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Immune thrombocytopenic purpura (ITP)
Ali Al Khader, M.D. Faculty of Medicine Al-Balqa’ Applied University
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ITP 2 clinical subtypes 1-Chronic…relatively common
…women between 20 & 40 2-Acute…self-limited …mostly in children after viral infection
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Chronic ITP Antibodies against platelet membrane glycoproteins IIb/IIIa or Ib/IX …detected in roughly 80% of cases of chronic ITP The spleen is an important site of: -anti-platelet antibody production -destruction of the IgG-coated platelets The bone marrow usually contains increased numbers of megakaryocytes …a finding common to all forms of thrombocytopenia caused by accelerated platelet destruction
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Chronic ITP, clinical features
Petechiae, easy bruising, epistaxis, gum bleeding, and hemorrhages after minor trauma …more serious intracerebral or subarachnoid hemorrhages are uncommon
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ITP, diagnosis Clinical features The presence of thrombocytopenia
Examination of the marrow The exclusion of secondary ITP…due to drugs or autoimmune disease
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Chronic ITP, treatment Treatment usually involves the use of immunosuppressive agents and, in some cases, splenectomy Splenomegaly is not a feature of uncomplicated chronic ITP …However, splenectomy: …normalizes the platelet count …induces a complete remission in more than two-thirds of patients
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Thank You
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