[Relapsing polychondritis, interstitial granulomatous dermatitis and antiphospholipid syndrome: an unusual clinical association]

Acta Reumatol Port. 2011 Jul-Sep;36(3):292-7.
[Article in Portuguese]

Abstract

The authors describe the case of a 49 year-old male patient with a 3-year history of antiphospholipid syndrome, admitted after presenting in the emergency room with erythematous nodular skin lesions, affecting the face and neck, with a week's duration. Local biopsies were suggestive of interstitial granulomatous dermatitis. The patient described lesions compatible with bilateral auricular chondritis, two weeks prior to the appearance of the nodules, which resolved spontaneously after 3 days. There was a previous episode of nasal chondritis, two years previously, and another episode starting at the 7th day of hospitalization. These findings, taken together with a diagnosis of seronegative polyarthritis established 5 years before the current events, lead to a diagnosis of relapsing polychondritis.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Antiphospholipid Syndrome / complications*
  • Antiphospholipid Syndrome / diagnosis
  • Dermatitis / complications*
  • Dermatitis / diagnosis
  • Granuloma / complications
  • Granuloma / diagnosis
  • Humans
  • Male
  • Middle Aged
  • Polychondritis, Relapsing / complications*
  • Polychondritis, Relapsing / diagnosis