Systemic sclerosis with sarcoidosis: case report and review of the published work

J Dermatol. 2014 May;41(5):421-3. doi: 10.1111/1346-8138.12438. Epub 2014 Mar 12.

Abstract

Sarcoidosis and systemic sclerosis (SSc) rarely coexist. Here, we report a Japanese female SSc patient who developed systemic sarcoidosis. Her SSc was a limited type negative for anti-Scl-70 antibody and positive for anticentromere antibody (ACA). Moreover, we performed a review of the English-language published work that described cases of concurrent SSc and sarcoidosis. Then, we found that most SSc and sarcoidosis concurrent patients positive for anti-Scl-70 antibody were male (77.8%). On the other hand, most patients positive for ACA were female (87.5%). These results suggest some relationships between autoantibody profiles and sex in SSc and sarcoidosis concurrence.

Keywords: autoantibody; concurrent; sarcoidosis; sex; systemic sclerosis.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Antibodies, Antinuclear / blood
  • DNA Topoisomerases, Type I
  • Female
  • Humans
  • Male
  • Middle Aged
  • Nuclear Proteins / immunology
  • Sarcoidosis / complications*
  • Sarcoidosis / immunology
  • Scleroderma, Systemic / complications*
  • Scleroderma, Systemic / immunology
  • Sex Characteristics

Substances

  • Antibodies, Antinuclear
  • Nuclear Proteins
  • Scl 70 antigen, human
  • anticentromere antibody
  • DNA Topoisomerases, Type I