Please use this identifier to cite or link to this item: https://repositorio.ufrn.br/handle/123456789/21203
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dc.contributor.authorSantos, Pedro Paulo de Andrade-
dc.contributor.authorSantos, Bruna Rafaela Martins dos-
dc.contributor.authorFreitas, Valéria Souza-
dc.contributor.authorFreitas, Roseana de Almeida-
dc.contributor.authorSouza, Lélia Batista de-
dc.date.accessioned2016-08-22T12:47:00Z-
dc.date.available2016-08-22T12:47:00Z-
dc.date.issued2012-
dc.identifier.citationSANTOS, Pedro Paulo de Andrade et al. Neurilemmoma of the oral cavity in pediatric patient. RGO. Revista Gaúcha de Odontologia, v. 60, n. 3, p. 381-383, 2012.pt_BR
dc.identifier.urihttps://repositorio.ufrn.br/jspui/handle/123456789/21203-
dc.languageengpt_BR
dc.rightsAcesso Abertopt_BR
dc.subjectMouthpt_BR
dc.subjectNeurilemmomapt_BR
dc.subjectPediatricspt_BR
dc.titleNeurilemmoma of the oral cavity in pediatric patientpt_BR
dc.title.alternativeNeurilemoma em cavidade oral acometendo paciente pediátricopt_BR
dc.typearticlept_BR
dc.description.resumoNeurilemmomas arising from Schwann cells, rarely found in oral cavity, are characterized by solitary occurrence, slow growth and smooth surface with variable clinical aspects, depending on the nerve origin. Most instances are typically asymptomatic. Microscopically, the histopathological characteristic consists of alternating regions of hypercellularity and hypocellularity such as Antoni A and Antoni B, respectively. The prognosis is favorable; complete surgical removal is the treatment of choice, no recurrence should be expected. The present report shows the case of neurilemmoma in bucal mucosa, in a 9-year-old child. Patient was referred to the Stomatology Clinic of School of Dentistry, Universidade Federal do Rio Grande do Norte, with complaint of nodular mass, with approximately one year development. Patient was submitted to excisional biopsy, with histopathological exam showing diagnosis of neurilemmoma. After 1 year follow-up there has been no recurrence of lesion.pt_BR
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