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S1 神经根症状性特发性非交通性硬脊膜蛛网膜囊肿:一例报告。

Symptomatic idiopathic noncommunicating intradural arachnoid cyst of the S1 nerve root: a case report.

机构信息

Department of Neurosurgery, Military Medical Academy, Belgrade, Serbia.

出版信息

Spine (Phila Pa 1976). 2011 Jun 15;36(14):E979-82. doi: 10.1097/BRS.0b013e3181fd679a.

Abstract

STUDY DESIGN

A case report of a rare symptomatic, idiopathic, noncommunicating intradural arachnoid cyst (IAC) of the proximal part of the S1 nerve root (NR).

OBJECTIVE

To discuss the possible pathophysiology, clinical and magnetic resonance imaging (MRI) presentation, intraoperative findings, and follow-up of IAC of the proximal part of the S1 NR.

SUMMARY OF BACKGROUND DATA

Rare variety of the Nabors's Type 3 spinal IAC. The etiopathogenesis are uncertain. Surgical NR decompression with extirpation of the cyst is the treatment of choice.

METHODS

A 37-year-old woman clinically presented as monoradiculopathy with a 9-month history of progressive, posture-dependent radicular pain, paresthesia and hypoesthesia in the right S1 dermatome, and mild weakness of the ipsilateral plantar flexors. Magnetic resonance imaging (MRI) showed a noncommunicating IAC of the proximal part of the S1 NR on the right side. Surgical exploration through the ipsilateral L5-S1 hemilaminectomy was performed with microsurgical arachnolysis of the compressed and stretched S1 NR fascicles that surrounded the cyst, during which the cyst spontaneously collapsed. The remnant of the cyst wall was extirpated and histopathology confirmed the diagnosis.

RESULTS

After surgery an excellent clinical outcome was archived: the leg pain was no longer present and the paraesthesia, hypoesthesia, and motor weakness were resolved within 3 months. At 12 months of follow-up, the patient continues to be completely asymptomatic with no evidence of recurrence on MRI.

CONCLUSION

A rare case of symptomatic, idiopathic, noncommunicating IAC of the proximal part of the S1 NR has been presented. Early recognition and treatment resulted in complete symptom resolution, with preservation of the full working capacity and good quality of life. Isolated monoradiculopathy with progressive, posture-dependent radicular pain seem to be typical clinical findings for such a lesion. Attending physicians should always be mindful of this fact in the total clinical evaluation of such cases.

摘要

研究设计

罕见的症状性、特发性、非交通性 S1 神经根(NR)近端硬脊膜下蛛网膜囊肿(IAC)的病例报告。

目的

讨论 IAC 近端 S1NR 的可能病理生理学、临床和磁共振成像(MRI)表现、术中发现和随访。

背景资料摘要

Nabors 型 3 型脊髓 IAC 的罕见变体。其病因学尚不确定。手术 NR 减压和囊肿切除术是首选治疗方法。

方法

一名 37 岁女性,表现为单根神经根病,病史 9 个月,进行性、姿势依赖性神经根痛,右侧 S1 皮区感觉异常和感觉减退,同侧跖屈肌无力。磁共振成像(MRI)显示右侧 S1NR 近端非交通性 IAC。通过同侧 L5-S1 半椎板切除术进行手术探查,对受压和拉伸的 S1NR 束进行显微蛛网膜松解,在此过程中囊肿自发塌陷。切除囊肿壁的残余部分,并通过组织病理学证实诊断。

结果

手术后获得了极好的临床结果:腿部疼痛不再存在,感觉异常、感觉减退和运动无力在 3 个月内得到解决。在 12 个月的随访中,患者继续完全无症状,MRI 无复发迹象。

结论

报告了一例罕见的症状性、特发性、非交通性 S1NR 近端 IAC。早期识别和治疗导致完全缓解症状,保留了完整的工作能力和良好的生活质量。孤立性单根神经根病,进行性、姿势依赖性神经根痛,似乎是此类病变的典型临床发现。在对这些病例进行全面临床评估时,主治医生应始终牢记这一事实。

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