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Multifocal cardiac myxoma: report of a rare clinical entity
P K Goel1, K V Anand, A K Srivastava
1Department of Cardiology, Sanjay Gandhi Post Graduate Institute of Medical Sciences, Lucknow. pkgoel@sgpgi.ac.in
Insights
Primary cardiac tumors are rare, with myxomas being most common. This study details a rare case of multiple myxomas across three heart chambers, including ventricles, successfully treated with surgery.
Area of Science:
- Cardiology
- Cardiac Surgery
- Oncology
Background:
- Primary tumors of the heart and pericardium are uncommon, with cardiac myxomas constituting the majority of these rare neoplasms.
- Multiple myxomas are typically found in both atria (biatrial location).
Observation:
- A rare clinical case is presented involving a patient with four cardiac myxomas.
- These tumors were distributed across three of the heart's four chambers, uniquely involving both ventricles.
Findings:
- Transthoracic echocardiography was instrumental in accurately identifying the location and extent of the four cardiac tumors.
- Surgical intervention was successfully performed, leading to the complete removal of all identified myxomas.
Implications:
- This case expands the known spectrum of cardiac myxoma presentation, particularly regarding multiplicity and ventricular involvement.
- Highlights the importance of comprehensive echocardiographic evaluation for diagnosing complex cardiac tumor cases.
- Demonstrates the efficacy of surgical resection in managing extensive cardiac myxoma burdens.
Abstract:
Primary tumors of the heart and pericardium are rare, with myxomas representing the majority. Myxomas, if multiple, are mostly biatrial in location. We report a case with four tumors in three chambers of the heart, including both ventricles, which were identified by transthoracic echocardiography and successfully operated.
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