M Rambausek, H P Seelig, K Andrassy, R Waldherr, V Lenhard, E Ritz
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引用次数: 0
摘要
iga -肾小球肾炎(IgA-GN)约占我们单位所有肾小球肾炎的20%。50例IgA-GN患者中有17例出现肾衰竭,在平均68个月的随访过程中,17例患者中有11例出现肾衰竭。3例患者需要血液透析。50例患者中有22例高血压,5例为恶性高血压。在29%的IgA-GN患者和19%的其他GN患者的皮肤活检中发现了血管周围IgA沉积,但在健康对照中没有发现。粘膜(唾液和鼻腔)分泌IgA浓度正常。在皮肤和肾小球IgA/IgM沉积物中,用单克隆抗体证实IgA1。未发现HLA-A、B、DR抗原过量,临床病程与HLA-Bw35无相关性。
Clinical and serological features of mesangial IgA glomerulonephritis.
IgA-glomerulonephritis (IgA-GN) accounts for approximately 20 per cent of all glomerulonephritis in our unit. Seventeen out of 50 patients with IgA-GN developed renal failure, which appeared in 11 out of 17 over the course of a mean follow-up of 68 months. Haemodialysis was required in three patients. Twenty-two out of 50 patients had hypertension, five with malignant hypertension. Perivascular IgA deposits were found in skin biopsies of 29 per cent of patients with IgA-GN and also in 19 per cent of patients with other GN, but not in healthy controls. Mucosal (salivary and nasal) secretory IgA concentrations were normal. In cutaneous and glomerular IgA/IgM deposits, IgA1 was demonstrated using monoclonal antibodies. No excess of HLA-A, B or DR antigens and no relation of clinical course and HLA-Bw35 were found.