1例唐氏综合征相关急性巨核细胞白血病中存在两条21号等臂染色体的21号染色体五体病例。 - Suppr

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A case of pentasomy 21 with two isochromosome 21s in acute megakaryoblastic leukemia associated with Down syndrome.

作者信息

Park Yeongchun, Lim Jinsook, Ko Yong Hyun, Kim Jimyung, Kwon Gye Cheol, Koo Sun Hoe

机构信息

Department of Laboratory Medicine, Chungnam National University Hospital, Daejeon, Korea.

出版信息

Ann Lab Med. 2015 May;35(3):373-5. doi: 10.3343/alm.2015.35.3.373. Epub 2015 Apr 1.

DOI:10.3343/alm.2015.35.3.373

PMID:25932450

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4390710/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d159/4390710/3d06e5aa1adb/alm-35-373-g001.jpg

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A case of pentasomy 21 with two isochromosome 21s in acute megakaryoblastic leukemia associated with Down syndrome.

Ann Lab Med. 2015 May;35(3):373-5. doi: 10.3343/alm.2015.35.3.373. Epub 2015 Apr 1.

Pentasomy 21 with two isochromosomes 21 in a case of acute myeloid leukemia without maturation.

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Down syndrome-like acute megakaryoblastic leukemia in a patient with Cornelia de Lange syndrome.

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Acute megakaryoblastic leukemia and clonal trisomy 21 in a phenotypically normal infant.

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Myelodysplasia and acute megakaryoblastic leukemia in Down's syndrome.

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GATA1 as a new target to detect minimal residual disease in both transient leukemia and megakaryoblastic leukemia of Down syndrome.

Leuk Res. 2005 Nov;29(11):1353-6. doi: 10.1016/j.leukres.2005.04.007.

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Acute megakaryoblastic leukemia in Down syndrome: orbital infiltration.

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Trisomy 8 as a secondary genetic change in acute megakaryoblastic leukemia associated with Down's syndrome.

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引用本文的文献

Mosaic complete tetrasomy 21 in a fetus with complete atrioventricular septal defect and minor morphological variations.

Mol Genet Genomic Med. 2019 Nov;7(11):e00895. doi: 10.1002/mgg3.895. Epub 2019 Sep 7.

本文引用的文献

The role of chromosome 21 in hematology and oncology.

Genes Chromosomes Cancer. 2010 Jun;49(6):497-508. doi: 10.1002/gcc.20764.

Duplication of isodicentric chromosome 21, idic(21)(p11.2), leading to pentasomy 21q in acute myeloid leukemia with multilineage dysplasia.

Cancer Genet Cytogenet. 2009 Oct;194(1):38-43. doi: 10.1016/j.cancergencyto.2009.04.019.

Acute megakaryoblastic leukaemia (AMKL) and transient myeloproliferative disorder (TMD) in Down syndrome: a multi-step model of myeloid leukaemogenesis.

Br J Haematol. 2009 Oct;147(1):3-12. doi: 10.1111/j.1365-2141.2009.07789.x. Epub 2009 Jul 6.

Intrachromosomal amplification of chromosome 21 (iAMP21) may arise from a breakage-fusion-bridge cycle.

Genes Chromosomes Cancer. 2007 Apr;46(4):318-26. doi: 10.1002/gcc.20412.

Chromosome 19 abnormalities are commonly seen in AML, M7.

Blood. 2002 Nov 15;100(10):3838; author reply 3838-9. doi: 10.1182/blood-2002-07-2225.

Tetrasomy 21 as a sole chromosome abnormality in acute myeloid leukemia. fluorescence in situ hybridization and spectral karyotyping analyses.

Cancer Genet Cytogenet. 2002 Apr 1;134(1):60-4. doi: 10.1016/s0165-4608(01)00604-5.

Frequent gain of chromosome 19 in megakaryoblastic leukemias detected by comparative genomic hybridization.

Genes Chromosomes Cancer. 2001 Nov;32(3):285-93. doi: 10.1002/gcc.1192.

Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2.

Br J Haematol. 2001 May;113(2):305-17. doi: 10.1046/j.1365-2141.2001.02723.x.

Clinical and prognostic significance of trisomy 21 in adult patients with acute myelogenous leukemia and myelodysplastic syndromes.

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A case of pentasomy 21 with two isochromosome 21s in acute megakaryoblastic leukemia associated with Down syndrome.

作者信息

Park Yeongchun, Lim Jinsook, Ko Yong Hyun, Kim Jimyung, Kwon Gye Cheol, Koo Sun Hoe

机构信息

Department of Laboratory Medicine, Chungnam National University Hospital, Daejeon, Korea.

出版信息

Ann Lab Med. 2015 May;35(3):373-5. doi: 10.3343/alm.2015.35.3.373. Epub 2015 Apr 1.

DOI:10.3343/alm.2015.35.3.373

PMID:25932450

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4390710/

Abstract

摘要

相似文献

A case of pentasomy 21 with two isochromosome 21s in acute megakaryoblastic leukemia associated with Down syndrome.

Ann Lab Med. 2015 May;35(3):373-5. doi: 10.3343/alm.2015.35.3.373. Epub 2015 Apr 1.

Pentasomy 21 with two isochromosomes 21 in a case of acute myeloid leukemia without maturation.

Cancer Genet Cytogenet. 2002 Jan 1;132(1):71-3. doi: 10.1016/s0165-4608(01)00529-5.

Down syndrome-like acute megakaryoblastic leukemia in a patient with Cornelia de Lange syndrome.

Haematologica. 2018 Jun;103(6):e274-e276. doi: 10.3324/haematol.2017.178590. Epub 2017 Dec 7.

Acute megakaryoblastic leukemia and clonal trisomy 21 in a phenotypically normal infant.

Blood. 1991 Jun 1;77(11):2542-3.

Myelodysplasia and acute megakaryoblastic leukemia in Down's syndrome.

Leuk Res. 1994 Mar;18(3):163-71. doi: 10.1016/0145-2126(94)90111-2.

GATA1 as a new target to detect minimal residual disease in both transient leukemia and megakaryoblastic leukemia of Down syndrome.

Leuk Res. 2005 Nov;29(11):1353-6. doi: 10.1016/j.leukres.2005.04.007.

[Megakaryoblastic leukemia and transient abnormal myelopoiesis with Down's syndrome].

Rinsho Ketsueki. 1988 Aug;29(8):1200-6.

Acute megakaryoblastic leukemia in Down syndrome: orbital infiltration.

Am J Ophthalmol. 2000 Jul;130(1):128-30. doi: 10.1016/s0002-9394(00)00459-1.

Dicentric chromosome in the bone marrow of a child with megakaryoblastic leukaemia and Down's syndrome.

J Clin Pathol. 1988 Apr;41(4):378-80. doi: 10.1136/jcp.41.4.378.

Trisomy 8 as a secondary genetic change in acute megakaryoblastic leukemia associated with Down's syndrome.

Leukemia. 1999 Mar;13(3):491-2. doi: 10.1038/sj.leu.2401330.

引用本文的文献

Mosaic complete tetrasomy 21 in a fetus with complete atrioventricular septal defect and minor morphological variations.

Mol Genet Genomic Med. 2019 Nov;7(11):e00895. doi: 10.1002/mgg3.895. Epub 2019 Sep 7.

本文引用的文献

The role of chromosome 21 in hematology and oncology.

Genes Chromosomes Cancer. 2010 Jun;49(6):497-508. doi: 10.1002/gcc.20764.

Duplication of isodicentric chromosome 21, idic(21)(p11.2), leading to pentasomy 21q in acute myeloid leukemia with multilineage dysplasia.

Cancer Genet Cytogenet. 2009 Oct;194(1):38-43. doi: 10.1016/j.cancergencyto.2009.04.019.

Acute megakaryoblastic leukaemia (AMKL) and transient myeloproliferative disorder (TMD) in Down syndrome: a multi-step model of myeloid leukaemogenesis.

Br J Haematol. 2009 Oct;147(1):3-12. doi: 10.1111/j.1365-2141.2009.07789.x. Epub 2009 Jul 6.

Intrachromosomal amplification of chromosome 21 (iAMP21) may arise from a breakage-fusion-bridge cycle.

Genes Chromosomes Cancer. 2007 Apr;46(4):318-26. doi: 10.1002/gcc.20412.

Chromosome 19 abnormalities are commonly seen in AML, M7.

Blood. 2002 Nov 15;100(10):3838; author reply 3838-9. doi: 10.1182/blood-2002-07-2225.

Tetrasomy 21 as a sole chromosome abnormality in acute myeloid leukemia. fluorescence in situ hybridization and spectral karyotyping analyses.

Cancer Genet Cytogenet. 2002 Apr 1;134(1):60-4. doi: 10.1016/s0165-4608(01)00604-5.

Frequent gain of chromosome 19 in megakaryoblastic leukemias detected by comparative genomic hybridization.

Genes Chromosomes Cancer. 2001 Nov;32(3):285-93. doi: 10.1002/gcc.1192.

Br J Haematol. 2001 May;113(2):305-17. doi: 10.1046/j.1365-2141.2001.02723.x.

Clinical and prognostic significance of trisomy 21 in adult patients with acute myelogenous leukemia and myelodysplastic syndromes.

Leukemia. 1995 Jan;9(1):115-7.