Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
Department of Diagnostic Radiology, American University of Beirut Medical Center, Beirut, Lebanon.
J Int Med Res. 2021 May;49(5):3000605211018595. doi: 10.1177/03000605211018595.
Diffuse large B-cell lymphoma (DLBCL) commonly presents with systemic manifestations including fever, weight loss, and night sweats. Uncommonly, patients with DLBCL can present with musculoskeletal manifestations mimicking polymyalgia rheumatica (PMR). Herein, the case of a 61-year-old woman who presented with pain in the bilateral shoulders, arms, hands, knees, pelvic girdle, and neck with bouts of fever, is presented. Laboratory workup for infectious and connective tissue diseases was non-revealing, except for elevated inflammatory markers. A positron emission tomography (PET)/computed tomography (CT) scan was suggestive of PMR, but also revealed enlarged lymph nodes initially thought to be reactive in nature. However, a lymph node biopsy showed findings consistent with DLBCL. This case highlights the importance of a thorough investigational workup when cases with features of PMR do not meet the proper criteria for this diagnosis to be made, in order not to miss a hematopoietic neoplasm with a PMR-like presentation.
弥漫性大 B 细胞淋巴瘤 (DLBCL) 常表现为全身症状,包括发热、体重减轻和盗汗。不常见的是,DLBCL 患者可表现为类似于风湿性多肌痛 (PMR) 的肌肉骨骼表现。本文报告了一例 61 岁女性,双侧肩部、手臂、手部、膝盖、骨盆带和颈部疼痛,伴有发热发作。除了炎症标志物升高外,感染和结缔组织疾病的实验室检查结果无异常。正电子发射断层扫描 (PET)/计算机断层扫描 (CT) 扫描提示 PMR,但也显示最初认为是反应性的增大淋巴结。然而,淋巴结活检显示符合 DLBCL 的发现。本病例强调了在具有 PMR 特征的病例不符合该诊断标准时,进行彻底的调查性检查的重要性,以免漏诊表现为 PMR 样的血液系统恶性肿瘤。