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先天性孤立肾近年文献屡见报道,且先天性孤立肾伴输尿管、膀胱等先天性畸形亦有报道,而先天性孤立肾伴精囊腺囊肿文献报道极少。其发病机制亦不清楚,本院于1991年10月至11月间连续收治2例,现报告如下。【例1】男性,20岁。小便不畅,蹲位小便20余天。20余天来小便费力,站立位时明显,有小便不尽感,有时伴淋漓,蹲位时减轻,小便每日20次左右,无血精及射精障碍,无血尿、尿急、尿痛。门诊因肛诊、B超提示先天性孤立肾伴盆腔占位性病变收住院。
Congenital solitary kidney frequently reported in recent years, and reports of congenital solitary kidney with ureter, bladder and other congenital malformations have also been reported, and the literature of congenital solitary kidney with seminal vesicle rarely reported. Its pathogenesis is also not clear, the hospital in October 1991 to November consecutive cases of 2 cases, the report is as follows. [Example 1] Male, 20 years old. Poor urine, squat urine more than 20 days. More than 20 days to urinate effortlessly, standing position obviously, there is urine sense, sometimes accompanied by dripping, squatting relief, urine 20 times a day, no blood and ejaculation disorders, no hematuria, urgency, dysuria. Outpatient clinic due to anorexia, B-ultrasound prompted congenital solitary kidney pelvic space lesions admitted to hospital.