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双角子宫和单角子宫合并单侧肾发育不全及孤立肾异常:3例报告

Bicornuate and unicornuate uterus associated with unilateral renal aplasia and abnormal solitary kidneys: report of 3 cases.

作者信息

Sayer T, O'Reilly P H

出版信息

J Urol. 1986 Jan;135(1):110-1. doi: 10.1016/s0022-5347(17)45534-0.

DOI:10.1016/s0022-5347(17)45534-0
PMID:3941441
Abstract

We present 3 cases of a genital abnormality associated with unilateral renal aplasia in which the single kidney was abnormal. Renal aplasia associated with unicornuate uterus or uterus didelphia is rare but it has been reported previously. However, except for vesicoureteral reflux the single kidney usually is normal. Modern methods of evaluating renal function and urodynamics will be helpful when abnormal kidneys are found and will avoid unnecessary surgery. It is mandatory to suspect abnormalities of the urinary tract when genital maldevelopment is encountered and vice versa.

摘要

我们报告了3例与单侧肾发育不全相关的生殖器异常病例,其中单肾存在异常。肾发育不全与单角子宫或双子宫相关的情况较为罕见,但此前已有报道。然而,除了膀胱输尿管反流外,单肾通常是正常的。当发现异常肾脏时,现代评估肾功能和尿动力学的方法将有所帮助,并可避免不必要的手术。当遇到生殖器发育异常时,必须怀疑泌尿系统存在异常,反之亦然。

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