Biology and genetics of extranodal mature T-cell and NK-cell lymphomas and lymphoproliferative disorders

被引:0
|
作者
Lewis, Natasha E. [1 ]
Zhou, Ting [2 ]
Dogan, Ahmet [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Pathol & Lab Med, Hematopathol Serv, New York, NY 10065 USA
[2] MD Anderson Canc Ctr, Dept Hematopathol, Mol Diagnost Lab, Houston, TX USA
关键词
REFRACTORY CELIAC-DISEASE; TUMOR-SUPPRESSOR GENES; CLINICOPATHOLOGICAL FEATURES; INTRAEPITHELIAL LYMPHOCYTES; SIGNALING PATHWAYS; PROGNOSTIC-FACTORS; LUPUS PROFUNDUS; HIGH PREVALENCE; FOLLOW-UP; PANNICULITIS;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The extranodal mature T-cell and NK-cell lymphomas and lymphoproliferative disorders represent a unique group of rare neoplasms with both overlapping and distinct clinicopathological, biological, and genomic features. Their predilection for specific sites, such as the gastrointestinal tract, aerodigestive tract, liver, spleen, and skin/soft tissues, underlies their classification. Recent genomic advances have furthered our understanding of the biology and pathogenesis of these diseases, which is critical for accurate diagnosis, prognostic assessment, and therapeutic decision-making. Here we review clinical, pathological, genomic, and biological features of the following extranodal mature T-cell and NK-cell lymphomas and lymphoproliferative disorders: primary intestinal T-cell and NK-cell neoplasms, hepatosplenic T-cell lymphoma, extranodal NK/T-cell lymphoma, nasal type, and subcutaneous panniculitis-like T-cell lymphoma.
引用
收藏
页码:3261 / 3277
页数:17
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