Conus medullaris syndrome as a presenting feature of MOG-associated disease

Pract Neurol. 2023 Aug;23(4):314-316. doi: 10.1136/pn-2022-003560. Epub 2023 Jan 13.

Abstract

We report a case of conus medullaris syndrome presenting with lower limb and bladder symptoms. MR imaging showed an abnormality in the lowest part of the spinal cord as a first presentation of myelin oligodendrocyte glycoprotein (MOG)-associated disease. While such cord swelling can mimic a tumour, these patients respond well to corticosteroids, with good outcomes. MOG-associated disease is an immune-mediated syndrome distinct from aquaporin 4 antibody positive neuromyelitis optica syndrome and is now considered an independent entity. Although there can be overlapping phenotypes, there are also differences, and MOG-associated disease generally has a much better prognosis compared with aquaporin 4 antibody-positive neuromyelitis optica syndrome.

Keywords: MYELOPATHY.

Publication types

  • Case Reports

MeSH terms

  • Aquaporin 4
  • Autoantibodies
  • Humans
  • Myelin-Oligodendrocyte Glycoprotein
  • Neuromyelitis Optica* / complications
  • Neuromyelitis Optica* / diagnostic imaging
  • Neuromyelitis Optica* / drug therapy
  • Spinal Cord Compression* / diagnostic imaging
  • Spinal Cord Compression* / etiology

Substances

  • Myelin-Oligodendrocyte Glycoprotein
  • Aquaporin 4
  • Autoantibodies