Сочетание ишемической болезни сердца и идиопатической тромбоцитопенической пурпуры: литературная справка и клинический случай коронарной ангиопластики


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Abstract

Idiopathic (or immune) thrombocytopenic purpura is rare autoimmune disease, characterized with forming of antithrombocytic antibodies leading to thrombocyte destruction in the spleen and bleeding tendency. Chronic form of ITP commonly occur in adults, and characterized with decreased number of circulating platelets (isolated thrombocytopenia) and manifests as bleeding from mucous membranes and skin symptoms. A 52-year patient presented with ITP, ischemic heart disease and indications for coronary angioplasty. We studied the problem of concomitant antithrombotic therapy safety in patients with ITP, undergoing coronary angioplasty.

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Chief Editor

Leo A. Bockeria, MD, PhD, DSc, Professor, Academician of Russian Academy of Sciences, President of Bakoulev National Medical Research Center for Cardiovascular Surgery