Hemophagocytic syndrome: a rare but fatal complication after liver transplantation

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摘要Hemophagocytic syndrome (HPS) is recognized as a disorder characterized by a variety of symptoms including fever,jaundice,skin rash,lymphadenopathy,and hepatosplenomegaly related to uncontrolled systemic T-cell activation.1 Two forms of HPS have been characterized:primary/familial hemophagocytic lymphohistiocytosis and secondary/reactive HPS.Reactive HPS was first described in 1979 by Risdall et al.

作者单位 Liver Transplantation Center, Third Affiliated Hospital of Sun Yat-sen University, Transplantation Research Institute of Sun Yat-sen University, Guangzhou, Guangdong 510630, China ^[1]

关键词 bone marrow biopsy hemophagocytic syndrome infection liver transplantation pancytopenia

栏目名称

CLINICAL PRACTICE

DOI 10.3760/cma.j.issn.0366-6999.20130979

发布时间 2013-11-01

基金项目

This study was supported by grants from the Major State Basic Research Development Program (973 Program) of China（2009CB522404）； the National Eleventh Five Year Science and Technology Plan Major Projects of China（2008ZX10002-02）； the Sci-tech Research Development Program of Guangdong Province（2007A032000001）

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