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Z. Frikha, et al., “Cardiac Tamponade and Paroxysmal Third-Degree Atrioventricular Block Revealing a Primary Cardiac Non-Hodgkin Large B-Cell Lymphoma of the Right Ventricle: A Case Report,” Journal of Medical Case Reports, Vol. 5, 2011, p. 433. doi:10.1186/1752-1947-5-433

has been cited by the following article:

• TITLE: Cardiac Mass and Hypertrophic Cardiomyopathy as Aggressive Presentation of Primary Cardiac Lymphoma: A Case Report

  AUTHORS: Mehandi Haran, Evbu Enakpene, Ankur Lodha

  KEYWORDS: Primary Cardiac Lymphoma; Asymmetric Left Ventricular Hypertrophy; Chemotherapy

  JOURNAL NAME: Journal of Cancer Therapy, Vol.3 No.3, June 20, 2012

  ABSTRACT: Primary cardiac lymphoma is very rare. This disease occurs mainly in immunocompromised patients and rarely in the immunocompetent. With the advent of echocardiogram, computed tomography and magnetic resonance imaging, more cases are being diagnosed ante-mortem although the prognosis still remains poor. These cardiac tumors provide unique diagnostic and therapeutic challenges. We present an interesting case of primary cardiac lymphoma diagnosed antemortem in an 81 year old immunocompetent female presenting as a large mass in the right atrium, right ventricle and encasing the right coronary artery; and asymmetric left ventricular hypertrophy, a variant of hypertrophic cardiomyopathy. Patient responded very well to chemotherapy with subsequent regression of the cardiac mass and ventricular hypertrophy.