A case of anti-myelin oligodendrocyte glycoprotein antibody-positive multiphasic disseminated encephalomyelitis showing significant recovery after immunoadsorption plasmapheresis
Author:
Affiliation:
1. Department of Internal Medicine IV, Division of Neurology, Osaka Medical and Pharmaceutical University
2. Blood Purification Center, Osaka Medical and Pharmaceutical University
Publisher
Societas Neurologica Japonica
Subject
Neurology (clinical)
Link
https://www.jstage.jst.go.jp/article/clinicalneurol/63/8/63_cn-001868/_pdf
Reference20 articles.
1. 1) Reindl M, Di Pauli F, Rostásy K, et al. The spectrum of MOG autoantibody-associated demyelinating diseases. Nat Rev Neurol 2013;9:455-461.
2. 2) 宮本勝一.抗ミエリンオリゴデンドロサイト糖タンパク質抗体関連疾患の病態と治療.神経治療 2022;39:183-185.
3. 3) Jarius S, Ruprecht K, Kleiter I, et al. MOG-IgG in NMO and related disorders: a multicenter study of 50 patients. Part 2: epidemiology, clinical presentation, radiological and laboratory features, treatment responses, and long-term outcome. J Neuroinflamm 2016;13:280.
4. 4) Cobo-Calvo A, Sepúlveda M, Rollot F, et al. Evaluation of treatment response in adults with relapsing MOG-Ab-associated disease. J Neuroinflammation 2019;16:134.
5. 5) Hennes EM, Baumann M, Schanda K, et al. Prognostic relevance of MOG antibodies in children with an acquired demyelinating syndrome. Neurology 2017;89:900-908.
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