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Composite haemangioendothelioma in the heart: a case report
BACKGROUND: Primary cardiac neoplasm is rare and generally benign. Epithelioid haemangioendothelioma, a potentially malignant tumour of vascular origin, has been occasionally described in the heart. Composite haemangioendothelioma, characterized by a heterogeneous architecture of vascular components...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10408359/ https://www.ncbi.nlm.nih.gov/pubmed/37559782 http://dx.doi.org/10.1093/ehjcr/ytad343 |
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author | Schaeffer, Thibault Glatz, Katharina Eckstein, Friedrich S Matt, Peter |
author_facet | Schaeffer, Thibault Glatz, Katharina Eckstein, Friedrich S Matt, Peter |
author_sort | Schaeffer, Thibault |
collection | PubMed |
description | BACKGROUND: Primary cardiac neoplasm is rare and generally benign. Epithelioid haemangioendothelioma, a potentially malignant tumour of vascular origin, has been occasionally described in the heart. Composite haemangioendothelioma, characterized by a heterogeneous architecture of vascular components and usually located in soft tissue of the extremities, has only been reported twice in the heart. We herein report another case of this extremely uncommon cardiac tumour. CASE SUMMARY: Comprehensive cardiac examination of a 59-year-old female patient with palpitations and personal history of Hodgkin’s lymphoma and chest radiation revealed a mass in the left atrium. After surgical resection, histopathological and immunohistochemical analysis identified a composite haemangioendothelioma. After two years, repeated imaging revealed neither signs of local relapse nor metastasis. CONCLUSIONS: Composite haemangioendothelioma, a very uncommon form of potentially malignant vascular tumour, can also be encountered in the heart. In this present case, the outcome was favourable two years after surgical resection without adjuvant therapy. |
format | Online Article Text |
id | pubmed-10408359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-104083592023-08-09 Composite haemangioendothelioma in the heart: a case report Schaeffer, Thibault Glatz, Katharina Eckstein, Friedrich S Matt, Peter Eur Heart J Case Rep Case Report BACKGROUND: Primary cardiac neoplasm is rare and generally benign. Epithelioid haemangioendothelioma, a potentially malignant tumour of vascular origin, has been occasionally described in the heart. Composite haemangioendothelioma, characterized by a heterogeneous architecture of vascular components and usually located in soft tissue of the extremities, has only been reported twice in the heart. We herein report another case of this extremely uncommon cardiac tumour. CASE SUMMARY: Comprehensive cardiac examination of a 59-year-old female patient with palpitations and personal history of Hodgkin’s lymphoma and chest radiation revealed a mass in the left atrium. After surgical resection, histopathological and immunohistochemical analysis identified a composite haemangioendothelioma. After two years, repeated imaging revealed neither signs of local relapse nor metastasis. CONCLUSIONS: Composite haemangioendothelioma, a very uncommon form of potentially malignant vascular tumour, can also be encountered in the heart. In this present case, the outcome was favourable two years after surgical resection without adjuvant therapy. Oxford University Press 2023-07-21 /pmc/articles/PMC10408359/ /pubmed/37559782 http://dx.doi.org/10.1093/ehjcr/ytad343 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Case Report Schaeffer, Thibault Glatz, Katharina Eckstein, Friedrich S Matt, Peter Composite haemangioendothelioma in the heart: a case report |
title | Composite haemangioendothelioma in the heart: a case report |
title_full | Composite haemangioendothelioma in the heart: a case report |
title_fullStr | Composite haemangioendothelioma in the heart: a case report |
title_full_unstemmed | Composite haemangioendothelioma in the heart: a case report |
title_short | Composite haemangioendothelioma in the heart: a case report |
title_sort | composite haemangioendothelioma in the heart: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10408359/ https://www.ncbi.nlm.nih.gov/pubmed/37559782 http://dx.doi.org/10.1093/ehjcr/ytad343 |
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