The Pan African Medical Journal (Jul 2016)

Myositis ossificans progressive: case report

  • Sofia Talbi,
  • Nassira Aradoini,
  • Iman El Mezouar,
  • Fatima Ezzahra Abourazzak,
  • Taoufik Harzy

DOI
https://doi.org/10.11604/pamj.2016.24.264.6670
Journal volume & issue
Vol. 24, no. 264

Abstract

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Myositis ossificansprogressiva (MOP) is an autosomal dominant disorder. There is a progressive ectopic ossification and skeletal malformation, mainly in the connective tissue of muscle. The diagnosis is based on the clinical findings and radiological demonstration of the skeletal malformations. A 38-year-old female patient was admitted to our department with progressive increase of the thigh. Results of laboratory studies were normal . The radiography of the right thigh showed multiple intramuscular calcifications. Myositis ossificansprogressiva should be diagnosed as early as possible and non-invasively, based upon history, clinical and radiological findings. Early and correct diagnosis is fundamental for indication of proper management of the disease. Key words: myositis ossificans progressive, ossification, ectopic bone.

Keywords