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输尿管异位开口是较少见的先天性泌尿系畸形,常与肾发育不全或重肾、重输尿管同时存在。我院自1978年至1991年共收治15例。报告如下。1 临床资料15例均为女性,年龄14岁以下10例,15~20岁5例。就诊原因:①自幼表现正常排尿伴持续溢尿者13例;②尿道肿物突出不能还纳2例,肿物反复突出分别为3及9个月,不能回缩,疼痛,排尿不畅已1~3天。全组15例异位开口来源于:一侧肾发育不全4例(左、右各2例);单侧重复肾7例(左3例、右4例);双侧
Ectopic ureter is a rare congenital urinary tract deformity, often associated with renal hypoplasia or kidney, ureter at the same time exist. Our hospital from 1978 to 1991 were treated 15 cases. The report is as follows. A clinical data of 15 cases were female, under the age of 14 years in 10 cases, 15 to 20 years in 5 cases. Reasons for treatment: ① normal performance of urination with persistent overflow in 13 cases; ② prominent urethral mass can not be returned in 2 cases, repeatedly highlighted the tumor were 3 and 9 months, can not be retracted, pain, poor urination has 1 ~ 3 days. The whole group of 15 cases of ectopic openings from: one side of renal dysplasia in 4 cases (left and right in 2 cases); unilateral repeated kidney in 7 cases (left 3 cases, right 4 cases); bilateral