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膜增殖性肾小球肾炎(MPGN)在病理形态学上以肾小球基膜(GBM)增厚和亲膜细胞及系膜基质增殖为特点。以往曾称它为混合型膜性-增殖性肾小球肾炎或慢性小叶性肾小球肾炎。在英国多称之为系膜毛细血管性肾小球肾炎。West等发现本病具有持续低补体血症,故又称为低补体血性慢性肾小球肾炎。近年来,本病逐渐引起人们的重视,认为是慢性弥漫
Membranoproliferative glomerulonephritis (MPGN) is characterized by thickening of the glomerulus basement membrane (GBM) and proliferation of the progenitor cells and mesangial matrix in the pathomorphology. It has been previously described as a mixed membranous proliferative glomerulonephritis or chronic lobular glomerulonephritis. More in the United Kingdom called mesangial capillary glomerulonephritis. West and other found that the disease has persistent hypocomplementemia, it is also known as hypocomplementemic chronic glomerulonephritis. In recent years, the disease gradually attracted people’s attention, that is chronic diffuse