MOG antibody associated demyelinating syndrome presenting as aseptic meningitis in a 6-year-old boy

Johanna Leinert1, Eva Neumaier-Probst2, Georg Kutschke1

  • 1Department of Pediatrics, Heidelberg University, Mannheim, Germany.

Insights

Myelin oligodendrocyte glycoprotein antibody (MOG-Ab) associated demyelinating syndrome can mimic aseptic meningitis in children. This is the first reported pediatric case, showing improvement with methylprednisolone treatment.

Area of Science:

  • Neuroimmunology
  • Pediatric Neurology
  • Demyelinating Diseases

Background:

  • Myelin oligodendrocyte glycoprotein antibody (MOG-Ab) associated demyelinating syndrome is an immune-mediated condition affecting the central nervous system.
  • While MOG-Ab associated demyelinating syndrome is recognized, its presentation can vary, with some cases mimicking infectious meningitis.

Observation:

  • A 6-year-old boy initially presented with symptoms suggestive of aseptic meningitis.
  • Cerebral and spinal lesions consistent with acute disseminated encephalomyelitis were identified via magnetic resonance imaging.
  • The patient experienced rapid clinical improvement following high-dose intravenous methylprednisolone therapy.

Findings:

  • This case represents the first documented pediatric instance of MOG-Ab associated demyelinating syndrome presenting as aseptic meningitis.
  • Previously, this specific clinical presentation of MOG-Ab associated demyelinating syndrome has been reported primarily in adults.

Implications:

  • Recognizing aseptic meningitis as a potential early sign of MOG-Ab associated demyelinating syndrome in children is crucial for timely diagnosis.
  • This finding expands the known spectrum of MOG-Ab associated demyelinating syndrome phenotypes in pediatric populations.
  • Early diagnosis and appropriate treatment, such as corticosteroids, can lead to favorable outcomes in pediatric MOG-Ab associated demyelinating syndrome.

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