Harpey J P, Renault F, Foncin J F, Gardeur D, Horn Y E, Roy C
Arch Fr Pediatr. 1983 May;40(5):407-9.
A 14 year-old boy presented, at a 3 month interval, with 2 episodes of hemiplegia of rapid onset. The first time, CT scan revealed a large parietal "tumor", shown to be pseudocystic at surgery, and histologically proven as a demyelinating disease. During the second attack, CT scan showed a similar but contralateral lesion, regressing completely under steroid treatment. 40 months after the onset of the disease, the child's life and intelligence are normal.
一名14岁男孩每隔3个月出现2次快速发作的偏瘫。第一次发作时,CT扫描显示一个大的顶叶“肿瘤”,手术中显示为假性囊肿,组织学证实为脱髓鞘疾病。第二次发作时,CT扫描显示一个类似但位于对侧的病变,在类固醇治疗下完全消退。疾病发作40个月后,孩子的生活和智力正常。