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组织细胞坏死性淋巴结炎的临床病理特征及免疫表型:84例分析

[Clinicopathologic characteristics and immunophenotypes of histiocytic necrotizing lymphadenitis: an analysis of 84 cases].

作者信息

Du Hua, Shi Yonghong, Shi Yingxu

机构信息

Department of Pathology, Affiliated Hospital of Inner Mongolia Medical University/Inner Mongolia Medical University, Hohehot 010050, China.

出版信息

Zhonghua Bing Li Xue Za Zhi. 2016 Feb;45(2):86-90. doi: 10.3760/cma.j.issn.0529-5807.2016.02.004.

DOI:10.3760/cma.j.issn.0529-5807.2016.02.004
PMID:26879428
Abstract

OBJECTIVE

To study the clinical manifestation, pathologic features and immunophenotype of histiocytic necrotizing lymphadenitis (HNL).

METHODS

The clinicopathologic data of 84 patients with HNL from 2005 to 2014 were retrospectively studied. Immunohistochemical staining using EliVision method for CD20, PAX5, CD3, CD45RO, CD4, CD8, CD56, CD68, CD123, granzyme-B, TIA1 and MPO was carried out. In-situ hybridization for Epstein-Barr virus RNA was performed on archival lymph node biopsy tissue.

RESULTS

Immunohistochemical study showed that the lesional cells were predominantly histiocytes (CD68+), plasmacytoid dendritic cells (CD123+) and T lymphocytes (CD3+ and CD45RO+). Clusters of CD68-positive cells with strong and diffuse MPO expression were identified. T lymphocytes with CD4 and CD8 positivity were noted. CD56+ natural killer cells and CD20+/PAX5 B cells were rare. Apoptosis-related markers, including TIA1 and granzyme B were expressed by T lymphocytes and histiocytes in lymph nodes of HNL. In-situ hybridization for Epstein-Barr virus RNA was positive in only 10.0% of the cases.

CONCLUSIONS

HNL shows no specific clinical and laboratory findings. Recognition of the characteristic histopathologic changes in lymph node biopsy of HNL is the key to correct diagnosis. Immunohistochemical study using a panel of markers, including CD3, CD4, CD8, MPO, CD123, granzyme-B and TIA1, is helpful in the differential diagnosis of HNL.

摘要

目的

研究组织细胞坏死性淋巴结炎(HNL)的临床表现、病理特征及免疫表型。

方法

回顾性分析2005年至2014年84例HNL患者的临床病理资料。采用EliVision法对CD20、PAX5、CD3、CD45RO、CD4、CD8、CD56、CD68、CD123、颗粒酶B、TIA1和MPO进行免疫组化染色。对存档的淋巴结活检组织进行爱泼斯坦-巴尔病毒RNA原位杂交。

结果

免疫组化研究显示,病变细胞主要为组织细胞(CD68+)、浆细胞样树突状细胞(CD123+)和T淋巴细胞(CD3+和CD45RO+)。发现CD68阳性细胞簇伴有强弥漫性MPO表达。注意到CD4和CD8阳性的T淋巴细胞。CD56+自然杀伤细胞和CD20+/PAX5 B细胞罕见。HNL淋巴结中的T淋巴细胞和组织细胞表达凋亡相关标志物,包括TIA1和颗粒酶B。爱泼斯坦-巴尔病毒RNA原位杂交仅在10.0%的病例中呈阳性。

结论

HNL无特异性临床和实验室检查结果。认识HNL淋巴结活检的特征性组织病理学改变是正确诊断的关键。使用包括CD3、CD4、CD8、MPO、CD123、颗粒酶B和TIA1在内的一组标志物进行免疫组化研究有助于HNL的鉴别诊断。

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