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,…