PRES-like presentation in MOG antibody-related demyelination (MARD)

J Clin Neurosci. 2020 Feb:72:453-455. doi: 10.1016/j.jocn.2020.01.034. Epub 2020 Jan 22.

Abstract

A 33-year-old male presented with a progressive four-week history of frontal headache and left visual field impairment. MRI brain confirmed bilateral, asymmetric, occipital vasogenic oedema, suggestive of posterior reversible encephalopathy syndrome (PRES). Serum testing for MOG antibodies was positive, confirming a diagnosis of MOG antibody-related demyelination (MARD). A similar PRES-like pattern of white matter inflammation has been reported previously in neuromyelitis optica spectrum disorder but has not previously been reported in MARD.

Keywords: Myelin oligodendrocyte glycoprotein; Posterior reversible encephalopathy syndrome.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Autoantibodies / blood
  • Brain / diagnostic imaging
  • Demyelinating Autoimmune Diseases, CNS / diagnosis*
  • Demyelinating Autoimmune Diseases, CNS / diagnostic imaging
  • Demyelinating Autoimmune Diseases, CNS / immunology
  • Diagnosis, Differential
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Myelin-Oligodendrocyte Glycoprotein / immunology*
  • Posterior Leukoencephalopathy Syndrome / diagnosis*
  • Posterior Leukoencephalopathy Syndrome / diagnostic imaging
  • Posterior Leukoencephalopathy Syndrome / immunology

Substances

  • Autoantibodies
  • Myelin-Oligodendrocyte Glycoprotein