Immune Thrombocytopenia is a topic covered in the Pediatric Surgery NaT.

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Introduction

Immune thrombocytopenia (ITP), previously called idiopathic thrombocytopenia, is a relatively rare autoimmune disorder that is characterized by isolated thrombocytopenia. As a result of the humoral antibody response against platelets, platelets are destroyed in a matter of hours instead of eight to ten days [1]. In some patients there may also be suppression of the megakaryocytes resulting in decreased production of platelets as well [1].

see alsoSplenic Disorders

Content in this topic is referenced in SCORE Splenic Diseases overviewHematologic Diseases: Spherocytosis, Sickle Cell, ITP, HSP overview

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Introduction

Immune thrombocytopenia (ITP), previously called idiopathic thrombocytopenia, is a relatively rare autoimmune disorder that is characterized by isolated thrombocytopenia. As a result of the humoral antibody response against platelets, platelets are destroyed in a matter of hours instead of eight to ten days [1]. In some patients there may also be suppression of the megakaryocytes resulting in decreased production of platelets as well [1].

see alsoSplenic Disorders

Content in this topic is referenced in SCORE Splenic Diseases overviewHematologic Diseases: Spherocytosis, Sickle Cell, ITP, HSP overview

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Last updated: August 3, 2018