Results 11 to 20 of about 3,402 (214)

Complement in hemolytic anemia [PDF]

Hematology, 2015
Complement is increasingly being recognized as an important driver of human disease, including many hemolytic anemias. Paroxysmal nocturnal hemoglobinuria (PNH) cells are susceptible to hemolysis because of a loss of the complement regulatory proteins CD59 and CD55.
openaire   +4 more sources

Immune hemolytic anemia in a patient with tuberculous lymphadenitis

Journal of Global Infectious Diseases, 2011
Anemia in tuberculosis is usually anemia of chronic disease. Severe hemolytic anemia is exceedingly rare in tuberculosis patients. We report a patient diagnosed with tubercular lymphadenitis complicated by Coomb′s positive hemolytic anemia.
Manjunath Nandennavar, Sanju Cyriac, Krishnakumar, T G Sagar   +3 more
doaj   +1 more source

Hemolysis From Intravenous Immunoglobulin in Obese Patients With Kawasaki Disease

Frontiers in Pediatrics, 2020
Objective: We assessed the risk of IVIG-associated hemolytic anemia in patients with acute Kawasaki disease (KD) and evaluated the risk of weight-based dosing in our obese patients.Methods: IVIG-associated hemolytic anemia was assessed in acute KD ...
Khanh-Van Y. Van Anh, Saloni Shah, Adriana H. Tremoulet   +2 more
doaj   +1 more source

A 22-month-old Boy with Acute Glomerulonephritis Coexistent with Hemolytic Anemia and Idiopathic Thrombocytopenia [PDF]

Childhood Kidney Diseases, 2015
Hemolytic anemia and thrombocytopenia are rare clinical manifestations of acute glomerulonephritis. Initially, in all such cases, a diagnosis of hemolytic uremic syndrome, thrombotic thrombocytopenic purpura, systemic lupus erythematosus, and amyloidosis
Hye Won Park, Bo Seon Seo, Su Jin Jung, Jun Ho Lee   +3 more
doaj   +1 more source

Complement inhibitors to treat IgM-mediated autoimmune hemolysis

Haematologica, 2015
Complement activation in autoimmune hemolytic anemia may exacerbate extravascular hemolysis and may occasionally result in intravascular hemolysis. IgM autoantibodies as characteristically found in cold autoantibody autoimmune hemolytic anemia, in cold ...
Diana Wouters, Sacha Zeerleder
doaj   +1 more source

Identification of hemolytic anemia in Korean indigenous cattle with a criteria value of reticulocyte count, indirect bilirubin, and L-lactate concentration

Frontiers in Veterinary Science
Bovine hemolytic anemia has a negative impact on animal welfare and productivity due to its associated clinical symptoms. Hemolysis is generally known to cause reticulocytosis, increased indirect bilirubin, decreased concentration of haptoglobin, and ...
Youngwoo Jung, Ji-Yeong Ku, Youngjun Kim, Youngjun Kim, WooChan Kim, Hyungjae So, Lianfu Piao, Ji-Seon Yoon, Jinho Park   +8 more
doaj   +1 more source

Donath-landsteiner hemolytic anemia with erythrophagocytosis and platelet phagocytosis in peripheral smear: Rare findings

Medical Journal of Dr. D.Y. Patil Vidyapeeth, 2022
The Donath-Landsteiner (DL) hemolytic anemia or paroxysmal cold hemoglobinuria (PCH) is a rare subtype of autoimmune hemolytic anemia (AIHA). We report here a case of a 22-year-old young female who presented with acute onset shortness of breath.
Majed Abdul Basit Momin, Anamika Aluri, P M Bala Bhaskar   +2 more
doaj   +1 more source

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

Journal 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, Abdulmohsen AlSubhi, Ibrahim Bali, Abdullah Alsarrani, Arwa AlHujaili, Ahmad Tarwah   +5 more
doaj   +1 more source

Cold Agglutinin-induced Hemolytic Anemia as the Primary Presentation in Systematic Lupus Erythematosus (SLE) in Pregnancy Triggered by Infection: A Case Report

Case Reports in Clinical Practice, 2022
Autoimmune hemolytic anemia (AIHA) may be the first manifestation of systematic lupus erythematosus (SLE). Antierythrocyte antibodies in SLE are mainly warm-type Immunoglobulin G (IgG), but mixed-type AIHA is also reported.
Vajihe Marsusi, Ashraf Sadat Jamal, Laleh Eslamian, Maasoumeh Saleh, Behnaz Nouri, Danial Dehghan   +5 more
doaj  

Early Impact of Childhood Opportunity on Neurocognitive Outcomes in Sickle Cell Disease

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Introduction Neurocognitive impairment is a well‐recognized complication of sickle cell disease (SCD) that begins early in childhood and persists across development. While cerebrovascular injury contributes substantially to risk, neurocognitive deficits are also observed in children without overt or silent cerebral infarctions, suggesting ...
Julia E. LaMotte, Hannah Koch, Olivia A. Coughlin, Jillian R. Bouck, Allie Carter, Seethal A. Jacob   +5 more
wiley   +1 more source