Clinical Features of Hepatic Manifestations among Adult Patients with Hemophagocytic Lymphohistiocytosis: A Retrospective Study

被引:1
作者
Bao, Qiongling [1 ,2 ]
Xu, Zhengqing [3 ]
Yang, Fengling [1 ,2 ]
Lu, Juan [1 ,2 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 1, State Key Lab Diag & Treatment Infect Dis, Hangzhou, Peoples R China
[2] Collaborat Innovat Ctr Diag & Treatment Infect Dis, Hangzhou, Peoples R China
[3] Anji Cty Peoples Hosp, Dept Resp Med, Huzhou, Peoples R China
关键词
Hemophagocytic lymphohistiocytosis; Acute liver failure; CLIF-SOFA; ACUTE LIVER-FAILURE; PROGNOSTIC-FACTORS; EARLY DEATH; SECONDARY; VALIDATION; MORTALITY; CHILDREN; DISEASE; SCORE;
D O I
10.1159/000535535
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Liver dysfunction is common in patients with hemophagocytic lymphohistiocytosis (HLH). However, whether the severity of liver injury is associated with the prognosis of patients with HLH remains to be determined. This study aims to assess the association of the severity of liver involvement with short-term prognosis among adult patients with HLH. Methods: A retrospective study was performed from January 2012 to December 2020, including 150 patients with newly diagnosed HLH and liver injury. Results: The majority of our cohort suffered from mild to moderate hepatic damage, presenting with Child-Turcotte-Pugh (CTP) class A (55, 36.7%) or B (74, 49.3%). The prevalence of acute liver failure (ALF) was 9.3% in our cohort. The overall 30-day mortality rate was 49.3% among the study population. HLH patients with ALF showed an extremely adverse prognosis, with a mortality rate as high as 92.9%. In a multivariate analysis, age >= 60 years (p = 0.016), blood urea nitrogen (BUN) >= 7 mu mol/L (p < 0.001), and malignancy-associated HLH (p < 0.001) at the diagnosis of HLH were identified as being strongly correlated with 30-day prognosis. An excellent predictive power was found. Among the predictive scores used to assess early death of HLH patients with liver injury, the prognostic efficiency of chronic liver failure-sequential organ failure assessment (CLIF-SOFA) (AUROC: 0.936 +/- 0.0211) and SOFA score (0.901 +/- 0.026) were significantly better than those of the APACHE II (p < 0.001), model for end-stage liver disease score (p < 0.001) and CTP scores (p < 0.001). Conclusion: Patients with old age, elevated BUN, and malignancy had inferior survival. CLIF-SOFA and SOFA enable more accurate prediction of early death in HLH patients with liver injury than other liver-specific and general prognostic models.
引用
收藏
页码:525 / 533
页数:9
相关论文
共 24 条
  • [1] Hemophagocytic Lymphohistiocytosis
    Al-Samkari, Hanny
    Berliner, Nancy
    [J]. ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 13, 2018, 13 : 27 - 49
  • [2] Pathophysiology and epidemiology of hemophagocytic lymphohistiocytosis
    Allen, Carl E.
    McClain, Kenneth L.
    [J]. HEMATOLOGY-AMERICAN SOCIETY OF HEMATOLOGY EDUCATION PROGRAM, 2015, : 177 - 182
  • [3] Liver transplantation for children with acute liver failure associated with secondary hemophagocytic lymphohistiocytosis
    Amir, Achiya Z.
    Ling, Simon C.
    Naqvi, Ahmed
    Weitzman, Sheila
    Fecteau, Annie
    Grant, David
    Ghanekar, Anand
    Cattral, Mark
    Nalli, Nadya
    Cutz, Ernest
    Kamath, Binita
    Jones, Nicola
    De Angelis, Maria
    Ng, Vicky
    Avitzur, Yaron
    [J]. LIVER TRANSPLANTATION, 2016, 22 (09) : 1245 - 1253
  • [4] Prognostic factors of early death in a cohort of 162 adult haemophagocytic syndrome: impact of triggering disease and early treatment with etoposide
    Arca, Marc
    Fardet, Laurence
    Galicier, Lionel
    Riviere, Sebastien
    Marzac, Christophe
    Aumont, Cedric
    Lambotte, Olivier
    Coppo, Paul
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2015, 168 (01) : 63 - 68
  • [5] The clinical and laboratory evaluation of familial hemophagocytic lymphohistiocytosis and the importance of hepatic and spinal cord involvement: a single center experience
    Beken, Burcin
    Aytac, Selin
    Balta, Gunay
    Kuskonmaz, Baris
    Uckan, Duygu
    Unal, Sule
    Cetin, Mualla
    Gumruk, Fatma
    [J]. HAEMATOLOGICA, 2018, 103 (02) : 231 - 236
  • [6] Acute liver failure secondary to severe systemic disease from fatal hemophagocytic lymphohistiocytosis: Case report and systematic literature review
    Cappell, Mitchell S.
    Hader, Ismail
    Amin, Mitual
    [J]. WORLD JOURNAL OF HEPATOLOGY, 2018, 10 (09) : 629 - 636
  • [7] Hepatic manifestations of hemophagocytic syndrome:: A study of 30 cases
    de Kerguenec, C
    Hillaire, S
    Molinié, V
    Gardin, C
    Degott, C
    Erlinger, S
    Valla, D
    [J]. AMERICAN JOURNAL OF GASTROENTEROLOGY, 2001, 96 (03) : 852 - 857
  • [8] Clinical characteristics of liver failure with hemophagocytic lymphohistiocytosis
    Dong, Jinling
    Xie, Fang
    Jia, Lin
    Li, Juan
    Hu, Zhongjie
    Zhu, Yueke
    Yu, Hongwei
    Zhao, Yujuan
    Yao, Qinwei
    Meng, Qinghua
    [J]. SCIENTIFIC REPORTS, 2019, 9 (1)
  • [9] Development and Validation of the HScore, a Score for the Diagnosis of Reactive Hemophagocytic Syndrome
    Fardet, Laurence
    Galicier, Lionel
    Lambotte, Olivier
    Marzac, Christophe
    Aumont, Cedric
    Chahwan, Doumit
    Coppo, Paul
    Hejblum, Gilles
    [J]. ARTHRITIS & RHEUMATOLOGY, 2014, 66 (09) : 2613 - 2620
  • [10] Jagtap N, 2017, J CLIN EXP HEPATOL, V7, P184, DOI 10.1016/j.jceh.2017.01.119