Department of Biomedical Sciences, Humanitas University, Via Rita Levi Montalcini 4, 20090 Pieve Emanuele, Milan, Italy.
Neurosurgery Department, IRCCS Humanitas Research Hospital, Via Manzoni 56, 20089 Rozzano, Milan, Italy.
Acta Neurochir (Wien). 2023 Sep;165(9):2513-2518. doi: 10.1007/s00701-023-05632-4. Epub 2023 May 24.
Ependymomas are glial cell tumors whose recommended treatment, according to the recent European guidelines, is surgical. Patient outcomes, in terms of progression-free survival and overall survival, are strongly related to the extent of resection. However, in some cases, critical locations and/or large dimensions could make a gross total resection challenging. In this article, we describe the surgical anatomy and technique of a combined telovelar-posterolateral approach for the resection of a giant posterior fossa ependymoma.
A 24-year-old patient who presented to our institution complaining of a 3-month history of headache, vertigo, and imbalance. Preoperative MRI scans showed a large mass within the fourth ventricle, extending towards the left cerebellopontine angle and perimedullary space through the homolateral Luschka foramen. Surgical treatment was proposed with the aims of releasing the preoperative symptoms, obtaining the tumor's histopathological and molecular definition, and preventing any future neurological deterioration. The patient gave his written consent for surgery and consented to the publication of his images. A combined telovelar-posterolateral approach was then performed to maximize the tumor's exposure and resection. Surgical technique and anatomical exposure have been extensively described, and a 2-dimensional operative video has been included.
The postoperative MRI scan demonstrated an almost complete resection of the lesion, with only a millimetric tumor remnant infiltrating the uppermost portion of the inferior medullary velum. Histo-molecular analysis revealed a grade 2 ependymoma. The patient was discharged home neurologically intact.
The combined telovelar-posterolateral approach allowed to achieve a near total resection of a giant multicompartimental mass within the posterior fossa in a single surgical stage.
室管膜瘤是一种神经胶质细胞瘤,根据最近的欧洲指南,其推荐的治疗方法是手术。患者的无进展生存期和总生存期的结果与切除范围密切相关。然而,在某些情况下,关键位置和/或大尺寸可能使大体全切除具有挑战性。本文描述了一种联合经穹窿后外侧入路切除巨大后颅窝室管膜瘤的手术解剖和技术。
一名 24 岁的患者因头痛、眩晕和失衡 3 个月来我院就诊。术前 MRI 扫描显示第四脑室有一个大肿块,向左侧桥小脑角和同侧面神经孔经侧 Luschka 孔延伸至延髓周围间隙。手术治疗的目的是缓解术前症状,获得肿瘤的组织病理学和分子定义,并防止任何未来的神经功能恶化。患者签署了手术同意书,并同意出版其图像。然后采用联合经穹窿后外侧入路最大限度地暴露和切除肿瘤。手术技术和解剖暴露已得到广泛描述,并包括了一个二维手术视频。
术后 MRI 扫描显示病变几乎完全切除,只有毫米级肿瘤残留浸润下髓帆的最上部。组织分子分析显示为 2 级室管膜瘤。患者出院时神经功能完整。
联合经穹窿后外侧入路可在单个手术阶段实现对后颅窝巨大多腔室肿块的近全切除。