A case of Ollier disease with non-small cell lung cancer and review of the literature

Rheumatol Int. 2010 Mar;30(5):699-703. doi: 10.1007/s00296-009-0983-7. Epub 2009 Jun 6.

Abstract

Ollier disease is a rare, non-hereditary mesodermal dysphasia, characterized by multiple enchondromas, which demonstrate asymmetric involvement of the metaphyses of the long bones. Many malignancies, especially chondrosarcomas, may be observed in association with this disease. The clinical and radiologic characteristics of a case involving a 44-year-old male patient with non-small cell lung cancer are presented together with the clinical characteristics of other cases reported in the literature.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adolescent
  • Adult
  • Amputation, Surgical
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Arthralgia / etiology
  • Biopsy
  • Bone Neoplasms / diagnosis
  • Bone Neoplasms / etiology
  • Bone Neoplasms / secondary*
  • Bone and Bones / diagnostic imaging
  • Bone and Bones / pathology
  • Carcinoma, Non-Small-Cell Lung / diagnosis
  • Carcinoma, Non-Small-Cell Lung / etiology
  • Carcinoma, Non-Small-Cell Lung / secondary*
  • Carcinoma, Non-Small-Cell Lung / therapy
  • Child
  • Enchondromatosis / complications
  • Enchondromatosis / diagnosis*
  • Enchondromatosis / therapy
  • Fatigue / etiology
  • Female
  • Humans
  • Lung Neoplasms / diagnosis
  • Lung Neoplasms / etiology
  • Lung Neoplasms / pathology*
  • Lung Neoplasms / therapy
  • Male
  • Tomography, X-Ray Computed
  • Young Adult

Substances

  • Anti-Inflammatory Agents, Non-Steroidal