Results 41 to 50 of about 65,798 (270)

Diagnostic and therapeutic considerations in idiopathic hypereosinophilia with warm autoimmune hemolytic anemia. [PDF]

open access: yes, 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
core   +1 more source

Mixed autoimmune hemolytic anemia in a 2-year-old girl

open access: yesJournal of Applied Hematology, 2023
Immune hemolytic anemia is diagnosed when it exhibits the clinical symptoms and laboratory findings of hemolytic anemia, such as pallor, jaundice, anemia, high indirect bilirubin, increased reticulocyte count, and a positive direct antiglobulin test ...
Asim Abdullah Alamri   +5 more
doaj   +1 more source

New Insights in Autoimmune Hemolytic Anemia: From Pathogenesis to Therapy

open access: yesJournal of Clinical Medicine, 2020
Autoimmune hemolytic anemia (AIHA) is a highly heterogeneous disease due to increased destruction of autologous erythrocytes by autoantibodies with or without complement involvement. Other pathogenic mechanisms include hyper-activation of cellular immune
W. Barcellini   +3 more
semanticscholar   +1 more source

Successful therapeutic plasma exchange in cold autoimmune hemolytic anemia in patient with disseminated tuberculosis

open access: yesReumatismo, 2021
An association of autoimmune hemolytic anemia with disseminated tuberculosis is an exceedingly rare entity. We describe herein a case of cold hemolytic autoimmune anemia associated with miliary tuberculosis resolved with blood transfusions, therapeutic ...
N. Belfeki   +7 more
doaj   +1 more source

Autoimmune hemolytic anemia: current knowledge and perspectives

open access: yesImmunity & 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.
S. Michalak   +5 more
semanticscholar   +1 more source

Severe autoimmune hemolytic anemia following receipt of SARS‐CoV‐2 mRNA vaccine

open access: yesTransfusion, 2021
Large clinical trials have demonstrated the overall safety of vaccines for severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2). However, reports have emerged of autoimmune phenomena, including vaccine‐associated myocarditis, immune ...
S. Gadi   +8 more
semanticscholar   +1 more source

Severe autoimmune hemolytic anemia complicating hereditary spherocytosis treated successfully with glucocorticoids and cyclosporine: a case report

open access: yesHematology, 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

Warm Autoimmune Hemolytic Anemia Associated With Asymptomatic SARS-CoV-2 Infection

open access: yesCureus, 2021
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the resultant coronavirus disease 2019 (COVID-19) are associated with several hematologic abnormalities, including immune thrombocytopenia, antiphospholipid syndrome, and autoimmune ...
Joseph R Liput   +3 more
semanticscholar   +1 more source

Warm Autoimmune Hemolytic Anemia as the Initial Presentation of Systemic Lupus Erythematosus (SLE): A Case Report

open access: yesThe 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 Kander   +4 more
semanticscholar   +1 more source

Intravascular Large B-Cell Lymphoma Presenting as Dementia and Hemolytic Anemia [PDF]

open access: yes, 2010
Background: Intravascular lymphoma (IVL) is an uncommon disease characterized by atypical lymphoid cells growing inside the lumina of small vessels. The diversity of clinical presentation due to possible involvement of multiple organs often complicates ...
Ahle, Guido   +6 more
core   +1 more source

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