Metastatic Cardiac Angiosarcoma in a 26-Year-Old Male

Elizabeth S Ellent1, Ronald Chong-Yik2, Abdul Mukhtadir Khan3

  • 1Department of Internal Medicine, Ochsner Clinic Foundation, New Orleans, LA.

Ochsner Journal
|September 24, 2016
PubMed

Insights

Cardiac angiosarcoma is a rare heart tumor. This case highlights that common symptoms like chest pain and hemoptysis can indicate this rare cancer, emphasizing broad diagnostic considerations.

Area of Science:

  • Cardiology
  • Oncology
  • Pathology

Background:

  • Cardiac angiosarcomas are exceptionally rare, occurring in 0.056% of cases.
  • Diagnosis is challenging due to varied presentations based on tumor location.
  • Symptoms can mimic heart failure or arrhythmias depending on proximity to cardiac structures.

Observation:

  • A young male presented with extensive lung cardiac angiosarcoma.
  • Key symptoms included pleuritic chest pain and hemoptysis.
  • The patient did not exhibit typical right-sided heart failure signs.

Findings:

  • The patient's primary complaint was hemoptysis, not heart failure.
  • This presentation deviates from classic cardiac angiosarcoma symptoms.

Implications:

  • Clinicians must maintain a broad differential diagnosis for common symptoms.
  • Consider rare conditions like cardiac angiosarcoma in patients with chest pain and hemoptysis.
  • Early and accurate diagnosis is crucial for rare cardiac tumors.
Abstract

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