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Immune thrombocytopenic purpura, can be triggered by drugs, or associated with infection, pregnancy, or immune disorders such as systemic lupus erythematosus. About half of all cases are classified as "idiopathic," meaning the cause is unknown. The ,abbreviation, ",ITP," is much used.
Immune thrombocytopenia (,ITP,) is a bleeding disorder caused by decrease in the number of platelets (thrombocytes) that occurs in a person who does not have another disorder that affects platelets. In ,ITP,, the immune system produces antibodies again a person's own platelets and destroys them. Immune ...
11/1/2020, · ,Immune thrombocytopenic purpura, (,ITP,)—also known as ,idiopathic thrombocytopenic purpura, and, more recently, as immune thrombocytopenia—is a clinical syndrome in which a decreased number of circulating platelets (thrombocytopenia) manifests as a bleeding tendency, easy bruising (purpura), or extravasation of blood from capillaries into skin an...
ITP, that arises suddenly is known as acute ,ITP,, if the platelet count remains low after three months it will be called persistent ,ITP,, and if the platelet count has not returned to normal after 12 months it will be called chronic ,ITP,. The severity of the condition is noted by adding the ,term, severe or mild.
The two types of ,ITP, are acute (temporary or short-,term,) and chronic (long-lasting). Acute ,ITP, generally lasts less than 6 months. It mainly occurs in children—both boys and girls—and is the most common type of ,ITP,. Acute ,ITP, often occurs after a viral infection. Chronic ,ITP, lasts 6 …