Results 61 to 70 of about 400,917 (195)
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
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Scientific Reports, 2016 Hemolytic anemia intensity has been suggested as a vital factor for the growth of certain clinical complications of sickle cell disease. However, there is no effective and rapid diagnostic method.
S. Sang +7 more
semanticscholar +1 more source
Hemolytic Anemia in Cirrhosis: A Case of Spur-Cell Anemia
Annals of Internal Medicine: Clinical CasesAnemia is a common complication of cirrhosis; therefore, its evaluation must be thorough and tailored to a patient's history. In this case, a 67-year-old woman with metabolic dysfunction–associated cirrhosis presented with transfusion-refractory ...
Blake H. Bentley +2 more
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Concurrent Atypical Hemolytic Uremic Syndrome and Autoimmune Hemolytic Anemia: a case report
Caspian Journal of Pediatrics, 2018 Background: Atypical hemolytic uremic syndrome (aHUS) is a life-threatening and scarce disorder characterized by acute renal failure and disease, non-immune microangiopathic hemolytic anemia and thrombocytopenia, leading to end-stage renal failure or ...
Sayed Yousef Mojtahedi +1 more
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Autoimmune Hemolytic Anemia as a Complication of Nivolumab Therapy
Case Reports in Oncology, 2016 Recently, immunotherapeutic drugs, including PD-1 inhibitors (nivolumab, pembrolizumab), PD-L1 inhibitors (atezolizumab, avelumab), and CTLA4 inhibitors (ipiliumumab), have emerged as important additions to the armamentarium against certain malignancies ...
Amruth R. Palla +3 more
semanticscholar +1 more source
Hemolytic Anemia and Reactive Thrombocytosis Associated With Cefoperazone/Sulbactam
Frontiers in Pharmacology, 2019 Background: Cefoperazone/sulbactam is a broad-spectrum antibacterial agent. Drug-induced immune hemolytic anemia is a rare but serious condition, and reactive thrombocytosis is caused by processes extrinsic to the megakaryocyte.
Ling Zhou, Jianan Bao, Jingjing Ma
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New Insights in the Pathogenesis of Autoimmune Hemolytic Anemia
Transfusion Medicine and Hemotherapy, 2015 Autoimmune hemolytic anemia (AIHA) is caused by the increased destruction of red blood cells (RBCs) by anti-RBC autoantibodies with or without complement activation.
W. Barcellini
semanticscholar +1 more source
DETECTION OF OCCULT GLOMERULAR DYSFUNCTION IN GLUCOSE SIX PHOSPHATE DEHYDROGENASE DEFICIENCY ANEMIA
Mediterranean Journal of Hematology and Infectious Diseases, 2016 Background: Glucose six phosphate dehydrogenase deficiency (G6PD) anemia is associated with intravascular hemolysis. The freely filtered hemoglobin can damage the kidney. We aimed to assess gloumerular status in G6PD children.
Gehan Abdel Hakeem +6 more
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Acute hemolysis in association with hepatitis B infection in a child with beta-thalassemia trait
The Turkish Journal of Pediatrics, 1994 Autoimmune hemolytic anemia may occur in the course of some viral diseases such as Coxsackie virus, cytomegalovirus, Epstein Barr virus, Influenza A, herpes simplex virus, and rarely hepatitis B virus infection.
A Gürgey, A Yüce, N Ozbek, N Koçak
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Babesiosis-induced warm autoimmune hemolytic anemia, from infection to hemolysis: a case report
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
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