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[两例先天性尿道狭窄合并膀胱输尿管反流]

[Two cases of congenital urethral stenosis complicated with vesicoureteral reflux].

作者信息

Watanabe J, Omatsu M, Kounami T, Takeuchi H, Tomoyoshi T

机构信息

Department of Urology, Uji Tokushukai Hospital.

出版信息

Hinyokika Kiyo. 1990 Sep;36(9):1081-3.

PMID:2239616
Abstract

Secondary vesicoureteral reflux (VUR) is not uncommon, but is rarely accompanied by congenital urethral stenosis in children. We report 2 cases. Case 1 was in a 3-year-old boy who had congenital anterior urethral stenosis accompanied by VUR. Urethroplasty by Johanson's operation was performed and 6 years later VUR disappeared. Case 2 was in a 7-year-old girl, who had congenital peripheral urethral stenosis accompanied by VUR. The urethra was dilated by a balloon-dilator and about 1 year later VUR disappeared.

摘要

继发性膀胱输尿管反流(VUR)并不罕见,但在儿童中很少伴有先天性尿道狭窄。我们报告2例病例。病例1为一名3岁男孩,患有先天性前尿道狭窄并伴有VUR。通过约翰森手术进行了尿道成形术,6年后VUR消失。病例2为一名7岁女孩,患有先天性周围性尿道狭窄并伴有VUR。用球囊扩张器对尿道进行了扩张,约1年后VUR消失。

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