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交叉性输尿管异位伴异位盲端输尿管。

Crossed ureteral ectopia with an ectopic blind-ending ureter.

作者信息

Chida N, Orikasa S, Konda R, Takahashi M, Ishidoya S, Ogata Y

机构信息

Department of Urology, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Urol Int. 1995;55(3):169-72. doi: 10.1159/000282779.

Abstract

A rare case of multiple urological anomalies is presented. The chief complaint of the patient, a 12-year-old girl, was urinary incontinence. Radiologic and endoscopic examinations revealed that the patient had a normal left kidney and ureter, a left ectopic blind-ending ureter that opened near the neck of the bladder, and right complete double ureters with an ectopic orifice that opened on the left of the external urethral meatus. This orifice was responsible for her urinary incontinence. Right ureteroneocystostomy was performed and the incontinence was cured. An attempt was made to explain the embryological origin of the anomalies observed in this case. We postulated that during development, on the left, there were three ureteral buds on the mesonephric duct. The first bud was at the normal position and drained the left kidney in a normal manner. The second bud was cranial from the normal position on the mesonephric duct and was associated with growth in an abnormal direction. This bud made contact with the upper portion of the right metanephric mass. The last bud grew between the two aforementioned buds. This bud was not draped by the metanephric mass and became the blind-ending ureter. On the right, one ureteral bud was located on the mesonephric duct and it made contact with a metanephric mass that became the right kidney. The upper part of the right kidney was drained by the ureter that had originally been located on the left mesonephric duct. This condition should be termed crossed ureteral ectopia rather than crossed renal ectopia, since the ureter was the structure that crossed.

摘要

本文报告一例罕见的多发性泌尿系统异常病例。患者为一名12岁女孩,主要症状为尿失禁。影像学和内镜检查显示,患者左肾和输尿管正常,左侧异位盲端输尿管开口于膀胱颈部附近,右侧为完全性双输尿管,异位开口于尿道外口左侧。该开口导致了她的尿失禁。实施了右侧输尿管膀胱吻合术,尿失禁得以治愈。本文尝试解释该病例中所观察到的异常的胚胎学起源。我们推测,在发育过程中,左侧中肾管上有三个输尿管芽。第一个芽位于正常位置,以正常方式引流左肾。第二个芽位于中肾管上正常位置的头侧,且生长方向异常。这个芽与右后肾组织的上部接触。最后一个芽在上述两个芽之间生长。这个芽未被后肾组织覆盖,形成了盲端输尿管。右侧,一个输尿管芽位于中肾管上,它与一个后肾组织接触,该后肾组织发育成右肾。右肾上部由原本位于左中肾管上的输尿管引流。这种情况应称为交叉输尿管异位,而非交叉肾异位,因为是输尿管发生了交叉。

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