论文部分内容阅读
重复肾双输尿管可合并输尿管异位开口.本病易误诊及漏诊.我院从1977～1990年共收治15例,现报告如下.[1]临床资料本组15例全部为女性,年龄5～24岁.单侧重复肾双输尿管10例,双侧重复肾双输尿管、单侧异位开口 5例.异位开口部位;前庭10例,阴道内5例.全部病例都自幼正常排尿伴漏尿.15例均手术治疗,9例作半肾(上位肾)连同输尿管大部切除,6例行输尿管膀胱吻合术.漏尿均消失.[2]讨论先天性输尿管异位开口多发生于重复肾与重复
Duplication of renal double ureter may be combined with ureteral ectopic opening. The disease is misdiagnosed and missed diagnosis .1977-1990 years admitted to our hospital a total of 15 cases, are as follows. [1] Clinical data All 15 patients in this group were female, aged 5 ~ 24 years old.Reciprocal double renal ureter in 10 cases, bilateral double renal ureter, unilateral ectopic opening in 5. Ectopic opening site, 10 cases of vestibule, 5 cases of intravaginal.All cases were normal childhood urinary leakage Urine .15 cases were treated surgically, 9 cases of semi-kidney (upper kidney) together with the removal of the ureter, ureteral calcification in 6 cases anastomosis. Leakage are disappeared. [2] Discussion Congenital ureter opening occurred in the repeat Kidney and repeat