Autor: |
Sinclair EJ; Centre for Human Genetics, Sheffield, United Kingdom., Potter AM, Watmore AE, Fitchett M, Ross F |
Jazyk: |
angličtina |
Zdroj: |
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1998 Aug; Vol. 105 (1), pp. 20-3. |
DOI: |
10.1016/s0165-4608(98)00003-x |
Abstrakt: |
Trisomy 15 as a single autosomal abnormality is a rare finding in hematological disorders and has not as yet been associated with any specific disease type. We report 20 cases of trisomy 15 observed in the bone marrow of patients referred for a suspected hematological malignancy. Most patients were elderly, and a marked male predominance was evident. Aneuploidy for the Y chromosome was observed in addition to +15 in 11 out of 15 male patients. A myelodysplastic disorder (MDS) was confirmed in six cases, and acute myeloid leukemia (AML) in one. There was no evidence of malignant hematological diseases in the remaining 13 patients. We propose that there may be an association between loss of the Y chromosome and trisomy 15 and that trisomy 15, like missing Y, may not always be a marker of malignancy, but may reflect an underlying age effect. The possibility that its presence may herald the development of a malignant condition cannot, however, be excluded. |
Databáze: |
MEDLINE |
Externí odkaz: |
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