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   How is ITP diagnosed?

   • To diagnose ITP, your provider will ask about your medical and family history. They will also ask about your symptoms and do a physical exam to look for signs of bleeding. Your provider may order one or more of the following blood tests.

   Platelet Disorders - Immune Thrombocytopenia (ITP) | NHLBI, NIH

   www.nhlbi.nih.gov/health/immune-thrombocytopenia

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   How do you know if you have ITP?

   • Because platelets help stop bleeding, the symptoms of ITP are related to increased bleeding. However, each person may experience symptoms differently. Symptoms may include: The purple color of the skin after blood has "leaked" under it. A bruise is blood under the skin. Persons with ITP may have large bruises from no known injury.

   Idiopathic Thrombocytopenic Purpura | Johns Hopkins Medicine

   www.hopkinsmedicine.org/health/conditions-and-diseases/idiopathic-thrombocytopenic-purpura

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   Is ITP a serious condition?

   • For most children and adults, ITP is not a serious condition. Acute ITP in children often goes away on its own within a few weeks or months and does not return. For a small number of children, ITP does not go away on its own, and the child may need treatment. Chronic ITP varies from person to person and can last for many years.

   Platelet Disorders - Immune Thrombocytopenia (ITP) | NHLBI, NIH

   www.nhlbi.nih.gov/health/immune-thrombocytopenia

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2. www.mayoclinic.org › diseases-conditionsImmune thrombocytopenia (ITP) - Diagnosis and treatment ...

   www.mayoclinic.org › diseases-conditions

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   Jun 8, 2023 · To diagnose immune thrombocytopenia, a health care provider will try to rule out other possible causes of bleeding and a low platelet count. No one test can prove the diagnosis. Blood tests can check platelet levels. Rarely, adults might need a bone marrow biopsy to rule out other problems.

3. my.clevelandclinic.org › health › diseasesImmune Thrombocytopenia (ITP): Symptoms, Diagnosis & Treatment

   my.clevelandclinic.org › health › diseases

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   Aug 24, 2023 · Immune thrombocytopenia happens when your immune system clears your platelets from circulation and your platelet level goes down. In some cases, ITP goes away on its own or with treatment. Other times, immune thrombocytopenia is a chronic condition, which means symptoms can be treated, but not cured. People with chronic ITP may need treatment ...

4. www.hopkinsmedicine.org › health › conditions-andIdiopathic Thrombocytopenic Purpura | Johns Hopkins Medicine

   www.hopkinsmedicine.org › health › conditions-and

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   Immune thrombocytopenic purpura (ITP) is a blood disorder characterized by a decrease in the number of platelets in the blood. Platelets are cells in the blood that help stop bleeding. A decrease in platelets can cause easy bruising, bleeding gums, and internal bleeding. This disease is caused by an immune reaction against one's own platelets.

5. www.nhlbi.nih.gov › health › immune-thrombocytopeniaPlatelet Disorders - Immune Thrombocytopenia (ITP) | NHLBI, NIH

   www.nhlbi.nih.gov › health › immune-thrombocytopenia

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   Mar 24, 2022 · Español. IN THIS ARTICLE. What is ITP? What are the symptoms? How is it diagnosed? What causes ITP? How is ITP treated? What health problems can ITP cause? What is ITP? Immune thrombocytopenia (ITP) is a type of platelet disorder. In ITP, your blood does not clot as it should, because you have a low platelet count.

6. www.uptodate.com › contents › immuneImmune thrombocytopenia (ITP) in adults: Clinical ... - UpToDate

   www.uptodate.com › contents › immune

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   Jul 26, 2023 · Immune thrombocytopenia (ITP, also called idiopathic thrombocytopenic purpura, immune thrombocytopenic purpura) is an acquired thrombocytopenia caused by autoantibodies against platelet antigens. It is one of the more common causes of thrombocytopenia in otherwise asymptomatic adults.

7. www.ncbi.nlm.nih.gov › books › NBK537240ITP-Immune Thrombocytopenic Purpura - StatPearls - NCBI Bookshelf

   www.ncbi.nlm.nih.gov › books › NBK537240

   May 5, 2024 · Immune thrombocytopenic purpura (ITP) is an autoimmune disease characterized by a low platelet count, purpura, and hemorrhagic episodes caused by antiplatelet autoantibodies. The diagnosis is typically made by excluding the known causes of thrombocytopenia. IgG autoantibodies sensitize the circulating platelets.