Analysis of the prevalence of von Hippel-Lindau Syndrome in patients with hemangioblastomas of the Central Nervous System

Detalhes bibliográficos
Autor(a) principal: Fonseca, Gustavo Soares Gomes Barros
Data de Publicação: 2022
Outros Autores: Freire, Vivianne Maria Laranjeiras Monte, Bonfim, Lais Lima, Penha, Elana Cristina da Silva, Guimarães, João Victor Araújo, Pereira, Raphael Erick Lima, Macedo, Gabriel de Sousa, Britto, Filipe Augusto Lopes Cajubá de, Murad, Letícia Muniz de Abreu, Brito, Alessandra do Rosário, Reis, Lara Letícia Teixeira, Santos, Amanda Cordeiro, Mesquita Neto, Agostinho Rodrigues, Prazeres, Julianne Souza, Cunha, Luiza Mariana Batista Lima, Maia, Ana Vitória Feitosa Barroso, Silva, Carolynne Weba da, Borges, Fernando de Abreu, Almeida, Monaliza Brito de, Vieira, Samantha Cunha, Soares, Isabela Coelho Brito, Tapety Sá, Liciana, Pereira, Lucca Adriano, Bezerra, Thalita Martins, Soares, Ivana Mota, Sousa, Rebeca Machado Castro, Coelho, Maria Beatriz Celedonio, Caldeira, Felipe Ramos
Tipo de documento: Artigo
Idioma: por
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/26018
Resumo: Hemangioblastomas (HBs) are benign neoplasms commonly located in the cerebellum and spinal cord and may arise sporadically or related to von Hippel-Lindau Syndrome (VHL). When there is an association with VHL, multifocal tumors may arise, unlike sporadic tumors, which are isolated. VHL is a hereditary disease related to the development of benign and malignant tumors, the most common being central nervous system hemangioblastomas and retinal angiomas. The disease is caused by the inefficacy of the Tumor Suppressor Gene VHL (pVHL) in an allolo on chromosome 3p25-26. The presence of VHL in patients with HBs leads the patient to a worse prognosis, as it facilitates metastatization. Thus, the aim of the following review is to analyze the prevalence of von Hippel-Lindau syndrome in patients with central nervous system (CNS) hemangioblastomas. This is a systematic bibliographic review that used the PubMed, SciELO and Google Scholar platforms as databases for research of scientific articles, with a time frame between 2016 and 2022, in English. According to the search engine, 4 results were found after the exclusion criteria in the PubMed and Google Scholar databases. It was found, therefore, that there is a moderate prevalence of HLV in patients with CNS HBs. Among the studies, the lowest prevalence rate of HlV in patients with HBs was 23%, while the highest rate was approximately 60%, with an overall average of ± 39.2%, when considering all studies involving these patients.
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spelling Analysis of the prevalence of von Hippel-Lindau Syndrome in patients with hemangioblastomas of the Central Nervous SystemAnálisis de la prevalencia del Síndrome de von Hippel-Lindau en pacientes con hemangioblastomas del Sistema Nervioso CentralAnálise da prevalência da Síndrome de von Hippel-Lindau em pacientes portadores de hemangioblastomas do Sistema Nervoso CentralHemangioblastomaVon Hippel-Lindau syndromePrevalence.HemangioblastomaSíndrome de Von Hippel-LindauPrevalencia.HemangioblastomaSíndrome de Von Hippel-LindauPrevalência.Hemangioblastomas (HBs) are benign neoplasms commonly located in the cerebellum and spinal cord and may arise sporadically or related to von Hippel-Lindau Syndrome (VHL). When there is an association with VHL, multifocal tumors may arise, unlike sporadic tumors, which are isolated. VHL is a hereditary disease related to the development of benign and malignant tumors, the most common being central nervous system hemangioblastomas and retinal angiomas. The disease is caused by the inefficacy of the Tumor Suppressor Gene VHL (pVHL) in an allolo on chromosome 3p25-26. The presence of VHL in patients with HBs leads the patient to a worse prognosis, as it facilitates metastatization. Thus, the aim of the following review is to analyze the prevalence of von Hippel-Lindau syndrome in patients with central nervous system (CNS) hemangioblastomas. This is a systematic bibliographic review that used the PubMed, SciELO and Google Scholar platforms as databases for research of scientific articles, with a time frame between 2016 and 2022, in English. According to the search engine, 4 results were found after the exclusion criteria in the PubMed and Google Scholar databases. It was found, therefore, that there is a moderate prevalence of HLV in patients with CNS HBs. Among the studies, the lowest prevalence rate of HlV in patients with HBs was 23%, while the highest rate was approximately 60%, with an overall average of ± 39.2%, when considering all studies involving these patients.Los hemangioblastomas (HB) son neoplasias benignas comúnmente localizadas en el cerebelo y la médula espinal y pueden surgir esporádicamente o relacionadas con el síndrome de von Hippel-Lindau (VHL). Cuando hay una asociación con VHL, pueden surgir tumores multifocales, a diferencia de los tumores esporádicos, que se aíslan. La VHL es una enfermedad hereditaria relacionada con el desarrollo de tumores benignos y malignos, siendo los más comunes los hemangioblastomas del sistema nervioso central y los angiomas retinianos. La enfermedad es causada por la ineficacia del gen supresor de tumores VHL (pVHL) en un alolo en el cromosoma 3p25-26. La presencia de VHL en pacientes con HB lleva al paciente a un peor pronóstico, ya que facilita la metastatización. Por lo tanto, el objetivo de la siguiente revisión es analizar la prevalencia del síndrome de von Hippel-Lindau en pacientes con hemangioblastomas del sistema nervioso central (SNC). Se trata de una revisión bibliográfica sistemática que utilizó las plataformas PubMed, SciELO y Google Scholar como bases de datos para la investigación de artículos científicos, con un marco temporal entre 2016 y 2022, en inglés. Según el buscador, se encontraron 4 resultados tras los criterios de exclusión en las bases de datos PubMed y Google Scholar. Se encontró, por lo tanto, que existe una prevalencia moderada de HLV en pacientes con HB del SNC. Entre los estudios, la tasa de prevalencia más baja de HlV en pacientes con HB fue del 23%, mientras que la tasa más alta fue de aproximadamente el 60%, con un promedio general de ± 39,2%, al considerar todos los estudios con estos pacientes.Hemangioblastomas (HBs) são neoplasias benignas comumente localizadas no cerebelo e medula espinhal e podem surgir de forma esporádica ou relacionados à Síndrome de von Hippel-Lindau (VHL). Quando há associação com a VHL, tumores multifocais podem surgir, diferentemente dos esporádicos, que são isolados. A VHL é uma doença hereditária relacionada ao desenvolvimento de tumores benignos e malignos, sendo os mais comuns os hemangioblastomas do Sistema Nervoso Central e os angiomas de retina. A doença é causada pela ineficácia do gene supressor de tumor VHL (pVHL) em um alelo no cromossomo 3p25-26. A presença da VHL em pacientes com HBs leva o paciente a um pior prognóstico, por facilitar a metastatização. Dessa forma, o objetivo da seguinte revisão é analisar a prevalência da Síndrome de von Hippel-Lindau em pacientes portadores de hemangioblastomas do Sistema Nervoso Central (SNC). Trata-se de uma revisão bibliográfica sistemática que utilizou as plataformas PubMed, SciELO e Google Scholar como bases de dados para pesquisa de artigos científicos, com recorte temporal entre 2016 e 2022, na língua inglesa. De acordo com o mecanismo de busca, 4 resultados foram encontrados após os critérios de exclusão nas bases de dados PubMed e Google Scholar. Constatou-se, portanto, que há moderada prevalência da VHL em pacientes portadores de HBs do SNC. Dentre os estudos, a menor taxa de prevalência da VHL em pacientes com HBs foi de 23%, enquanto a maior taxa foi de aproximadamente 60%, com uma média geral de ± 39,2%, ao serem considerados todos os estudos que envolveram esses pacientes.Research, Society and Development2022-02-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/2601810.33448/rsd-v11i2.26018Research, Society and Development; Vol. 11 No. 2; e44311226018Research, Society and Development; Vol. 11 Núm. 2; e44311226018Research, Society and Development; v. 11 n. 2; e443112260182525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIporhttps://rsdjournal.org/index.php/rsd/article/view/26018/22770Copyright (c) 2022 Gustavo Soares Gomes Barros Fonseca; Vivianne Maria Laranjeiras Monte Freire; Lais Lima Bonfim; Elana Cristina da Silva Penha; João Victor Araújo Guimarães; Raphael Erick Lima Pereira; Gabriel de Sousa Macedo; Filipe Augusto Lopes Cajubá de Britto; Letícia Muniz de Abreu Murad; Alessandra do Rosário Brito; Lara Letícia Teixeira Reis; Amanda Cordeiro Santos; Agostinho Rodrigues Mesquita Neto; Julianne Souza Prazeres; Luiza Mariana Batista Lima Cunha; Ana Vitória Feitosa Barroso Maia; Carolynne Weba da Silva; Fernando de Abreu Borges; Monaliza Brito de Almeida; Samantha Cunha Vieira; Isabela Coelho Brito Soares; Liciana Tapety Sá; Lucca Adriano Pereira; Thalita Martins Bezerra; Ivana Mota Soares; Rebeca Machado Castro Sousa; Maria Beatriz Celedonio Coelho; Felipe Ramos Caldeirahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessFonseca, Gustavo Soares Gomes Barros Freire, Vivianne Maria Laranjeiras Monte Bonfim, Lais LimaPenha, Elana Cristina da Silva Guimarães, João Victor Araújo Pereira, Raphael Erick Lima Macedo, Gabriel de Sousa Britto, Filipe Augusto Lopes Cajubá de Murad, Letícia Muniz de Abreu Brito, Alessandra do Rosário Reis, Lara Letícia Teixeira Santos, Amanda Cordeiro Mesquita Neto, Agostinho Rodrigues Prazeres, Julianne Souza Cunha, Luiza Mariana Batista Lima Maia, Ana Vitória Feitosa Barroso Silva, Carolynne Weba da Borges, Fernando de Abreu Almeida, Monaliza Brito de Vieira, Samantha Cunha Soares, Isabela Coelho Brito Tapety Sá, LicianaPereira, Lucca AdrianoBezerra, Thalita Martins Soares, Ivana Mota Sousa, Rebeca Machado Castro Coelho, Maria Beatriz Celedonio Caldeira, Felipe Ramos 2022-02-07T01:42:50Zoai:ojs.pkp.sfu.ca:article/26018Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2024-01-17T09:44:09.857450Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Analysis of the prevalence of von Hippel-Lindau Syndrome in patients with hemangioblastomas of the Central Nervous System
Análisis de la prevalencia del Síndrome de von Hippel-Lindau en pacientes con hemangioblastomas del Sistema Nervioso Central
Análise da prevalência da Síndrome de von Hippel-Lindau em pacientes portadores de hemangioblastomas do Sistema Nervoso Central
title Analysis of the prevalence of von Hippel-Lindau Syndrome in patients with hemangioblastomas of the Central Nervous System
spellingShingle Analysis of the prevalence of von Hippel-Lindau Syndrome in patients with hemangioblastomas of the Central Nervous System
Fonseca, Gustavo Soares Gomes Barros
Hemangioblastoma
Von Hippel-Lindau syndrome
Prevalence.
Hemangioblastoma
Síndrome de Von Hippel-Lindau
Prevalencia.
Hemangioblastoma
Síndrome de Von Hippel-Lindau
Prevalência.
title_short Analysis of the prevalence of von Hippel-Lindau Syndrome in patients with hemangioblastomas of the Central Nervous System
title_full Analysis of the prevalence of von Hippel-Lindau Syndrome in patients with hemangioblastomas of the Central Nervous System
title_fullStr Analysis of the prevalence of von Hippel-Lindau Syndrome in patients with hemangioblastomas of the Central Nervous System
title_full_unstemmed Analysis of the prevalence of von Hippel-Lindau Syndrome in patients with hemangioblastomas of the Central Nervous System
title_sort Analysis of the prevalence of von Hippel-Lindau Syndrome in patients with hemangioblastomas of the Central Nervous System
author Fonseca, Gustavo Soares Gomes Barros
author_facet Fonseca, Gustavo Soares Gomes Barros
Freire, Vivianne Maria Laranjeiras Monte
Bonfim, Lais Lima
Penha, Elana Cristina da Silva
Guimarães, João Victor Araújo
Pereira, Raphael Erick Lima
Macedo, Gabriel de Sousa
Britto, Filipe Augusto Lopes Cajubá de
Murad, Letícia Muniz de Abreu
Brito, Alessandra do Rosário
Reis, Lara Letícia Teixeira
Santos, Amanda Cordeiro
Mesquita Neto, Agostinho Rodrigues
Prazeres, Julianne Souza
Cunha, Luiza Mariana Batista Lima
Maia, Ana Vitória Feitosa Barroso
Silva, Carolynne Weba da
Borges, Fernando de Abreu
Almeida, Monaliza Brito de
Vieira, Samantha Cunha
Soares, Isabela Coelho Brito
Tapety Sá, Liciana
Pereira, Lucca Adriano
Bezerra, Thalita Martins
Soares, Ivana Mota
Sousa, Rebeca Machado Castro
Coelho, Maria Beatriz Celedonio
Caldeira, Felipe Ramos
author_role author
author2 Freire, Vivianne Maria Laranjeiras Monte
Bonfim, Lais Lima
Penha, Elana Cristina da Silva
Guimarães, João Victor Araújo
Pereira, Raphael Erick Lima
Macedo, Gabriel de Sousa
Britto, Filipe Augusto Lopes Cajubá de
Murad, Letícia Muniz de Abreu
Brito, Alessandra do Rosário
Reis, Lara Letícia Teixeira
Santos, Amanda Cordeiro
Mesquita Neto, Agostinho Rodrigues
Prazeres, Julianne Souza
Cunha, Luiza Mariana Batista Lima
Maia, Ana Vitória Feitosa Barroso
Silva, Carolynne Weba da
Borges, Fernando de Abreu
Almeida, Monaliza Brito de
Vieira, Samantha Cunha
Soares, Isabela Coelho Brito
Tapety Sá, Liciana
Pereira, Lucca Adriano
Bezerra, Thalita Martins
Soares, Ivana Mota
Sousa, Rebeca Machado Castro
Coelho, Maria Beatriz Celedonio
Caldeira, Felipe Ramos
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Fonseca, Gustavo Soares Gomes Barros
Freire, Vivianne Maria Laranjeiras Monte
Bonfim, Lais Lima
Penha, Elana Cristina da Silva
Guimarães, João Victor Araújo
Pereira, Raphael Erick Lima
Macedo, Gabriel de Sousa
Britto, Filipe Augusto Lopes Cajubá de
Murad, Letícia Muniz de Abreu
Brito, Alessandra do Rosário
Reis, Lara Letícia Teixeira
Santos, Amanda Cordeiro
Mesquita Neto, Agostinho Rodrigues
Prazeres, Julianne Souza
Cunha, Luiza Mariana Batista Lima
Maia, Ana Vitória Feitosa Barroso
Silva, Carolynne Weba da
Borges, Fernando de Abreu
Almeida, Monaliza Brito de
Vieira, Samantha Cunha
Soares, Isabela Coelho Brito
Tapety Sá, Liciana
Pereira, Lucca Adriano
Bezerra, Thalita Martins
Soares, Ivana Mota
Sousa, Rebeca Machado Castro
Coelho, Maria Beatriz Celedonio
Caldeira, Felipe Ramos
dc.subject.por.fl_str_mv Hemangioblastoma
Von Hippel-Lindau syndrome
Prevalence.
Hemangioblastoma
Síndrome de Von Hippel-Lindau
Prevalencia.
Hemangioblastoma
Síndrome de Von Hippel-Lindau
Prevalência.
topic Hemangioblastoma
Von Hippel-Lindau syndrome
Prevalence.
Hemangioblastoma
Síndrome de Von Hippel-Lindau
Prevalencia.
Hemangioblastoma
Síndrome de Von Hippel-Lindau
Prevalência.
description Hemangioblastomas (HBs) are benign neoplasms commonly located in the cerebellum and spinal cord and may arise sporadically or related to von Hippel-Lindau Syndrome (VHL). When there is an association with VHL, multifocal tumors may arise, unlike sporadic tumors, which are isolated. VHL is a hereditary disease related to the development of benign and malignant tumors, the most common being central nervous system hemangioblastomas and retinal angiomas. The disease is caused by the inefficacy of the Tumor Suppressor Gene VHL (pVHL) in an allolo on chromosome 3p25-26. The presence of VHL in patients with HBs leads the patient to a worse prognosis, as it facilitates metastatization. Thus, the aim of the following review is to analyze the prevalence of von Hippel-Lindau syndrome in patients with central nervous system (CNS) hemangioblastomas. This is a systematic bibliographic review that used the PubMed, SciELO and Google Scholar platforms as databases for research of scientific articles, with a time frame between 2016 and 2022, in English. According to the search engine, 4 results were found after the exclusion criteria in the PubMed and Google Scholar databases. It was found, therefore, that there is a moderate prevalence of HLV in patients with CNS HBs. Among the studies, the lowest prevalence rate of HlV in patients with HBs was 23%, while the highest rate was approximately 60%, with an overall average of ± 39.2%, when considering all studies involving these patients.
publishDate 2022
dc.date.none.fl_str_mv 2022-02-03
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/26018
10.33448/rsd-v11i2.26018
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identifier_str_mv 10.33448/rsd-v11i2.26018
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dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/26018/22770
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info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Research, Society and Development
publisher.none.fl_str_mv Research, Society and Development
dc.source.none.fl_str_mv Research, Society and Development; Vol. 11 No. 2; e44311226018
Research, Society and Development; Vol. 11 Núm. 2; e44311226018
Research, Society and Development; v. 11 n. 2; e44311226018
2525-3409
reponame:Research, Society and Development
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repository.name.fl_str_mv Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)
repository.mail.fl_str_mv rsd.articles@gmail.com
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