Pathophysiology and medical treatment of pain in fibrous dysplasia of bone

Orphanet J Rare Dis. 2012 May 24;7 Suppl 1(Suppl 1):S3. doi: 10.1186/1750-1172-7-S1-S3. Epub 2012 May 24.

Abstract

One of the most common complications of fibrous dysplasia of bone (FD) is bone pain. Usual pain killers are often of inadequate efficacy to control this bone pain. The mechanism of bone pain in FD remains uncertain, but by analogy with bone tumors one may consider that ectopic sprouting and formation of neuroma-like structures by sensory and sympathetic nerve fibers also occur in the dysplastic skeleton. Bone pain has been reported in up to 81% of adults and 49% of children. It affects predominantly the lower limbs and the spine. The degree of pain is highly variable and adults reports more pain than children. Bisphosphonates have been shown to reduce bone pain in uncontrolled studies. Their influence on bone strength remains unknown. In a randomized trial testing alendronate, bone pain was not significantly improved. Another trial assessing the effect of risedronate is ongoing. Possible future therapies include tocilizumab, denosumab and drugs targeting nerve growth factor and its receptor TrkA.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Alendronate / pharmacology
  • Antibodies, Monoclonal, Humanized / pharmacology
  • Bone Neoplasms / physiopathology
  • Bone and Bones / innervation
  • Bone and Bones / physiopathology
  • Fibrous Dysplasia of Bone / drug therapy
  • Fibrous Dysplasia of Bone / physiopathology*
  • Humans
  • Nerve Fibers / pathology
  • Pain / drug therapy*
  • Pain / physiopathology*
  • Pain Management / methods*
  • Pain Measurement / methods
  • Self Report
  • Sensory Receptor Cells / pathology

Substances

  • Antibodies, Monoclonal, Humanized
  • tocilizumab
  • Alendronate