Key result
Surgical resection successfully resolves a rare cardiac epithelioid hemangioma in a young woman.
Case Report (n=1)
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Cardiac epithelioid hemangioma is an extremely rare benign vascular tumor that can present with supraventricular arrhythmia and peripheral eosinophilia, and is amenable to surgical resection.
Epithelioid hemangioma (EH) is a rare benign vascular lesion, characterized by endothelial cells with epithelioid/histiocytoid appearance. Heart involvement is extremely rare. We present an unusual case of cardiac EH in a young woman with supraventricular arrhythmia, nephrotic syndrome (membranous glomerulopathy), and peripheral eosinophilia after a pregnancy and normal partum resembling Kimura disease. Echocardiogram showed a large tumor mass in the right cardiac ventricle. The cardiac tumor was removed and the histopathology revealed an endothelial proliferation associated with abundant eosinophils. The neoplastic endothelial cells were eosinophilic and polygonal with epithelioid/histiocytoid morphology. Lymphoid nodules were occasionally seen. The neoplastic cells were positive for CD34, CD31, ERG, and factor VIII and negative for CK. A diagnosis of EH was rendered. The patient was alive and well after surgical resection. EH and Kimura disease represent separate entities, but clinical and/or histological overlapping can be observed. Epithelioid/histiocytoid endothelial cells constitute the hallmark feature that favors a final diagnosis of EH.
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Machado et al. (2015) conducted a case report in Cardiac epithelioid hemangioma (n=1). Surgical resection was evaluated on Patient survival and well-being. Surgical resection of a rare cardiac epithelioid hemangioma in a young woman was successful, with the patient remaining alive and well post-operatively.
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