Abstract
Hemophagocytic syndrome (HPS), also known as hemophagocytic
lymphohistiocytosis (HLH), is a group of syndromes in which multiple
pathogenic factors lead to the proliferation of activated lymphocytes
and histiocytes that secrete large amounts of inflammatory
cytokines[[1]](#ref-0001).HLH is a multi-organ
hyperinflammatory syndrome caused by the secretion of large amounts of
inflammatory cytokines from