메뉴 건너뛰기




Volumn 33, Issue 9, 2009, Pages

Acute lymphoblastic leukemia following severe congenital neutropenia or de novo ALL?

Author keywords

Cancer; Childhood leukemia; Congenital neutropenia; Leukemogenesis; MLL rearrangement

Indexed keywords

CELL PROTEIN; GENOMIC DNA; GRANULOCYTE COLONY STIMULATING FACTOR; LEUKOCYTE ELASTASE; LEUKOCYTE ELASTASE 2; MIXED LINEAGE LEUKEMIA PROTEIN; PROTEIN CSF3R; PROTEIN G6PC3; PROTEIN HAX 1; UNCLASSIFIED DRUG;

EID: 67549094663     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.leukres.2009.03.039     Document Type: Letter
Times cited : (2)

References (25)
  • 1
    • 0022414091 scopus 로고
    • Acute lymphoblastic leukemia in infants less than one year of age: a cumulative experience of the Children's Cancer Study Group
    • Reaman G., Zeltzer P., Bleyer W.A., Amendola B., Level C., Sather H., et al. Acute lymphoblastic leukemia in infants less than one year of age: a cumulative experience of the Children's Cancer Study Group. J Clin Oncol 3 (1985) 1513-1521
    • (1985) J Clin Oncol , vol.3 , pp. 1513-1521
    • Reaman, G.1    Zeltzer, P.2    Bleyer, W.A.3    Amendola, B.4    Level, C.5    Sather, H.6
  • 2
    • 0028946875 scopus 로고
    • Incidence of cancer in children in the United States. Sex-, race-, and 1-year age-specific rates by histologic type
    • Gurney J.G., Severson R.K., Davis S., and Robison L.L. Incidence of cancer in children in the United States. Sex-, race-, and 1-year age-specific rates by histologic type. Cancer 75 (1995) 2186-2195
    • (1995) Cancer , vol.75 , pp. 2186-2195
    • Gurney, J.G.1    Severson, R.K.2    Davis, S.3    Robison, L.L.4
  • 3
    • 85069403880 scopus 로고    scopus 로고
    • Acute leukemia in infants
    • Nathan D.G., et al. (Ed), Saunders, Philadelphia
    • Reaman G.H. Acute leukemia in infants. In: Nathan D.G., et al. (Ed). Nathan and Oski's hematology of infancy and childhood (2003), Saunders, Philadelphia 1210-1218
    • (2003) Nathan and Oski's hematology of infancy and childhood , pp. 1210-1218
    • Reaman, G.H.1
  • 4
    • 0032717039 scopus 로고    scopus 로고
    • The role of chromosome translocations in leukemogenesis
    • Rowley J.D. The role of chromosome translocations in leukemogenesis. Semin Hematol 36 (1999) 59-72
    • (1999) Semin Hematol , vol.36 , pp. 59-72
    • Rowley, J.D.1
  • 5
    • 77049235105 scopus 로고
    • Infantile genetic agranulocytosis; agranulocytosis infantilis hereditaria
    • Kostmann R. Infantile genetic agranulocytosis; agranulocytosis infantilis hereditaria. Acta Paediatr 45 Suppl. (1956) 1-78
    • (1956) Acta Paediatr , vol.45 , Issue.SUPPL , pp. 1-78
    • Kostmann, R.1
  • 6
    • 42049117271 scopus 로고    scopus 로고
    • Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations
    • Germeshausen M., Grudzien M., Zeidler C., Abdollahpour H., Yetgin S., Rezaei N., et al. Novel HAX1 mutations in patients with severe congenital neutropenia reveal isoform-dependent genotype-phenotype associations. Blood 111 (2008) 4954-4957
    • (2008) Blood , vol.111 , pp. 4954-4957
    • Germeshausen, M.1    Grudzien, M.2    Zeidler, C.3    Abdollahpour, H.4    Yetgin, S.5    Rezaei, N.6
  • 7
    • 51649109108 scopus 로고    scopus 로고
    • Transformation of severe congenital neutropenia to early acute lymphoblastic leukemia in a patient with HAX1 mutation and without G-CSF administration or receptor mutation
    • Yetgin S., Olcay L., Koç A., and Germeshausen M. Transformation of severe congenital neutropenia to early acute lymphoblastic leukemia in a patient with HAX1 mutation and without G-CSF administration or receptor mutation. Leukemia 22 (2008) 1797
    • (2008) Leukemia , vol.22 , pp. 1797
    • Yetgin, S.1    Olcay, L.2    Koç, A.3    Germeshausen, M.4
  • 10
    • 0035525791 scopus 로고    scopus 로고
    • Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease
    • Ancliff P.J., Gale R.E., Liesner R., Hann I.M., and Linch D.C. Mutations in the ELA2 gene encoding neutrophil elastase are present in most patients with sporadic severe congenital neutropenia but only in some patients with the familial form of the disease. Blood 98 (2001) 2645-2650
    • (2001) Blood , vol.98 , pp. 2645-2650
    • Ancliff, P.J.1    Gale, R.E.2    Liesner, R.3    Hann, I.M.4    Linch, D.C.5
  • 11
    • 33845972945 scopus 로고    scopus 로고
    • Incidence of CSF3R mutations in severe congenital neutropenia and relevance for leukemogenesis: results of a long-term survey
    • Germeshausen M., Ballmaier M., and Welte K. Incidence of CSF3R mutations in severe congenital neutropenia and relevance for leukemogenesis: results of a long-term survey. Blood 109 (2007) 93-99
    • (2007) Blood , vol.109 , pp. 93-99
    • Germeshausen, M.1    Ballmaier, M.2    Welte, K.3
  • 12
    • 4444272669 scopus 로고    scopus 로고
    • Screening for G-CSF receptor mutations in patients with secondary myeloid or lymphoid transformation of severe congenital neutropenia. A report from the French Neutropenia Register
    • Cassinat B., Bellanné-Chantelot C., Notz-Carrère A., Menot M.L., Vaury C., Micheau M., et al. Screening for G-CSF receptor mutations in patients with secondary myeloid or lymphoid transformation of severe congenital neutropenia. A report from the French Neutropenia Register. Leukemia 18 (2004) 1553-1555
    • (2004) Leukemia , vol.18 , pp. 1553-1555
    • Cassinat, B.1    Bellanné-Chantelot, C.2    Notz-Carrère, A.3    Menot, M.L.4    Vaury, C.5    Micheau, M.6
  • 13
    • 0035254525 scopus 로고    scopus 로고
    • Granulocyte colony-stimulating factor receptor mutations in a patient with acute lymphoblastic leukemia secondary to severe congenital neutropenia
    • Germeshausen M., Ballmaier M., Schulze H., Welte K., Flohr T., Beiske K., et al. Granulocyte colony-stimulating factor receptor mutations in a patient with acute lymphoblastic leukemia secondary to severe congenital neutropenia. Blood 97 (2001) 829-831
    • (2001) Blood , vol.97 , pp. 829-831
    • Germeshausen, M.1    Ballmaier, M.2    Schulze, H.3    Welte, K.4    Flohr, T.5    Beiske, K.6
  • 14
    • 26944451745 scopus 로고    scopus 로고
    • Acute lymphoblastic leukemia in a patient with congenital neutropenia without G-CSF-R and ELA2 mutations
    • Yetgin S., Germeshausen M., Touw I., Koç A., and Olcay L. Acute lymphoblastic leukemia in a patient with congenital neutropenia without G-CSF-R and ELA2 mutations. Leukemia 19 (2005) 1710-1711
    • (2005) Leukemia , vol.19 , pp. 1710-1711
    • Yetgin, S.1    Germeshausen, M.2    Touw, I.3    Koç, A.4    Olcay, L.5
  • 16
    • 14744268243 scopus 로고    scopus 로고
    • Identification of various MLL gene aberrations that lead to MLL gene mutation in patients with acute lymphoblastic leukemia (ALL) and infants with acute leukemia
    • Pais A., Amare Kadam P., Raje G., Sawant M., Kabre S., Jain H., et al. Identification of various MLL gene aberrations that lead to MLL gene mutation in patients with acute lymphoblastic leukemia (ALL) and infants with acute leukemia. Leuk Res 29 (2005) 517-526
    • (2005) Leuk Res , vol.29 , pp. 517-526
    • Pais, A.1    Amare Kadam, P.2    Raje, G.3    Sawant, M.4    Kabre, S.5    Jain, H.6
  • 17
    • 34249663344 scopus 로고    scopus 로고
    • Genomic DNA of leukemic patients: target for clinical diagnosis of MLL rearrangements
    • Meyer C., Kowarz E., Schneider B., Oehm C., Klingebiel T., Dingermann T., et al. Genomic DNA of leukemic patients: target for clinical diagnosis of MLL rearrangements. Biotechnol J 1 (2006) 656-663
    • (2006) Biotechnol J , vol.1 , pp. 656-663
    • Meyer, C.1    Kowarz, E.2    Schneider, B.3    Oehm, C.4    Klingebiel, T.5    Dingermann, T.6
  • 18
    • 0028349911 scopus 로고
    • 11q23/MLL rearrangement confers a poor prognosis in infants with acute lymphoblastic leukemia
    • Pui C.H., Behm F.G., Downing J.R., Hancock M.L., Shurtleff S.A., Ribeiro R.C., et al. 11q23/MLL rearrangement confers a poor prognosis in infants with acute lymphoblastic leukemia. J Clin Oncol 12 (1994) 909-915
    • (1994) J Clin Oncol , vol.12 , pp. 909-915
    • Pui, C.H.1    Behm, F.G.2    Downing, J.R.3    Hancock, M.L.4    Shurtleff, S.A.5    Ribeiro, R.C.6
  • 19
    • 34249810636 scopus 로고    scopus 로고
    • Incidence of submicroscopic deletions vary according to disease entities and chromosomal translocations in hematologic malignancies: investigation by fluorescence in situ hybridization
    • Moon H.W., Chang Y.H., Kim T.Y., Oh B.R., Min H.C., Kim B.K., et al. Incidence of submicroscopic deletions vary according to disease entities and chromosomal translocations in hematologic malignancies: investigation by fluorescence in situ hybridization. Cancer Genet Cytogenet 175 (2007) 166-168
    • (2007) Cancer Genet Cytogenet , vol.175 , pp. 166-168
    • Moon, H.W.1    Chang, Y.H.2    Kim, T.Y.3    Oh, B.R.4    Min, H.C.5    Kim, B.K.6
  • 20
    • 17844401738 scopus 로고    scopus 로고
    • The incidence of submicroscopic deletions in reciprocal translocations is similar in acute myeloid leukemia, BCR-ABL positive acute lymphoblastic leukemia, and chronic myeloid leukemia
    • Bacher U., Schnittger S., Kern W., Hiddemann W., Haferlach T., and Schoch C. The incidence of submicroscopic deletions in reciprocal translocations is similar in acute myeloid leukemia, BCR-ABL positive acute lymphoblastic leukemia, and chronic myeloid leukemia. Haematologica 90 (2005) 558-559
    • (2005) Haematologica , vol.90 , pp. 558-559
    • Bacher, U.1    Schnittger, S.2    Kern, W.3    Hiddemann, W.4    Haferlach, T.5    Schoch, C.6
  • 21
    • 0035383839 scopus 로고    scopus 로고
    • Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis
    • Kolomietz E., Al-Maghrabi J., Brennan S., Karaskova J., Minkin S., Lipton J., et al. Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis. Blood 97 (2001) 3581-3588
    • (2001) Blood , vol.97 , pp. 3581-3588
    • Kolomietz, E.1    Al-Maghrabi, J.2    Brennan, S.3    Karaskova, J.4    Minkin, S.5    Lipton, J.6
  • 22
    • 0027184681 scopus 로고
    • Acute leukemias of different lineages have similar MLL gene fusions encoding related chimeric proteins resulting from chromosomal translocation
    • Corral J., Forster A., Thompson S., Lampert F., Kaneko Y., Slater R., et al. Acute leukemias of different lineages have similar MLL gene fusions encoding related chimeric proteins resulting from chromosomal translocation. Proc Natl Acad Sci USA 90 (1993) 8538-8542
    • (1993) Proc Natl Acad Sci USA , vol.90 , pp. 8538-8542
    • Corral, J.1    Forster, A.2    Thompson, S.3    Lampert, F.4    Kaneko, Y.5    Slater, R.6
  • 23
    • 0027283999 scopus 로고
    • Heterogeneity of breakpoints of 11q23 rearrangements in hematologic malignancies identified with fluorescence in situ hybridization
    • Kobayashi H., Espinosa III R., Thirman M.J., Gill H.J., Fernald A.A., Diaz M.O., et al. Heterogeneity of breakpoints of 11q23 rearrangements in hematologic malignancies identified with fluorescence in situ hybridization. Blood 82 (1993) 547-551
    • (1993) Blood , vol.82 , pp. 547-551
    • Kobayashi, H.1    Espinosa III, R.2    Thirman, M.J.3    Gill, H.J.4    Fernald, A.A.5    Diaz, M.O.6
  • 24
    • 33750306281 scopus 로고    scopus 로고
    • A case of acute myelogenous leukemia with MLL-AF10 fusion caused by insertion of 5′ MLL into 10p12, with concurrent 3′ MLL deletion
    • Matsuda K., Hidaka E., Ishida F., Yamauchi K., Makishima H., Ito T., et al. A case of acute myelogenous leukemia with MLL-AF10 fusion caused by insertion of 5′ MLL into 10p12, with concurrent 3′ MLL deletion. Cancer Genet Cytogenet 171 (2006) 24-30
    • (2006) Cancer Genet Cytogenet , vol.171 , pp. 24-30
    • Matsuda, K.1    Hidaka, E.2    Ishida, F.3    Yamauchi, K.4    Makishima, H.5    Ito, T.6
  • 25
    • 9944227139 scopus 로고    scopus 로고
    • Overlapping deletion regions at 11q23 in myelodysplastic syndrome and chronic lymphocytic leukemia, characterized by a novel BAC probe
    • Siew-Gek Lee A., Rudduck-Sivaswaren C., Khun-Hong Lie D., Li-Ming Chua C., Tien S.L., Morsberger L., et al. Overlapping deletion regions at 11q23 in myelodysplastic syndrome and chronic lymphocytic leukemia, characterized by a novel BAC probe. Cancer Genet Cytogenet 153 (2004) 151-157
    • (2004) Cancer Genet Cytogenet , vol.153 , pp. 151-157
    • Siew-Gek Lee, A.1    Rudduck-Sivaswaren, C.2    Khun-Hong Lie, D.3    Li-Ming Chua, C.4    Tien, S.L.5    Morsberger, L.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.