特发性脊髓空洞伴隐蔽性蛛网膜网:神经病理特征、鉴别诊断和手术策略。

IF 3.6 2区 医学 Q1 CLINICAL NEUROLOGY
Neurospine Pub Date : 2025-09-01 Epub Date: 2025-09-30 DOI:10.14245/ns.2550278.139
Chunli Lu, Min Yin, Fan Yuan, Chenyuan Ding, Xingwen Wang, Fengzeng Jian
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引用次数: 0

摘要

目的:特发性脊髓空洞伴隐蔽性蛛网膜病变是一种相对罕见的疾病,其特点是发病微妙,临床表现不典型,诊断和治疗具有重大挑战。本研究旨在评估IS的影像学和临床病理特征,以改善手术治疗和患者预后。方法:在本研究中,回顾性地从2020年12月至2025年3月的单中心脊髓空洞数据库(N=1,039)中提取临床和放射学数据。其中,15例确诊为IS的患者术前进行了磁共振成像和脊髓造影,以准确确定负责的脊柱节段。收集围手术期综合评估及临床结果。术中,充分探查蛛网膜下腔(SAS),彻底切除增厚和附着的蛛网膜组织,恢复脑脊液(CSF)的正常循环。此外,将IS的临床资料、病理特征和手术结果与创伤后迟发性脊髓空洞(PTDS)进行比较,以评估潜在的差异。结果:在本研究中,所有患者术前均行脊髓造影,显示不同程度的SAS梗阻。对于接受精确和全面蛛网膜溶解的IS病例,总体术后结果良好。术中病理证实所有IS病例均以非感染性、非急性炎症为特征。术前最大喉喉/脐带比值平均为0.70±0.07(范围0.54 ~ 0.88),喉喉分辨率为12.2% ~ 100%,平均改善29.6%。PTDS患者表现出相对较高的感觉不良发生率和较大的注射器张力指数。然而,IS和PTDS在鼻管长度、偏差或位置方面没有显著差异。值得注意的是,与PTDS组相比,IS组表现出明显更好的术后脊髓空洞缓解和脊髓空洞相关症状的改善。结论:虽然IS和PTDS有共同的蛛网膜粘连机制,但它们在病理特征、治疗方法和临床结果上存在显著差异。在IS病例中,在患节段进行彻底的脊髓蛛网膜溶解可以恢复正常的脊髓搏动和脑脊液循环,从而有效地解决鼻塞问题,获得良好的长期预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Novel Clinical Insight Into Idiopathic Syringomyelia With Occult Arachnoid Webs: Neuropathological Features, Differential Diagnosis, and Surgical Strategy.

A Novel Clinical Insight Into Idiopathic Syringomyelia With Occult Arachnoid Webs: Neuropathological Features, Differential Diagnosis, and Surgical Strategy.

A Novel Clinical Insight Into Idiopathic Syringomyelia With Occult Arachnoid Webs: Neuropathological Features, Differential Diagnosis, and Surgical Strategy.

A Novel Clinical Insight Into Idiopathic Syringomyelia With Occult Arachnoid Webs: Neuropathological Features, Differential Diagnosis, and Surgical Strategy.

Objective: Idiopathic syringomyelia (IS) associated with occult arachnoid pathology is a relatively rare condition characterized by a subtle onset, atypical clinical manifestations, and significant diagnostic and therapeutic challenges. This study aims to evaluate the radiographic and clinicopathological features of IS to improve surgical management and patient outcomes.

Methods: In this study, clinical and radiologic data were retrospectively extracted from a single-center syringomyelia database (N=1,039) spanning December 2020 to March 2025. Among these, 15 patients diagnosed with IS underwent preoperative magnetic resonance imaging and myelography to identify the responsible spinal segments precisely. Comprehensive perioperative assessments and clinical outcomes were collected. During surgery, the subarachnoid space (SAS) was thoroughly explored, with complete removal of thickened and adherent arachnoid tissue to restore normal cerebrospinal fluid (CSF) circulation. Additionally, clinical data, pathological features, and surgical outcomes of IS were compared to those of posttraumatic delayed syringomyelia (PTDS) to evaluate potential differences.

Results: In this series, all patients underwent preoperative myelography, revealing varying degrees of SAS obstruction. For IS cases that received precise and comprehensive arachnoid lysis, overall postoperative outcomes were favorable. Intraoperative pathology confirmed that all IS cases were characterized by noninfectious, nonacute inflammation. The preoperative maximal syrinx/cord ratio averaged 0.70±0.07 (range, 0.54-0.88), while the syrinx resolution rate varied from 12.2% to 100%, with a mean improvement of 29.6%. Patients with PTDS exhibited a relatively higher incidence of hypesthesia and a greater syrinx tension index. However, no significant differences were observed between IS and PTDS in terms of syrinx length, deviation, or location. Notably, the IS group demonstrated significantly better postoperative syrinx resolution and improvement in syringomyelia-related symptoms compared to the PTDS group.

Conclusion: While both IS and PTDS share a common underlying mechanism of arachnoid adhesions, they differ significantly in pathological features, treatment approaches, and clinical outcomes. In cases of IS, thorough spinal arachnoid lysis at the affected segment could restore normal spinal cord pulsation and CSF circulation, leading to effective syrinx resolution and a favorable long-term prognosis.

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Neurospine
Neurospine Multiple-
CiteScore
5.80
自引率
18.80%
发文量
93
审稿时长
10 weeks
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