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

Joel Corbett1, Sandeep Bhuta2, Kerri Prain3

  • 1Department of Neurology, Gold Coast University Hospital, Southport, QLD 4215, Australia.

Insights

Posterior reversible encephalopathy syndrome (PRES) was observed in a patient with MOG antibody-related demyelination (MARD). This PRES-like pattern is a novel finding in MARD, previously only seen in neuromyelitis optica spectrum disorder.

Area of Science:

  • Neuroimmunology
  • Neurology
  • Radiology

Background:

  • Posterior reversible encephalopathy syndrome (PRES) is a neurological condition characterized by vasogenic edema.
  • It has been associated with neuromyelitis optica spectrum disorder (NMOSD).
  • MOG antibody-related demyelination (MARD) is an autoimmune disorder affecting the central nervous system.

Observation:

  • A 33-year-old male presented with headache and visual field impairment.
  • Brain MRI revealed bilateral occipital vasogenic edema, consistent with PRES.
  • The patient tested positive for MOG antibodies, confirming MARD.

Findings:

  • This case presents a PRES-like pattern of white matter inflammation in MARD.
  • This radiological finding has not been previously reported in MARD.
  • The presentation mimics patterns seen in NMOSD.

Implications:

  • This finding expands the spectrum of clinical and radiological presentations of MARD.
  • It suggests potential overlapping pathophysiological mechanisms between MARD and NMOSD.
  • Further research is needed to understand the relationship between MOG antibodies and PRES-like phenomena.

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