نتایج جستجو برای: cold autoimmune hemolytic anemia

تعداد نتایج: 228165  

Journal: :international journal of hematology-oncology and stem cell research 0
behzad nazel khosroshahi emam reza hospital, hamadan university of medical sciences, hamadan, iran ; blood transfusion research center, high institute for research and education in transfusion medicine, tehran, iran. mohammad jafari department of pathology, school of medicine, hamadan university of medical sciences, hamadan, iran. hossein vazini department of nursing, hamedan branch, islamic azad university, hamedan, iran. alireza ahmadi department of hematology and oncology, school of medicine, hamadan university of medical sciences, hamadan, iran. keivan shams department of immunology, school of medicine, shiraz university of medical sciences, shiraz, iran. mahdi kholoujini department of mycology, school of medicine, tarbiat modares university, tehran, iran.

autoimmune hemolytic anemia (aiha) is characterized by shortening of red blood cell (rbc) survival and the presence of autoantibodies directed against autologous rbcs. approximately 20% of autoimmune hemolytic anemia cases are associated with cold-reactive antibody. about half of patients with aiha have no underlying associated disease; these cases are termed primary or idiopathic. secondary ca...

Journal: :Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie 2015
Sigbjørn Berentsen

The classification of autoimmune hemolytic anemias and the complement system are reviewed. In autoimmune hemolytic anemia of the warm antibody type, complement-mediated cell lysis is clinically relevant in a proportion of the patients but is hardly essential for hemolysis in most patients. Cold antibody-mediated autoimmune hemolytic anemias (primary cold agglutinin disease, secondary cold agglu...

Journal: :Hematology/oncology clinics of North America 1976
L C Jefferies

Autoimmune hemolytic anemias include warm and cold reactive autoimmune hemolytic anemias (WAIHA and CAD), paroxysmal cold hemoglobinuria (PCH), and drug-induced hemolytic anemias. If autoimmune hemolytic anemia is suspected, the clinical history should be communicated to the transfusion service, because specific tests to confirm these diagnoses are not routinely performed. This includes evaluat...

2015
Behzad Nazel Khosroshahi Mohammad Jafari Hossein Vazini Alireza Ahmadi Keivan Shams Mahdi Kholoujini

Autoimmune hemolytic anemia (AIHA) is characterized by shortening of red blood cell (RBC) survival and the presence of autoantibodies directed against autologous RBCs. Approximately 20% of autoimmune hemolytic anemia cases are associated with cold-reactive antibody. About half of patients with AIHA have no underlying associated disease; these cases are termed primary or idiopathic. Secondary ca...

2011
Shilpi Gupta Anita Szerszen Fadi Nakhl Seema Varma Aaron Gottesman Frank Forte Meekoo Dhar

INTRODUCTION Mixed warm and cold autoimmune hemolytic anemia runs a chronic course with severe intermittent exacerbations. Therapeutic options for the treatment of hemolysis associated with autoimmune hemolytic anemia are limited. There have been only two reported cases of the effective use of rituximab in the treatment of patients with mixed autoimmune hemolytic anemia. We report a case of sev...

Journal: :Turk pediatri arsivi 2017
Zeynep Canan Özdemir Özcan Bör Ener Çağrı Dinleyici Eylem Kıral

Autoimmune hemolytic anemia is a picture of hemolysis which is caused by autoantibodies against red blood cell surface antigens. It is classified as primary, secondary or warm and cold autoimmune hemolytic anemia according to the temperature at which antibodies react. It is usually an acute and self-limiting condition. Here, we present a three-year-old male patient who presented with malaise, p...

2016
Jean François Lesesve

Cold agglutinin disease arising in the context of chronic lymphocytic leukemia can misdiagnose a warm autoimmune hemolytic anemia.

Journal: :The New England Journal of Medicine 2021

Cold agglutinin disease is a rare autoimmune hemolytic anemia characterized by hemolysis that caused activation of the classic complement pathway. Sutimlimab, humanized monoclonal antibody, selectively targets C1s protein, C1 complex serine protease responsible for activating this

Journal: :Asian Journal of Transfusion Science 2010

Journal: :iranian red crescent medical journal 0
zahra nikousefat department of clinical sciences, veterinary faculty, razi university, kermanshah, ir iran moosa javdani department of veterinary surgery and radiology, veterinary faculty, shahrekord university, shahrekord, ir iran mohammad hashemnia department of pathobiology, veterinary faculty, razi university, kermanshah, ir iran; department of pathobiology, veterinary faculty, razi university, kermanshah, ir iran. tel: +98-8318322599 abbas haratyan department of pathology, sajad hospital, kermanshah, ir iran ali jalili department of clinical sciences, veterinary faculty, razi university, kermanshah, ir iran

introduction autoimmune haemolytic anemia (aiha) is a complex process characterized by an immune reaction against red blood cell self-antigens. the analysis of specimens, drawn from patients with cold auto-immune hemolytic anemia is a difficult problem for automated hematology analyzer. this paper was written to alert technologists and pathologists to the presence of cold agglutinins and its ef...

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