ArticleCureus2026
Left Ventricular Myxoma in a Young Adult: An Unusual Presentation of a Rare Cardiac Tumor.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
5 authors.
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No grant is acknowledged in the PubMed record.
Abstract
Cardiac myxomas are rare primary tumors, generally benign, and predominantly located in the atria, especially the left. Their clinical presentation is variable, and they can manifest with embolic events, intracardiac obstruction, or as an incidental finding. We present a case of a 25-year-old patient with fatigue and atypical chest pain, in whom transthoracic echocardiography revealed a pedunculated, irregular-bordered, highly mobile intracavitary mass in the left ventricle, attached to the interventricular septum. Given the unusual location and the potential risk of complications, complete surgical resection was performed, with no adverse postoperative events. Histopathological examination confirmed the diagnosis of cardiac myxoma. This case highlights an uncommon presentation of this entity, underscoring the importance of considering cardiac tumors in the differential diagnosis of ventricular masses and the fundamental role of echocardiography in their timely detection and therapeutic planning.
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