Urethrocavernous fistula: a case report and systematic review.

Revista internacional de andrologia Pub Date : 2025-03-01 Epub Date: 2025-03-30 DOI:10.22514/j.androl.2025.012
Javier Fernández Siles, Sergio Correa Portillo, Rodrigo España Navarro
{"title":"Urethrocavernous fistula: a case report and systematic review.","authors":"Javier Fernández Siles, Sergio Correa Portillo, Rodrigo España Navarro","doi":"10.22514/j.androl.2025.012","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Urethrocavernous fistulas are rare pathological communications between the urethra and corpora cavernosa, primarily associated with trauma or iatrogenic interventions (<i>e.g.</i>, priapism shunt surgery). Their nonspecific symptomatology (urethrorrhagia, purulent discharge, or urinary retention) often delays diagnosis. The objective of this paper is to analyze the clinical and therapeutic profile of urethrocavernous fistulas through a case report and systematic literature review to establish evidence-based management insights.</p><p><strong>Case: </strong>A 22-year-old male presented with recurrent urethrorrhagia during erection and acute urinary retention secondary to clots. The initial urethroscopy and CT angiography were inconclusive. Subsequent arteriography revealed a right internal pudendal artery-cavernosal fistula. After two non-permanent embolizations failed, definitive occlusion was achieved via non-absorbable coils, resolving symptoms without recurrence or other complications at 23 months.</p><p><strong>Conclusions: </strong>Urethrocavernous fistulas are rare with limited literature descriptions. Systematic review of 17 cases reveals marked heterogeneity in the clinical presentations and the therapeutic outcomes, emphasizing the imperative for standardized diagnostic and therapeutic protocols. They are predominantly diagnosed incidentally through retrograde urethrography and urethroscopy. Conservative management with urinary diversion may be considered as the initial approach, while surgery is reserved for refractory cases or those with associated injuries. Embolization is a poorly studied treatment option.</p>","PeriodicalId":519907,"journal":{"name":"Revista internacional de andrologia","volume":"23 1","pages":"102-107"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista internacional de andrologia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22514/j.androl.2025.012","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/30 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Urethrocavernous fistulas are rare pathological communications between the urethra and corpora cavernosa, primarily associated with trauma or iatrogenic interventions (e.g., priapism shunt surgery). Their nonspecific symptomatology (urethrorrhagia, purulent discharge, or urinary retention) often delays diagnosis. The objective of this paper is to analyze the clinical and therapeutic profile of urethrocavernous fistulas through a case report and systematic literature review to establish evidence-based management insights.

Case: A 22-year-old male presented with recurrent urethrorrhagia during erection and acute urinary retention secondary to clots. The initial urethroscopy and CT angiography were inconclusive. Subsequent arteriography revealed a right internal pudendal artery-cavernosal fistula. After two non-permanent embolizations failed, definitive occlusion was achieved via non-absorbable coils, resolving symptoms without recurrence or other complications at 23 months.

Conclusions: Urethrocavernous fistulas are rare with limited literature descriptions. Systematic review of 17 cases reveals marked heterogeneity in the clinical presentations and the therapeutic outcomes, emphasizing the imperative for standardized diagnostic and therapeutic protocols. They are predominantly diagnosed incidentally through retrograde urethrography and urethroscopy. Conservative management with urinary diversion may be considered as the initial approach, while surgery is reserved for refractory cases or those with associated injuries. Embolization is a poorly studied treatment option.

尿道海绵瘘1例报告及系统回顾。
背景:尿道海绵体瘘是尿道和海绵体之间罕见的病理性交通,主要与创伤或医源性干预(如阴茎分流手术)有关。其非特异性症状(尿道出血、脓性排出物或尿潴留)常延误诊断。本文的目的是通过一个病例报告和系统的文献综述来分析尿道海绵窦瘘的临床和治疗概况,以建立基于证据的管理见解。病例:一名22岁男性,在勃起期间出现复发性尿道出血和继发于血栓的急性尿潴留。最初的尿道镜检查和CT血管造影结果不确定。随后的动脉造影显示右侧阴部动脉-海绵体内瘘。在两次非永久性栓塞失败后,通过不可吸收线圈实现最终闭塞,在23个月时消除症状,无复发或其他并发症。结论:尿道海绵窦瘘是罕见的,文献描述有限。对17例病例的系统回顾揭示了临床表现和治疗结果的显著异质性,强调了标准化诊断和治疗方案的必要性。它们主要通过逆行尿道造影和尿道镜检查偶然诊断。保守治疗泌尿分流可被视为初始方法,而手术则保留给顽固性病例或伴有损伤的患者。栓塞是一种研究较少的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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