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[先天性输尿管中段狭窄:一例报告]

[Congenital mid-ureteral stricture: report of a case].

作者信息

Miyoshi Y, Inoue Y, Matsuzaki J, Fukuda M, Satomi Y

机构信息

Department of Urology, Yokosuka Kyosai Hospital.

出版信息

Hinyokika Kiyo. 1997 Sep;43(9):669-71.

PMID:9365849
Abstract

A rare case of congenital mid-ureteral stricture is reported. A 17-year-old woman was admitted with sudden onset of right flank pain. Intravenous urography demonstrated bilateral small renal calculi, left hydronephrosis and a stricture of the left ureter at the level of the pelvic brim. The diagnosis was determined as congenital mid-ureteral stricture because the ureter tapered smoothly from 25 mm to 5 mm in diameter at the stenotic site. She was successfully treated by partial ureterectomy with end-to-end anastomosis. Histopathologically, no dysplasia of muscular layer was recognized.

摘要

报告了一例罕见的先天性输尿管中段狭窄病例。一名17岁女性因突发右侧腰痛入院。静脉肾盂造影显示双侧小肾结石、左肾积水以及左侧输尿管在骨盆边缘水平处狭窄。诊断为先天性输尿管中段狭窄,因为在狭窄部位输尿管直径从25毫米平滑地逐渐变细至5毫米。她通过输尿管部分切除术加端端吻合术成功治愈。组织病理学检查未发现肌层发育异常。

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