IgG4-related disease: nomenclature, clinical features, and treatment

被引:100
作者
Stone, John H. [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Rheumatol Unit,Dept Med, Boston, MA 02114 USA
关键词
IgG4-related disease; Autoimmune pancreatitis; Chronic sclerosing sialadenitis; Retroperitoneal fibrosis; Rituximab; HEPATIC INFLAMMATORY PSEUDOTUMOR; CHRONIC SCLEROSING SIALADENITIS; IMMUNOGLOBULIN G4-ASSOCIATED CHOLANGITIS; EOSINOPHILIC ANGIOCENTRIC FIBROSIS; IGG4-POSITIVE PLASMA-CELLS; AUTOIMMUNE PANCREATITIS; RETROPERITONEAL FIBROSIS; SYSTEMIC-DISEASE; SERUM IGG4; MULTIFOCAL FIBROSCLEROSIS;
D O I
10.1053/j.semdp.2012.08.002
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Concepts about IgG4-related disease (IgG4-RD) are now emerging swiftly. The condition has been identified in virtually every organ system, and its features are often excellent mimickers of malignancies, infections, and other immune-mediated disorders. Recommendations for nomenclature were proposed by the Organizing Committee of the 2011 International IgG4-related disease Symposium, and guidelines for the pathologic diagnosis of this condition have been published by an international group of experts. Experience with treatment regimens is growing. Glucocorticoids and B-cell depletion strategies both appear to be effective and are the subject of ongoing studies. This article reviews the current thought and understanding of this disease with regard to nomenclature, organ system involvement, and approaches to therapy. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:177 / 190
页数:14
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