Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2111966 | Cancer Genetics and Cytogenetics | 2006 | 6 Pages |
Abstract
Chronic myeloid leukemia (CML) is a clonal malignant disorder of a pluripotent hematopoetic stem cell characterized by the presence of the Philadelphia (Ph) chromosome in more than 90% of patients. Cryptic or “masked” BCR/ABL gene rearrangements may be found in cases with a normal karyotype and in cases with the complex karyotype, in which typical t(9;22) is not visible at the microscopic level. Those rearrangements can now be detected by fluorescence in situ hybridization. Here, we report on a novel and complex Ph chromosome-negative CML case with a t(6;9)(p21;q34.1) in which the BCR/ABL fusion gene is located at 6p21.
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Authors
Biljana Todorić-Zivanović, Dragomir Marisavljević, Cecilia Surace, Vesna Čemerikić, Olivera Marković, Koviljka Krtolica, Željka Tatomirović, Bojana Cikota, Zvonko Magić, Mariano Rocchi,