Decreased production of platelets Congenital bone marrow failure (Fanconi anemia, Wiskott-Aldrich syndrome; congenital amegakaryocytic thrombocytopenia) Acquired bone marrow failure (aplastic anemia, myelodysplasia, leukemia) Exposure to chemotherapy, irradiation, medications (https://ouhsc.edu/platelets/ditp.html) Marrow infiltration (neoplastic, infectious) Nutritional (deficiency of vitamin B12, folate) Other: HIV infection, alcohol Increased destruction of platelets Immune thrombocytopenia (primary) Immune thrombocytopenia (secondary), including drug-induced or related to lymphoproliferative disorders (eg, CLL, hepatitis C virus, Epstein-Barr virus, or HIV) Heparin-induced thrombocytopenia Thrombotic microangiopathy Disseminated intravascular coagulation Posttransfusion purpura Neonatal alloimmune thrombocytopenia Mechanical (aortic valvular dysfunction; extracorporeal bypass) von Willebrand disease, type 2B Hemophagocytosis Increased sequestration of platelets Hypersplenism (eg, related to cirrhosis, myeloproliferative disorders, lymphoma) Other conditions causing thrombocytopenia Gestational thrombocytopenia Bernard-Soulier syndrome, gray platelet syndrome, May-Hegglin anomaly Pseudothrombocytopenia |