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

被引：0
|
作者：
Ming-jun Zhang [1 ]
Yu-lan Liu [1 ]
机构：
[1] Department of Gastroenterology, Peking University People’s Hospital
来源：
ChineseMedicalSciencesJournal | 2014年 / 29卷 / 03期
关键词：
hemophagocytic lymphohistiocytosis; liver dysfunction;
D O I：
暂无
中图分类号：
R575 [肝及胆疾病];
学科分类号：
1002 ; 100201 ;
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 hemophagocytosis in the bone marrow or other tissues.We report an adult HLH case admitted to hepatology department.
引用
收藏
页码：191 / 193
页数：3
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