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导致脊髓压迫且术前影像学检查结果不明确的脊髓硬膜内蛛网膜网:3例报告及文献复习

Spinal Intradural Arachnoid Webs Causing Spinal Cord Compression with Inconclusive Preoperative Imaging: A Report of 3 Cases and a Review of the Literature.

作者信息

Zhang Dafang, Papavassiliou Efstathios

机构信息

Department of Orthopaedic Surgery, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.

Department of Orthopaedic Surgery, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.

出版信息

World Neurosurg. 2017 Mar;99:251-258. doi: 10.1016/j.wneu.2016.12.015. Epub 2016 Dec 18.

Abstract

OBJECTIVE

Spinal arachnoid webs are a rare variant of spinal arachnoid cysts where 1 or multiple focal membranes of arachnoid tissue obstruct the subarachnoid space. Only 11 prior cases of arachnoid webs have been reported in the literature. We present a series of 3 consecutive cases of arachnoid webs from our institution and review the literature on this rare condition to provide recommendations for its management.

METHODS

Retrospective chart review was performed for 3 consecutive cases of intradural arachnoid webs causing spinal cord compression at our institution, with inconclusive preoperative imaging, treatment with surgical decompression, and resection. There were no external sources of funding.

RESULTS

Our cases occurred dorsally in the thoracic spine and were associated with syringomyelia. Preoperative magnetic resonance imaging, computed tomography myelography, and cine magnetic resonance imaging were inconclusive, and the definitive diagnosis was made with intraoperative ultrasound. Patients underwent laminectomies and resection of arachnoid webs. Unique from prior reports of arachnoid webs, the webs in the present cases were composed of multiple septated longitudinal membranes rather than a transverse band. All patients had improvement of presenting symptoms postoperatively.

CONCLUSIONS

Intradural arachnoid webs causing spinal cord compression are rare. Preoperative imaging may be inconclusive. Because of the septated longitudinal nature of the visualized membranes, we propose a 1-way valve mechanism of cerebrospinal fluid obstruction causing gradual cord compression and resultant syringomyelia.

摘要

目的

脊髓蛛网膜网是脊髓蛛网膜囊肿的一种罕见变异形式,其中蛛网膜组织的1个或多个局灶性膜阻塞蛛网膜下腔。文献中仅报道过11例蛛网膜网病例。我们展示了本机构连续3例蛛网膜网病例,并回顾了关于这种罕见病症的文献,以提供其治疗建议。

方法

对本机构3例导致脊髓受压的硬膜内蛛网膜网连续病例进行回顾性病历审查,术前影像学检查结果不明确,采用手术减压和切除术治疗。无外部资金来源。

结果

我们的病例发生在胸椎背侧,与脊髓空洞症相关。术前磁共振成像、计算机断层脊髓造影和电影磁共振成像结果不明确,术中超声做出明确诊断。患者接受了椎板切除术和蛛网膜网切除术。与既往蛛网膜网报道不同的是,本病例中的网由多个分隔的纵向膜组成,而非横向带。所有患者术后出现症状均有改善。

结论

导致脊髓受压的硬膜内蛛网膜网罕见。术前影像学检查结果可能不明确。由于所见膜的纵向分隔性质,我们提出一种脑脊液阻塞的单向瓣膜机制,导致脊髓逐渐受压并引发脊髓空洞症。

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