Coexistence of recurrent chromosomal abnormalities and the Philadelphia chromosome in acute and chronic myeloid leukemias: report of five cases and review of literature
- PMID: 32831907
- PMCID: PMC7437057
- DOI: 10.1186/s13039-020-00501-6
Coexistence of recurrent chromosomal abnormalities and the Philadelphia chromosome in acute and chronic myeloid leukemias: report of five cases and review of literature
Abstract
Progression of chronic myelogenous leukemia (CML) is frequently accompanied by cytogenetic evolution. Additional genetic abnormalities are seen in 10-20% of CML cases at the time of diagnosis, and in 60-80% of cases of advanced disease. Unbalanced chromosomal changes such as an extra copy of the Philadelphia chromosome (Ph), trisomy 8, and i(17)(q10) are common. Balanced chromosomal translocations, such as t(3;3), t(8;21), t(15;17), and inv(16) are typically found in acute myeloid leukemia, but rarely occur in CML. Translocations involving 11q23, t(8;21), and inv(16) are relatively common genetic abnormalities in acute leukemia, but are extremely rare in CML. In the literature to date, there are at least 76 Ph+ cases with t(3;21), 47 Ph+ cases with inv(16), 16 Ph+ cases with t(8;21), and 9 Ph+ cases with t(9;11). But most of what has been published is now over 30 years old, without the benefit of modern immunophenotyping to confirm diagnosis, and before the introduction of treatment regimes such as TKI. In this study, we explored the rare concomitant occurrence of coexistence current chromosomal translocation and t(9;22) in CML or acute myeloid leukemia (AML).
Keywords: Acute myeloid leukemia; Balanced chromosomal abnormalities; Chronic myelogenous leukemia; Clonal evolution; t(9;22).
© The Author(s) 2020.
Conflict of interest statement
Competing interestsThe authors declare no conflicts of interest.
Figures





Similar articles
-
Chromosomal rearrangement involving 11q23 locus in chronic myelogenous leukemia: a rare phenomenon frequently associated with disease progression and poor prognosis.J Hematol Oncol. 2015 Apr 8;8:32. doi: 10.1186/s13045-015-0128-2. J Hematol Oncol. 2015. PMID: 25888368 Free PMC article.
-
Cytogenetic and molecular genetic evolution of chronic myeloid leukemia.Acta Haematol. 2002;107(2):76-94. doi: 10.1159/000046636. Acta Haematol. 2002. PMID: 11919388 Review.
-
Philadelphia chromosome-negative acute myeloid leukemia with 11q23/MLL translocation in a patient with chronic myelogenous leukemia.Stem Cell Investig. 2015 Jul 1;2:13. doi: 10.3978/j.issn.2306-9759.2015.06.01. eCollection 2015. Stem Cell Investig. 2015. PMID: 27358881 Free PMC article.
-
Clinical implications of clonal chromosomal abnormalities in Philadelphia negative cells in CML patients after treated with tyrosine kinase inhibitors.Cancer Genet. 2019 Oct;238:44-49. doi: 10.1016/j.cancergen.2019.07.008. Epub 2019 Jul 24. Cancer Genet. 2019. PMID: 31425925
-
Relapse and cytogenetic evolution in myeloid neoplasms.Panminerva Med. 2017 Dec;59(4):308-319. doi: 10.23736/S0031-0808.17.03380-8. Panminerva Med. 2017. PMID: 29144072 Review.
Cited by
-
Transformation into acute myeloid leukemia with t(8;21)(q22;q22.1); RUNX1::RUNX1T1 from JAK2-mutated essential thrombocythemia: a case report.J Med Case Rep. 2024 Aug 18;18(1):372. doi: 10.1186/s13256-024-04691-0. J Med Case Rep. 2024. PMID: 39154170 Free PMC article.
References
-
- Zaccaria A, Testoni N, Valenti AM, Luatti S, Tonelli M, Marzocchi G, et al. Chromosome abnormalities additional to the Philadelphia chromosome at the diagnosis of chronic myelogenous leukemia: pathogenetic and prognostic implications. Cancer Genet Cytogenet. 2010;199:76–80. doi: 10.1016/j.cancergencyto.2010.02.003. - DOI - PubMed
-
- Gabert J, Beillard E, van der Velden VH, Bi W, Grimwade D, Pallisgaard N, et al. Standardization and quality control studies of ‘real-time’ quantitative reverse transcriptase polymerase chain reaction of fusion gene transcripts for residual disease detection in leukemia – a Europe against Cancer program. Leukemia. 2003;17:2318–2357. doi: 10.1038/sj.leu.2403135. - DOI - PubMed
LinkOut - more resources
Full Text Sources