Skull base chordomas presenting with abducens nerve deficits: clinical characteristics and predictive factors for deficit improvement or resolution.

IF 3.5 2区 医学 Q1 CLINICAL NEUROLOGY
Nallammai Muthiah, Zachary C Gersey, Laura Le, Hussein Abdallah, Hussam Abou-Al-Shaar, S Tonya Stefko, Gabrielle R Bonhomme, Can Kocasarac, Eric W Wang, Carl H Snyderman, Paul A Gardner, Georgios A Zenonos
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引用次数: 0

Abstract

Objective: Skull base chordomas (SBCs) often present with cranial nerve (CN) VI deficits. Studies have not assessed the prognosis and predictive factors for CN VI recovery among patients presenting with CN VI deficits.

Methods: The medical records of patients who underwent resection for primary chordoma from 2001 to 2020 were reviewed. Those presenting with CN VI palsy were identified. The extent of CN VI deficit was determined to be partial or complete based on the Scott-Kraft score. The change in deficit from baseline was recorded within 3 days of surgery and at the 6-month follow-up. The postoperative course was followed until partial and/or complete deficit recovery. Univariate logistic regression models were created to predict improvement or resolution of CN VI deficit.

Results: A total of 113 patients with primary SBC were identified, 34 of whom presented with CN VI deficits: 24 (73%) with partial and 9 (27%) with complete deficits. The extent of deficit in 1 patient was unable to be determined. The median duration of deficit preoperatively was 3.6 months, and CN VI was most commonly radiographically abutted at the prepontine cistern and Dorello's canal. Twenty-three (68%) patients experienced at least partial CN VI recovery (mean 61 days, range 2-174 days). Nineteen (56%) patients experienced complete CN VI recovery (mean 162 days, range 2-469 days). No patients whose CN VI deficit worsened immediately after surgery achieved improvement in CN VI function at 6 months (p = 0.001). Preoperative partial (relative to complete) CN VI deficit was associated with greater odds of CN VI deficit improvement by 6 months (OR 7.7, p = 0.028). Factors not associated with deficit resolution included duration of deficit, CN VI involvement by tumor, total segments abutted by tumor, sex, age at diagnosis, gross-total resection, tumor volume, and adjuvant radiation therapy, although this analysis may have been underpowered to detect small differences.

Conclusions: Overall, 68% of patients achieved at least partial recovery in CN VI function after endoscopic skull base surgery. Among patients with partial CN VI palsy at baseline, 83% achieved CN VI recovery within 6 months and 75% achieved complete recovery within 14 months. For patients who presented with a complete CN VI deficit, within those same time frames, 33% and 11% achieved partial and complete recovery, respectively. Complete preoperative CN VI deficit was associated with lower odds of CN VI recovery by 6 months. The duration of preoperative deficit does not predict functional CN VI recovery.

以外展神经缺损为表现的颅底脊索瘤:临床特征和缺损改善或解决的预测因素。
目的:颅底脊索瘤(sbc)常表现为颅神经(CN) VI缺损。研究尚未评估CN VI缺损患者CN VI恢复的预后和预测因素。方法:回顾2001 ~ 2020年本院原发性脊索瘤切除术患者的病历。确定了患有CN VI麻痹的患者。根据Scott-Kraft评分确定CN VI缺陷的程度是部分或完全。在手术后3天和6个月的随访中记录了从基线开始的赤字变化。随访至部分和/或完全缺损恢复。建立了单变量logistic回归模型来预测CN VI缺陷的改善或解决。结果:共有113例原发性SBC患者被确定,其中34例表现为CN VI缺损:24例(73%)为部分缺损,9例(27%)为完全缺损。1例患者的缺损程度无法确定。术前缺损的中位持续时间为3.6个月,ccvi最常在术前池和Dorello管处毗邻。23例(68%)患者经历了至少部分CN VI恢复(平均61天,范围2-174天)。19例(56%)患者CN VI完全恢复(平均162天,范围2-469天)。术后CN VI缺损立即加重的患者在6个月时CN VI功能均未改善(p = 0.001)。术前部分(相对于完全)CN VI缺损与6个月CN VI缺损改善的几率较大相关(OR 7.7, p = 0.028)。与缺损解决无关的因素包括缺损持续时间、肿瘤累及的CN VI、肿瘤毗邻的总节段、性别、诊断时年龄、总切除量、肿瘤体积和辅助放射治疗,尽管该分析可能不足以发现微小的差异。结论:总体而言,68%的患者在内窥镜颅底手术后至少部分恢复了中冠VI功能。在基线时CN VI部分麻痹的患者中,83%的患者在6个月内恢复CN VI, 75%的患者在14个月内完全恢复。在相同的时间框架内,表现为完全CN VI缺损的患者,分别有33%和11%实现了部分和完全恢复。术前CN VI完全缺损与6个月CN VI恢复的几率较低相关。术前缺损的持续时间不能预测CN VI功能恢复。
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来源期刊
Journal of neurosurgery
Journal of neurosurgery 医学-临床神经学
CiteScore
7.20
自引率
7.30%
发文量
1003
审稿时长
1 months
期刊介绍: The Journal of Neurosurgery, Journal of Neurosurgery: Spine, Journal of Neurosurgery: Pediatrics, and Neurosurgical Focus are devoted to the publication of original works relating primarily to neurosurgery, including studies in clinical neurophysiology, organic neurology, ophthalmology, radiology, pathology, and molecular biology. The Editors and Editorial Boards encourage submission of clinical and laboratory studies. Other manuscripts accepted for review include technical notes on instruments or equipment that are innovative or useful to clinicians and researchers in the field of neuroscience; papers describing unusual cases; manuscripts on historical persons or events related to neurosurgery; and in Neurosurgical Focus, occasional reviews. Letters to the Editor commenting on articles recently published in the Journal of Neurosurgery, Journal of Neurosurgery: Spine, and Journal of Neurosurgery: Pediatrics are welcome.
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