2013
DOI: 10.1097/mph.0b013e318271f457
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ITP in Children

Abstract: Primary immune thrombocytopenia (ITP) is one of the most common bleeding disorders of childhood. In most cases, it presents with sudden widespread bruising and petechiae in an otherwise well child. Thought to be mainly a disorder of antibody-mediated platelet destruction, ITP can be self-limited or develop into a chronic condition. In this review, we discuss current concepts of the pathophysiology and treatment approaches to pediatric ITP.

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Cited by 58 publications
(31 citation statements)
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“…Approximately 80% of pediatric patients will respond to a single treatment or combination of first line therapies, which include watchful waiting, corticosteroids, IVIG, or anti-D ( 4 , 5 ). For the remaining patients, additional second line treatments are needed.…”
Section: Introductionmentioning
confidence: 99%
“…Approximately 80% of pediatric patients will respond to a single treatment or combination of first line therapies, which include watchful waiting, corticosteroids, IVIG, or anti-D ( 4 , 5 ). For the remaining patients, additional second line treatments are needed.…”
Section: Introductionmentioning
confidence: 99%
“…The disease is essentially antibody mediated platelet destruction [19], and manifests as acute and rapidly occurring bruising and petechiae in previously healthy children.…”
Section: Discussionmentioning
confidence: 99%
“…Pediatric immune thrombocytopenia (ITP) is an acquired immune mediated disorder characterized by isolated thrombocytopenia (1)(2)(3). ITP is characterized by autoreactive antibodies that bind to platelets targeting them for phagocytosis by macrophages in the spleen and liver (4,5). Other mechanisms, including B-cell hyperreactivity, T-cell-mediated cytotoxicity and impaired platelet production, have also been demonstrated to cause ITP (6)(7)(8)(9)(10)(11).…”
Section: Introductionmentioning
confidence: 99%