Molecular Diagnostics of T-Cell Lymphoproliferative Disorders

被引:2
|
作者
Bailey, Nathanael G. [1 ]
Elenitoba-Johnson, Kojo S. J. [1 ]
机构
[1] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
来源
CANCER JOURNAL | 2014年 / 20卷 / 01期
关键词
T-cell lymphoma; T-cell leukemia; genomics; gene rearrangement; FISH; polymerase chain reaction; molecular diagnostics; ACUTE LYMPHOBLASTIC-LEUKEMIA; EPSTEIN-BARR-VIRUS; GAMMA-GENE REARRANGEMENTS; MINIMAL RESIDUAL DISEASE; POLYMERASE-CHAIN-REACTION; IN-SITU HYBRIDIZATION; CHRONIC LYMPHOCYTIC-LEUKEMIA; OF-FUNCTION MUTATIONS; GENOME-WIDE ANALYSIS; LYMPHOMA KINASE ALK;
D O I
10.1097/PPO.0000000000000016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
T-cell neoplasms include both mature T-cell leukemias and lymphomas and immature proliferations of precursor T cells. Molecular laboratories routinely assay suspected T-cell proliferations for evidence of clonality. In addition, some T-cell neoplasms are characterized by recurrent structural abnormalities that can be readily identified by such techniques as fluorescence in situ hybridization. New massively parallel sequencing technologies have led to the identification of numerous recurrent gene mutations in T-cell neoplasms. These findings are reviewed. As new technologies become implemented in molecular diagnostic laboratories and as targeted therapies are developed, it is anticipated that more extensive genomic characterization of T-cell neoplasms will be routinely performed in the future.
引用
收藏
页码:48 / 60
页数:13
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