Chinese Medical Sciences Journal ›› 2014, Vol. 29 ›› Issue (3): 191-193.doi: 10.1016/S1001-9294(14)60068-7

• Case Reports • 上一篇    下一篇

A Hemophagocytic Lymphohistiocytosis Patient Initiated with Prominent Liver Dysfunction: a Case Report

Ming-jun Zhang, Yu-lan Liu*   

  1. Department of Gastroenterology, Peking University People's Hospital, Beijing 100044, China
  • 出版日期:2014-09-29 发布日期:2014-09-29
  • 通讯作者: *Corresponding author Tel: 86-10-88325559, E-mail: liuyulan@ E-mail:liuyulan@pkuph.edu.cn

A Hemophagocytic Lymphohistiocytosis Patient Initiated with Prominent Liver Dysfunction: a Case Report

Ming-jun Zhang, Yu-lan Liu*   

  1. Department of Gastroenterology, Peking University People's Hospital, Beijing 100044, China
  • Published:2014-09-29 Online:2014-09-29
  • Contact: *Corresponding author Tel: 86-10-88325559, E-mail: liuyulan@pkuph.edu.cn E-mail:liuyulan@pkuph.edu.cn

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.

关键词: hemophagocytic lymphohistiocytosis, liver dysfunction

Abstract: 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.

Key words: hemophagocytic lymphohistiocytosis, liver dysfunction

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