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[皮下脂膜炎样T细胞淋巴瘤:细胞毒性颗粒相关蛋白TIA-1的表达及其与爱泼斯坦-巴尔病毒感染的关系]

[Subcutaneous panniculitis-like T-cell lymphoma: expression of cytotoxic-granule-associated protein TIA-1 and its relation with Epstein-Barr virus infection].

作者信息

Wang L, Yang Y, Liu W, Li G, Liao Q, Lai R, Li F, Ran Y, Zhou G

机构信息

Department of Dermatoverneology, First University Hospital, West China University of Medical Sciences, Chengdu 610041, China.

出版信息

Zhonghua Bing Li Xue Za Zhi. 2000 Apr;29(2):103-6.

Abstract

OBJECTIVE

To study the clinicopathologic features, the expression of cytotoxic-granule-associated protein TIA-1 and Epstein-Barr virus (EBV) infection in subcutaneous panniculitis-like T-cell lymphoma (SPTCL).

METHODS

Totally 17 cases of SPTCL were studied. Immunohistochemical staining was done for TIA-1, CD45RO, CD3, CD20 and CD68, and in situ hybridization for EBV encoded small nuclear RNA (EBER1/2).

RESULTS

In the 17 cases of SPTCL, the ratio of male-to-female was 1:1.1 and the median age was 24 years old. The main clinical manifestations were asymptomatic plaques, nodules and masses. Histologically, the pattern of lymphoid cells infiltration was panniculitis. The infiltrated lymphoid cells were pleomorphic and their mitotic figures were few (0 - 2/hpt). In the tumor tissue, there might be epithilioid granulomas, multinuclear cells, beanbag cells, small pieces of necrosis and small vessels with lymphoid cells infiltration in the vascular wall. Immunohistochemically, all the cases showed a T-cell phenotype and the expression rate of TIA-1 was 100% (16/16). By in situ hybridization, the positive rate of EBV-EBER1/2 was 29.4% (5/17).

CONCLUSIONS

SPTCL has a specific histopathologic picture. It may originate from cytotoxic T lymphocytes or NK cells. Some of them may be accompanying with EBV latent infection.

摘要

目的

研究皮下脂膜炎样T细胞淋巴瘤(SPTCL)的临床病理特征、细胞毒性颗粒相关蛋白TIA-1的表达及EB病毒(EBV)感染情况。

方法

对17例SPTCL进行研究。采用免疫组织化学法检测TIA-1、CD45RO、CD3、CD20和CD68,采用原位杂交法检测EBV编码的小核RNA(EBER1/2)。

结果

17例SPTCL中,男女比例为1:1.1,中位年龄为24岁。主要临床表现为无症状性斑块、结节和肿块。组织学上,淋巴细胞浸润模式为脂膜炎。浸润的淋巴细胞多形性,核分裂象少见(0 - 2个/高倍视野)。肿瘤组织中可见上皮样肉芽肿、多核巨细胞、豆袋细胞、小片坏死及血管壁有淋巴细胞浸润的小血管。免疫组织化学显示,所有病例均呈T细胞表型,TIA-1表达率为100%(16/16)。原位杂交显示,EBV-EBER1/2阳性率为29.4%(5/17)。

结论

SPTCL具有独特的组织病理学表现。它可能起源于细胞毒性T淋巴细胞或NK细胞。部分病例可能伴有EBV潜伏感染。

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