论文部分内容阅读
多睾畸形是一极为罕见的先天性反常,现将我院收治一例报告如下。患者,男,28岁。因右腹股沟触及蚕豆大小肿块一年余,于1984年12月29日入院。一年前患者在一次重体力劳动后,偶然发现右腹股沟区有一蚕豆大小肿块,因局部无疼痛及其它不适,故未作诊治。近两个月来患者时感右腹股沟区疼痛且放射至腰部酸痛,但无畏寒发热,亦无尿频尿痛。体检:右腹股沟处可触及蚕豆大肿块,表面光滑,无压痛,质中等硬,可轻微活动,肿块上界不清。阴囊内两睾丸大小正常,无触痛,两侧精索无增粗。入院诊断①右侧股疝。②右腹股沟淋巴结炎。
Multiple testicular deformity is a very rare congenital anomaly, now admitted to our hospital a case report is as follows. Patient, male, 28 years old. Due to the right groin touched the size of broad bean tumors more than a year, in December 29, 1984 admission. A year ago, after a heavy manual work, he accidentally discovered that there was a broad bean mass in the right groin area. Because of no local pain or other discomfort, no diagnosis or treatment was done. In the past two months, the patient felt pain in the right groin area and radiates to the waist with pain, but no chills and fever, nor dysuria. Physical examination: the right groin can reach the broad masses of broad beans, smooth surface, no tenderness, medium hard, can be mild activity, unclear upper bound. Scrotal testicular two normal size, no tenderness, stenosis on both sides without thickening. Admission diagnosis ① right femoral hernia. ② right inguinal lymphadenitis.