Letter to the Editor
Idiopathic Thrombocytopenic Purpura in Individuals Older than 75 Years: A Rare Series
Abstract
To the Editor: Idiopathic thrombocytopenic purpura (ITP), currently referred to as primary immune thrombocytopenic purpura, is an autoimmune disease linked to the presence of autoantibodies responsible for the peripheral destruction and central inhibition of platelet growth.1 Bleeding results from unusually low levels of platelets, the cells that help blood coagulate.2 Treatment of ITP is based on the recommendations of experts2; however, in 2017, no such recommendations exist for adults older than 75 years.This content is limited to qualifying members.
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