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Published in: Journal of Cardiothoracic Surgery 1/2008

Open Access 01-12-2008 | Case report

Large asymptomatic Left Atrial Myxoma with ossification: case report

Authors: Mattheos Panagiotou, Nikolaos D Panagopoulos, Panagiota Ravazoula, Loukas Kaklamanis, Efstratios N Koletsis

Published in: Journal of Cardiothoracic Surgery | Issue 1/2008

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Abstract

Background

Atrial myxomas are the most common primary cardiac tumors. They are usually small or moderate in size by the time of the diagnosis, exhibiting non specific cardiac or systemic symptoms, and are most frequently soft and friable without microscopic signs of ossification. We describe herein an extremely rare case of an asymptomatic giant left atrial myxoma with angiographic neovascularization and ossification.

Case presentation

An asymptomatic 58-year-old male with a giant left atrial tumor, was transferred to our Unit for surgical treatment. The tumor was an incidental finding during a work-up for hemoptysis due to bronchectasis. The coronary angiogram showed tumor vessels originating from the RCA. The tumor macroscopically did not resemble a myxoma, considering its dimensions (12 × 10 cm) and its solid substance. The mass was excised together with the interatrial septum and the right lateral LA wall close to the right pulmonary veins orifices. The defect was closed with Dacron patches in order to prevent malformation of both atria. The pathology study revealed a benign myxoma with excessive osteoid (mature bone) content.

Conclusion

We consider our case as extremely rare because of the asymptomatic course despite the large size of the tumor, the blood supply from the right coronary artery and the bone formation.
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Metadata
Title
Large asymptomatic Left Atrial Myxoma with ossification: case report
Authors
Mattheos Panagiotou
Nikolaos D Panagopoulos
Panagiota Ravazoula
Loukas Kaklamanis
Efstratios N Koletsis
Publication date
01-12-2008
Publisher
BioMed Central
Published in
Journal of Cardiothoracic Surgery / Issue 1/2008
Electronic ISSN: 1749-8090
DOI
https://doi.org/10.1186/1749-8090-3-19

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