Risdall R J, Brunning R D, Sibley R K, Dehner L P, McKenna R W
Am J Surg Pathol. 1980 Oct;4(5):439-50.
The light- and electron-microscopic features and histochemical characterization of three consecutive cases of malignant histiocytosis (MH) are reported. Each case demonstrated involvement of lymph nodes and bone marrow. In the lymph node, the characteristic destructive sinusoidal pattern of involvement by cytologically malignant cells was present. Phagocytosis by malignant cells was rare and most readily appreciated in the imprint preparations. The major problem in differential diagnosis related to defining the histiocytic nature of the malignant cells. This question was resolved by the demonstration of diffuse cytoplasmic staining with the nonspecific esterase and acid phosphatase reactions as well as the ultrastructural demonstration of histiocytes. Although benign, reactive histiocytes were positive, malignant histiocytes did not stain for lysozyme by an immunoperoxidase technique. In contrast to the uniform appearance of these cases, many reports of MH in the past have consisted of heterogeneous cases with variable histologic appearances from a proliferation of predominantly mature histiocytes with marked phagocytosis to cytologically malignant cells with little apparent functional activity. This variation in histologic appearance is due in part to inclusion of cases of reactive histiocytic proliferations, including the recently described virus-associated hemophagocytic syndrome.
报告了三例连续的恶性组织细胞增多症(MH)的光镜和电镜特征以及组织化学特征。每例均显示有淋巴结和骨髓受累。在淋巴结中,存在特征性的由细胞学上恶性细胞构成的破坏性窦状模式。恶性细胞的吞噬现象罕见,在印片标本中最易观察到。鉴别诊断的主要问题在于确定恶性细胞的组织细胞性质。通过非特异性酯酶和酸性磷酸酶反应显示弥漫性胞质染色以及组织细胞的超微结构显示,解决了这个问题。尽管良性反应性组织细胞呈阳性,但恶性组织细胞通过免疫过氧化物酶技术检测溶菌酶不着色。与这些病例的一致表现不同,过去许多关于MH的报告包含了组织学表现各异的异质性病例,从以显著吞噬作用为主的成熟组织细胞增生到几乎没有明显功能活性的细胞学上的恶性细胞。组织学表现的这种差异部分归因于纳入了反应性组织细胞增生的病例,包括最近描述的病毒相关性噬血细胞综合征。