摘要
报告6例外周T细胞淋巴瘤的新亚型-组织细胞样T细胞淋巴瘤。6例均发生于颈部淋巴结(其中颈右4例,颈左2例)。组织学上完全是组织细胞特点-细胞大,胞浆丰富,有吞噬。但免疫组化为T细胞表型(UCHL1(+)),1例基因重排为TCRr(+),证实为T细胞来源。
Six cases with a new subtype of peripheral T-cell lymphoma, histiocytoid T-cell lymphoma, were reported. The lymphoma occurred in cervical lymph nodes in all the cases (right in 4 and left in 2 cases).Histopathologically. the cells were large, rich in cytoplasm and capable of phagocytosis, but immunohistochemically, the cells had T-cell phenotype (UCHL1+).Gene rearrangement was TLCRr (+) in one case,demonstrating T-cell origin.
出处
《诊断病理学杂志》
CSCD
1996年第4期203-204,共2页
Chinese Journal of Diagnostic Pathology
关键词
外周T细胞淋巴瘤
组织细胞样T
免疫组化
Peripheral T-cell lymphoma
Histiocytoid T-cell
Immunohistochemistry