IgG4-related disease: 2013 update

被引:8
|
作者
Monach P.A. [1 ]
机构
[1] Vasculitis Center, Section of Rheumatology, Boston University School of Medicine, 72 East Concord Street, E-533, Boston
关键词
Aortitis; Autoimmune pancreatitis; IgG4-Related disease; Periaortitis; Retroperitoneal fibrosis;
D O I
10.1007/s11936-013-0232-y
中图分类号
学科分类号
摘要
Opinion statement: Having diagnosed a patient as having IgG4-related disease, I would have a low threshold for recommending immune-suppressive treatment, and would make that recommendation for any patient with vascular involvement. My initial approach would be prednisone at 40-60 mg/day with a plan to reduce the dose every two weeks, e.g., 40, 30, 20, 15, 10, 7.5, 5, and 2.5 mg for 2 weeks each. In the event of relapse, I would double the current prednisone dose, slow the taper, and add azathioprine, anticipating using that drug for one year if the patient were to remain in remission. In the event or subsequent relapse, I would stop azathioprine and use rituximab. In a patient with large artery involvement, I would consult a vascular surgeon soon after diagnosis, anticipating a need for surgical repair. © 2013 Springer Science+Business Media New York.
引用
收藏
页码:214 / 223
页数:9
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