Type 1 Neurofibromatosis and effects on the stomatognatic system

Detalhes bibliográficos
Autor(a) principal: Noronha, Anariely
Data de Publicação: 2018
Outros Autores: Cardoso, Inês Lopes
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10284/8595
Resumo: Neurofibromatosis is a systemic hereditary disorder that mainly affects the skin and nervous system. It was identified for the first time by Friedrich Von Recklinghausen, being called the Von Recklinghausen syndrome. Some of the clinical symptoms can be visible since birth, however, most of them start to show up during childhood and adolescence and, in women, phenotype becomes evident during pregnancy, due to the severe hormonal changes that occur. The goal of this research was to understand the way type I neurofibromatosis can affect the oral cavity and how the dental doctor can help. For that, several papers were selected from the search on the websites Pubmed, Elsevier and UptoDate using the following keywords: neurofibromatosis, oral health, neurofibroma, oral cancer, GTP, type 1 neurofibromatosis. Concerning clinical features at the oral cavity, more than one fourth of patients with this disorder can show neurofibromas in the mouth, usually isolated. Phenotype can include increased fungiform papillae, head and neck polyps, nodules in the posterior portion of the back of the tongue, dental mobility caused by lesions in the gingival-dental-alveolar complex, changes in the number of teeth, molar retention, dental calculus, aplasia of the second bottom molars and advanced periodontal disease. Bone changes can be present like subperiosteal erosion, hyperplasia, hypoplasia, dysplasia in the wings of the sphenoid and short size. Concerning therapeutic strategies, some studies suggest that proteins of the mTOR pathway (mammalian target of rapamycin) can be the target for therapy of this disease in case of malignant transformation.
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spelling Type 1 Neurofibromatosis and effects on the stomatognatic systemNeurofibromatosisOral healthNeurofibromaOral cancerType 1 NeurofibromatosisNeurofibromatosis is a systemic hereditary disorder that mainly affects the skin and nervous system. It was identified for the first time by Friedrich Von Recklinghausen, being called the Von Recklinghausen syndrome. Some of the clinical symptoms can be visible since birth, however, most of them start to show up during childhood and adolescence and, in women, phenotype becomes evident during pregnancy, due to the severe hormonal changes that occur. The goal of this research was to understand the way type I neurofibromatosis can affect the oral cavity and how the dental doctor can help. For that, several papers were selected from the search on the websites Pubmed, Elsevier and UptoDate using the following keywords: neurofibromatosis, oral health, neurofibroma, oral cancer, GTP, type 1 neurofibromatosis. Concerning clinical features at the oral cavity, more than one fourth of patients with this disorder can show neurofibromas in the mouth, usually isolated. Phenotype can include increased fungiform papillae, head and neck polyps, nodules in the posterior portion of the back of the tongue, dental mobility caused by lesions in the gingival-dental-alveolar complex, changes in the number of teeth, molar retention, dental calculus, aplasia of the second bottom molars and advanced periodontal disease. Bone changes can be present like subperiosteal erosion, hyperplasia, hypoplasia, dysplasia in the wings of the sphenoid and short size. Concerning therapeutic strategies, some studies suggest that proteins of the mTOR pathway (mammalian target of rapamycin) can be the target for therapy of this disease in case of malignant transformation.Repositório Institucional da Universidade Fernando PessoaNoronha, AnarielyCardoso, Inês Lopes2020-03-03T12:38:37Z2020-02-28T16:15:27Z2018-01-01T00:00:00Z2018-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10284/8595eng2349-0748cv-prod-36872210.15520/jmbas.v6i4.107info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-09-06T02:07:58Zoai:bdigital.ufp.pt:10284/8595Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T15:45:28.504276Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Type 1 Neurofibromatosis and effects on the stomatognatic system
title Type 1 Neurofibromatosis and effects on the stomatognatic system
spellingShingle Type 1 Neurofibromatosis and effects on the stomatognatic system
Noronha, Anariely
Neurofibromatosis
Oral health
Neurofibroma
Oral cancer
Type 1 Neurofibromatosis
title_short Type 1 Neurofibromatosis and effects on the stomatognatic system
title_full Type 1 Neurofibromatosis and effects on the stomatognatic system
title_fullStr Type 1 Neurofibromatosis and effects on the stomatognatic system
title_full_unstemmed Type 1 Neurofibromatosis and effects on the stomatognatic system
title_sort Type 1 Neurofibromatosis and effects on the stomatognatic system
author Noronha, Anariely
author_facet Noronha, Anariely
Cardoso, Inês Lopes
author_role author
author2 Cardoso, Inês Lopes
author2_role author
dc.contributor.none.fl_str_mv Repositório Institucional da Universidade Fernando Pessoa
dc.contributor.author.fl_str_mv Noronha, Anariely
Cardoso, Inês Lopes
dc.subject.por.fl_str_mv Neurofibromatosis
Oral health
Neurofibroma
Oral cancer
Type 1 Neurofibromatosis
topic Neurofibromatosis
Oral health
Neurofibroma
Oral cancer
Type 1 Neurofibromatosis
description Neurofibromatosis is a systemic hereditary disorder that mainly affects the skin and nervous system. It was identified for the first time by Friedrich Von Recklinghausen, being called the Von Recklinghausen syndrome. Some of the clinical symptoms can be visible since birth, however, most of them start to show up during childhood and adolescence and, in women, phenotype becomes evident during pregnancy, due to the severe hormonal changes that occur. The goal of this research was to understand the way type I neurofibromatosis can affect the oral cavity and how the dental doctor can help. For that, several papers were selected from the search on the websites Pubmed, Elsevier and UptoDate using the following keywords: neurofibromatosis, oral health, neurofibroma, oral cancer, GTP, type 1 neurofibromatosis. Concerning clinical features at the oral cavity, more than one fourth of patients with this disorder can show neurofibromas in the mouth, usually isolated. Phenotype can include increased fungiform papillae, head and neck polyps, nodules in the posterior portion of the back of the tongue, dental mobility caused by lesions in the gingival-dental-alveolar complex, changes in the number of teeth, molar retention, dental calculus, aplasia of the second bottom molars and advanced periodontal disease. Bone changes can be present like subperiosteal erosion, hyperplasia, hypoplasia, dysplasia in the wings of the sphenoid and short size. Concerning therapeutic strategies, some studies suggest that proteins of the mTOR pathway (mammalian target of rapamycin) can be the target for therapy of this disease in case of malignant transformation.
publishDate 2018
dc.date.none.fl_str_mv 2018-01-01T00:00:00Z
2018-01-01T00:00:00Z
2020-03-03T12:38:37Z
2020-02-28T16:15:27Z
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