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Hemophagocytic Lymphohistiocytosis
New England Journal of MedicineKonkol S, Killeen RB, Rai M.
europepmc +14 more sources
Hemophagocytic lymphohistiocytosis [PDF]
Baylor University Medical Center Proceedings, 2018 Hemophagocytic lymphohistiocytosis (HLH) is a rare syndrome of widespread inflammation due to massive amounts of cytokines released from activated macrophages. The most common trigger for HLH is infection from a virus, most commonly Epstein-Barr virus. Here we report an adult case of this rare and life-threatening syndrome.
Jasmine, Gowarty +2 more
exaly +10 more sources
Hemophagocytic Lymphohistiocytosis. [PDF]
Archives of Pathology & Laboratory Medicine, 2021 CONTEXT.— Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening disorder of immune regulation that can eventually result in end-organ damage and death.
T. S. Ponnatt, C. Lilley, K. Mirza
semanticscholar +4 more sources
Approaching hemophagocytic lymphohistiocytosis
Frontiers in Immunology, 2023 Hemophagocytic Lymphohistiocytosis (HLH) is a rare clinical condition characterized by sustained but ineffective immune system activation, leading to severe and systemic hyperinflammation.
A. Chinnici +7 more
semanticscholar +5 more sources
Pediatric Hemophagocytic Lymphohistiocytosis (HLH). [PDF]
Blood, 2020 Hemophagocytic lymphohistiocytosis (HLH) is a syndrome describing patients with severe systemic hyperinflammation. Characteristic features include unremitting fever, cytopenias, hepatosplenomegaly, and elevation of typical HLH biomarkers.
S. Canna, R. Marsh
semanticscholar +3 more sources
Secondary hemophagocytic lymphohistiocytosis following blood transfusion in the absence of an identifiable trigger [PDF]
SAGE Open Medical Case ReportsHemophagocytic lymphohistiocytosis is a life-threatening inflammatory syndrome resulting from uncontrolled immune activation. Secondary hemophagocytic lymphohistiocytosis is typically triggered by infection, malignancy, or autoimmune disease, though ...
Ashley M. Tuin +2 more
doaj +2 more sources
Lymphoma-associated hemophagocytic lymphohistiocytosis [PDF]
Hematology, Transfusion and Cell TherapyHemophagocytic lymphohistiocytosis is a severe, rare condition characterized by excessive immune activation, leading to significant morbidity and mortality.
Thomás de Souza Patto Marcondes +2 more
doaj +2 more sources
Fulminant hemophagocytic lymphohistiocytosis induced by pandemic A (H1N1) influenza: a case report [PDF]
Journal of Medical Case Reports, 2011 Introduction Hemophagocytic lymphohistiocytosis induced by viral diseases is a well recognized entity. Severe forms of H5N1 influenza are known to be associated with symptoms very similar to a reactive hemophagocytic syndrome.
Wacrenier Agnès +4 more
doaj +2 more sources
Secondary hemophagocytic lymphohistiocytosis in a patient with severe leptospirosis: a case report [PDF]
Journal of Medical Case ReportsBackground Hemophagocytic lymphohistiocytosis is a rare but life-threatening hyperinflammatory syndrome that can be triggered by infections, malignancies, and autoimmune diseases.
Mariana R. Basurto-Hurtado +3 more
doaj +2 more sources
Hemophagocytic Lymphohistiocytosis
Pediatrics In Review, 2022 Hemophagocytic lymphohistiocytosis (HLH) is an aggressive life-threatening disease that consists of uncontrolled activated lymphocytes and macrophages that secrete excessive cytokines. Symptoms and laboratory findings of HLH include prolonged fever, cytopenia, hepatosplenomegaly, liver dysfunction, hypertriglyceridemia, hyperferritinemia, increased ...
Hannah, Major-Monfried +2 more
openaire +6 more sources