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Rapidly progressive glomerulonephritis due to anti-glomerular basement membrane disease accompanied by IgA nephropathy: A case report

机译:抗肾小球基底膜疾病伴IgA肾病引起的快速进行性肾小球肾炎1例

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摘要

Anti-glomerular basement membrane (anti-GBM) disease is characterized by autoantibodies against antigenic site on type IV collagen of the GBM. The coexistence of anti-GBM disease and other immune complex mediated glomerulonephritis is common. Herein, we describe a patient presented with rapidly progressive glomerulonephritis, who was diagnosed as IgA-mediated nephropathy and was found to have abundant serum anti-glomerular basement membrane IgG antibodies. The patient's renal function improved considerably with intensive immunosuppressive therapy.
机译:抗肾小球基底膜(抗GBM)疾病的特征在于针对GBM的IV型胶原上的抗原位点的自身抗体。抗GBM疾病与其他免疫复合物介导的肾小球肾炎并存是常见的。本文中,我们描述了一名患有快速进行性肾小球肾炎的患者,该患者被诊断为IgA介导的肾病,并且发现其血清抗肾小球基底膜IgG抗体丰富。强化免疫抑制治疗可大大改善患者的肾功能。

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