Pathologic and Molecular Genetic Features of Chronic Lymphocytic Leukemia

被引:4
作者
Hsi, Eric D. [1 ]
机构
[1] Cleveland Clin, Dept Clin Pathol, Cleveland, OH 44195 USA
关键词
B-CELL LYMPHOCYTOSIS; CD38; EXPRESSION; MUTATION STATUS; GENOMIC ABERRATIONS; ZAP-70; FLOW-CYTOMETRY; DISTINCT; CLL; PATHOGENESIS; DISORDERS;
D O I
10.1053/j.seminoncol.2011.11.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chronic lymphocytic leukemia (CLL) is an indolent B-cell leukemia. While many patients may not require therapy, some patients will suffer a progressive course and die of their disease. This clinical heterogeneity is reflected in the molecular genetic heterogeneity that is becoming apparent through studies of immunoglobulin heavy chain gene mutational status, chromosomal numerical abnormalities, microRNA abnormalities, and genetic abnormalities identified by whole genome sequencing. Indeed, many of these studies are becoming routine in the assessment of patients with CLL or being incorporated into clinical trials to further stratify patients for appropriate therapies. Here, we will review the morphologic, immunophenotypic, and molecular genetic features of CLL and touch upon the concept of monoclonal B-cell lymphocytosis. © 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:74 / 79
页数:6
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