Cardiac Lymphoma: A Case Report.

IF 1.9
Arquivos brasileiros de cardiologia Pub Date : 2025-03-24 eCollection Date: 2025-01-01 DOI:10.36660/abc.20240299
Leticia Ferraz Pamplona, Kelly Barnabé Serpa de Oliveira, João Ancelmo Dos Reis Neto, Luis Antelo Bustamante, Januário Manoel de Souza, Flávia Fernandes Silva Zacchi, Juliana Brenande de Oliveira Brito, Salomon Soriano Ordinola Rojas
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Abstract

Cardiac tumors are rare. Primary cardiac lymphoma is defined as non-Hodgkin lymphoma that involves only the heart and/or pericardium. It is an aggressive tumor with a poor prognosis and its symptoms may be nonspecific. A definitive diagnosis can only be obtained through histopathological study, and chemotherapy is the main treatment strategy. This case is about a 71-year-old male patient, with a rare form of primary cardiac tumor. He had postoperative complications such as acute pulmonary edema and the need for a pacemaker, which occurred after tumor resection requiring reconstruction of the vena cava and suture of the right atrium. Primary cardiac lymphoma is a tumor that is difficult to diagnose because it has a vague and non-specific symptomatic presentation. However, it should always be included as a differential diagnosis of cardiac masses. Early diagnosis can significantly improve the prognosis and increase the survival rate of patients by quickly referring them for specific treatment.

心脏淋巴瘤1例报告。
心脏肿瘤很少见。原发性心脏淋巴瘤定义为仅累及心脏和/或心包的非霍奇金淋巴瘤。它是一种侵袭性肿瘤,预后差,其症状可能是非特异性的。只有通过组织病理学检查才能得到明确的诊断,化疗是主要的治疗策略。这个病例是一个71岁的男性患者,患有一种罕见的原发性心脏肿瘤。他有术后并发症,如急性肺水肿和需要起搏器,这发生在肿瘤切除后需要重建腔静脉和缝合右心房。原发性心脏淋巴瘤是一种难以诊断的肿瘤,因为它具有模糊和非特异性的症状表现。然而,它应该作为心脏肿块的鉴别诊断。早期诊断可迅速转诊进行特异性治疗,显著改善预后,提高患者生存率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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