Chronic immune thrombocytopenic purpura (ITP) is characterized by easy bruising and petechiae that persists for more than 6-12 months. The spleen plays a key role in the pathophysiology by destroying antibody-coated platelets. Treatment options include wait and watch if platelets are above 50,000, intravenous immunoglobulins, corticosteroids, intravenous anti-D therapy, splenectomy, rituximab, and thrombopoietin receptor agonists like romiplostim and eltrombopag. The choice of treatment depends on the severity of symptoms, platelet count, and prior treatment history.