IgG4-related disease: what do we know after 20 years

被引：1
|
作者：
Sokol, E., V [1 ]
机构：
[1] Nasonova Res Inst Rheumatol, Moscow, Russia
来源：
TERAPEVTICHESKII ARKHIV | 2020年 / 92卷 / 05期
关键词：
IgG4-related disease; diagnostic criteria; classification criteria; pathogenesis; CD4+T cytotoxic cells; plasmabalsts; malignancy; lymphoma; allergy; abatacept; rituximab; AUTOIMMUNE PANCREATITIS; CANCER; RISK; SIALADENITIS; MALIGNANCIES; ASSOCIATION; STATEMENT; DIAGNOSIS; CRITERIA;
D O I：
10.26442/00403660.2020.05.000632
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
IgG4-related disease is immunomediated fibroinflammatory condition, characterized by tumefective lesions in different organs with distinctive pathomorphological features and IgG4 hypersecretion in serum and tissues in the majority of patients. IgG4-RD has been established as a separate clinical in the early 2000s. In the review we focus on the evolution of views on ethiopathogenesis of the disease, therapeutic and diagnostic options and classification of the disease.
引用
收藏
页码：104 / 109
页数：6
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