Results 11 to 20 of about 21,425 (243)
Thymoma with Autoimmune Hemolytic Anemia
Case Reports in Oncology, 2014 A 38-year-old Japanese male was referred to our hospital with abnormal chest X-ray results and severe Coombs-positive hemolytic anemia. He was diagnosed with a stage IV, WHO type A thymoma and was treated with oral prednisolone (1 mg/kg/day) and ...
Kensuke Suzuki +4 more
doaj +4 more sources
Babesiosis-induced warm autoimmune hemolytic anemia, from infection to hemolysis: a case report [PDF]
Journal of Medical Case ReportsBackground Warm autoimmune hemolytic anemia is characterized by destruction of red blood cells mediated by autoantibodies, which can be triggered by various underlying factors including tick-borne infections. Babesia spp.
Jenna Davison +6 more
doaj +2 more sources
Immunotherapy-associated autoimmune hemolytic anemia
Journal for ImmunoTherapy of Cancer, 2017 Background Immunotherapy has been widely used in the treatment of several solid and hematologic malignancies. Checkpoint inhibitors have been the forefront of cancer immunotherapy in recent years.
Uqba Khan +4 more
doaj +2 more sources
Cold versus warm autoimmune hemolytic anemia in diffuse large B cell lymphoma: pathogenic and therapeutic implications: a case series [PDF]
Journal of Medical Case ReportsBackground Autoimmune hemolytic anemia-associated diffuse large B cell lymphoma is rare, with distinct pathogenic mechanisms and therapeutic responses in cold agglutinin syndrome (CAS) and warm autoimmune hemolytic anemia subtypes poorly characterized ...
Zhiye Zhang +3 more
doaj +2 more sources
Current Opinion in Immunology, 1994 Autoimmune hemolytic anemia (AHA) is characterized by the production of Coombs' antibodies, which are responsible for the destruction of red blood cells (RBCs). Analysis of both monoclonal anti-RBC autoantibodies derived from autoimmune New Zealand black
Izui, Shozo
core +4 more sources
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
Management of autoimmune hemolytic anemia. [PDF]
Hematology Am Soc Hematol Educ ProgramAbstract Autoimmune hemolytic anemia (AIHA) is caused by premature erythrocyte destruction mediated by autoantibodies (auto-Ab) with or without complement activation. The most frequent form (60%-70% of cases) is warm AIHA (wAIHA), driven by immunoglobulin G auto-Ab that react at body temperature. Cold agglutinin disease (CAD, 20%-25%)
Barcellini W, Fattizzo B.
europepmc +3 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
Atypical autoimmune hemolytic anemia
Haematologica, 2011 9/L (10-90), bilirubin 1.5 mg/dL (0-1.0), lactate dehydrogenase 1715 U/L (normal < 210) and ferritin 697 ng/mL. The blood film showed microcytosis and coarse basophilic stippling consistent with β-thalassemia trait. Only very occasional spherocytes were noted and there was no agglutination.
David Telio +4 more
doaj +3 more sources