Chronic immune thrombocytopenic purpura in childhood

Citation
T. Kuhne et P. Imbach, Chronic immune thrombocytopenic purpura in childhood, SEM THROMB, 24(6), 1998, pp. 549-553
Citations number
49
Categorie Soggetti
Hematology,"Cardiovascular & Hematology Research
Journal title
SEMINARS IN THROMBOSIS AND HEMOSTASIS
ISSN journal
00946176 → ACNP
Volume
24
Issue
6
Year of publication
1998
Pages
549 - 553
Database
ISI
SICI code
0094-6176(1998)24:6<549:CITPIC>2.0.ZU;2-4
Abstract
Immune thrombocytopenic purpura (ITP) is a bleeding disorder and is traditi onally divided in acute and chronic forms based on the duration of the dise ase. Chronic ITP is characterized by a persistence of thrombocytopenia for more than 6 months. Ten to 20% of children with ITP and almost all adults w ill develop the chronic condition. Pathophysiology of chronic ITP suggests an autoimmune process and a dysregulated immune response. There are no risk factors to predict the clinical course of ITP, Controlled clinical trials are needed to clarify many diagnostic and therapeutic aspects of chronic IT P, as recently stated by a panel of pediatric and adult hematologists on be half of The American Society of Hematology (ASH). In this article, we will focus on pathophysiological, diagnostic, and management aspects of chronic childhood ITP.