Tetrasomy 8 as a primary chromosomal abnormality in a child with acute megakaryoblastic leukemia: a case report and review of the literature

被引:8
|
作者
Aktas, D [1 ]
Tuncbilek, E
Cetin, M
Hicsonmez, G
机构
[1] Hacettepe Univ, Ihsan Dogramaci Childrens Hosp, Dept Genet, TR-06100 Ankara, Turkey
[2] Hacettepe Univ, Ihsan Dogramaci Childrens Hosp, Dept Hematol, TR-06100 Ankara, Turkey
关键词
D O I
10.1016/S0165-4608(00)00403-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. (C) 2001 Elsevier Science Inc. All rights reserved.
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收藏
页码:166 / 168
页数:3
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