Ulman I, Avanoğlu A, Erdener A, Sahin A H, Gökdemir A
Department of Pediatric Surgery, Ege University Faculty of Medicine, Izmir, Turkey.
J Pediatr Surg. 1996 Dec;31(12):1680-1. doi: 10.1016/s0022-3468(96)90047-0.
Caudal duplication is a rare anomaly with less than 30 reported cases. For those patients who also have double bladders, there are not enough data regarding the function of the lower urinary tract. A boy with caudal duplication anomaly was evaluated fluoroscopically and urodynamically. The results of the evaluation showed that the bladders were filling and emptying synchronously with normal and almost identical detrusor pressures. The child did not require either or both bladders to be resected. Because the level of the duplication in dipygus cases varies, thorough evaluation of the lower urinary tract, including urodynamics, should be considered for every case.
尾端重复畸形是一种罕见的异常情况,报告病例不足30例。对于那些同时患有双膀胱的患者,关于下尿路功能的数据并不充足。对一名患有尾端重复畸形的男孩进行了荧光镜检查和尿动力学评估。评估结果显示,两个膀胱的充盈和排空是同步的,逼尿肌压力正常且几乎相同。该患儿不需要切除任何一个或两个膀胱。由于双臀畸形病例中重复的水平各不相同,因此对于每一例病例都应考虑对下尿路进行全面评估,包括尿动力学评估。