[Sneddon syndrome with anti-mitochondrial type M5 antibodies]

Presse Med. 2005 Aug 27;34(14):1011-2. doi: 10.1016/s0755-4982(05)84103-x.
[Article in French]

Abstract

Introduction: Antimitochondrial type M5 antibodies (AMA-M5) are among the immunological abnormalities associated with Sneddon syndrome.

Case: A 45 year-old woman, hospitalized for diplopia and with a 20-year history of obstetrical accidents, internuclear ophthalmoplegia and livedo, was diagnosed with Sneddon syndrome associated with primary antiphospholipid syndrome (APS) aggravated by the presence of AMA-M5.

Discussion: AMA-M5 are immunological markers of APS to the same extent as antiphospholipid antibodies. This case demonstrates the interest of screening for AMA-M5 in cases of strong clinical suspicion of APS when the anticoagulant lupus test is normal and no anti-cardiolipin, anti-b2 glycoprotein I or antiprothrombin antibodies are found.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Antiphospholipid Syndrome / complications*
  • Antiphospholipid Syndrome / diagnosis
  • Antiphospholipid Syndrome / immunology
  • Autoantibodies / immunology*
  • Diagnosis, Differential
  • Female
  • Humans
  • Middle Aged
  • Mitochondria / immunology*
  • Sneddon Syndrome / complications*
  • Sneddon Syndrome / diagnosis

Substances

  • Autoantibodies