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具有内皮下沉积物的系膜毛细血管性肾小球肾炎(Ⅰ型)并不是一种同源的疾病。Peters等认为这种肾炎的发生可能由于抗原抗体免疫复合物的清除缺陷所致,是一种免疫缺陷综合征。我们报导1例具有肾小球系膜毛细血管性肾小球肾炎和免疫缺乏的患者,此例可能是最近发现的。此为一个55岁男性患者,诉有晕厥发作。血压170/100mmHg。常规尿检查显示蛋白尿。血浆尿素浓度为7.9mmol/1(474mg/100ml),血浆肌酐160μmol/l(1.8mg/100ml),血清总蛋白67g/l,血清白蛋白43g/l(两者均正常)。血清IgG7.55g/l(正常
Mesangiocapillary glomerulonephritis (type I) with subendothelial deposits is not a homologous disease. Peters believes that the occurrence of this nephritis may be due to the removal of antigen-antibody immune complexes due to defects, is an immunodeficiency syndrome. We report 1 patient with glomerular mesangial capillary glomerulonephritis and immunodeficiency, and this case may have been recently discovered. This is a 55-year-old male patient who v. Syncope. Blood pressure 170 / 100mmHg. Routine urinalysis shows proteinuria. Plasma urea concentrations were 7.9 mmol / l (474 mg / 100 ml), plasma creatinine 160 μmol / l (1.8 mg / 100 ml), serum total protein 67 g / l and serum albumin 43 g / l both normal. Serum IgG7.55g / l (normal