Improvement in recurrent anti-myelin oligodendrocyte glycoprotein antibody - positive cerebral cortical encephalitis not requiring anti - inflammatory therapy following the decrease in cytokine/chemokine levels

2020; Elsevier BV; Volume: 43; Linguagem: Inglês

10.1016/j.msard.2020.102168

ISSN

2211-0356

Autores

Tomoko Takamatsu, Gaku Yamanaka, Hideko Uryu, Mika Takeshita, Natsumi Morishita, Shinichiro Morıchı, Yu Ishida, Shingo Oana, Hiroo Terashi, Hiroyuki Shichino, Hiroshi Sakuma, Hisashi Kawashima,

Tópico(s)

RNA regulation and disease

Resumo

Anti-myelin oligodendrocyte glycoprotein antibody (MOG-Ab)-positive cerebral cortical encephalitis (CCE) is a recently reported condition, which reportedly improves with anti-inflammatory therapy including steroids or intravenous immunoglobulin (IVIG) treatment ( Mariotto et al., 2017 Mariotto S. Monaco S. Peschl P. Coledan I. Mazzi R. Hoftberger R. Reindl M. Ferrari S. MOG antibody seropositivity in a patient with encephalitis: beyond the classical syndrome. BMC Neurol. 2017; 17: 190 Crossref PubMed Scopus (19) Google Scholar ; Ogawa et al., 2017 Ogawa R. Nakashima I. Takahashi T. Kaneko K. Akaishi T. Takai Y. Sato D.K. Nishiyama S. Misu T. Kuroda H. Aoki M. Fujihara K. MOG antibody-positive, benign, unilateral, cerebral cortical encephalitis with epilepsy. Neurol Neuroimmunol Neuroinflamm. 2017; 4: e322 Crossref PubMed Scopus (258) Google Scholar ). Recently, a 22-year-old woman with MOG-Ab-positive CCE presented with a considerably benign clinical course and improved rapidly without immunotherapy ( Otani et al., 2020 Otani T. Irioka T. Igarashi S. Kaneko K. Takahashi T. Yokota T. Self-remitting cerebral cortical encephalitis associated with myelin oligodendrocyte glycoprotein antibody mimicking acute viral encephalitis: A case report. Mult Scler Relat Disord. 2020; 41102033 Abstract Full Text Full Text PDF PubMed Scopus (12) Google Scholar ). Herein, we present the case of a pediatric patient with recurrent CCE, who recovered from recurrent episodes, with the administration of an antiepileptic drug (carbamazepine) only, without the need for immunotherapy. Moreover, various cytokines/chemokines, especially Th 17-related inflammatory cytokines, which were elevated, decreased after the MOG-Ab disappeared following the third recurrence.

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