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Published in 2017 at "Hematological Oncology"
DOI: 10.1002/hon.2314
Abstract: Adult onset hemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory syndrome, which can develop as a complication of many disorders. Early diagnosis is essential in order to avoid a fatal outcome. To confirm the diagnosis of acquired…
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Keywords:
onset hemophagocytic;
adult onset;
institution series;
hemophagocytic lymphohistiocytosis ... See more keywords
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recommendations!
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Published in 2018 at "Multiple sclerosis and related disorders"
DOI: 10.1016/j.msard.2018.07.031
Abstract: Familial hemophagocytic lymphohistiocytosis (HLH) is a rare autosomal recessive life-threatening multisystem inflammatory disorder. It is characterized by excessive production of cytokines and uncontrolled activation of lymphocytes and macrophages leading to widespread organ infiltration and tissue…
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Keywords:
onset hemophagocytic;
adult onset;
disease;
hemophagocytic lymphohistiocytosis ... See more keywords