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
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How I treat warm autoimmune hemolytic anemia [PDF]
Blood, 2021 Warm autoimmune hemolytic anemia (wAIHA) is caused by increased erythrocyte destruction by IgG autoantibodies, with or without complement activation.
Wilma Barcellini, Bruno Fattizzo
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Autoimmune hemolytic anemia: current knowledge and perspectives [PDF]
Immunity & Ageing, 2020 Autoimmune hemolytic anemia (AIHA) is an acquired, heterogeneous group of diseases which includes warm AIHA, cold agglutinin disease (CAD), mixed AIHA, paroxysmal cold hemoglobinuria and atypical AIHA.
Sylwia Sulimiera Michalak +5 more
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Diagnostic and therapeutic considerations in idiopathic hypereosinophilia with warm autoimmune hemolytic anemia. [PDF]
, 2015 Hypereosinophilic syndrome (HES) encompasses numerous diverse conditions resulting in peripheral hypereosinophilia that cannot be explained by hypersensitivity, infection, or atopy and that is not associated with known systemic diseases with specific ...
Brys, Adam K +3 more
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Development of New Drugs for Autoimmune Hemolytic Anemia
Pharmaceutics, 2022 Autoimmune hemolytic anemia (AIHA) is a rare disorder characterized by the autoantibody-mediated destruction of red blood cells, and treatments for it still remain challenging.
Zhengrui Xiao, Irina Murakhovskaya
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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
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The American journal of case reports, 2021 Patient: Female, 32-year-old Final Diagnosis: Anemia • hemolytic anemia • systemic lupus erythematosus Symptoms: Fatigue • weakness Medication: — Clinical Procedure: — Specialty: Hematology • Immunology Objective: Unknown etiology Background: Autoimmune ...
Tejaswi Kanderi +4 more
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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
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Refractory cold autoimmune hemolytic anemia as initial presentation of gastric B cell lymphoma: a case report [PDF]
Journal of Medical Case ReportsBackground Cold agglutinin disease is one of main two types of cold-antibody autoimmune hemolytic anemias, which can be either primary or, commonly, secondary to an infection or underlying lymphoproliferative disease [1].
Gayathri Fernando +4 more
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Epstein-Barr virus-associated autoimmune hemolytic anemia: a clinical report and review of literature [PDF]
Italian Journal of PediatricsBackground Epstein-Barr virus (EBV) infection is a common disease both in children and adults, but can lead to several complications; involvement of the blood system is often described, particularly neutropenia and thrombocytopenia, but autoimmune ...
Salvatore Accomando +5 more
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