• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

症状性Ⅰ型Chiari畸形的手术治疗:25例采用小脑扁桃体缩窄术治疗的成年患者系列研究

Surgical Treatment in Symptomatic Chiari Malformation Type I: A Series of 25 Adult Patients Treated with Cerebellar Tonsil Shrinkage.

作者信息

Villa Alessandro, Imperato Alessia, Maugeri Rosario, Visocchi Massimiliano, Iacopino Domenico Gerardo, Francaviglia Natale

机构信息

Division of Neurosurgery, ARNAS Civico Hospital, Palermo, Italy.

Division of Neurosurgery, IRCCS Neuromed, Pozzilli, Italy.

出版信息

Acta Neurochir Suppl. 2019;125:125-131. doi: 10.1007/978-3-319-62515-7_18.

DOI:10.1007/978-3-319-62515-7_18
PMID:30610312
Abstract

BACKGROUND

The variety of symptoms and radiological findings in patients with Chiari malformation type I makes both the indication for surgery and the technical modality controversial. We report our 5-year experience, describing our technique and critically evaluating the clinical results.

METHODS

Between 2012 and 2016, 25 patients (15 female and 10 male; mean age 39.2 years) underwent posterior fossa decompression for Chiari malformation type I. Their clinical complaints included headache, nuchalgia, upper limb weakness or numbness, instability, dizziness and diplopia. Syringomyelia was present in 12 patients (48%). Suboccipital craniectomy was completed in all cases with C1 laminectomy and shrinkage of the cerebellar tonsils by bipolar coagulation; duraplasty was performed with a suturable dura substitute.

RESULTS

Gratifying results were observed in our series. Symptoms and signs were resolved in 52% of patients, and 20% of patients had an improvement in their preoperative deficits. The symptoms of six patients (24%) were essentially unchanged, and one patient (4%) deteriorated despite undergoing surgery. Generally, patients with syringomyelia on magnetic resonance imaging (MRI) showed less symptomatic improvement after surgery. The syrinx disappeared in seven of 12 patients, and complications occurred in three patients (12%).

CONCLUSION

Cerebellar tonsil reduction and restoration of cerebrospinal fluid (CSF) circulation provided clinical improvement and a stable reduction in the syrinx size in the vast majority of treated patients, with a low rate of complications.

摘要

背景

I型Chiari畸形患者的症状和影像学表现多样,这使得手术指征和技术方式都存在争议。我们报告了我们5年的经验,描述了我们的技术并对临床结果进行了批判性评估。

方法

2012年至2016年期间,25例患者(15例女性和10例男性;平均年龄39.2岁)接受了I型Chiari畸形的后颅窝减压术。他们的临床症状包括头痛、颈部疼痛、上肢无力或麻木、共济失调、头晕和复视。12例患者(48%)存在脊髓空洞症。所有病例均完成枕下颅骨切除术并进行C1椎板切除术,通过双极电凝使小脑扁桃体缩小;使用可缝合的硬脑膜替代物进行硬脑膜成形术。

结果

我们的系列观察到了令人满意的结果。52%的患者症状和体征得到缓解,20%的患者术前缺陷有所改善。6例患者(24%)的症状基本未变,1例患者(4%)尽管接受了手术但病情恶化。一般来说,磁共振成像(MRI)显示有脊髓空洞症的患者术后症状改善较少。12例患者中有7例脊髓空洞消失,3例患者(12%)出现并发症。

结论

小脑扁桃体缩小和脑脊液(CSF)循环恢复使绝大多数接受治疗的患者临床症状改善,脊髓空洞大小稳定缩小,并发症发生率低。

相似文献

1
Surgical Treatment in Symptomatic Chiari Malformation Type I: A Series of 25 Adult Patients Treated with Cerebellar Tonsil Shrinkage.症状性Ⅰ型Chiari畸形的手术治疗:25例采用小脑扁桃体缩窄术治疗的成年患者系列研究
Acta Neurochir Suppl. 2019;125:125-131. doi: 10.1007/978-3-319-62515-7_18.
2
Effects of posterior fossa decompression with and without duraplasty on Chiari malformation-associated hydromyelia.后颅窝减压术联合或不联合硬脑膜成形术对Chiari畸形相关脊髓空洞症的影响。
Neurosurgery. 2000 Jun;46(6):1384-9; discussion 1389-90. doi: 10.1097/00006123-200006000-00018.
3
Treatment of Chiari I malformation in patients with and without syringomyelia: a consecutive series of 66 cases.伴有和不伴有脊髓空洞症的Chiari I型畸形患者的治疗:66例连续病例系列
Neurosurg Focus. 2001 Jul 15;11(1):E3. doi: 10.3171/foc.2001.11.1.4.
4
Various manifestation of Chiari I malformation in children and improvement after surgery.儿童 Chiari I 畸形的各种表现及术后改善。
J Integr Neurosci. 2022 May 30;21(4):100. doi: 10.31083/j.jin2104100.
5
Decompression of the spinal subarachnoid space as a solution for syringomyelia without Chiari malformation.脊髓蛛网膜下腔减压作为治疗无Chiari畸形的脊髓空洞症的一种方法。
Spinal Cord. 2002 Oct;40(10):501-6. doi: 10.1038/sj.sc.3101322.
6
Posterior fossa decompression for Chiari malformation type I: clinical and radiological presentation, outcome and complications in a retrospective series of 105 procedures.后颅窝减压术治疗 Chiari 畸形 I 型:105 例回顾性系列的临床和影像学表现、结果和并发症。
Acta Neurol Belg. 2019 Jun;119(2):245-252. doi: 10.1007/s13760-019-01086-7. Epub 2019 Feb 8.
7
Elucidating the pathophysiology of syringomyelia.阐明脊髓空洞症的病理生理学。
J Neurosurg. 1999 Oct;91(4):553-62. doi: 10.3171/jns.1999.91.4.0553.
8
Surgical outcomes after posterior fossa decompression with and without duraplasty in Chiari malformation-I.Chiari畸形I型行后颅窝减压术伴或不伴硬脑膜成形术的手术结果。
Clin Neurol Neurosurg. 2014 Oct;125:182-8. doi: 10.1016/j.clineuro.2014.07.027. Epub 2014 Aug 12.
9
Bony Decompression for Chiari Malformation Type I: Long-Term Follow-Up.I型Chiari畸形的骨性减压:长期随访
Acta Neurochir Suppl. 2019;125:119-124. doi: 10.1007/978-3-319-62515-7_17.
10
Surgical results of arachnoid-preserving posterior fossa decompression for Chiari I malformation with associated syringomyelia.保留蛛网膜的后颅窝减压术治疗 Chiari I 畸形伴脊髓空洞症的手术效果。
J Clin Neurosci. 2012 Apr;19(4):557-60. doi: 10.1016/j.jocn.2011.06.034. Epub 2012 Feb 1.

引用本文的文献

1
Chiari Formation or Malformation? Trends in the Pathophysiology and Surgical Treatment of an Ever-Elusive Entity.Chiari畸形还是Chiari形成?一个难以捉摸的实体的病理生理学和外科治疗趋势。
Brain Sci. 2024 Oct 5;14(10):1006. doi: 10.3390/brainsci14101006.
2
Post-Operative Complications after Foramen Magnum Decompression with Duraplasty Using Different Graft Materials in Adults Patients with Chiari I Malformation: A Systematic Review and Meta-Analysis.成人 Chiari I 畸形患者使用不同移植材料行枕大孔减压及硬脑膜成形术后的并发症:一项系统评价和荟萃分析
J Clin Med. 2023 May 10;12(10):3382. doi: 10.3390/jcm12103382.
3
Acquired Chiari I malformation due to lumboperitoneal shunt: A case report and review of literature.
腰大池-腹腔分流术所致获得性Chiari I畸形:一例报告并文献复习
Surg Neurol Int. 2019 May 10;10:78. doi: 10.25259/SNI-234-2019. eCollection 2019.