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18 Possible Causes for Thrombocytopenia Post Hemolytic Anemia

  • Evan's Syndrome

    Cold-reacting autoantibodies associated with hemolytic anemia usually have a broad thermal range that enables them to bind target antigens at near-physiologic temperatures[blogs.nejm.org] Tags: anemia , Case Records of the Massachusetts General Hospital , thrombocytopenia Posted in Physicians-In-Training Permalink 2 Comments This entry was posted on Thursday[blogs.nejm.org]

  • Myeloproliferative Disease

    , infections, inflammatory diseases, tissue damage, iron deficiency, hemolytic anemia, post splenectomy, cryoglobulinemia, medications (steroids, adrenaline, trans-retinoic[scielo.br] Differential diagnosis ET must be distinguished from other MPN and the processes that lead to transient reactive thrombocytosis: acute hemorrhage, recovery of thrombocytopenia[scielo.br]

  • HIV-induced Thrombocytopenia

    thrombocytopenia, Drug-induced thrombocytopenia, Post-infectious, HIV, other autoimmune (lupus, antiphospholipid syndrome) 3.[errolozdalga.com] Increased destruction: a) Microangiopathic Hemolytic Anemias (MAHA): DIC, TTP/HUS, HELLP syndrome - see Ellen Eaton's recent MR summary for more b) Immune-mediated: ITP, Heparin-induced[errolozdalga.com]

  • Autoimmune Hemolytic Anemia

    Overview of Evans syndrome (Coombs’-positive autoimmune hemolytic anemia and thrombocytopenia) AIHA: Results when IgG present which reacts with RBC antigens at room temperature[errolozdalga.com] SLE), immune deficiency, liquid tumors, post-hematopoietic stem cell transplant Pathophysiology: IgG (and subsequently fixed complement) adhere to phagocytes, resulting in[errolozdalga.com]

  • Immune Hemolytic Anemia

    Overview of Evans syndrome (Coombs’-positive autoimmune hemolytic anemia and thrombocytopenia) AIHA: Results when IgG present which reacts with RBC antigens at room temperature[errolozdalga.com] SLE), immune deficiency, liquid tumors, post-hematopoietic stem cell transplant Pathophysiology: IgG (and subsequently fixed complement) adhere to phagocytes, resulting in[errolozdalga.com]

  • Hemolytic Uremic Syndrome

    Laboratory findings revealed that the patient had hemolytic anemia, thrombocytopenia, and acute renal failure.[ncbi.nlm.nih.gov] anemia with fragmented erythrocytes, thrombocytopenia and acute renal failure.[doi.org] Post-mortem examination confirmed that the patient had PHUS.[ncbi.nlm.nih.gov]

  • Traumatic Hemolytic Anemia

    Overview of Evans syndrome (Coombs’-positive autoimmune hemolytic anemia and thrombocytopenia) AIHA: Results when IgG present which reacts with RBC antigens at room temperature[errolozdalga.com] SLE), immune deficiency, liquid tumors, post-hematopoietic stem cell transplant Pathophysiology: IgG (and subsequently fixed complement) adhere to phagocytes, resulting in[errolozdalga.com]

  • Erythrocytosis

    , infections, inflammatory diseases, tissue damage, iron deficiency, hemolytic anemia, post splenectomy, cryoglobulinemia, medications (steroids, adrenaline, trans-retinoic[ncbi.nlm.nih.gov] Differential diagnosis ET must be distinguished from other MPN and the processes that lead to transient reactive thrombocytosis: acute hemorrhage, recovery of thrombocytopenia[ncbi.nlm.nih.gov]

  • Microangiopathic Hemolytic Anemia

    Microangiopathic Hemolytic Anemia and Thrombocytopenia Questions The ASCO Post is pleased to present Hematology Expert Review, an occasional feature that includes a case report[ascopost.com] Overview of Evans syndrome (Coombs’-positive autoimmune hemolytic anemia and thrombocytopenia) AIHA: Results when IgG present which reacts with RBC antigens at room temperature[errolozdalga.com] Gruppo RA, Rother RP: Eculizumab for congenital atypical hemolytic-uremic syndrome. N Engl J Med 360:544-546, 2009.[ascopost.com]

  • Atypical Hemolytic Uremic Syndrome

    anemia with fragmented erythrocytes, thrombocytopenia and acute renal failure.[doi.org] In children, the most frequent form (90% of patients), called typical or post-diarrheal (D ) HUS, is caused by infection with Shiga-toxin (Stx)-producing Escherichia coli[doi.org] Factor I Factor B Membrane cofactor protein Plasma infusion Plasma exchange Transplantation Introduction Hemolytic uremic syndrome (HUS) is characterized by the triad of hemolytic[doi.org]

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