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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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Uterus didelphys with unilateral hematocolpos, ipsilateral renal agenesis and menses. A case report and literature review.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。
J Reprod Med. 1987 Jan;32(1):47-58.
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Successful pregnancy following surgery in the obstructed uterus in a uterus didelphys with unilateral distal vaginal agenesis and ipsilateral renal agenesis: case report and literature review.双子宫合并单侧远端阴道闭锁及同侧肾缺如患者梗阻性子宫手术后成功妊娠:病例报告及文献综述
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[Uterus duplex with hematometrocolpos and ipsilateral agenesis of the kidney].双子宫伴阴道积血及同侧肾缺如
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Uterus duplex with a unilaterally imperforate vagina--diagnosis and treatment. Report of two cases and review of the literature.双子宫合并单侧阴道闭锁——诊断与治疗。两例报告并文献复习。
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Didelphic uterus and obstructed hemivagina with renal agenesis: case report and review of the literature.双子宫合并梗阻性半阴道及肾缺如:病例报告及文献复习
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