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肝脾γδ T细胞淋巴瘤:与爱泼斯坦-巴尔病毒及活化细胞毒性分子的关系

Hepatosplenic gammadelta T-cell lymphoma: relation to Epstein-Barr virus and activated cytotoxic molecules.

作者信息

Ohshima K, Haraoka S, Harada N, Kamimura T, Suzumiya J, Kanda M, Kawasaki C, Sugihara M, Kikuchi M

机构信息

Department of Pathology, School of Medicine, Fukuoka University, Kyushu University, Fukuoka, Japan.

出版信息

Histopathology. 2000 Feb;36(2):127-35. doi: 10.1046/j.1365-2559.2000.00804.x.

Abstract

AIMS

Hepatosplenic gammadelta T-cell lymphoma (TCL) is a rare, aggressive subset of peripheral TCL that presents with hepatosplenomegaly and cytopenia. Epstein-Barr virus (EBV) infection and activated cytotoxic molecules (granzyme and perforin) are uncommon in hepatosplenic gammadelta CTL. EBV infection and activated cytotoxic molecules are occasionally detected in non-hepatosplenic gammadelta TCL. We describe the clinicopathological features of three Japanese cases who were not immunodeficient.

METHODS AND RESULTS

All cases showed gammadelta T-cell type (CD2+, CD3+, T-cell receptor (TCR)delta-1+, betaF1-). Two cases expressed natural killer (NK) cell-associated antigens (CD8-, CD16+, CD56+; CD8-, CD16-, CD56+), and one expressed CD8 (CD8+, CD16-, CD56-). All cases expressed cytotoxicity-associated molecules (perforin, granzyme B, TIA-1 and Fas ligand). However, perforin and Fas ligand were not detected in one case. In-situ hybridization analysis with EBER probes revealed strong nuclear positivity in all neoplastic cells. In addition, two cases showed clonal bands of the EBV terminal repeat (TR) gene. Cytologically, instead of the presence of monomorphic medium-sized cells, our three cases showed pleomorphic medium-sized and large cells.

CONCLUSIONS

Our gammadelta TCL cases were clinicopathologically considered to be compatible with hepatosplenic gammadelta T-cell lymphoma. However, with regard to EBV association, activated cytotoxic profile and cytological features they resembled non-hepatosplenic gammadelta TCL. EBV may play a role in this disease by inducing cellular activation.

摘要

目的

肝脾γδT细胞淋巴瘤(TCL)是外周TCL中一种罕见的侵袭性亚型,表现为肝脾肿大和血细胞减少。爱泼斯坦 - 巴尔病毒(EBV)感染和活化的细胞毒性分子(颗粒酶和穿孔素)在肝脾γδTCL中并不常见。EBV感染和活化的细胞毒性分子偶尔在非肝脾γδTCL中被检测到。我们描述了3例非免疫缺陷日本患者的临床病理特征。

方法与结果

所有病例均显示γδT细胞类型(CD2 +、CD3 +、T细胞受体(TCR)δ - 1 +、βF1 - )。2例表达自然杀伤(NK)细胞相关抗原(CD8 - 、CD16 +、CD56 +;CD8 - 、CD16 - 、CD56 +),1例表达CD8(CD8 +、CD16 - 、CD56 - )。所有病例均表达细胞毒性相关分子(穿孔素、颗粒酶B、TIA - 1和Fas配体)。然而,1例未检测到穿孔素和Fas配体。用EBER探针进行原位杂交分析显示所有肿瘤细胞均有强核阳性。此外,2例显示EBV末端重复(TR)基因的克隆条带。细胞学上,我们的3例病例并非出现单形性中等大小细胞,而是显示多形性中等大小和大细胞。

结论

我们的γδTCL病例在临床病理上被认为与肝脾γδT细胞淋巴瘤相符。然而,在EBV关联、活化的细胞毒性谱和细胞学特征方面,它们类似于非肝脾γδTCL。EBV可能通过诱导细胞活化在这种疾病中发挥作用。

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