Chronic Immune Thrombocytopenia in Children: Epidemiology and Clinical Presentation

被引:10
作者
Bennett, Carolyn M. [1 ,2 ,3 ]
Tarantino, Michael [4 ]
机构
[1] Emory Univ, Sch Med, Aflac Canc Ctr, Atlanta, GA 30342 USA
[2] Emory Univ, Sch Med, Blood Disorders Serv, Atlanta, GA 30342 USA
[3] Childrens Healthcare Atlanta, Atlanta, GA 30342 USA
[4] Univ Illinois, Coll Med Peoria, Peoria, IL 61656 USA
关键词
Chronic childhood immune thrombocytopenic purpura; ITP; Bleeding; Splenectomy; Intracranial hemorrhage; AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME; COMMON VARIABLE IMMUNODEFICIENCY; ITP-STUDY-GROUP; SYSTEMIC-LUPUS-ERYTHEMATOSUS; INTRAVENOUS GAMMA-GLOBULIN; LONG-TERM EFFICACY; MYCOPHENOLATE-MOFETIL; ANTI-D; EVANS-SYNDROME; CHILDHOOD-ITP;
D O I
10.1016/j.hoc.2009.08.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immune thrombocytopenic purpura (ITP) is one of the most common acquired bleeding disorders in children. Most children with ITP will have acute disease, self-limited thrombocytopenia that resolves completely within weeks or months, with or without therapy. A small subset of children with ITP has clinically significant disease with severe thrombocytopenia and/or bleeding that requires intervention. Treatment for these children is an ongoing clinical challenge, as few therapies offer long-term remission, and all have significant side effects and toxicities. This article focuses on the management of clinically significant chronic ITP in the pediatric population.
引用
收藏
页码:1223 / +
页数:17
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