Brachial plexus tumours: Diagnosis, treatment, surgical approach, and outcomes in a series of 47 patients

Neurocirugia (English Edition) Pub Date : 2026-09-01 Epub Date: 2026-03-20 DOI:10.1016/j.neucie.2026.500755
Alberto Isla, Sabela Vázquez, Beatriz Mansilla, María Santiago, Susana Santiago, Pablo Garcia-Feijoo
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Abstract

Introduction

Brachial plexus tumours are uncommon, with a prevalence of less than 5% of upper extremity tumours, and their surgical resection represents a major challenge due to the anatomical complexity of the region. The aim of this retrospective study is to analyze, in a large patient series, the clinical, radiological, and surgical characteristics of brachial plexus tumours, as well as to evaluate the different surgical approaches used according to tumour location and characteristics.

Material and methods

A retrospective study was conducted of all patients operated on for brachial plexus tumours between 2000 and 2025 at a tertiary center. Clinical, radiological, histological, surgical, and follow-up variables were collected. Approaches were classified as supraclavicular, infraclavicular, supra-infraclavicular, and posterior. Mild and severe neurological deficits were defined. Descriptive statistics and χ2 tests were used to analyze the relationship between tumour size and malignancy.

Results

Forty-seven patients were included (mean age: 48.5 years; 55.3% women). The most common symptom was pain (72.3%). The tumours were: schwannomas 29.8%, neurofibromas 27.7%, malignant 25.5%, metastases 4.3%, and miscellaneous 12.8%. Complete resection was achieved in 53.2%, being more frequent in schwannomas. The most frequent locations were the posterior cord and the inferior trunk. The size-malignancy relationship showed a non-significant trend towards higher malignancy in tumours >50 mm (p = 0.072). After surgery, 46.8% were left without sequelae; new motor deficit was more common in patients without prior deficits. Recurrences were recorded in 23.4% and progression of residual tumour in 14.9%.

Conclusions

Surgical resection of brachial plexus tumours depends on histological type, size, and their relationship with neurovascular structures. Schwannomas allowed a higher rate of total resection, unlike neurofibromas and malignant tumours, which were limited by infiltration and size. We highlight the usefulness of surgery for functional improvement, as most patients improved in this aspect, aided by intraoperative neurophysiological monitoring.
臂丛肿瘤:47例患者的诊断、治疗、手术入路和预后。
臂丛肿瘤并不常见,患病率不到上肢肿瘤的5%,由于该区域的解剖复杂性,其手术切除是一个重大挑战。本回顾性研究的目的是在大量患者中分析臂丛肿瘤的临床、放射学和外科特征,并根据肿瘤的位置和特征评估不同的手术入路。材料和方法:回顾性研究了2000年至2025年间在三级中心接受臂丛肿瘤手术的所有患者。收集临床、放射学、组织学、外科和随访变量。入路分为锁骨上入路、锁骨下入路、锁骨上-锁骨下入路和后路。定义轻度和重度神经功能缺损。采用描述性统计和χ2检验分析肿瘤大小与恶性程度的关系。结果:纳入47例患者(平均年龄48.5岁,女性55.3%)。最常见的症状是疼痛(72.3%)。其中:神经鞘瘤29.8%,神经纤维瘤27.7%,恶性25.5%,转移性4.3%,杂性12.8%。53.2%的患者完全切除,在神经鞘瘤中更为常见。最常见的部位是后束和下干。肿瘤大小与恶性程度的关系显示,bbb50 mm肿瘤的恶性程度增高趋势不显著(P=072)。术后无后遗症46.8%;新的运动障碍在先前没有运动障碍的患者中更为常见。复发占23.4%,残余肿瘤进展占14.9%。结论:臂丛肿瘤的手术切除取决于其组织学类型、大小及其与神经血管结构的关系。神经鞘瘤与受浸润和大小限制的神经纤维瘤和恶性肿瘤不同,神经鞘瘤的全切除率更高。我们强调手术对功能改善的有用性,因为大多数患者在术中神经生理监测的帮助下在这方面有所改善。
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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