先天性脑穿通畸形又名空洞脑畸形,是一种少见的脑发育障碍疾病。我院收治1例伴有偏瘫和癫痫,经手术切除病灶侧大脑半球,顽固性癫痫得到控制,兹报告如下。 患儿 男,12岁,因反复抽搐8年,于1985年1月10日入院。患儿足月顺产,产后3个月发现右下肢活动 Congenital brain perforating deformity, also known as empty brain deformity, is a rare brain development disorders. In our hospital, one case was treated with hemiplegia and epilepsy. The lesion side hemisphere was excised surgically and the intractable epilepsy was controlled. The report is as follows. Male, 12 years old, was admitted to hospital on January 10, 1985 because of repeated convulsions for 8 years. Children with full-term follow-up, 3 months postpartum found that the right lower limb activity