1.
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.
2.
West Indian med. j
; 34(3): 167-71, Sept. 1985. tab
Artículo
en Inglés
| LILACS
| ID: lil-32192