论文部分内容阅读
目的 :进一步明确小儿 Fisher氏综合征的病因及诊断标准。方法 :对 2 2例小儿 Fisher氏综合征的临床表现、脑脊液进行对比研究。结果 :2 2例患儿均以眼肌麻痹和小脑共济失调为主征 ,伴有肢体不同程度的不完全的弛缓性瘫痪 ,约半数以上病儿脑脊液出现蛋白、细胞分离现象。结论 :Fisher氏综合征是急性感染性神经根神经炎 ( AIP)一种特殊型或变异型 ,是以小脑共济失调为主的颅神经受损的AIP。
Objective: To further clarify the etiology and diagnostic criteria of pediatric Fisher’s syndrome. Methods: The clinical manifestations of 22 pediatric Fisher’s syndrome, cerebrospinal fluid were compared. Results: Twenty-two children were mainly characterized by ophthalmoplegia and cerebellar ataxia, incomplete flaccid paralysis with varying degrees of limbs, and protein and cell separation in the cerebrospinal fluid of more than half of children. Conclusion: Fisher’s syndrome is a special type or variant of acute infective nerve root neuritis (AIP). It is a type of AIP with cranial nerves predominantly affected by cerebellar ataxia.