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The many faces of hemophagocytic lymphohistiocytosis — a challenge in diagnosis and therapy

✍ Scribed by Moshous, Despina


Book ID
124119946
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
256 KB
Volume
47
Category
Article
ISSN
0009-9120

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## Abstract Hemophagocytic lymphohistiocytosis (HLH) is a rare and severe inflammatory disorder marked by abnormal cytotoxic T and natural killer cell activity, resulting in impaired clearance of pathogen, excessive cytokine production, and continued immune system activation. Soluble IL‐2 receptor