Thrombocytopenic purpura belongs to an immune syndrome, which is a more serious bleeding disorder. It is mainly due to the presence of anti-platelet antibodies in the blood circulation, resulting in massive destruction of platelets and eventually causing purpura. If not actively treated, thrombocytopenic purpura is likely to cause hemorrhagic anemia and even intracranial hemorrhage if the symptoms are severe. The actual fact is that you can use medication, surgery and other methods. A, drug treatment 1, platelet-raising drugs: such as Etripopat, Romistatin and other drugs, can effectively promote the production of platelets, to help the remission of the disease; 2, glucocorticoids: such as prednisolone, has the effect of inhibiting the destruction of platelets, slowing down the rate of reduction of platelets; 3, platelet preparations: intravenous infusion of platelet preparations, can effectively increase the number of platelets in the blood; 4. Gammaglobulin: high doses of gammaglobulin can be used in case of emergency bleeding; 5. Immunosuppressants: vincristine, cyclophosphamide, azathioprine, etc., can act on patients who are not suitable for glucocorticoid therapy or splenectomy. Second, surgical treatment such as splenectomy, mainly to inhibit the destruction of platelets by the spleen. During the treatment period, more attention should be paid to rest, and the disease has a certain degree of recurrence, so attention should be paid to regular review after treatment.