What's new in NMOSD and MOGAD?

被引：3

作者：

Marignier, R. ^{[1
]}

机构：

[1] Hop Neurol & Neurochirurg P Wertheimer, Ctr Reference Malad Inflammatoires Rares Cerveau &, Serv Neurol Sclerose Plaques Pathol Myeline & Neur, Bron, France

来源：

REVUE NEUROLOGIQUE | 2024年 / 180卷 / 09期

关键词：

Neuromyelitis optica; Myelin oligodendrocyte glycoprotein; Multiple sclerosis; Antibodies myelitis; Optic neuritis;

D O I：

10.1016/j.neurol.2024.08.004

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

In this mini-review, we focus on novelties in the field of neuromyelitis optica spectrum disorders (NMOSD) and myelin oligodendrocyte glycoprotein antibody associated disease (MOGAD). We first describe the proposed criteria for MOGAD and evaluate their impact and potential limitations, with a highlight on the subgroups of patients tested MOG-antibody positive only in the cerebrospinal fluid. We then propose a brief state of the art on the current knowledge on the so-call "double seronegative" NMOSD group, regarding nosology, clinical, biological and imaging features and the unmet need in this field. The last part is dedicating to the present and future of acute treatment in NMSOD and MOGAD. (c) 2024 The Author(s). Published by Elsevier Masson SAS. This is an open access article under the CC BY-NC license (http://creativecommons.org/licenses/by-nc/4.0/).

引用

页码：957 / 962

页数：6

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