Generalized lymphadenopathy as an atypical initial clinical manifestation in rheumatoid arthritis and a possible hypothetical mechanism

José Eugenio Vázquez‐Meraz, C. Duarte-Salazar, R. Franco-Cendejas, David Antonio Argüelles-Pérez, G. Aristi-Urista, J. Arellano-Galindo
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Abstract

Objective: To describe a 60-year-old male with diffuse generalized lymphadenopathy preceding a diagnosis of rheumatoid arthritis.Case presentation: The patient was admitted on suspicion of lymphoma. Chest positron emission/computed tomography showed enlarged lymph nodes bilaterally, mediastinum in the perihilar, retroperitoneum, and inguinal regions, with normal hematopoiesis of bone marrow. Lymph node biopsy revealed reactive follicular lymphadenopathy. Polyarthritis was present, and a rheumatoid factor test was positive eight months after the initial medical evaluation. A diagnosis of rheumatoid arthritis associated with generalized lymph node involvement was made. The patient was treated with leflunomide and corticosteroids and showed complete recovery without recurrence at 18 months of follow-up.Conclusions: Once histological findings of reactive lymph node hyperplasia are established as primarily related to rheumatic disease activity, clinicians should consider a possible diagnosis of rheumatoid arthritis.
全身性淋巴结病作为类风湿关节炎的一种非典型初始临床表现及其可能的假说机制
目的:描述一名60岁男性弥漫性全身性淋巴结病,诊断为类风湿关节炎。病例描述:患者因怀疑淋巴瘤而入院。胸部正电子发射/计算机断层扫描显示双侧淋巴结肿大,门周纵隔、腹膜后和腹股沟区,骨髓造血功能正常。淋巴结活检显示反应性滤泡性淋巴结病。存在多发性关节炎,在最初的医疗评估后8个月类风湿因子测试呈阳性。诊断为类风湿关节炎伴全身淋巴结受累。患者接受来氟米特和皮质类固醇治疗,在18个月的随访中显示完全恢复,无复发。结论:一旦组织学发现反应性淋巴结增生主要与风湿病活动有关,临床医生应考虑类风湿关节炎的可能诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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