Beyond Beck's Triad: A Rare Cause of Cardiac Tamponade and Hemoptysis.
Journal: 2018/November - Ochsner Journal
ISSN: 1524-5012
Abstract:
UNASSIGNED
Primary cardiac angiosarcoma (CAS) is a rare tumor with a dismal prognosis. Many patients present with noncardiac symptoms related to metastatic disease that could delay the diagnosis and deteriorate the outcome.
UNASSIGNED
A 36-year-old male presented with hemoptysis. Initial imaging and biopsies were inconclusive, but a repeat transthoracic echocardiogram to evaluate the patient's pericardial effusion showed a mass inferior to the right atrium and invading the wall. Biopsy results from 3 different sites confirmed the diagnosis of CAS. However, the patient's course was complicated with respiratory failure that ultimately led to his death. Autopsy demonstrated CAS involving the full thickness of the right atrium and pericardial tissue, with a diffuse metastatic process involving the lung, brain, and stomach.
UNASSIGNED
The case highlights the importance of having an increased level of suspicion for cardiac malignancy among young patients presenting with noncardiac symptoms.
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Ochsner J 18(3): 271-273

Beyond Beck's Triad: A Rare Cause of Cardiac Tamponade and Hemoptysis

Background:

Primary cardiac angiosarcoma (CAS) is a rare tumor with a dismal prognosis. Many patients present with noncardiac symptoms related to metastatic disease that could delay the diagnosis and deteriorate the outcome.

Case Report:

A 36-year-old male presented with hemoptysis. Initial imaging and biopsies were inconclusive, but a repeat transthoracic echocardiogram to evaluate the patient's pericardial effusion showed a mass inferior to the right atrium and invading the wall. Biopsy results from 3 different sites confirmed the diagnosis of CAS. However, the patient's course was complicated with respiratory failure that ultimately led to his death. Autopsy demonstrated CAS involving the full thickness of the right atrium and pericardial tissue, with a diffuse metastatic process involving the lung, brain, and stomach.

Conclusion:

The case highlights the importance of having an increased level of suspicion for cardiac malignancy among young patients presenting with noncardiac symptoms.

Department of Internal Medicine, MedStar Washington Hospital Center, Washington, DC
Wayne State University, Detroit Medical Center Heart Hospital, Detroit, MI
Address correspondence to M. Chadi Alraies, Wayne State University, Detroit Medical Center Heart Hospital, 311 Mack Ave., Detroit, MI 48201 Tel: (216) 255-0008. Email: moc.liamtoh@seiarla

Abstract

Background:

Primary cardiac angiosarcoma (CAS) is a rare tumor with a dismal prognosis. Many patients present with noncardiac symptoms related to metastatic disease that could delay the diagnosis and deteriorate the outcome.

Case Report:

A 36-year-old male presented with hemoptysis. Initial imaging and biopsies were inconclusive, but a repeat transthoracic echocardiogram to evaluate the patient's pericardial effusion showed a mass inferior to the right atrium and invading the wall. Biopsy results from 3 different sites confirmed the diagnosis of CAS. However, the patient's course was complicated with respiratory failure that ultimately led to his death. Autopsy demonstrated CAS involving the full thickness of the right atrium and pericardial tissue, with a diffuse metastatic process involving the lung, brain, and stomach.

Conclusion:

The case highlights the importance of having an increased level of suspicion for cardiac malignancy among young patients presenting with noncardiac symptoms.

Keywords: Heart neoplasms, hemoptysis, sarcoma
Abstract

ACKNOWLEDGMENTS

The authors have no financial or proprietary interest in the subject matter of this article.

ACKNOWLEDGMENTS

REFERENCES

REFERENCES

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