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皮下脂膜炎样T细胞淋巴瘤:源于T/NK表型大颗粒淋巴细胞的一种独特肿瘤的进一步证据

Subcutaneous panniculitis-like T-cell lymphoma: further evidence for a distinct neoplasm originating from large granular lymphocytes of T/NK phenotype.

作者信息

Dargent J L, Roufosse C, Delville J P, Kentos A, Delplace J, Kornreich A, Cochaux P, Hilbert P, Pradier O, Feremans W

机构信息

Department of Pathology, CHU St Pierre/ULB-Institut Jules Bordet, Brussels, Belgium.

出版信息

J Cutan Pathol. 1998 Aug;25(7):394-400. doi: 10.1111/j.1600-0560.1998.tb01764.x.

DOI:10.1111/j.1600-0560.1998.tb01764.x
PMID:9765026
Abstract

We report the case of a 20 year-old caucasian woman who presented a primary subcutaneous panniculitis-like T-cell lymphoma (SPTCL) as an invasive tumor of the chest wall. Herein, the neoplastic cells were found to express a CD3+CD8+ phenotype but also displayed variably the natural killer (NK)-associated antigens CD56 and CD57 as well as granzyme B. On cytological examination, these cells showed a large granular lymphocyte (LGL)-like morphology with presence of azurophilic granules in their cytoplasm. Electron dense and membrane bound granules like those found in cytotoxic T lymphocytes (CTL) were also demonstrated by electron microscopy. Neither rearrangement of the T-cell receptor subunits nor Epstein-Barr virus (EBV) genome was observed at the molecular level. The LGL-like features of the neoplastic cells found in this case and the presence of NK-associated antigens provide additional support to the cytotoxic derivation of most SPTCL.

摘要

我们报告了一例20岁的白种女性病例,该患者的原发性皮下脂膜炎样T细胞淋巴瘤(SPTCL)表现为胸壁的侵袭性肿瘤。在此病例中,肿瘤细胞被发现表达CD3 + CD8 +表型,但也可变地表达自然杀伤(NK)相关抗原CD56和CD57以及颗粒酶B。在细胞学检查中,这些细胞显示出大颗粒淋巴细胞(LGL)样形态,其细胞质中存在嗜天青颗粒。电子显微镜也证实了存在类似于细胞毒性T淋巴细胞(CTL)中的电子致密和膜结合颗粒。在分子水平上未观察到T细胞受体亚基的重排或爱泼斯坦-巴尔病毒(EBV)基因组。该病例中发现的肿瘤细胞的LGL样特征以及NK相关抗原的存在为大多数SPTCL的细胞毒性起源提供了额外的支持。

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