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Gliofibromas (including malignant forms), and gliosarcomas: a comparative study and review of the literature.胶质纤维瘤(包括恶性形式)与胶质肉瘤:一项比较研究及文献综述
Acta Neuropathol. 1993;85(4):349-61. doi: 10.1007/BF00334444.
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Primary osteosarcoma of the cerebrum with immunohistochemical and ultrastructural studies: report of a case.大脑原发性骨肉瘤的免疫组织化学和超微结构研究:一例报告
Acta Neuropathol. 1994;88(4):384-8. doi: 10.1007/BF00310384.
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Osteogenic sarcoma of the somatic soft tissues. Clinicopathologic study of 26 cases and review of literature.躯体软组织骨肉瘤。26例临床病理研究及文献复习
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Extraosseous osteogenic sarcoma.骨外骨肉瘤
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9
Histogenesis of sarcomatous component of the gliosarcoma: an ultrastructural study.胶质肉瘤肉瘤成分的组织发生:一项超微结构研究。
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10
Primary intracerebral osteosarcoma.原发性颅内骨肉瘤。
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硬脊膜内原发性软骨母细胞性骨肉瘤:病例报告

Intradural primary chondroblastic osteosarcoma: case report.

作者信息

Walker M T, Toye L R, Coons S W, Porter R W, Wallace R C

机构信息

Division of Neuroradiology, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, AZ, USA.

出版信息

AJNR Am J Neuroradiol. 2001 Nov-Dec;22(10):1960-2.

PMID:11733332
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7973820/
Abstract

We report a rare case of intradural primary osteosarcoma (IPOS) in a 74-year-old man with aphasia and right-sided hemiparesis. Radiologic workup revealed a large, partially calcified, left-sided frontotemporal intracranial mass lesion. At surgery, the tumor was found to be entirely intradural; it involved the brain and subarachnoid space of the left sylvian fissure. The adjacent dura was uninvolved. Neuropathologic findings confirmed the diagnosis of chondroblastic osteosarcoma. To our knowledge, this is the sixth reported case of IPOS and the first reported case of the chondroblastic subtype.

摘要

我们报告了一例罕见的硬脊膜内原发性骨肉瘤(IPOS),患者为一名74岁男性,伴有失语和右侧偏瘫。影像学检查发现左侧额颞部颅内有一个大的、部分钙化的肿块病变。手术中发现肿瘤完全位于硬脊膜内;它累及左侧外侧裂的脑和蛛网膜下腔。相邻的硬脑膜未受累。神经病理学检查结果证实为软骨母细胞性骨肉瘤。据我们所知,这是第六例报告的IPOS病例,也是第一例报告的软骨母细胞亚型病例。