神经胶质瘤治疗的循证进展

M. A. Samad, K. Nathani, U. K. Choudry, M. Waqas, S. Khan, S. Enam
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引用次数: 1

摘要

胶质瘤是起源于神经胶质的原发性脑肿瘤。多形性胶质母细胞瘤传统上被归类为IV级胶质肿瘤,预后最差。在过去的几十年里,诊断和治疗的重点逐渐转向分子和基因分析。这伴随着放射学、放射学和医学肿瘤学的进步。尽管在个别学科方面取得了重大进展,但总体预后并没有显著增加。对于大多数此类肿瘤需要最大限度的安全切除已达成共识。通过术前成像获得的解剖细节和白质束。这些详细的放射学模式允许外科医生计划一个安全的轨迹到病变,避免神经系统并发症。五氨基乙酰丙酸和荧光素引导有助于增加切除范围。清醒开颅与脑测绘已重新流行的安全切除低级别胶质瘤,特别是那些位于流利区。在这篇综述文章中,我们讨论了胶质瘤治疗的各个方面,包括诊断和手术切除。
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Evidence-based advances in glioma management
Glioma is primary brain tumors of the glial origin. Glioblastoma multiforme traditionally classified as Grade IV glial tumor carries the worst prognosis. Over the past decades, focus of the diagnosis and management has gradually shifted toward molecular and genetic profiling. This has been accompanied by advancement in radiology, radiation, and medical oncology. Despite significant progress in the individual disciplines, the overall prognosis has not increased significantly. There is consensus on the need of maximum safe resection for most of these tumors. Details of anatomy and white matter tracts obtained through preoperative imaging. These detailed radiological modalities allow the surgeons to plan a safe trajectory to the lesion, avoiding neurological complications. Five aminolevulinic acid and fluorescein guidance help increasing the extent of resection. Awake craniotomy with brain mapping has regained popularity for the safe resection of low-grade glioma, especially those located in eloquent areas. In this review article, we have discussed various aspect of glioma management including diagnosis and surgical resection.
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