INTRODUCTION: Primary cardiac lymphoma is rare. CASE PRESENTATION: We report the case of a 64-year-old non-immunodeficient Caucasian man, with cardiac tamponade and paroxysmal third-degree atrioventricular block. Echocardiography revealed the presence of a large pericardial effusion with signs of tamponade and a right ventricular mass was suspected. Scanner investigations clarified the sites, extension and anatomic details of myocardial and pericardial infiltration. Surgical resection was performed due to the rapid impairment of his cardiac function. Analysis of the pericardial fluid and histology confirmed the diagnosis of non-Hodgkin large B-cell lymphoma. He was treated with chemotherapy. CONCLUSION: The prognosis remains poor for this type of tumor due to delays in diagnosis and the importance of the site of disease.
INTRODUCTION:Primary cardiac lymphoma is rare. CASE PRESENTATION: We report the case of a 64-year-old non-immunodeficient Caucasian man, with cardiac tamponade and paroxysmal third-degree atrioventricular block. Echocardiography revealed the presence of a large pericardial effusion with signs of tamponade and a right ventricular mass was suspected. Scanner investigations clarified the sites, extension and anatomic details of myocardial and pericardial infiltration. Surgical resection was performed due to the rapid impairment of his cardiac function. Analysis of the pericardial fluid and histology confirmed the diagnosis of non-Hodgkin large B-cell lymphoma. He was treated with chemotherapy. CONCLUSION: The prognosis remains poor for this type of tumor due to delays in diagnosis and the importance of the site of disease.
Authors: Michael M Quigley; Eric Schwartzman; Pamela D Boswell; Rebecca L Christensen; Lisa A Gleason; Robert W Sharpe; Thomas A D'Amato Journal: Blood Date: 2003-01-30 Impact factor: 22.113