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Published in 2017 at "American Journal of Hematology"
DOI: 10.1002/ajh.24828
Abstract: To the Editor: Hemophagocytic lymphohistiocytosis (HLH) is a rare disorder that is characterized by overactive natural-killer and cytotoxic T cells that improperly trigger macrophages and subsequently leads to hemophagocytosis in bone marrow, spleen, liver, and…
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Keywords:
osteonecrosis;
secondary hlh;
diagnosis;
prevalence ... See more keywords
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Published in 2020 at "Rheumatology"
DOI: 10.1093/rheumatology/keaa109.017
Abstract: Haemophagocytic lymphohistiocytosis (HLH) is a rare, life threatening syndrome characterised by severe immune activation. The primary form occurs in early childhood and is fatal without treatment. Secondary HLH can occur at any age, usually in…
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Keywords:
secondary hlh;
treatment;
haemophagocytic lymphohistiocytosis;
none ... See more keywords
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Published in 2020 at "Blood"
DOI: 10.1182/blood.2019003664
Abstract: Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening hyperinflammatory condition. Primary HLH occurs early in life as a result of monogenic biallelic mutations affecting lymphocyte cytotoxicity. Secondary HLH occurs mostly in adults secondary to infection, lymphoma, or…
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Keywords:
cell cytotoxicity;
cytotoxicity;
secondary hlh;
lymphocyte cytotoxicity ... See more keywords
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Published in 2021 at "Journal of Clinical Oncology"
DOI: 10.1200/jco.2021.39.15_suppl.e19578
Abstract: e19578 Background: Secondary HLH in adults is associated to infections, malignancies, and autoimmune disorders. HLH in children has been the basis for the management and treatment of HLH in adults. Despite their clinical similarities there…
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Keywords:
lymphohistiocytosis hlh;
hemophagocytic lymphohistiocytosis;
secondary hemophagocytic;
secondary hlh ... See more keywords