Lin Ting-Shen, Tsao Tang-Yi, Chen Shih-Wei, Ko Min-Cheng, Tsai Stella Chin-Shaw
Department of Otolaryngology, Tungs' Taichung MetroHarbor Hospital, Taichung 435, Taiwan.
Department of Pathology, Tungs' Taichung MetroHarbor Hospital, Taichung 435, Taiwan.
Diagnostics (Basel). 2025 Jun 14;15(12):1517. doi: 10.3390/diagnostics15121517.
Methotrexate is widely used as a disease-modifying antirheumatic drug for rheumatoid arthritis (RA), yet prolonged immunosuppression may lead to rare complications, including Epstein-Barr virus (EBV)-positive lymphoproliferative disorders (LPDs). We present the case of a 70-year-old woman with RA on chronic immunosuppressive therapy who developed symptoms resembling recurrent tonsillitis. CT imaging revealed bilateral necrotic palatine tonsils and extensive necrotic lymphadenopathy involving the cervical, mediastinal, and axillary regions. Bilateral tonsillectomy was performed due to concerns about malignancy or infection, and histopathology confirmed a polymorphic EBV-positive LPD with Hodgkin-like features, consistent with iatrogenic immunodeficiency-associated LPD. Methotrexate was subsequently discontinued, and the patient was managed conservatively without systemic chemotherapy. Clinical recovery was observed during follow-up. This case highlights the importance of considering methotrexate-associated LPDs in the differential diagnosis of atypical tonsillar infections in immunosuppressed patients, particularly when necrotic features or systemic lymphadenopathy are present. The pathogenesis may involve EBV reactivation under impaired immune surveillance due to methotrexate, leading to abnormal B-cell proliferation and clonal expansion. This case is contextualized through a comparative analysis of published reports, highlighting clinical features and treatment responses of methotrexate-associated EBV-positive LPDs in the form of a focused literature review.
甲氨蝶呤作为一种改善病情的抗风湿药物,被广泛用于治疗类风湿关节炎(RA),然而长期免疫抑制可能导致罕见的并发症,包括 Epstein-Barr 病毒(EBV)阳性淋巴增殖性疾病(LPDs)。我们报告了一例 70 岁患有 RA 的女性患者,她接受慢性免疫抑制治疗,出现了类似复发性扁桃体炎的症状。CT 成像显示双侧坏死性腭扁桃体以及累及颈部、纵隔和腋窝区域的广泛坏死性淋巴结病。由于担心恶性肿瘤或感染,进行了双侧扁桃体切除术,组织病理学证实为具有霍奇金样特征的多形性 EBV 阳性 LPD,符合医源性免疫缺陷相关的 LPD。随后停用了甲氨蝶呤,患者接受保守治疗,未进行全身化疗。随访期间观察到临床恢复。该病例强调了在免疫抑制患者非典型扁桃体感染的鉴别诊断中考虑甲氨蝶呤相关 LPD 的重要性,特别是当出现坏死特征或全身淋巴结病时。其发病机制可能涉及由于甲氨蝶呤导致免疫监视受损下的 EBV 重新激活,从而导致异常 B 细胞增殖和克隆性扩增。通过对已发表报告的比较分析将该病例进行背景化,以聚焦文献综述的形式突出了甲氨蝶呤相关 EBV 阳性 LPD 的临床特征和治疗反应。