Results 11 to 20 of about 21,508 (259)
Pancytopenia with autoimmune hemolytic anemia
Apollo Medicine, 2021 Payal Bargujar +2 more
doaj +2 more sources
Autoimmune hemolytic anemia [PDF]
Hematology, 2018 AbstractThe diagnosis of autoimmune hemolytic anemia (AIHA) can be made with a stepwise approach that aims to identify laboratory and clinical evidence of hemolysis and then determine the immune nature of hemolysis with the direct anti-globulin test. Once alternative causes for these findings have been excluded, AIHA is established, and the clinician ...
Anita, Hill, Quentin A, Hill
openaire +5 more sources
Acute Tubular Necrosis Associated with Autoimmune Hemolytic Anemia due to Acute Gastroenteritis
Turkish Journal of Internal Medicine, 2021 Autoimmune hemolytic anemia (AIHA) is a rare disease with a rate of 1-3 in 100,000 in adults. AIHA are defined as primary (idiopathic) or secondary depending on the presence or absence of accompanying disease.
Mehmet Sezen +7 more
doaj +1 more source
Complement inhibitors to treat IgM-mediated autoimmune hemolysis
Haematologica, 2015 Complement activation in autoimmune hemolytic anemia may exacerbate extravascular hemolysis and may occasionally result in intravascular hemolysis. IgM autoantibodies as characteristically found in cold autoantibody autoimmune hemolytic anemia, in cold ...
Diana Wouters, Sacha Zeerleder
doaj +1 more source
Anemia hemolítica autoimune e colite ulcerosa.
Acta Médica Portuguesa, 1995 Although several associations of autoimmune disorders with ulcerative colitis have been reported, autoimmune hemolytic anemia is extremely rare. We report a case of a 35 year-old white woman with a twelve-year history of mild ulcerative colitis treated ...
L Rebocho, M Lucas, R M Victorino
doaj +1 more source
Problem of the diagnosis of acquired hemolytic anemia in childhood
Zdorovʹe Rebenka, 2020 Autoimmune hemolytic anemia is a heterogeneous group of diseases that are associated with decompensated acquired hemolysis. Autoimmune hemolytic anemia in children is most commonly observed after a viral illness. However, it is quite a rare disorder with
S.O. Nykytyuk +4 more
doaj +1 more source
CAQ Corner: Immune‐mediated complications
, 2022 Liver Transplantation, EarlyView.
Mary Thomson, John R. Lake
wiley +1 more source
Hematology, 2023 Background Severe autoimmune hemolytic anemia complicating hereditary spherocytosis is life threatening and has not been described in a case report. Here, we report a case in which this intractable disease was treated successfully with glucocorticoids ...
Na Wang +4 more
doaj +1 more source
RASGRP1 Deficiency Manifesting as Severe Vasculopathy and Fatal Autoimmune Hemolytic Anemia. [PDF]
EJHaemABSTRACT Background RASGRP1 deficiency is a rare inborn error of immunity characterized by immunodeficiency, autoimmunity, and lymphoproliferation. Results We report a 5‐year‐old male with novel homozygous splice‐donor mutations in RASGRP1(c.1720+1G>A and c.1720+2T>C) who presented with severe vasculopathy (ischemic stroke and thrombosis), secondary ...
Ashari KA +5 more
europepmc +2 more sources
Autoimmune hemolytic anemia as an initial manifestation of Hodgkin’s Disease: Case report [PDF]
, 2016 This paper presents the case of an 11 year-old male who attended the Internal Medicine Service at a high complexity pediatric hospital. Initially, the patient attended due to a clinical profile consisting of autoimmune hemolytic anemia that was partially
Urrego-Díaz, José Augusto +11 more
core +1 more source