The latest on IgG4-RD: a rapidly emerging disease

被引:86
作者
Carruthers, Mollie N. [1 ]
Stone, John H. [1 ]
Khosroshahi, Arezou [1 ]
机构
[1] Massachusetts Gen Hosp, Rheumatol Unit, Div Rheumatol, Dept Med, Boston, MA 02114 USA
关键词
autoimmune pancreatitis; IgG4; IgG4 related disease; IgG4 related systemic disease; IGG4-RELATED SYSTEMIC-DISEASE; ANGIOMATOID-NODULAR-TRANSFORMATION; EOSINOPHILIC ANGIOCENTRIC FIBROSIS; INFLAMMATORY MYOFIBROBLASTIC TUMOR; PLASMA-CELLS; TUBULOINTERSTITIAL NEPHRITIS; AUTOIMMUNE PANCREATITIS; MEMBRANOUS NEPHROPATHY; SCLEROSING MESENTERITIS; MULTIFOCAL FIBROSCLEROSIS;
D O I
10.1097/BOR.0b013e32834ddb4a
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review Provide an update of the developments in IgG4 related disease within the last year in terms of nomenclature, diagnostic criteria and clinical features. Recent findings The number of diseases associated with IgG4 related disease continues to grow. The entities of idiopathic orbital inflammation, idiopathic cervical fibrosis, eosinophilic angiocentric fibrosis, reactive nodular fibrous pseudotumor, sclerosing mesenteritis, and membranous glomerulonephritis should all be added to the list of diseases associated with the IgG4 related disease spectrum. The issues of nomenclature and diagnostic criteria for IgG4 related disease have important recent developments as well. Summary The diagnosis of IgG4 related disease continues to be challenging. Increasing recognition of IgG4 related disease has led to a large body of literature on organ sites of involvement. Understanding how the disease manifests itself is critical to diagnosis and ultimately treatment.
引用
收藏
页码:60 / 69
页数:10
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