[Diagnosis and treatment of neuromyelitis optica]

Ugeskr Laeger. 2014 Jun 23;176(26):V02130104.
[Article in Danish]

Abstract

Neuromyelitis optica (NMO) is an inflammatory demyelinating disease characterized by antibodies against aquaporin-4 in up to 80% of the cases and even less in the NMO spectrum disorders, which may be difficult to distinguish from early multiple sclerosis. While immunosuppressive therapy should be introduced in definite NMO, treatment strategies of NMO spectrum disorders are less clearly defined. Here, we review the current guidelines for treatment of NMO and NMO spectrum disorders in the light of two cases, and suggest a practical approach to the management of these disorders.

Publication types

  • Case Reports
  • English Abstract
  • Review

MeSH terms

  • Adult
  • Algorithms
  • Aquaporin 4 / immunology
  • Azathioprine / therapeutic use
  • Female
  • Humans
  • Immunosuppressive Agents / therapeutic use
  • Magnetic Resonance Imaging
  • Male
  • Methylprednisolone / therapeutic use
  • Middle Aged
  • Neuromyelitis Optica* / diagnosis
  • Neuromyelitis Optica* / drug therapy
  • Neuromyelitis Optica* / immunology
  • Neuromyelitis Optica* / therapy
  • Plasmapheresis
  • Practice Guidelines as Topic
  • Steroids / therapeutic use

Substances

  • Aquaporin 4
  • Immunosuppressive Agents
  • Steroids
  • Azathioprine
  • Methylprednisolone