Development of facial palsy during immunoadsorption plasmapheresis in Miller Fisher syndrome: a clinical report of two cases

被引:14
|
作者
Chida, K
Takase, S
Itoyama, Y
机构
[1] Kohnan Hosp, Dept Neurol, Taihaku Ku, Sendai, Miyagi 982, Japan
[2] Tohoku Univ, Sch Med, Dept Neurol, Sendai, Miyagi 980, Japan
关键词
Miller Fisher syndrome; immunoadsorption; plasmapheresis; facial palsy;
D O I
10.1136/jnnp.64.3.399
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Immunoadsorption plasmapheresis (IAP) using a tryptophan linked gel column has been shown to effectively remove serum IgG anti-GQ1b antibody which may contribute to the pathogenesis of Miller Fisher syndrome. Two patients are reported on with Miller Fisher syndrome, who developed bilateral facial palsy during LAP using a tryptophan column, while ophthalmoplegia, ataxia, and, areflexia were improving. In these patients, the titre of anti-GQ1b antibodies was reduced. The LAP using a tryptophan column has a beneficial effect on Miller Fisher syndrome but may not inhibit the development of facial palsy. The mechanism of such a dissociated effect of IAP on Miller Fisher syndrome is discussed.
引用
收藏
页码:399 / 401
页数:3
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