Shintaku I, Ono Y, Katoh N, Takeda A, Ohshima S
Department of Urology Komaki Shimin Hospital, Aichi, Japan.
Int J Urol. 1996 Sep;3(5):412-3. doi: 10.1111/j.1442-2042.1996.tb00568.x.
A case of congenital urethral diverticulum is presented. The patient was a 16-year-old boy with the chief complaint of dribbling urine since he was 14 years old. A retrograde urethrogram revealed a diverticulum of the bulbar urethra, which had been produced by a cystic dilation of the Cowper's gland duct. The walls of the diverticulum were resected endoscopically.
本文报告一例先天性尿道憩室病例。患者为一名16岁男孩，自14岁起主要症状为滴尿。逆行尿道造影显示球部尿道憩室，由考珀腺导管的囊性扩张所致。通过内镜切除憩室壁。
