Angiosarcoma of the heart predominantly involving the pericardium: A clinicopathologic study with
R Ruffolo1, S Suster1, M Sivina1
1From the Department of Pathology and Laboratory Medicine, Mount Sinai Medical Center and University of Miami, School of Medicine, Miami Beach, Florida, USA; Department of Cardiovascular Surgery, Mount Sinai Medical Center and University of Miami, School of Medicine, Miami Beach, Florida, USA.
Abstract:
A case of angiosarcoma of the heart with predominant involvement of the pericardium and diffuse bilateral lymphangitic spread to both lungs is presented. The patient was a 32-year-old man admitted for cough, dyspnea, and intermittent hemoptysis. Chest x-ray and computed tomography scans revealed bilateral pulmonary infiltrates and pericardial effusion. An echocardiogram showed a large oval mass overlying and compressing the right atrium and ventricle. At autopsy, multiple hemorrhagic tumor nodules were present in the pericardial sac, and an 8-cm hemorrhagic tumor mass was found overlying and compressing the right atrial appendage and infiltrating the heart muscle. Histological, immunohistochemical, and electron-microscopic examination revealed the features of angiosarcoma. The predominant pericardial location observed in this case was a source of difficulty both in the clinical and pathological differential diagnosis and raised the question of possible primary pericardial angiosarcoma with secondary involvement of the heart. A review of the literature on this topic is presented.
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