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IgA 介导的抗肾小球基底膜病的不寻常病例。

An unusual case of IgA-mediated anti-glomerular basement membrane disease.

机构信息

Division of Nephrology, Changhua Christian Hospital, 135, Nanhsiao Street, Changhua, 500, Taiwan.

出版信息

Int Urol Nephrol. 2013 Aug;45(4):1229-34. doi: 10.1007/s11255-012-0162-8. Epub 2012 Mar 29.

Abstract

Anti-glomerular basement membrane (GBM) disease is mediated by circulating autoantibodies, principally IgG, targeted at the type IV collagen of GBM. The IgA variant of anti-GBM disease has rarely been described. We report a 65-year-old man with uremia, undergoing hemodialysis, who was referred because of hemoptysis. A chest X-ray showed diffuse infiltration in the right lung field. Laboratory data were remarkable for renal failure, anemia, and thrombocytopenia. Furthermore, laboratory evidence of microangiopathic hemolytic anemia was present. A kidney biopsy revealed diffuse crescentic glomerulonephritis. Circulating IgA anti-GBM antibody was found, as well as the presence of significant IgA deposition in a linear pattern along the GBM, suggesting an anti-GBM antibody-mediated disease. The patient was treated with plasmapheresis and pulse steroid therapy, which resulted in an immediate improvement in the pulmonary hemorrhage and hematological abnormalities. However, the patient did not regain renal function and remained on hemodialysis.

摘要

抗肾小球基底膜 (GBM) 病是由循环自身抗体介导的,主要是靶向 GBM 型 IV 胶原的 IgG。IgA 型抗 GBM 病很少被描述。我们报告了一例 65 岁男性,患有尿毒症,正在接受血液透析,因咯血而被转介。胸部 X 线显示右肺野弥漫性浸润。实验室数据显示肾功能衰竭、贫血和血小板减少。此外,还存在微血管性溶血性贫血的实验室证据。肾脏活检显示弥漫性新月体肾小球肾炎。发现循环 IgA 抗 GBM 抗体,以及在 GBM 上呈线性模式存在大量 IgA 沉积,提示为抗 GBM 抗体介导的疾病。患者接受了血浆置换和脉冲类固醇治疗,这立即改善了肺部出血和血液学异常。然而,患者的肾功能没有恢复,仍需进行血液透析。

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