Abstract Idiopathic thrombocytopenic purpura (ITP), now commonly termed immune thrombocytopenia, is an acquired autoimmune disorder characterized by isolated thrombocytopenia resulting from increased platelet destruction and impaired platelet production. It may occur at any age and can present with petechiae, purpura, easy bruising, mucosal bleeding, or, in severe cases, internal hemorrhage. Diagnosis is primarily based on clinical assessment, complete blood count,…
ABSTRACT Immune thrombocytopenia (ITP) is an autoimmune condition in which body’s immune system destroys platelets which leads to a low platelet count and increased risk of bleeding. It affects approximately 2–4 adults per 100,000 people every year and it can occur at any age. In children, ITP often develops after a viral infection, while in adults it may become persistent…