NMDA receptor antibody in teratoma-related opsoclonus-myoclonus syndrome

被引:4
作者
Urriola, Nicolas X. [1 ,2 ]
Helou, Jacob [3 ]
Maamary, Joel [4 ]
Pogson, Jacob [4 ]
Lee, Frederick [5 ]
Parratt, Kaitlyn [4 ]
Gillis, David [6 ]
Fulham, Michael J. [6 ]
Halmagyi, G. Michael [4 ]
机构
[1] Royal Prince Alfred Hosp, Dept Neurol, Sydney, NSW, Australia
[2] Royal Prince Alfred Hosp, Dept Immunol, Sydney, NSW, Australia
[3] Royal Prince Alfred Hosp, Dept Neurol, Sydney, NSW, Australia
[4] Royal Prince Alfred Hosp, Dept Immunol, Sydney, NSW, Australia
[5] Royal Brisbane & Womens Hosp, Dept Immunol, Brisbane, Qld, Australia
[6] Royal Prince Alfred Hosp, Dept Med Imaging, Sydney, NSW, Australia
关键词
Neuroimmunology; NMDAR antibody encephalitis; Opsoclonus-myoclonus syndrome; Oscillopsia; PET scan; Video pupil tracking; ENCEPHALITIS;
D O I
10.1016/j.jocn.2018.10.011
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Opsoclonus-myoclonus syndrome (OMS) is a brainstem/cerebellar syndrome producing disabling multidirectional saccadic oscillations with oscillopsia, with or without somatic myoclonus and cerebellar ataxia (Wong et al., 2001; Armangue et al., 2016). OMS is presumed to have an autoimmune basis and patients with it are tested for antineuronal antibodies and have imaging to locate any tumors. Here we report a unusual case of a young woman who had NMDAR antibody (NMDAR-ab) positive, teratomarelated, isolated OMS without encephalopathy. Removal of her ovarian teratoma, and immunotherapy with steroids, intravenous immunoglobulin (IVIg), plasma exchange (PLEX), and ultimately with B-cell depletion with rituximab resulted in total recovery after 3 months. Patients with teratoma-related OMS very rarely have NMDAR-ab which suggests that it is not the NMDAR-ab per se that causes the OMS. Crown Copyright (C) 2018 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:203 / 204
页数:2
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