<abstract xmlns="http://www.w3.org/1999/xhtml"><p>Immune thrombocytopenic purpura (ITP) is an acquired disease in which autoantibodies to platelets cause their sequestration and destruction by mononuclear macrophages, principally in the spleen. If increased production of platelets by megakaryocytes does not compensate for platelet destruction, the number of circulating platelets decreases (thrombocytopenia), resulting in a characteristic bleeding tendency (purpura). While most children with the disease experience a relatively short and benign clinical course, ITP in adults often lasts more than 6 months (chronic ITP) and is resistant to conventional treatment (corticosteroids, intravenous immune globulin, or splenectomy). The goal of medical management is to increase the platelet count to a safe level, without the risks of bacterial infections associated with splenectomy or toxicity from prolonged corticosteroid therapy. Splenectomy increases platelet counts in hours to days in most patients with acute ITP, but nearly 50 percent experience recurrent thrombocytopenia by 5 years postsplenectomy.</p></abstract>

Immune thrombocytopenic purpura (ITP) is an acquired disease in which autoantibodies to platelets cause their sequestration and destruction by mononuclear macrophages, principally in the spleen. If increased production of platelets by megakaryocytes does not compensate for platelet destruction, the number of circulating platelets decreases (thrombocytopenia), resulting in a characteristic bleeding tendency (purpura). While most children with the disease experience a relatively short and benign clinical course, ITP in adults often lasts more than 6 months (chronic ITP) and is resistant to conventional treatment (corticosteroids, intravenous immune globulin, or splenectomy). The goal of medical management is to increase the platelet count to a safe level, without the risks of bacterial infections associated with splenectomy or toxicity from prolonged corticosteroid therapy. Splenectomy increases platelet counts in hours to days in most patients with acute ITP, but nearly 50 percent experience recurrent thrombocytopenia by 5 years postsplenectomy.

Review: immune thrombocytopenic purpura: an update for immunohematologists

Immunohematology

{"article-title":"Review: immune thrombocytopenic purpura: an update for immunohematologists"}

Immune thrombocytopenic purpura (ITP) is an acquired disease in which autoantibodies to platelets cause their sequestration and destruction by mononuclear...

Review: immune thrombocytopenic purpura: an update for immunohematologists

Pubblicato online: 15 mag 2020

Pagine: 112 - 117

DOI: https://doi.org/10.21307/immunohematology-2019-432

Parole chiave
platelets, thrombocytopenia, platelet antibodies, reticuloendothelial system, macrophage Fc receptors, splenectomy, intravenous immune globulin, IV Rh immune globulin, rituximab

© 2004 S.G. Sandler., published by Sciendo

Review: immune thrombocytopenic purpura: an update for immunohematologists

Pubblicato online: 15 mag 2020

Pagine: 112 - 117

DOI: https://doi.org/10.21307/immunohematology-2019-432

Parole chiaveplatelets, thrombocytopenia, platelet antibodies, reticuloendothelial system, macrophage Fc receptors, splenectomy, intravenous immune globulin, IV Rh immune globulin, rituximab

© 2004 S.G. Sandler., published by Sciendo

Parole chiave
platelets, thrombocytopenia, platelet antibodies, reticuloendothelial system, macrophage Fc receptors, splenectomy, intravenous immune globulin, IV Rh immune globulin, rituximab