Künzig H J, Engelking R, Gharib M
Geburtshilfe Frauenheilkd. 1982 Aug;42(8):597-801. doi: 10.1055/s-2008-1036928.
A case of malformation of the urogenital system with a persistent urogenital sinus and a cloaca is reported. There was unilateral agenesis of the kidney, megaureter and a double ureter with an ureteral orifice into the vagina and the clitoris. There was a double uterus and vagina with an orifice into the terminal gut. The patient had chronic recurrent urinary tract infections which required a colostomy during childhood. The operation largely restored a normal urogenital area and a functional anus.
报告了一例泌尿生殖系统畸形病例,伴有持续性泌尿生殖窦和泄殖腔。存在单侧肾缺如、巨输尿管以及一条双输尿管,其输尿管口开口于阴道和阴蒂。有双子宫和双阴道,开口于终末肠道。该患者患有慢性复发性尿路感染,童年时期需要进行结肠造口术。手术在很大程度上恢复了正常的泌尿生殖区域和功能性肛门。