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同时存在 L1-2 椎间盘膨出和移动性脊神经鞘瘤导致马尾综合征:一例罕见病例报告。

Simultaneous L1-2 Bulged Disc and Mobile Spinal Schwannoma Causing Cauda Equina Syndrome: A Rare Case Report.

机构信息

Bone & Joint Diseases Research Center, Department of Orthopedic Surgery, Shiraz University of Medical Sciences, Shiraz, Iran.

Department of Neurosurgery, Georgetown University, Comprehensive Brain Tumor Center, MedStar Georgetown, Washington, DC, USA.

出版信息

Am J Case Rep. 2024 May 25;25:e942717. doi: 10.12659/AJCR.942717.

Abstract

BACKGROUND Aside from the rarity of mobile spinal schwannomas, the coexistence of these tumors with herniated intervertebral disc is also scarce. Furthermore, cauda equina syndrome (CES), as a manifestation of intraspinal schwannomas has been reported rarely. Described here is a case of simultaneous lumbar disc bulge and mobile spinal schwannoma presented with intermittent symptoms of CES. CASE REPORT A 62-year-old man presented with severe but intermittent leg pain for 2 weeks, which later progressed to an episode of lower extremity weakness and difficulty in urination. Magnetic resonance imaging revealed an intraspinal tumor that moved in position relative to the L1-2 disc bulge on scans 6 h apart, with associated spontaneous regression in symptoms. The tumor was found to be a mobile spinal schwannoma, originated from a nerve root. A standard microdissection technique was used to remove the tumor through a spinous process-sparing unilateral approach, with complete laminectomy of L1. Use of intraoperative ultrasound facilitated the accurate tumor localization. Postoperatively, the patient no longer had symptoms. CONCLUSIONS This report presents a combination of a common spinal pathology, intervertebral disc herniation, alongside a rare condition, mobile spinal schwannoma, whose uncommon clinical manifestations, such as CES can cause irreversible neurological deficits. Surgeons need to remain vigilant of potential atypical scenarios when treating patients. Surgical treatment challenges regarding the mobility of tumors, such as accurate localization, should be addressed using intraoperative imaging to avoid wrong-level surgery. To mitigate the irreversible neurological complications, patients should receive comprehensive information for alarming signs of CES.

摘要

背景

除了脊髓神经鞘瘤罕见的移动性外,这些肿瘤与椎间盘突出并存也很少见。此外,马尾综合征(CES)作为椎管内神经鞘瘤的一种表现形式也很少有报道。本文描述了一例同时存在腰椎间盘膨出和脊髓神经鞘瘤的病例,表现为 CES 的间歇性症状。

病例报告

一名 62 岁男性因严重但间歇性腿部疼痛持续 2 周就诊,随后进展为下肢无力和排尿困难。磁共振成像显示椎管内肿瘤在相隔 6 小时的扫描中相对于 L1-2 椎间盘膨出移动,症状自发缓解。肿瘤被发现是一个移动的脊髓神经鞘瘤,起源于神经根。采用标准的显微解剖技术,通过棘突保留的单侧入路切除肿瘤,对 L1 进行全椎板切除术。术中超声的使用有助于肿瘤的准确定位。术后,患者不再有症状。

结论

本报告介绍了一种常见的脊柱病理,即椎间盘突出症,以及一种罕见的情况,即移动性脊髓神经鞘瘤,其不常见的临床表现,如 CES,可能导致不可逆的神经功能缺损。外科医生在治疗患者时需要警惕潜在的非典型情况。对于肿瘤的移动性等手术治疗挑战,如准确的定位,应使用术中影像学来避免错误的手术水平。为了减轻不可逆的神经并发症,应向患者提供 CES 报警信号的全面信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d508/11138359/3141deb1737e/amjcaserep-25-e942717-g001.jpg

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