Diffuse idiopathic skeletal hyperostosis (Forestier's disease) - a case report

Authors

  • Ivan Milanov UHATNP "St.Naum"; Medical university – Sofia
  • N. Topalov UHATNP „St. Naum”
  • B. Popivanova UHATNP „St. Naum”
  • A. Shokova UHATNP „St. Naum”

Keywords:

diffuse idiopathic skeletal hyperostosis, Forestier’s disease, dysphagia, fractures of spine

Abstract

The diffuse idiopathic skeletal hyperostosis is a disease predominantly affecting the elderly. It was described for the first time by Forestier as a senile ankylosing spondylosis, and ankylosing hyperostosis. The condition is characterized by specific ossification of the spine without signs of spondyloarthropathy or degenerative spondylosis. Rarely, it can cause dysphagia, dysphonia or stridor. In the late stages of the disease, specific fractures can be seen even after a minimal trauma event.
Even though, the disease is known for ages, it is often unrecognized or misdiagnosed as deforming spondylosis in the clinical practice. This is a clinical case and a review of the clinical features of Forestier’s disease aiming to improve and ease diagnosing.

References

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Published

30.12.2015

How to Cite

Milanov, Ivan, et al. “Diffuse Idiopathic Skeletal Hyperostosis (Forestier’s Disease) - a Case Report ”. Cephalgia, vol. 17, no. 1-2, Dec. 2015, pp. 34-38, https://cephalgia.org/index.php/ce/article/view/40.

Issue

Section

CEPHALGIA