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Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

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Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
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Laparoscopic Anatomical Right Hemihepatectomy via the In Situ Anterior Approach
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Cardiac hemangioma: a case report.

Sung-Yong Hong1, Kyung-Taek Park1, Yang-Haeng Lee1

  • 1Department of Thoracic and Cardiovascular Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine, Korea.

The Korean Journal of Thoracic and Cardiovascular Surgery
|May 1, 2014
PubMed
Summary

This study reports a rare case of cardiac hemangioma, a benign heart tumor, misdiagnosed as a myxoma. Successful surgical removal confirmed the capillary hemangioma diagnosis, highlighting diagnostic challenges.

Keywords:
Heart neoplasmsHemangiomaLeft atriumMyxoma

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Area of Science:

  • Cardiology
  • Pathology

Background:

  • Primary cardiac tumors are rare, with hemangiomas accounting for only 2% of resected cases.
  • Cardiac hemangiomas originating from the left atrial wall are exceptionally uncommon.

Observation:

  • A patient presented with a cardiac mass initially misdiagnosed as a left atrial myxoma.
  • The tumor was located at the orifice of the right lower pulmonary vein.

Findings:

  • Pathological examination confirmed the mass to be a cardiac capillary hemangioma, not a myxoma.
  • This case highlights the potential for misdiagnosis of left atrial hemangiomas as myxomas due to similar presentations.

Implications:

  • Accurate preoperative diagnosis of cardiac hemangiomas is crucial to avoid misdiagnosis and ensure appropriate treatment.
  • This case underscores the importance of considering rare differential diagnoses in cardiac oncology.