A Rare Cause of Abdominal Pain in Childhood: Cardiac Angiosarcoma

Detalhes bibliográficos
Autor(a) principal: Citak,Elvan Caglar
Data de Publicação: 2018
Outros Autores: Ozeren,Murat, Karaca,M. Kerem, Karpuz,Derya, Karahan,Feryal, Yilmaz,Eda Bengi, Balci,Yuksel, Kara,Pelin Ozcan, Arpaci,Rabia Bozdogan
Tipo de documento: Relatório
Idioma: eng
Título da fonte: Brazilian Journal of Cardiovascular Surgery (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-76382018000100104
Resumo: Abstract Cardiac angiosarcomas are extremely rare in childhood, they are rapidly progressive tumours that often present themselves as diagnostic dilemmas, resulting in delayed diagnosis. Also, extracardiac manifestations, including abdominal pain, are extremely rare in patients with intracardiac tumors. We herein present the case of a 15-year-old girl who presented with abdominal pain. Echocardiography and thoracic computed tomography showed right atrial mass. The patient underwent surgery, chemotherapy, and radiotherapy. Eight months after treatment, abdominal recurrence was detected. The abdominal mass was resected, and radiotherapy and new chemotherapy protocol were given. The present case illustrates a rare case of primary cardiac angiosarcoma posing a diagnostic dilemma in an adolescent girl.
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spelling A Rare Cause of Abdominal Pain in Childhood: Cardiac AngiosarcomaHemangiosarcomaHeartHeart neoplasmsChildAbstract Cardiac angiosarcomas are extremely rare in childhood, they are rapidly progressive tumours that often present themselves as diagnostic dilemmas, resulting in delayed diagnosis. Also, extracardiac manifestations, including abdominal pain, are extremely rare in patients with intracardiac tumors. We herein present the case of a 15-year-old girl who presented with abdominal pain. Echocardiography and thoracic computed tomography showed right atrial mass. The patient underwent surgery, chemotherapy, and radiotherapy. Eight months after treatment, abdominal recurrence was detected. The abdominal mass was resected, and radiotherapy and new chemotherapy protocol were given. The present case illustrates a rare case of primary cardiac angiosarcoma posing a diagnostic dilemma in an adolescent girl.Sociedade Brasileira de Cirurgia Cardiovascular2018-02-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-76382018000100104Brazilian Journal of Cardiovascular Surgery v.33 n.1 2018reponame:Brazilian Journal of Cardiovascular Surgery (Online)instname:Sociedade Brasileira de Cirurgia Cardiovascular (SBCCV)instacron:SBCCV10.21470/1678-9741-2017-0095info:eu-repo/semantics/openAccessCitak,Elvan CaglarOzeren,MuratKaraca,M. KeremKarpuz,DeryaKarahan,FeryalYilmaz,Eda BengiBalci,YukselKara,Pelin OzcanArpaci,Rabia Bozdoganeng2018-03-27T00:00:00Zoai:scielo:S0102-76382018000100104Revistahttp://www.rbccv.org.br/https://old.scielo.br/oai/scielo-oai.php||rosangela.monteiro@incor.usp.br|| domingo@braile.com.br|| brandau@braile.com.br1678-97410102-7638opendoar:2018-03-27T00:00Brazilian Journal of Cardiovascular Surgery (Online) - Sociedade Brasileira de Cirurgia Cardiovascular (SBCCV)false
dc.title.none.fl_str_mv A Rare Cause of Abdominal Pain in Childhood: Cardiac Angiosarcoma
title A Rare Cause of Abdominal Pain in Childhood: Cardiac Angiosarcoma
spellingShingle A Rare Cause of Abdominal Pain in Childhood: Cardiac Angiosarcoma
Citak,Elvan Caglar
Hemangiosarcoma
Heart
Heart neoplasms
Child
title_short A Rare Cause of Abdominal Pain in Childhood: Cardiac Angiosarcoma
title_full A Rare Cause of Abdominal Pain in Childhood: Cardiac Angiosarcoma
title_fullStr A Rare Cause of Abdominal Pain in Childhood: Cardiac Angiosarcoma
title_full_unstemmed A Rare Cause of Abdominal Pain in Childhood: Cardiac Angiosarcoma
title_sort A Rare Cause of Abdominal Pain in Childhood: Cardiac Angiosarcoma
author Citak,Elvan Caglar
author_facet Citak,Elvan Caglar
Ozeren,Murat
Karaca,M. Kerem
Karpuz,Derya
Karahan,Feryal
Yilmaz,Eda Bengi
Balci,Yuksel
Kara,Pelin Ozcan
Arpaci,Rabia Bozdogan
author_role author
author2 Ozeren,Murat
Karaca,M. Kerem
Karpuz,Derya
Karahan,Feryal
Yilmaz,Eda Bengi
Balci,Yuksel
Kara,Pelin Ozcan
Arpaci,Rabia Bozdogan
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Citak,Elvan Caglar
Ozeren,Murat
Karaca,M. Kerem
Karpuz,Derya
Karahan,Feryal
Yilmaz,Eda Bengi
Balci,Yuksel
Kara,Pelin Ozcan
Arpaci,Rabia Bozdogan
dc.subject.por.fl_str_mv Hemangiosarcoma
Heart
Heart neoplasms
Child
topic Hemangiosarcoma
Heart
Heart neoplasms
Child
description Abstract Cardiac angiosarcomas are extremely rare in childhood, they are rapidly progressive tumours that often present themselves as diagnostic dilemmas, resulting in delayed diagnosis. Also, extracardiac manifestations, including abdominal pain, are extremely rare in patients with intracardiac tumors. We herein present the case of a 15-year-old girl who presented with abdominal pain. Echocardiography and thoracic computed tomography showed right atrial mass. The patient underwent surgery, chemotherapy, and radiotherapy. Eight months after treatment, abdominal recurrence was detected. The abdominal mass was resected, and radiotherapy and new chemotherapy protocol were given. The present case illustrates a rare case of primary cardiac angiosarcoma posing a diagnostic dilemma in an adolescent girl.
publishDate 2018
dc.date.none.fl_str_mv 2018-02-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-76382018000100104
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0102-76382018000100104
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.21470/1678-9741-2017-0095
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Cirurgia Cardiovascular
publisher.none.fl_str_mv Sociedade Brasileira de Cirurgia Cardiovascular
dc.source.none.fl_str_mv Brazilian Journal of Cardiovascular Surgery v.33 n.1 2018
reponame:Brazilian Journal of Cardiovascular Surgery (Online)
instname:Sociedade Brasileira de Cirurgia Cardiovascular (SBCCV)
instacron:SBCCV
instname_str Sociedade Brasileira de Cirurgia Cardiovascular (SBCCV)
instacron_str SBCCV
institution SBCCV
reponame_str Brazilian Journal of Cardiovascular Surgery (Online)
collection Brazilian Journal of Cardiovascular Surgery (Online)
repository.name.fl_str_mv Brazilian Journal of Cardiovascular Surgery (Online) - Sociedade Brasileira de Cirurgia Cardiovascular (SBCCV)
repository.mail.fl_str_mv ||rosangela.monteiro@incor.usp.br|| domingo@braile.com.br|| brandau@braile.com.br
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