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Case Report Open Access
Hemophagocytic lymphohistiocytosis (HLH), also known as hemophagocytic syndrome (HPS), is a rare life threatening hematologic disorder manifested by clinical findings of extreme inflammation and unregulated immune activation. HLH can occur as a familial or sporadic disorder, and it can be triggered by a variety of events that disrupts immune haemostasis. Infection is a common trigger both in those with a genetic predisposition and in sporadic cases. Often the greatest barrier to a successful outcome is delay in diagnosis, which is difficult because of the rarity of this syndrome. Here we, present a case of a young male who presented with enteric fever and confirmed as acute hemophagocytic syndrome and deteriorated rapidly inspite of quick diagnosis and treatment.
Hemophagocytic lymphohistiocytosis, Hemophagocytic syndrome, Enteric (Typhoid) fever, Liver Cancer Case Reports, Bone cancer, Skin Cancer