论文部分内容阅读
1968年 Berger 及 Hinglais 在法国首先描述 IgA 肾病以来,许多作者作了进一步的研究。证实本病在免疫病理及临床表现上均具有特点,构成了原发性肾小球疾病中一种独立的类型。各个学者根据本病的主要临床病理特点作了不同的命名,如血管系膜性 IgA 肾小球肾炎(Mesangial IgA glomerulonephri-tis);IgA-IgG 肾病(IgA-IgG Nephropathy);Berger’s 病(Berger’s disease);IgA 相关的肾小球肾炎(IgA Associated glomerulo-nephri-tis)等。这些别名都反映此一类型肾小球肾炎
Many authors made further research since Berger and Hinglais first described IgA nephropathy in France in 1968. Confirmed the disease in the immune pathology and clinical manifestations are characterized by the formation of the primary glomerular disease in a separate type. Various scholars have given different names according to the main clinicopathological features of the disease, such as Mesangial IgA glomerulonephritis; IgA-IgG nephropathy; Berger’s disease ); IgA-associated glomerulo-nephri-tis and the like. These aliases reflect this type of glomerulonephritis