PROMOTING ACCESS TO AFRICAN RESEARCH

Pan African Medical Journal

Log in or Register to get access to full text downloads.

Remember me or Register



Myositis ossificans progressive: case report

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

Abstract


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.

The Pan African Medical Journal 2016;24



http://dx.doi.org/10.11604/pamj.2016.24.264.6670
AJOL African Journals Online