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Frequently Asked Questions

What is the prognosis of cardiac angiosarcoma?

Background: Primary cardiac angiosarcoma is rare, but it is the most aggressive type of cardiac malignant tumor. When disease is confirmed it is often late in its stage resulting in a poor prognosis.

What is primary cardiac angiosarcoma?

Rationale: Primary cardiac angiosarcoma is a rare malignant cardiac neoplasm with early metastasis and poor prognosis. As there are currently no guidelines or effective therapeutic strategies, management of this condition depends on previous experiences of the clinician treating and the consideration of reported cases.

How is cardiac angiosarcoma diagnosed?

Echocardiography, CT and cardiac MRI, are all excellent imaging tools that may enable early detection and diagnosis of cardiac angiosarcoma. Clinicians should remember to keep this rare disease in the differential diagnosis of patients being evaluated for recurrent pericardial effusions of unknown etiology.

What is the most common complication of right-sided angiosarcoma?

The pericardium is frequently involved with right-sided angiosarcoma; cardiac tamponade and pericardial effusion are common complications. In a study by Hong et al. [2], 56% of the patients presented with pericardial effusion with or without cardiac tamponade.


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