Myositis Ossificans Progressiva in the Whole Spine: A Case Report
Myositis ossificans progressiva is a rare inherited disease characterized by progressive ectopic ossifications associated with thumb and big toe anomalies. Ossification usually progresses from central to the peripheral, proximal to distal, cranial to caudal, and from dorsal to ventral directions and leading to activity limitation, significant eating disability, recurrent pulmonary infection, and atelectasis. In this report, we present a 7-year-old boy with a total spine stiffness (wooden spine) seriously limited his activity of daily living.
Abdallah A, Gokcedag A, Ofluoglu AE, Emel E. Non-traumatic myositis ossificans in the lumbar spine. Am J Case Rep 2014;15:421-5.
Connor JM, Evans DA. Fibrodysplasia ossificans progressiva: the clinical features and natural history of 34 patients. J Bone Joint Surg 1982;64B:76-83.
Al-Salmi I, Raniga S, Hadidi AA. Fibrodysplasia ossificans progressiva - radiological findings: a case report. Oman Med J 2014;29:368-70.
Pignolo RJ, Shore EM, Kaplan FS. Fibrodysplasia ossificans progressiva: diagnosis, management, and therapeutic horizons. Pediatr Endocrinol Rev 2013;10:437-48.
Lutwak L. Myositis ossificans progressiva. Mineral, metabolic and radioactive calcium studies of the effects of hormones. Am J Med 1964;37:269-93.
Talbi S, Aradoini N, Mezouar IE, Abourazzak FE, Harzy T. Myositis ossificans progressive: case report. Pan Afr Med J 2016;24:264.
Illingworth RS. Myositis ossificans progressiva (Munchmeyer's disease). Brief review with report of two cases treated with corticosteroids and observed for 16 years. Arch Dis Child 1971;46:264-8.
|Issue||Vol 56, No 2 (2018)|
|Myositis ossificans Heterotopic ossification Paraspinal muscles|
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