Paraganglioma – Predictors factors of major aggressivity
Autor(a) principal: | |
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Data de Publicação: | 2024 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Texto Completo: | https://rponcologia.com/index.php/rpo/article/view/70 |
Resumo: | Paragangliomas are rare neuroendocrine tumors whose clinic and presentation depend on secretory profile, size, and location. About 40% of paragangliomas are associated with genetic syndromes with the succinate dehydrogenase enzyme complex (SDH) mutation being the most frequent. Mutation in SDHB is associated with a worse prognosis and increased risk of metastatic disease. We present a clinical case of a 45-year-old man, with a germline mutation in the SDHB gene, who initially underwent excision of paraganglioma with 10 cm that recurred with disseminated disease. He underwent several systemic treatments with some response but unfortunately died in the context of oncologic disease. Regarding this case, we review some predictors of poor prognosis. |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
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Paraganglioma – Predictors factors of major aggressivityParaganglioma – Fatores preditores de maior agressividadeparagangliomasuccinate dehydrogenase mutationmetastatic diseaseprognosisParagangliomamutação da succinato desidrogenasedoença metastáticaprognósticoParagangliomas are rare neuroendocrine tumors whose clinic and presentation depend on secretory profile, size, and location. About 40% of paragangliomas are associated with genetic syndromes with the succinate dehydrogenase enzyme complex (SDH) mutation being the most frequent. Mutation in SDHB is associated with a worse prognosis and increased risk of metastatic disease. We present a clinical case of a 45-year-old man, with a germline mutation in the SDHB gene, who initially underwent excision of paraganglioma with 10 cm that recurred with disseminated disease. He underwent several systemic treatments with some response but unfortunately died in the context of oncologic disease. Regarding this case, we review some predictors of poor prognosis. Os paragangliomas são tumores neuroendrócrinos raros cuja clínica e apresentação dependem do perfil secretor, tamanho e localização. Cerca de 40% dos paragangliomas estão associados a síndromes genéticos, sendo a mutação do complexo enzimático succinato desidrogenase (SDH) a mais frequente. A presença de mutação no SDHB está associada a pior prognóstico com risco aumentado de metastização. Apresentamos um caso clínico de um homem de 45 anos, com mutação germinativa no gene SDHB, submetido inicialmente a exérese de paraganglioma com 10 cm que recidivou com doença disseminada. Realizou diversos tratamentos sistémicos com resposta parcial, mas acabou por falecer no contexto da doença oncológica. A propósito deste caso, revemos alguns fatores preditores de mau prognóstico.Sociedade Portuguesa de Oncologia2024-06-26info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://rponcologia.com/index.php/rpo/article/view/70Portuguese Journal of Oncology; Vol. 7 No. 1-2 (2024): Revista Portuguesa de Oncologia; 42-45Revista Portuguesa de Oncologia; Vol. 7 N.º 1-2 (2024): Revista Portuguesa de Oncologia; 42-452976-0062reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAPporhttps://rponcologia.com/index.php/rpo/article/view/70https://rponcologia.com/index.php/rpo/article/view/70/31Direitos de Autor (c) 2024 Revista Portuguesa de Oncologiainfo:eu-repo/semantics/openAccessTeixeira, CarinaBarbosa, MiguelRibeiro, Maria JoãoFernandes, Catarina2024-06-29T05:12:28Zoai:ojs.rponcologia.com:article/70Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T17:57:04.095647Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Paraganglioma – Predictors factors of major aggressivity Paraganglioma – Fatores preditores de maior agressividade |
title |
Paraganglioma – Predictors factors of major aggressivity |
spellingShingle |
Paraganglioma – Predictors factors of major aggressivity Teixeira, Carina paraganglioma succinate dehydrogenase mutation metastatic disease prognosis Paraganglioma mutação da succinato desidrogenase doença metastática prognóstico |
title_short |
Paraganglioma – Predictors factors of major aggressivity |
title_full |
Paraganglioma – Predictors factors of major aggressivity |
title_fullStr |
Paraganglioma – Predictors factors of major aggressivity |
title_full_unstemmed |
Paraganglioma – Predictors factors of major aggressivity |
title_sort |
Paraganglioma – Predictors factors of major aggressivity |
author |
Teixeira, Carina |
author_facet |
Teixeira, Carina Barbosa, Miguel Ribeiro, Maria João Fernandes, Catarina |
author_role |
author |
author2 |
Barbosa, Miguel Ribeiro, Maria João Fernandes, Catarina |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Teixeira, Carina Barbosa, Miguel Ribeiro, Maria João Fernandes, Catarina |
dc.subject.por.fl_str_mv |
paraganglioma succinate dehydrogenase mutation metastatic disease prognosis Paraganglioma mutação da succinato desidrogenase doença metastática prognóstico |
topic |
paraganglioma succinate dehydrogenase mutation metastatic disease prognosis Paraganglioma mutação da succinato desidrogenase doença metastática prognóstico |
description |
Paragangliomas are rare neuroendocrine tumors whose clinic and presentation depend on secretory profile, size, and location. About 40% of paragangliomas are associated with genetic syndromes with the succinate dehydrogenase enzyme complex (SDH) mutation being the most frequent. Mutation in SDHB is associated with a worse prognosis and increased risk of metastatic disease. We present a clinical case of a 45-year-old man, with a germline mutation in the SDHB gene, who initially underwent excision of paraganglioma with 10 cm that recurred with disseminated disease. He underwent several systemic treatments with some response but unfortunately died in the context of oncologic disease. Regarding this case, we review some predictors of poor prognosis. |
publishDate |
2024 |
dc.date.none.fl_str_mv |
2024-06-26 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://rponcologia.com/index.php/rpo/article/view/70 |
url |
https://rponcologia.com/index.php/rpo/article/view/70 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://rponcologia.com/index.php/rpo/article/view/70 https://rponcologia.com/index.php/rpo/article/view/70/31 |
dc.rights.driver.fl_str_mv |
Direitos de Autor (c) 2024 Revista Portuguesa de Oncologia info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Direitos de Autor (c) 2024 Revista Portuguesa de Oncologia |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Sociedade Portuguesa de Oncologia |
publisher.none.fl_str_mv |
Sociedade Portuguesa de Oncologia |
dc.source.none.fl_str_mv |
Portuguese Journal of Oncology; Vol. 7 No. 1-2 (2024): Revista Portuguesa de Oncologia; 42-45 Revista Portuguesa de Oncologia; Vol. 7 N.º 1-2 (2024): Revista Portuguesa de Oncologia; 42-45 2976-0062 reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia instacron:RCAAP |
instname_str |
FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
collection |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
repository.name.fl_str_mv |
Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia |
repository.mail.fl_str_mv |
info@rcaap.pt |
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