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
Staged repair of Effmann type IIA2Y urethral duplication using composite tissue tubularization: A case report 复合组织管化分阶段修复Effmann IIA2Y型尿道重复1例
IF 0.5
Urology Case Reports Pub Date : 2025-07-21 DOI: 10.1016/j.eucr.2025.103137
P.R. Saju, H. Balabhaskar, Sunil Ashok, S.J. Aquil Faris, Maradana Prudhvi Vasanth, Sharoo Shaneej, Jinesh Jayadevan
{"title":"Staged repair of Effmann type IIA2Y urethral duplication using composite tissue tubularization: A case report","authors":"P.R. Saju,&nbsp;H. Balabhaskar,&nbsp;Sunil Ashok,&nbsp;S.J. Aquil Faris,&nbsp;Maradana Prudhvi Vasanth,&nbsp;Sharoo Shaneej,&nbsp;Jinesh Jayadevan","doi":"10.1016/j.eucr.2025.103137","DOIUrl":"10.1016/j.eucr.2025.103137","url":null,"abstract":"<div><div>Effmann type IIA2Y urethral duplication is a rare congenital anomaly requiring individualized surgical management. We report a pediatric case managed with initial buccal mucosa grafting and perineal urethrostomy, followed by a 9-year loss to follow-up. On return, the graft remained viable, and definitive repair was performed using composite tissue tubularization with buccal mucosa, perineal, and scrotal skin. The patient achieved continent, complication-free voiding. This case highlights the durability of multi-tissue grafts and demonstrates the feasibility of delayed reconstruction in complex urethral anomalies.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"Article 103137"},"PeriodicalIF":0.5,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144686962","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
Spontaneous rupture of the upper urinary tract (fornix) secondary to ureteropelvic junction obstruction: A case report of a rare condition 肾盂输尿管连接处梗阻致上尿路（穹窿）自发性破裂1例
IF 0.4
Urology Case Reports Pub Date : 2025-07-21 DOI: 10.1016/j.eucr.2025.103134
Idriss Ziani , Salim Ouskri , Imad Boualaoui , Ahmed Ibrahimi , Hachem EL-Sayegh , Yassine Nouini
{"title":"Spontaneous rupture of the upper urinary tract (fornix) secondary to ureteropelvic junction obstruction: A case report of a rare condition","authors":"Idriss Ziani ,&nbsp;Salim Ouskri ,&nbsp;Imad Boualaoui ,&nbsp;Ahmed Ibrahimi ,&nbsp;Hachem EL-Sayegh ,&nbsp;Yassine Nouini","doi":"10.1016/j.eucr.2025.103134","DOIUrl":"10.1016/j.eucr.2025.103134","url":null,"abstract":"<div><div><u>Spontaneous rupture of the renal fornix (SRF) is a rare condition, usually caused by acute upper urinary tract obstruction, most commonly from kidney stones</u>. Its association with ureteropelvic junction obstruction (UPJO), whether congenital or acquired, is very uncommon. We report a case of a 29-year-old man with fever and right lumbar pain. Imaging showed a fornix rupture without stones, indicating possible UPJO. Emergency drainage with a double-J stent quickly improved his condition, followed by laparoscopic pyeloplasty, leading to full recovery. <u>This case highlights the importance of timely management of UPJO to prevent serious complications like fornix rupture.</u></div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"Article 103134"},"PeriodicalIF":0.4,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144763828","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
Massive congenital bladder diverticulum in a teenager: Navigating an uncommon clinical entity through an exceptional therapeutic challenge – A case report 一个青少年的巨大先天性膀胱憩室：通过一个特殊的治疗挑战来导航一个不寻常的临床实体-一个病例报告
IF 0.5
Urology Case Reports Pub Date : 2025-07-21 DOI: 10.1016/j.eucr.2025.103139
W. Salama , M. Tetou , M. Mrabti , M.A. Sobhi , A. Elbahri , M. Alami , A. Ameur
{"title":"Massive congenital bladder diverticulum in a teenager: Navigating an uncommon clinical entity through an exceptional therapeutic challenge – A case report","authors":"W. Salama ,&nbsp;M. Tetou ,&nbsp;M. Mrabti ,&nbsp;M.A. Sobhi ,&nbsp;A. Elbahri ,&nbsp;M. Alami ,&nbsp;A. Ameur","doi":"10.1016/j.eucr.2025.103139","DOIUrl":"10.1016/j.eucr.2025.103139","url":null,"abstract":"<div><div>Primary congenital bladder diverticula, rare in pediatric populations and particularly in females, often justify surgery for symptomatic cases. We report a 15-year-old girl with a giant bladder diverticulum, significant post-void residual urine, and preserved renal function without vesicoureteral reflux. Conservative care included antibiotic prophylaxis, surveillance imaging, and lifestyle modifications was adopted due to family refusal of surgery. Clinical stability (reduced infections, no complications) and anatomical stability were observed, supporting the hypothesis of residual muscular fibers as a stabilizing factor, suggesting potential nosological reclassification. This case underscores individualized therapeutic decisions integrating family preferences and rigorous monitoring.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"Article 103139"},"PeriodicalIF":0.5,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144694833","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
When scoliosis surgery in a child unexpectedly resolves hydronephrosis: A case report and review of the literature 当儿童脊柱侧凸手术意外地解决肾积水：一个病例报告和文献回顾
IF 0.4
Urology Case Reports Pub Date : 2025-07-21 DOI: 10.1016/j.eucr.2025.103138
Peranzoni Francesca, Zambelli Pierre-Yves, Broennimann Enrico
{"title":"When scoliosis surgery in a child unexpectedly resolves hydronephrosis: A case report and review of the literature","authors":"Peranzoni Francesca,&nbsp;Zambelli Pierre-Yves,&nbsp;Broennimann Enrico","doi":"10.1016/j.eucr.2025.103138","DOIUrl":"10.1016/j.eucr.2025.103138","url":null,"abstract":"<div><div>Hydronephrosis, defined as dilation of the renal pelvis and calyces, may occur with scoliosis or after corrective surgery. However, spontaneous resolution of pre-existing hydronephrosis following scoliosis correction has not been previously reported. We present a 12-year-old girl with a <em>ZMYM2</em> mutation, severe thoracolumbar scoliosis (Cobb 103°), and bilateral hydronephrosis. After posterior spinal fusion (T4–L3), hydronephrosis resolved completely. Just as the spinal angle, likely the angle between the renal pelvis and ureter was similarly adjusted, facilitating improved urinary drainage. This rare case highlights a possible dual therapeutic effect of scoliosis correction on spinal alignment and urinary drainage in selected cases.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"Article 103138"},"PeriodicalIF":0.4,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144779989","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 rare case of inflammatory myofibroblastic tumour mimicking retained prostatic tissue following HoLEP 一例罕见的炎性肌纤维母细胞肿瘤，类似于HoLEP后保留的前列腺组织
IF 0.4
Urology Case Reports Pub Date : 2025-07-21 DOI: 10.1016/j.eucr.2025.103135
Jae Won Yun , Muhammad-Kabir Ali , Christopher Anderson , Tevita Aho , Tamer El-Husseiny
{"title":"A rare case of inflammatory myofibroblastic tumour mimicking retained prostatic tissue following HoLEP","authors":"Jae Won Yun ,&nbsp;Muhammad-Kabir Ali ,&nbsp;Christopher Anderson ,&nbsp;Tevita Aho ,&nbsp;Tamer El-Husseiny","doi":"10.1016/j.eucr.2025.103135","DOIUrl":"10.1016/j.eucr.2025.103135","url":null,"abstract":"<div><div>Retained prostatic tissue following HoLEP is rare but requires prompt surgical intervention. We present the case of rapidly growing inflammatory myofibroblastic tumour of the bladder presenting shortly after HoLEP, successfully resected in an en-bloc fashion with Holmium-YAG laser. Further prospective data is required for genitourinary inflammatory myofibroblastic tumours to standardise oncological management.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"Article 103135"},"PeriodicalIF":0.4,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144739329","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
Giant adrenal calcification: rare case report and literature review 巨大肾上腺钙化：罕见病例报告及文献复习
IF 0.5
Urology Case Reports Pub Date : 2025-07-19 DOI: 10.1016/j.eucr.2025.103131
Zaiqing Jiang , Yunfeng Li , Kai Zhao , Xinbao Yin , Ke Wang , Zongliang Zhang
{"title":"Giant adrenal calcification: rare case report and literature review","authors":"Zaiqing Jiang ,&nbsp;Yunfeng Li ,&nbsp;Kai Zhao ,&nbsp;Xinbao Yin ,&nbsp;Ke Wang ,&nbsp;Zongliang Zhang","doi":"10.1016/j.eucr.2025.103131","DOIUrl":"10.1016/j.eucr.2025.103131","url":null,"abstract":"<div><div>We report the largest documented case of idiopathic giant adrenal calcification in a middle-aged woman, incidentally detected during imaging. Preoperative CT revealed an 8.5 × 7.0 × 5.0 cm left adrenal mass. Retroperitoneal laparoscopic adrenalectomy was successfully performed, with no recurrence at 18-month follow-up. This rare condition lacks evidence-based guidelines, necessitating multicenter studies to refine diagnosis and management.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"Article 103131"},"PeriodicalIF":0.5,"publicationDate":"2025-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144694288","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
Immunotherapy-related cystitis induced by nivolumab: A case report and review of the literature 纳武单抗诱导的免疫治疗相关性膀胱炎：1例报告和文献回顾
IF 0.5
Urology Case Reports Pub Date : 2025-07-19 DOI: 10.1016/j.eucr.2025.103132
Yingying Yuan , Lianqing Lou , Siheng Zhu , Dong Yan
{"title":"Immunotherapy-related cystitis induced by nivolumab: A case report and review of the literature","authors":"Yingying Yuan ,&nbsp;Lianqing Lou ,&nbsp;Siheng Zhu ,&nbsp;Dong Yan","doi":"10.1016/j.eucr.2025.103132","DOIUrl":"10.1016/j.eucr.2025.103132","url":null,"abstract":"<div><div>Immune checkpoint inhibitors (ICIs) like nivolumab have revolutionized cancer treatment but can cause immune-related adverse events (irAEs), including rare cystitis. This case report describes a gastric cancer patient who developed urinary symptoms, such as hematuria and frequent urination, after nivolumab treatment. Despite initial antibiotics, symptoms worsened, leading to a diagnosis of immune-related cystitis. Intravenous methylprednisolone provided rapid relief and restored renal function. Early recognition and corticosteroid treatment are crucial for managing ICI-induced cystitis and preventing unnecessary antibiotics.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"Article 103132"},"PeriodicalIF":0.5,"publicationDate":"2025-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144694289","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
Cough-associated detrusor overactivity resolved after intravesical onabotulinumtoxin A injection: A case report 膀胱内注射肉毒杆菌毒素A后，咳嗽相关逼尿肌过度活动得以缓解：1例报告
IF 0.5
Urology Case Reports Pub Date : 2025-07-18 DOI: 10.1016/j.eucr.2025.103129
Rie Yoshimura , Nobutaka Shimizu , Mio Togo , Shinkuro Yamamoto , Tomoya Nao , Tsutomu Shimamoto , Hideo Fukuhara , Satoshi Fukata , Shingo Ashida , Takashi Karashima , Motoaki Saito , Keiji Inoue
{"title":"Cough-associated detrusor overactivity resolved after intravesical onabotulinumtoxin A injection: A case report","authors":"Rie Yoshimura ,&nbsp;Nobutaka Shimizu ,&nbsp;Mio Togo ,&nbsp;Shinkuro Yamamoto ,&nbsp;Tomoya Nao ,&nbsp;Tsutomu Shimamoto ,&nbsp;Hideo Fukuhara ,&nbsp;Satoshi Fukata ,&nbsp;Shingo Ashida ,&nbsp;Takashi Karashima ,&nbsp;Motoaki Saito ,&nbsp;Keiji Inoue","doi":"10.1016/j.eucr.2025.103129","DOIUrl":"10.1016/j.eucr.2025.103129","url":null,"abstract":"<div><div>A 68-year-old woman developed urgency urinary incontinence (UUI) one month after tension-free vaginal tape (TVT) surgery for stress urinary incontinence. Pharmacological treatment was ineffective. Pressure-flow study revealed cough-associated detrusor overactivity (CADO). An intravesical injection of 100 U botulinum toxin resolved symptoms and normalized bladder sensation. Six months later, CADO recurred and was successfully treated with a second injection. No adverse events occurred. CADO is often misdiagnosed as stress incontinence, and accurate diagnosis requires urodynamic evaluation. This case highlights the potential of intravesical botulinum toxin for managing CADO, including recurrence. Further studies should establish optimal diagnostic strategies and long-term efficacy.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"Article 103129"},"PeriodicalIF":0.5,"publicationDate":"2025-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144665665","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
Late-presenting congenital anterior urethral diverticulum causing renal impairment in a male child 迟发性先天性前尿道憩室导致男童肾功能损害
IF 0.5
Urology Case Reports Pub Date : 2025-07-17 DOI: 10.1016/j.eucr.2025.103127
Yasmine Houas , Arije Zouaoui , Riadh Jouini
{"title":"Late-presenting congenital anterior urethral diverticulum causing renal impairment in a male child","authors":"Yasmine Houas ,&nbsp;Arije Zouaoui ,&nbsp;Riadh Jouini","doi":"10.1016/j.eucr.2025.103127","DOIUrl":"10.1016/j.eucr.2025.103127","url":null,"abstract":"<div><div>We report the case of a 6-year-old boy who presented with lower urinary tract obstruction and chronic renal impairment due to a delayed diagnosis of isolated CAUD. The diagnosis was eventually made by voiding cystourethrography, which revealed a large anterior diverticulum. This case illustrates a rare late presentation of CAUD with significant renal dysfunction, highlighting a crucial diagnostic pitfall. Clinicians should actively consider and investigate for anterior urethral diverticulum in any male child presenting with unexplained renal insufficiency or voiding symptoms, as early detection is essential to prevent irreversible upper urinary tract damage.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"Article 103127"},"PeriodicalIF":0.5,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144694832","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 mid-segment ureteral duplication: Uncovering a rare developmental anomaly 输尿管中段重复1例：揭示罕见的发育异常
IF 0.5
Urology Case Reports Pub Date : 2025-07-17 DOI: 10.1016/j.eucr.2025.103128
Yazan Dibas , Jana Dibas , Motaz Daraghma , Zaid Sawaftah
{"title":"A case of mid-segment ureteral duplication: Uncovering a rare developmental anomaly","authors":"Yazan Dibas ,&nbsp;Jana Dibas ,&nbsp;Motaz Daraghma ,&nbsp;Zaid Sawaftah","doi":"10.1016/j.eucr.2025.103128","DOIUrl":"10.1016/j.eucr.2025.103128","url":null,"abstract":"<div><div>Ureteral duplication is a congenital anomaly often associated with urinary complications. We report a case of a 54-year-old female presenting with recurrent urinary tract infections and right flank pain. Imaging revealed a rare mid-segment ureteral duplication, where the ureter bifurcates and rejoins before entering the bladder. The anomaly was complicated by ESBL-producing <em>Escherichia coli</em> infection. Conservative management with antibiotics was chosen after the patient declined surgery. This case underscores the diagnostic challenges of mid-segment duplications and highlights the importance of advanced imaging in adults with unexplained recurrent urinary tract infections.</div></div>","PeriodicalId":38188,"journal":{"name":"Urology Case Reports","volume":"62 ","pages":"Article 103128"},"PeriodicalIF":0.5,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144679671","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
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