Idiopathic Thrombocytopenic Purpura (ITP)
- AKA Autoimmune Thrombocytopenic Purpura
- Acute or gradual onset of petechiae or ecchymoses in skin and mucous membranes
- Epistaxis and conjunctival hemorrhage common
- Melena hematemesis and menorrhagia
- Non-palpable spleen (97%) - although splenectomy is a treatment
- Mechanism
- IgG autoantibodies coat platelets and triggers splenic clearance
- Bleeding occurs when platelets <50.000/mm3
- Serious hemorrhage <10.000
- Intracranial hemorrhage <2.000
- Exams
- Bleeding time prolonged; coagulation time normal
- Bone marrow increased megakaryocytes
- Chronic Variant
- More in adult females, cyclical associated with H. pylori and varicella in adults
- Acute variant
- Children
- Follows viral illness in 50% (parvo B19)
- Most resolve spontaneously
- Treatment
- Corticosteroids
- Splenectomy
- IVIg
- IV anti-D (anti-Rho), danazol, rituximab, other immunosuppressive agents
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