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Multiple lipomata of the tricuspid valve and papillary muscle: case report
BACKGROUND: Cardiac lipomas are rare benign primary tumours of the heart. Due to the nature of these tumours, they are often asymptomatic and diagnosed incidentally. Whether asymptomatic patients with cardiac lipomas should perform surgery still remains controversial. CASE SUMMARY: A 34-year-old Asi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343444/ https://www.ncbi.nlm.nih.gov/pubmed/34377909 http://dx.doi.org/10.1093/ehjcr/ytab260 |
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author | Zhao, Yixin Li, Guoliang Wang, Shun Yan, Yang |
author_facet | Zhao, Yixin Li, Guoliang Wang, Shun Yan, Yang |
author_sort | Zhao, Yixin |
collection | PubMed |
description | BACKGROUND: Cardiac lipomas are rare benign primary tumours of the heart. Due to the nature of these tumours, they are often asymptomatic and diagnosed incidentally. Whether asymptomatic patients with cardiac lipomas should perform surgery still remains controversial. CASE SUMMARY: A 34-year-old Asian male who was incidentally found hyperechoic masses in the right ventricle (RV) on the transthoracic echocardiogram by annually routine physical examination was admitted to our cardiology department. His medical history was unremarkable. The repeated transthoracic and transoesophageal echocardiogram showed multiple solitary and well-demarcated masses in the RV. On the cardiac magnetic resonance imaging, four discrete masses (considering the possibility of it being a lipoma) partially occluding the right ventricular outflow tract (RVOT) were observed. During the open-heart resection surgery, it was found that the tricuspid valve and papillary muscle were covered by multiple adipose masses in the RV that arose from the interventricular septum and the free wall, resulting in partial RVOT obstruction. These excised masses were histopathologically confirmed as lipomata characterized by the mature adipocytes with entrapped myocardial cells. The patient had no cardiac abnormality in the 1-month follow-up after the surgery. DISCUSSION: This rare clinical case of multiple lipomata of the tricuspid valve and papillary muscle acknowledges that multimodality imaging is the cornerstone for the assessment and diagnosis. Surgery should be performed in cases of symptomatic or large lipomas as well as when a lipoma is considered to be high risk because of RVOT obstruction. |
format | Online Article Text |
id | pubmed-8343444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-83434442021-08-09 Multiple lipomata of the tricuspid valve and papillary muscle: case report Zhao, Yixin Li, Guoliang Wang, Shun Yan, Yang Eur Heart J Case Rep Case Report BACKGROUND: Cardiac lipomas are rare benign primary tumours of the heart. Due to the nature of these tumours, they are often asymptomatic and diagnosed incidentally. Whether asymptomatic patients with cardiac lipomas should perform surgery still remains controversial. CASE SUMMARY: A 34-year-old Asian male who was incidentally found hyperechoic masses in the right ventricle (RV) on the transthoracic echocardiogram by annually routine physical examination was admitted to our cardiology department. His medical history was unremarkable. The repeated transthoracic and transoesophageal echocardiogram showed multiple solitary and well-demarcated masses in the RV. On the cardiac magnetic resonance imaging, four discrete masses (considering the possibility of it being a lipoma) partially occluding the right ventricular outflow tract (RVOT) were observed. During the open-heart resection surgery, it was found that the tricuspid valve and papillary muscle were covered by multiple adipose masses in the RV that arose from the interventricular septum and the free wall, resulting in partial RVOT obstruction. These excised masses were histopathologically confirmed as lipomata characterized by the mature adipocytes with entrapped myocardial cells. The patient had no cardiac abnormality in the 1-month follow-up after the surgery. DISCUSSION: This rare clinical case of multiple lipomata of the tricuspid valve and papillary muscle acknowledges that multimodality imaging is the cornerstone for the assessment and diagnosis. Surgery should be performed in cases of symptomatic or large lipomas as well as when a lipoma is considered to be high risk because of RVOT obstruction. Oxford University Press 2021-07-30 /pmc/articles/PMC8343444/ /pubmed/34377909 http://dx.doi.org/10.1093/ehjcr/ytab260 Text en © The Author(s) 2021. 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 Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (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 Zhao, Yixin Li, Guoliang Wang, Shun Yan, Yang Multiple lipomata of the tricuspid valve and papillary muscle: case report |
title | Multiple lipomata of the tricuspid valve and papillary muscle: case report |
title_full | Multiple lipomata of the tricuspid valve and papillary muscle: case report |
title_fullStr | Multiple lipomata of the tricuspid valve and papillary muscle: case report |
title_full_unstemmed | Multiple lipomata of the tricuspid valve and papillary muscle: case report |
title_short | Multiple lipomata of the tricuspid valve and papillary muscle: case report |
title_sort | multiple lipomata of the tricuspid valve and papillary muscle: case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343444/ https://www.ncbi.nlm.nih.gov/pubmed/34377909 http://dx.doi.org/10.1093/ehjcr/ytab260 |
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