非显性坏死性菊池病和藤本病的病理分析。

Y Takano, M Saegusa, M Okudaira
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引用次数: 21

摘要

本文对28例非显性坏死性型菊池-藤本病(KF病,组织细胞坏死性淋巴结炎)进行临床病理、免疫组织化学和电镜检查,以分析该病的性质。此外,利用聚合酶链反应(PCR)和原位杂交(ISH)检测eb病毒(EBV)的存在也进行了调查,因为在检查的病例中发现EBV阳性的血清免疫反应率很高。临床特征为男女比例相等,平均年龄26岁,轻度白细胞减少,约40%伴有38℃以上的发热。主要的特殊病理特征是:(1)病理区域有不同数量的核碎片,电镜下鉴定为细胞凋亡;(ii)存在中大型转化淋巴细胞(免疫母细胞),其中极少数同时对UCHL1和L26呈阳性,以及浆细胞样细胞,其中一些对UCHL1呈阳性;(iii)特征性形状的组织细胞在病理区域占主导地位,细胞核不规则,抗溶菌酶和抗α 1-抗胰蛋白酶抗体强烈阳性。PCR和ISH调查显示,这些病例中完全没有EBV,尽管阳性对照的结果很好。因此,认为EBV不是KF病的致病病毒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pathologic analyses of non-overt necrotizing type Kikuchi and Fujimoto's disease.

Twenty-eight cases of non-overt necrotizing type Kikuchi-Fujimoto disease (KF disease, histiocytic necrotizing lymphadenitis) were investigated clinicopathologically, immunohistochemically and electron microscopically in order to analyze the nature of this disease. In addition, investigations to detect the presence of Epstein-Barr virus (EBV) using the polymerase chain reaction (PCR) and in situ hybridization (ISH) were also performed as a high incidence of positive serum immunoreactivity to EBV had been revealed in the cases examined. The clinical features were an equal male to female ratio, mean age of 26 years, mild leukopenia and about 40% association with fever over 38 degrees C. The major particular pathologic features were: (i) varying amounts of nuclear debris in the pathologic areas, identified as apoptosis by electron microscopy; (ii) presence of medium to large sized transformed lymphocytes (immunoblasts), a very small number of them positive for both UCHL1 and L26, and plasmacytoid cells, some of them positive for UCHL1; and (iii) characteristically shaped histiocytes predominant in the pathologic areas, with irregular nuclei and strongly positive for anti-lysozyme and anti-alpha 1-antitrypsin antibodies. Investigations with PCR and ISH revealed a complete absence of EBV in these cases despite excellent results for positive controls. It was therefore considered that EBV was not a causative virus for KF disease.

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