Renal Involvement in Antineutrophil Cytoplasmic Antibody-Associated Vasculitis

被引:17
|
作者
Zonozi, Reza [1 ]
Niles, John L. [1 ]
Cortazar, Frank B. [1 ]
机构
[1] Massachusetts Gen Hosp, Vasculitis & Glomerulonephritis Ctr, Div Nephrol, 101 Merrimac St, Boston, MA 02114 USA
关键词
ANCA-associated vasculitis; Granulomatosis with polyangiitis; Microscopic polyangiitis; Rapidly progressive glomerulonephritis; ANCA-ASSOCIATED VASCULITIS; SMALL-VESSEL VASCULITIS; DAILY ORAL CYCLOPHOSPHAMIDE; LATE-ONSET NEUTROPENIA; B-CELL DEPLETION; RHEUMATOID-ARTHRITIS; MAINTENANCE THERAPY; TREATMENT RESISTANCE; RITUXIMAB THERAPY; RANDOMIZED-TRIAL;
D O I
10.1016/j.rdc.2018.06.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is the most common cause of rapidly progressive glomerulonephritis. ANCAs play an important role in the pathogenesis and diagnosis of AAV. The classic renal lesion in AAV is a pauci-immune necrotizing and crescentic glomerulonephritis. Treatment is divided into 2 phases: (1) induction of remission to eliminate disease activity and (2) maintenance of remission to prevent disease relapse. Patients with AAV with end-stage renal disease require modification of immunosuppressive strategies and consideration for kidney transplant. An improved understanding of disease pathogenesis has led to new treatment strategies being tested in clinical trials.
引用
收藏
页码:525 / +
页数:20
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