Diagnosis and treatment of cardiac angiosarcoma

Primary cardiac tumors are very rare in the population. About 20% of it are malignant. The most common type of cardiac malignant tumor is angiosarcoma. This tumor has the ability to infiltrate surrounding tissues and form distant metastases. Angiosarcoma is most often located in the right atrium and...

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Main Authors: Aleksandra Ołownia, Jakub Orczyk, Agata Tokarzewska, Halina Piecewicz-Szczęsna
Format: Article
Language:English
Published: Kazimierz Wielki University 2023-06-01
Series:Journal of Education, Health and Sport
Subjects:
Online Access:https://apcz.umk.pl/JEHS/article/view/43962
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author Aleksandra Ołownia
Jakub Orczyk
Agata Tokarzewska
Halina Piecewicz-Szczęsna
author_facet Aleksandra Ołownia
Jakub Orczyk
Agata Tokarzewska
Halina Piecewicz-Szczęsna
author_sort Aleksandra Ołownia
collection DOAJ
description Primary cardiac tumors are very rare in the population. About 20% of it are malignant. The most common type of cardiac malignant tumor is angiosarcoma. This tumor has the ability to infiltrate surrounding tissues and form distant metastases. Angiosarcoma is most often located in the right atrium and it mostly attacks men. This neoplasm is difficult to diagnose, because it has no specific symptoms. Patients with this tumor may complain of a chest pain, cardiac arrhythmias, suffocation and distal oedema. The rarity of occurrence and the lack of specyfic symptoms contribute to late diagnosis of the disease and worse prognosis of patients. Angiosarcoma can also be misdiagnosed as pneumonia or more common cardiovascular disease for example coronary artery disease. In advanced stage, this tumor can even lead to myocardial rupture. Various imaging methods are used in the diagnostics of this neoplasm for example: CT, MRI, PET-CT or Echocardiography. Histopathological examinations are less frequently used due to the risk of serious complications like hemothorax. Due to the very uncommon occurrence of the angiosarcoma, guidelines describing treatment of patients with this neoplasm, have not been developed yet. Currently, surgical removal of the tumor (if it is possible), chemiotherapy and radiotherapy are used. Reaserches on the genetic mutations which cause angiosarcoma and the development of appropriate drugs may give patients a chance for more effective treatment in the future
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spelling doaj.art-1fa01cceb2f846f0bb18d5939aa4a3f62023-06-19T10:46:38ZengKazimierz Wielki UniversityJournal of Education, Health and Sport2391-83062023-06-0140110.12775/JEHS.2023.40.01.002Diagnosis and treatment of cardiac angiosarcomaAleksandra Ołownia0Jakub Orczyk1Agata Tokarzewska2Halina Piecewicz-Szczęsna3Student Scientific Association at Department of Epidemiology and Clinical Research Methodology Medical University of Lublin, ul. Radziwiłłowska 11, Lublin 20-080, PolandStudent Scientific Association at Department of Epidemiology and Clinical Research Methodology Medical University of Lublin, ul. Radziwiłłowska 11, Lublin 20-080, PolandStudent Scientific Association at Department of Epidemiology and Clinical Research Methodology Medical University of Lublin, ul. Radziwiłłowska 11, Lublin 20-080, PolandDepartment of Epidemiology and Clinical Research Methodology of the Medical University of Lublin, ul. Radziwiłłowska 11, Lublin 20-080, PolandPrimary cardiac tumors are very rare in the population. About 20% of it are malignant. The most common type of cardiac malignant tumor is angiosarcoma. This tumor has the ability to infiltrate surrounding tissues and form distant metastases. Angiosarcoma is most often located in the right atrium and it mostly attacks men. This neoplasm is difficult to diagnose, because it has no specific symptoms. Patients with this tumor may complain of a chest pain, cardiac arrhythmias, suffocation and distal oedema. The rarity of occurrence and the lack of specyfic symptoms contribute to late diagnosis of the disease and worse prognosis of patients. Angiosarcoma can also be misdiagnosed as pneumonia or more common cardiovascular disease for example coronary artery disease. In advanced stage, this tumor can even lead to myocardial rupture. Various imaging methods are used in the diagnostics of this neoplasm for example: CT, MRI, PET-CT or Echocardiography. Histopathological examinations are less frequently used due to the risk of serious complications like hemothorax. Due to the very uncommon occurrence of the angiosarcoma, guidelines describing treatment of patients with this neoplasm, have not been developed yet. Currently, surgical removal of the tumor (if it is possible), chemiotherapy and radiotherapy are used. Reaserches on the genetic mutations which cause angiosarcoma and the development of appropriate drugs may give patients a chance for more effective treatment in the future https://apcz.umk.pl/JEHS/article/view/43962hearthistopathologyangiosarcomaprimary cardiac tumormalignant tumorcardiology
spellingShingle Aleksandra Ołownia
Jakub Orczyk
Agata Tokarzewska
Halina Piecewicz-Szczęsna
Diagnosis and treatment of cardiac angiosarcoma
Journal of Education, Health and Sport
heart
histopathology
angiosarcoma
primary cardiac tumor
malignant tumor
cardiology
title Diagnosis and treatment of cardiac angiosarcoma
title_full Diagnosis and treatment of cardiac angiosarcoma
title_fullStr Diagnosis and treatment of cardiac angiosarcoma
title_full_unstemmed Diagnosis and treatment of cardiac angiosarcoma
title_short Diagnosis and treatment of cardiac angiosarcoma
title_sort diagnosis and treatment of cardiac angiosarcoma
topic heart
histopathology
angiosarcoma
primary cardiac tumor
malignant tumor
cardiology
url https://apcz.umk.pl/JEHS/article/view/43962
work_keys_str_mv AT aleksandraołownia diagnosisandtreatmentofcardiacangiosarcoma
AT jakuborczyk diagnosisandtreatmentofcardiacangiosarcoma
AT agatatokarzewska diagnosisandtreatmentofcardiacangiosarcoma
AT halinapiecewiczszczesna diagnosisandtreatmentofcardiacangiosarcoma