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以心脏肿物为表现的弥漫性大B细胞淋巴瘤

Diffuse Large B-cell Lymphoma Presenting as a Cardiac Mass.

作者信息

Nasir Abdullah, Patel Yash B

机构信息

Internal Medicine, Trinity Health Ann Arbor Hospital, Ann Arbor, USA.

出版信息

Cureus. 2024 May 6;16(5):e59755. doi: 10.7759/cureus.59755. eCollection 2024 May.

Abstract

Cardiac involvement as the initial presentation of lymphoma is a rare occurrence. The most common type of cardiac lymphoma is diffuse large B-cell lymphoma (DLBCL), which often affects the right atrium. Cardiac lymphoma can either be mediastinal DLBCL invading the heart or primary cardiac lymphoma. We describe the case of an 84-year-old female who presented with an eight-week history of dyspnea. Computed tomography angiography (CTA) of the chest showed a right-sided pleural effusion with collapse of the right middle and lower lobes as well as a large mass-like density within the anterior pericardium, compressing the right atrium and right ventricle and encasing the right coronary artery. A transthoracic echocardiogram (TTE) showed a multilocular hypoechoic mass in the right atrium with invasion into the wall of the right atrium. The patient underwent diagnostic and therapeutic thoracentesis. Pleural fluid cytology revealed diffuse large B-cell lymphoma, with positive stains for CD20, PAX5, CD10, BCL6, and Mum-1. Fluorescence in situ hybridization (FISH) revealed an abnormality of BCL2/18q (16%). A staging positron emission tomography (PET) scan showed a large mediastinal mass involving the right pericardium, focal uptake in the left thyroid lobe, left skull base, and musculature around the proximal left femur. Chemotherapy was initiated with R-mini-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone). PET scans after three cycles of chemotherapy showed a complete metabolic response with the resolution of previously noted hypermetabolic lesions. The patient completed all six cycles of chemotherapy without issues. The differential diagnosis of a right atrial cardiac mass should include lymphoma. TTE is usually the initial imaging test, and a tissue biopsy is required for a definitive diagnosis. DLBCL is highly aggressive and carries a poor prognosis if untreated. Early diagnosis and treatment with standard chemotherapy are crucial for favorable outcomes.

摘要

心脏受累作为淋巴瘤的首发表现较为罕见。最常见的心脏淋巴瘤类型是弥漫性大B细胞淋巴瘤(DLBCL),常累及右心房。心脏淋巴瘤可以是侵犯心脏的纵隔DLBCL,也可以是原发性心脏淋巴瘤。我们描述了一例84岁女性患者,有8周的呼吸困难病史。胸部计算机断层血管造影(CTA)显示右侧胸腔积液伴右中、下叶肺不张,以及心包前部有一个大的肿块样密度影,压迫右心房和右心室,并包绕右冠状动脉。经胸超声心动图(TTE)显示右心房有一个多房性低回声肿块,侵犯右心房壁。患者接受了诊断性和治疗性胸腔穿刺术。胸水细胞学检查显示为弥漫性大B细胞淋巴瘤,CD20、PAX5、CD10、BCL6和Mum-1染色阳性。荧光原位杂交(FISH)显示BCL2/18q异常(16%)。分期正电子发射断层扫描(PET)显示一个大的纵隔肿块累及右心包,左甲状腺叶、左颅底和左股骨近端周围肌肉组织有局灶性摄取。开始使用R-mini-CHOP(利妥昔单抗、环磷酰胺、阿霉素、长春新碱和泼尼松)进行化疗。三个化疗周期后的PET扫描显示完全代谢缓解,之前发现的高代谢病变消失。患者顺利完成了所有六个周期的化疗。右心房心脏肿块的鉴别诊断应包括淋巴瘤。TTE通常是初始影像学检查,明确诊断需要进行组织活检。DLBCL具有高度侵袭性,如果不治疗,预后较差。早期诊断并采用标准化化疗对取得良好疗效至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a562/11152600/a491a324eab1/cureus-0016-00000059755-i01.jpg

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