Takano Y, Saegusa M, Okudaira M
Department of Pathology, Kitasato University School of Medicine, Sagamihara, Japan.
Acta Pathol Jpn. 1993 Nov;43(11):635-45. doi: 10.1111/j.1440-1827.1993.tb02547.x.
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.
为分析非典型坏死型菊池-藤本病(KF病,组织细胞坏死性淋巴结炎)的本质,对28例患者进行了临床病理、免疫组化及电镜研究。此外,鉴于已检测的病例中EB病毒(EBV)血清免疫反应阳性率较高,还采用聚合酶链反应(PCR)和原位杂交(ISH)检测EBV的存在。临床特征为男女比例均等,平均年龄26岁,轻度白细胞减少,约40%患者伴有体温超过38℃的发热。主要的特殊病理特征为:(i)病理区域有不同数量的核碎片,电镜下确定为凋亡;(ii)存在中等至大型转化淋巴细胞(免疫母细胞),其中极少数UCHL1和L26均呈阳性,还有浆细胞样细胞,部分UCHL1呈阳性;(iii)病理区域以特征性形态的组织细胞为主,核不规则,抗溶菌酶和抗α1-抗胰蛋白酶抗体呈强阳性。PCR和ISH检测显示这些病例中完全不存在EBV,尽管阳性对照结果良好。因此认为EBV不是KF病的致病病毒。