A novel t (5; 17) (q35; q21) associated with t (8; 21) (q22; q22) in a patient with acute myeloid leukemia: case report and review of literature-Reference-Cited by-同舟云学术

A novel t (5; 17) (q35; q21) associated with t (8; 21) (q22; q22) in a patient with acute myeloid leukemia: case report and review of literature

Published:2023-06-28 Issue: Volume:14 Page:50-55
ISSN:1947-6027
Container-title:Genes & Cancer
language:en
Short-container-title:Genes Cancer

Author:

Zahra Kmira¹,Cherif Wided¹,Ahmed Gereisha²,Regaieg Haifa¹,Nesrine Ben Sayed¹,Zaier Monia¹,Mootamri Wided²,Youssef Yosra Ben¹,Brahem Nejia²,Sennana Halima³,Khelif Abderrahim¹

Affiliation:

1. Department of Clinical Hematology, Farhat Hached University Hospital-Sousse-Tunisia, Sousse 4081, Tunisia

2. Department of Cytology, Farhat Hached University Hospital-Sousse-Tunisia, Sousse 4081, Tunisia

3. Department of Cytogenetics, Farhat Hached University Hospital-Sousse-Tunisia, Sousse 4081, Tunisia

Publisher

Impact Journals, LLC

Subject

Cancer Research,Genetics

Reference21 articles.

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2. De Kouchkovsky I, Abdul-Hay M. ‘Acute myeloid leukemia: a comprehensive review and 2016 update’. Blood Cancer J. 2016; 6:e441. https://doi.org/10.1038/bcj.2016.50. [Pubmed]

3. Redner RL, Rush EA, Faas S, Rudert WA, Corey SJ. The t(5;17) variant of acute promyelocytic leukemia expresses a nucleophosmin-retinoic acid receptor fusion. Blood. 1996; 87:882–86. [Pubmed]

4. Brunel V, Sainty D, Carbuccia N, Arnoulet C, Costello R, Mozziconacci MJ, Simonetti J, Coignet L, Gabert J, Stoppa AM. Unbalanced translocation t(5;17) in an typical acute promyelocytic leukemia. Genes Chromosomes Cancer. 1995; 14:307–12. https://doi.org/10.1002/gcc.2870140410. [Pubmed]

5. Arber DA, Stein AS, Carter NH, Ikle D, Forman SJ, Slovak ML. Prognostic impact of acute myeloid leukemia classification. Importance of detection of recurring cytogenetic abnormalities and multilineage dysplasia on survival. Am J Clin Pathol. 2003; 119:672–80. https://doi.org/10.1309/EM7K-CQR4-GLMH-RCX4. [Pubmed]

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