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表现为心脏肿物并伴有房性心律失常的弥漫性大B细胞淋巴瘤

Diffuse Large B Cell Lymphoma Presenting as a Cardiac Mass Complicated by Atrial Arrhythmia.

作者信息

Lee Julie Jiyun, Jandali Ramzy

机构信息

Department of Internal Medicine Olive View-UCLA Medical Center.

Department of Internal Medicine University of California, Los Angeles.

出版信息

J Brown Hosp Med. 2025 Apr 1;4(2):1-5. doi: 10.56305/001c.133593. eCollection 2025.

Abstract

Cardiac involvement in diffuse large B-cell lymphoma (DLBCL) is uncommon and often presents with nonspecific symptoms, such as chest pain and dyspnea, which can lead to challenges in diagnosis. Cardiac lymphomas most often arise in the right atrium or the pericardium, and can thus result in tachyarrhythmias, pericardial effusions, and heart failure symptoms, all of which can further complicate clinical management. Diagnosis typically requires comprehensive imaging such as cardiac magnetic resonance imaging (MRI) or positron emission tomography-computed tomography (PET-CT), as transthoracic echocardiography (TTE) alone is limited in the diagnosis of intracardiac masses, as well as tissue biopsy for histopathological confirmation. Treatment typically involves systemic chemotherapy, though outcomes are generally poor, as cardiac involvement is generally a late manifestation of DLBCL. This case underscores the importance of early recognition, need for comprehensive imaging and tissue diagnosis, and multidisciplinary care in managing cardiac lymphoma, as well as the challenges associated with refractory disease.

摘要

弥漫性大B细胞淋巴瘤(DLBCL)累及心脏并不常见,常表现为胸痛和呼吸困难等非特异性症状,这会给诊断带来挑战。心脏淋巴瘤最常起源于右心房或心包,因此可导致快速性心律失常、心包积液和心力衰竭症状,所有这些都会使临床管理进一步复杂化。诊断通常需要心脏磁共振成像(MRI)或正电子发射断层扫描-计算机断层扫描(PET-CT)等综合成像检查,因为仅经胸超声心动图(TTE)在诊断心内肿块方面存在局限性,还需要组织活检进行组织病理学确诊。治疗通常采用全身化疗,不过总体预后较差,因为心脏受累通常是DLBCL的晚期表现。该病例强调了早期识别、综合成像和组织诊断的必要性以及多学科护理在管理心脏淋巴瘤中的重要性,同时也凸显了难治性疾病相关的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10ab/11967343/e68e0476bee3/bhm_2025_4_2_133593_273922.jpg

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