Autoimmune hemolytic anemia (AIHA) occurs when antibodies directed against the person’s own red blood cells (RBCs) cause them to burst (lyse), leading to. Autoimmune hemolytic anemia (AIHA) is an uncommon disorder characterized by hemolysis mediated by autoantibodies directed against. Autoimmune hemolytic anemia is characterized by shortened red blood cell survival and a positive Coombs test. The responsible autoantibodies may be either.

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How I treat autoimmune hemolytic anemia. Of these developments, the antiglobulin test described by Coombs, Mourant, and Race in has proved to be one of the more important, useful tools now available for the detection of immune hemolytic states. Chronic cold agglutinin disease is marked by the presence of a cold agglutinin in high titer and a DAT positive anekia complement and not IgG. Autoimmune hemolytic anemia with both cold and warm autoantibodies.

Autoimmune haemolytic hwmolitik associated with alpha-methyldopa therapy. The family history in HS, however, often identifies other affected individuals.

Mild leukocytosis and neutrophilia are typical. Received Jun 1; Accepted Aug In paroxysmal cold hemoglobinuria, surviving RBCs are generally coated with complement.

In CAS, red cell transfusions are only indicated when there is a life-threatening anemia causing crisis. Sang Adalha ParkM.

Autoimmune hemolytic anemia with monoclonal IgM Hemoltiik anti-P cold autohemolysins. Thromboembolic episodes are relatively common during active phases of the disease, frequently associated with anti-phospholipid antibodies [ 555657 ]. Blood films from patients with AIHA. Hemoglobinuria is rare in warm antibody AIHA but is more common in patients with cold agglutinin disease, and especially in patients with paroxysmal cold hemoglobinuria and with some types of drug-induced immune hemolytic anemia.


Patients with primary or secondary cold AIHA have a mild, chronic hemolytic anemia producing pallor and fatigue, however there is exacerbation of the condition in a cold environment. Annual incidence of warm antibody AIHA is estimated at one per 75, population, occurring in people of all ages [ 3 ].

Autoimmune hemolytic anemia

Alloadsorption, alloantibody, autoadsorption, autoantibody, autoimmune hemolytic anemia, best match blood, flow cytometry, gel technology. The determination of thermal amplitude of the causative autoantibody correlates with the severity of the episodes of hemolysis in patients with AIHA following their exposure to warm or cold.

Coombs-negative AIHA has been reviewed elsewhere [ 26 ]. Factors influencing prognosis in childhood autoimmune hemolytic anemia. Other therapies such as plasmapheresis, IVIG, danazol have been tried with variable success. Serum haptoglobin levels are low, and lactate dehydrogenase levels are increased. Studies on the biosynthetic pathway of human P erythrocyte antigens using somatic cells in culture. The more the molecules of IgG, the more the activation of complement, the more is the red cell destruction.

Support Center Support Center. The constitutional symptoms and hemoglobinuria generally last a few hours. Cases associated with symptomatic lymphoproliferative disorders are said to represent secondary cold agglutinin disease.

Idiopathic primary chronic cold agglutinin disease associated with clonal B-lymphocyte proliferation with or without symptomatic lymphoma. Factors affecting the pathogenicity of red cell auto and alloantibodies. Author information Article notes Copyright and License information Disclaimer. Megaloblastic anemia Pernicious anemia. These hemolytic episodes were thought to be due to infectious agents.

In patients with refractory warm AIHA, administration of high dose cyclophosphamide, alemtuzumab anti-CD52 monoclonal antibodyor ofatumumab anti-CD20 monoclonal antibody that targets different epitope compared to rituximab can be considered as the “last option” treatments, although the toxicity of alemtuzumab hinder the wide application of this drug [ 28 ].


Autoimmune hemolytic anemia – Wikipedia

As a result, the DAT is positive with anti-C3, but it is generally negative with anti IgG unless performed at colder temperatures. There are autiomun principle causes for the negative DAT: Cold hemagglutinin disease associated with IgG cold-reactive antibody. Novel drugs can be considered as the final option in AIHA patients who are refractory to all other drugs.

Occasionally patients have a combination of warm and cold autoantibodies. Rossi’s Principles of Transfusion Medicine. Autoimmune hemolytic anemia AIHA exhibits two important characteristics: InLederer and Brill described cases of acute hemolysis with rapid onset of anemia and rapid recovery after transfusion therapy.

Arndt PA, Garratty G.

Anemia Hemolitik Autoimun by erfan andrianto on Prezi

The manual method has the disadvantage that it is least sensitive for detection of red cell bound Ig. Thiopental- related immune hemolytic anemia and renal failure. Oxford, Blackwell Science,p Autoimmune hemolytic anemia associated with anti-Sc 1. Autoimmune hemolytic anemia with reticulocytopenia.

The Clinical Pictures of Autoimmune Hemolytic Anemia

Even patients with severe hemolysis may have only mild splenomegaly. Cipto Mangunkusumo, Jakarta Indonesia. Retrieved 28 December This is a type II immune response in which the drug binds to macromolecules on the surface of the RBCs and acts as an antigen.