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埃勒斯-当洛综合征患者的腰椎人工椎间盘置换术:一例病例报告及临床管理探讨

Lumbar artificial disc replacement in Ehlers-Danlos syndrome: A case report and discussion of clinical management.

作者信息

Lindley Emily M, Patti Brianna N, Taylor Matthew, Burger Evalina L, Patel Vikas V

机构信息

Department of Orthopaedics, University of Colorado Denver, Anschutz Medical Campus, Denver, CO.

Adult Clinical Genetics, Department of Medicine, University of Colorado Denver, Anschutz Medical Campus, Denver, CO.

出版信息

Int J Spine Surg. 2012 Dec 1;6:124-9. doi: 10.1016/j.ijsp.2012.02.006. eCollection 2012.

Abstract

BACKGROUND

Ehlers-Danlos syndrome (EDS) is a heterogeneous collection of connective tissue disorders characterized by varying degrees of skin hyperextensibility, joint hypermobility, and tissue fragility. Surgical treatment of EDS patients is complicated by the extreme fragility of their vessels and tissues. The purpose of this case report is to present the management of an EDS patient with debilitating low-back pain.

METHODS

A 52-year-old woman with a clinical diagnosis of EDS presented with degenerative disc disease at L4-5 that had not been alleviated by previous microdiscectomies. The clinical course, decision-making process, and treatment are discussed in this case report.

RESULTS

The patient was referred for genetic evaluation, which classified her with type III EDS, or hypermobility type. We presented the patient with the risks and benefits of fusion versus artificial disc replacement (ADR), particularly with regard to her EDS diagnosis of the hypermobility subtype. Given the patient's lack of extreme spinal hypermobility on examination and the absence of clear contraindications regarding ADR in type III EDS, the decision was made to proceed with ADR. There were no surgical complications, and the patient's low-back pain and radicular symptoms resolved with no evidence of implant migration or hypermobility at 1 year postoperatively.

CONCLUSIONS

In this case report, the referral to a geneticist and consultation with a vascular surgeon were integral steps in the decision to proceed with surgery. Although the clarified diagnosis of type III EDS did not eliminate the potential risk for vascular compromise during surgery, it placed the patient at lower risk than patients with other subtypes of EDS. Similarly, her lack of extreme hypermobility made us more comfortable with pursuing ADR. Although we emphasize extreme caution when considering surgical treatment, this case report suggests that some patients with less severe forms of EDS may be able to successfully undergo anterior spine surgery, including ADR.

摘要

背景

埃勒斯-当洛综合征(EDS)是一组结缔组织疾病的统称,其特征为不同程度的皮肤过度伸展、关节活动过度以及组织脆弱性。EDS患者的手术治疗因血管和组织的极度脆弱而变得复杂。本病例报告的目的是介绍一名患有使人衰弱的下背痛的EDS患者的治疗情况。

方法

一名临床诊断为EDS的52岁女性,患有L4 - 5节段的椎间盘退变疾病,此前的显微椎间盘切除术未能缓解该症状。本病例报告讨论了其临床病程、决策过程和治疗方法。

结果

该患者被转诊进行基因评估,结果将她归类为III型EDS,即活动过度型。我们向患者介绍了融合手术与人工椎间盘置换(ADR)的风险和益处,特别是考虑到她的EDS活动过度亚型诊断。鉴于患者检查时未出现脊柱极度活动过度,且III型EDS中ADR没有明确的禁忌证,因此决定进行ADR。手术无并发症,患者的下背痛和神经根症状得到缓解,术后1年无植入物移位或活动过度的迹象。

结论

在本病例报告中,转诊至遗传学家处并咨询血管外科医生是决定进行手术的重要步骤。虽然明确诊断为III型EDS并不能消除手术期间血管受损的潜在风险,但与其他亚型的EDS患者相比,该患者的风险较低。同样,她没有极度活动过度的情况使我们更放心地进行ADR。虽然我们在考虑手术治疗时强调要极其谨慎,但本病例报告表明,一些病情较轻的EDS患者可能能够成功接受前路脊柱手术,包括ADR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9064/4300890/8719ecf59476/IJSS-6-2012-02-006-g001.jpg

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