Gut mediated syncope
Main Author: | |
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Publication Date: | 2019 |
Other Authors: | , , |
Format: | Article |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | https://revista.spcir.com/index.php/spcir/article/view/718 |
Summary: | 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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Gut mediated syncopeSíncope de causa intestinalgastrointestinal stromal tumorsyncopeimatinibtumor estroma gastrointestinalsíncopeimatinibGastrointestinal 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; N.º 45 (2019): Número 45 - Novembro 2019; 31-362183-11651646-6918reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron: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, Anabela2024-10-24T16:53:22Zoai:revista.spcir.com:article/718Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T19:00:42.682036Repositórios 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 |
Gut mediated syncope Síncope de causa intestinal |
title |
Gut mediated syncope |
spellingShingle |
Gut mediated syncope Azevedo, Pedro gastrointestinal stromal tumor syncope imatinib tumor estroma gastrointestinal síncope imatinib |
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 |
dc.subject.por.fl_str_mv |
gastrointestinal stromal tumor syncope imatinib tumor estroma gastrointestinal síncope imatinib |
topic |
gastrointestinal stromal tumor syncope imatinib tumor estroma gastrointestinal síncope imatinib |
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 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/article |
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article |
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publishedVersion |
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https://revista.spcir.com/index.php/spcir/article/view/718 |
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https://revista.spcir.com/index.php/spcir/article/view/718 |
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eng |
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eng |
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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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Copyright (c) 2019 Revista Portuguesa de Cirurgia info:eu-repo/semantics/openAccess |
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Copyright (c) 2019 Revista Portuguesa de Cirurgia |
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Sociedade Portuguesa de Cirurgia |
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Sociedade Portuguesa de Cirurgia |
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Revista Portuguesa de Cirurgia; No. 45 (2019): Number 45 - June 2018; 31-36 Revista Portuguesa de Cirurgia; N.º 45 (2019): Número 45 - Novembro 2019; 31-36 2183-1165 1646-6918 reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia instacron:RCAAP |
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