Author:
Chen Ke-Wei,Chang Ju-Hsin,Yeh Su-Peng,Lu Chiung-Ray
Abstract
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.
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine,General Medicine,Surgery,Pulmonary and Respiratory Medicine
Reference9 articles.
1. Gowda RM, Khan IA: Clinical perspectives of primary cardiac lymphoma. Angiology. 2003, 54: 599-604. 10.1177/000331970305400510.
2. Sheppard MN, Angelini A, Raad M, Savelieva I: Tumours of the heart. The ESC Textbook of Cardiovascular Medicine. Edited by: Camm AJF, Luscher T, Serruys PW. 2006, Blackwell, London, 535-552.
3. Reynen K: Frequency of primary tumors of the heart. Am J Cardiol. 1996, 77: 107-10.1016/S0002-9149(97)89149-7.
4. Miguel CE, Bestetti RB: Primary cardiac lymphoma. Int J Cardiol. 2011, 149: 358-363. 10.1016/j.ijcard.2010.02.016.
5. Miyashita T, Miyzawa I, Kiyosawa K: A case of primary cardiac B cell lymphoma associated with ventricular tachycardia, successfully treated with systemic chemotherapy and radiotherapy. Jpn Circ J. 2000, 64: 135-138. 10.1253/jcj.64.135.
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