Vaquerizo-Madrid J
Departamento y Cátedra de Pediatría, Hospital Universitario Regional Infanta Cristina, Universidad de Extremadura, Badajoz, España.
Rev Neurol. 1999;29(12):1188-9.
The authors describe a 14 year-old boy with bilateral arachnoid cysts of the sylvian area and temporal lobe hypoplasia. Also showed vermis and brainstem hypoplasia. Clinically manifest a severe encephalopathy with tetraparesia, autism and late onset polymorphic epilepsy. He presented a favorable outcome with valproate and vigabatrine. To the best of our knowledge only one case like ours has been reported.
作者描述了一名14岁男孩，患有双侧外侧裂区蛛网膜囊肿和颞叶发育不全。还表现出小脑蚓部和脑干发育不全。临床上表现为严重脑病，伴有四肢瘫痪、自闭症和迟发性多形性癫痫。他使用丙戊酸盐和氨己烯酸治疗后预后良好。据我们所知，仅有一例与我们的病例类似的报告。
