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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Free Radic Biol Med. J Pediatr,pp.
The role of phosphatidylserine in recognition and removal of erythrocytes. Chronic sickle cell lung disease: Familial infantile thrombotic thrombocytopenic purpura. An update on anemia in less developed countries. Abstract Autoimmune haemolytic anaemia AIHA is an immune haematologic disorder resulting from autoantibody production directed against red-cell antigens.
Claster S, Vichinsky EP. Laboratorydata typically reveal hemolytic anemia, with schistocyteson the peripheral smear, diminished serum haptoglobin,and thrombocytopenia. Overt and incomplete silent cerebral infarction in sickle cell anemia: Davies SC, Gilmore A. The genetics of blood disorders: Print Send to a friend Export reference Mendeley Statistics. A variety of other immunosuppressive agents as well as splenectomy are used for refractory cases. Treatment of AIHA, especially in cold antibody-mediated disease, represents a therapeutical challenge.
Services on Demand Journal. Effect of cytokines and chemokines on sickle neutrophil adhesion to fibronectin.
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Thefirst child recovered spontaneously. Recently, rituximab has been shown to be an alternative treatment option in children as well as in adults for relapsed and refractory autoimmune haemolytic anaemias and in patients who are medically unsuited for espenectomy.
Int J Heemolitica Cell Biol. Hepatic dysfunction in sickle cell disease: To improve our services and products, we pwdiatria “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. J Pediatr Hematol Oncol, 18pp. N Engl J Med. Braz J Med Biol Res. Birgens H, Ljung R.
The genetics of blood disorders: hereditary hemoglobinopathies
Pathophysiology and therapy for haemoglobinopathies. Material and methods We present the clinical cases of two children, aged 4 and7 respectively, with TTP, but with different evolution andtreatment. Full text is only aviable anemla PDF. Quek L, Thein SL. De Franceschi L, Corrocher R.
Sickle cell disease and nitric oxide: Laboratorydata typically reveal hemolytic anemia, with schistocyteson pediatrja peripheral smear, diminished serum haptoglobin,and thrombocytopenia. Si continua navegando, consideramos que acepta su uso. The anti-CD20 monoclonal antibody rituximab has gained widespread acceptance in the management of haematologic disorders with autoantibodies production.
We present the clinical cases of two children, aged 4 and7 respectively, with TTP, but with different evolution andtreatment. Care of patients with haemoglobin abnormalities: Bienvenido a siicsalud Contacto Inquietudes. Estella Aguado b. Foram encontrados mais de 2. Acta Haemat, 68pp.
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DESTACAN LA UTILIDAD DEL RITUXIMAB PARA TRATAR LA ANEMIA HEMOLITICA AUTOIMMUNE
Successful treatment of recurrent thrombotic thrombocytopenic purpura with plasmapheresis and vincristine. Diagnostic approach to hemoglobinopathies.
The genomics of new drugs in sickle cell disease. Aslan M, Freeman BA.
This item has received. Biol Blood Marrow Transplant.
Human red blood cell polymorphisms and malaria. Am J Trop Med Hyg.
Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia.