Gut mediated syncope

Detalhes bibliográficos
Autor(a) principal: Azevedo, Pedro
Data de Publicação: 2019
Outros Autores: Custódio, Marta, Sequeira, Carolina, Marques, Anabela
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://revista.spcir.com/index.php/spcir/article/view/718
Resumo: Gastrointestinal stromal tumor (GIST) is a rare mesenchymal tumor (0,3-3% of all gastrointestinal tumors), mostly found in the stomach and small intestine. In most cases, GIST is caused by a gain-of-function mutation in KIT gene, resulting in an abnormal proliferation of interstitial Cajal cells. We report the case of a 74-year-old man, with a history of ischemic heart disease, under double antiaggregation, who went to the hospital after an episode of syncope. Physical examination was unremarkable, and his exams only revealed an iron deficiency anemia (9.2 g/dL). Subsequent diagnostic investigation showed a colon adenoma that was excised endoscopically. He presented a new episode of syncope, associated with acute hemoglobin decrease (4.5 g/dL), without clinical evidence of blood loss. We repeated the studies (endoscopic and tomography), which were negative. In the meantime, a videocapsule study was performed, which found a mass in the jejunum, surgically excised, confirming the diagnosis of GIST; the true cause of anemia and syncope. One year passed, our patient is taking imatinib, with no evidence of relapse. Presenting this case report, we do a brief review of this theme. The diagnosis of GIST is not always linear. They are manifested mainly by gastrointestinal hemorrhage and anemia, and most are detected in endoscopic examinations or by computed tomography. Whenever possible, complete surgical resection is the treatment of choice, with adjunctive treatment with imatinib in high-risk patients. In the presence of an unresectable GIST or whose excision may result in great morbidity, imatinib may also be used as neoadjuvant. In advanced metastatic disease, treatment is only done with tyrosine-kinase inhibitors, and surgery is done only for some of the complications.
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spelling Gut mediated syncopeSíncope de causa intestinalGastrointestinal stromal tumor (GIST) is a rare mesenchymal tumor (0,3-3% of all gastrointestinal tumors), mostly found in the stomach and small intestine. In most cases, GIST is caused by a gain-of-function mutation in KIT gene, resulting in an abnormal proliferation of interstitial Cajal cells. We report the case of a 74-year-old man, with a history of ischemic heart disease, under double antiaggregation, who went to the hospital after an episode of syncope. Physical examination was unremarkable, and his exams only revealed an iron deficiency anemia (9.2 g/dL). Subsequent diagnostic investigation showed a colon adenoma that was excised endoscopically. He presented a new episode of syncope, associated with acute hemoglobin decrease (4.5 g/dL), without clinical evidence of blood loss. We repeated the studies (endoscopic and tomography), which were negative. In the meantime, a videocapsule study was performed, which found a mass in the jejunum, surgically excised, confirming the diagnosis of GIST; the true cause of anemia and syncope. One year passed, our patient is taking imatinib, with no evidence of relapse. Presenting this case report, we do a brief review of this theme. The diagnosis of GIST is not always linear. They are manifested mainly by gastrointestinal hemorrhage and anemia, and most are detected in endoscopic examinations or by computed tomography. Whenever possible, complete surgical resection is the treatment of choice, with adjunctive treatment with imatinib in high-risk patients. In the presence of an unresectable GIST or whose excision may result in great morbidity, imatinib may also be used as neoadjuvant. In advanced metastatic disease, treatment is only done with tyrosine-kinase inhibitors, and surgery is done only for some of the complications.O tumor do estroma gastrointestinal (GIST) é um tumor mesenquimatoso, de ocorrência rara (0,3-3% de todos os tumores gastrointestinais), sendo mais vezes diagnosticados no estômago e intestino delgado. Na maioria dos casos, o GIST é causado por uma mutação com ganho de função do gene KIT, originando uma proliferação anormal de células intersticiais de Cajal. Reportamos o caso de um homem de 74 anos, com antecedentes de cardiopatia isquémica, duplamente antiagregado, que recorreu ao hospital após episódio de síncope. O exame físico foi inespecífico e os seus exames apenas revelaram anemia ferropénica (9,2 gr/dL). A investigação diagnóstica subsequente mostrou um adenoma do cólon que foi excisado endoscopicamente. Apresentou novo episódio de síncope, associado a descida aguda da hemoglobina (4,5 gr/dL), sem evidência clínica das perdas hemáticas. Repetiram-se os estudos (endoscópicos e tomografias), que foram negativos. Realizou, entretanto, estudo por vídeocápsula que revelou uma massa no jejuno, que foi excisada cirurgicamente confirmando o diagnóstico de GIST como a verdadeira causa da anemia e das síncopes. Passado um ano, o doente encontra-se sob imatinib, sem qualquer evidência de recidiva. Faz-se uma breve revisão do tema a propósito deste caso clínico. O diagnóstico do GIST nem sempre é linear. Manifestam-se usualmente por hemorragia gastrointestinal e anemia, sendo maioritariamente detectados em exames endoscópicos ou pela tomografia computorizada. Sempre que possível, a ressecção cirúrgica completa é o tratamento de eleição, com tratamento adjuvante com imatinib em doentes de alto risco. Perante um GIST irressecável ou cuja excisão pode resultar em grande morbilidade, o imatinib também é usado como neoadjuvante. No caso de doença metastática avançada, o tratamento é feito apenas com inibidores da tirosina-cinase, ficando a cirurgia para algumas das complicações.Sociedade Portuguesa de Cirurgia2019-12-28info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://revista.spcir.com/index.php/spcir/article/view/718Revista Portuguesa de Cirurgia; No 45 (2019): Number 45 - June 2018; 31-36Revista Portuguesa de Cirurgia; No 45 (2019): Number 45 - June 2018; 31-362183-11651646-6918reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttps://revista.spcir.com/index.php/spcir/article/view/718https://revista.spcir.com/index.php/spcir/article/view/718/534Copyright (c) 2019 Revista Portuguesa de Cirurgiainfo:eu-repo/semantics/openAccessAzevedo, PedroCustódio, MartaSequeira, CarolinaMarques, Anabela2024-03-14T22:05:43Zoai:revista.spcir.com:article/718Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T04:00:57.876744Repositório 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 Gut mediated syncope
Síncope de causa intestinal
title Gut mediated syncope
spellingShingle Gut mediated syncope
Azevedo, Pedro
title_short Gut mediated syncope
title_full Gut mediated syncope
title_fullStr Gut mediated syncope
title_full_unstemmed Gut mediated syncope
title_sort Gut mediated syncope
author Azevedo, Pedro
author_facet Azevedo, Pedro
Custódio, Marta
Sequeira, Carolina
Marques, Anabela
author_role author
author2 Custódio, Marta
Sequeira, Carolina
Marques, Anabela
author2_role author
author
author
dc.contributor.author.fl_str_mv Azevedo, Pedro
Custódio, Marta
Sequeira, Carolina
Marques, Anabela
description Gastrointestinal stromal tumor (GIST) is a rare mesenchymal tumor (0,3-3% of all gastrointestinal tumors), mostly found in the stomach and small intestine. In most cases, GIST is caused by a gain-of-function mutation in KIT gene, resulting in an abnormal proliferation of interstitial Cajal cells. We report the case of a 74-year-old man, with a history of ischemic heart disease, under double antiaggregation, who went to the hospital after an episode of syncope. Physical examination was unremarkable, and his exams only revealed an iron deficiency anemia (9.2 g/dL). Subsequent diagnostic investigation showed a colon adenoma that was excised endoscopically. He presented a new episode of syncope, associated with acute hemoglobin decrease (4.5 g/dL), without clinical evidence of blood loss. We repeated the studies (endoscopic and tomography), which were negative. In the meantime, a videocapsule study was performed, which found a mass in the jejunum, surgically excised, confirming the diagnosis of GIST; the true cause of anemia and syncope. One year passed, our patient is taking imatinib, with no evidence of relapse. Presenting this case report, we do a brief review of this theme. The diagnosis of GIST is not always linear. They are manifested mainly by gastrointestinal hemorrhage and anemia, and most are detected in endoscopic examinations or by computed tomography. Whenever possible, complete surgical resection is the treatment of choice, with adjunctive treatment with imatinib in high-risk patients. In the presence of an unresectable GIST or whose excision may result in great morbidity, imatinib may also be used as neoadjuvant. In advanced metastatic disease, treatment is only done with tyrosine-kinase inhibitors, and surgery is done only for some of the complications.
publishDate 2019
dc.date.none.fl_str_mv 2019-12-28
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dc.identifier.uri.fl_str_mv https://revista.spcir.com/index.php/spcir/article/view/718
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://revista.spcir.com/index.php/spcir/article/view/718
https://revista.spcir.com/index.php/spcir/article/view/718/534
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info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2019 Revista Portuguesa de Cirurgia
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Sociedade Portuguesa de Cirurgia
publisher.none.fl_str_mv Sociedade Portuguesa de Cirurgia
dc.source.none.fl_str_mv Revista Portuguesa de Cirurgia; No 45 (2019): Number 45 - June 2018; 31-36
Revista Portuguesa de Cirurgia; No 45 (2019): Number 45 - June 2018; 31-36
2183-1165
1646-6918
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