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单侧阴道积血与同侧肾缺如:两例报告并文献复习

Unilateral hematocolpos and ipsilateral renal agenesis: report of two cases and review of the literature.

作者信息

Yoder I C, Pfister R C

出版信息

AJR Am J Roentgenol. 1976 Aug;127(2):303-8. doi: 10.2214/ajr.127.2.303.

Abstract

Two cases are presented of a partially duplicated vagina characterized by a one-sided hematocolpos associated with renal agenesis on the same side. A review of the English literature reveals 39 previously reported cases. Invariably this complex of anomalies is seen in adolescents and young women with progressively severe abdominal pain, menstrual irregularities, and a pelvic mass. It is important to make an early accurate diagnosis since they are usually managed as having an ovarian mass and submitted to multiple laparotomies and occasionally to mutilating surgery. An analysis is presented of the salient embryologic, clinical, and radiologic features of the 41 cases gathered. The need for definitive preoperative evaluation of both the urinary tract (urography and cystoscopy) and the genital tract (hysterosalpingography) cannot be overemphasized.

摘要

本文报告了两例部分重复阴道的病例,其特征为单侧阴道积血并伴有同侧肾缺如。回顾英文文献发现,此前已有39例相关病例报道。这种复杂的异常情况总是出现在青少年和年轻女性中,伴有进行性加重的腹痛、月经不规律和盆腔肿块。早期准确诊断很重要,因为这类患者通常被当作患有卵巢肿块来处理,从而接受多次剖腹手术,偶尔还会接受致残性手术。本文对收集到的41例病例的重要胚胎学、临床和放射学特征进行了分析。强调对泌尿系统(尿路造影和膀胱镜检查)和生殖道(子宫输卵管造影)进行明确术前评估的必要性。

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