A Rare Case of Idiopathic Thrombocytopenic Purpura with Unusual Clinical Manifestations
Abstract
Idiopathic thrombocytopenic purpura (ITP) is an autoimmune condition marked by isolated thrombocytopenia, which makes people more likely to hemorrhage. We provide a case of a 45-year-old female patient with ITP who displayed unusual clinical symptoms, emphasizing the diagnostic difficulties and treatment options in such circumstances.