Endoscope-assisted Trans-lamina Terminalis Resection of Chordoid Glioma at the Third Ventricle: A Case Report.

NMC case report journal Pub Date : 2023-10-14 eCollection Date: 2023-01-01 DOI:10.2176/jns-nmc.2023-0107
Yuichi Oda, Kosaku Amano, Kentaro Chiba, Kenta Masui, Takakazu Kawamata
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Abstract

As per the 2021 World Health Organization (WHO) Classification of Tumors of the Central Nervous System, chordoid glioma (CG) is defined as a slow-growing glial neoplasm categorized as grade II tumor. This tumor is primarily located in the anterior part of the third ventricle, often adheres to important surrounding structures, and is hemorrhagic in nature. Therefore, dissecting this tumor is extremely difficult. In this study, we present the case of a 44-year-old man who initially complained of mild headache and was diagnosed with a homogeneous gadolinium-enhanced lesion in the third ventricle via magnetic resonance imaging. The pathological diagnosis based on his biopsy at the previous hospital was CG. The patient demonstrated no neurological deficit at that time, but the tumor had gradually grown, hydrocephalus appeared 2 years after the tumor was detected, and the patient developed short memory disorder and daytime sleepiness. We resected the tumor via the anterior interhemispheric trans-lamina terminalis approach using a microscope and an endoscope. The residual tumor at the blind spot of the microscopic view was resected under an angled rigid endoscopic view using dedicated tools for transsphenoidal surgery. The tumor was grossly resected, and the histopathological diagnosis was CG. Postoperative neurological findings included slight memory disorder and hypothalamic adrenal dysfunction. No tumor recurrence was reported 3 years post resection. The endoscope-assisted anterior interhemispheric trans-lamina terminalis approach was determined useful for CG resection with minimal surgical complications and without tumor recurrence.

内窥镜辅助经终板切除第三脑室脊索样胶质瘤1例。
根据2021年世界卫生组织(WHO)中枢神经系统肿瘤分类,脊索样胶质瘤(CG)被定义为一种生长缓慢的神经胶质肿瘤,被归类为II级肿瘤。该肿瘤主要位于第三脑室前部,常附着于重要的周围结构,具有出血性。因此,解剖这个肿瘤是非常困难的。在本研究中,我们报告了一名44岁男性的病例,他最初抱怨轻微头痛,并通过磁共振成像诊断为第三脑室均匀钆增强病变。先前医院活检病理诊断为CG。患者当时无神经功能障碍,但肿瘤逐渐生长,发现肿瘤2年后出现脑积水,患者出现短时记忆障碍及白天嗜睡。我们在显微镜和内窥镜下经前半球间经终末板入路切除肿瘤。在经过蝶窦手术的专用工具下,在有角度的刚性内镜下切除显微镜视图盲点处的残留肿瘤。大体切除肿瘤,组织病理诊断为CG。术后神经学表现包括轻微记忆障碍和下丘脑肾上腺功能障碍。术后3年未见肿瘤复发。内窥镜辅助的前半球间经终末板入路被确定为CG切除术的有效方法,手术并发症少,肿瘤无复发。
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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