专家笔谈

成人巨噬细胞活化综合征诊断困境和个体化治疗

  • 贾园 ,
  • 栗占国
展开
  • 北京大学人民医院风湿免疫科,北京 100044

收稿日期: 2020-07-03

  网络出版日期: 2020-12-13

本文引用格式

贾园 , 栗占国 . 成人巨噬细胞活化综合征诊断困境和个体化治疗[J]. 北京大学学报(医学版), 2020 , 52(6) : 991 -994 . DOI: 10.19723/j.issn.1671-167X.2020.06.001

参考文献

[1] Ramos-Casals M, Brito-Zerón P, López-Guillermo A, et al. Adult haemophagocytic Syndrome[J]. Lancet, 2014,383(9927):1503-1516.
[2] 黄文秋, 王旖旎, 王晶石, 等. 192例成人噬血细胞淋巴组织细胞增生症患者的临床分析[J]. 中华血液学杂志, 2014,35(9):796-801.
[3] Atteritano M, David A, Bagnato G, et al. Haemophagocytic syndrome in rheumatic patients. A systematic review[J]. Eur Rev Med Pharmacol Sci, 2012,16(10):1414-1424.
[4] Ahn SS, Yoo BW, Jung SM, et al. In-hospital mortality in febrile lupus patients based on 2016 EULAR/ACR/PRINTO classificationcriteria for macrophage activation syndrome[J]. Semin Arthritis Rheum, 2017,47(2):216-221.
[5] Ravelli A, Minoia F, Davì S, et al. 2016 classification criteria for macrophage activation syndrome complicating systemic juve-nile idiopathic arthritis: A European League Against Rheumatism / American College of Rheumatology / Paediatric Rheumatology International Trials Organisation Collaborative Initiative[J]. Ann Rheum Dis, 2016,75(3):481-489.
[6] Ahn SS, Yoo BW, Jung SM, et al. Application of the 2016 EULAR/ACR/PRINTO classification criteria for macrophage activation syndrome in patients with adult-onset Still disease[J]. J Rheumatol, 2017,44(7):996-1003.
[7] Liu AC, Yang Y, Li MT, et al. Macrophage activation syndrome in systemic lupus erythematosus: A multicenter, case-controlstudy in China[J]. Clin Rheumatol, 2018,37(1):93-100.
[8] Zhang M, Behrens EM, Atkinson TP, et al. Genetic defects in cytolysis in macrophage activation syndrome[J]. Curr Rheumatol Rep, 2014,16(9):439.
[9] Wang Y, Wang Z, Zhang J, et al. Genetic features of late onset primary hemophagocytic lymphohistiocytosis in adolescence or adulthood[J]. PLoS One, 2014,9(9):e107386.
[10] 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.
[11] Davì S, Minoia F, Pistorio A, et al. Performance of current guidelines for diagnosis of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis[J]. Arthritis Rheumatol, 2014,66(10):2871-2880.
[12] Ravelli A, Magni-Manzoni S, Pistorio A, et al. Preliminary diagnostic guidelines for macrophage activation syndrome complicating systemic juve-nile idiopathic arthritis[J]. J Pediatr, 2005,146(5):598-604.
[13] La Rosee P, Horne A, Hines M, et al. Recommendations of the management of hemophagocytic lymphohistiocytosis in adults[J]. Blood, 2019,133(23):2465-2477.
[14] Tada Y, Inokuchi S, Maruyama A, et al. Are the 2016 EULAR/ACR/PRINTO classification criteria for macrophage activation syndrome applicable to patients with adult-onset Still’s disease?[J]. Rheumatol Int, 2019,39(1):97-104.
[15] Minoia F, Bovis F, Davì S, et al. Development and initial validation of the MS score for diagnosis of macrophage activation syndrome in systemic juvenile idiopathic arthritis[J]. Ann Rheum Dis, 2019,78(10):1357-1362.
[16] Wang R, Li T, Ye S, et al. Application of MS score in macrophage activation syndrome patients associated with adult onset Still’s disease [J/OL]. Ann Rheum Dis, (2019-10-14) [2020-06-25]. doi: 10.1136/annrheumdis-2019-216286.
[17] 姚海红, 王旖旎, 张霞, 等. 67例成人巨噬细胞活化综合征的临床特征及治疗转归[J]. 北京大学学报(医学版), 2019,51(6):996-1002.
[18] Grom AA, Horne A, De Benedetti F. Macrophage activation syndrome in the era of biologic therapy[J]. Nat Rev Rheumatol, 2016,12(5):259-268.
[19] Weiss ES, Girard-Guyonvarc’h C, Holzinger D, et al. Interleukin-18 diagnostically distinguishes and pathogenically promotes human and murine macrophage activation syndrome[J]. Blood, 2018,131(13):1442-1455.
文章导航

/