RESUMEN
Myositis ossificans is defined as a self-limiting pseudotumor composed of reactive hypercellular fibrous tissue and bone. USP6 rearrangements have been identified as a consistent genetic driving event in aneurysmal bone cyst and nodular fasciitis. It is therefore an integral part of the diagnostic workup when dealing with (myo)fibroblastic lesions of soft tissue and bone. Two cases of myositis ossificans with USP6 rearrangement were published so far. We determine herein the incidence of USP6 rearrangement in myositis ossificans using USP6 fluorescence in situ hybridization analysis (FISH). Of the 11 cases included, seven patients were female and four were male. Age ranged from 6 to 56â¯years (mean 27â¯years). Lesions were located in the thigh (nâ¯=â¯5), knee (nâ¯=â¯1), lower leg (nâ¯=â¯1), lower arm (nâ¯=â¯1), perineum (nâ¯=â¯1), gluteal (nâ¯=â¯1) and thoracic wall (nâ¯=â¯1). All assessable cases except one (8/9) showed rearrangement of USP6 providing evidence that myositis ossificans is genetically related to nodular fasciitis and aneurysmal bone cyst.