Manzoni Carlo
Divisione di Chirurgia Pediatrica, Università Cattolica del S. Cuore, Policlinico A. Gemelli, Largo A. Gemelli 8, 00168 Roma, Italy.
Rays. 2002 Apr-Jun;27(2):87-8.
Ureteral valves together with stenosis and diverticula represent congenital malformations of the ureteral tract between the pyeloureteral junction and the ureterovesical junction. They are rare malformations and even more rarely they cause an obstacle to urine flow. The proximal subjejunal ureteral tract is more frequently involved. The most reliable pathogenetic hypotheses suggest a delay in the canalization of fetal ureter or an ischemic damage. The true ureteral valves should be distinguished from Ostling embryonic folds that can be documented in 5% of newborns and disappear with growth. Treatment, when necessary, consists in the resection of the affected ureteral tract followed by ureteral or pelviureteral end-to-end anastomosis.
输尿管瓣膜连同狭窄和憩室代表肾盂输尿管连接处和输尿管膀胱连接处之间输尿管通道的先天性畸形。它们是罕见的畸形,更罕见的是它们会导致尿流障碍。近端空肠下输尿管通道更常受累。最可靠的发病机制假说是胎儿输尿管管道化延迟或缺血性损伤。真正的输尿管瓣膜应与奥斯特林胚胎皱襞相区分,后者在5%的新生儿中可被记录到,并随生长而消失。必要时,治疗方法是切除受影响的输尿管通道,然后进行输尿管或肾盂输尿管端端吻合术。