平山症的静脉病理学手术治疗:探索潜在病因的九例综合病例系列。

IF 1.4 Q2 OTORHINOLARYNGOLOGY Journal of Craniovertebral Junction and Spine Pub Date : 2024-01-01 Epub Date: 2024-03-13 DOI:10.4103/jcvjs.jcvjs_179_23
Deepak Nandkishore Sharma, Vamsi Krishna Yerramneni, Thirumal Yerragunta, Govind B Gaikwad, Vasundhara S Rangan, Sasank Akurati
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引用次数: 0

摘要

目的:平山症是一种罕见的颈椎病,主要影响年轻人。该病的典型特征是上肢远端肌肉萎缩。虽然硬膜囊发育不良、神经根发育不良、脊柱韧带结构异常和静脉发育不良等各种发病机制已被提出,但本研究探讨了静脉病变的潜在作用以及在此基础上的手术治疗:本研究是一项前瞻性描述性病例系列研究,共9例。诊断依据华山诊断标准,包括临床表现、影像学和电生理学。在磁共振成像(MRI)无法显示充血静脉的病例中,颈椎的计算机断层扫描(CT)静脉造影被用作成像工具。所有患者都接受了颈椎椎板切除术和硬膜外后静脉丛凝固术,并进行或不进行椎板成形术。对所有患者进行定期随访,评估临床改善情况和颈部残疾指数:所有九名患者均为男性,具有典型的临床特征、电生理异常和核磁共振成像检查结果,只有一名患者因核磁共振成像检查结果不确定而通过 CT 静脉造影帮助确诊。术后,所有患者的神经功能都得到了改善,病情也趋于稳定。除一名患者出现脊柱后凸外,所有接受 CT 静脉造影和颈椎 X 光检查的患者在中立位和动态位时均未再出现充血的静脉丛或明显的不稳定性。一名患者的另一侧肢体出现症状,接受了第二次手术:这一综合病例系列有力地证明了静脉病理学是平山症的潜在病因。手术治疗包括椎板切除术和静脉凝固术,同时进行或不进行扩张性椎板成形术,可持续改善神经功能预后,长期稳定病情,且不限制活动,并发症较少。然而,还需要进一步的研究来阐明颈椎静脉扩张的内在机制。
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Venous pathology targeted surgical management in Hirayama disease: A comprehensive case series of nine cases exploring this potential etiology.

Objective: Hirayama disease is a rare cause of cervical myelopathy predominantly affecting young individuals. The disease is classically characterized by muscle atrophy in the distal upper limbs. While various etiopathogenesis such as dural sac dysplasia, nerve root dysplasia, structural abnormalities of the spinal ligament, and venous dysplasia have been proposed, this study explores the potential role of venous pathology and surgical management on the basis of it.

Methodology: This is a prospective descriptive case series of nine cases. The diagnosis was made based on the Huashan diagnostic criteria which includes clinical manifestation, imaging, and electrophysiology. In cases where magnetic resonance imaging (MRI) failed to demonstrate engorged veins, a computed tomography (CT) venogram of the cervical spine was used as an imaging tool. All patients underwent cervical laminectomy and coagulation of the posterior epidural venous plexus with or without laminoplasty. All the patients were followed up regularly; clinical improvement and neck disability index were assessed.

Results: All nine patients were male and exhibited classical clinical features, electrophysiological abnormalities, and MRI findings except, in one patient where a CT venogram helped in establishing the diagnosis as the MRI was inconclusive. Postoperatively, all patients had neurological improvement and stabilization of the disease. All patients who underwent CT venogram and cervical spine X-ray in neutral and dynamic position demonstrated no recurrence of engorged venous plexus or significant instability except one patient developing kyphosis. One patient experiencing symptoms in the other limb underwent a second surgery.

Conclusion: This comprehensive case series strongly supports venous pathology as a potential etiology of Hirayama disease. Surgical management with laminectomy and venous coagulation with or without expansile laminoplasty has delivered consistent improvement in neurological outcomes and long-term disease stabilization without the restriction of movements and lesser complications. However, further research is warranted to elucidate the mechanism underlying cervical venous dilatation.

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来源期刊
CiteScore
1.90
自引率
9.10%
发文量
57
审稿时长
12 weeks
期刊最新文献
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