Primary Mediastinal B-Cell Lymphoma Presenting as Cardiac Tamponade.

Alexander T Phan, Johnny S Randhawa, Brandon Johnston, Chayanne Khosravi, Aldin Malkoc, Sarkis Arabian
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Abstract

Primary mediastinal B-cell lymphoma (PMBCL) is a rare subtype of non-Hodgkin lymphoma. Typical symptoms include cough, chest pain, and dyspnea; however, cardiac tamponade as the primary manifestation is exceedingly rare. We hereby present a case of a 34-year-old male with a past medical history of obesity, who presented to our emergency department with a chronic dry cough for 4 months. On admission, computed tomography demonstrated a large 11.1-cm diameter anterior mediastinal mass, and echocardiography demonstrated cardiac tamponade physiology. The patient underwent further workup including pericardiocentesis, subsequent pericardial window, and mediastinal biopsy, which demonstrated histopathology consistent with PMBCL. Our case highlights the importance of a complete and thorough workup for patients with chronic untraditional symptoms. This case is unique in that PMBCL is rarely associated with cardiac tamponade as the primary clinical presentation. Additionally, we recommend an extensive cardiac workup for patients presenting with a large mediastinal mass, as failure to do so may result in patient morbidity and mortality.

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原发性纵隔b细胞淋巴瘤表现为心脏填塞。
原发性纵隔b细胞淋巴瘤(PMBCL)是一种罕见的非霍奇金淋巴瘤亚型。典型症状包括咳嗽、胸痛和呼吸困难;然而,以心包填塞为主要表现是极为罕见的。我们在此报告一例34岁男性,既往有肥胖病史,因慢性干咳4个月来急诊科就诊。入院时,计算机断层扫描显示前纵隔直径11.1 cm的大肿块,超声心动图显示心脏填塞生理学。患者接受了进一步的检查,包括心包穿刺,随后的心包窗和纵隔活检,结果显示组织病理学符合PMBCL。我们的病例强调了对慢性非传统症状患者进行全面彻底检查的重要性。本病例的独特之处在于,PMBCL很少以心脏填塞为主要临床表现。此外,我们建议对出现较大纵隔肿块的患者进行广泛的心脏检查,因为不这样做可能导致患者发病率和死亡率。
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