Abstract
Background: Hemophagocytic lymphohistocytosis (HLH) is a potentially fatal multiple organ inflammatory response syndrome that is characterized by proliferation of histiocytes and inflammatory factor storm. The disease progress varies fast and has a high death rate. Disseminated intravascular coagulation (DIC) is one of the leading causes of death in HLH. Here, we reported a child suffered from secondary HLH with the early symptom of DIC.
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