Misdiagnosis of Congenital Posterior Urethroperineal Fistula and Comparison With Urethral Duplications and Rectourethral Fistula

被引：1

作者：

Cheng, Julie W. ^{[1
]}

Ahn, Jennifer J.

Cain, Mark P.

Anderson, Jamie E.

Smith, Caitlin A.

Rice-Townsend, Samuel E.

机构：

[1] Seattle Childrens Hosp, Div Urol, 4800 Sand Point Way NE M-S OA-9-220, Seattle, WA 98105 USA

来源：

UROLOGY | 2021年 / 158卷

关键词：

urethra; perineum; urinary fistula; congenital abnormalities; urinary tract;

D O I：

10.1016/j.urology.2021.09.013

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

Congenital posterior urethroperineal fistula (CUPF) is a urothelium-lined tract between the posterior urethra and perineum. This condition is rare and has been proposed to be a urethral duplication variant. A case of CUPF that was misdiagnosed and surgically treated as a rectourethral fistula is presented. The clinical presentation, diagnosis, and treatment of CUPF are discussed and compared with those of Y-type urethral duplications and H-type rectourethral fistulas. UROLOGY 158: 193-196, 2021. (c) 2021 Elsevier Inc.

引用

页码：193 / 196

页数：4

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