Primary cardiac angiosarcoma: a case report
Primary cardiac angiosarcoma is relatively rare, and most cases involve metastasis at the time of diagnosis. The median survival time is 14 months for patients who can be treated surgically, versus 3.8 ± 2.5 months for patients with metastasis who could not undergo surgery. Radical surgical resectio...
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doaj-af9e12d142d9451db080e2356794a7822021-08-26T23:33:30ZengSAGE PublishingJournal of International Medical Research1473-23002021-08-014910.1177/03000605211033261Primary cardiac angiosarcoma: a case reportXin FangSong ZhengPrimary cardiac angiosarcoma is relatively rare, and most cases involve metastasis at the time of diagnosis. The median survival time is 14 months for patients who can be treated surgically, versus 3.8 ± 2.5 months for patients with metastasis who could not undergo surgery. Radical surgical resection, radiotherapy, chemotherapy, and targeted therapy are the main treatments, but prognosis remains poor because of rapid progression and high recurrence and metastasis rates. At present, there is no unified standard treatment, and selecting the correct treatment plan and improving patient survival and quality of life remain challenging. We have reported the case of a 45-year-old woman with a primary heart tumor that infiltrated the right atrial wall and pericardium. Angiosarcoma was verified histologically. After palliative resection of the primary tumor followed by concurrent chemoradiotherapy and targeted therapy, the patient exhibited overall survival of 23 months, highlighting the potential utility of this treatment strategy.https://doi.org/10.1177/03000605211033261 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xin Fang Song Zheng |
spellingShingle |
Xin Fang Song Zheng Primary cardiac angiosarcoma: a case report Journal of International Medical Research |
author_facet |
Xin Fang Song Zheng |
author_sort |
Xin Fang |
title |
Primary cardiac angiosarcoma: a case report |
title_short |
Primary cardiac angiosarcoma: a case report |
title_full |
Primary cardiac angiosarcoma: a case report |
title_fullStr |
Primary cardiac angiosarcoma: a case report |
title_full_unstemmed |
Primary cardiac angiosarcoma: a case report |
title_sort |
primary cardiac angiosarcoma: a case report |
publisher |
SAGE Publishing |
series |
Journal of International Medical Research |
issn |
1473-2300 |
publishDate |
2021-08-01 |
description |
Primary cardiac angiosarcoma is relatively rare, and most cases involve metastasis at the time of diagnosis. The median survival time is 14 months for patients who can be treated surgically, versus 3.8 ± 2.5 months for patients with metastasis who could not undergo surgery. Radical surgical resection, radiotherapy, chemotherapy, and targeted therapy are the main treatments, but prognosis remains poor because of rapid progression and high recurrence and metastasis rates. At present, there is no unified standard treatment, and selecting the correct treatment plan and improving patient survival and quality of life remain challenging. We have reported the case of a 45-year-old woman with a primary heart tumor that infiltrated the right atrial wall and pericardium. Angiosarcoma was verified histologically. After palliative resection of the primary tumor followed by concurrent chemoradiotherapy and targeted therapy, the patient exhibited overall survival of 23 months, highlighting the potential utility of this treatment strategy. |
url |
https://doi.org/10.1177/03000605211033261 |
work_keys_str_mv |
AT xinfang primarycardiacangiosarcomaacasereport AT songzheng primarycardiacangiosarcomaacasereport |
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