal priapism is an exceptionally rare and usually benign condition, most commonly representing a non-ischemic (high-flow) state that resolves spontaneously. We report a 5-day-old Somali neonate who presented with a painless penile erection persisting for more than 48 hours. Physical examination revealed no penile discoloration, rigidity, or tenderness, and <u>laboratory evaluation</u> showed no hematological abnormalities. Doppler ultrasonography was unavailable; however, clinical findings were consistent with non-ischemic priapism. The infant was managed conservatively with close observation, resulting in complete spontaneous resolution without complications. This case highlights that careful clinical assessment and conservative management are sufficient, even in resource-limited settings.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103355"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146038746","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 pheochromocytomas with locally advanced right adrenal tumor extending into the inferior vena cava in a suspected Von Hippel–Lindau syndrome: A case report 怀疑Von Hippel-Lindau综合征的双侧嗜铬细胞瘤伴局部进展的右肾上腺肿瘤延伸至下腔静脉1例
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-01-10 DOI: 10.1016/j.eucr.2026.103343
Sami Chebbi , Houssem Bel Hadj Alouane , Mohamed Amine Oueslati , Nidham Eddine Kchir , Sami Ben Rhouma
{"title":"Bilateral pheochromocytomas with locally advanced right adrenal tumor extending into the inferior vena cava in a suspected Von Hippel–Lindau syndrome: A case report","authors":"Sami Chebbi ,&nbsp;Houssem Bel Hadj Alouane ,&nbsp;Mohamed Amine Oueslati ,&nbsp;Nidham Eddine Kchir ,&nbsp;Sami Ben Rhouma","doi":"10.1016/j.eucr.2026.103343","DOIUrl":"10.1016/j.eucr.2026.103343","url":null,"abstract":"<div><div>We report a case of bilateral pheochromocytomas in a 45-year-old man with cutaneous findings suggestive of a hereditary disease. Imaging revealed a large right adrenal tumor extending into the inferior vena cava (IVC) and a smaller contralateral lesion. The patient underwent right adrenalectomy with IVC thrombectomy, while the left lesion was managed conservatively. Histopathology confirmed pheochromocytoma with extensive IVC tumor thrombus and no distant metastases. A residual IVC thrombus was treated with anticoagulation and remained stable on follow-up imaging. This case highlights the complexity of managing hereditary pheochromocytomas with vascular invasion.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103343"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145980325","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
Metastatic castrate-resistant prostate cancer to the penis resulting in malignant priapism and urethral obstruction 阴茎转移性去势抵抗性前列腺癌，导致恶性阴茎勃起和尿道阻塞。
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-02-16 DOI: 10.1016/j.eucr.2026.103380
Courtney Stewart , Joon Yau Leong , W. Kevin Kelly , Mihir S. Shah
{"title":"Metastatic castrate-resistant prostate cancer to the penis resulting in malignant priapism and urethral obstruction","authors":"Courtney Stewart ,&nbsp;Joon Yau Leong ,&nbsp;W. Kevin Kelly ,&nbsp;Mihir S. Shah","doi":"10.1016/j.eucr.2026.103380","DOIUrl":"10.1016/j.eucr.2026.103380","url":null,"abstract":"<div><div>A 76-year-old male with metastatic castrate-resistant prostate cancer was found to have metastatic disease to the urethra and penis on PSMA PET scan. This resulted in constant pain due to obstruction of blood flow through the corpora cavernosum resulting in priapism and urethral obstruction. The patient underwent a radical penectomy, partial urethrectomy and perineal urethrostomy creation. Final pathology confirmed metastatic prostatic adenocarcinoma. Although rare, prostate cancer can metastasize to the corpora spongiosum or cavernosa. Treatment options are limited, and surgical excision with urinary diversion is likely to provide the most durable outcomes for one's quality of life.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103380"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147285357","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
Corrigendum to: Phentolamine rescue for glanular ischemia in the setting of inadvertent administration of high-dose 1:1,000 epinephrine to glans in distal hypospadias surgery [Urol Case Rep, (59), March 2025, 102941. PMID: 39925745] 对远端尿道下裂手术中不小心给药高剂量1:10 00肾上腺素的情况下，酚度拉明对glu缺血的抢救[ul Case Rep， （59）， March 2025, 102941]的更正。PMID: 39925745)
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-01-07 DOI: 10.1016/j.eucr.2026.103338
Victoria Schulte , Alexandra Carolan , Irina Stanasel , Bruce Schlomer
{"title":"Corrigendum to: Phentolamine rescue for glanular ischemia in the setting of inadvertent administration of high-dose 1:1,000 epinephrine to glans in distal hypospadias surgery [Urol Case Rep, (59), March 2025, 102941. PMID: 39925745]","authors":"Victoria Schulte ,&nbsp;Alexandra Carolan ,&nbsp;Irina Stanasel ,&nbsp;Bruce Schlomer","doi":"10.1016/j.eucr.2026.103338","DOIUrl":"10.1016/j.eucr.2026.103338","url":null,"abstract":"","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103338"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145929221","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
A case of isolated testicular Tuberculosis: Approach and management 孤立性睾丸结核1例：方法与处理
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2025-12-23 DOI: 10.1016/j.eucr.2025.103328
Ismail Mahad Abdullahi, Ismail Ahmed Ali, Abdirahin Mohamed Abdulkadir, Rahma Abdukadir Ahmed, Abdullahi Hassan Elmi
{"title":"A case of isolated testicular Tuberculosis: Approach and management","authors":"Ismail Mahad Abdullahi,&nbsp;Ismail Ahmed Ali,&nbsp;Abdirahin Mohamed Abdulkadir,&nbsp;Rahma Abdukadir Ahmed,&nbsp;Abdullahi Hassan Elmi","doi":"10.1016/j.eucr.2025.103328","DOIUrl":"10.1016/j.eucr.2025.103328","url":null,"abstract":"<div><div>Testicular tuberculosis is a rare form of genitourinary TB that often mimics conditions such as neoplasms or chronic epididymo-orchitis, making diagnosis challenging. We report a 60-year-old man with longstanding right testicular pain and swelling, no systemic symptoms, and a history of household TB exposure. Imaging showed a large hydrocele with suspected underlying pathology. Intraoperative findings revealed necrotic testicular tissue, prompting orchiectomy. Histopathology confirmed granulomatous inflammation with caseous necrosis consistent with TB. The patient began standard anti-tubercular therapy. This case highlights the need to consider testicular TB in chronic scrotal swelling, particularly in TB-endemic settings.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103328"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145929223","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
Primary renal sclerosing epithelioid fibrosarcoma: A case report 原发性肾硬化上皮样纤维肉瘤1例
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2025-12-31 DOI: 10.1016/j.eucr.2025.103324
Faisl Alslimah , Maher Moazin , Abdulrahman Alshehri , Yasser Alharbi , Ali Howaidi , Saif Alqahtani , Salman Almalki
{"title":"Primary renal sclerosing epithelioid fibrosarcoma: A case report","authors":"Faisl Alslimah ,&nbsp;Maher Moazin ,&nbsp;Abdulrahman Alshehri ,&nbsp;Yasser Alharbi ,&nbsp;Ali Howaidi ,&nbsp;Saif Alqahtani ,&nbsp;Salman Almalki","doi":"10.1016/j.eucr.2025.103324","DOIUrl":"10.1016/j.eucr.2025.103324","url":null,"abstract":"<div><div>Sclerosing epithelioid fibrosarcoma (SEF) is a rare variant of fibrosarcoma that primarily arises in the deep soft tissue of the extremities and trunk. Primary SEF in the visceral organs is rare, and only a few cases have been reported. A 20-year-old man was diagnosed with primary renal SEF metastatic to the lymph nodes and bone, which was managed with open right radical nephrectomy and ongoing chemotherapy. Immunohistochemical staining for MUC-4, vimentin, BCL-2, and EMA was positive in tumor cells. Next-generation sequencing revealed the presence of EWSR–CREB3L1 gene fusions and SMARCB1 rearrangement in exon 6.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103324"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145898021","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
Intrascrotal extratesticular schwannoma in a 10-year-old boy: A case report of an extremely rare benign tumor 10岁男童腹囊内睾丸外神经鞘瘤：一罕见良性肿瘤
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-01-23 DOI: 10.1016/j.eucr.2026.103352
Alhareth Baarimah , Nahid Osman , Ziyad Althobaiti , Mohammed Althobaiti , Bader Alzahrani , Ashraf Soliman
{"title":"Intrascrotal extratesticular schwannoma in a 10-year-old boy: A case report of an extremely rare benign tumor","authors":"Alhareth Baarimah ,&nbsp;Nahid Osman ,&nbsp;Ziyad Althobaiti ,&nbsp;Mohammed Althobaiti ,&nbsp;Bader Alzahrani ,&nbsp;Ashraf Soliman","doi":"10.1016/j.eucr.2026.103352","DOIUrl":"10.1016/j.eucr.2026.103352","url":null,"abstract":"<div><div>Extratesticular schwannoma (neurilemmoma) is an exceedingly rare benign paratesticular tumor, the diagnosis of which is usually challenging. We present the case of a 10-year-old boy presenting with a painless scrotal mass. Scrotal ultrasonography confirmed the extratesticular location but offered nonspecific findings. A definitive diagnosis was established via histopathology after complete surgical excision. This case highlights the need to include schwannoma in the differential diagnosis of pediatric paratesticular masses. To our knowledge, this is the third documented pediatric intrascrotal extratesticular schwannoma and involved the youngest patient reported in the literature.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103352"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146078542","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
A case report of testicular plasmacytoma misdiagnosed as lymphoma by ultrasound 睾丸浆细胞瘤超声误诊为淋巴瘤1例
IF 0.4
Urology Case Reports Pub Date : 2026-03-01 Epub Date: 2026-01-10 DOI: 10.1016/j.eucr.2026.103345
Danhong Yu , Nianyu Xue
{"title":"A case report of testicular plasmacytoma misdiagnosed as lymphoma by ultrasound","authors":"Danhong Yu ,&nbsp;Nianyu Xue","doi":"10.1016/j.eucr.2026.103345","DOIUrl":"10.1016/j.eucr.2026.103345","url":null,"abstract":"<div><div>Testicular plasmacytoma is an extremely rare malignant tumour whose clinical manifestations resemble those of common testicular tumours, making preoperative diagnosis challenging. This paper reports a case of a 63-year-old male patient who presented for consultation due to'unintentionally discovering enlargement of the right scrotum for four days’. The ultrasound findings bear a striking resemblance to lymphoma, leading to misdiagnosis as lymphoma on ultrasound. Following radical orchiectomy, pathological and immunohistochemical examination confirmed the diagnosis of plasmacytoma. Although rare, testicular plasmacytoma should be considered as part of the differential diagnosis for testicular masses.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"65 ","pages":"Article 103345"},"PeriodicalIF":0.4,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145980326","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
首页 上一页 下一页 尾页
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整，为了账户安全，请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们：info@booksci.cn Book学术提供免费学术资源搜索服务，方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号：604180095
Book学术官方微信
小红书