Trisomy 1q in a patient with severe aplastic anemia

被引:8
|
作者
Angelidis, Prodromos
Kojouri, Kiarash
Lee, Jiyun
Kern, William
Mulvihill, John J.
Li, Shibo [1 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Pediat, Oklahoma City, OK 73190 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Dept Pathol, Oklahoma City, OK 73190 USA
[3] Univ Oklahoma, Hlth Sci Ctr, Dept Med, Oklahoma City, OK 73104 USA
关键词
D O I
10.1016/j.cancergencyto.2006.03.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aplastic anemia is a rare, serious disease characterized by hypocellular bone marrow and pancytopenia in the peripheral blood. Most cases are acquired, idiopathic, and without gross cytogenetic abnormalities. A few chromosome abnormalities have recurred among a small subset of patients, most commonly trisomy 8 and monosomy 7. Some of these chromosome abnormalities have prognostic and therapeutic significance, although for most the clinical relevance is not known. We present the case of a 40-year-old man with idiopathic severe aplastic anemia in bone marrow cells with trisomy of the whole long arm of chromosome 1 due to an unbalanced translocation between chromosomes 1 and 15 at breakpoints of q10 and 15q10. This clonal abnormality (which, to our knowledge, has not been previously reported in a patient with aplastic anemia) suggests that genes on 1q may be involved in marrow aplasia. (c) 2006 Elsevier Inc. All rights reserved.
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收藏
页码:73 / 75
页数:3
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