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自发性脊髓蛛网膜下腔出血伴蛛网膜囊肿形成——病例报告及文献复习

Spontaneous Spinal Subarachnoid Hemorrhage with Development of an Arachnoid Cyst-A Case Report and Review of the Literature.

作者信息

Velz Julia, Fierstra Jorn, Regli Luca, Germans Menno R

机构信息

Department of Neurosurgery, Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland; University of Zurich, Zurich, Switzerland.

Department of Neurosurgery, Clinical Neuroscience Center, University Hospital Zurich, Zurich, Switzerland; University of Zurich, Zurich, Switzerland.

出版信息

World Neurosurg. 2018 Nov;119:374-380. doi: 10.1016/j.wneu.2018.08.108. Epub 2018 Aug 24.

Abstract

BACKGROUND

Spontaneous spinal subarachnoid hemorrhage (SAH) is extremely rare and occurs in <1% of all cases of SAH. To the best of our knowledge, only 1 case of spontaneous spinal SAH with later development of a symptomatic spinal arachnoid cyst (SAC) has been described in the literature to date. The objective of the present study was to report the challenging clinical management of SAC based on a literature review.

CASE DESCRIPTION

We report the case of a 51-year-old woman with acute onset of back pain, neck pain, and headaches with an angiogram-negative supratentorial SAH. Further magnetic resonance imaging screening of the spine revealed additional subarachnoid blood at the level of the thoracic spine, without evidence of vascular malformations. Several weeks after the hemorrhage, the patient developed progressive numbness in her trunk and lower extremities and weakness in her lower extremities. A follow-up magnetic resonance imaging study revealed a large arachnoid cyst at level T4-T7 with spinal cord compression. The patient underwent left hemilaminectomy at T4-T6 and fenestration of the SAC. In a second surgery, right-sided hemilaminectomy at T7 was performed with complete marsupialization of the larger cyst and placement of an intradural shunt. At the 6-month clinical follow-up examination, she showed improvement of her clinical symptoms.

CONCLUSIONS

Treatment of secondary SAC is challenging, and surgery of the SAC with or without placement of a shunt is a possible treatment option.

摘要

背景

自发性脊髓蛛网膜下腔出血(SAH)极为罕见,在所有SAH病例中发生率低于1%。据我们所知,迄今为止,文献中仅描述了1例自发性脊髓SAH后出现有症状的脊髓蛛网膜囊肿(SAC)的病例。本研究的目的是在文献综述的基础上报告SAC具有挑战性的临床管理情况。

病例描述

我们报告了1例51岁女性病例,该患者急性起病,出现背痛、颈痛和头痛,脑血管造影显示幕上SAH阴性。进一步的脊柱磁共振成像筛查显示胸椎水平有额外的蛛网膜下腔出血,未发现血管畸形证据。出血数周后,患者躯干和下肢逐渐出现麻木,下肢无力。随访磁共振成像研究显示T4 - T7水平有一个大的蛛网膜囊肿并伴有脊髓受压。患者接受了T4 - T6左侧半椎板切除术及SAC开窗术。在第二次手术中,进行了T7右侧半椎板切除术,将较大囊肿完全袋形化并置入硬膜内分流管。在6个月的临床随访检查中,她的临床症状有所改善。

结论

继发性SAC的治疗具有挑战性,SAC手术无论是否置入分流管都是一种可能的治疗选择。

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