Molecular pathology of lymphoma

被引:40
作者
Coupland, S. E. [1 ]
机构
[1] Univ Liverpool, Dept Mol & Clin Canc Med, Liverpool L69 3GA, Merseyside, England
关键词
ocular adnexal lymphoma; extranodal marginal zone lymphoma; diffuse large B-cell lymphoma; ABC DLBCL; GCB DLBCL; vitreoretinal lymphoma; B-CELL LYMPHOMA; PRIMARY INTRAOCULAR LYMPHOMA; CENTRAL-NERVOUS-SYSTEM; CLASS SWITCH RECOMBINATION; CYTIDINE DEAMINASE AID; GERMINAL-CENTER; GENE-EXPRESSION; SOMATIC HYPERMUTATION; MALT LYMPHOMA; OUTCOME PREDICTION;
D O I
10.1038/eye.2012.247
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Ocular lymphomas can be divided into intraocular lymphomas and ocular adnexal lymphomas. The vitreoretinal lymphomausually a diffuse large B-cell lymphoma (DLBCL) of high-grade malignancy-is the most common lymphoid malignancy arising in the eye, while the extranodal marginal zone B-cell lymphoma (EMZL), an indolent often recurrent tumour, occurs most frequently in the ocular adnexal tissue. The two lymphoma subtypes differ significantly in their clinical presentation, subsequent course and outcome as well as in their underlying morphological, immunophenotypical and genetic features. The molecular processes involved in DLBCL and EMZL development are complex, and include chromosomal translocations, mutations caused by aberrant somatic hypermutation, sporadic somatic mutations, and copy number alterations, characterized by deletions and amplifications. These lead to alterations in particular signalling pathways, which in turn activate transcription factors, such as nuclear factor NF-kappa B. This review provides an overview of the histological features of DLBCL and EMZL, and discusses the current insights into the molecular mechanisms underlying the development of these tumours, when they occur systemically and particularly when they arise in ocular tissues. Eye (2013) 27, 180-189; doi:10.1038/eye.2012.247; published online 7 December 2012
引用
收藏
页码:180 / 189
页数:10
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