Jaffe R, Santamaria M, Yunis E J, Tannery N H, Agostini R M, Medina J, Goodman M
Am J Surg Pathol. 1984 Dec;8(12):885-98. doi: 10.1097/00000478-198412000-00001.
Four small round cell malignant tumors of bone occurring in children are described. There was no catecholamine secretion and the clinical, radiologic, and biopsy diagnosis in each was Ewing's sarcoma. Glycogen was sparse both on imprints and in tissue sections. The tumors, when extensively sampled, had areas of a lobular growth pattern and Homer Wright rosettes. The rosettes were always focal and varied in complexity from case to case; they were rudimentary in one instance and markedly fibrillar in the most obvious instance. Neuron-specific enolase was demonstrated in tissue sections and in longterm cell cultures from three of the tumors. The cultured cells put out moderately long beaded processes in serum-free medium but had no catecholamine fluorescence. Electron microscopy of the tumor rosettes and the cultured cells showed processes containing aggregates of microtubules and only one case had rare neurosecretory granules. This study suggests that some small round cell tumors of bone and soft tissue in children, which present as Ewing's sarcoma, are neuroectodermal in nature.
本文描述了4例发生于儿童的骨小圆细胞恶性肿瘤。这些肿瘤均无儿茶酚胺分泌,每例的临床、放射学及活检诊断均为尤因肉瘤。印片及组织切片中糖原均稀少。肿瘤经广泛取材后,可见小叶状生长模式区域及霍纳·赖特玫瑰花结。玫瑰花结总是局灶性的,不同病例其复杂程度各异;其中1例较为原始,最典型的1例则有明显的纤维状结构。在3例肿瘤的组织切片及长期细胞培养物中均检测到神经元特异性烯醇化酶。培养细胞在无血清培养基中伸出适度长的串珠状突起,但无儿茶酚胺荧光。肿瘤玫瑰花结及培养细胞的电子显微镜检查显示,突起内含有微管聚集物,仅1例有罕见的神经分泌颗粒。本研究提示,一些表现为尤因肉瘤的儿童骨及软组织小圆细胞肿瘤本质上为神经外胚层来源。