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[先天性腹壁发育不全中的尿道。关于15例(作者译)]

[The urethra in congenital aplasia of the abdominal wall. Concerning 15 cases (author's transl)].

作者信息

Beurton D, Pascal B, Cukier J

出版信息

J Urol Nephrol (Paris). 1976 Mar;82(3):173-85.

PMID:137988
Abstract

The authors have collected in 13 years, 15 cases of congenital aplasia of the abdominal wall. All of the patients had involvement of the urinary apparatus of varying degree of severity, megalo-ureter, megabladder and dilatation of the posterior urethra being the most constant lesions. Twelve patients with renal failure, benefited from reparatory surgery of the excretory pathway. Eleven patients had complete or incomplete retention: in 5 cases there was a urethral valve. In 6 cases the megalo-urethra was apparently idiopathic. In all of these cases, endoscopic treatment was carried out, constituted either of resection of valves, or internal urethro-sphincterotomy using a cutting electrode: 9 times, the result obtained was excellent. One patient was improved; in one case the result could not be assessed. For the authors, obstructive urethral pathology is a frequently unrecognized or badly understood fact. It is accessible to endoscopic treatment, which must precede or accompany correction of the ureteral abnormalities.

摘要

作者在13年里共收集了15例先天性腹壁发育不全病例。所有患者均有不同程度的泌尿系统受累,其中巨输尿管、巨膀胱和后尿道扩张是最常见的病变。12例肾衰竭患者受益于排泄途径修复手术。11例患者存在完全或不完全尿潴留:5例存在尿道瓣膜。6例巨尿道显然为特发性。在所有这些病例中,均进行了内镜治疗,包括瓣膜切除术或使用切割电极进行内尿道括约肌切开术:9次治疗效果极佳。1例患者病情改善;1例患者的治疗结果无法评估。对作者而言,梗阻性尿道病变是一个经常未被认识或理解不足的问题。它可通过内镜治疗,且在内镜治疗应先于或伴随输尿管异常的纠正。

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