Complex Variant t(9;22) Chromosome Translocations in Five Cases of Chronic Myeloid Leukemia

Author:

Valencia Ana1,Cervera José1,Such Esperanza1,Barragán Eva2,Bolufer Pascual2,Fuster Oscar2,Collado Rosa3,Martínez Jesús1,Sanz Miguel A.1

Affiliation:

1. Department of Hematology, La Fe University Hospital, 46009 Valencia, Spain

2. Molecular Biology Laboratory, Department of Medical Biopathology, La Fe University Hospital, 46009 Valencia, Spain

3. Department of Hematology, Hospital General Universitario de Valencia, 46014 Valencia, Spain

Abstract

The Philadelphia (Ph1) chromosome arising from the reciprocal t(9;22) translocation is found in more than 90% of chronic myeloid leukemia (CML) patients and results in the formation of the chimeric fusion geneBCR-ABL. However, a small proportion of patients with CML have simple or complex variants of this translocation, involving various breakpoints in addition to 9q34 and 22q11. We report five CML cases carrying variant Ph translocations involving both chromosomes 9 and 22 as well as chromosomes 3, 5, 7, 8, or 10. G-banding showed a reciprocal three-way translocation involving 3q21, 5q31, 7q32, 8q24, and 10q22 bands.BCR-ABLfusion signal on der(22) was found in all of the cases by FISH.

Publisher

Hindawi Limited

Subject

Hematology

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