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先天性孤立肾临床上少见,迄今为止国内仅报导8例,我院共收治7例,现介绍如下。 临 床 资 料 (1)本组7例年龄在24～59岁之间,其中男5例,女2例,左侧5例,右侧2例。 (2)多数病例均作系统的泌尿系检查;包括同位素肾图,超声波,静脉肾盂造影,膀胱镜等。其中2例行腹膜后充气造影,2例作腹主动脉造影,2例经手术探查证实。 (3)7例均有腰痛或血尿、尿频等症状,1例合并附睾结核,2例并发肾结石。 (4)2例女性患者同时合并双子宫畸形,男性5例均未发现生殖系统及其他器官异常。
Clinically isolated neoplasms rare, so far only 8 cases reported in China, our hospital were treated in 7 cases, are described below. Clinical data (1) The group of 7 patients aged 24 to 59 years old, including 5 males and 2 females, left in 5 cases, right in 2 cases. (2) The majority of cases are for urinary system examination; including isotope nephrogram, ultrasound, intravenous pyelography, cystoscopy and so on. Two cases underwent retroperitoneal gasification angiography, two cases of abdominal aorta angiography, 2 cases confirmed by surgical exploration. (3) All 7 cases had symptoms of lumbago or hematuria and frequent urination. One case had epididymal tuberculosis and two cases had kidney stones. (4) Two cases of female patients with double uterus deformity were also combined, and no abnormalities of reproductive system and other organs were found in 5 males.