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Use este identificador para citar o ir al link de este elemento: http://hdl.handle.net/1843/78740
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Campo DCValorIdioma
dc.creatorBruno Ramos Chrcanovicpt_BR
dc.creatorPeter A. Brennanpt_BR
dc.creatorSiavash Rahimipt_BR
dc.creatorRicardo Santiago Gomezpt_BR
dc.date.accessioned2024-12-17T20:19:03Z-
dc.date.available2024-12-17T20:19:03Z-
dc.date.issued2018-04-
dc.citation.volume47pt_BR
dc.citation.issue4pt_BR
dc.citation.spage315pt_BR
dc.citation.epage325pt_BR
dc.identifier.doihttps://doi.org/10.1111/jop.12622pt_BR
dc.identifier.issn1600-0714pt_BR
dc.identifier.urihttp://hdl.handle.net/1843/78740-
dc.description.resumoPurpose: To integrate the available data published to date on ameloblastic fibromas (AF) and ameloblastic fibrosarcomas (AFS) into a comprehensive analysis of their clinical/radiological features. Methods: An electronic search was undertaken in July 2017. Eligibility criteria included publications having enough clinical, radiological and histological information to confirm a definite diagnosis. Results: A total of 244 publications (279 central AF tumours, 10 peripheral AF, 103 AFS) were included. AF and AFS differed significantly with regard to the occurrence of patients' mean age, bone expansion, cortical bone perforation and lesion size. Recurrence rates were as follows: central AF (19.2%), peripheral AF (12.5%), AFS (all lesions, 35%), primary (de novo) AFS (28.8%) and secondary AFS (occurring after an AF, 50%). Larger lesions and older patients were more often treated by surgical resections for central AF. Segmental resection resulted in the lowest rate of recurrence for most of the lesion types. AFS treated by segmental resection had a 70.5% lower probability to recur (OR 0.295; P = .049) than marginal resection; 21.3% of the AFS patients died due to complications related to the lesion. Conclusions: Very long follow-up is recommended for AF lesions, due to the risk of recurrence and malignant change into AFS. Segmental resection is the most recommended therapy for AFS.pt_BR
dc.format.mimetypepdfpt_BR
dc.languageengpt_BR
dc.publisherUniversidade Federal de Minas Geraispt_BR
dc.publisher.countryBrasilpt_BR
dc.publisher.departmentFAO - DEPARTAMENTO DE CLÍNICApt_BR
dc.publisher.initialsUFMGpt_BR
dc.relation.ispartofJournal of Oral Pathology & Medicinept_BR
dc.rightsAcesso Restritopt_BR
dc.subjectAmeloblastic fibromapt_BR
dc.subjectAmeloblastic fibrosarcomapt_BR
dc.subjectClinical featurespt_BR
dc.subjectOdontogenic tumourspt_BR
dc.subjectRecurrence ratept_BR
dc.subject.otherMargins of excisionpt_BR
dc.subject.otherRecurrencept_BR
dc.subject.otherClinical studypt_BR
dc.subject.otherRadiologypt_BR
dc.subject.otherProbabilitypt_BR
dc.subject.otherWounds and injuriespt_BR
dc.titleAmeloblastic fibroma and ameloblastic fibrosarcoma: a systematic reviewpt_BR
dc.typeArtigo de Periódicopt_BR
dc.url.externahttps://onlinelibrary.wiley.com/doi/10.1111/jop.12622pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0002-3460-3374pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0003-4804-3264pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0002-8282-1480pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0001-8770-8009pt_BR
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