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Hemophagocytic lymphohistiocytosis [PDF]

open access: yesBaylor 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

Secondary hemophagocytic lymphohistiocytosis following blood transfusion in the absence of an identifiable trigger [PDF]

open access: yesSAGE Open Medical Case Reports
Hemophagocytic 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

Fulminant hemophagocytic lymphohistiocytosis induced by pandemic A (H1N1) influenza: a case report [PDF]

open access: yesJournal 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]

open access: yesJournal of Medical Case Reports
Background 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

Lymphoma-associated hemophagocytic lymphohistiocytosis [PDF]

open access: yesHematology, Transfusion and Cell Therapy
Hemophagocytic 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

Hemophagocytic Lymphohistiocytosis [PDF]

open access: yesArchives 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. HLH is characterized by uncontrolled activation of cytotoxic T lymphocytes, natural killer cells, and macrophages that can lead to a cytokine storm ...
Tanya Sajan, Ponnatt   +2 more
openaire   +3 more sources

Hemophagocytic Lymphohistiocytosis

open access: yesPediatrics 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

Neurological symptoms of familial hemophagocytic lymphohistiocytosis type 2 [PDF]

open access: yesJournal of Integrative Neuroscience, 2020
Hemophagocytic lymphohistiocytosis with central nervous system involvement is caused by inflammatory factor storms. The inflammatory factors invade the blood-brain barrier and further infiltrate brain tissue resulting in associated neurological and/or ...
Jingshi Wang, Houzhen Tuo, Lin Wu, Xinkai Wang, Zhao Wang
doaj   +1 more source

Hemophagocytic lymphohistiocytosis during pregnancy: a review of the literature in epidemiology, pathogenesis, diagnosis and treatment

open access: yesOrphanet Journal of Rare Diseases, 2021
Hemophagocytic lymphohistiocytosis during pregnancy is rare; it is often misdiagnosed, resulting in a high maternal and foetal mortality rate. Herein, based on limited case reports including antepartum and postpartum cases, we reviewed the current ...
Lidong Liu   +4 more
doaj   +1 more source

Hemophagocytic Lymphohistiocytosis [PDF]

open access: yesIndian Journal of Hematology and Blood Transfusion, 2012
Hemophagocytic lymphohistiocytosis (HLH) is an immune disorder characterized by uncontrolled inflammation due to defective immune response. It may be familial or acquired, but both share a common feature of threatening the life of a patient and may lead to death unless treated by appropriate treatment. Here in we report a case of adult HLH.
A M V R, Narendra   +5 more
openaire   +2 more sources

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