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Immune thrombocytopenic purpura (ITP) is a blood disorder. With this disease, you have a lower amount of platelets than normal in your blood. Platelets are blood cell fragments that help with blood clotting. Having fewer platelets can cause easy bruising, bleeding gums, and internal bleeding. ITP is caused by an immune reaction against your own platelets. This means that your body's immune system attacks your platelets by mistake.
ITP is a rare autoimmune blood disorder that both children and adults can develop.
There are two forms of ITP:
With ITP, your immune system attacks your body's own platelets by mistake. Most often, this is a result of antibody production against platelets. In a small number of cases, a type of white blood cell called T-cells will directly attack platelets. This immune system mistake may happen due to:
Sometimes the cause of ITP is not known.
A normal platelet count is about 150,000 to 450,000 per microliter (µL) of blood. With ITP, the platelet count is less than 100,000. By the time major bleeding occurs, you may have a platelet count of less than 10,000. The lower your platelet count, the greater your risk of bleeding.
Because platelets help stop bleeding, ITP symptoms are linked to increased bleeding. Each person's symptoms may vary depending on how low their platelet count is. Symptoms may include:
ITP symptoms may look like other health problems. Always see your doctor for a diagnosis.
Your doctor will take your health history and give you a physical exam. Your doctor may ask about any medicines you are taking that may cause bleeding or lower your platelet count. You may also have these tests:
Treatment will depend on your symptoms, age, and general health. It will also depend on how severe the condition is.
When treatment is needed, the two most common forms of immediate treatment are steroids and intravenous immunoglobulin (IVIG):
Other treatments for ITP may include:
Tips to help you get the most from a visit to your doctor: