Cho K J, Lee S S, Khang S K
Department of Anatomic Pathology, Korea Cancer Center Hospital, Seoul, Korea.
J Korean Med Sci. 1996 Oct;11(5):409-14. doi: 10.3346/jkms.1996.11.5.409.
Forty-five cases of histiocytic necrotizing lymphadenitis (HNL) or Kikuchi-Fujimoto disease were reviewed clinico-pathologically and studied for Epstein-Barr virus (EBV) and hepatitis B virus (HBV) by in situ hybridization to assess their causative role. Histologically, the lymph nodes typically showed relatively well defined paracortical lesions composed of large atypical mononuclear cells, histiocytes, and karyorrhectic nuclear debris. Mild to moderate degree of coagulation type necrosis was present in 24 cases. Clinical features did not vary greatly from previously described female preponderance, young age onset, subacute cervical lymphadenopathy, and frequent leukopenia, except for a few cases with recurrent disease over 8-9 years. Serologic tests revealed EBV IgG antibody in one case, HBV surface antibody in 11 cases and HBV surface antigen in 2 cases. In situ hybridization was performed on 41 cases using internal repeat 1 fragment DNA and EBV-coded small RNA (EBER-1) for EBV, and pan-HBV DNA probe for HBV detection, and showed that all cases were negative for EBV or HBV genome. Our results suggest EBV or HBV may not have causative role in the pathogenesis of HNL.
对45例组织细胞坏死性淋巴结炎(HNL)或菊池-藤本病进行了临床病理回顾,并通过原位杂交研究了爱泼斯坦-巴尔病毒(EBV)和乙型肝炎病毒(HBV),以评估它们的致病作用。组织学上,淋巴结通常表现为相对界限清楚的副皮质区病变,由大的非典型单核细胞、组织细胞和核碎裂的核碎片组成。24例出现轻度至中度的凝固性坏死。临床特征与先前描述的女性占优势、发病年龄较轻、亚急性颈部淋巴结病和频繁的白细胞减少症相比变化不大,除了少数病例在8至9年期间疾病复发。血清学检测显示1例有EBV IgG抗体,11例有HBV表面抗体,2例有HBV表面抗原。对41例使用内部重复1片段DNA和EBV编码的小RNA(EBER-1)进行EBV原位杂交,使用泛HBV DNA探针进行HBV检测,结果显示所有病例的EBV或HBV基因组均为阴性。我们的结果表明EBV或HBV可能在HNL的发病机制中不具有致病作用。