Type 1 Neurofibromatosis and effects on the stomatognatic system
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | |
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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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 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
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publishedVersion |
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http://hdl.handle.net/10284/8595 |
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http://hdl.handle.net/10284/8595 |
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eng |
language |
eng |
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2349-0748 cv-prod-368722 10.15520/jmbas.v6i4.107 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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application/pdf |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1817553544216051712 |