Gingival neurofibroma in a neurofibromatosis type 1 patient.
作者
José Antonio García-de Marcos,Alicia Dean Ferrer,Alamillos Granados F,Juan José Ruiz Masera,García de Marcos Mj,Alfredo Vidal Jiménez,Borja Valenzuela Salas,Ana García Lainez
出处
期刊:PubMed [National Institutes of Health] 日期:2007-08-01卷期号:12 (4): E287-91被引量:34
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 (cafe 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.