메뉴 건너뛰기




Volumn 37, Issue 8, 2015, Pages e490-e493

Management of acute myeloblastic leukemia in a child with biallelic mismatch repair deficiency

Author keywords

Acute myeloblastic leukemia; bMMRD; Bone marrow transplantation

Indexed keywords

CD33 ANTIGEN; CD34 ANTIGEN; CYCLOSPORIN; CYTARABINE; ETOPOSIDE; FLUDARABINE; IDARUBICIN; MICROSOMAL AMINOPEPTIDASE; MITOXANTRONE; NUCLEOPHOSMIN; PROTEIN MSH6; RITUXIMAB; STEM CELL FACTOR RECEPTOR; ANTINEOPLASTIC AGENT; DNA BINDING PROTEIN; G-T MISMATCH-BINDING PROTEIN; NUCLEAR PROTEIN;

EID: 84945958510     PISSN: 10774114     EISSN: 15363678     Source Type: Journal    
DOI: 10.1097/MPH.0000000000000415     Document Type: Article
Times cited : (9)

References (19)
  • 1
    • 40549106508 scopus 로고    scopus 로고
    • Diagnosis, genetics, and management of inherited bone marrow failure syndromes
    • Alter BP. Diagnosis, genetics, and management of inherited bone marrow failure syndromes. Hematology Am Soc Hematol Educ Program. 2007;29-39.
    • (2007) Hematology Am Soc Hematol Educ Program. , pp. 29-39
    • Alter, B.P.1
  • 2
    • 84885423998 scopus 로고    scopus 로고
    • Subgroupspecific prognostic implications of TP53 mutation in medulloblastoma
    • Zhukova N, Ramaswamy V, Remke M, et al. Subgroupspecific prognostic implications of TP53 mutation in medulloblastoma. J Clin Oncol. 2013;31:2927-2935.
    • (2013) J Clin Oncol. , vol.31 , pp. 2927-2935
    • Zhukova, N.1    Ramaswamy, V.2    Remke, M.3
  • 3
    • 84876900933 scopus 로고    scopus 로고
    • Revised guidelines for the clinical management of Lynch syndrome (HNPCC): Recommendations by a group of European experts
    • Vasen HF, Blanco I, Aktan-Collan K, et al. Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts. Gut. 2013; 62:812-823.
    • (2013) Gut. , vol.62 , pp. 812-823
    • Vasen, H.F.1    Blanco, I.2    Aktan-Collan, K.3
  • 4
    • 33646187811 scopus 로고    scopus 로고
    • The multifaceted mismatch-repair system
    • Jiricny J. The multifaceted mismatch-repair system. Nat Rev Mol Cell Biol. 2006;7:335-346.
    • (2006) Nat Rev Mol Cell Biol. , vol.7 , pp. 335-346
    • Jiricny, J.1
  • 5
    • 0033556009 scopus 로고    scopus 로고
    • Neurofibromatosis and early onset of cancers in hMLH1-deficient children
    • Wang Q, Lasset C, Desseigne F, et al. Neurofibromatosis and early onset of cancers in hMLH1-deficient children. Cancer Res. 1999;59:294-297.
    • (1999) Cancer Res. , vol.59 , pp. 294-297
    • Wang, Q.1    Lasset, C.2    Desseigne, F.3
  • 6
    • 0345222475 scopus 로고    scopus 로고
    • Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type 1
    • Ricciardone MD, Ozcelik T, Cevher B, et al. Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type 1. Cancer Res. 1999;59:290-293.
    • (1999) Cancer Res. , vol.59 , pp. 290-293
    • Ricciardone, M.D.1    Ozcelik, T.2    Cevher, B.3
  • 7
    • 34249723181 scopus 로고    scopus 로고
    • Constitutive deficiency in DNA mismatch repair
    • Felton KE, Gilchrist DM, Andrew SE. Constitutive deficiency in DNA mismatch repair. Clin Genet. 2007;71:483-498.
    • (2007) Clin Genet. , vol.71 , pp. 483-498
    • Felton, K.E.1    Gilchrist, D.M.2    Andrew, S.E.3
  • 8
    • 50649111364 scopus 로고    scopus 로고
    • Constitutional mismatch repair-deficiency syndrome: Have we so far seen only the tip of an iceberg?
    • Wimmer K, Etzler J. Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg? Hum Genet. 2008;124:105-122.
    • (2008) Hum Genet. , vol.124 , pp. 105-122
    • Wimmer, K.1    Etzler, J.2
  • 9
    • 84901470161 scopus 로고    scopus 로고
    • Diagnostic criteria for constitutional mismatch repair deficiency syndrome: Suggestions of the European consortium 'Care for CMMRD' (C4CMMRD)
    • Wimmer K, Kratz CP, Vasen FA, et al. Diagnostic criteria for constitutional mismatch repair deficiency syndrome: suggestions of the European consortium 'Care for CMMRD' (C4CMMRD). J Med Genet. 2014;51:355-365.
    • (2014) J Med Genet. , vol.51 , pp. 355-365
    • Wimmer, K.1    Kratz, C.P.2    Vasen, F.A.3
  • 10
    • 84899494138 scopus 로고    scopus 로고
    • Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium "Care for CMMR-D" (C4CMMR-D)
    • Vasen HFA, Ghorbanoghli Z, Bourdeaut F, et al. Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium "Care for CMMR-D" (C4CMMR-D). J Med Genet. 2014;51: 283-293.
    • (2014) J Med Genet. , vol.51 , pp. 283-293
    • Vasen, H.F.A.1    Ghorbanoghli, Z.2    Bourdeaut, F.3
  • 11
    • 38949127061 scopus 로고    scopus 로고
    • RNA-based mutation analysis identifies an unusual MSH6 splicing defect and circumvents PMS2 pseudo gene interference
    • Etzler J, Peyrl A, Zatkova A, et al. RNA-based mutation analysis identifies an unusual MSH6 splicing defect and circumvents PMS2 pseudo gene interference. Hum Mutat. 2008;29:299-305.
    • (2008) Hum Mutat. , vol.29 , pp. 299-305
    • Etzler, J.1    Peyrl, A.2    Zatkova, A.3
  • 12
    • 33846660119 scopus 로고    scopus 로고
    • Medulloblastoma, acute myelocytic leukemia and colonic carcinomas in a child with biallelic MSH6 mutations
    • Scott RH, Mansour S, Pritchard-Jones K, et al. Medulloblastoma, acute myelocytic leukemia and colonic carcinomas in a child with biallelic MSH6 mutations. Nat Clin Pract Oncol. 2007;l:130-134.
    • (2007) Nat Clin Pract Oncol. , vol.1 , pp. 130-134
    • Scott, R.H.1    Mansour, S.2    Pritchard-Jones, K.3
  • 13
    • 84896717941 scopus 로고    scopus 로고
    • Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: Report from the constitutional mismatch repair deficiency consortium
    • Bakry D, Aronson M, Durno C, et al. Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: report from the constitutional mismatch repair deficiency consortium. Eur J Cancer. 2014;50:987-996.
    • (2014) Eur J Cancer. , vol.50 , pp. 987-996
    • Bakry, D.1    Aronson, M.2    Durno, C.3
  • 14
    • 77952674566 scopus 로고    scopus 로고
    • Pathophysiology and management of inherited bone marrow failure syndromes
    • Shimamura A, Alter BP. Pathophysiology and management of inherited bone marrow failure syndromes. Blood Rev. 2010;24: 101-122.
    • (2010) Blood Rev. , vol.24 , pp. 101-122
    • Shimamura, A.1    Alter, B.P.2
  • 15
    • 42149116279 scopus 로고    scopus 로고
    • Cancer risks in Fanconi anemia: Findings from the German Fanconi Anemia Registry
    • Rosenberg PS, Alter BP. Cancer risks in Fanconi anemia: findings from the German Fanconi Anemia Registry. Haematologica. 2008;93:511-517.
    • (2008) Haematologica. , vol.93 , pp. 511-517
    • Rosenberg, P.S.1    Alter, B.P.2
  • 16
    • 77952484840 scopus 로고    scopus 로고
    • Child with ataxia telangiectasia developing acute myeloid leukemia
    • Lin CH, Lin WC. Child with ataxia telangiectasia developing acute myeloid leukemia. J Clin Oncol. 2010;28:213-214.
    • (2010) J Clin Oncol. , vol.28 , pp. 213-214
    • Lin, C.H.1    Lin, W.C.2
  • 18
    • 0035396754 scopus 로고    scopus 로고
    • Chromosomal aberrations in Bloom syndrome patients with myeloid malignancies
    • Poppe B. Chromosomal aberrations in Bloom syndrome patients with myeloid malignancies. Cancer Genet Cytogenet. 2001;128:39-42.
    • (2001) Cancer Genet Cytogenet. , vol.128 , pp. 39-42
    • Poppe, B.1
  • 19
    • 65349086151 scopus 로고    scopus 로고
    • Mechanisms in the pathogenesis of malignant tumours in neurofibromatosis type 1
    • Brems H. Mechanisms in the pathogenesis of malignant tumours in neurofibromatosis type 1. Lancet Oncol. 2009;10: 508-515.
    • (2009) Lancet Oncol. , vol.10 , pp. 508-515
    • Brems, H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.