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Immune Thrombocytopenia (ITP): Symptoms, Diagnosis & Treatment
Immune thrombocytopenia (ITP) is a rare blood disorder that affects how your blood clots. When your blood can’t clot, you may bruise easily, bleed more than normal when you’re hurt or start bleeding for no reason. Sometimes, ITP goes away without treatment. Other times, it’s a chronic condition, meaning treatment eases symptoms but doesn’t cure it.
Immune Thrombocytopenic Purpura - StatPearls - NCBI Bookshelf
The American Society of Hematology defines immune thrombocytopenic purpura (ITP) as isolated thrombocytopenia (platelet count less than 100,000/microL) with normal white blood cells and normal hemoglobin in the setting of a generalized purpuric rash. ITP was previously known as idiopathic thrombocytopenic purpura or immune thrombocytopenic purpura.
Platelet Disorders - Immune Thrombocytopenia (ITP) | NHLBI, NIH
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.
Idiopathic Thrombocytopenic Purpura | Johns Hopkins Medicine
Idiopathic thrombocytopenic purpura is a blood disorder characterized by an abnormal decrease in the number of platelets in the blood. A decrease in platelets can result in easy bruising, bleeding gums, and internal bleeding. ITP may be acute and resolve in less than 6 months, or chronic and last longer than 6 months.
Immune thrombocytopenia (ITP) - Diagnosis and treatment - Mayo Clinic
Questions about ITP might include: How many platelets do I have in my blood? Is my platelet count too low? What is causing my ITP? Do I need more tests? Is this condition temporary or long lasting? What treatments are there? What do you recommend? What are the possible side effects of these treatments? What will happen if I do nothing?
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