Mar 24, 2022 · Immune thrombocytopenia (ITP) is a platelet disorder caused by problems with your immune system. Learn about the symptoms, causes, and treatments for ITP.

ITP is a rare autoimmune blood disorder that both children and adults can develop. There are 2 forms of ITP: Acute thrombocytopenic purpura. This is the most common type of ITP and mainly affects younger children. Less commonly, it may occur in older children and adults. Symptoms often appear after a virus, such as chickenpox.

The two types of Idiopathic thrombocytopenic purpura (ITP) are acute (temporary or short-term) and chronic (long-lasting). Acute ITP generally lasts less than six months. It mainly occurs in children, both boys and girls, and is the most common type of ITP.

Types of immune thrombocytopenia. The two ITP types are: Primary ITP: This is when your immune system attacks your platelets. About 80% of all cases are primary ITP. Healthcare providers may call immune thrombocytopenia an autoimmune disorder.

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.

Immune thrombocytopenic purpura (ITP), also known as idiopathic thrombocytopenic purpura or immune thrombocytopenia, is an autoimmune primary disorder of hemostasis characterized by a low platelet count in the absence of other causes. [1][2] ITP often results in an increased risk of bleeding from mucosal surfaces (such as the nose or gums) or th...

Jun 8, 2023 · Immune thrombocytopenia usually happens when the immune system makes a mistake. It attacks and destroys the cells that help blood clot, also known as platelets. In adults, an infection with HIV, hepatitis or the bacteria that causes stomach ulcers, known as …

May 5, 2024 · Immune thrombocytopenia (ITP) is an autoimmune disorder characterized by a low platelet count, purpura, and hemorrhagic episodes. ITP without an underlying disorder is known as primary ITP. Secondary ITP typically has an external cause, including drugs and other autoimmune conditions like systemic lupus erythematosus.

ITP affects approximately four to eight per 100,000 children under the age of 15 each year in the U.S. There are two forms of ITP: Acute thrombocytopenic purpura — This is most commonly seen in young children (2 to 6 years old). The symptoms may follow a viral illness, such as chickenpox.

Immune thrombocytopenia (ITP) is an autoimmune disorder characterized by an abnormally low number of platelets (<100,000/µL) in the blood. The low platelet count is attributed to a dysfunctional immune system that targets both platelets and their precursors.