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婴儿型 Müller 管缺陷伴孤立肾及单侧异位输尿管开口于前庭 1 例：膀胱缺如吗？

A Case of Solitary Kidney and Single-system Ectopic Ureter Draining Into the Vestibule in an Infant With Müllerian Duct Defect: Was the Bladder Missing?

机构信息

Department of Urology, Osaka Woman's and Children's Hospital, Izumi, Osaka, Japan.

Department of Urology, Osaka Woman's and Children's Hospital, Izumi, Osaka, Japan.

出版信息

Urology. 2023 Nov;181:144-146. doi: 10.1016/j.urology.2023.08.002. Epub 2023 Aug 12.

DOI:10.1016/j.urology.2023.08.002
PMID:37579854
Abstract

We report a case of a solitary kidney and a single-system ectopic ureter draining into the vestibule in an infant with a Müllerian duct defect. Due to the absence of the upper vagina and uterus, an extremely underdeveloped bladder masqueraded as the vagina, and bladder agenesis was suspected preoperatively. Urinary continence was achieved using staged bladder surgery without augmentation or urinary diversion.

摘要

我们报告了一例患有 Müllerian 管缺陷的婴儿，其为孤立肾和单系统异位输尿管，开口于前庭。由于上阴道和子宫缺失，一个发育极差的膀胱被误认为是阴道，术前怀疑膀胱发育不全。通过分期膀胱手术实现了尿控，无需扩张或尿流改道。

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