Chinese Medical Sciences Journal ›› 2014, Vol. 29 ›› Issue (3): 191-193.doi: 10.1016/S1001-9294(14)60068-7
Ming-jun Zhang, Yu-lan Liu*
Ming-jun Zhang, Yu-lan Liu*
摘要: HEMOPHAGOCYTIC lymphohistiocytosis (HLH) is an aggressive and potentially fatal syndrome that results from inappropriate activation of lymphocytes and macrophages. It is characterized by fever, hepatosplenomegaly, cytopenias, hypertriglyceridemia, hypofibrinogenemia, and pathologic findings of hemo- phagocytosis in the bone marrow or other tissues. We report an adult HLH case admitted to hepatology department.