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首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Glioblastoma multiforme and cerebral cavernous malformations: Intersection of pathophysiologic pathways
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Glioblastoma multiforme and cerebral cavernous malformations: Intersection of pathophysiologic pathways

机译:多形性胶质母细胞瘤和脑海绵状畸形:病理生理学途径的交集

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摘要

Cerebral cavernous malformations (CCM) are known to occur in both sporadic and familial forms. To date, there has been no identified association of CCM with glioblastoma multiforme. We present a 69-year-old woman with a 14 year history of multiple CCM who developed progressive aphasia. She had no radiation exposure and had only undergone a single computed tomography scan in her entire life. MRI demonstrated irregular gadolinium enhancement in the area of a prior stable CCM, suspicious for a high grade tumor. Stereotactic biopsy revealed a glioblastoma multiforme. This is a unique case of glioblastoma multiforme arising from the "site" of a known CCM. We review the literature on the genetics of cavernous malformations and propose a mechanism for the tumorigenic potential of these vascular malformations.
机译:已知脑海绵状畸形(CCM)以散发和家族形式均发生。迄今为止,还没有发现CCM与多形性胶质母细胞瘤的关联。我们介绍了一位患有多发性CCM 14年病史的69岁女性,她发展为进行性失语。她没有任何辐射暴露,并且一生只接受了一次计算机断层扫描。 MRI显示先前稳定的CCM区域中g的不规则增强,可疑为高度肿瘤。立体定向活检显示多形性胶质母细胞瘤。这是由已知CCM的“部位”引起的多形胶质母细胞瘤的独特案例。我们回顾了海绵畸形的遗传学文献,并提出了这些血管畸形的潜在致瘤机制。

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