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The In ovo CAM-assay as a Xenograft Model for Sarcoma

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Published on: July 17, 2013

Primary cardiac epithelioid angiosarcoma: A case report.

Thanh Hoa Do¹, Xuan Duong Le¹, Thu Thuy Vu²

¹Department of Emergency, Hanoi, Vietnam.

Radiology Case Reports

|July 22, 2022

Summary

This summary is machine-generated.

Primary cardiac angiosarcoma, a rare cancer, was diagnosed in a 44-year-old male. Imaging revealed a left atrial tumor with significant pericardial effusion, confirmed by pathology as epithelioid angiosarcoma.

Keywords:

Computed tomography (CT)Heart tumor Magnetic resonance imaging (MRI)Primary cardiac epithelioid angiosarcoma Transthoracic echocardiography (TTE)

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Area of Science:

Cardiovascular Pathology
Oncology
Medical Imaging

Background:

Primary cardiac angiosarcoma is an exceedingly rare and aggressive malignancy originating in the heart.
Early diagnosis is challenging due to nonspecific symptoms and rarity.

Observation:

A 44-year-old male presented with a left atrial heart tumor.
Significant pericardial effusion and local invasion were noted on imaging.
Diagnostic modalities included transthoracic echocardiography, computed tomography, and magnetic resonance imaging.

Findings:

Postoperative histopathological examination confirmed the tumor as primary cardiac epithelioid angiosarcoma.
The findings highlight the importance of advanced imaging in diagnosing rare cardiac tumors.

Implications:

This case underscores the diagnostic challenges and aggressive nature of primary cardiac angiosarcoma.
Accurate histopathological diagnosis is crucial for appropriate patient management and treatment strategies.
Further research into rare cardiac malignancies is warranted.