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多睾畸形是一极为少见的先天性反常。现将我们收治一例报告如下: 患者,4岁,因右侧阴囊内肿物发现10天,于91年8月13日入院,患儿母亲在给患儿穿衣时发现右侧阴囊大于左侧,用手触摸时,在右睾丸的上方触到一肿块而就诊。体检:阴茎呈幼儿形,发育正常。两侧阴囊发育尚好,右侧明显下垂,两侧睾丸大小,质均正常。右侧睾丸的上方可触到一约3×2cm肿物,外形似鸭梨状,表面光滑囊性感。透光试验(+),无触痛,牵拉睾丸时肿物随之上下活动。初步诊断:右侧精索鞘膜积液。在基础加局麻
Polysexal deformity is a very rare congenital anomaly. We now treat a case of the report as follows: The patient, 4 years old, because the right side of the scrotal mass was found 10 days, admitted on August 13, 91, the mother of the child found that the right scrotum is larger than the left when dressing the child , Touch by hand, touch the top of the right testis and a doctor. Physical examination: the penis was a child-shaped, normal development. On both sides of the scrotum development is still good, the right side of the obvious droop, both sides of the testicular size, quality are normal. The top of the right testis can touch about 3 × 2cm tumor, shaped like a pear-shaped, smooth surface capsule sexy. Light transmission test (+), no tenderness, when pulling the testicular mass along the upper and lower activities. Initial diagnosis: right spermatic cord effusion. In the foundation plus local anesthesia