Неврология, нейропсихиатрия, психосоматика (Jun 2020)

Anti-MOG associated myelitis

  • A. I. Isaykin,
  • O. N. Voskresenskaya,
  • T. I. Kuzminova,
  • E. V. Ermilova,
  • O. V. Stezhko

DOI
https://doi.org/10.14412/2074-2711-2020-3-87-92
Journal volume & issue
Vol. 12, no. 3
pp. 87 – 92

Abstract

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There is now increasing evidence that demyelinating disease with anti-myelin oligodendrocyte glycoprotein (anti-MOG) antibodies is an independent nosological unit. The paper describes a clinical case of anti-MOG associated myelitis at the CI-TXlevel. Differential diagnosis was made between multiple sclerosis, Devic's myelitis optica, and idiopathic transverse myelitis. The clinical, morphopathological, and diagnostic features of anti-MOG associated myelitis are discussed. There are new diagnostic criteria for neuromyelitis optica spectrum diseases (NMOSD), as well as red flags, in the absence of which the diagnosis of NMOSD can be established as a diagnosis of exclusion.

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