메뉴 건너뛰기




Volumn 93, Issue 2, 1999, Pages 459-466

Myelodysplastic and myeloproliferative disorders of childhood: A study of 167 patients

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CANCER SUSCEPTIBILITY; CHILDHOOD DISEASE; CLINICAL FEATURE; COMORBIDITY; DOWN SYNDROME; FEMALE; HEPATOSPLENOMEGALY; HUMAN; INCIDENCE; INFANT; MAJOR CLINICAL STUDY; MALE; MALIGNANT TRANSFORMATION; MYELODYSPLASTIC SYNDROME; MYELOPROLIFERATIVE DISORDER; ONSET AGE; PRESCHOOL CHILD; PRIORITY JOURNAL;

EID: 0033555976     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v93.2.459.402k19_459_466     Document Type: Article
Times cited : (209)

References (52)
  • 1
    • 0345600172 scopus 로고
    • Classification and clinical manifestations of the hematopoietic stem cell disorders
    • Williams W, Beutler E, Erslev A, Lichtmann M (eds): New York, NY, McGraw-Hill
    • Lichtmann M: Classification and clinical manifestations of the hematopoietic stem cell disorders, in Williams W, Beutler E, Erslev A, Lichtmann M (eds): Hematology. New York, NY, McGraw-Hill, 1990, p 148
    • (1990) Hematology , pp. 148
    • Lichtmann, M.1
  • 6
    • 0026569705 scopus 로고
    • Bone marrow dysfunctions preceding acute leukemia in children: A clinical study
    • Wegelius R: Bone marrow dysfunctions preceding acute leukemia in children: A clinical study. Leuk Res 16:71, 1992
    • (1992) Leuk Res , vol.16 , pp. 71
    • Wegelius, R.1
  • 7
    • 0028069002 scopus 로고
    • The chronic myeloid leukaemias: Guidelines for distinguishing chronic granulocytic, atypical chronic myeloid, and chronic myelomonocytic leukaemia. Proposals by the French-American-British cooperative Leukaemia group
    • Bennett J, Catovsky D, Daniel M, Flandrin G, Galton D, Gralnick H, Sultan C, Cox C: The chronic myeloid leukaemias: Guidelines for distinguishing chronic granulocytic, atypical chronic myeloid, and chronic myelomonocytic leukaemia. Proposals by the French-American-British Cooperative Leukaemia Group. Br J Haematol 87:746, 1994
    • (1994) Br J Haematol , vol.87 , pp. 746
    • Bennett, J.1    Catovsky, D.2    Daniel, M.3    Flandrin, G.4    Galton, D.5    Gralnick, H.6    Sultan, C.7    Cox, C.8
  • 9
    • 0026063878 scopus 로고
    • Selective hypersensitivity to granulocyte-macrophage colony stimulating factor by juvenile chronic myeloid leukemia hematopoietic progenitors
    • Emanuel PD, Bates LJ, Castleberry RP, Gualtieri RJ, Zuckerman KS: Selective hypersensitivity to granulocyte-macrophage colony stimulating factor by juvenile chronic myeloid leukemia hematopoietic progenitors. Blood 77:925, 1991
    • (1991) Blood , vol.77 , pp. 925
    • Emanuel, P.D.1    Bates, L.J.2    Castleberry, R.P.3    Gualtieri, R.J.4    Zuckerman, K.S.5
  • 10
    • 0026756459 scopus 로고
    • Myelodysplastic syndromes in childhood: A population based study of nine cases
    • Hasle H, Jacobsen BB, Pedersen NT: Myelodysplastic syndromes in childhood: A population based study of nine cases. Br J Haematol 81:495, 1992
    • (1992) Br J Haematol , vol.81 , pp. 495
    • Hasle, H.1    Jacobsen, B.B.2    Pedersen, N.T.3
  • 13
    • 0028910402 scopus 로고
    • Childhood monosomy 7: Epidemiology, biology and mechanistic implications
    • Luna-Fineman S, Shannon K, Lange B: Childhood monosomy 7: Epidemiology, biology and mechanistic implications. Blood 85:1985, 1995
    • (1995) Blood , vol.85 , pp. 1985
    • Luna-Fineman, S.1    Shannon, K.2    Lange, B.3
  • 15
    • 0030280090 scopus 로고    scopus 로고
    • Juvenile myelomonocytic leukemia: Molecular understanding and prospects of therapy
    • Emanuel P, Shannon K, Castelberry R: Juvenile myelomonocytic leukemia: molecular understanding and prospects of therapy. Mol Med Today 2:468, 1996
    • (1996) Mol Med Today , vol.2 , pp. 468
    • Emanuel, P.1    Shannon, K.2    Castelberry, R.3
  • 16
    • 0030843626 scopus 로고    scopus 로고
    • Juvenile myelomonocytic leukemia
    • Arico M, Biondi A, Pui C: Juvenile myelomonocytic leukemia. Blood 90:479, 1997
    • (1997) Blood , vol.90 , pp. 479
    • Arico, M.1    Biondi, A.2    Pui, C.3
  • 17
    • 0142099097 scopus 로고    scopus 로고
    • Response: Differentiating juvenile myelomonocytic leukemia from infectious disease
    • Niemeyer C, Fenu S, Hasle H, Mann G, Stary J, van Wering E: Response: Differentiating juvenile myelomonocytic leukemia from infectious disease. Blood 91:365, 1998
    • (1998) Blood , vol.91 , pp. 365
    • Niemeyer, C.1    Fenu, S.2    Hasle, H.3    Mann, G.4    Stary, J.5    Van Wering, E.6
  • 18
    • 0021162175 scopus 로고
    • Bone marrow histology in myelodysplastic syndromes. II prognostic value of abnormal localization of immature precursors in MDS
    • Tricot G, De Wolf-Peeters C, Vlietinck P, Werwilghen R: Bone marrow histology in myelodysplastic syndromes. II Prognostic value of abnormal localization of immature precursors in MDS. Br J Haematol 58:217, 1984
    • (1984) Br J Haematol , vol.58 , pp. 217
    • Tricot, G.1    De Wolf-Peeters, C.2    Vlietinck, P.3    Werwilghen, R.4
  • 19
    • 33845382806 scopus 로고
    • Nonparametric estimation from incomplete observations
    • Kaplan E, Meier P: Nonparametric estimation from incomplete observations. J Am Stat Assoc 53:457, 1958
    • (1958) J Am Stat Assoc , vol.53 , pp. 457
    • Kaplan, E.1    Meier, P.2
  • 24
    • 0027979146 scopus 로고
    • Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders
    • Shannon KM, O'Connell P, Martin GA, Paderanga D, Olson K, Dinndorf P, McCormick F: Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders. N Engl J Med 330:597, 1994
    • (1994) N Engl J Med , vol.330 , pp. 597
    • Shannon, K.M.1    O'Connell, P.2    Martin, G.A.3    Paderanga, D.4    Olson, K.5    Dinndorf, P.6    McCormick, F.7
  • 25
    • 0028224348 scopus 로고
    • Fusion of PDGF receptor β to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation
    • Golub TR, Barker GF, Lovett M, Gilliland DG: Fusion of PDGF receptor β to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation. Cell 77:307, 1994
    • (1994) Cell , vol.77 , pp. 307
    • Golub, T.R.1    Barker, G.F.2    Lovett, M.3    Gilliland, D.G.4
  • 30
    • 0030947237 scopus 로고    scopus 로고
    • Homozygous inactivation of the NF1 gene in bone marrow cells from children with neurofibromatosis type 1 and malignant myeloid disorders
    • Side L, Taylor B, Cayouett M, Conner E, Thompson P, Luce M, Shannon K: Homozygous inactivation of the NF1 gene in bone marrow cells from children with neurofibromatosis type 1 and malignant myeloid disorders. N Engl J Med 336:1713, 1997
    • (1997) N Engl J Med , vol.336 , pp. 1713
    • Side, L.1    Taylor, B.2    Cayouett, M.3    Conner, E.4    Thompson, P.5    Luce, M.6    Shannon, K.7
  • 32
    • 0032125716 scopus 로고    scopus 로고
    • Mutations of the NF1 gene in children with juvenile myelomonocytic leukemia without clinical evidence of neurofibromatosis, type 1
    • Side L, Emanuel P, Taylor B, Franklin J, Thompson P, Castleberry R, Shannon K: Mutations of the NF1 gene in children with juvenile myelomonocytic leukemia without clinical evidence of neurofibromatosis, type 1. Blood 92:267, 1998
    • (1998) Blood , vol.92 , pp. 267
    • Side, L.1    Emanuel, P.2    Taylor, B.3    Franklin, J.4    Thompson, P.5    Castleberry, R.6    Shannon, K.7
  • 33
    • 16744366910 scopus 로고    scopus 로고
    • Distinctive demography, biology, and outcome of acute myeloid leukemia and myelodysplastic syndrome in children with Down syndrome: Children's cancer group studies 2861 and 2891
    • Lange B, Kobrinsky N, Barnard D, Arthur D, Buckley J, Howells W, Gold S, Sanders J, Neudorf S, Smith F, Woods W: Distinctive demography, biology, and outcome of acute myeloid leukemia and myelodysplastic syndrome in children with Down syndrome: Children's Cancer Group Studies 2861 and 2891. Blood 91:608, 1998
    • (1998) Blood , vol.91 , pp. 608
    • Lange, B.1    Kobrinsky, N.2    Barnard, D.3    Arthur, D.4    Buckley, J.5    Howells, W.6    Gold, S.7    Sanders, J.8    Neudorf, S.9    Smith, F.10    Woods, W.11
  • 34
    • 0025959243 scopus 로고
    • Leukemia and preleukemia in Fanconi anemia patients. A review of the literature and report of the international fanconi anemia registry
    • Auerbach A, Allen R: Leukemia and preleukemia in Fanconi anemia patients. A review of the literature and report of the International Fanconi Anemia Registry. Cancer Genet Cytogenet 51:1, 1991
    • (1991) Cancer Genet Cytogenet , vol.51 , pp. 1
    • Auerbach, A.1    Allen, R.2
  • 36
    • 0028206608 scopus 로고
    • Granulocyte colony-stimulating factor (G-CSF) production and G-CSF receptor structure in patients with congenital neutropenia
    • Guba S, Sartor C, Hutchinson R, Boxer L, Emerson S: Granulocyte colony-stimulating factor (G-CSF) production and G-CSF receptor structure in patients with congenital neutropenia. Blood 83:1486, 1994
    • (1994) Blood , vol.83 , pp. 1486
    • Guba, S.1    Sartor, C.2    Hutchinson, R.3    Boxer, L.4    Emerson, S.5
  • 38
    • 0027372507 scopus 로고
    • Cytogenetic analysis has strong independent prognostic value in de novo myelodysplastic syndromes and can be incorporated in a new scoring system: A report on 408 cases
    • Morel P, Hebbar M, Lai JL, Duhamel A, Preudomme C, Wattel E, Bauters F, Fenaux P: Cytogenetic analysis has strong independent prognostic value in de novo myelodysplastic syndromes and can be incorporated in a new scoring system: A report on 408 cases. Leukemia 7:1315, 1993
    • (1993) Leukemia , vol.7 , pp. 1315
    • Morel, P.1    Hebbar, M.2    Lai, J.L.3    Duhamel, A.4    Preudomme, C.5    Wattel, E.6    Bauters, F.7    Fenaux, P.8
  • 40
    • 0022368551 scopus 로고
    • Childhood bone marrow monosomy 7 syndrome: A familial disorder?
    • Carroll WL, Morgan R, Glader BE: Childhood bone marrow monosomy 7 syndrome: A familial disorder? J Pediatr 107:578, 1985
    • (1985) J Pediatr , vol.107 , pp. 578
    • Carroll, W.L.1    Morgan, R.2    Glader, B.E.3
  • 41
    • 0026655447 scopus 로고
    • Evidence implicating heterozygous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monosomy 7
    • Shannon KM, Turhan AG, Rogers PC, Kan YW: Evidence implicating heterozygous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monosomy 7. Genomics 14:121, 1992
    • (1992) Genomics , vol.14 , pp. 121
    • Shannon, K.M.1    Turhan, A.G.2    Rogers, P.C.3    Kan, Y.W.4
  • 42
    • 0026591778 scopus 로고
    • Recombinant human granulocyte-colony stimulating factor in the treatment of patients with chronic benign granulocytopenia and congenital agranulocytosis (Kostmann's syndrome)
    • Imashuku S, Tsuchida M, Sasaki M, Shimokawa T, Nakamura H, Matsuyama T, Taniguchi N, Oda M, Higuchi S, Ishimoto K: Recombinant human granulocyte-colony stimulating factor in the treatment of patients with chronic benign granulocytopenia and congenital agranulocytosis (Kostmann's syndrome). Acta Paediatr 81:133, 1992
    • (1992) Acta Paediatr , vol.81 , pp. 133
    • Imashuku, S.1    Tsuchida, M.2    Sasaki, M.3    Shimokawa, T.4    Nakamura, H.5    Matsuyama, T.6    Taniguchi, N.7    Oda, M.8    Higuchi, S.9    Ishimoto, K.10
  • 44
    • 0023551999 scopus 로고
    • Molecular characterization of chromosome 7 long arm deletions in myeloid disorders
    • Kere J, Ruutu T, Lahtinen R, de la Chapelle A: Molecular characterization of chromosome 7 long arm deletions in myeloid disorders. Blood 70:1349, 1987
    • (1987) Blood , vol.70 , pp. 1349
    • Kere, J.1    Ruutu, T.2    Lahtinen, R.3    De La Chapelle, A.4
  • 45
    • 0024495676 scopus 로고
    • Chromosome 7 long arm deletion in myeloid disorders: A narrow breakpoint region in 7q22 defined by molecular mapping
    • Kere J, Ruutu T, Davies KA, Roninson IB, Watkins PC, Winqvist R, de la Chapelle A: Chromosome 7 long arm deletion in myeloid disorders: A narrow breakpoint region in 7q22 defined by molecular mapping. Blood 73:230, 1989
    • (1989) Blood , vol.73 , pp. 230
    • Kere, J.1    Ruutu, T.2    Davies, K.A.3    Roninson, I.B.4    Watkins, P.C.5    Winqvist, R.6    De La Chapelle, A.7
  • 46
    • 0029821113 scopus 로고    scopus 로고
    • Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted in malignant myeloid diseases
    • LeBeau M, Espinosa R, Davis E, Eisenbart J, Larson R, Green E: Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted in malignant myeloid diseases. Blood 88:1930, 1996
    • (1996) Blood , vol.88 , pp. 1930
    • LeBeau, M.1    Espinosa, R.2    Davis, E.3    Eisenbart, J.4    Larson, R.5    Green, E.6
  • 47
    • 0029743347 scopus 로고    scopus 로고
    • Intensive chemotherapy in childhood myelodysplastic syndrome. A comparison with results in acute myeloid leukemia
    • Hasle H, Kerndrup G, Yssing M, Clausen N, Ostergaard E, Jacobsen N, Brock Jacobsen B: Intensive chemotherapy in childhood myelodysplastic syndrome. A comparison with results in acute myeloid leukemia. Leukemia 10:1269, 1996
    • (1996) Leukemia , vol.10 , pp. 1269
    • Hasle, H.1    Kerndrup, G.2    Yssing, M.3    Clausen, N.4    Ostergaard, E.5    Jacobsen, N.6    Brock Jacobsen, B.7
  • 48
    • 0030765385 scopus 로고    scopus 로고
    • Effect of diagnosis (refractory anemia with excess blasts, refractory anemia with excess blasts in transformation, or acute myeloid leukemia [AML]) on outcome of AML-type chemotherapy
    • Estey E, Thall P, Beran M, Kantarjian H, Pierce S, Keating M: Effect of diagnosis (refractory anemia with excess blasts, refractory anemia with excess blasts in transformation, or acute myeloid leukemia [AML]) on outcome of AML-type chemotherapy. Blood 90:2969, 1997
    • (1997) Blood , vol.90 , pp. 2969
    • Estey, E.1    Thall, P.2    Beran, M.3    Kantarjian, H.4    Pierce, S.5    Keating, M.6
  • 51
    • 18844465770 scopus 로고    scopus 로고
    • Allogeneic bone marrow transplantation for chronic myelomonocytic leukemia in childhood: A report from the European working group on Myelodysplastic syndrome in childhood
    • Locatelli F, Niemeyer C, Angelucci E, Bender-Gotze C, Burdach S, Ebell W, Friedrich W, Hasle H, Herman J, Jacobsen N: Allogeneic bone marrow transplantation for chronic myelomonocytic leukemia in childhood: A report from the European Working Group on Myelodysplastic Syndrome in Childhood. J Clin Oncol 15:566, 1997
    • (1997) J Clin Oncol , vol.15 , pp. 566
    • Locatelli, F.1    Niemeyer, C.2    Angelucci, E.3    Bender-Gotze, C.4    Burdach, S.5    Ebell, W.6    Friedrich, W.7    Hasle, H.8    Herman, J.9    Jacobsen, N.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.