Abstract Immune thrombocytopenia (ITP) formerly known as Idiopathic Thrombocytopenic Purpura , is an acquired autoimmune hematological disorder characterized by a persistently or intermittently reduced platelet count resulting from immune-mediated platelet destruction and impaired platelet production. The condition affects individuals across all age groups and presents with a wide spectrum of clinical manifestations, ranging from asymptomatic thrombocytopenia and cutaneous purpura to…