Acute promyelocytic leukemia with tetraploid karyotype and multiple PML-RARA fusion signals
Author:
Affiliation:
1. Department of Hematology, Tenri Hospital
2. Tenri Institute of Medical Research
Publisher
Tenri Foundation, Tenri Institute of Medical Research
Link
https://www.jstage.jst.go.jp/article/tenrikiyo/23/2/23_23-018/_pdf
Reference9 articles.
1. 1 Manola KN, Karakosta M, Sambani C, et al. Isochromosome der(17)(q10)t(15;17) in acute promyelocytic leukemia resulting in an additional copy of the RARA-PML fusion gene: report of 4 cases and review of the literature. Acta Haematol 2010;123:162-170.
2. 2 Lo-Coco F, Avvisati G, Vignetti M, et al. Front-line treatment of acute promyelocytic leukemia with AIDA induction followed by risk-adapted consolidation for adults younger than 61 years: results of the AIDA-2000 trial of the GIMEMA Group. Blood 2010;116:3171-3179.
3. 3 Sanz MA, Lo Coco F, Martin G, et al. Definition of relapse risk and role of nonanthracycline drugs for consolidation in patients with acute promyelocytic leukemia: a joint study of the PETHEMA and GIMEMA cooperative groups. Blood 2000;96:1247-1253.
4. 4 Lo-Coco F, Cicconi L, Breccia M. Current standard treatment of adult acute promyelocytic leukaemia. Br J Haematol 2016;172:841-854.
5. 5 Storchova Z, Kuffer C. The consequences of tetraploidy and aneuploidy. J Cell Sci 2008;121:3859-3866.
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