Indrabhinduwat Manasawee, Arciniegas Calle Maria C, Colgan Joseph P, Villarraga Hector R
Cardiovascular Diseases Department, Mayo Clinic, Rochester, Minnesota, USA.
Bhumibol Adulyadej Hospital, Bangkok, Thailand.
Echo Res Pract. 2018 Sep;5(3):K53-K58. doi: 10.1530/ERP-18-0023. Epub 2018 Jun 12.
SummaryThirty-seven-year-old male presented with cough, dyspnea, significant weight loss (20 kg) and subacute fever for the past 2 months. Physical examination revealed inspiratory and expiratory wheezing bilaterally. A normal S1, S2 and a 3/6 systolic ejection murmur at the left upper parasternal border with respiratory variation were found during cardiac auscultation. Kidney and bone marrow biopsy reported a high-grade B-cell lymphoma. Echocardiography and cardiac CT findings consisted of multiple intracardiac masses affecting the right ventricular (RV) outflow track, RV apex, medial portion of the right atrium and posterior left atrium, as well as mild impairment of the RV systolic function. The masses in the RV outflow track caused partial obstruction (pulmonary valve peak velocity 2.3 m/s) with a RV systolic pressure of 43 mmHg. The infiltrative mass in the interatrial septum extended into both the right and left atrial cavities. The right superior pulmonary vein was occluded. This patient was treated with aggressive chemotherapy and had a good clinical response that resulted in mass size reduction after the first course of chemotherapy. Multimodality imaging techniques such as echocardiography, cardiac CT and PET scan can provide complementary information to better evaluate, stage and manage these patients.
Lymphoma can be found as a primary tumor in cardiac tissue, but secondary cardiac lymphoma is far more common.Appropriate investigation, histopathology, immunophenotype, staging and risk assessment are required for definite diagnosis and treatment.Cardiac lymphoma frequently manifests as an ill-defined, infiltrative mass. Typical location is in the atrium (right atrium is the most common site). Pericardial thickening or effusion is also common.Echocardiography is a quick, bedside, non-invasive assessment of anatomical involvement and hemodynamics affected by cardiac lymphoma. Echocardiographic findings of cardiac lymphoma include a hypoechoic, ill-defined infiltrative masses in the myocardium, nodular protrusion into cardiac chambers and pericardial effusion. Obstruction of inflow/outflow track can also be found.If a diagnosis of cardiac lymphoma is made, the most effective treatment is chemotherapy. Surgical treatment may have a role when hemodynamic compromise does not respond to chemotherapy and radiotherapy.
总结
一名37岁男性,在过去2个月出现咳嗽、呼吸困难、显著体重减轻(20千克)及亚急性发热。体格检查发现双侧吸气和呼气时均有哮鸣音。心脏听诊发现S1、S2正常,在胸骨左缘上方可闻及3/6级收缩期喷射性杂音,随呼吸变化。肾脏和骨髓活检报告为高级别B细胞淋巴瘤。超声心动图和心脏CT检查发现多个心内肿块,累及右心室流出道、右心室心尖、右心房内侧部分和左心房后部,同时右心室收缩功能轻度受损。右心室流出道的肿块导致部分梗阻(肺动脉瓣峰值流速2.3米/秒),右心室收缩压为43毫米汞柱。房间隔的浸润性肿块延伸至右心房和左心房腔。右上肺静脉闭塞。该患者接受了积极化疗,临床反应良好,首个化疗疗程后肿块缩小。超声心动图、心脏CT和PET扫描等多模态成像技术可提供补充信息,以更好地评估、分期和管理这些患者。
淋巴瘤可作为心脏组织的原发性肿瘤出现,但继发性心脏淋巴瘤更为常见。
明确诊断和治疗需要进行适当的检查、组织病理学、免疫表型、分期和风险评估。
心脏淋巴瘤常表现为边界不清的浸润性肿块。典型部位在心房(右心房最常见)。心包增厚或积液也很常见。
超声心动图是对心脏淋巴瘤累及的解剖结构和血流动力学进行快速、床边、无创评估的方法。心脏淋巴瘤的超声心动图表现包括心肌内低回声、边界不清的浸润性肿块、向心腔内的结节状突出和心包积液。也可发现流入/流出道梗阻。
如果诊断为心脏淋巴瘤,最有效的治疗方法是化疗。当血流动力学障碍对化疗和放疗无反应时,手术治疗可能起作用。