[Pachydermoperiostosis. A case report]

Rev Med Interne. 2006 Sep;27(9):710-2. doi: 10.1016/j.revmed.2006.04.019. Epub 2006 Jun 5.
[Article in French]

Abstract

Introduction: The pachydermoperiostosis (PDP) or primitive hypertrophic osteoarthropathy (HOA) is a rare hereditary disease.

Case record: We report a 22-year-old man born to consanguineous marriage who presented presented with PDP. This patient disclosed an arthropathy, a clubbing, a diffuse periostosis, and a pachyderma of the hands, the feet and the forehead. All the examinations that were performed to look for an etiology remained negative. Diagnosis of PDP was considered and the patient treated with colchicine.

Discussion: We discuss the diagnostic issues raised by PDP, especially with the secondary HOA and chronic inflammatory rheumatisms.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Colchicine / administration & dosage
  • Colchicine / therapeutic use
  • Gout Suppressants / administration & dosage
  • Gout Suppressants / therapeutic use
  • Humans
  • Male
  • Osteoarthropathy, Primary Hypertrophic* / diagnosis
  • Osteoarthropathy, Primary Hypertrophic* / diagnostic imaging
  • Osteoarthropathy, Primary Hypertrophic* / drug therapy
  • Radiography

Substances

  • Gout Suppressants
  • Colchicine