dc.contributorHosp Novo Julho
dc.contributorSanta Casa Misericordia Juiz Fora
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:30:37Z
dc.date.accessioned2022-10-05T17:00:09Z
dc.date.available2014-05-20T15:30:37Z
dc.date.available2022-10-05T17:00:09Z
dc.date.created2014-05-20T15:30:37Z
dc.date.issued2009-03-01
dc.identifierInternational Journal of Oral and Maxillofacial Surgery. Edinburgh: Churchill Livingstone, v. 38, n. 3, p. 289-292, 2009.
dc.identifier0901-5027
dc.identifierhttp://hdl.handle.net/11449/39947
dc.identifier10.1016/j.ijom.2008.11.025
dc.identifierWOS:000264629000016
dc.identifier7595315660858413
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3910988
dc.description.abstractThis paper reports one case, of an ameloblastic fibro-odontosarcoma (AFOS) affecting the mandible, in a 12-year-old girl. This neoplasm is a rare odontogenic neoplasm. To the authors' knowledge this is the fifteenth case of AFOS reported in English. The patient's chief complaint was a swelling in the face For 6 months. An incisional biopsy was performed diagnosing the case as all ameloblastic fibroma. After radiography ameloblastic fibro-odontoma was diagnosed. Computed tomography was performed and a stereolithography model made to plan the surgical procedures. A hemimandibulectomy followed by a vascularized fibular flap was then proposed. The surgery was uneventful. Microscopic features diagnosed an AFOS. After 23 months of close follow-up there is no sign of recurrence or metastasis. Dental implants were recently placed in the fibular flap.
dc.languageeng
dc.publisherChurchill Livingstone
dc.relationInternational Journal of Oral and Maxillofacial Surgery
dc.relation2.164
dc.relation1,137
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectameloblastic fibro-odontosarcoma
dc.subjecthemimandibulectomy
dc.subjectreconstruction
dc.subjectfibula
dc.subjectstereolithography
dc.titleAmeloblastic fibro-odontosarcoma: a case report
dc.typeArtigo


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