[An 11 year old woman with myelin-oligodendrocyte glycoprotein antibody showing various phenotypes of central nervous system disorders in one year]

Rinsho Shinkeigaku. 2022 Mar 29;62(3):211-216. doi: 10.5692/clinicalneurol.cn-001685. Epub 2022 Mar 25.
[Article in Japanese]

Abstract

An 11-year-old woman with myelin-oligodendrocyte glycoprotein (MOG) antibody developed cortical encephalitis twice, followed by acute disseminated encephalomyelitis (ADEM) and optic neuritis in one year. Although optic neuritis was refractory after corticosteroid therapy, plasma exchange was effective and complete remission was achieved. We considered that episodes of cortical encephalitis, ADEM and optic neuritis occurred in the present patient can be included in MOG IgG-associated disorders. Also, we recommend plasma exchange for refractory MOG IgG-associated optic neuritis, even in pediatric patient.

Keywords: MOG antibody; acute disseminated encephalomyelitis (ADEM); cortical encephalitis; optic neuritis; plasma exchange.

Publication types

  • Case Reports

MeSH terms

  • Autoantibodies
  • Child
  • Encephalomyelitis, Acute Disseminated* / complications
  • Encephalomyelitis, Acute Disseminated* / diagnosis
  • Encephalomyelitis, Acute Disseminated* / therapy
  • Female
  • Humans
  • Myelin-Oligodendrocyte Glycoprotein
  • Optic Neuritis* / diagnosis
  • Optic Neuritis* / therapy
  • Phenotype

Substances

  • Autoantibodies
  • Myelin-Oligodendrocyte Glycoprotein