Published: 7 February 2021
Author(s): Marco Tana, Claudio Tana, Giulia Rizzo, Fabrizio Ricci, Ettore Porreca
Issue: May 2021

immune thrombocytopenic purpura (ITP) is a rare hematologic disorder characterized by isolated thrombocytopenia due to platelet destruction, without abnormalities of erythrocyte or leukocyte number or morphology. The incidence ranges between 1.6 to 3.9 per 100.000 patient-years, with higher rates among the elderly [1].


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