Hemophagocytic lymphohistiocytosis (HLH) is a severe hyperinflammatory syndrome
induced by aberrantly activated macrophages and cytotoxic T cells. The primary (genetic) …

Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of pathologic immune activation,
often associated with genetic defects of lymphocyte cytotoxicity. Though a distinctive …

Background T cell mediated hyperinflammatory responses such as cytokine release
syndrome (CRS) and immune effector cell associated neurotoxicity syndrome (ICANS) are …

Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening state of immune
hyperactivation that arises in the setting of genetic mutations and infectious, inflammatory, or …

Hemophagocytic lymphohistiocytosis is a life-threatening disorder characterized by
unbridled activation of cytotoxic T lymphocytes, natural killer (NK) cells, and macrophages …

Haemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory syndrome, which if not
promptly treated, can lead rapidly to critical illness and death. HLH is termed macrophage …

Hemophagocytic lymphohistiocytosis (HLH) is a devastating disorder of uncontrolled
immune activation characterized by clinical and laboratory evidence of extreme …

Purpose Hemophagocytic lymphohistiocytosis (HLH) is a severe hyperinflammatory
syndrome emerging from a deregulated immune response due to various triggers. In adults …

Most knowledge of hemophagocytic syndromes (HPSs) including hemophagocytic
lymphohistiocytosis (HLH) is derived from pediatric studies; literature on adult HPS/HLH …

Abstract Background Adult-onset Still's disease (AOSD) is rare inflammatory disease of
unknown etiology that usually affects young adults. The more common clinical …