Aragona F, Glazel G P, Zaramella P, Zorzi C, Talenti E, Perale R, Marigo A
Institute of Urology, University of Padua, Italy.
Urol Radiol. 1988;10(4):207-9. doi: 10.1007/BF02926571.
Agenesis of the bladder is a rare congenital anomaly, recorded most often in stillborn infants. Renal agenesis and other severe malformations are frequently associated. An apparent failure of the infraureteral tissue of the mesonephric duct to develop into trigone and proximal urethra seems to be the cause of this anomaly. We report a case of bladder agenesis with anal atresia, left renal dysplasia, and bicornuate uterus.
膀胱缺如是一种罕见的先天性异常，最常记录于死产婴儿。常伴有肾缺如及其他严重畸形。中肾管输尿管下段组织明显未能发育成三角区和近端尿道似乎是这种异常的原因。我们报告一例伴有肛门闭锁、左肾发育不良和双角子宫的膀胱缺如病例。
