[PM-Scl antibody positive systemic sclerosis associated with inclusion-body myositis]

Z Rheumatol. 2005 Oct;64(7):499-502. doi: 10.1007/s00393-005-0664-1.
[Article in German]

Abstract

We describe a 72- year-old patient with a ten year history of anti-PM-Scl positive systemic sclerosis associated with inclusion-body myositis. While the association of dermatomyositis and polymyositis with anti-PM-Scl positive systemic sclerosis is frequently reported, inclusion-body myositis was, to the best of our knowledge, only previously described once in association with anti-PM-Scl-positive systemic sclerosis. The distinction between inclusion-body myositis and other forms of inflammatory myopathy, like the histopathologically well distinguishable polymyositis or dermatomyositis, is relevant because of the poor response of inclusion- body myositis to immunosuppressive treatment. Our case underlines that in patients with anti-PM-Scl-positive systemic sclerosis and treatment resistant progressive myopathy the diagnosis of inclusion body myositis should be considered.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Aged
  • Autoantigens / blood*
  • Autoantigens / immunology
  • Biomarkers / blood
  • Diagnosis, Differential
  • Exoribonucleases
  • Exosome Multienzyme Ribonuclease Complex
  • Female
  • Humans
  • Myositis, Inclusion Body / blood*
  • Myositis, Inclusion Body / complications
  • Myositis, Inclusion Body / diagnosis*
  • Myositis, Inclusion Body / immunology
  • Scleroderma, Systemic / blood*
  • Scleroderma, Systemic / complications
  • Scleroderma, Systemic / diagnosis*
  • Scleroderma, Systemic / immunology

Substances

  • Autoantigens
  • Biomarkers
  • Exoribonucleases
  • Exosome Multienzyme Ribonuclease Complex
  • EXOSC10 protein, human