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梅耶-罗基坦斯基综合征。5例报告。

The Mayer-Rokitansky syndrome. Report of 5 cases.

作者信息

Guys J M, Borella F, Panuel M, Coquet M, Monfort G

机构信息

Department of Pediatric Surgery, CHU Timone, Marseille, France.

出版信息

Eur Urol. 1988;14(4):301-4. doi: 10.1159/000472965.

Abstract

Five cases of uterus didelphys, unilateral imperforate vagina and ipsilateral renal agenesis are reported with a follow-up from 1 to 5 years. Diagnosis included typical revelation at puberty (2 cases) but also in the first months of life (2 cases). One case was only diagnosed at the age of 6 years, and the presence of an ectopic ureter was noted in the imperforate vagina. The authors point out the necessity of precise evaluation and careful management in order to maintain an intact reproductory tract. Simple excision of the septum is recommended which can most of the time be done by the vaginal approach.

摘要

报告了5例双子宫、单侧阴道闭锁并同侧肾缺如的病例,随访时间为1至5年。诊断包括青春期典型表现(2例),但也有出生后最初几个月出现症状的情况(2例)。1例直到6岁才被诊断出来,在闭锁的阴道中发现了异位输尿管。作者指出,为了维持完整的生殖道,进行精确评估和仔细管理很有必要。建议进行隔膜简单切除术,大多数情况下可通过阴道途径完成。

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