Rambausek M, Seelig H P, Andrassy K, Waldherr R, Lenhard V, Ritz E
Proc Eur Dial Transplant Assoc. 1983;19:663-8.
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.
在我们科室,IgA 肾病(IgA-GN)约占所有肾小球肾炎的 20%。50 例 IgA-GN 患者中有 17 例发展为肾衰竭,其中 11 例在平均 68 个月的随访过程中出现肾衰竭。3 例患者需要进行血液透析。50 例患者中有 22 例患有高血压,其中 5 例为恶性高血压。在 29%的 IgA-GN 患者皮肤活检中发现血管周围 IgA 沉积,在 19%的其他肾小球肾炎患者中也发现了这种沉积,但在健康对照中未发现。黏膜(唾液和鼻腔)分泌型 IgA 浓度正常。在皮肤和肾小球 IgA/IgM 沉积物中,使用单克隆抗体证实为 IgA1。未发现 HLA-A、B 或 DR 抗原过量,且未发现临床病程与 HLA-Bw35 之间存在关联。