Furiya Yoshiko, Hirano Makito, Kusunoki Susumu, Ueda Masami, Sugie Kazuma, Nishiwaki Tomohisa, Ueno Satoshi
Department of Neurology, Nara Medical University, Kashihara, Nara 634-8521, Japan.
Muscle Nerve. 2008 Dec;38(6):1630-3. doi: 10.1002/mus.21131.
In this report we describe a 72-year-old woman who had cytomegalovirus infection-related Guillain-Barré syndrome (GBS) associated with multiple immunoglobulin M (IgM) anti-ganglioside antibodies. She became tetraplegic with respiratory failure, but recovered completely after intravenous immunoglobulin therapy and plasmapheresis. The serum contained high-titer IgM antibody activities to several gangliosides with disialosyl residues (GD1b, GD3, GT1b, GQ1b, and GT1a) and GD1a. These antibodies are often found in sera from patients with chronic sensory ataxic neuropathy, but they occur rarely in GBS.
在本报告中,我们描述了一名72岁女性,她患有与巨细胞病毒感染相关的吉兰 - 巴雷综合征(GBS),伴有多种免疫球蛋白M(IgM)抗神经节苷脂抗体。她出现四肢瘫痪并伴有呼吸衰竭,但在接受静脉注射免疫球蛋白治疗和血浆置换后完全康复。血清中含有针对几种带有双唾液酸残基的神经节苷脂(GD1b、GD3、GT1b、GQ1b和GT1a)以及GD1a的高滴度IgM抗体活性。这些抗体常在慢性感觉性共济失调性神经病患者的血清中发现,但在GBS中很少出现。