切换至 "中华医学电子期刊资源库"

中华肾病研究电子杂志 ›› 2019, Vol. 08 ›› Issue (03) : 142 -144. doi: 10.3877/cma.j.issn.2095-3216.2019.03.009

所属专题: 经典病例 经典病例 文献

病例报告

非典型溶血尿毒综合征一例报告并文献复习
涂天琪1, 涂晓文2,(), 王欢2, 李娟2, 许倬2   
  1. 1. 100088 北京,解放军火箭军特色医学中心肾脏内科;100029 北京大学医学部中日友好临床医学院
    2. 100088 北京,解放军火箭军特色医学中心肾脏内科
  • 收稿日期:2019-01-16 出版日期:2019-06-28
  • 通信作者: 涂晓文

A case report of atypical hemolytic uremic syndrome with literature review

Tianqi Tu1, Xiaowen Tu2(), Huan Wang2   

  • Received:2019-01-16 Published:2019-06-28
  • Corresponding author: Xiaowen Tu
引用本文:

涂天琪, 涂晓文, 王欢, 李娟, 许倬. 非典型溶血尿毒综合征一例报告并文献复习[J]. 中华肾病研究电子杂志, 2019, 08(03): 142-144.

Tianqi Tu, Xiaowen Tu, Huan Wang. A case report of atypical hemolytic uremic syndrome with literature review[J]. Chinese Journal of Kidney Disease Investigation(Electronic Edition), 2019, 08(03): 142-144.

[1]
George JN, Nester CM. Syndromes of thrombotic microangiopathy [J]. N Engl J Med, 2014, 371(19): 1847-1848.
[2]
彭娜,佟芳. 非典型溶血尿毒综合征的研究进[J]. 临床肾脏病杂志,2018,18(6): 381-383.
[3]
Yoshida Y, Kato H, Ikeda Y, et al. Pathogenesis of atypical hemolytic uremic syndrome [J]. J Atheroscler Thromb, 2019, 26(2): 99-110.
[4]
Noris M, Remuzzi G. Atypical hemolytic uremic syndrome [J]. N Engl J Med, 2009, 361(17): 1676-1687.
[5]
Cataland SR, Wu HM. Atypical hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: clinically differentiating the thrombotic microangiopathies [J]. Eur J Intern Med, 2013, 24(6): 486-491.
[6]
Sawai T, Nangaku M, Ashida A, et al. Diagnostic criteria for atypical hemolytic uremic syndrome proposed by the Joint Committee of the Japanese Society of Nephrology and the Japan Pediatric Society [J]. Clin Exp Nephrol, 2014, 18(1): 4-9.
[7]
Bhuyan UN. Thrombotic microangiopathy with hypertension and acute renal failure in children (a typical hemolytic uremic syndrome) [J]. J Postgrad Med, 1994, 40(3): 120-122.
[8]
Kavanagh D, Kemp EJ, Mayland E, et al. Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome [J]. J Am Soc Nephrol, 2005, 16(7): 2150-2155.
[9]
Caprioli J, Noris M, Brioschi S, et al. Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome [J]. Blood, 2006, 108(4): 1267-1279.
[10]
Moore I, Strain L, Pappworth I, et al. Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome [J]. Blood, 2010, 115(2): 379-387.
[11]
de Jorge EG, Harris CL, Esparza-Gordillo J, et al. Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome [J]. Proc Natl Acad Sci USA, 2007, 104(1): 240-245.
[12]
Kato H, Nangaku M, Hataya H, et al. Clinical guides for atypical hemolytic uremic syndrome in Japan[J]. Clin Exp Nephrol, 2016, 20(4): 536-543.
[13]
Nickavar A, Sotoudeh K. Assesment, treatment and prevention of atypical hemolytic uremic syndrome [J]. Int J Prev Med, 2013, 4(1): 6-14.
[14]
Licht C, Greenbaum LA, Muus P, et al. Efficacy and safety of eculizumab in atypical hemolytic uremic syndrome from 2-year extensions of phase 2 studies [J]. Kidney Int, 2015, 87(5): 1061-1073.
[15]
Cao M, Leite BN, Ferreiro T, et al. Eculizumab modifies outcomes in adults with atypical hemolytic uremic syndrome with acute kidney injury [J]. Am J Nephrol, 2018, 48(3): 225-233.
No related articles found!
阅读次数
全文


摘要