메뉴 건너뛰기




Volumn 32, Issue 10, 2008, Pages 1615-1619

Tetrasomy 21 as a sole acquired abnormality without GATA1 gene mutation in pediatric acute megakaryoblastic leukemia: A case report and review of the literature

Author keywords

Acute megakaryoblastic leukemia; GATA1; Tetrasomy 21

Indexed keywords

CD33 ANTIGEN; CD34 ANTIGEN; CD61 ANTIGEN; CD7 ANTIGEN; FIBRINOGEN RECEPTOR; MICROSOMAL AMINOPEPTIDASE; STEM CELL FACTOR RECEPTOR; TRANSCRIPTION FACTOR GATA 1; TRANSCRIPTION FACTOR RUNX1;

EID: 44749093964     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.leukres.2008.02.010     Document Type: Article
Times cited : (9)

References (31)
  • 2
    • 0028910557 scopus 로고
    • Clinical and prognostic significance of trisomy 21 in adult patients with acute myelogenous leukemia and myelodysplastic syndromes
    • Cortes J.E., Kantarjian H., O'Brien S., Keating M., Pierce S., Freireich E.J., et al. Clinical and prognostic significance of trisomy 21 in adult patients with acute myelogenous leukemia and myelodysplastic syndromes. Leukemia 9 (1995) 115-117
    • (1995) Leukemia , vol.9 , pp. 115-117
    • Cortes, J.E.1    Kantarjian, H.2    O'Brien, S.3    Keating, M.4    Pierce, S.5    Freireich, E.J.6
  • 3
  • 5
    • 0025945301 scopus 로고
    • Acute megakaryocytic leukemia in children. Clinical, immunologic, and cytogenetic findings in two patients
    • Slavc I., Urban C., Haas O.A., Kroisel P.M., and Koller U. Acute megakaryocytic leukemia in children. Clinical, immunologic, and cytogenetic findings in two patients. Cancer 68 (1991) 2266-2272
    • (1991) Cancer , vol.68 , pp. 2266-2272
    • Slavc, I.1    Urban, C.2    Haas, O.A.3    Kroisel, P.M.4    Koller, U.5
  • 6
    • 0028805799 scopus 로고
    • Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia
    • Rogan P.K., Close P., Blouin J.-L., Seip J.R., Gannutz L., Ladda R.L., et al. Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia. Am J Med Genet 59 (1995) 174-181
    • (1995) Am J Med Genet , vol.59 , pp. 174-181
    • Rogan, P.K.1    Close, P.2    Blouin, J.-L.3    Seip, J.R.4    Gannutz, L.5    Ladda, R.L.6
  • 7
    • 0030999555 scopus 로고    scopus 로고
    • A breakpoint map of recurrent chromosomal rearrangements in human neoplasia
    • Mitelman F., Mertens F., and Johansson B. A breakpoint map of recurrent chromosomal rearrangements in human neoplasia. Nat Genet 15 (1997) 417-474
    • (1997) Nat Genet , vol.15 , pp. 417-474
    • Mitelman, F.1    Mertens, F.2    Johansson, B.3
  • 8
    • 0023689044 scopus 로고    scopus 로고
    • Groupe Francais de Cytogenetique Hematologique. Cytogenetics of acutely transformed chronic myeloproliferative syndromes without a Philadelphia chromosome. A multicenter study of 55 patients. Cancer Genet Cytogenet 1988;32:157-68.
    • Groupe Francais de Cytogenetique Hematologique. Cytogenetics of acutely transformed chronic myeloproliferative syndromes without a Philadelphia chromosome. A multicenter study of 55 patients. Cancer Genet Cytogenet 1988;32:157-68.
  • 9
    • 0024692819 scopus 로고
    • Transient myeloproliferative disorder (TMD) with transiently increased tetrasomy-21 cells in a phenotypically normal newborn
    • Takeda T., Murano K., Chihara H., Taki M., Watanabe A., Yamada K., et al. Transient myeloproliferative disorder (TMD) with transiently increased tetrasomy-21 cells in a phenotypically normal newborn. Jpn J Clin Hematol 30 (1989) 1010-1015
    • (1989) Jpn J Clin Hematol , vol.30 , pp. 1010-1015
    • Takeda, T.1    Murano, K.2    Chihara, H.3    Taki, M.4    Watanabe, A.5    Yamada, K.6
  • 13
    • 0029559117 scopus 로고
    • Tetrasomy 21 as a sole abnormality in erythroleukemia
    • Udayakumar A.M., and Sundareshan T.S. Tetrasomy 21 as a sole abnormality in erythroleukemia. Cancer Genet Cytogenet 85 (1995) 85-87
    • (1995) Cancer Genet Cytogenet , vol.85 , pp. 85-87
    • Udayakumar, A.M.1    Sundareshan, T.S.2
  • 14
    • 0029781419 scopus 로고    scopus 로고
    • Chronic neutrophil leukaemia in adolescence and young adulthood
    • Hasle H., Olesen G., Kerndrup G., Philip P., and Jacobsen N. Chronic neutrophil leukaemia in adolescence and young adulthood. Br J Haematol 94 (1996) 628-630
    • (1996) Br J Haematol , vol.94 , pp. 628-630
    • Hasle, H.1    Olesen, G.2    Kerndrup, G.3    Philip, P.4    Jacobsen, N.5
  • 15
    • 0032832959 scopus 로고    scopus 로고
    • Trisomy 21 as the sole acquired karyotypic abnormality in acute myeloid anemia and myelodysplastic syndrome
    • Wan T.S.K., Au W.Y., Chan J.C.W., Chan L.C., and Ma S.K. Trisomy 21 as the sole acquired karyotypic abnormality in acute myeloid anemia and myelodysplastic syndrome. Leuk Res 23 (1999) 1079-1083
    • (1999) Leuk Res , vol.23 , pp. 1079-1083
    • Wan, T.S.K.1    Au, W.Y.2    Chan, J.C.W.3    Chan, L.C.4    Ma, S.K.5
  • 16
    • 0034667690 scopus 로고    scopus 로고
    • High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2B gene in M0 acute leukemia and in myeloid malignancies with acquired trisomy 21
    • Preudhomme C., Warot-Loze D., Roumier C., Grardel-Duflos N., Garand R., Lai J.L., et al. High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2B gene in M0 acute leukemia and in myeloid malignancies with acquired trisomy 21. Blood 96 (2000) 2862-2869
    • (2000) Blood , vol.96 , pp. 2862-2869
    • Preudhomme, C.1    Warot-Loze, D.2    Roumier, C.3    Grardel-Duflos, N.4    Garand, R.5    Lai, J.L.6
  • 17
    • 0035878532 scopus 로고    scopus 로고
    • Tetrasomy 21 as the sole acquired karyotypic abnormality in acute myeloblastic leukemia
    • Odagaki T., Sugimoto T., Matsuo M., Tatsumi E., and Saigo K. Tetrasomy 21 as the sole acquired karyotypic abnormality in acute myeloblastic leukemia. Cancer Genet Cytogenet 128 (2001) 158-160
    • (2001) Cancer Genet Cytogenet , vol.128 , pp. 158-160
    • Odagaki, T.1    Sugimoto, T.2    Matsuo, M.3    Tatsumi, E.4    Saigo, K.5
  • 18
    • 0036540239 scopus 로고    scopus 로고
    • Tetrasomy 21 as a sole chromosome abnormality in acute myeloid leukemia: fluorescence in situ hybridization and spectral karyotyping analyses
    • Ohsaka A., Hisa T., Watanabe N., Kojima H., and Nagasawa T. Tetrasomy 21 as a sole chromosome abnormality in acute myeloid leukemia: fluorescence in situ hybridization and spectral karyotyping analyses. Cancer Genet Cytogenet 134 (2002) 60-64
    • (2002) Cancer Genet Cytogenet , vol.134 , pp. 60-64
    • Ohsaka, A.1    Hisa, T.2    Watanabe, N.3    Kojima, H.4    Nagasawa, T.5
  • 19
    • 10044256729 scopus 로고    scopus 로고
    • Tetrasomy 21 transient leukemia with a GATA1 mutation in a phenotypically normal trisomy 21 mosaic infant: case report and review of the literature
    • Sandoval C., Pine S.R., Guo Q., Sastry S., Stewart J., Kronn D., et al. Tetrasomy 21 transient leukemia with a GATA1 mutation in a phenotypically normal trisomy 21 mosaic infant: case report and review of the literature. Pediatr Blood Cancer 44 (2005) 85-91
    • (2005) Pediatr Blood Cancer , vol.44 , pp. 85-91
    • Sandoval, C.1    Pine, S.R.2    Guo, Q.3    Sastry, S.4    Stewart, J.5    Kronn, D.6
  • 22
    • 0036156276 scopus 로고    scopus 로고
    • Transient myeloproliferative disorder, a disorder with too few data and many unanswered questions: does it contain an important piece of the puzzle to understanding hematopoiesis and acute myelogenous leukemia?
    • Gamis A.S., and Hilden J.M. Transient myeloproliferative disorder, a disorder with too few data and many unanswered questions: does it contain an important piece of the puzzle to understanding hematopoiesis and acute myelogenous leukemia?. J Pediatr Hematol Oncol 24 (2002) 2-5
    • (2002) J Pediatr Hematol Oncol , vol.24 , pp. 2-5
    • Gamis, A.S.1    Hilden, J.M.2
  • 23
    • 0037071383 scopus 로고    scopus 로고
    • Transcriptional regulation of erythropoiesis: an affair involving multiple partners
    • Cantor A.B., and Orkin S.H. Transcriptional regulation of erythropoiesis: an affair involving multiple partners. Oncogene 21 (2002) 3368-3376
    • (2002) Oncogene , vol.21 , pp. 3368-3376
    • Cantor, A.B.1    Orkin, S.H.2
  • 25
    • 0034812344 scopus 로고    scopus 로고
    • Molecular and transcriptional regulation of megakaryocyte differentiation
    • Shivdasani R.A. Molecular and transcriptional regulation of megakaryocyte differentiation. Stem Cells 19 (2001) 397-407
    • (2001) Stem Cells , vol.19 , pp. 397-407
    • Shivdasani, R.A.1
  • 28
    • 0042243593 scopus 로고    scopus 로고
    • Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21
    • Rainis L., Bercovich D., Strehl S., Schlegel A.T., Stark B., Trka J., et al. Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21. Blood 102 (2003) 981-986
    • (2003) Blood , vol.102 , pp. 981-986
    • Rainis, L.1    Bercovich, D.2    Strehl, S.3    Schlegel, A.T.4    Stark, B.5    Trka, J.6
  • 29
    • 0034988869 scopus 로고    scopus 로고
    • Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia
    • Minelli A., Morerio C., Maserati E., Olivieri C., Panarello C., Bonvini L., et al. Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia. Leukemia 15 (2001) 971-975
    • (2001) Leukemia , vol.15 , pp. 971-975
    • Minelli, A.1    Morerio, C.2    Maserati, E.3    Olivieri, C.4    Panarello, C.5    Bonvini, L.6
  • 30
    • 0032935506 scopus 로고    scopus 로고
    • Isolated tetrasomy 8 in minimally differentiated acute myeloid leukemia (AML-M0)
    • Xue Y., Guo Y., Zhou Y., Xie X., Zheng L., and Shen M. Isolated tetrasomy 8 in minimally differentiated acute myeloid leukemia (AML-M0). Leuk Lymphoma 33 (1999) 581-585
    • (1999) Leuk Lymphoma , vol.33 , pp. 581-585
    • Xue, Y.1    Guo, Y.2    Zhou, Y.3    Xie, X.4    Zheng, L.5    Shen, M.6
  • 31
    • 0026748638 scopus 로고
    • Formation of a hyperdiploid karyotype in childhood acute lymphoblastic leukemia
    • Onodera N., McCabe N.R., and Rubin C.M. Formation of a hyperdiploid karyotype in childhood acute lymphoblastic leukemia. Blood 80 (1992) 203-208
    • (1992) Blood , vol.80 , pp. 203-208
    • Onodera, N.1    McCabe, N.R.2    Rubin, C.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.