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Artículo | IMSEAR | ID: sea-219749

RESUMEN

Desmoidfibromatosisis a rare tumor affectingbone.This tumorhistologically and biologically mimics the extra-abdominal desmoid tumor of soft tissue. This is locally infiltrative and aggressive in nature. The reported incidence ofsuch cases is around 2–4 per million population whichaccountsfor 0.03% of all neoplasms. In maxillofacial region, incidence is less than 3% of all cases. Treatment of such tumors is surgical excision and chances of recurrence are more. Weherebyreport a case of a 23-year-old female patient withdesmoid fibromatosis in the mandibular posterior region.

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