Central nervous system aquaporin-4 autoimmunity presenting with an isolated cerebral abnormality

Mult Scler. 2012 Sep;18(9):1340-3. doi: 10.1177/1352458512441271. Epub 2012 Jul 3.

Abstract

Advances in the understanding of central nervous system aquarporin-4 autoimmunity have promoted the recognition of diverse clinical presentations beyond the traditional view of neuromyelitis optica. We describe a patient who developed hemiparesis caused by an extensive cerebral lesion as an initial manifestation of central nervous system aquarporin-4 autoimmunity. Although the patient had no history of optic neuritis or myelitis, not only was serum anti-aquarporin-4 antibody positive, but an imaging, treatment response and histopathological features also revealed characteristic findings suggestive of central nervous system aquarporin-4 autoimmunity. The present case highlights the importance of a comprehensive evaluation for anti-aquarporin-4 antibody even in patients presenting with isolated cerebral lesions.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aquaporin 4 / immunology*
  • Autoantibodies / blood*
  • Autoimmunity*
  • Biopsy
  • Brain / immunology*
  • Brain / pathology*
  • Disability Evaluation
  • Disease Progression
  • Female
  • Humans
  • Immunohistochemistry
  • Magnetic Resonance Imaging
  • Middle Aged
  • Neuromyelitis Optica / complications
  • Neuromyelitis Optica / diagnosis
  • Neuromyelitis Optica / immunology*
  • Neuromyelitis Optica / pathology
  • Neuromyelitis Optica / therapy
  • Paresis / etiology
  • Predictive Value of Tests
  • Prognosis

Substances

  • AQP4 protein, human
  • Aquaporin 4
  • Autoantibodies