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2号染色体短臂2区3带缺失:急性髓系白血病中一种常见的复发性异常。

del(2)(p23): a consistent recurrent abnormality in acute myelogenous leukemia.

作者信息

Verma R S, Macera M J, da Costa M, Bradley T, Christodoulidou F

机构信息

Division of Genetics, Long Island College Hospital, Brooklyn, N.Y. 11201.

出版信息

Cancer Genet Cytogenet. 1991 Dec;57(2):175-9. doi: 10.1016/0165-4608(91)90149-o.

Abstract

A case of acute myelogenous leukemia (AML-M2) with an unusual chromosomal finding is presented. In addition to the most frequently observed translocation in this neoplasia, involving the long arms of chromosomes 8 and 21, there was a partial deletion of the short arm of chromosome 2 band (p23), i.e., 46,XX,del(2)(p23),t(8;21)(q22;q22). Deletion of the short arm of chromosome 2 has been described in association with other chromosome abnormalities in two other cases of AML and as the sole abnormality in three cases of AML, indicating that this abnormality is nonrandom and may be associated with leukemic transformation of hematopoietic cells. Therefore, we propose that the del(2)(p23),t(8;21)(q22;q22) abnormality be accorded status III and possibly considered a subset of AML (M2).

摘要

本文报告一例伴有异常染色体发现的急性髓性白血病(AML-M2)。除了该肿瘤中最常观察到的涉及8号和21号染色体长臂的易位外,还存在2号染色体短臂2区带(p23)的部分缺失,即46,XX,del(2)(p23),t(8;21)(q22;q22)。2号染色体短臂的缺失在另外两例AML中曾与其他染色体异常相关联,在三例AML中作为唯一异常被描述,这表明该异常并非随机出现,可能与造血细胞的白血病转化有关。因此,我们建议将del(2)(p23),t(8;21)(q22;q22)异常归为III类,并且可能将其视为AML(M2)的一个子集。

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