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终丝动静脉瘘合并退行性腰骶椎管狭窄:3 例报告并文献复习。

Filum Terminale Arteriovenous Fistula in Association with Degenerative Lumbosacral Spinal Canal Stenosis: Report of 3 Cases and Review of the Literature.

机构信息

Department of Neurosurgery, Prasat Neurological Institute, Bangkok, Thailand.

Department of Neurosurgery, Prasat Neurological Institute, Bangkok, Thailand.

出版信息

World Neurosurg. 2020 Jun;138:231-241. doi: 10.1016/j.wneu.2020.03.011. Epub 2020 Mar 10.

DOI:10.1016/j.wneu.2020.03.011
PMID:32169619
Abstract

BACKGROUND

Filum terminale arteriovenous fistulas (FTAVFs) are rare, and the pathogenesis of these fistulas remains unclear. They may be either congenital or acquired in origin. The authors report 3 cases of FTAVFs in association with severe spinal canal stenosis. The authors also review literature of FTAVFs associated with spinal canal stenosis.

CASE DESCRIPTION

All 3 cases harboring FTAVFs manifested with progressive myelopathy and bowel/bladder dysfunction following long history of back pain, sciatica, and/or intermittent claudication. The fistulas were located around or at the level of spinal canal stenosis and supplied by the anterior spinal and/or lateral sacral arteries with cranial drainage from the dilated vein of the filum terminale to the perimedullary veins. The first and third cases were treated concomitantly by performing instrumented fusion with decompressive laminectomy along with occlusion of the fistula with good results. The second case was unsuccessfully treated by endovascular treatment through the lateral sacral artery and denied further surgical treatment.

CONCLUSIONS

Our 3 case reports may provide additional evidence supporting an acquired etiology of FTAVFs, probably secondary to the severe central canal stenosis. From our review, the level of the fistulas in most patients is correlated with the level of spinal canal stenosis. The authors preferred the concomitant surgical treatment by performing decompressive laminectomy and obliteration of the fistula in the same surgical session.

摘要

背景

终丝动静脉瘘(FTAVFs)较为罕见,其发病机制尚不清楚。它们可能是先天性的,也可能是后天获得的。作者报告了 3 例与严重椎管狭窄相关的 FTAVFs 病例。作者还回顾了与椎管狭窄相关的 FTAVFs 的文献。

病例描述

所有 3 例存在 FTAVFs 的患者均表现为长期背痛、坐骨神经痛和/或间歇性跛行后出现进行性脊髓病和肠/膀胱功能障碍。瘘管位于椎管狭窄处或其附近,由脊髓前动脉和/或侧骶动脉供血,颅侧引流从扩张的终丝静脉到髓周静脉。第一例和第三例患者同时接受了经皮融合减压术,同时通过瘘管闭塞治疗,取得了良好的效果。第二例患者经侧骶动脉血管内治疗失败,并拒绝进一步手术治疗。

结论

我们的 3 例病例报告可能为 FTAVFs 的获得性病因提供了更多证据,可能继发于严重的中央管狭窄。根据我们的回顾,大多数患者的瘘管水平与椎管狭窄水平相关。作者更倾向于在同一手术中同时进行减压和瘘管闭塞的手术治疗。

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