Open Access Case report

Primary cardiac B-cell lymphoma with atrioventricular block and paroxysmal ventricular tachycardia

Ke-Wei Chen1, Ju-Hsin Chang2, Su-Peng Yeh3 and Chiung-Ray Lu1*

Author Affiliations

1 Division of Cardiology, Department of Internal Medicine, China Medical University Hospital, 2 Yuh-Der Rd, Taichung, 40447, Taiwan

2 Departments of Anesthesia, and Pain Service and Critical Care Medicine, China Medical University Hospital, Taichung, 40402, Taiwan

3 China Medical University Hospital, Taichung, 40402, Taiwan

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Journal of Cardiothoracic Surgery 2012, 7:70 doi:10.1186/1749-8090-7-70

Published: 18 July 2012

Abstract

Primary cardiac lymphoma (PCL) is very rare, and is extremely challenging to diagnose due to nonspecific symptoms. When discovered, the right atrium and ventricle are most commonly affected, while diffuse cardiac involvement is uncommon. PCL is fatal unless promptly diagnosed and treated. Herein, we present the case of a 36-year-old immunocompetent male who presented with a 5-year history of non-specific chest symptoms and was diagnosed with primary diffuse cardiac large B-cell lymphoma involving the entire heart.

Keywords:
Primary cardiac lymphoma; AV block; PVT