Immune Thrombocytopenic Purpura (Itp)

The immune thrombocytopenic purpura (ITP) is a conditional by thrombocytopenia hemorrhagic disorder that is not associated with a systemic disease. Usually, however, it runs in the adult chronic, in children acute and self-limiting. The size of the spleen is normal in the absence of other underlying disease. Diagnosis requires the exclusion of other diseases by appropriate tests. Treatment includes corticosteroids, splenectomy, immunosuppressive and Thrombopoietinrezeptoragonisten. For life-threatening bleeding platelet transfusions can i.v. Corticosteroids, iv Anti-immunoglobulin E or i.v. Immunoglobulin be used individually or in combination.

The immune thrombocytopenic purpura (ITP) is a conditional by thrombocytopenia hemorrhagic disorder that is not associated with a systemic disease. Usually, however, it runs in the adult chronic, in children acute and self-limiting. The size of the spleen is normal in the absence of other underlying disease. Diagnosis requires the exclusion of other diseases by appropriate tests. Treatment includes corticosteroids, splenectomy, immunosuppressive and Thrombopoietinrezeptoragonisten. For life-threatening bleeding platelet transfusions can i.v. Corticosteroids, iv Anti-immunoglobulin E or i.v. Immunoglobulin be used individually or in combination.

(Idiopathic thrombocytopenic purpura, immune thrombocytopenic purpura; ITP) The immune thrombocytopenic purpura (ITP) is a conditional by thrombocytopenia hemorrhagic disorder that is not associated with a systemic disease. Usually, however, it runs in the adult chronic, in children acute and self-limiting. The size of the spleen is normal in the absence of other underlying disease. Diagnosis requires the exclusion of other diseases by appropriate tests. Treatment includes corticosteroids, splenectomy, immunosuppressive and Thrombopoietinrezeptoragonisten. For life-threatening bleeding platelet transfusions can i.v. Corticosteroids, iv Anti-immunoglobulin E or i.v. Immunoglobulin be used individually or in combination. The immune thrombocytopenia is caused in most cases by a platelet-specific autoantibodies. When immune thrombocytopenia in childhood formation of the autoantibody can be triggered by viral antigen. The trigger in adults is unknown. ITP tends to deteriorate during pregnancy and increases the risk of maternal morbidity (immune thrombocytopenic purpura (ITP) in pregnancy). Symptoms and complaints Clinically, immune thrombocytopenia manifested by petechiae, purpura and mucosal bleeding. Massive gastrointestinal bleeding and hematuria are less common. The spleen is of normal size, unless a parallel present viral infection or autoimmune hemolytic anemia leads to an increase. Like other diseases with increased platelet dismantling the immune thrombocytopenia is associated with an increased risk of thrombosis. Petechiae (hard palate) DR P. MARAZZI / SCIENCE PHOTO LIBRARY var model = {thumbnailUrl ‘/-/media/manual/professional/images/m2400600-petechiae-on-the-palate-science-photo-library-high_de.jpg ? lang = en & thn = 0 & mw = 350 ‘, imageUrl:’ /-/media/manual/professional/images/m2400600-petechiae-on-the-palate-science-photo-library-high_de.jpg?la=de&thn=0 ‘ , title: ‘petechiae (hard palate) “, description:’ u003Ca id = ” v38396068 “”class = “” anchor “” u003e u003c / a u003e u003cdiv class = “” para “” u003e u003cp u003ePetechien are characterized by small red spots as seen here on the palate of this patient u003c / p u003e u003c / div u003e ‘credits’. DR P. MARAZZI / SCIENCE PHOTO LIBRARY’

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