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出 处:《现代肿瘤医学》2010年第3期557-560,共4页Journal of Modern Oncology
摘 要:目的:探讨Kikuchi淋巴结炎的病因及临床特征,提高对Kikuchi淋巴结炎的认识,减少误诊。方法:对31例病理确诊为Kikuchi淋巴结炎的病例,结合临床特点和免疫组化进行分析观察。结果:31例中男性14例,女性17例,临床表现均为发热和浅表淋巴结肿大。所有的病例可见核碎片及淋巴细胞凋亡;淋巴结内出现片状或灶状形态多样的组织细胞增生。免疫组化标记CD45、CD68及CD3均为阳性表达。结论:本病病理形态以组织细胞增生为特征,主要是与组织细胞来源的淋巴瘤进行鉴别,免疫组化标记CD68及CD3阳性表达,对本病诊断有很重要的价值。该病属自限性疾病,预后多良好。Objective:To investigate the cause of Kikuchi's lymphadenitis and clinical characteristics. Methods: Thirty one cases with Kikuchi lymphadenitis, were analysed for the clinical features. Results: Among 31 cases, 14 male, 17 female. High fever and superficial lymph nodes can be seen in all cases also lymphocyte apoptosis nuclear debris;numerous polymorphical histiocyte proliferation in focal or lange areas were visualized. CD45, CD68 and CD3 were positive in 31 cases. Conclusion:Lymphnode focal necrosis and histiocytic proliferation are featares of Kikuchig lymphadenitis. CD68 and CD3 expression has very important value for HNl's diagnosis. The disease is self - limited disease, most patients have good prognosis.
关 键 词:组织细胞性坏死性淋巴结炎 免疫组化 KIKUCHI病
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