Secondary hemophagocytic lymphohistiocytosis induced by cholecystitis: A case report and a review of the literature

被引:1
|
作者
Jin, Cheng-Qiang [1 ]
Dong, Hai-Xin [1 ]
Zhou, Jian-Wei [1 ]
Jia, Yan-xia [2 ]
机构
[1] Attached Hosp, Analyt Sect, Jining Med Coll, Jining City, Shandong, Peoples R China
[2] Jining 1 Peoples Hosp, Dept Radiol, Jining, Shandong, Peoples R China
关键词
Hemophagocytic lymphohistiocytosis; Hemophagocytic syndrome; Anemia; Cholecystitis; PATHOGENESIS; DIAGNOSIS;
D O I
10.1016/j.cca.2016.07.007
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening disease resulting from excessive activation and non-malignant proliferation of macrophages and T lymphocytes. Whether it can be caused by cholecystitis has not yet been reported in the world. Case report: A 4-year-old girl was admitted to hospital with cholecystitis. The patient was diagnosed with hemophagocytic lymphohistiocytosis after 3 days of admission based on the results of laboratory tests showing hypofibrinogenemia, hypertriglyceridemia, thrombocytopenia, anemia and leulcopenia. Conclusions: From this case experience, if a timely symptomatic treatment is given, the condition of the patient with secondary HLH can be alleviated. This is the first report of cholecystitis-induced hemophagocytic syndrome in the world also. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:236 / 239
页数:4
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