Tovar J A, Barriola M, Paisan L
Chir Pediatr. 1978;19(2):113-4.
This paper reports a very unusual variety of female ano-rectal agenesis without fistula associated with severe urogenital malformations. The patient died of renal failure and, at autopsy, both ureters draining dysplastic ectopic kidneys and two vaginas, either with its corresponding uterus and annexa were found opening to s single perineal orifice through a very narrow conduit. Bladder and urachus were absent and a single left umbilical artery was found. This infant had also thoracic vertebral anomalies.
本文报道了一种非常罕见的女性肛门直肠闭锁类型，无瘘管，伴有严重的泌尿生殖系统畸形。患者死于肾衰竭，尸检发现，引流发育异常的异位肾的两条输尿管以及两个阴道，分别与其对应的子宫和附件，通过一条非常狭窄的管道开口于单一的会阴口。膀胱和脐尿管缺失，发现一条单一的左脐动脉。该婴儿还存在胸椎异常。
