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Pericardial angiosarcoma simulating pericardial effusion by echocardiography

Chest
|June 1, 1978
PubMed

Insights

A rapidly growing angiosarcoma led to a boy's incapacitation and death within three months. Echocardiograms documented the aggressive tumor's cardiac encasement and metastasis, highlighting a rare cause of echo-free space.

Area of Science:

  • Cardiovascular Pathology
  • Pediatric Oncology
  • Medical Imaging

Background:

  • Angiosarcoma is a rare and aggressive malignant vascular tumor.
  • Pediatric cardiac tumors are uncommon, with angiosarcoma being particularly rare and aggressive.
  • Echocardiography is a crucial non-invasive tool for diagnosing cardiac and pericardial abnormalities.

Observation:

  • A fast-growing angiosarcoma caused rapid incapacitation and death in a pediatric patient over three months.
  • Serial echocardiograms revealed extensive tumor growth encasing the heart within a thick, purplish vascular neoplasm.
  • The tumor showed extracardiac metastasis, and the heart weighed significantly at 2,000 gm.

Findings:

  • The case demonstrates the aggressive nature of angiosarcoma in a pediatric patient, leading to rapid deterioration.
  • Echocardiographic findings included a thick pericardial neoplasm encasing the heart, distinct from pericardial effusion.
  • Autopsy confirmed angiosarcoma with significant cardiac involvement and metastasis.

Implications:

  • This case underscores the importance of considering pericardial tumors in the differential diagnosis of echo-free spaces on echocardiograms.
  • Early recognition and diagnosis of pediatric cardiac angiosarcoma are critical for potential therapeutic interventions, despite its poor prognosis.
  • Further research into the pathogenesis and treatment of pediatric angiosarcoma is warranted.

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