Cargando…
Cardiac endothelial sarcoma with hypereosinophilia of children: a case report
Cardiac malignancies in children are extremely rare and they with hypereosinophilia are rather relatively uncommon. The majority of individuals may survive over the long term even with heart tumors provided they don't have any significant symptoms and their hemodynamics are unaffected. But we s...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10080960/ https://www.ncbi.nlm.nih.gov/pubmed/37029383 http://dx.doi.org/10.1186/s13019-023-02206-4 |
_version_ | 1785021022688247808 |
---|---|
author | Zhang, Wei He, Mengyuan Wang, Qiang |
author_facet | Zhang, Wei He, Mengyuan Wang, Qiang |
author_sort | Zhang, Wei |
collection | PubMed |
description | Cardiac malignancies in children are extremely rare and they with hypereosinophilia are rather relatively uncommon. The majority of individuals may survive over the long term even with heart tumors provided they don't have any significant symptoms and their hemodynamics are unaffected. But we should nevertheless be aware of them, especially when they are coupled with persistent hypereosinophilia and the development of a hemodynamic anomaly. The case of a malignant heart tumor with hypereosinophilia in a 13-year-old girl is presented in this paper. She exhibited an echocardiographic deficit and a heart murmur. Additionally, it was difficult to treat her hypereosinophilia. Nevertheless, it was resolved the day after the operation. We presume that there is a certain relationship between them. This study gives clinicians a wide range of options for analyzing the connections between malignancy and hypereosinophilia. |
format | Online Article Text |
id | pubmed-10080960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100809602023-04-08 Cardiac endothelial sarcoma with hypereosinophilia of children: a case report Zhang, Wei He, Mengyuan Wang, Qiang J Cardiothorac Surg Case Report Cardiac malignancies in children are extremely rare and they with hypereosinophilia are rather relatively uncommon. The majority of individuals may survive over the long term even with heart tumors provided they don't have any significant symptoms and their hemodynamics are unaffected. But we should nevertheless be aware of them, especially when they are coupled with persistent hypereosinophilia and the development of a hemodynamic anomaly. The case of a malignant heart tumor with hypereosinophilia in a 13-year-old girl is presented in this paper. She exhibited an echocardiographic deficit and a heart murmur. Additionally, it was difficult to treat her hypereosinophilia. Nevertheless, it was resolved the day after the operation. We presume that there is a certain relationship between them. This study gives clinicians a wide range of options for analyzing the connections between malignancy and hypereosinophilia. BioMed Central 2023-04-07 /pmc/articles/PMC10080960/ /pubmed/37029383 http://dx.doi.org/10.1186/s13019-023-02206-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Zhang, Wei He, Mengyuan Wang, Qiang Cardiac endothelial sarcoma with hypereosinophilia of children: a case report |
title | Cardiac endothelial sarcoma with hypereosinophilia of children: a case report |
title_full | Cardiac endothelial sarcoma with hypereosinophilia of children: a case report |
title_fullStr | Cardiac endothelial sarcoma with hypereosinophilia of children: a case report |
title_full_unstemmed | Cardiac endothelial sarcoma with hypereosinophilia of children: a case report |
title_short | Cardiac endothelial sarcoma with hypereosinophilia of children: a case report |
title_sort | cardiac endothelial sarcoma with hypereosinophilia of children: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10080960/ https://www.ncbi.nlm.nih.gov/pubmed/37029383 http://dx.doi.org/10.1186/s13019-023-02206-4 |
work_keys_str_mv | AT zhangwei cardiacendothelialsarcomawithhypereosinophiliaofchildrenacasereport AT hemengyuan cardiacendothelialsarcomawithhypereosinophiliaofchildrenacasereport AT wangqiang cardiacendothelialsarcomawithhypereosinophiliaofchildrenacasereport |