Parente Alberto, Ortiz Ruben, Burgos Laura, Angulo Jose Maria
Department of Pediatric Urology, Gregorio Marañon University Hospital, Madrid, Spain.
J Endourol Case Rep. 2018 Apr 1;4(1):45-47. doi: 10.1089/cren.2018.0019. eCollection 2018.
Urethral triplication is a rare congenital anomaly of the lower urinary system, with <15 cases reported so far. We present a 24-month-old boy with accessory hypoplastic urethra ending in glans. At the beginning of toilet training, urine output was observed along the rectum. Rigid cystoscopy shows a perineal urethra starting in the posterior urethra. Subsequently, flexible cystoscopy showed entry of epispadic urethra in the bladder immediately superior to the bladder neck. It was running parallel to primary urethra. Then, we observed two most frequent types of urethral duplication in the sagittal plane in a single patient.
尿道重复是下泌尿系统一种罕见的先天性异常,迄今为止报道的病例少于15例。我们报告一名24个月大的男孩,其附属尿道发育不全,止于龟头。在开始如厕训练时,发现尿液从直肠排出。硬性膀胱镜检查显示会阴尿道起自后尿道。随后,软性膀胱镜检查显示耻骨上尿道在膀胱颈上方紧邻处进入膀胱,与主尿道平行。然后,我们在一名患者的矢状面上观察到了两种最常见的尿道重复类型。