Tancoš Vladimír, Bohuš Peter, Fröhlichová Lucia, Blichárová Alžbeta, Sopková Dorota
Department of Forensic Medicine, Faculty of Medicine, Pavol Jozef Šafárik University in Košice, Slovakia;
Rom J Morphol Embryol. 2025 Jan-Mar;66(1):245-250. doi: 10.47162/RJME.66.1.23.
Primary cardiac lymphoma (PCL), defined as extranodal non-Hodgkin's lymphoma involving exclusively the heart and∕or pericardium, is a neoplasm with an extremely low incidence, a high degree of malignancy, and a poor prognosis. It comprises 0.5% of all extranodal lymphomas and 1-2% of all primary cardiac tumors, while the most commonly reported subtype is diffuse large B-cell lymphoma (DLBCL). The tumor is more common in immunocompromised patients compared with those who are immunocompetent. Modern imaging methods now allow for earlier detection of these tumors, despite their variable clinical manifestation, which is often a cause of misdiagnosis. We present an autopsy case of undiagnosed PCL in an immunocompetent 72-year-old man, where postmortem examination revealed massive tumor infiltration of the right-sided heart chambers extending to the left ventricle. Histological analysis showed microscopic tumor infiltration within the left atrium as well. A diagnosis of DLBCL of non-germinal subtype was made based on immunohistochemistry.
原发性心脏淋巴瘤(PCL)定义为仅累及心脏和/或心包的结外非霍奇金淋巴瘤,是一种发病率极低、恶性程度高且预后不良的肿瘤。它占所有结外淋巴瘤的0.5%,占所有原发性心脏肿瘤的1-2%,而最常报道的亚型是弥漫性大B细胞淋巴瘤(DLBCL)。与免疫功能正常的患者相比,该肿瘤在免疫功能低下的患者中更为常见。尽管这些肿瘤临床表现多样,常导致误诊,但现代成像方法现在能够更早地检测到它们。我们报告一例72岁免疫功能正常男性未确诊的PCL尸检病例,尸检显示右侧心腔有大量肿瘤浸润,并延伸至左心室。组织学分析还显示左心房内有微观肿瘤浸润。根据免疫组织化学诊断为非生发亚型的DLBCL。