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Rheumatism as a cause of cardiac hemangioma: a rare case report and review of literature with special focus on etiology
BACKGROUND: Cardiac hemangioma is a very rare benign tumor of the heart which accounts for 1–2% of all primary cardiac tumors. Multiple cardiac hemangiomas are even rarer with only three cases published in the literature. Pathologically it can be divided into cavernous hemangioma, capillary hemangio...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10122334/ https://www.ncbi.nlm.nih.gov/pubmed/37085767 http://dx.doi.org/10.1186/s12872-023-03241-8 |
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author | Xie, Ting Masroor, Matiullah Chen, Xuan Liu, Fujin Zhang, Jie Yang, Dayan Liu, Cong Xiang, Mei |
author_facet | Xie, Ting Masroor, Matiullah Chen, Xuan Liu, Fujin Zhang, Jie Yang, Dayan Liu, Cong Xiang, Mei |
author_sort | Xie, Ting |
collection | PubMed |
description | BACKGROUND: Cardiac hemangioma is a very rare benign tumor of the heart which accounts for 1–2% of all primary cardiac tumors. Multiple cardiac hemangiomas are even rarer with only three cases published in the literature. Pathologically it can be divided into cavernous hemangioma, capillary hemangioma, arteriovenous hemangioma, mixed-type hemangioma, and so on. At present, the etiology of cardiac hemangioma is not completely clear. In this study, we present multiple cardiac hemangiomas located in the right atrium and discuss the new unreported possible cause (rheumatism) of cardiac hemangioma. This is the fourth case of multiple cardiac hemangiomas in the medical literature and the first time to present rheumatism as the cause of cardiac hemangioma. CASE PRESENTATION: A 53-year-old man presented to the clinic with intermittent chest tightness and shortness of breath for 2 years. On echocardiography, multiple soft tissue masses in the right atrium were found. The patient had rheumatic heart disease with severe mitral stenosis and moderate tricuspid regurgitation. Two masses with a diameter of about 20 mm and 15 mm were seen in the right atrium. One mass was located on the inferior margin of the fossa ovalis and the other was adjacent to the inferior vena cava. Both masses were successfully removed surgically. The mitral valve replacement and tricuspid valve plasty were performed at the same time. The postoperative histopathology results confirmed the diagnosis of cavernous hemangioma. CONCLUSION: The occurrence of multiple hemangiomas in the heart is possible, especially in the presence of rheumatism. Rheumatism is one of the possible etiologies of cardiac hemangioma. Cardiologists and cardiac surgeons should be aware of its occurrence and should consider cardiac hemangioma as a differential diagnosis especially in rheumatic heart disease patients when they present with soft tissue cardiac masses for accurate management. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-023-03241-8. |
format | Online Article Text |
id | pubmed-10122334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101223342023-04-23 Rheumatism as a cause of cardiac hemangioma: a rare case report and review of literature with special focus on etiology Xie, Ting Masroor, Matiullah Chen, Xuan Liu, Fujin Zhang, Jie Yang, Dayan Liu, Cong Xiang, Mei BMC Cardiovasc Disord Case Report BACKGROUND: Cardiac hemangioma is a very rare benign tumor of the heart which accounts for 1–2% of all primary cardiac tumors. Multiple cardiac hemangiomas are even rarer with only three cases published in the literature. Pathologically it can be divided into cavernous hemangioma, capillary hemangioma, arteriovenous hemangioma, mixed-type hemangioma, and so on. At present, the etiology of cardiac hemangioma is not completely clear. In this study, we present multiple cardiac hemangiomas located in the right atrium and discuss the new unreported possible cause (rheumatism) of cardiac hemangioma. This is the fourth case of multiple cardiac hemangiomas in the medical literature and the first time to present rheumatism as the cause of cardiac hemangioma. CASE PRESENTATION: A 53-year-old man presented to the clinic with intermittent chest tightness and shortness of breath for 2 years. On echocardiography, multiple soft tissue masses in the right atrium were found. The patient had rheumatic heart disease with severe mitral stenosis and moderate tricuspid regurgitation. Two masses with a diameter of about 20 mm and 15 mm were seen in the right atrium. One mass was located on the inferior margin of the fossa ovalis and the other was adjacent to the inferior vena cava. Both masses were successfully removed surgically. The mitral valve replacement and tricuspid valve plasty were performed at the same time. The postoperative histopathology results confirmed the diagnosis of cavernous hemangioma. CONCLUSION: The occurrence of multiple hemangiomas in the heart is possible, especially in the presence of rheumatism. Rheumatism is one of the possible etiologies of cardiac hemangioma. Cardiologists and cardiac surgeons should be aware of its occurrence and should consider cardiac hemangioma as a differential diagnosis especially in rheumatic heart disease patients when they present with soft tissue cardiac masses for accurate management. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12872-023-03241-8. BioMed Central 2023-04-21 /pmc/articles/PMC10122334/ /pubmed/37085767 http://dx.doi.org/10.1186/s12872-023-03241-8 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 Xie, Ting Masroor, Matiullah Chen, Xuan Liu, Fujin Zhang, Jie Yang, Dayan Liu, Cong Xiang, Mei Rheumatism as a cause of cardiac hemangioma: a rare case report and review of literature with special focus on etiology |
title | Rheumatism as a cause of cardiac hemangioma: a rare case report and review of literature with special focus on etiology |
title_full | Rheumatism as a cause of cardiac hemangioma: a rare case report and review of literature with special focus on etiology |
title_fullStr | Rheumatism as a cause of cardiac hemangioma: a rare case report and review of literature with special focus on etiology |
title_full_unstemmed | Rheumatism as a cause of cardiac hemangioma: a rare case report and review of literature with special focus on etiology |
title_short | Rheumatism as a cause of cardiac hemangioma: a rare case report and review of literature with special focus on etiology |
title_sort | rheumatism as a cause of cardiac hemangioma: a rare case report and review of literature with special focus on etiology |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10122334/ https://www.ncbi.nlm.nih.gov/pubmed/37085767 http://dx.doi.org/10.1186/s12872-023-03241-8 |
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