Simms Roslyn, Kipgen David, Dahill Stephen, Marshall David, Rodger R Stuart
Renal Unit, Western Infirmary, Glasgow, Scotland, UK.
Am J Kidney Dis. 2008 Mar;51(3):e11-4. doi: 10.1053/j.ajkd.2007.10.043.
We report the case of a 62-year-old woman with rheumatoid arthritis treated with adalimumab, an anti-tumor necrosis factor alpha drug, who presented with 4 weeks of lethargy, upper respiratory tract symptoms, a vasculitic skin rash, and rapidly deteriorating renal function. She had cytoplasmic antineutrophil cytoplasmic antibodies and skin and renal biopsy specimens diagnostic of small vessel vasculitis and necrotizing crescentic glomerulonephritis, respectively. After immunosuppressive therapy and discontinuation of adalimumab therapy, vasculitis resolved and renal function recovered. This is the first report of antineutrophil cytoplasmic antibody associated necrotizing glomerulonephritis with adalimumab.
我们报告了一例62岁患类风湿关节炎的女性病例,该患者接受抗肿瘤坏死因子α药物阿达木单抗治疗,出现了4周的乏力、上呼吸道症状、血管炎性皮疹以及迅速恶化的肾功能。她存在胞浆型抗中性粒细胞胞浆抗体,皮肤和肾脏活检标本分别诊断为小血管血管炎和坏死性新月体性肾小球肾炎。在接受免疫抑制治疗并停用阿达木单抗治疗后,血管炎消退,肾功能恢复。这是阿达木单抗相关的抗中性粒细胞胞浆抗体相关性坏死性肾小球肾炎的首例报告。