An extranodal Richter's syndrome presenting with cardiac diffuse large B-cell lymphoma: a case report

Richter's syndrome (RS) defines the transformation of chronic lymphocytic leukemia into high-grade lymphoma, which usually involves lymph nodes and bone marrow. Extranodal involvement of the heart is an extremely rare condition. Patients with heart involvement tended to have a low response to c...

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Veröffentlicht in:BMC cardiovascular disorders 2023-12, Vol.23 (1), p.624-624, Article 624
Hauptverfasser: Wang, Hua, Yan, Wei-Hong, Sun, Jun-Jie, Dong, Mei, Zhang, Nan, Liu, Tong, Song, Nian-Peng, Zhong, Lin
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Sprache:eng
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Zusammenfassung:Richter's syndrome (RS) defines the transformation of chronic lymphocytic leukemia into high-grade lymphoma, which usually involves lymph nodes and bone marrow. Extranodal involvement of the heart is an extremely rare condition. Patients with heart involvement tended to have a low response to chemotherapy and relative poor prognosis. The transformation process of RS is often insidious and nonspecific making it challenging to diagnose. A 64-year-old woman wih a history of chronic lymphocytic leukemia (CLL) presented with intermittent chest pain and was diagnosed with non-ST-elevation myocardial infarction (NSTEMI). However, the contrast enhanced echocardiography revealed a large irregular mass, measuring about 75.4 mm × 37.5 mm, located on the lateral and posterior wall of the right ventricle. Biopsy of the cardiac mass and the results revealed diffuse large B-cell lymphoma. We present a case of a 64-year-old woman with aggressive diffuse large B-cell lymphoma involving the heart. This case could provide some insights in the diagnosis of cardiac lymphoma.
ISSN:1471-2261
1471-2261
DOI:10.1186/s12872-023-03663-4