Brooks H, Taylor H G, Nichol F E
Department of Rheumatology, Leicester Royal Infirmary, United Kingdom.
Clin Rheumatol. 1992 Dec;11(4):566-8. doi: 10.1007/BF02283121.
We report a 53-year-old man with sero-negative rheumatoid arthritis who developed a fever, rash and hepatitis 3 weeks after starting sulphasalazine therapy. This was associated with a T cell lymphocytosis, eosinophilia and evidence of classical complement pathway activation. He responded to high dose corticosteroids. This is a rare but characteristic reaction which is likely to be encountered by rheumatologists more frequently with the increasing use of sulphasalazine. It should be recognized promptly as it may be fatal and can be confused with other systemic diseases.
我们报告一名53岁血清阴性类风湿关节炎男性患者,在开始柳氮磺胺吡啶治疗3周后出现发热、皮疹和肝炎。这与T细胞淋巴细胞增多、嗜酸性粒细胞增多以及经典补体途径激活的证据有关。他对高剂量皮质类固醇治疗有反应。这是一种罕见但具有特征性的反应,随着柳氮磺胺吡啶使用的增加,风湿病学家可能会更频繁地遇到。应迅速识别,因为它可能是致命的,并且可能与其他全身性疾病混淆。