메뉴 건너뛰기




Volumn 16, Issue , 2015, Pages 110-114

Atypical hemolytic-uremic syndrome: A case report and literature review

Author keywords

ADAM proteins; Hemolytic uremic syndrome; Purpura, thrombotic thrombocytopenic; Thrombotic microangiopathies

Indexed keywords

ANTIHYPERTENSIVE AGENT; COCAINE; CREATININE; ECULIZUMAB; GLYCERYL TRINITRATE; HAPTOGLOBIN; HYDRALAZINE; ISOSORBIDE MONONITRATE; LACTATE DEHYDROGENASE; METHADONE; METRONIDAZOLE; NIFEDIPINE; OPIATE; UREA; VON WILLEBRAND FACTOR CLEAVING PROTEINASE;

EID: 84923825067     PISSN: None     EISSN: 19415923     Source Type: Journal    
DOI: 10.12659/AJCR.892907     Document Type: Article
Times cited : (16)

References (36)
  • 1
    • 84879350647 scopus 로고    scopus 로고
    • Atypical hemolytic uremic syndrome: What is it, how is it diagnosed, and how is it treated?
    • Nester CM, Thomas CP: Atypical hemolytic uremic syndrome: what is it, how is it diagnosed, and how is it treated? Hematology Am Soc Hematol Educ Program, 2012; 2012: 617–25.
    • (2012) Hematology am Soc Hematol Educ Program , vol.2012 , pp. 617-625
    • Nester, C.M.1    Thomas, C.P.2
  • 2
    • 0037158606 scopus 로고    scopus 로고
    • Thrombotic microangiopathies
    • Moake JL: Thrombotic microangiopathies. N Engl J Med, 2002; 347(8): 589–600.
    • (2002) N Engl J Med , vol.347 , Issue.8 , pp. 589-600
    • Moake, J.L.1
  • 3
    • 2542490269 scopus 로고    scopus 로고
    • Effect of plasma exchange on plasma ADAMTS13 metalloprotease activity, inhibitor level, and clinical outcome in patients with idiopathic and nonidiopathic thrombotic thrombocytopenic purpura
    • Zheng XL1, Kaufman RM, Goodnough LT, Sadler JE: Effect of plasma exchange on plasma ADAMTS13 metalloprotease activity, inhibitor level, and clinical outcome in patients with idiopathic and nonidiopathic thrombotic thrombocytopenic purpura. Blood, 2004; 103(11): 4043–9.
    • (2004) Blood , vol.103 , Issue.11 , pp. 4043-4049
    • Xl1, Z.1    Kaufman, R.M.2    Goodnough, L.T.3    Sadler, J.E.4
  • 4
    • 77949903692 scopus 로고    scopus 로고
    • Survival and relapse in patients with thrombotic thrombocytopenic purpura
    • quiz 1662
    • Kremer Hovinga JA, Vesely SK, Terrell DR et al: Survival and relapse in patients with thrombotic thrombocytopenic purpura. Blood, 2010; 115 (8): 1500–11; quiz 1662.
    • (2010) Blood , vol.115 , Issue.8 , pp. 1500-1511
    • Kremer Hovinga, J.A.1    Vesely, S.K.2    Terrell, D.R.3
  • 5
    • 34547633064 scopus 로고    scopus 로고
    • Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome
    • Sellier-Leclerc AL, Fremeaux-Bacchi V, Dragon-Durey MA et al: Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome. J Am Soc Nephrol, 2007; 18(8): 2392–400.
    • (2007) J am Soc Nephrol , vol.18 , Issue.8 , pp. 2392-2400
    • Sellier-Leclerc, A.L.1    Fremeaux-Bacchi, V.2    Dragon-Durey, M.A.3
  • 6
    • 0029823536 scopus 로고    scopus 로고
    • Typical and atypical hemolytic uremic syndrome
    • Proesmans, W: Typical and atypical hemolytic uremic syndrome. Kidney Blood Press Res, 1996; 19(3–4): 205–8.
    • (1996) Kidney Blood Press Res , vol.19 , Issue.34 , pp. 205-208
    • Proesmans, W.1
  • 7
    • 70350279315 scopus 로고    scopus 로고
    • Atypical hemolytic-uremic syndrome
    • Noris M, Remuzzi G: Atypical hemolytic-uremic syndrome. N Engl J Med, 2009; 361(17): 1676–87.
    • (2009) N Engl J Med , vol.361 , Issue.17 , pp. 1676-1687
    • Noris, M.1    Remuzzi, G.2
  • 8
    • 84883557853 scopus 로고    scopus 로고
    • Atypical hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: Clinically differentiating the thrombotic microangiopathies
    • Cataland SR, Wu HM: Atypical hemolytic uremic syndrome and thrombotic thrombocytopenic purpura: clinically differentiating the thrombotic microangiopathies. Eur J Intern Med, 2013; 24(6): 486–91.
    • (2013) Eur J Intern Med , vol.24 , Issue.6 , pp. 486-491
    • Cataland, S.R.1    Wu, H.M.2
  • 9
    • 84896695246 scopus 로고    scopus 로고
    • Diagnostic criteria for atypical hemolytic uremic syndrome proposed by the Joint Committee of the Japanese Society of Nephrology and the Japan Pediatric Society
    • 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. Clin Exp Nephrol, 2014; 18(1): 4–9.
    • (2014) Clin Exp Nephrol , vol.18 , Issue.1 , pp. 4-9
    • Sawai, T.1    Nangaku, M.2    Ashida, A.3
  • 10
    • 0031970553 scopus 로고    scopus 로고
    • Genetic studies into inherited and sporadic hemolytic uremic syndrome
    • Warwicker P, Goodship TH, Donne RL et al: Genetic studies into inherited and sporadic hemolytic uremic syndrome. Kidney Int, 1998; 53(4): 836–44.
    • (1998) Kidney Int , vol.53 , Issue.4 , pp. 836-844
    • Warwicker, P.1    Goodship, T.H.2    Donne, R.L.3
  • 11
    • 0035128326 scopus 로고    scopus 로고
    • Factor H mutations in hemolytic uremic syndrome cluster in exons 18–20, a domain important for host cell recognition
    • Richards A, Buddles MR, Donne RL et al: Factor H mutations in hemolytic uremic syndrome cluster in exons 18–20, a domain important for host cell recognition. Am J Hum Genet, 2001; 68(2): 485–90.
    • (2001) Am J Hum Genet , vol.68 , Issue.2 , pp. 485-490
    • Richards, A.1    Buddles, M.R.2    Donne, R.L.3
  • 12
    • 2342650263 scopus 로고    scopus 로고
    • Mutations in CD46, a complement regulatory protein, predispose to atypical HUS
    • Goodship TH, Liszewski MK, Kemp EJ et al: Mutations in CD46, a complement regulatory protein, predispose to atypical HUS. Trends Mol Med, 2004; 10(5): 226–31.
    • (2004) Trends Mol Med , vol.10 , Issue.5 , pp. 226-231
    • Goodship, T.H.1    Liszewski, M.K.2    Kemp, E.J.3
  • 13
    • 0242331610 scopus 로고    scopus 로고
    • Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome
    • Richards A, Kemp EJ, Liszewski MK et al: Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome. Proc Natl Acad Sci USA, 2003; 100(22): 12966–71.
    • (2003) Proc Natl Acad Sci USA , vol.100 , Issue.22 , pp. 12966-12971
    • Richards, A.1    Kemp, E.J.2    Liszewski, M.K.3
  • 14
    • 27744452766 scopus 로고    scopus 로고
    • Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome
    • Kavanagh D, Kemp EJ, Mayland E et al: Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome. J Am Soc Nephrol, 2005; 16(7): 2150–15.
    • (2005) J am Soc Nephrol , vol.16 , Issue.7 , pp. 2150-2215
    • Kavanagh, D.1    Kemp, E.J.2    Mayland, E.3
  • 15
    • 33747159590 scopus 로고    scopus 로고
    • Genetics of HUS: The impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome
    • 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. Blood, 2006; 108(4): 1267–79.
    • (2006) Blood , vol.108 , Issue.4 , pp. 1267-1279
    • Caprioli, J.1    Noris, M.2    Brioschi, S.3
  • 16
    • 75649133611 scopus 로고    scopus 로고
    • 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
    • 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. Blood, 2010; 115(2): 379–87.
    • (2010) Blood , vol.115 , Issue.2 , pp. 379-387
    • Moore, I.1    Strain, L.2    Pappworth, I.3
  • 17
    • 34047200899 scopus 로고    scopus 로고
    • Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome
    • e41
    • Zipfel PF, Edey M, Heinen S et al: Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome. PLoS Genet, 2007; 3(3): e41.
    • (2007) Plos Genet , vol.3 , Issue.3
    • Zipfel, P.F.1    Edey, M.2    Heinen, S.3
  • 18
    • 33846094404 scopus 로고    scopus 로고
    • Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome
    • Goicoechea de Jorge E, Harris CL, Esparza-Gordillo J et al: Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome. Proc Natl Acad Sci USA, 2007; 104(1): 240–45.
    • (2007) Proc Natl Acad Sci USA , vol.104 , Issue.1 , pp. 240-245
    • De Goicoechea Jorge, E.1    Harris, C.L.2    Esparza-Gordillo, J.3
  • 19
    • 67651166873 scopus 로고    scopus 로고
    • Thrombomodulin mutations in atypical hemolytic-uremic syndrome
    • Delvaeye M, Noris M, De Vriese A et al: Thrombomodulin mutations in atypical hemolytic-uremic syndrome. N Engl J Med, 2009; 361(4): 345–57.
    • (2009) N Engl J Med , vol.361 , Issue.4 , pp. 345-357
    • Delvaeye, M.1    Noris, M.2    De Vriese, A.3
  • 20
    • 84883054621 scopus 로고    scopus 로고
    • Diagnosis of atypical hemolytic uremic syndrome: A review of case studies
    • Laurence J: Diagnosis of atypical hemolytic uremic syndrome: a review of case studies. Clin Adv Hematol Oncol, 2012; 10(10 Suppl.17): 9–11.
    • (2012) Clin Adv Hematol Oncol , vol.10 , Issue.10 , pp. 9-11
    • Laurence, J.1
  • 21
    • 77953008442 scopus 로고    scopus 로고
    • Myocardial infarction is a complication of factor H-associated atypical HUS
    • Sallée M, Daniel L, Piercecchi MD et al: Myocardial infarction is a complication of factor H-associated atypical HUS. Nephrol Dial Transplant, 2010; 25(6): 2028–32.
    • (2010) Nephrol Dial Transplant , vol.25 , Issue.6 , pp. 2028-2032
    • Sallée, M.1    Daniel, L.2    Piercecchi, M.D.3
  • 22
    • 78650517945 scopus 로고    scopus 로고
    • New insights into postrenal transplant hemolytic uremic syndrome
    • Zuber J, Le Quintrec M, Sberro-Soussan R et al: New insights into postrenal transplant hemolytic uremic syndrome. Nat Rev Nephrol, 2011; 7(1): 23–35.
    • (2011) Nat Rev Nephrol , vol.7 , Issue.1 , pp. 23-35
    • Zuber, J.1    Le Quintrec, M.2    Sberro-Soussan, R.3
  • 23
    • 0032956162 scopus 로고    scopus 로고
    • Thrombotic microangiopathy manifesting as thrombotic thrombocytopenic purpura/hemolytic uremic syndrome in the cancer patient
    • Gordon LI, Kwaan HC: Thrombotic microangiopathy manifesting as thrombotic thrombocytopenic purpura/hemolytic uremic syndrome in the cancer patient. Semin Thromb Hemost, 1999; 25(2): 217–21.
    • (1999) Semin Thromb Hemost , vol.25 , Issue.2 , pp. 217-221
    • Gordon, L.I.1    Kwaan, H.C.2
  • 24
    • 0028012915 scopus 로고
    • Haemolytic-uraemic syndrome in practice
    • Neild GH: Haemolytic-uraemic syndrome in practice. Lancet, 1994; 343(8894): 398–401.
    • (1994) Lancet , vol.343 , Issue.8894 , pp. 398-401
    • Neild, G.H.1
  • 25
    • 22544461682 scopus 로고    scopus 로고
    • Hemolytic uremic syndrome
    • Noris, M, Remuzzi G: Hemolytic uremic syndrome. J Am Soc Nephrol, 2005; 16(4): 1035–50.
    • (2005) J am Soc Nephrol , vol.16 , Issue.4 , pp. 1035-1050
    • Noris, M.1    Remuzzi, G.2
  • 26
    • 84867993256 scopus 로고    scopus 로고
    • Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies
    • Zuber J, Fakhouri F, Roumenina LT et al: Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies. Nat Rev Nephrol, 2012; 8(11): 643–57.
    • (2012) Nat Rev Nephrol , vol.8 , Issue.11 , pp. 643-657
    • Zuber, J.1    Fakhouri, F.2    Roumenina, L.T.3
  • 27
    • 84874777659 scopus 로고    scopus 로고
    • Assesment, treatment and prevention of atypical hemolytic uremic syndrome
    • Nickavar A, Sotoudeh K: Assesment, treatment and prevention of atypical hemolytic uremic syndrome. Int J Prev Med, 2013; 4(1): 6–14.
    • (2013) Int J Prev Med , vol.4 , Issue.1 , pp. 6-14
    • Nickavar, A.1    Sotoudeh, K.2
  • 28
    • 79151471122 scopus 로고    scopus 로고
    • AHUS caused by complement dysregulation: New therapies on the horizon
    • Waters AM, Licht C: aHUS caused by complement dysregulation: new therapies on the horizon. Pediatr Nephrol, 2011; 26(1): 41–57.
    • (2011) Pediatr Nephrol , vol.26 , Issue.1 , pp. 41-57
    • Waters, A.M.1    Licht, C.2
  • 29
    • 34247381485 scopus 로고    scopus 로고
    • Complete factor H deficiency-associated atypical hemolytic uremic syndrome in a neonate
    • Cho HY, Lee BS, Moon KC et al: Complete factor H deficiency-associated atypical hemolytic uremic syndrome in a neonate. Pediatr Nephrol, 2007; 22(6): 874–80.
    • (2007) Pediatr Nephrol , vol.22 , Issue.6 , pp. 874-880
    • Cho, H.Y.1    Lee, B.S.2    Moon, K.C.3
  • 30
    • 59449088846 scopus 로고    scopus 로고
    • Eculizumab for congenital atypical hemolytic-uremic syndrome
    • Gruppo RA, Rother RP: Eculizumab for congenital atypical hemolytic-uremic syndrome. N Engl J Med, 2009; 360(5): 544–46.
    • (2009) N Engl J Med , vol.360 , Issue.5 , pp. 544-546
    • Gruppo, R.A.1    Rother, R.P.2
  • 31
    • 70349907791 scopus 로고    scopus 로고
    • Complement inhibitor eculizumab in atypical hemolytic uremic syndrome
    • Mache CJ, Acham-Roschitz B, Frémeaux-Bacchi V et al: Complement inhibitor eculizumab in atypical hemolytic uremic syndrome. Clin J Am Soc Nephrol, 2009; 4(8): 1312–16.
    • (2009) Clin J am Soc Nephrol , vol.4 , Issue.8 , pp. 1312-1316
    • Mache, C.J.1    Acham-Roschitz, B.2    Frémeaux-Bacchi, V.3
  • 32
    • 77956252835 scopus 로고    scopus 로고
    • Thrombotic microangiopathy: Atypical HUS: Current diagnostic and therapeutic approaches
    • Rosales A, Riedl M, Zimmerhackl LB: Thrombotic microangiopathy: atypical HUS: current diagnostic and therapeutic approaches. Nat Rev Nephrol, 2010; 6(9): 504–6.
    • (2010) Nat Rev Nephrol , vol.6 , Issue.9 , pp. 504-506
    • Rosales, A.1    Riedl, M.2    Zimmerhackl, L.B.3
  • 33
    • 81255130615 scopus 로고    scopus 로고
    • Eculizumab safely reverses neurologic impairment and eliminates need for dialysis in severe atypical hemolytic uremic syndrome
    • Ohanian M, Cable C, Halka K: Eculizumab safely reverses neurologic impairment and eliminates need for dialysis in severe atypical hemolytic uremic syndrome. Clin Pharmacol, 2011; 3: 5–12.
    • (2011) Clin Pharmacol , vol.3 , pp. 5-12
    • Ohanian, M.1    Cable, C.2    Halka, K.3
  • 34
    • 78649513705 scopus 로고    scopus 로고
    • Eculizumab therapy in an adult with plasma exchange-refractory atypical hemolytic uremic syndrome
    • Prescott HC, Wu HM, Cataland SR, Baiocchi RA et al: Eculizumab therapy in an adult with plasma exchange-refractory atypical hemolytic uremic syndrome. Am J Hematol, 2010; 85(12): 976–77.
    • (2010) Am J Hematol , vol.85 , Issue.12 , pp. 976-977
    • Prescott, H.C.1    Wu, H.M.2    Cataland, S.R.3    Baiocchi, R.A.4
  • 35
    • 84906522458 scopus 로고    scopus 로고
    • [Eculizumab for the treatment of atypical hemolytic uremic syndrome: Case report and revision of the literature.]
    • [in Portuguese]
    • Vaisbich MH, Henriques Ldos S, Watanabe A et al: [Eculizumab for the treatment of atypical hemolytic uremic syndrome: case report and revision of the literature.] J Bras Nefrol, 2013; 35(3): 237–41 [in Portuguese].
    • (2013) J Bras Nefrol , vol.35 , Issue.3 , pp. 237-241
    • Vaisbich, M.H.1    Henriques Ldos, S.2    Watanabe, A.3
  • 36
    • 84890548424 scopus 로고    scopus 로고
    • Long-term remission of atypical HUS with anti-factor H antibodies after cyclophosphamide pulses
    • Sana G, Dragon-Durey MA, Charbit M et al: Long-term remission of atypical HUS with anti-factor H antibodies after cyclophosphamide pulses. Pediatr Nephrol, 2014; 29(1): 75–83.
    • (2014) Pediatr Nephrol , vol.29 , Issue.1 , pp. 75-83
    • Sana, G.1    Dragon-Durey, M.A.2    Charbit, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.