Alpers C E, Beckstead J H
Am J Surg Pathol. 1985 Jan;9(1):57-64. doi: 10.1097/00000478-198501000-00010.
We report a case of a neuroendocrine tumor of the jejunum metastatic to the liver in a 26-year-old woman. Light and electron microscopy of this tumor revealed a poorly differentiated neoplasm composed of clusters of round to polygonal cells compatible with a diagnosis of neuroendocrine tumor. In the absence of identifiable silver-staining granules or immunocytochemical demonstration of a specific hormone product in tumor cells, this tumor cannot be further classified among the various neuroendocrine tumors that may arise in this location. However, interspersed among tumor cells was a distinct population of multinucleate giant cells having an appearance similar to benign osteoclasts. Enzyme histochemistry for 5'-nucleotidase, acid phosphatase, and nonspecific esterase each showed a dichotomous staining pattern for the small tumor cells and giant cells and suggest that the giant cells are not tumor derived, but represent a second, presumably reactive, cell population.
我们报告了一例26岁女性空肠神经内分泌肿瘤转移至肝脏的病例。该肿瘤的光镜和电镜检查显示为低分化肿瘤,由圆形至多边形细胞簇组成,符合神经内分泌肿瘤的诊断。由于肿瘤细胞中未发现可识别的嗜银颗粒或特定激素产物的免疫细胞化学证据,该肿瘤无法在这个部位可能出现的各种神经内分泌肿瘤中进一步分类。然而,在肿瘤细胞之间散布着一群独特的多核巨细胞,其外观类似于良性破骨细胞。对5'-核苷酸酶、酸性磷酸酶和非特异性酯酶的酶组织化学分析显示,小肿瘤细胞和巨细胞均呈现二分染色模式,提示巨细胞并非肿瘤来源,而是代表第二种可能具有反应性的细胞群体。