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J Neurol Neurosurg Psychiatry 2006;77:290-295 doi:10.1136/jnnp.2005.075861
  • Review

Demyelination in rheumatic diseases

  1. A Theodoridou,
  2. L Settas
  1. Rheumatology Unit of the 1st Internal Medicine Department, AHEPA University Hospital, Thessaloniki, Greece
  1. Correspondence to:
 Athina Theodoridou
 Rheumatology Unit of the 1st Internal Medicine department, AHEPA University Hospital, 54006 Thessaloniki, Greece; atheodori{at}yahoo.gr
  • Received 17 July 2005
  • Accepted 17 October 2005
  • Revised 10 October 2005

Abstract

Multiple sclerosis (MS) is a chronic inflammatory disease of the central nervous system (CNS) characterised by multifocal areas of demyelination in the white matter of the brain and spinal cord. Autoantibodies, for example antinuclear antibodies, can also be present. MS and other demyelinating processes, such as transverse myelitis and optic neuritis (which may be clinically isolated cases or be part of the clinical spectrum of MS), are sometimes difficult to differentiate from CNS involvement in systemic autoimmune diseases like systemic lupus erythematosus (SLE), antiphospholipid syndrome (APS), Sjoegren’s syndrome (SS), and Adamantiades-Behcet disease (BD). An acute isolated neurological syndrome presents the biggest diagnostic problem, since it is common in MS, but can also be the only feature or first manifestation in SLE, APS, SS, and BD. Indeed, the clinical presentation and lesions evidenced by magnetic resonance imaging may be similar.

Footnotes

  • Competing interests: none declared

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