[1]常腾武 王继超.Chiari畸形Ⅰ型的诊治现状[J].中国临床神经外科杂志,2021,26(07):564-566.[doi:10.13798/j.issn.1009-153X.2021.07.024]
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Chiari畸形Ⅰ型的诊治现状()
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《中国临床神经外科杂志》[ISSN:1009-153X/CN:42-1603/TN]

卷:
26
期数:
2021年07期
页码:
564-566
栏目:
综述
出版日期:
2021-07-25

文章信息/Info

文章编号:
1009-153X(2021)07-0564-03
作者:
常腾武 王继超
183000 乌鲁木齐,新疆医科大学研究生院(常腾武);183001 乌鲁木齐,新疆维吾尔自治区人民医院神经外科(王继超)
关键词:
Chiari畸形I型诊断手术治疗
分类号:
R 742.8+2; R 651.1+1
DOI:
10.13798/j.issn.1009-153X.2021.07.024
文献标志码:
A

参考文献/References:

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[2] Aitken LA, Lindan CE, Sidney S, et al. Chiari type I malfor-mation in a pediatric population [J]. Pediatr Neurol, 2009, 40(6): 449-54.
[3] Pascual J, Oterino A, Berciano J. Headache in type I Chiari malformation [J]. Neurology, 1992, 42(8): 1519-1521.
[4] Mcvige JW, Leonardo J. Imaging of Chiari type I malforma-tion and syringohydromyelia [J]. Neurol Clin, 2014, 32(1): 95-126.
[5] Deng X, Yang C, Gan J, et al. Long-term outcomes after small-bone-window posterior fossa decompression and duraplasty in adults with Chiari malformation type I [J]. World Neurosurg, 2015, 84(4): 998-1004.
[6] Hida K, Iwasaki Y, Koyanagi I, et al. Pediatric syringomy-elia with chiari malformation: its clinical characteristics andsurgical outcomes [J]. Surg Neurol, 1999, 51(4): 383-391.
[7] Strahle J, Muraszko K M, Kapurch J, et al. Natural history of Chiari malformation Type I following decision for conserva-tive treatment [J]. J Neurosurg Pediatr, 2011, 8(2): 214-221.
[8] Fakhri A, Shah MN, Goyal MS. Advanced imaging of Chiari 1 malformations [J]. Neurosurg Clin N Am, 2015, 26(4): 519-526.
[9] Haughton V, Mardal KA. Spinal fluid biomechanics andimaging: an update for neuroradiologists [J]. AJNR Am J Neuroradiol, 2014, 35(10): 1864-1869.
[10] Haughton VM, Korosec FR, Medow JE, et al. Peak systolic and diastolic CSF velocity in the foramen magnum in adult patients with Chiari I malformations and in normal control participants [J]. AJNR Am J Neuroradiol, 2003, 24(2): 169-176.
[11] 张 成,石长斌. 磁共振相位对比电影成像法在ChiariⅠ型畸形诊断与治疗中的应用[J]. 临床神经外科杂志,2018,15(3):232-235.
[12] Leung V, Magnussen JS, Stoodley MA, et al. Cerebellar and hindbrain motion in Chiari malformation with and without syringomyelia [J]. J Neurosurg Spine, 2016, 24(4): 546-555.
[13] Doruk E, Ozay R, Sekerci Z, et al. Cervico-medullary com-pression ratio: a novel radiological parameter correlating with clinical severity in Chiari type 1 malformation [J]. Clin Neurol Neurosurg, 2018, 174: 123-128.
[14] Hatem SM, Attal N, Ducreux D, et al. Assessment of spinal somatosensory systems with diffusion tensor imaging in syringomyelia [J]. J Neurol Neurosurg Psychiatry, 2009, 80(12): 1350-1356.
[15] Mcvige JW, Leonardo J. Neuroimaging and the clinical man-ifestations of Chiari malformation type Ⅰ (CM-Ⅰ) [J]. Curr Pain Headache Rep, 2015, 19(6): 18.
[16] Kahn EN, Muraszko KM, Maher CO. Prevalence of Chiari I malformation and syringomyelia [J]. Neurosurg Clin N Am, 2015, 26(4): 501-507.
[17] Aghakhani N, Parker F, David P, et al. Long-term follow-upof Chiari-related syringomyelia in adults: analysis of 157 surgically treated cases [J]. Neurosurgery, 2009, 64(2): 308-315.
[18] Leon TJ, Kuhn EN, Arynchyna AA, et al. Patients with"benign" Chiari I malformations require surgical decom-pression at a low rate [J]. J Neurosurg Pediatr, 2019: 23(4):498-506.
[19] Genitori L, Peretta P, Nurisso C, et al. Chiari type I anoma-lies in children and adolescents: minimally invasive mana-gement in a series of 53 cases [J]. Childs Nerv Syst, 2000, 16(10-11): 707-718.
[20] Weinberg JS, Freed DL, Sadock J, et al. Headache andChiari I malformation in the pediatric population [J]. PediatrNeurosurg, 1998, 29(1): 14-18.
[21] Raza-Knight S, Mankad K, Prabhakar P, et al. Headache outcomes in children undergoing foramen magnum decom-pression for Chiari I malformation [J]. Arch Dis Child, 2017,102(3): 238-243.
[22] Shweikeh F, Sunjaya D, Nuno M, et al. National trends,complications, and hospital charges in pediatric patients with Chiari malformation type I treated with posterior fossa decompression with and without duraplasty [J]. Pediatr Neurosurg, 2015, 50(1): 31-37.
[23] Lu VM, Phan K, Crowley SP, et al. The addition of duraplas-ty to posterior fossa decompression in the surgical treatment of pediatric Chiari malformation Type I: a systematic review and meta-analysis of surgical and performance outcomes[J]. J Neurosurg Pediatr, 2017, 20(5): 439-449.
[24] Lin W, Duan G, Xie J, et al. Comparison of results between posterior fossa decompression with and without duraplasty for the surgical treatment of Chiari malformation type I: asystematic review and meta-analysis [J]. World Neurosurg, 2018, 110: 460-474.
[25] Milhorat TH, Nishikawa M, Kula RW, et al. Mechanisms of cerebellar tonsil herniation in patients with Chiari malfor-mations as guide to clinical management [J]. Acta Neurochir(Wien), 2010, 152(7): 1117-1127.
[26] Dyste GN, Menezes AH, Vangilder JC. Symptomatic Chiari malformations: an analysis of presentation, management, and long-term outcome [J]. J Neurosurg, 1989, 71(2): 159-168.
[27] Zhao JL, Li MH, Wang CL, et al. A systematic review ofChiari I malformation: techniques and outcomes [J]. World Neurosurg, 2016, 88: 7-14.
[28] Klekamp J. Surgical treatment of Chiari I malformation--analysis of intraoperative findings, complications, and out-come for 371 foramen magnum decompressions [J]. Neuro-surgery, 2012, 71(2): 365-380.
[29] 刘 彬,王振宇,谢京诚,等. Chiari畸形合并脊髓空洞症术中不同大小后颅窝减压窗近期疗效的比较[J]. 中国临床神经外科杂志,2016,21(1):10-12,16.

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备注/Memo

备注/Memo:
通讯作者:王继超,E-mail:xjsjwk@163.com
更新日期/Last Update: 2021-07-25