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Gingival neurofibroma in a neurofibromatosis type 1 patient : case report

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Gingival neurofibroma in a neurofibromatosis type 1 patient : case report

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dc.contributor.author García de Marcos, J.A. es
dc.contributor.author Dean Ferrer, Alicia es
dc.contributor.author Alamillos Granados, Francisco es
dc.contributor.author Ruiz Masera, J.J. es
dc.contributor.author García de Marcos, M.J. es
dc.contributor.author Vidal Jiménez, A. es
dc.contributor.author Valenzuela Salas, B. es
dc.contributor.author García Lainez, Ana es
dc.date.accessioned 2017-11-21T13:44:26Z
dc.date.available 2017-11-21T13:44:26Z
dc.date.issued 2007 es
dc.identifier.citation García de Marcos, J.A. ; Dean Ferrer, Alicia ; Alamillos Granados, Francisco ; Ruiz Masera, J.J. ; García de Marcos, M.J. ; Vidal Jiménez, A. ; Valenzuela Salas, B. ; García Lainez, Ana. Gingival neurofibroma in a neurofibromatosis type 1 patient : case report. En: Medicina oral, patología oral y cirugía bucal. Ed. inglesa, 12 4 2007: 5- es
dc.identifier.uri http://hdl.handle.net/10550/63212
dc.description.abstract Neurofibroma is a benign peripheral nerve sheath tumour. It is one of the most frequent tumours of neural origin and its presence is one of the clinical criteria for the diagnosis of type 1 neurofibromatosis (NF-I). Neurofibromatosis type 1 is an autosomal dominantly inherited disease due to an alteration in the long arm of chromosome 17. About 50% of NF-I patients have no family history of the disease. NF-I patients have skin lesions (café au lait spots and neurofibromas) as well as bone malformations and central nervous system tumours. Diagnosis is based on a series of clinical criteria. Gingival neurofibroma in NF-I is uncommon. Treatment of neurofibromas is surgical resection. The aim of this paper is to report a case of NF-I with gingival involvement and to review the literature. es
dc.title Gingival neurofibroma in a neurofibromatosis type 1 patient : case report es
dc.type journal article es_ES
dc.subject.unesco UNESCO::CIENCIAS MÉDICAS es
dc.identifier.doi es
dc.type.hasVersion VoR es_ES

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