Department of Neurosurgery, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Department of Neurology, St. Josef-Hospital Bochum, Ruhr University Bochum, Bochum, Germany.
BMC Neurol. 2020 Feb 13;20(1):55. doi: 10.1186/s12883-020-01637-z.
Perineuriomas are rare benign peripheral nerve sheath tumours of perineurial cell origin and can be classified into intraneural and extraneural perineuriomas. They most commonly present a mononeuropathy of gradual onset and slow progression, resulting in progressive neurological deficits like hypoesthesia or motor weakness. Therapy is still variable. Aim of the study was to compare our surgical treatment and our follow-up regime including high-resolution nerve sonography with the current literature to evaluate best treatment of perineuriomas.
Retrospective analysis of our dataset "peripheral nerve lesion" to identify patients suffering from perineuriomas between 01.01.2012 until 31.12.2018. Surgical treatment and the follow-up examination of three patients were described. Additionally, a systematic review including PubMed, the Cochrane Collaboration Library, Scopus and Google Scholar was performed for literature published between January 1, 1990 and October 31, 2019 independently by 2 authors.
In the first case, the left ulnar nerve was affected. In the second case, the left peroneal nerve and in the third case the right median nerve was affected. High-resolution nerve sonography was performed in each case. All patients underwent interfascicular neurolysis combined with a targeted fascicular biopsy under electrophysiological monitoring. Neurological deficits improved subsidized by rehabilitation. Surgical therapy and the neurological outcome were compared with literature. Systematic review revealed 22 articles, which met the inclusion criteria. Therefore, demographics, surgical treatment and neurological outcome of 77 patients were analysed.
Perineuriomas are rare benign nerve sheath tumours with a slow progression, sometimes difficult to diagnose. Decompression and neurolysis may improve neurological deficits. High resolution nerve sonography might serve as a helpful additional diagnostic tool in this process.
神经鞘瘤是一种起源于神经鞘雪旺细胞的罕见良性周围神经鞘肿瘤,可分为神经内和神经外神经鞘瘤。它们最常表现为逐渐发作和缓慢进展的单神经病,导致感觉减退或运动无力等进行性神经功能缺损。治疗仍存在差异。本研究的目的是比较我们的手术治疗和我们的随访方案,包括高分辨率神经超声检查,并结合当前文献,以评估神经鞘瘤的最佳治疗方法。
回顾性分析我们的“周围神经病变”数据集,以确定 2012 年 1 月 1 日至 2018 年 12 月 31 日期间患有神经鞘瘤的患者。描述了三名患者的手术治疗和随访检查。此外,我们还独立地通过两位作者在 PubMed、Cochrane 协作图书馆、Scopus 和 Google Scholar 上进行了文献的系统评价,文献发表时间为 1990 年 1 月 1 日至 2019 年 10 月 31 日。
在第一个病例中,左侧尺神经受到影响。在第二个病例中,左侧腓总神经受到影响,在第三个病例中,右侧正中神经受到影响。在每种情况下都进行了高分辨率神经超声检查。所有患者均在电生理监测下接受束间神经松解术联合靶向束活检。神经功能缺损在康复的辅助下得到改善。将手术治疗和神经学结果与文献进行比较。系统评价显示,有 22 篇文章符合纳入标准。因此,分析了 77 例患者的人口统计学、手术治疗和神经学结果。
神经鞘瘤是一种罕见的良性神经鞘肿瘤,进展缓慢,有时难以诊断。减压和神经松解术可能改善神经功能缺损。高分辨率神经超声检查在这一过程中可能作为一种有用的辅助诊断工具。