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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Secondary cold type AIHA is also caused primarily by lymphoproliferative disorders, but is also commonly caused by infection, especially by mycoplasma, viral pneumonia, autoimuj mononucleosis, and other respiratory infections. Hemolytic anemia is the hemolytic state in which anemia is present, and bone marrow function is inferentially unable to compensate for the shortened life-span of the red cell.

In another example, a patient presented with acrocyanosis and a high-titer, high-thermal-amplitude, complement-fixing IgM cold agglutinin, without evidence for hemolysis.

Most of the cold addalah are directed against I antigen and I antigen negative donor units are extremely rare, so red cell transfusion may potentiate hemolysis. The typical case of an infectious etiology involves mycoplasmal pneumonia or infectious mononucleosis in an adolescent or young adult.

Clinical and serological characterization of autoimmune hemolytic anemia in a tertiary care hospital in North India. Patients with paroxysmal cold hemoglobinuria exhibit a rapid fall in hematocrit during a paroxysm. Anti-i specificity is predominant in patients with infectious mononucleosis and in some patients with lymphoma. Anti-Wr b and other autoantibodies responsible for positive direct antiglobulin test hemolitii individuals. This study was conducted to identify the profile of autoimmune hemolytic anemia AIHA patients and their response of treatment after receiving corticosteroid treatment.

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In context to Indian scenario Das et al opined that decision to transfuse in AIHA should be based on the clinical condition of the patient.

Anemia Hemolitik Autoimun by erfan andrianto on Prezi

Studies on the biosynthetic pathway of human P erythrocyte antigens using somatic cells in culture. Das SS, Chaudhary R. This technique demonstrated that a rabbit antibody against human globulin would induce agglutination of human red cells “coated with an incomplete variety of rhesus antibody”. The typical tests used for this are a complete blood count CBC with peripheral smear, bilirubin, lactate dehydrogenase LDH in particular with isoenzyme 1haptoglobin and urine hemoglobin.

Rossi’s Principles of Transfusion Medicine.

Autoimmune hemolytic anemia with predominance of IgA autoantibody. Tes Coombs menunjukkan anti-C3 dan ditemukannya cold antibody. Clinical history is also important to elucidate any underlying illness or medications that may have led to the disease. Idiopathic primary chronic autoinun agglutinin disease has its peak incidence after age 50 years. On the mechanisms of sensitization and attachment of antibodies to RBCs in drug-induced immune hemolytic anemia.

The Clinical Pictures of Autoimmune Hemolytic Anemia

Immune hemolysis in vivo begins with opsonization of red cells by autoantibody. Each has its own advantages and disadvantages.

Efficacy of treatment depends on the correct diagnosis of either warm- or cold-type AIHA. Idiopathic acquired hemolytic anemia: Autoimmune hemolytic anemia in India: In secondary AIHA, the symptoms and signs of the underlying disease may overshadow the hemolytic anemia and associated features.


A century of exciting progress in understanding. Associated with ingestion of certain drugs e.

Autoimmune hemolytic anemia – Wikipedia

Donath-Landsteiner hemolytic anemia in children. Lymphoproliferative disorders such as chronic lymphocytic leukemia, Hodgkin’s disease, non-Hodgkin’s lymphoma and Waldenstorm’s macroglobulinemia are the leading causes of secondary cases. Primary warm antibody AIHA accounts for about half of the cases [ 34 ]. Autoimmune hemolytic anemia with reticulocytopenia: Find articles by Sang Hyuk Park. Acrocyanosis involving the fingers, toes, nose, and ears is caused by sludging of RBCs in the cutaneous microvasculature fig.

Support Center Support Center. Exacerbation of autoantibody-mediated hemolytic anemia by viral infection. It was observed by Sokol et al. The causes of AIHA are poorly understood. Occasionally immune thrombocytopenia is seen in patients with warm antibody AIHA, a condition termed Evans syndrome [ 17 ].

Children with chronic AIHA tend to be older [ 60 ]. The direct antiglobulin reaction may be positive for complement during and briefly following an acute attack. Alpha-interferon for severe cold agglutinin disease.