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Primary IgA Vasculitis with Nephritis in a Patient with Rheumatoid Arthritis Diagnosed by Anti-galactose-deficient IgA1 Immunostaining

机译:抗半乳糖缺陷型IgA1免疫染色诊断类风湿关节炎患者的原发性IgA血管炎合并肾炎

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摘要

Renal disease is a common complication of rheumatoid arthritis (RA) and can occur secondary to RA or be induced by therapeutic agents. Recently, glomerular deposition of galactose-deficient IgA1 (Gd-IgA1) was identified as a feature of primary IgA vasculitis with nephritis (IgA-VN). We herein report a case of IgA-VN in an RA patient whose disease activity was controlled by treatment with etanercept. To distinguish between primary IgA-VN and secondary IgA-VN caused by RA or etanercept, we performed immunostaining of renal biopsy sections with the Gd-IgA1-specific antibody KM55. Positive KM55 staining confirmed the diagnosis of primary IgA-VN in a patient with RA.
机译:肾脏疾病是类风湿关节炎(RA)的常见并发症,可继发于RA或由治疗剂引起。最近,半乳糖缺陷型IgA1(Gd-IgA1)的肾小球沉积被确定为原发性IgA血管炎合并肾炎(IgA-VN)的特征。我们在此报告了RA患者的IgA-VN病例,该患者的疾病活动受依那西普治疗控制。为了区分由RA或依那西普引起的原发性IgA-VN和继发性IgA-VN,我们用Gd-IgA1特异性抗体KM55进行了肾脏活检切片的免疫染色。 KM55阳性染色证实了RA患者的原发性IgA-VN诊断。

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