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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 |