A comprehensive analysis of ganglioneuromas: a 30-year experience of 101 patients.

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY
Journal of neurosurgery Pub Date : 2026-07-31 Print Date: 2026-10-01 DOI:10.3171/2026.2.JNS252992
Pavlos Texakalidis, Rahul Gogoi, Robert J Spinner
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引用次数: 0

Abstract

Objective: Ganglioneuromas (GNs) are rare benign tumors arising from sympathetic neural crest derivatives, with limited large-scale data guiding management. The objective of this study was to characterize the clinical presentation, imaging features, surgical management, and long-term outcomes of patients with GN treated at a single institution over a 30-year period.

Methods: The authors conducted a retrospective review of all patients diagnosed with GN between 1995 and 2025 at a single institution. Clinical data, imaging characteristics, operative details, perioperative complications, and long-term outcomes were abstracted.

Results: A total of 101 patients (62.3% female, mean age 26.9 ± 15.9 years) were identified. Tumors most commonly arose in the retroperitoneum (n = 46, 45.5%), thoracic paraspinal/mediastinal region (n = 33, 32.7%), presacral space (n = 18, 17.8%), and cervical region (n = 4, 4%). The mean tumor dimensions on MRI were 8.5 ± 3.8 × 6.6 ± 3.2 × 5.8 ± 3.7 cm. Most lesions (72%) were incidental findings. Seventy patients underwent 72 surgeries, of which 69.4% had preoperative biopsy confirmation. Gross-total resection (GTR) was achieved in 73.6% of cases (53/72) and subtotal resection (STR) was performed in 26.4% (19/72). Short-term postoperative complications occurred in 43.1% of cases, most commonly neurological deficits (22.2%). The mean hospital length of stay was 4.6 ± 3.7 days. At the final follow-up (mean duration 33.8 ± 42.6 months), 46.5% of patients were stable, 42.3% had improved, and 11.3% had worsened from baseline. Two patients experienced recurrence (2.9%, 2/70). No malignant transformations were observed. Thirty-one patients were managed with observation (mean age 32.3 ± 17.7 years; mean follow-up duration 90.9 ± 151 months). Observation was chosen primarily due to proximity to major vascular or neural structures (74.2%). No patient in the observation group developed new symptoms, and 2 tumors exhibited minimal interval growth (0.08-0.17 cm/year).

Conclusions: GNs demonstrate indolent behavior, low recurrence rates, and no observed malignant transformation in this large cohort. GTR is achievable in most cases, but STR provides excellent long-term control when required to avoid morbidity. Observation is safe for asymptomatic tumors, particularly when adjacent to critical structures, with no growth observed on long-term follow-up, except for minimal growth in few cases. These findings support an individualized, risk-based approach to management.

神经节神经瘤的综合分析:30年101例患者的经验。
目的:神经节神经瘤(Ganglioneuromas, GNs)是一种罕见的交感神经嵴衍生的良性肿瘤,缺乏大规模的数据指导治疗。本研究的目的是描述在单一机构治疗的GN患者在30年期间的临床表现、影像学特征、手术处理和长期结果。方法:作者对1995年至2025年间在单一机构诊断为GN的所有患者进行了回顾性分析。总结临床资料、影像学特征、手术细节、围手术期并发症及远期预后。结果:共发现101例患者,其中女性62.3%,平均年龄26.9±15.9岁。肿瘤最常发生在腹膜后(n = 46, 45.5%)、胸椎旁/纵隔区域(n = 33, 32.7%)、骶前间隙(n = 18, 17.8%)和颈椎区域(n = 4, 4%)。MRI平均肿瘤尺寸为8.5±3.8 × 6.6±3.2 × 5.8±3.7 cm。大多数病变(72%)是偶然发现的。70例患者共进行了72次手术,其中69.4%的患者术前活检证实。73.6%(53/72)的病例实现了总切除(GTR), 26.4%(19/72)的病例实现了次全切除(STR)。术后短期并发症发生率为43.1%,最常见的是神经功能缺损(22.2%)。平均住院时间4.6±3.7天。在最后的随访中(平均持续时间33.8±42.6个月),46.5%的患者病情稳定,42.3%的患者病情好转,11.3%的患者病情较基线恶化。2例复发(2.9%,2/70)。未见恶性转化。31例患者接受观察,平均年龄(32.3±17.7)岁,平均随访时间(90.9±151)个月。选择观察主要是因为靠近主要血管或神经结构(74.2%)。观察组患者无新症状出现,2例肿瘤间期生长极小(0.08 ~ 0.17 cm/年)。结论:在这个庞大的队列中,GNs表现出惰性行为,低复发率,未观察到恶性转化。在大多数情况下,GTR是可以实现的,但STR在需要时提供了良好的长期控制,避免了发病率。对于无症状的肿瘤,特别是与关键结构相邻的肿瘤,观察是安全的,在长期随访中没有观察到生长,除了少数病例有微小的生长。这些发现支持个体化的、基于风险的管理方法。
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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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