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膜增生性肾小球肾炎是一种临床少见的原发性肾小球疾病（约占原发性肾小球疾病10％～20％）[1]。其病理特点为肾小球基低膜增厚，系膜细胞增生及系膜基质扩张，光镜下：毛细血管增厚和双轨状，重者可伴有间质纤维化，小管萎缩和间质单核细胞浸润，临床上常表现为肾病综合征伴血
Membrane proliferative glomerulonephritis is a clinically rare primary glomerular disease (about 10% to 20% of primary glomerular disease) [1]. The pathological features of glomerular basement membrane thickening, mesangial cell proliferation and mesangial matrix expansion, light microscopy: capillary thickening and double rail-like, severe cases may be associated with interstitial fibrosis, tubular atrophy and interstitial Monocyte infiltration, the clinical manifestations of nephrotic syndrome with blood