Clinicopathologic analysis of 7 cases of oral schwannoma and review of the literature?

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dc.contributor.authorSantos, Pedro Paulo de Andrade
dc.contributor.authorFreitas, Valéria Souza
dc.contributor.authorPinto, Leão Pereira
dc.contributor.authorFreitas, Roseana de Almeida
dc.contributor.authorSouza, Lelia Batista de
dc.date.accessioned2017-01-30T11:47:32Z
dc.date.available2017-01-30T11:47:32Z
dc.date.issued2010
dc.description.resumoSchwannomas, also known as neurilemmomas, are uncommon neoplasms apparently derived from Schwann cells. The growth of these tumors causes displacement and compression of the nerve of origin. Schwannomas are usually solitary lesions but can be multiple when associated with neurofibromatosis. Anti-S100 protein is the most widely used antibody for the identification of this neoplasm. Surgical excision is the treatment of choice for schwannomas, with few and controversial reports of recurrence or malignant transformation. The present article reports 7 additional cases of oral schwannoma, and the literature is reviewed regarding clinicopathologic features, immunohistochemical findings, differential diagnosis, and therapeutic management of this benign neural tumor.pt_BR
dc.identifier.citationSANTOS, Pedro Paulo de Andrade et al. Clinicopathologic analysis of 7 cases of oral schwannoma and review of the literature?. Annals of Diagnostic Pathology, v. 14, n. 4, p. 235-239, 2010.pt_BR
dc.identifier.urihttps://repositorio.ufrn.br/jspui/handle/123456789/21786
dc.languageengpt_BR
dc.rightsAcesso Abertopt_BR
dc.subjectNeurilemmomapt_BR
dc.subjectSchwannomapt_BR
dc.subjectNeural tumorpt_BR
dc.subjectBenign tumorpt_BR
dc.titleClinicopathologic analysis of 7 cases of oral schwannoma and review of the literature?pt_BR
dc.typearticlept_BR

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