Division of Plastic and Reconstructive Surgery, Department of Surgery, University of Florida.
Lilian S. Wells Department of Neurosurgery, University of Florida College of Medicine, Gainesville, Florida, USA.
Int J Surg. 2023 Apr 1;109(4):972-981. doi: 10.1097/JS9.0000000000000309.
Various treatment options have been introduced for the management of primary tumors of the brachial plexus (BP), ranging from conservative therapy to wide local excision with/without postoperative chemoradiotherapy. However, no consensus exists regarding optimal treatment strategies based on collated and published data.
The aim of this study was to investigate the clinicopathological characteristics and outcome of patients with primary tumors of the BP who underwent surgical treatment.
A systematic search of the four main online databases, including Web of Science (WOS), PubMed, Scopus, and Google Scholar, was conducted.
All related articles addressing the clinical outcome and role of surgical interventions for management of primary tumors of the BP.
Optimal surgical and radiotherapeutic interventions for benign and malignant lesions based on the pathologic characteristics and location of primary BP tumors.
A total of 687 patients (693 tumors) with a mean age of 41.7±8.7 years old were evaluated. In total, 629 (90.8%) tumors were benign, and 64 (9.2%) were malignant, with a mean tumor size of 5.4±3.1 cm. The location of the tumor was reported for 639 patients. For these tumors, 444 (69.5%) originated from the supraclavicular region, and 195 (30.5%) were infraclavicular. The trunks were the most common location for tumor involvement, followed by the roots, cords, and terminal branches. Gross total resection was achieved in 432 patients and subtotal resection (STR) was performed in 109 patients. With neurofibromas, STR still resulted in good outcomes. The outcomes following treatment of malignant peripheral nerve sheath tumors were poor regardless of the type of resection. In general, symptoms related to pain and sensory issues resolved rapidly postoperatively. However, the resolution of motor deficits was often incomplete. Local tumor recurrence occurred in 15 (2.2%), patients and distant metastasis was observed in only eight (1.2%) cases. The overall mortality was 21 (3.1%) patients among the study population.
The main limitation was the lack of level I and II evidence.
The ideal management strategy for primary BP tumors is complete surgical resection. However, in some cases, particularly for neurofibromas, STR may be preferable to preserve maximal neurological function. The degree of surgical excision (total or subtotal) mainly depends on the pathological characteristics and primary location of the tumor.
对于臂丛原发性肿瘤的治疗,已经提出了各种治疗方案,包括从保守治疗到广泛局部切除加/或术后放化疗。然而,基于已发表的数据,目前还没有关于最佳治疗策略的共识。
本研究旨在探讨接受手术治疗的臂丛原发性肿瘤患者的临床病理特征和结局。
对包括 Web of Science(WOS)、PubMed、Scopus 和 Google Scholar 在内的四个主要在线数据库进行了系统检索。
所有涉及臂丛原发性肿瘤临床结局和手术干预作用的相关文章。
根据臂丛原发性肿瘤的病理特征和位置,对良性和恶性病变进行最佳的手术和放射治疗干预。
共评估了 687 例(693 个肿瘤)平均年龄为 41.7±8.7 岁的患者。其中 629 例(90.8%)肿瘤为良性,64 例(9.2%)为恶性,肿瘤平均大小为 5.4±3.1cm。报告了 639 例患者的肿瘤位置。对于这些肿瘤,444 例(69.5%)起源于锁骨上区,195 例(30.5%)起源于锁骨下区。肿瘤最常累及干,其次是根、索和终末支。432 例患者实现了全切除,109 例患者行次全切除术(STR)。对于神经纤维瘤,STR 仍能获得良好的结果。无论切除类型如何,恶性外周神经鞘瘤的治疗结局均较差。一般来说,与疼痛和感觉问题相关的症状术后迅速缓解。然而,运动功能缺损的恢复往往不完全。15 例(2.2%)患者出现局部肿瘤复发,8 例(1.2%)患者出现远处转移。研究人群中总的死亡率为 21 例(3.1%)。
主要的局限性在于缺乏 I 级和 II 级证据。
对于臂丛原发性肿瘤,理想的治疗策略是完全手术切除。然而,在某些情况下,特别是对于神经纤维瘤,STR 可能更有利于保留最大的神经功能。手术切除的程度(完全或次全)主要取决于肿瘤的病理特征和原发部位。