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[先天性尿道狭窄]

[Congenital urethral strictures].

作者信息

Katz G, Landau E H, Pode D

机构信息

Urology Dept., Hadassah-University Hospital, Jerusalem.

出版信息

Harefuah. 1994 Nov 1;127(9):298-300, 360.

PMID:7843653
Abstract

We present 12 patients with presumed congenital urethral stricture (mean age at diagnosis 20 years). They complained of various urological symptoms, including dysuria, transient urinary retention, urgency and reduced flow. The time from onset of symptoms to diagnosis averaged 18 months. The strictures were presumed congenital because no patient had a history of urethral infection or of instrumentation, and all the strictures were at the proximal bulbar urethra, as has been described for congenital, bulbar, urethral stricture. We treated 5 patients initially by internal urethrotomy, of whom 2 required transurethral dilatation at follow-up. 7 others were treated initially by transurethral dilatation, 4 of whom required more than 1 treatment. Follow-up has averaged 21 months. In 8 of 10 patients the maximal urinary flow at latest follow-up is greater than 20 ml/sec.

摘要

我们报告了12例疑似先天性尿道狭窄患者(诊断时平均年龄20岁)。他们主诉各种泌尿系统症状,包括排尿困难、短暂性尿潴留、尿急和尿流减少。从症状出现到诊断的时间平均为18个月。这些狭窄被推测为先天性,因为没有患者有尿道感染或器械操作史,并且所有狭窄均位于球部尿道近端,正如先天性球部尿道狭窄所描述的那样。我们最初对5例患者进行了尿道内切开术,其中2例在随访时需要经尿道扩张。另外7例最初接受经尿道扩张治疗,其中4例需要不止一次治疗。平均随访21个月。在10例患者中的8例中,最新随访时的最大尿流率大于20 ml/秒。

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