Antón-Pacheco J, Ruiz de la Roja J C, Martín Oses E, Sánchez Sánchez E, Luján Galán M
Servicio de Cirugía Pediátrica, Hospital Universitario de Getafe, Madrid.
Actas Urol Esp. 1996 Jul-Aug;20(7):669-71.
Urethral duplication is a very rare malformation which occurs almost exclusively in males. Associated genital and urinary malformations are frequent, and the approach in symptomatic cases in surgical management. This paper presents one case of a full double urethra in a 9-year old girl with repeat urinary infections and incontinence. The accessory urethra was surgically removed using perianal and abdominal access. Evolution has been favourable with disappearance of symptomatology.
尿道重复畸形是一种非常罕见的畸形,几乎仅发生于男性。常伴有生殖系统和泌尿系统畸形,对于有症状的病例需采取手术治疗。本文报道了一例9岁女童完全性双尿道病例,该女童反复出现泌尿系统感染和尿失禁。通过经肛门和经腹入路手术切除了副尿道。术后症状消失,恢复良好。