Title of article
Tetrasomy 8 as a primary chromosomal abnormality in a child with acute megakaryoblastic leukemia: a case report and review of the literature
Author/Authors
Aktas، نويسنده , , Dilek and Tuncbilek، نويسنده , , Ergul and Cetin، نويسنده , , Mualla and Hicsonmez، نويسنده , , Gonul، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2001
Pages
3
From page
166
To page
168
Abstract
Tetrasomy 8 is a relatively rare chromosomal abnormality in hematological disorders, and is mostly associated with myeloid malignancies and poor prognosis. In a number of cases, tetrasomy 8 has been reported as an accompanying anomaly with other chromosomal changes. In this report, we describe a 14-year-old girl with acute megakaryoblastic leukemia associated with tetrasomy 8 (primary) and trisomy 6, 19 and 20. She died 6 months after diagnosis, suggesting a relatively poor prognosis for AML with tetrasomy 8. To the best of our knowledge, this is the first report of a tetrasomy 8 abnormality associated with subtype FAB M7. Interestingly, this abnormality has not been previously reported in childhood AML patients.
Journal title
Cancer Genetics and Cytogenetics
Serial Year
2001
Journal title
Cancer Genetics and Cytogenetics
Record number
1823591
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