Congenital Anterior Urethrocutaneous Fistula: A Case Report

Changkai Deng, Qiang Peng, Xianliang Hu, Yang Lin, Fulin Li, Chao Ma, Feng Liu
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引用次数: 1

Abstract

Congenital anterior urethrocutaneous fistula (CAUF), is a uncommon anomaly characterised by fistulisation of penile urethra to skin. It’s usually seen as an isolated deformity or may accompany genitourinary or anorectal malformations. The cause is obscure, but probably reflects a focal defect in the urethral plate that prevents fusion of the urethral folds. This case reports states that CAUF is mainly located in subcoronal level and treatment of this entity is personalized according to size and locatiton of fistula. Success rates are high with the principles of hypospadias surgery
先天性前尿道瘘1例
先天性前尿道瘘(CAUF)是一种罕见的异常,其特征是阴茎尿道到皮肤的瘘管。它通常被视为孤立的畸形或可能伴随泌尿生殖系统或肛肠畸形。原因尚不清楚,但可能反映了尿道板的局灶性缺陷,阻止了尿道褶皱的融合。本病例报告指出,CAUF主要位于冠状下水平,根据瘘的大小和位置,对这种实体的治疗是个性化的。尿道下裂手术的成功率很高
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