Pirzada Faisal Masood, Nayyar Rishi, Yadav Devendra Kumar
Department of Urology, AIIMS, New Delhi, India.
Department of Paediatric Surgery, AIIMS, New Delhi, India.
Indian J Urol. 2025 Jan-Mar;41(1):69-72. doi: 10.4103/iju.iju_264_24. Epub 2025 Jan 1.
Urethral duplication is a rare congenital anomaly characterized by more than one urethral channel, with varied course, location of the external opening, and presentation. Presentations can be varied, depending upon individual anatomical dispensation but mostly present as obstruction, recurrent urinary infection, or double urinary stream. Treatment depends on the type of duplication and associated anomalies. Here, we report a case of urethral duplication which did not fit into any known reported type of urethral duplication forms and had five openings at the anal verge.
尿道重复畸形是一种罕见的先天性异常，其特征为存在一个以上的尿道通道，其走行、外口位置及表现各不相同。临床表现各异，取决于个体的解剖分布情况，但大多表现为梗阻、反复尿路感染或双尿流。治疗取决于重复畸形的类型及相关异常情况。在此，我们报告一例尿道重复畸形病例，该病例不符合任何已知报道的尿道重复畸形类型，且在肛门边缘有五个开口。
