Mixomas Cardíacos, 13 Anos de Experiência no seu Diagnóstico Ecocardiográfico

Detalhes bibliográficos
Autor(a) principal: Oliveira, R
Data de Publicação: 2010
Outros Autores: Branco, LM, Galrinho, A, Abreu, A, Abreu, J, Fiarresga, A, Mamede, A, Ramos, R, Leal, A, Pinto, E, Fragata, J, Cruz Ferreira, R
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.17/151
Resumo: INTRODUCTION: Transthoracic echocardiography is the method of choice for the diagnosis of cardiac myxomas, but the transesophageal approach provides a better definition of the location and characteristics of the tumor. The authors review their thirteen years' experience on the echocardiographic diagnosis of this pathology. METHODS: From 1994 to 2007, 41 cardiac tumors were diagnosed in our echocardiographic laboratory, of which 27 (65.85%) were cardiac myxomas. The exams and the patients' clinical files were retrospectively reviewed. RESULTS: Of the 27 patients, 22 (81.5%) were female, with a mean age of 62.1 +/- 13.6 years (25-84 years). The predominant clinical features were due to the obstruction caused by the tumor in more than two thirds of the patients, followed by constitutional symptoms in one third and embolic events in 30%. In the lab results, anemia was found in three patients and elevated sedimentation rate and CRP in two. In two patients the myxoma was found by chance. All the cases were of the sporadic type, although we found a prevalence of thyroid disease of 14% (4 patients). All patients underwent urgent surgical resection except one, in whom surgery was refused due to advanced age and comorbidities. The myxomas followed a typical distribution with 24 (88.8%) located in the left atrium, 18 of them attached to the atrial septum (AS) and two to the mitral valve. In one patient, the tumor involved both atria. The other two cases originated in the right atrium at the AS. Embolic phenomena were more frequent in small tumors (p = 0.027) and in those with a villous appearance (p = 0.032). Obstructive manifestations were associated with larger tumors (p = 0.046) and larger left atria (p = 0.048). In our series, there were no deaths during hospitalization or in the follow-up period of 5.2 +/- 3.7 years in 19 patients. There were two recurrences, both patients being successfully reoperated. CONCLUSION: Myxoma is the most common cardiac tumor. Transesophageal echocardiography provides excellent morphologic definition, aiding in diagnosis and follow-up. Most clinical manifestations are obstructive and are associated with larger tumors. Small tumors with a friable appearance have a higher chance of embolization. Surgical resection is usually curative and the long-term prognosis is excellent.
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spelling Mixomas Cardíacos, 13 Anos de Experiência no seu Diagnóstico EcocardiográficoCardiac Myxoma: a 13-Year Experience in Echocardiographic Diagnosis.AdultoIdosoNeoplasias CardíacasMixomaUltrassonografiaFactores de TempoHSM CARHSM CCTHSM ANPATINTRODUCTION: Transthoracic echocardiography is the method of choice for the diagnosis of cardiac myxomas, but the transesophageal approach provides a better definition of the location and characteristics of the tumor. The authors review their thirteen years' experience on the echocardiographic diagnosis of this pathology. METHODS: From 1994 to 2007, 41 cardiac tumors were diagnosed in our echocardiographic laboratory, of which 27 (65.85%) were cardiac myxomas. The exams and the patients' clinical files were retrospectively reviewed. RESULTS: Of the 27 patients, 22 (81.5%) were female, with a mean age of 62.1 +/- 13.6 years (25-84 years). The predominant clinical features were due to the obstruction caused by the tumor in more than two thirds of the patients, followed by constitutional symptoms in one third and embolic events in 30%. In the lab results, anemia was found in three patients and elevated sedimentation rate and CRP in two. In two patients the myxoma was found by chance. All the cases were of the sporadic type, although we found a prevalence of thyroid disease of 14% (4 patients). All patients underwent urgent surgical resection except one, in whom surgery was refused due to advanced age and comorbidities. The myxomas followed a typical distribution with 24 (88.8%) located in the left atrium, 18 of them attached to the atrial septum (AS) and two to the mitral valve. In one patient, the tumor involved both atria. The other two cases originated in the right atrium at the AS. Embolic phenomena were more frequent in small tumors (p = 0.027) and in those with a villous appearance (p = 0.032). Obstructive manifestations were associated with larger tumors (p = 0.046) and larger left atria (p = 0.048). In our series, there were no deaths during hospitalization or in the follow-up period of 5.2 +/- 3.7 years in 19 patients. There were two recurrences, both patients being successfully reoperated. CONCLUSION: Myxoma is the most common cardiac tumor. Transesophageal echocardiography provides excellent morphologic definition, aiding in diagnosis and follow-up. Most clinical manifestations are obstructive and are associated with larger tumors. Small tumors with a friable appearance have a higher chance of embolization. Surgical resection is usually curative and the long-term prognosis is excellent.Sociedade Portuguesa de CardiologiaRepositório do Centro Hospitalar Universitário de Lisboa Central, EPEOliveira, RBranco, LMGalrinho, AAbreu, AAbreu, JFiarresga, AMamede, ARamos, RLeal, APinto, EFragata, JCruz Ferreira, R2011-04-21T11:39:22Z20102010-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/151porRev Port Cardiol. 2010 Jul-Aug;29(7-8):1087-100.info: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:RCAAP2023-03-10T09:25:38ZPortal AgregadorONG
dc.title.none.fl_str_mv Mixomas Cardíacos, 13 Anos de Experiência no seu Diagnóstico Ecocardiográfico
Cardiac Myxoma: a 13-Year Experience in Echocardiographic Diagnosis.
title Mixomas Cardíacos, 13 Anos de Experiência no seu Diagnóstico Ecocardiográfico
spellingShingle Mixomas Cardíacos, 13 Anos de Experiência no seu Diagnóstico Ecocardiográfico
Oliveira, R
Adulto
Idoso
Neoplasias Cardíacas
Mixoma
Ultrassonografia
Factores de Tempo
HSM CAR
HSM CCT
HSM ANPAT
title_short Mixomas Cardíacos, 13 Anos de Experiência no seu Diagnóstico Ecocardiográfico
title_full Mixomas Cardíacos, 13 Anos de Experiência no seu Diagnóstico Ecocardiográfico
title_fullStr Mixomas Cardíacos, 13 Anos de Experiência no seu Diagnóstico Ecocardiográfico
title_full_unstemmed Mixomas Cardíacos, 13 Anos de Experiência no seu Diagnóstico Ecocardiográfico
title_sort Mixomas Cardíacos, 13 Anos de Experiência no seu Diagnóstico Ecocardiográfico
author Oliveira, R
author_facet Oliveira, R
Branco, LM
Galrinho, A
Abreu, A
Abreu, J
Fiarresga, A
Mamede, A
Ramos, R
Leal, A
Pinto, E
Fragata, J
Cruz Ferreira, R
author_role author
author2 Branco, LM
Galrinho, A
Abreu, A
Abreu, J
Fiarresga, A
Mamede, A
Ramos, R
Leal, A
Pinto, E
Fragata, J
Cruz Ferreira, R
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório do Centro Hospitalar Universitário de Lisboa Central, EPE
dc.contributor.author.fl_str_mv Oliveira, R
Branco, LM
Galrinho, A
Abreu, A
Abreu, J
Fiarresga, A
Mamede, A
Ramos, R
Leal, A
Pinto, E
Fragata, J
Cruz Ferreira, R
dc.subject.por.fl_str_mv Adulto
Idoso
Neoplasias Cardíacas
Mixoma
Ultrassonografia
Factores de Tempo
HSM CAR
HSM CCT
HSM ANPAT
topic Adulto
Idoso
Neoplasias Cardíacas
Mixoma
Ultrassonografia
Factores de Tempo
HSM CAR
HSM CCT
HSM ANPAT
description INTRODUCTION: Transthoracic echocardiography is the method of choice for the diagnosis of cardiac myxomas, but the transesophageal approach provides a better definition of the location and characteristics of the tumor. The authors review their thirteen years' experience on the echocardiographic diagnosis of this pathology. METHODS: From 1994 to 2007, 41 cardiac tumors were diagnosed in our echocardiographic laboratory, of which 27 (65.85%) were cardiac myxomas. The exams and the patients' clinical files were retrospectively reviewed. RESULTS: Of the 27 patients, 22 (81.5%) were female, with a mean age of 62.1 +/- 13.6 years (25-84 years). The predominant clinical features were due to the obstruction caused by the tumor in more than two thirds of the patients, followed by constitutional symptoms in one third and embolic events in 30%. In the lab results, anemia was found in three patients and elevated sedimentation rate and CRP in two. In two patients the myxoma was found by chance. All the cases were of the sporadic type, although we found a prevalence of thyroid disease of 14% (4 patients). All patients underwent urgent surgical resection except one, in whom surgery was refused due to advanced age and comorbidities. The myxomas followed a typical distribution with 24 (88.8%) located in the left atrium, 18 of them attached to the atrial septum (AS) and two to the mitral valve. In one patient, the tumor involved both atria. The other two cases originated in the right atrium at the AS. Embolic phenomena were more frequent in small tumors (p = 0.027) and in those with a villous appearance (p = 0.032). Obstructive manifestations were associated with larger tumors (p = 0.046) and larger left atria (p = 0.048). In our series, there were no deaths during hospitalization or in the follow-up period of 5.2 +/- 3.7 years in 19 patients. There were two recurrences, both patients being successfully reoperated. CONCLUSION: Myxoma is the most common cardiac tumor. Transesophageal echocardiography provides excellent morphologic definition, aiding in diagnosis and follow-up. Most clinical manifestations are obstructive and are associated with larger tumors. Small tumors with a friable appearance have a higher chance of embolization. Surgical resection is usually curative and the long-term prognosis is excellent.
publishDate 2010
dc.date.none.fl_str_mv 2010
2010-01-01T00:00:00Z
2011-04-21T11:39:22Z
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 http://hdl.handle.net/10400.17/151
url http://hdl.handle.net/10400.17/151
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Rev Port Cardiol. 2010 Jul-Aug;29(7-8):1087-100.
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Sociedade Portuguesa de Cardiologia
publisher.none.fl_str_mv Sociedade Portuguesa de Cardiologia
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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