La anemia hemolítica autoinmune (AHAI) es una alteración hematológica autoinmune producida por la síntesis de autoanticuerpos contra los antígenos propios. Estas representam as formas mais comuns de anemia hemolítica hereditária. .. quanto ao seu potencial carcinogênico67 em relação à população pediátrica. Recibido para publicación: Aceptado para publicación: Introducción. La anemia hemolítica microangiopática se describió por prime-.
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The treatment of these autoimmune haemolytic anaemias with rituximab requires authorisation by the Spanish Ministry of Health for compassionate use. Thrombotic thrombocytopenic purpura TTP or Moschovitzsyndrome is rare and is even rarer in childhood. nemolitica
The acute form is more frequent, anemka in most casesthe course is fulminant if treatment is not initiated. You can change the settings or obtain more information by clicking here. SRJ is a prestige metric based on the idea that not all citations are the same. Pulmonary hypertension in sickle cell disease.
Eur J Pediatr,pp. Cytokines and plasma factors in sickle cell disease. Related umbilical cord blood transplantation in patients with thalassemia and sickle cell disease. Hemoglobinopathies in newborns from Salvador, Bahia, Northeast Brazil. We present the clinical cases of two children, aged 4 and7 respectively, with TTP, but with different evolution andtreatment. Biol Blood Marrow Transplant. Increased adhesive properties of eosinophils in sickle cell disease. The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years.
Hematol Oncol Clin North Am. Continuing navigation will be considered as acceptance of this use. Diagnostic approach to hemoglobinopathies.
Davies SC, Gilmore A. Identification of differentially expressed genes induced by hydroxyurea in reticulocytes from sickle cell anaemia patients. A variety of other immunosuppressive agents as well as splenectomy are used for refractory cases.
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J Pediatr Rio J. Increased adhesive properties of neutrophils in sickle cell disease may be reversed by pharmacological nitric oxide donation. Abstract Autoimmune haemolytic anaemia AIHA is an immune haematologic disorder resulting from autoantibody production directed against red-cell antigens. Med Clin Barc96pp. Microangiopathic hemolytic anemia and thrombocytopenia.
Estella Aguado b. Current status of iron overload and chelation with deferasirox.
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Are you a health professional able to prescribe or dispense drugs? Corticoids represent the standard frontline therapeutic option for warm autoantibodies haemolytic anaemia. Indian J Med Sci. Foram encontrados mais de 2. Successful treatment of recurrent thrombotic thrombocytopenic purpura with plasmapheresis and vincristine.
Therapy with hydroxyurea is associated with reduced adhesion molecule gene and protein expression in sickle red cells with a concomitant reduction in adhesive properties.
Anemia hemolítica autoinmune por hemolisina bifásica | Anales de Pediatría (English Edition)
Induction of fetal hemoglobin in the treatment of sickle cell disease. Laboratorydata typically reveal hemolytic anemia, with schistocyteson the peripheral smear, diminished serum haptoglobin,and thrombocytopenia. Pulmonary hypertension in sickle cell disease: The etiology is still unknown,although different factors such as large von Willebrandfactor multimers and prostacyclin have been implicated.
Bienvenido a siicsalud Contacto Inquietudes. J Pediatr Hematol Oncol, 18pp. Singh SP, Gupta S. Recentemente, Canalli et al.