Granger J K, Houn H Y
Department of Pathology, University of Arkansas for Medical Sciences, Little Rock 72205.
Diagn Cytopathol. 1991;7(4):402-7. doi: 10.1002/dc.2840070413.
A case study of eosinophilic granuloma (Langerhans cell histiocytosis) of lymph node in a 32-year-old white man is presented. Clinical, cytologic, histologic, immunohistochemical, and flow cytometric findings are reported. Intraoperative cytologic findings can serve as valuable adjuncts to the frozen section, in this case serving as the sole method for diagnosis. This case is presented in light of the rarity of node-based eosinophilic granuloma and the absence of flow cytometric immunophenotypic findings in the literature.
本文报道了一名32岁白人男性淋巴结嗜酸性肉芽肿（朗格汉斯细胞组织细胞增多症）的病例研究。报告了临床、细胞学、组织学、免疫组织化学和流式细胞术检查结果。术中细胞学检查结果可作为冰冻切片的重要辅助手段，在本病例中是唯一的诊断方法。鉴于以淋巴结为基础的嗜酸性肉芽肿较为罕见，且文献中缺乏流式细胞术免疫表型检查结果，故呈现此病例。
