Ohara N, Hayashi K, Shinohara C, Kamitani M, Furuta T, Yoshino T, Takahashi K, Taguchi K, Akagi T
Second Department of Pathology, Okayama University Medical School, Japan.
Acta Neuropathol. 1994;88(4):384-8. doi: 10.1007/BF00310384.
A 57-year-old woman with primary intracerebral osteosarcoma is reported. The tumor was identified by computed tomography as a mass with hemorrhage in the right parietal lobe. The surgical and pathological examinations confirmed an osteosarcoma of intracerebral origin. She suffered from repeated local recurrence of the tumor and died about 1 year after the onset. The pathological findings showed features of osteoblastic osteosarcoma with numerous osteoclast-like multinucleated giant cells. Immunohistochemically, tumor cells were positive for vimentin, and partially for actin. Multinucleated giant cells were reactive with vimentin and CD68 antibodies. Ultrastructurally, tumor cells were rich with rough endoplasmic reticulum. These findings are consistent with the histological features of skeletal or extraskeletal osteosarcoma. This is the third case of primary intracerebral osteosarcoma reported in the literature and the first one analyzed ultrastructurally.
报告了一名57岁患有原发性脑内骨肉瘤的女性。通过计算机断层扫描将肿瘤确定为右顶叶有出血的肿块。手术和病理检查证实为脑源性骨肉瘤。她遭受肿瘤反复局部复发,发病后约1年死亡。病理结果显示为成骨细胞性骨肉瘤特征,伴有大量破骨细胞样多核巨细胞。免疫组织化学检查显示,肿瘤细胞波形蛋白阳性,肌动蛋白部分阳性。多核巨细胞对波形蛋白和CD68抗体呈反应性。超微结构上,肿瘤细胞富含粗面内质网。这些发现与骨骼或骨骼外骨肉瘤的组织学特征一致。这是文献中报道的第三例原发性脑内骨肉瘤病例,也是第一例进行超微结构分析的病例。