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A typical bilateral atrial myxoma: a case report
Zhenghua Xiao1, Wei Meng1, Da Zhu1
1Department of Thoracic and Cardiovascular Surgery, West China Hospital, Sichuan University, Sichuan, Chengdu 610041, China.
This case report details an extremely rare instance of bilateral myxoma, a type of heart tumor, occurring in a single male patient. Such dual-chamber myxomas are exceptionally uncommon in the general population.
Area of Science:
- Cardiology
- Oncology
- Rare Diseases
Background:
- Myxoma is a rare tumor with a general population incidence of 0.0017%.
- Cardiac myxomas are typically solitary tumors, making bilateral occurrences exceptionally rare.
- This report focuses on a unique case presentation in a male patient.
Purpose of the Study:
- To report a unique case of bilateral cardiac myxoma.
- To highlight the extreme rarity of myxomas affecting two distinct heart chambers.
- To contribute to the literature on rare cardiac tumors.
Main Methods:
- Case report.
- Review of patient medical history.
- Diagnostic imaging (specify if available, e.g., echocardiography, MRI).
Main Results:
- The patient presented with myxoma in two different heart chambers.
- This presentation represents an extremely rare manifestation of cardiac myxoma.
- Details of the patient's condition and diagnostic findings are presented.
Conclusions:
- Bilateral cardiac myxoma is an exceedingly rare clinical entity.
- This case underscores the importance of considering rare diagnoses in complex presentations.
- Further research may be warranted to understand the etiology of bilateral myxomas.
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