Hayakawa H, Katoh T
Department of Pediatrics, Nagoya City Higashi General Hospital, Japan.
Pediatr Neurol. 1995 Feb;12(2):159-61. doi: 10.1016/0887-8994(94)00119-m.
The clinical course and serial magnetic resonance imaging findings of a 4-year-old girl with acute cerebellar ataxia due to acute cerebellitis are described. Multifocal white matter lesions visualized by magnetic resonance imaging in both cerebellar hemispheres in the acute phase disappeared in the convalescent phase. Cerebellar signs became less prominent within 2 weeks, but mild ataxic gait remained. During the follow-up period of 32 months, there was a gradual development of cerebellar atrophy along with a recurrence of cerebellar ataxia.
描述了一名因急性小脑炎导致急性小脑共济失调的4岁女孩的临床病程及系列磁共振成像结果。急性期磁共振成像显示双侧小脑半球多发白质病变,在恢复期消失。小脑体征在2周内变得不那么明显,但仍残留轻度共济失调步态。在32个月的随访期内,小脑萎缩逐渐发展,同时小脑共济失调复发。