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双子宫伴单侧阴道积血、同侧肾缺如及月经。病例报告及文献复习。

Uterus didelphys with unilateral hematocolpos, ipsilateral renal agenesis and menses. A case report and literature review.

作者信息

Morgan M A, Thurnau G R, Smith M L

出版信息

J Reprod Med. 1987 Jan;32(1):47-58.

PMID:3560063
Abstract

A 13-year-old girl with signs and symptoms of an acute abdomen was found to have uterus didelphys, unilateral hematocolpos, ipsilateral renal agenesis and menses. A review of the literature in English revealed 115 reported cases. This complex congenital anomaly is seen most commonly in adolescents with dysmenorrhea of progressive severity, abdominal pain and a pelvic mass.

摘要

一名13岁有急腹症体征和症状的女孩被发现患有双子宫、单侧阴道积血、同侧肾缺如并伴有月经。对英文文献的回顾显示有115例报告病例。这种复杂的先天性异常最常见于患有进行性加重痛经、腹痛和盆腔肿块的青少年。

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