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

Ming-jun Zhang; Yu-lan Liu

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

中国医学科学杂志（英文版） 2014年29卷第3期页码：191-193

• Case Reports • | Updated：2024-04-10

- A Hemophagocytic Lymphohistiocytosis Patient Initiated with Prominent Liver Dysfunction: a Case Report
- Affiliations：
  
  Department of Gastroenterology, Peking University People's Hospital,Beijing,China,100044
- Author bio：
- Funds：
- DOI：
  中图分类号：
- 网络出版日期：2014-09-29，
  
  纸质出版日期：2014
- Accepted：
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Ming-jun Zhang, Yu-lan Liu. A Hemophagocytic Lymphohistiocytosis Patient Initiated with Prominent Liver Dysfunction: a Case Report[J]. 中国医学科学杂志（英文版）, 2014,29(3):191-193.

Ming-jun Zhang, Yu-lan Liu. A Hemophagocytic Lymphohistiocytosis Patient Initiated with Prominent Liver Dysfunction: a Case Report[J]. Chinese medical sciences journal, 2014, 29(3): 191-193.
Ming-jun Zhang, Yu-lan Liu. A Hemophagocytic Lymphohistiocytosis Patient Initiated with Prominent Liver Dysfunction: a Case Report[J]. 中国医学科学杂志（英文版）, 2014,29(3):191-193. DOI：

Ming-jun Zhang, Yu-lan Liu. A Hemophagocytic Lymphohistiocytosis Patient Initiated with Prominent Liver Dysfunction: a Case Report[J]. Chinese medical sciences journal, 2014, 29(3): 191-193. DOI：

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.

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.

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