Results 151 to 160 of about 65,798 (270)
Journal of Blood Medicine, 2019 Autoimmune hemolytic anemia (AIHA) is increasingly observed after allogeneic hematopoietic stem cell transplantation (allo-HSCT), with a reported incidence between 4% and 6%.
W. Barcellini, B. Fattizzo, A. Zaninoni
semanticscholar +1 more source
Clinical Case Reports, Volume 13, Issue 12, December 2025.ABSTRACT Adult‐onset Still's disease (AOSD) is a rare autoinflammatory disorder characterized by fever, rash, joint pain, and elevated ferritin levels. Systemic inflammation can trigger an exaggerated immune response, leading to secondary hemophagocytic lymphohistiocytosis (HLH).
Vasileios Patriarcheas +8 more
wiley +1 more source
False-positive fourth-generation HIV test associated with autoimmune hemolytic anemia. Case report
Case Reports, 2019 Introduction: The fourth-generation ELISA human immunodeficiency virus (HIV) screening test has a high sensitivity and specificity >99% to detect both antigens and antibodies. Estimates are that only 0.5% yield false positive results. Case description:
Santiago Sánchez-Pardo +4 more
doaj +1 more source
New Therapies for the Treatment of Warm Autoimmune Hemolytic Anemia.
Transfusion Medicine Reviews, 2022 B. Fattizzo, W. Barcellini
semanticscholar +1 more source
Clinical Case Reports, Volume 13, Issue 12, December 2025.ABSTRACT Severe autoimmune thrombocytopenia (ATP) in systemic lupus erythematosus (SLE) patients can be life‐threatening when refractory to standard treatments. Low‐dose splenic irradiation (LDSI) can provide temporary platelet recovery before definitive splenectomy.
Ryosuke Hanaoka
wiley +1 more source
Blood Advances, 2018 New-onset autoimmune hemolytic anemia (AIHA) occurs in 2% to 6% of pediatric patients post-hematopoietic stem cell transplantation (HSCT) and is a significant complication.
C. Schuetz +9 more
semanticscholar +1 more source
Health Science Reports, Volume 8, Issue 12, December 2025.ABSTRACT Background and Aims Systemic lupus erythematosus (SLE) is a chronic autoimmune disease, and recent findings reveal that fertility and ovarian reserve are reduced even in moderate illness, showing that SLE has a direct impact on ovarian function.
Shaghayegh Moradi Alamdarloo +6 more
wiley +1 more source
eJHaem, Volume 6, Issue 6, December 2025.ABSTRACT Background Castleman disease (CD) encompasses a range of heterogeneous non‐clonal lymphoproliferative disorders, including unicentric (UCD), and multicentric (MCD) forms. The latter is subdivided into HHV‐8+ MCD, POEMS‐MCD, and idiopathic‐MCD, not otherwise specified (iMCD‐NOS).
Caterina Cristinelli +14 more
wiley +1 more source
Vitamin B12 Deficiency with Pseudothrombotic Microangiopathy and Thrombotic Thrombocytopenic Purpura: Similarities and Differences [PDF]
, 2020 Buess, Charles +3 more
core +2 more sources
Hematologic disorders in systemic lupus erythematosus
Acta Médica del Centro, 2010 A total of 194 cases of patients suffering from systemic lupus erythematosus were reviewed. The hematologic disorders that appeared in the classification criteria were: autoimmune hemolytic anemia (Coombs-positive) in 14 patients (7%), leukopenia in 38 ...
José Francisco Martínez Delgado +2 more
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