Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5951938 | Cardiovascular Pathology | 2015 | 5 Pages |
Abstract
Primary cardiac neoplasms are rare. However, among them, cardiac myxoma is the most common tumor. In contrast, primary cardiac lymphoma within a cardiac myxoma is extremely rare and might be difficult to diagnose because of non-specific clinical manifestations. We report the case of a previously healthy 52-year-old man who presented with acute onset of transient dysarthria and left hemiplegia. A transthoracic echocardiography showed a 6Ã2.5-cm solid mass in the left atrium, which was subsequently resected. Histological, immunohistochemical, and molecular analyses revealed an EBV-associated CD30-positive large B-cell lymphoma with anaplastic morphology within a cardiac myxoma and fibrinous material. Staging studies showed no evidence of lymphoma elsewhere. The patient achieved complete remission and is alive 42Â months after diagnosis, and did not receive chemotherapy. We discuss the clinical and pathologic features of lymphoma arising in cardiac myxoma or in intra-atrial fibrinoid mass and the potential role of IL-6 in its pathogenesis.
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Authors
Cristian Aguilar, Brady Beltran, Pilar Quiñones, Tomas Carbajal, Jorge Vilcapaza, Alejandro Yabar, Pedro Segura, Leticia Quintanilla-Martinez, Roberto N. Miranda, Jorge J. Castillo,