Togral, GurayYildizgoren, Mustafa TurgutArikan, MuratGungor, Safak2024-09-182024-09-1820141937-8688https://doi.org/10.11604/pamj.2014.19.383.5693https://hdl.handle.net/20.500.12483/9457Desmoid tumors are rare, soft-tissue neoplasms that do not metastasize, but exhibit aggressive growth and local invasion. They originate most frequently from abdominal fascial structures, although they can also appear at extra-abdominal sites. The most common extra-abdominal locations include the shoulder, chest wall, back, thigh, and head and neck. In children, desmoid tumors are more infiltrative, having a tendency towards osseous involvement more frequently than in adult patients. We report acase of a supraspinatus muscle desmoid tumor in a female patient with clavicle destruction.eninfo:eu-repo/semantics/openAccessDesmoid tumorclavicleshoulderArticle1910.11604/pamj.2014.19.383.5693259957792-s2.0-84938857207Q2WOS:000216550200002N/A