Huge Left Atrial Myxoma and Concomitant Silent Coronary Artery Disease in a Young Man
Marco Gennari1, Mara Rubino2, Daniele Andreini3
1Department of Cardiovascular Disease, Development and Innovation Cardiac Surgery Unit, Centro Cardiologico Monzino, Milan, Italy.
Insights
Silent coronary artery disease can occur in young adults with cardiac tumors. Preoperative coronary assessment is crucial for patients with cardiovascular risk factors and family history, even with non-ischemic heart conditions.
Area of Science:
- Cardiology
- Cardiovascular Surgery
- Cardiac Oncology
Background:
- Severe coronary artery disease (CAD) is uncommon in young, low-risk individuals.
- A family history of CAD and cardiovascular risk factors can indicate silent CAD.
- Left atrial myxoma can cause symptoms mimicking ischemic heart disease.
Observation:
- A 33-year-old male presented with shortness of breath due to a large left atrial myxoma.
- Preoperative assessment revealed significant, previously undiagnosed coronary artery disease.
Findings:
- The patient successfully underwent resection of the left atrial myxoma and coronary artery bypass grafting (CABG).
- This case highlights the potential for severe CAD in young, seemingly low-risk individuals with specific risk factors.
Implications:
- Preoperative coronary evaluation should be considered in young patients with cardiac tumors or other non-ischemic pathologies, especially if they have a family history of CAD.
- This approach can prevent perioperative complications and ensure optimal patient outcomes.
Abstract:
Severe but silent coronary artery disease may rarely exist in young patients with a low-risk profile but with a family history of coronary artery disease. We describe the case of a 33-year-old Caucasian male with progressive shortness of breath caused by a huge left atrial myxoma who was diagnosed to have significant coronary artery disease in the preoperative assessment. After investigations, the patient underwent resection of the left atrial tumor and coronary artery bypass grafting (CABG) with a successful outcome. Even in the case of a young male, it may be prudent to investigate silent coronary artery disease in the presence of cardiovascular risk factors and family history of coronary artery disease. The learning objective of this case is to debate about the usefulness of a preoperative coronary study even in the young population with cardiac nonischemic pathologies (ie, valve pathology, cardiac tumors, etc.).
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