后肠管状重复畸形合并泌尿生殖系统异常。

Tubular duplication of the hindgut with genitourinary anomalies.

作者信息

Okur H, Keskin E, Zorludemir U, Olcay I

机构信息

Department of Pediatric Surgery, Cukurova University, Faculty of Medicine, Adana, Turkey.

出版信息

J Pediatr Surg. 1992 Sep;27(9):1239-40. doi: 10.1016/0022-3468(92)90799-d.

DOI:10.1016/0022-3468(92)90799-d

PMID:1432541

Abstract

Hindgut duplication including the colon and rectum as well as the genital and urinary organs are extremely rare. Only a few cases are noted in the medical literature. In this report, a newborn with exstrophy of the urinary bladder, double vagina and uterus, double anus, and complete duplication of rectum and colon with malrotation is presented.

摘要

包括结肠、直肠以及生殖和泌尿器官在内的后肠重复畸形极为罕见。医学文献中仅记载了少数病例。在本报告中，呈现了一名患有膀胱外翻、双阴道和双子宫、双肛门以及直肠和结肠完全重复并伴有旋转不良的新生儿。