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-.
|Published (Last):||26 October 2013|
|PDF File Size:||18.17 Mb|
|ePub File Size:||7.98 Mb|
|Price:||Free* [*Free Regsitration Required]|
Laboratorydata typically reveal hemolytic anemia, with schistocyteson the peripheral smear, diminished serum haptoglobin,and thrombocytopenia. Clinically, it is characterized by microangiopathic hemolyticanemia, thrombocytopenia, neurologic abnormalities,fever and renal dysfunction.
Subscribe to our Newsletter. The acute form is more frequent, and in most casesthe course is fulminant if treatment is not initiated. The Spanish Association of Pediatrics has as one of its main objectives the dissemination of rigorous and updated scientific information on the peeiatria areas of pediatrics.
Cytokines and plasma factors in sickle cell disease.
Recentemente, Canalli pediatriaa al. You can change the settings or obtain more information by clicking here. J Pediatrics, 81pp. Thrombotic thrombocytopenic purpura TTP or Moschovitzsyndrome is rare and is even rarer in childhood.
Annals of Pediatrics is the Body of Scientific Expression of the Hemolitixa and is the vehicle hhemolitica which members communicate.
Correction of the sickle cell mutation in embryonic stem cells. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.
A variety of other immunosuppressive agents as well as splenectomy are used for refractory cases. Resultados similares foram obtidos em modelos animais com clorotrimazol, que bloqueia o canal de Gardos.
Johnson C, Telen MJ.
Anemia hemolítica autoinmune por hemolisina bifásica | Anales de Pediatría (English Edition)
Ann N Y Acad Sci. You can change the settings or obtain more information by clicking here.
Ion transport pathology in the mechanism of sickle cell dehydration. Med Clin Barc96pp. Moi P, Sadelain M.
There was a problem providing the content you requested
J Pediatr Rio J. Diagnostic approach to hemoglobinopathies. Induction of fetal hemoglobin in the treatment of sickle cell disease. Am J Trop Med Hyg. Chronic liver abnormalities in sickle cell disease: Thefirst child recovered spontaneously. The etiology is still unknown,although different factors such as large von Willebrandfactor multimers and prostacyclin have been implicated.
Hematol Oncol Clin North Am. Panigrahi I, Agarwal S. N Engl J Med. Remission after cis retinoic acid hemklitica thrombotic thrombocytopenic purpura. Eur J Pediatr,pp.
DESTACAN LA UTILIDAD DEL RITUXIMAB PARA TRATAR LA ANEMIA HEMOLITICA AUTOIMMUNE
Birgens H, Ljung R. J Pediatr,pp. Genetic dissection and prognostic modeling of pediagria stroke in sickle cell anemia. Key words autoimmune haemolytic anaemia, cold agglutinin disease, rituximab. Laboratorydata typically reveal hemolytic anemia, with schistocyteson the peripheral smear, diminished serum haptoglobin,and thrombocytopenia.
Material and methods We present the clinical cases of two pediatrka, aged 4 and7 respectively, with TTP, but with different evolution andtreatment. CiteScore measures average citations received per document published. Ela foi descrita por Linus Pauling et al. Indian J Med Sci.