期刊文献+

自身炎症性疾病临床诊断 被引量:5

Clinical diagnosis of autoinflammatory disease.
原文传递
导出
摘要 自身炎症性疾病(autoinflammatory diseases or disorders,AIDs)是一组以反复发热、急性关节炎和急性期蛋白增加为特征的复发性非侵袭性炎症性疾病。以往由于认识不足以及缺乏诊断条件,对这类疾病估计不足。随着基因诊断技术的进步、炎症发生发展机制与信号通路研究的日益进展,近年来对自身炎症性疾病的研究有了飞速进展,这也对临床诊断提出了更新的挑战。 Autoinflammatory diseases or disorders(AIDs)area group of recurrent non-invasive inflammatory diseases characterized by fever,acute arthritis and elevated acute-phaseproteins. The disease was underestimated in large part duringthe past few years due to insufficient understanding and lackof means of diagnosis. With the increasing advance of geneticdiagnosis technology and of research on the mechanism of theinflammatory occurrence and the development and the signalpathway,study about the AIDs has made a rapid progress,which also proposed the new challenge to immunological pediatrician for clinical practice.
作者 宋红梅 李冀
出处 《中国实用儿科杂志》 CSCD 北大核心 2015年第1期5-8,共4页 Chinese Journal of Practical Pediatrics
基金 2014年度公益性行业科研专项(201402012)
关键词 自身炎症性疾病 临床诊断 中条-西村综合征 自身炎症性骨病 autoinflammatory diseases/disorders clinical diagnosis Nakajo-Nishimura syndrome autoinflammatory bone disease
  • 相关文献

参考文献18

  • 1McDermott MF, Aksentijevich I, Galon J, et al. Germline muta- tions in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammato-ry syndromes[J]. Cell, 1999,97( 1 ) : 133-144.
  • 2Ozkurede VU, Franchi I: Immunology in clinic review series; fo- cus on autoinflammatory diseases : role of inflammasomes in au- toinflammatory syndromes [J]. Clin Exper Immunol, 2011,167 : 382-390.
  • 3Standing A, Omoyinmi E, Brogan P. Gene hunting in autoinflam- mation [J]. Clin Transl Allergy, 2013,3 ( 1 ) : 32.
  • 4Giat E, Lidar M. Cryopyrin-assoeiated periodic syndrome [J]. Isr Med Assoe J,2014,16(10) :659-661.
  • 5李成荣.自身炎症性疾病[J].中华儿科杂志,2008,46(11):842-847. 被引量:11
  • 6苟丽娟,赵岩,张文.自身炎症性疾病[J].中华临床免疫和变态反应杂志,2010,4(2):131-135. 被引量:4
  • 7Naik HB, Cowen EW. Autoinflammatory pustular neutrophilic diseases [ J ]. Dermatol Clin, 2013,31 (3) : 405-425.
  • 8Fuchs-Telem D, Sarig O, Van-aSteensel M, et al. Familial Pity- riasis Rubra Pilaris is caused by nmtations in CARDI4[J]. Am J Hum Genet,2012,91 : 163-170.
  • 9Marrakehi S, Guigue P, Renshaw BR, et al. Interieukin-36 re- ceptor antagonist deficiency and generalized pustular psoria- sis[J]. N Engl J Med, 2011,365 : 620-628.
  • 10Kanazawa N, Arima K, do H, et al. Nakajo-Nishimura syn- drome[J]. Jpn J Clin hnmunol, 2011,34(5 ) :388-400.

二级参考文献44

  • 1Drenth JP, van der Meer JW. Hereditary periodic fever. N Engl J Med, 2001, 345: 1748-1757.
  • 2Grateau G. Clinical and genetic aspects of the hereditary periodic fever syndromes. Rheumatology, 2004,43:410-415.
  • 3Ting JP, Kastner DL, Hoffman HM. CATERPILLERs, pyrin and hereditary immunological disorders. Nat Rev Immunol, 2006,6 : 183-195.
  • 4Martinon F, Tschopp J. Inflammatory easpases: linking an intracellular innate immune system to autoinflammatory diseases. Cell, 2004,117:561-574.
  • 5Kanazawa N, Furukawa F. Autoinflammatory syndromes with a dermatological perspective. J Dermatol, 2007,34 : 601-618.
  • 6Geha RS, Notarangelo LD, Casanova JL, et al. Primary immunodeficiency diseases : an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee. J Allergy Clin Immunol, 2007, 120: 776-794.
  • 7Miceli-Richard C, Lesage S, Rybojad M,et al. CARD15 mutations in Blau syndrome. Nat Genet,2001, 29 : 19-20.
  • 8Inohara N, Chamaillard M, McDonald C, et al. NOD-LRR proteins: role in host-microbial interactions and inflammatory disease. Annu Rev Biochem ,2005,74:355-383.
  • 9Rose CD, Wouters CH, Meiorin S, et al. Pediatric granulomatous arthritis : an international registry, Arthritis Rheum, 2006, 54 : 3337-3344.
  • 10Kanazawa N, Okafuji I, Kambe N, et al. Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: common genetic etiology with Blau syndrome. Blood, 2005,105:1195-1197.

共引文献11

同被引文献45

  • 1李建国,肖慧捷,杨霁云.补体H因子研究进展[J].国外医学(儿科学分册),2005,32(3):143-146. 被引量:5
  • 2沈公印,陈超.家族性地中海热——附2例报道[J].中国罕少疾病杂志,1999,6(4):26-26. 被引量:6
  • 3李成荣.自身免疫性淋巴细胞增生综合征[J].实用儿科临床杂志,2005,20(11):1060-1061. 被引量:2
  • 4贾园,刘栩,刘传慧,栗占国.系统性红斑狼疮合并干燥综合征患者的临床及实验室特征分析[J].中华风湿病学杂志,2006,10(1):23-26. 被引量:6
  • 5杨京民,陈军.C-反应蛋白对炎症性疾病的诊断价值[J].国际检验医学杂志,2007,28(2):168-168. 被引量:14
  • 6Dias AM, do Couto MC, Duarte CC, et al. White blood cell count abnor- malities and infections in one-year follow-up of 124 patients with SLE [ J]. Ann N Y Acad Sci ,2009,1173 : 103 - 107.
  • 7Gilliam BE, Chauhan AK, Low JM, et al. Measurement of biomarkers in juvenile idiopathic arthritis patients and their significant association with disease severity : a comparative study [ J ]. Clin Exp Rheumatol, 2008,26 (3) :492 -497.
  • 8Tamaki K, Kogata Y, Sugiyama D, et al. Diagnostic accuracy of serum procalcitonin concentrations for detecting systemic bacterial infection in patients with systemic autoimmune diseases [ J ]. J Rheumatol, 2008,35 (1) :114 -119.
  • 9Okada Y, Minakami H, Tomomasa T, et al. Serum procalcitonin concen- tration in patients with Kawasaki disease [ J ]. J Infect, 2004,48 ( 2 ) : 199 - 205.
  • 10Hedrich CM, Brock N, Fiebig B, et al. Anakinra: a safe and effective first-line treatment in systemic onset juvenile idiopathic arthritis (SoJIA) [J]. Rheumatol Int ,2012,32 (11 ) :3525 - 3530.

引证文献5

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部