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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...

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Autores principales: Zhang, Wei, He, Mengyuan, Wang, Qiang
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
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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.
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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
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