Diagnosis and classification of neuromyelitis optica (Devic's Syndrome)

被引:34
作者
Drori, Tali [1 ]
Chapman, Joab [1 ,2 ]
机构
[1] Tel Aviv Univ, Sackler Fac Med, Dept Neurol, Sheba Med Ctr, IL-52621 Tel Hashomer, Israel
[2] Chaim Sheba Med Ctr, Zabludowicz Ctr Autoimmune Dis, IL-52621 Tel Hashomer, Israel
关键词
Neuromyelitis optica; Autoimmune CNS diseases; NMO-IgG antibodies; Autoimmunity; Diagnostic criteria; IGG PREDICTS; SPECTRUM; MARKER; NMO;
D O I
10.1016/j.autrev.2014.01.034
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Neuromyelitis optica (NMO) is an autoimmune disorder, predominantly characterized by severe optic neuritis (ON) and transverse myelitis (TM). Historically considered a variant of Multiple sclerosis, the discovery that most NMO patients have autoantibodies against aquaporin-4 (AQP4) or NMO-IgG, dramatically changed our understanding of the disease. The finding of NMO-IgG revealed wider array of clinical presentations, including patients with recurrent ON of TM alone, now considered part of the NMO spectrum. Furthermore, symptoms other than optic-spinal involvement and the presence of brain lesions, do not exclude the diagnosis of NMO as traditionally accepted. We present an overview of the epidemiology, clinical manifestations and current diagnostic criteria for NMO and NMO spectrum disorders. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:531 / 533
页数:3
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