Hemophagocytic lymphohistiocytosis (HLH) is a fatal, hyper-inflammatory syndrome that is characterized by untimely activation of macrophages, and manifests as cytopenia, organ dysfunction, and coagulopathy. Secondary HLH can be associated with infection, drugs, malignancy, and transplantation, and is mostly triggered by infection. Herein, we report the case of a patient with Henoch-Schönlein purpura (HSP) who developed severe HLH secondary to Varicella zoster infection.
All Keywords
【저자키워드】 hemophagocytic lymphohistiocytosis, Henoch-Schönlein Purpura, Varicella zoster virus,
【저자키워드】 hemophagocytic lymphohistiocytosis, Henoch-Schönlein Purpura, Varicella zoster virus,