Secondary IgA nephropathy

被引:97
作者
Saha, Manish K. [1 ,2 ]
Julian, Bruce A. [2 ,3 ]
Novak, Jan [3 ]
Rizk, Dana V. [2 ]
机构
[1] Univ N Carolina, Dept Med, Chapel Hill, NC USA
[2] Univ Alabama Birmingham, Dept Med, ZRB 614,1720 2nd Ave South, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
基金
美国国家卫生研究院;
关键词
autoimmune diseases; glomerulonephritis; inflammatory bowel disease; liver disease; post-infectious glomerulonephritis; INCREASED IMMUNOGLOBULIN-A; O-GLYCOSYLATION; ALCOHOLIC CIRRHOSIS; ALTERED EXPRESSION; CYSTIC-FIBROSIS; PATHOGENESIS; DISEASE; GLOMERULONEPHRITIS; CELLS; RISK;
D O I
10.1016/j.kint.2018.02.030
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
IgA nephropathy is the most common primary glomerulonephritis worldwide. Its frequent coexistence with inflammatory, infectious, or malignant processes raises the possibility of a pathologic rather than coincidental association. Major strides have been made to elucidate the underlying pathophysiologic events that culminate in the development of primary IgA nephropathy. Whether secondary forms of the disease share common pathways triggered by underlying disorders or different mechanisms leading to similar pathologic findings remains to be determined. In this article we describe the most frequent etiologies for secondary IgA nephropathy and review the available literature for the pathophysiology.
引用
收藏
页码:674 / 681
页数:8
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