类风湿性关节炎患者甲氨蝶呤相关淋巴细胞增生性疾病引发的巨噬细胞激活综合征

IF 2.7 Q3 IMMUNOLOGY
Immunological Medicine Pub Date : 2023-12-01 Epub Date: 2023-05-18 DOI:10.1080/25785826.2023.2212808
Hirotoshi Kato, Masafumi Suzuki, Kazuo Misumi, Hitoshi Kohsaka
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引用次数: 1

摘要

一名56岁女性因类风湿关节炎接受甲氨蝶呤(MTX)治疗17年。盗汗、发烧和体重减轻使她来了我们医院。虽然左氧氟沙星未能退烧,但由于全血细胞减少症、降钙素原升高和肺结节性病变,怀疑她患有败血症。经紧急住院治疗后,最终确诊为甲氨蝶呤相关淋巴细胞增生性疾病(MTX-LPD)伴巨噬细胞激活综合征(MAS)。停用甲氨蝶呤并给予5天大剂量糖皮质激素后,患者的一般情况得到改善。因此,即使患者患有MAS危重症,也不需要细胞毒性药物来控制MTX-LPD。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Macrophage activation syndrome triggered by methotrexate-related lymphoproliferative disease in a patient with rheumatoid arthritis.

A 56-year-old woman was treated for rheumatoid arthritis for 17 years with methotrexate (MTX). Night sweats, fever and weight loss made her visit our hospital. Although levofloxacin failed to resolve her fever, she was suspected of having sepsis because of pancytopenia, elevated procalcitonin and a nodular lesion in the lung. After urgent hospitalization, she was diagnosed finally with the methotrexate-related lymphoproliferative disorder (MTX-LPD) associated with macrophage activation syndrome (MAS). Her general condition was improved with MTX withdrawal and 5-day high-dose glucocorticoid administration. Thus, even when the patient was critically ill with MAS, no cytotoxic agents were required to control MTX-LPD.

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来源期刊
Immunological Medicine
Immunological Medicine Medicine-Immunology and Allergy
CiteScore
7.10
自引率
2.30%
发文量
19
审稿时长
19 weeks
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