Fujii Daiki, Manabe Yasuhiro, Takahasi Yosiaki, Narai Hisashi, Omori Nobuhiko, Kusunoki Susumu, Abe Koji
Department of Neurology, National Hospital Organization Okayama Medical Center, Okayama, Japan.
Case Rep Neurol. 2012 Sep;4(3):212-5. doi: 10.1159/000345847. Epub 2012 Sep 27.
We report a 72-year-old woman with overlapping Miller Fisher syndrome (MFS), Guillain-Barré syndrome (GBS) and Bickerstaff's brainstem encephalitis (BBE). She developed diplopia and unsteady gait a week after an upper respiratory infection on day 1. She had weakness of both upper limbs on day 3 and became drowsy, and her respiratory status worsened on day 5. Neurologic examination revealed ophthalmoplegia, ataxia, symmetrical weakness, areflexia, and consciousness disturbance. We diagnosed her with MFS on day 1, GBS on day 3 and overlapping BBE on day 5. She underwent immunoadsorption therapy and two courses of intravenous immunoglobulin therapy. Ten months after onset, her symptoms had fully recovered. Anti-GM1 IgG, GD1a IgG, GQ1b IgG, and GT1a IgG antibodies were positive. Our case supports the notion that MFS, GBS, and BBE are all part of a continuous clinical spectrum, which is an antibody-mediated process.
我们报告了一名72岁女性,她患有重叠性米勒·费雪综合征(MFS)、吉兰-巴雷综合征(GBS)和比克斯特法夫脑干脑炎(BBE)。第1天,她在上呼吸道感染一周后出现复视和步态不稳。第3天出现双上肢无力,第5天变得嗜睡,呼吸状况恶化。神经系统检查发现眼肌麻痹、共济失调、对称性无力、腱反射消失和意识障碍。我们在第1天诊断她为MFS,第3天诊断为GBS,第5天诊断为重叠性BBE。她接受了免疫吸附治疗和两个疗程的静脉注射免疫球蛋白治疗。发病十个月后,她的症状已完全恢复。抗GM1 IgG、GD1a IgG、GQ1b IgG和GT1a IgG抗体呈阳性。我们的病例支持以下观点:MFS、GBS和BBE均属于连续临床谱系的一部分,这是一个抗体介导的过程。