Primitive cardiac lymphoma (PCL) is a rare disease accounting for only 1-2% of primary cardiac tumors. Diffuse large B cell lymphoma is the most common type and shows a rapid progression with poor prognosis. The clinical presentation of PCL is nonspecific, and echocardiographic study is essential to the initial work-up. Magnetic resonance imaging and computed tomography scan are the methods of choice for the assessment of tumor extension. The definitive diagnosis is histopathology examination. Chemotherapy and radiotherapy represent the best treatment and should be started promptly after PCL diagnosis. We here report a case of PCL in a 59-year-old man complicated by pulmonary microembolism, atrial fibrillation and signs of right outflow tract obstruction.

[Primary cardiac lymphoma in an immunocompetent young adult: outcome with chemotherapy] / Perna, Gian Piero; Gini, Guido; Brambatti, Michela; Battistoni, Ilaria; Marini, Marco; Angelini, Luca; Francioni, Matteo; Goteri, Gaia; Dottori, Melissa. - In: GIORNALE ITALIANO DI CARDIOLOGIA. - ISSN 1827-6806. - 18:1(2017), pp. 7-10. [10.1714/2628.27021]

[Primary cardiac lymphoma in an immunocompetent young adult: outcome with chemotherapy]

GOTERI, Gaia;
2017-01-01

Abstract

Primitive cardiac lymphoma (PCL) is a rare disease accounting for only 1-2% of primary cardiac tumors. Diffuse large B cell lymphoma is the most common type and shows a rapid progression with poor prognosis. The clinical presentation of PCL is nonspecific, and echocardiographic study is essential to the initial work-up. Magnetic resonance imaging and computed tomography scan are the methods of choice for the assessment of tumor extension. The definitive diagnosis is histopathology examination. Chemotherapy and radiotherapy represent the best treatment and should be started promptly after PCL diagnosis. We here report a case of PCL in a 59-year-old man complicated by pulmonary microembolism, atrial fibrillation and signs of right outflow tract obstruction.
2017
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11566/247614
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