A rare case of metabolic bone disease

Ann Clin Biochem. 2007 Mar;44(Pt 2):192-5. doi: 10.1258/000456307780118145.

Abstract

A 26-year-old female overseas student was admitted to hospital with a fracture of her left humerus following minimal trauma. Biochemical abnormalities included hypercalcaemia, hypophosphataemia, raised alkaline phosphatase, raised parathyroid hormone and undetectable 25-hydroxy-vitamin D. Skeletal X-rays revealed multiple osteolytic lesions in the humerus as well as similar lesions in the femora and pelvis. Magnetic resonance imaging of her left shoulder showed a large soft tissue mass in the proximal humerus. Bone biopsy was reported as consistent with a brown tumour of primary hyperparathyroidism and a sestamibi scan confirmed the presence of a parathyroid adenoma. However, the isotope bone scan was reported as showing features typical of fibrous dysplasia involving multiple sites. The patient subsequently fractured her right femoral shaft, and a femoral nail was inserted. Parathyroidectomy was performed at the same time. Postoperatively she exhibited increased calcium and vitamin D requirements. Coexistence of primary hyperparathyroidism and polyostotic fibrous dysplasia is very rare.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Bone Diseases, Metabolic / diagnosis*
  • Bone and Bones / metabolism
  • Bone and Bones / pathology*
  • Diagnosis, Differential
  • Female
  • Fibrous Dysplasia, Polyostotic / diagnosis*
  • Fibrous Dysplasia, Polyostotic / metabolism
  • Humans
  • Hyperparathyroidism / diagnosis*
  • Magnetic Resonance Imaging