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.
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页码：193 / 196
页数：4
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