| [1] |
RAMOS-CASALS M, BRITO-ZERÓN P, LÓPEZ-GUILLERMO A, et al. Adult haemophagocytic syndrome[J]. Lancet, 2014, 383(9927): 1503-1516. DOI: 10.1016/S0140-6736(13)61048-X. |
| [2] |
LUO LT, ZHANG X, MA HM, et al. A case of hemophagocytic syndrome with liver failure as the main manifestation[J]. J Clin Hepatol, 2020, 36(2): 412-413. DOI:10.3969/ j.issn. 1001-5256.2020.02.038.
|
| [3] |
JAGTAP N, SHARMA M, RAJESH G, et al. Hemophagocytic lymphohistiocytosis masquerading as acute liver failure: A single center experience[J]. J Clin Exp Hepatol, 2017, 7(3): 184-189. DOI: 10.1016/j.jceh.2017.01.119. |
| [4] |
Chinese Expert Union of Hemophagocytic Syndrome, Hematology Group of Scientific Branch of Chinese Medical Association. Consensus of Chinese experts on the diagnosis and treatment of Hemophilus syndrome[J]. Chin Med J, 2018, 98(2): 91-95. DOI: 10.3760/cma.j.issn.0376-2491.2018.02.004. |
| [5] |
TAKAHASHI N, CHUBACHI A, KUME M, et al. A clinical analysis of 52 adult patients with hemophagocytic syndrome: The prognostic significance of the underlying diseases[J]. Int J Hematol, 2001, 74(2): 209-213. DOI: 10.1007/BF02982007. |
| [6] |
CETICA V, SIENI E, PENDE D, et al. Genetic predisposition to hemophagocytic lymphohistiocytosis: Report on 500 patients from the Italian registry[J]. J Allergy Clin Immunol, 2016, 137(1): 188-196. e4. DOI: 10.1016/j.jaci.2015.06.048. |
| [7] |
CHEN X, WANG F, ZHANG Y, et al. Genetic variant spectrum in 265 Chinese patients with hemophagocytic lymphohistiocytosis: Molecular analyses of PRF1, UNC13D, STX11, STXBP2, SH2D1A, and XIAP[J]. Clin Genet, 2018, 94(2): 200-212. DOI: 10.1111/cge.13363. |
| [8] |
BRISSE E, WOUTERS CH, ANDREI G, et al. How viruses contribute to the pathogenesis of hemophagocytic lymphohistiocytosis[J]. Front Immunol, 2017, 8: 1102. DOI: 10.3389/fimmu.2017.01102. |
| [9] |
KARASU Z, KILIC M, CAGIRGAN S, et al. Hemophagocytic syndrome after living-related liver transplantation[J]. Transplant Proc, 2003, 35(4): 1482-1484. DOI: 10.1016/s0041-1345(03)00511-6. |
| [10] |
SEPULVEDA FE, de SAINT BASILE G. Hemophagocytic syndrome: Primary forms and predisposing conditions[J]. Curr Opin Immunol, 2017, 49: 20-26. DOI: 10.1016/j.coi.2017.08.004. |
| [11] |
MORIMOTO A, NAKAZAWA Y, ISHⅡ E. Hemophagocytic lymphohistiocytosis: Pathogenesis, diagnosis, and management[J]. Pediatr Int, 2016, 58(9): 817-825. DOI:10.1016/ j.jpeds.2013.06.053.
|
| [12] |
AMMANN S, LEHMBERG K, ZUR STADT U, et al. Primary and secondary hemophagocytic lymphohistiocytosis have different patterns of T-cell activation, differentiation and repertoire[J]. Eur J Immunol, 2017, 47(2): 364-373. DOI: 10.1002/eji.201646686. |
| [13] |
HENTER JI, HORNE A, ARICÓ M, et al. HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis[J]. Pediatr Blood Cancer, 2007, 48(2): 124-131. DOI: 10.1002/pbc.21039. |
| [14] |
KOU JT, LIU Z, ZHU JQ, et al. Research on clinical efficacy of liver transplantation for severe liver disease[J]. Organ Transpl, 2020, 11(4): 482-486. DOI: 10.3969/j.issn.1674-7445.2020.04.010. |
| [15] |
FU BS, YI SH, YI HM, et al. Clinical analysis of hemophagocytic syndrome after liver transplantation[J]. J Organ Transplantation, 2013, 4(2): 68-74. DOI:10.3969/ j.issn.1674-7445.2013.02.002.
|
| [16] |
AMIR AZ, LING SC, NAQVI A, et al. Liver transplantation for children with acute liver failure associated with secondary hemophagocytic lymphohistiocytosis[J]. Liver Transplantation, 2016, 22(9): 1245-1253. DOI:10.1016/ S0168-8278(16)00374-3.
|
| [17] |
|
| [18] |
MATTHES-MARTIN S, PETERS C, FRITSCH G, et al. Successful stem cell transplantation following orthotopic liver transplantation from the same haploidentical family donor in a girl with hemophagocytic lymphohistiocytosis[J]. Blood, 2000, 96(12): 3997-3999. DOI:10.1182/ blood.V96.12.3997.
|
DownLoad: