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成人后颅窝胶质瘤。

Gliomas of the posterior fossa in adults.

机构信息

Department of Neurosurgery, Tel Aviv Medical Center, 6 Weizman Street, 64239, Tel Aviv, Israel.

出版信息

J Neurooncol. 2013 Dec;115(3):401-9. doi: 10.1007/s11060-013-1231-2. Epub 2013 Aug 27.

Abstract

Infratentorial gliomas are relatively rare tumors compared to their supratentorial counterparts. As such they have not been extensively characterized as a group and are usually excluded from clinical studies. Using our database we aimed to characterize adult gliomas involving the posterior fossa with respect to their clinical behavior and prognostic factors. We reviewed our neurosurgical and neuro-oncological data bases for adult patients diagnosed with gliomas involving the posterior fossa between 1996 and 2010. Of 1,283 glioma patients, 57 patients with gliomas involving the posterior fossa were identified (4.4 %). Tumors were further classified by location as primary brainstem (n = 21) and primary cerebellar (n = 18) tumors. On univariate analysis survival was correlated to tumor grade and KPS. In addition we have identified a unique group of patients (n = 18) with previously diagnosed supratentorial gliomas who subsequently developed noncontiguous secondary infratentorial extension of their tumors with subsequent rapid clinical deterioration. Gliomas of the posterior fossa comprise a heterogeneous group of tumors. Histological grade of the tumor was found to be the main prognostic factor. Survival of primary cerebellar gliomas is comparable to supra-tentorial gliomas, while brainstem gliomas in adults fare better than in the pediatric population. Secondary extension of supratentorial gliomas to the posterior fossa signifies a grave prognosis.

摘要

与幕上胶质瘤相比,小脑幕下胶质瘤较为少见。因此,它们并没有被广泛地作为一个整体进行描述,并且通常被排除在临床研究之外。我们利用数据库,旨在描述累及后颅窝的成人胶质瘤在临床行为和预后因素方面的特点。我们回顾了我们的神经外科和神经肿瘤学数据库,以确定 1996 年至 2010 年间诊断为累及后颅窝的胶质瘤的成年患者。在 1283 例胶质瘤患者中,发现了 57 例累及后颅窝的胶质瘤患者(4.4%)。肿瘤进一步根据位置分为原发性脑干(n=21)和原发性小脑(n=18)肿瘤。在单变量分析中,生存与肿瘤分级和 KPS 相关。此外,我们还发现了一组独特的患者(n=18),他们先前被诊断为幕上胶质瘤,随后肿瘤出现非连续的继发性小脑幕下延伸,随后临床迅速恶化。后颅窝的胶质瘤是一组异质性的肿瘤。肿瘤的组织学分级被发现是主要的预后因素。原发性小脑胶质瘤的生存率与幕上胶质瘤相当,而成人脑干胶质瘤的预后优于儿科人群。幕上胶质瘤向后颅窝的继发性延伸表明预后不良。

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