The Natural History and Treatment of Meningiomas: An Update.

IF 1.8 4区 医学 Q3 CLINICAL NEUROLOGY
Seminars in Neurology Pub Date : 2024-02-01 Epub Date: 2023-12-05 DOI:10.1055/s-0043-1777352
Arsene Daniel Nyalundja, Fabrice Mugisha, Claire Karekezi
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引用次数: 0

Abstract

Meningiomas are the most frequent nonmalignant tumors of the central nervous system (CNS). Despite their benign nature and slow-growing pattern, if not diagnosed early, these tumors may reach relatively large sizes causing significant morbidity and mortality. Some variants are located in hard-to-access locations, compressing critical neurovascular structures, and making the surgical management even more challenging. Although most meningiomas have a good long-term prognosis after treatment, there are still controversies over their management in a subset of cases. While surgery is the first-line treatment, the use of fractionated radiotherapy or stereotactic radiosurgery is indicated for residual or recurrent tumors, small lesions, and tumors in challenging locations. Advances in molecular genetics and ongoing clinical trial results have recently helped both to refine the diagnosis and provide hope for effective biomolecular target-based medications for treatment. This article reviews the natural history and current therapeutic options for CNS meningiomas.

脑膜瘤的自然史和治疗:最新进展。
脑膜瘤是中枢神经系统(CNS)最常见的非恶性肿瘤。尽管脑膜瘤是良性肿瘤,且生长缓慢,但如果不及早诊断,这些肿瘤可能会发展到相对较大的规模,导致严重的发病率和死亡率。有些变异瘤位于难以进入的位置,压迫重要的神经血管结构,使手术治疗更具挑战性。虽然大多数脑膜瘤经治疗后长期预后良好,但对部分病例的治疗仍存在争议。虽然手术是一线治疗方法,但对于残留或复发的肿瘤、小病灶和位置特殊的肿瘤,可采用分次放射治疗或立体定向放射外科治疗。最近,分子遗传学的进展和正在进行的临床试验结果有助于完善诊断,并为基于生物分子靶点的有效药物治疗带来了希望。本文回顾了中枢神经系统脑膜瘤的自然史和目前的治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Seminars in Neurology
Seminars in Neurology 医学-临床神经学
CiteScore
4.60
自引率
3.70%
发文量
65
审稿时长
6-12 weeks
期刊介绍: Seminars in Neurology is a review journal on current trends in the evaluation, diagnosis, and treatment of neurological diseases. Areas of coverage include multiple sclerosis, central nervous system infections, muscular dystrophy, neuro-immunology, spinal disorders, strokes, epilepsy, motor neuron diseases, movement disorders, higher cortical function, neuro-genetics and neuro-ophthamology. Each issue is presented under the direction of an expert guest editor, and invited contributors focus on a single, high-interest clinical topic. Up-to-the-minute coverage of the latest information in the field makes this journal an invaluable resource for neurologists and residents.
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