Childhood immune thrombocytopenic purpura: diagnosis and management
Title
Childhood immune thrombocytopenic purpura: diagnosis and management
Creator
Blanchette V; Bolton-Maggs P
Identifier
Publisher
Hematology/oncology Clinics Of North America
Date
2010
Subject
Child; Humans; Purpura; Thrombocytopenic; Disease Management; Disease Susceptibility; Idiopathic/diagnosis/etiology/therapy
Description
Immune thrombocytopenic purpura (ITP) is an autoimmune disorder characterized by a low circulating platelet count caused by destruction of antibody-sensitized platelets in the reticuloendothelial system. ITP can be classified as childhood versus adult, acute versus chronic, and primary versus secondary. Persistence of thrombocytopenia defines the chronic form of the disorder. Secondary causes of ITP include collagen vascular disorders, immune deficiencies, and some chronic infections. This review focuses on the diagnosis and management of children who have acute and chronic ITP. Emphasis is placed on areas of controversy and new therapies.
2010
Rights
Article information provided for research and reference use only. PedPalASCNET does not hold any rights over the resource listed here. All rights are retained by the journal listed under publisher and/or the creator(s).
Type
Journal Article
Citation List Month
Backlog
URL Address
Citation
Blanchette V; Bolton-Maggs P, “Childhood immune thrombocytopenic purpura: diagnosis and management,” Pediatric Palliative Care Library, accessed April 26, 2024, https://pedpalascnetlibrary.omeka.net/items/show/14401.