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Updated: Jun 27, 2026

Echocardiographic Evaluation of Atrial Communications before Transcatheter Closure
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[Huge right atrial myxoma].

M Sotokawa1, Y Nishiya, S Hoshino

  • 1Department of Cardiovascular Surgery, Toyama Prefectural Central Hospital, Toyama, Japan.

Kyobu Geka. the Japanese Journal of Thoracic Surgery
|December 4, 2008
PubMed
Summary

This case study details a rare right atrial myxoma, a type of heart tumor. Surgical removal was successful, and the patient recovered well, highlighting effective treatment for this unusual cardiac anomaly.

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Area of Science:

  • Cardiology
  • Oncology
  • Cardiac Surgery

Background:

  • Myxomas constitute about half of primary cardiac tumors.
  • Most cardiac myxomas (75%) typically originate in the left atrium.

Observation:

  • A 68-year-old woman presented with anorexia, fatigue, and facial edema.
  • Diagnostic imaging, including echocardiogram, CT, MRI, and catheter angiocardiogram, identified a large right atrial tumor.

Findings:

  • The tumor was completely resected from the right atrial free wall under cardiopulmonary bypass.
  • Pathological examination confirmed the tumor as myxomatous tissue.

Implications:

  • This case expands the understanding of cardiac myxoma presentation and location.
  • Successful surgical management of right atrial myxoma offers a positive prognosis.