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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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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
Aquest document és un/a article, creat/da en: 2007

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.
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