Hemophagocytic lymphohistiocytosis (HLH) is a clinical syndrome of life-threatening
inflammation caused by an excessive, prolonged and ineffective immune response. An …

Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disease due to a highly
stimulated but ineffective immune response, with uncontrolled proliferation of activated …

Background Hemophagocytic lymphohistiocytosis (HLH) is an exaggerated inflammatory
reaction secondary to a host's inadequate immune response causing a self-perpetuating …

Background Hemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory syndrome
characterized by excessive activation of macrophages and T cells resulting from defective …

Secondary hemophagocytic lymphohistiocytosis (HLH) is a rare but fatal condition with
various underlying disorders in adult patients and is diagnosed based on the HLH-2004 …

Objectives To detect gene mutation associated with hemophagocytic lymphohistiocytosis
(HLH) and to identify mutation spectrum and clinical feature in HLH in children. Methods …

Hemophagocytic lymphohistiocytosis (HLH) is a progressive and potentially life-threatening
disorder. It is classified into primary and secondary HLH. The objective of our study was to …

Objectives Neonatal hemophagocytic lymphohistiocytosis (HLH) is a rare entity. The
objective of the study was to describe the prevalence, clinical characteristics, interventions …

Hemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory state secondary to
impaired cytotoxicity and resultant cytokine storm, presenting with fever, multi-organ failure …

Hemophagocytic lymphohistiocytosis (HLH) is a potentially fatal hyperinflammatory disorder
characterized by hypercytokinemia caused by excessive activation of cytotoxic T cells and …