摘要
多重打击B细胞淋巴瘤是指累及MYC/8q24的染色体畸变同时伴其他一种或多种染色体异常的B细胞淋巴瘤.其中,最早发现、最常见的重现染色体畸变为累及BCL2的t(14;18)(q32;q21),还包括MYC^+/BCL2^+/BCL6^+、MYC^+/BCL6^+、CCND1^+/MYC^+、BCL3^+/MYC+等.文章概述了介于弥漫大B细胞淋巴瘤和伯基特淋巴瘤之间未分类淋巴瘤中的多重打击B细胞淋巴瘤,内容包括流行病学、发病机制、临床特点及预后、病理特点及治疗进展.
Double-hit B cell lymphoma refers to a group of mature B cell lymphoma presented with MYC/8q24 rearrangement with one or more concurrent chromosomal translocations.The first and most common translocation ever found is t(14;18)(q32;q21) involving BCL2.Other breakpoint types include MYC^+/ BCL2^+/BCL6^+,MYC^+/BCL6^+,CCND1^+/MYC^+,BCL3^+/MYC^+ et al.This article reviewed the recent publications about the double-hit B cell lymphoma with features intermediate between diffuse large B-cell lymphoma and Burkitt lymphoma.The contents of the review include epidemiology,clinical characteristics,histopathology,treatment,prognosis and some prospects for future work.
出处
《白血病.淋巴瘤》
CAS
2014年第10期626-629,共4页
Journal of Leukemia & Lymphoma
基金
首都健康培育项目