Common peroneal nerve schwannomas around the knee: a surgical case series of 44 patients and systematic review of the literature.

IF 3.6 2区 医学 Q1 CLINICAL NEUROLOGY
Godard C W de Ruiter, Kirsten M Hayford, Thomas F H Vissers, Robert J Spinner
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引用次数: 0

Abstract

Objective: Resection of common peroneal nerve (CPN) schwannomas is generally believed to be associated with a high risk of postoperative deficit, especially the chance for development of a foot drop. The goal of this study was to investigate the surgical results for resection of schwannomas from the CPN around the knee and specifically the chance of developing a postoperative motor deficit.

Methods: Data from 36 patients with sporadic schwannomas and 8 patients with schwannomatosis (12 schwannomas total) treated at two centers were retrospectively analyzed. For sporadic cases, different locations around the knee were compared (i.e., proximal to the fibular head [FH], at the FH, and distal to the FH), taking into account the preoperative duration of symptoms, size at presentation, and surgical results of resection. The literature was systematically reviewed for reported cases by searching the PubMed and Embase databases.

Results: A total of 24 schwannomas proximal to the FH were surgically treated: 11 at the FH, and 13 distal to the FH. For the entire cohort, the mean size of CPN schwannomas distal to the FH at presentation was smaller (1.4 × 1.8 cm) compared with those proximal to (2.0 × 2.2 cm) and at (2.2 × 2.3 cm) the FH, although these differences were not statistically significant. The mean preoperative duration of symptoms was slightly longer for schwannomas distal to the FH (35 months) than for those proximal to the FH (21 months) and at the FH (27 months); however, this difference was not significant. Postoperative deficits occurred in 3 sporadic cases: 2 patients with temporary weakness (Medical Research Council grade 4) that completely resolved within several months and 1 patient who had previously undergone surgery elsewhere and presented with deficits and in whom weakness increased after resection. Improvement in preoperative deficits was observed in 1 patient with extensor hallucis longus muscle paralysis that completely recovered. One patient with schwannomatosis developed muscle weakness after resection of a plexiform schwannoma. A systematic review of 21 previously reported cases in the literature showed that larger CPN schwannomas (> 5 cm) were more likely to result in permanent motor deficits.

Conclusions: This retrospective study of 44 patients shows that peroneal nerve schwannomas around the knee can be safely removed with a low risk of deficits. The systematic review of the literature suggests that larger schwannomas are more likely to result in permanent deficit. In the authors' opinion, CPN schwannomas can best be resected, preferably when the lesion is relatively small.

膝周围腓总神经鞘瘤:44例手术病例及文献系统回顾。
目的:腓总神经鞘瘤切除术通常被认为与术后缺陷的高风险相关,特别是发生足下垂的机会。本研究的目的是研究切除膝关节周围神经鞘瘤的手术结果,特别是术后发生运动障碍的机会。方法:回顾性分析36例散发性神经鞘瘤患者和8例神经鞘瘤病患者(共12例神经鞘瘤)的治疗资料。对于散发性病例,比较膝关节周围的不同位置(即腓骨头近端、腓骨头远端和腓骨头远端),同时考虑症状的术前持续时间、出现时的大小和手术切除结果。通过检索PubMed和Embase数据库,系统地回顾了文献中报告的病例。结果:共手术治疗了24例FH近端神经鞘瘤:FH 11例,FH远端13例。在整个队列中,与FH近端(2.0 × 2.2 cm)和FH近端(2.2 × 2.3 cm)相比,FH远端CPN神经鞘瘤的平均大小(1.4 × 1.8 cm)更小,尽管这些差异没有统计学意义。远端神经鞘瘤的平均术前症状持续时间(35个月)略长于近端神经鞘瘤(21个月)和远端神经鞘瘤(27个月);然而,这种差异并不显著。3例散发性病例出现术后缺陷:2例患者出现暂时性虚弱(医学研究委员会4级),在几个月内完全消失;1例患者先前在其他地方接受过手术,出现缺陷,切除后虚弱加重。1例拇长伸肌麻痹患者的术前缺陷得到改善,并完全恢复。一例神经鞘瘤患者在丛状神经鞘瘤切除后出现肌肉无力。对21例既往文献报道病例的系统回顾显示,较大的CPN神经鞘瘤(直径50 cm)更有可能导致永久性运动障碍。结论:这项对44例患者的回顾性研究表明,膝关节周围腓神经鞘瘤可以安全切除,缺损风险低。对文献的系统回顾表明,较大的神经鞘瘤更有可能导致永久性缺陷。笔者认为,CPN神经鞘瘤最好切除,切除时病灶相对较小为佳。
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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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