Asanuma H, Nakai H, Shishido S, Tajima E, Kawamura T, Kawamura T
Department of Urology, Tokyo Metropolitan Kiyose Children's Hospital, Japan.
Int J Urol. 2000 May;7(5):195-8. doi: 10.1046/j.1442-2042.2000.00164.x.
Congenital vesicovaginal fistula is a very rare entity, the etiology of which has not been clearly elucidated because pathologic features have not been mentioned in previous reports. The case of a 4-year-old girl having incontinence resulting from a congenital vesicovaginal fistula joining with the left ectopic ureter from the hypoplastic kidney is described. This is thought to be the first presentation of congenital vesicovaginal fistula joining with ectopic ureter. A microscopic examination revealed the fistula consisting of transitional cell epithelium, suggesting an abnormal fusion of the ureteral bud and caudal end of the müllerian duct with the urogenital sinus.
先天性膀胱阴道瘘是一种非常罕见的疾病,由于既往报道中未提及病理特征,其病因尚未明确阐明。本文描述了一名4岁女童的病例,该女童因先天性膀胱阴道瘘合并左肾发育不全的异位输尿管而出现尿失禁。这被认为是先天性膀胱阴道瘘合并异位输尿管的首例报道。显微镜检查显示瘘管由移行上皮细胞构成,提示输尿管芽与苗勒管尾端和泌尿生殖窦异常融合。