Fujiwara Shunya, Manabe Yasuhiro, Nakano Yumiko, Omote Yoshio, Narai Hisashi, Abe Koji
Department of Neurology, National Hospital Organization Okayama Medical Center, Okayama, Japan.
Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.
Case Rep Neurol. 2021 Jun 14;13(2):380-383. doi: 10.1159/000516919. eCollection 2021 May-Aug.
We report a 72-year-old woman with Miller-Fisher syndrome (MFS) with syndrome of inappropriate secretion of antidiuretic hormone (SIADH). She developed diplopia and unsteady gait a week after an upper respiratory infection. Neurologic examination revealed ophthalmoplegia, ataxia, symmetrical weakness, numbness, and areflexia. She underwent intravenous immunoglobulin therapy. Her serum sodium concentration decreased to 119 mEq/L on day 12. She had low plasma osmolarity (254 mosm/kg), high urine osmolarity (457 mosm/kg), and high urine sodium level (73 mEq/L), while the blood level of antidiuretic hormone was normal. Anti-GD1b immunoglobulin G (IgG), -GQ1b IgG, -GT1a IgG, and -Gal-C IgM antibodies were positive. We diagnosed her with MFS overlapping with SIADH. Four weeks after onset, her symptoms recovered. The elevation of anti-GD1b, -GQ1b, and -GT1a antibodies that recognize disialosyl residue may be pathologically related to SIADH.
我们报告一例患有伴有抗利尿激素分泌不当综合征(SIADH)的米勒-费希尔综合征(MFS)的72岁女性。她在上呼吸道感染一周后出现复视和步态不稳。神经系统检查显示眼肌麻痹、共济失调、对称性肌无力、麻木和无反射。她接受了静脉注射免疫球蛋白治疗。第12天时她的血清钠浓度降至119 mEq/L。她的血浆渗透压较低(254 mosm/kg),尿渗透压较高(457 mosm/kg),尿钠水平较高(73 mEq/L),而抗利尿激素的血液水平正常。抗GD1b免疫球蛋白G(IgG)、-GQ1b IgG、-GT1a IgG和-Gal-C IgM抗体呈阳性。我们诊断她为重叠有SIADH的MFS。发病四周后,她的症状恢复。识别二唾液酸残基的抗GD1b、-GQ1b和-GT1a抗体升高可能在病理上与SIADH相关。