Abstract
Myositis ossificans (MO) is a benign condition characterized by heterotopic bone formation in soft tissues, predominantly muscles, and consists of posttraumatic (75%), nontraumatic, and congenital subtypes. Risk factors include traumatic brain injury and prolonged mechanical ventilation. The condition is caused by a dysregulation of local stem cells in response to tissue injury, leading to an inappropriate differentiation of fibroblasts into osteogenic cells. Posttraumatic MO is a benign and self-limiting condition, which progresses through parallel clinical, histopathologic, and radiographic stages, the three commonly described overlapping stages of evolution being early, intermediate, and mature. This chapter describes and illustrates the clinical characteristics, stages, and imaging findings of MO on X-ray, bone SPECT/CT, and MR.
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Bhure, U., Hany, T.F., Strobel, K. (2023). Myositis Ossificans. In: Van den Wyngaert, T., Gnanasegaran, G., Strobel, K. (eds) Clinical Atlas of Bone SPECT/CT. Springer, Cham. https://doi.org/10.1007/978-3-031-26449-8_265
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DOI: https://doi.org/10.1007/978-3-031-26449-8_265
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