Phan Alexander T, Randhawa Johnny S, Johnston Brandon, Khosravi Chayanne, Malkoc Aldin, Arabian Sarkis
Department of Internal Medicine, Arrowhead Regional Medical Center, Colton, CA 92324, USA.
Department of Critical Care Medicine, Arrowhead Regional Medical Center, Colton, CA 92324, USA.
J Med Cases. 2023 Aug;14(8):277-281. doi: 10.14740/jmc4106. Epub 2023 Aug 28.
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.
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,以心脏压塞为主要表现极为罕见。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个月就诊于我院急诊科。入院时,计算机断层扫描显示前纵隔有一个直径达11.1厘米的巨大肿块,超声心动图显示有心脏压塞的生理表现。患者接受了包括心包穿刺术、随后的心包开窗术和纵隔活检在内的进一步检查,组织病理学检查结果与PMBCL一致。我们的病例强调了对有慢性非典型症状患者进行全面彻底检查的重要性。该病例的独特之处在于,PMBCL很少以心脏压塞作为主要临床表现。此外,我们建议对出现巨大纵隔肿块的患者进行广泛的心脏检查,否则可能导致患者发病和死亡。