Non-syndromic aortic valve myxoma in a teen, cause of angina symptoms
Abstract Background Cardiac myxoma, a common benign primary tumor of the heart can be categorized into syndromic (Carney Complex) and non-syndromic(isolated). Carney Complex associated myxomas can be found in any region and system (cardiac, cutaneous, osseous, genitalia), and may manifest at a tende...
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doaj-7e9dc4aab83c487d98ae8a1486882c432020-11-25T03:54:04ZengBMCJournal of Cardiothoracic Surgery1749-80902019-07-011411310.1186/s13019-019-0968-xNon-syndromic aortic valve myxoma in a teen, cause of angina symptomsGeoffrey Joseph Changwe0Tao Zhang1Haizhou Zhang2Chengwei Zou3Departments of Cardiovascular Surgery and Ultrasound, Shandong Provincial Hospital affiliated to Shandong UniversityDepartments of Cardiovascular Surgery and Ultrasound, Shandong Provincial Hospital affiliated to Shandong UniversityDepartments of Cardiovascular Surgery and Ultrasound, Shandong Provincial Hospital affiliated to Shandong UniversityDepartments of Cardiovascular Surgery and Ultrasound, Shandong Provincial Hospital affiliated to Shandong UniversityAbstract Background Cardiac myxoma, a common benign primary tumor of the heart can be categorized into syndromic (Carney Complex) and non-syndromic(isolated). Carney Complex associated myxomas can be found in any region and system (cardiac, cutaneous, osseous, genitalia), and may manifest at a tender age. On the contrary, non-syndromic cardiac myxomas are usually confined to the chambers, and symptoms often present from 5th decade of life. Aortic valve myxoma is a very unusual occurrence, and presentation in a teen is extremely rare. Case report We share a case of aortic valve myxoma, uncovered using echocardiography in a 16-year-old male, admitted with complaints of exertional chest pain, dyspnoea and systolic murmur. Patient underwent uneventful surgery for tumor excision, and discharged 6-days post operation. Conclusion Given the high risk of developing cardiogenic stroke, infective endocarditis, degenerative effects on aortic valve leaflets and possible sudden death, like many other centers, we advocate for immediate liquidation of aortic myxoma regardless of age and symptoms.http://link.springer.com/article/10.1186/s13019-019-0968-xCardiac myxomaAortic valve myxomaNon-syndromicCarney complex |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Geoffrey Joseph Changwe Tao Zhang Haizhou Zhang Chengwei Zou |
spellingShingle |
Geoffrey Joseph Changwe Tao Zhang Haizhou Zhang Chengwei Zou Non-syndromic aortic valve myxoma in a teen, cause of angina symptoms Journal of Cardiothoracic Surgery Cardiac myxoma Aortic valve myxoma Non-syndromic Carney complex |
author_facet |
Geoffrey Joseph Changwe Tao Zhang Haizhou Zhang Chengwei Zou |
author_sort |
Geoffrey Joseph Changwe |
title |
Non-syndromic aortic valve myxoma in a teen, cause of angina symptoms |
title_short |
Non-syndromic aortic valve myxoma in a teen, cause of angina symptoms |
title_full |
Non-syndromic aortic valve myxoma in a teen, cause of angina symptoms |
title_fullStr |
Non-syndromic aortic valve myxoma in a teen, cause of angina symptoms |
title_full_unstemmed |
Non-syndromic aortic valve myxoma in a teen, cause of angina symptoms |
title_sort |
non-syndromic aortic valve myxoma in a teen, cause of angina symptoms |
publisher |
BMC |
series |
Journal of Cardiothoracic Surgery |
issn |
1749-8090 |
publishDate |
2019-07-01 |
description |
Abstract Background Cardiac myxoma, a common benign primary tumor of the heart can be categorized into syndromic (Carney Complex) and non-syndromic(isolated). Carney Complex associated myxomas can be found in any region and system (cardiac, cutaneous, osseous, genitalia), and may manifest at a tender age. On the contrary, non-syndromic cardiac myxomas are usually confined to the chambers, and symptoms often present from 5th decade of life. Aortic valve myxoma is a very unusual occurrence, and presentation in a teen is extremely rare. Case report We share a case of aortic valve myxoma, uncovered using echocardiography in a 16-year-old male, admitted with complaints of exertional chest pain, dyspnoea and systolic murmur. Patient underwent uneventful surgery for tumor excision, and discharged 6-days post operation. Conclusion Given the high risk of developing cardiogenic stroke, infective endocarditis, degenerative effects on aortic valve leaflets and possible sudden death, like many other centers, we advocate for immediate liquidation of aortic myxoma regardless of age and symptoms. |
topic |
Cardiac myxoma Aortic valve myxoma Non-syndromic Carney complex |
url |
http://link.springer.com/article/10.1186/s13019-019-0968-x |
work_keys_str_mv |
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