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Multiple intracardiac masses: myxoma, thrombus or metastasis: a case report
INTRODUCTION: The incidence of multiple intracardiac mass is rare. The differential diagnosis of intracavitary mass lesions includes benign, malignant primary, secondary metastatic cardiac tumors, or thrombus. CASE PRESENTATION: We report the case of a 49-year-old Asian woman, who experienced a 2-we...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550069/ https://www.ncbi.nlm.nih.gov/pubmed/26307017 http://dx.doi.org/10.1186/s13256-015-0650-4 |
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author | Lee, Wei-Chieh Huang, Min-Ping Fu, Morgan |
author_facet | Lee, Wei-Chieh Huang, Min-Ping Fu, Morgan |
author_sort | Lee, Wei-Chieh |
collection | PubMed |
description | INTRODUCTION: The incidence of multiple intracardiac mass is rare. The differential diagnosis of intracavitary mass lesions includes benign, malignant primary, secondary metastatic cardiac tumors, or thrombus. CASE PRESENTATION: We report the case of a 49-year-old Asian woman, who experienced a 2-week history of progressive exertional dyspnea, orthopnea, bilateral lower limb edema and palpitations. Transthoracic echocardiography showed one fixed round hyperechoic mass with central necrosis over the left ventricular apex, one oscillating hyperechoic nodule over the anterior mitral annulus and one irregularly heterogeneous mass bulging out from the lateral wall of the right atrium. The incidence of multiple myxomas is rare. Unfortunately, high tumor marker, serum lactic dehydrogenase and serum uric acid levels were also present. We could not differentiate between diagnoses of multiple myxomas with thrombi or multiple metastatic tumors. CONCLUSIONS: Primary intracardiac tumors are rare. Approximately 75% are benign, and approximately 50% are myxomas, which have an incidence of 0.0017% in the general population. Multiple intracardiac myxomas account for less than 5% of all cases of myxoma. Our case was an atypical picture of right atrial (RA) myxoma, as it was located in the RA lateral wall and extended to the RA auricle at the junction among the superior and inferior vena cava. Two masses in the left ventricle (LV) were thrombi and resolved after heparinization. Initially, elevated tumor markers and high serum uric acid and high serum lactic dehydrogenase levels were related to necrotic tumor-derived tissue, decompensated heart failure with pleural effusion and renal insufficiency. We share our experience of multiple intracardiac masses. Whether the intracardiac mass is benign or malignant, we recommend surgery due to the possibilities of systemic or pulmonary massive embolism, infection, arrhythmia and sudden death if the thrombus ruptures or the mass dislodges. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13256-015-0650-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4550069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45500692015-08-27 Multiple intracardiac masses: myxoma, thrombus or metastasis: a case report Lee, Wei-Chieh Huang, Min-Ping Fu, Morgan J Med Case Rep Case Report INTRODUCTION: The incidence of multiple intracardiac mass is rare. The differential diagnosis of intracavitary mass lesions includes benign, malignant primary, secondary metastatic cardiac tumors, or thrombus. CASE PRESENTATION: We report the case of a 49-year-old Asian woman, who experienced a 2-week history of progressive exertional dyspnea, orthopnea, bilateral lower limb edema and palpitations. Transthoracic echocardiography showed one fixed round hyperechoic mass with central necrosis over the left ventricular apex, one oscillating hyperechoic nodule over the anterior mitral annulus and one irregularly heterogeneous mass bulging out from the lateral wall of the right atrium. The incidence of multiple myxomas is rare. Unfortunately, high tumor marker, serum lactic dehydrogenase and serum uric acid levels were also present. We could not differentiate between diagnoses of multiple myxomas with thrombi or multiple metastatic tumors. CONCLUSIONS: Primary intracardiac tumors are rare. Approximately 75% are benign, and approximately 50% are myxomas, which have an incidence of 0.0017% in the general population. Multiple intracardiac myxomas account for less than 5% of all cases of myxoma. Our case was an atypical picture of right atrial (RA) myxoma, as it was located in the RA lateral wall and extended to the RA auricle at the junction among the superior and inferior vena cava. Two masses in the left ventricle (LV) were thrombi and resolved after heparinization. Initially, elevated tumor markers and high serum uric acid and high serum lactic dehydrogenase levels were related to necrotic tumor-derived tissue, decompensated heart failure with pleural effusion and renal insufficiency. We share our experience of multiple intracardiac masses. Whether the intracardiac mass is benign or malignant, we recommend surgery due to the possibilities of systemic or pulmonary massive embolism, infection, arrhythmia and sudden death if the thrombus ruptures or the mass dislodges. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13256-015-0650-4) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-26 /pmc/articles/PMC4550069/ /pubmed/26307017 http://dx.doi.org/10.1186/s13256-015-0650-4 Text en © Lee et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/ (http://creativecommons.org/licenses/by/4.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Lee, Wei-Chieh Huang, Min-Ping Fu, Morgan Multiple intracardiac masses: myxoma, thrombus or metastasis: a case report |
title | Multiple intracardiac masses: myxoma, thrombus or metastasis: a case report |
title_full | Multiple intracardiac masses: myxoma, thrombus or metastasis: a case report |
title_fullStr | Multiple intracardiac masses: myxoma, thrombus or metastasis: a case report |
title_full_unstemmed | Multiple intracardiac masses: myxoma, thrombus or metastasis: a case report |
title_short | Multiple intracardiac masses: myxoma, thrombus or metastasis: a case report |
title_sort | multiple intracardiac masses: myxoma, thrombus or metastasis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550069/ https://www.ncbi.nlm.nih.gov/pubmed/26307017 http://dx.doi.org/10.1186/s13256-015-0650-4 |
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