继发性免疫性血小板减少症病因异质性及研究进展

• 作者: 张广森 贺怡子
• 来源期刊: 临床血液学杂志
• 学科: 医学
• 关键词: 继发性免疫性血小板减少 病因 临床特点
• 年，卷（期）: 2017,（3）
• 所属期刊栏目: 综述
• 页码范围: 240-244
• 页数: 5页
• 分类号: R558.2
• 语种: 中文
• DOI: 10.13201/j.issn.1004-2806.2017.03.023

摘要

Immune thrombocytopenic purpura (ITP) is an acquired disease with detectable autoantibodies against antigens on platelets' surface,which accelerate platelets' destruction and inhibit their production.In most cases,ITP are considered be idiopathic;whereas others are secondary to some well-defined causes including autoimmune disease,immunodeficiency and drug.Recent studies suggest that the proclivity to develop platelet-reactive antibodies in secondary ITP is resulted from diverse mechanisms.ITP secondary to an underlying condition is an exclusive diagnosis that is essential for improving treatment efficacy.Our review focuses on new advances of pathogenic and clinical diversity in several common secondary ITP.

作者信息

序号	姓名	单位	发文数	被引次数	H指数	G指数
1	张广森		80	423	10.0	16.0
2	贺怡子		2	0	0.0	0.0