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软骨发育不全患儿的动态颈髓压迫及脑脊液动力学改变:11年手术病例系列回顾

Dynamic cervicomedullary cord compression and alterations in cerebrospinal fluid dynamics in children with achondroplasia: review of an 11-year surgical case series.

作者信息

Mukherjee Debraj, Pressman Barry D, Krakow Deborah, Rimoin David L, Danielpour Moise

机构信息

Maxine Dunitz Neurosurgical Institute.

出版信息

J Neurosurg Pediatr. 2014 Sep;14(3):238-44. doi: 10.3171/2014.5.PEDS12614. Epub 2014 Jun 27.


DOI:10.3171/2014.5.PEDS12614
PMID:24971605
Abstract

OBJECT: Achondroplasia may be associated with compression at the cervicomedullary junction. Determining which patients are at greatest risk for neurological complications of cervicomedullary compression can be difficult. In the current study the authors reviewed their records to determine the incidence and clinical significance of dynamic cervicomedullary stenosis and obstruction of CSF flow along with surgical outcomes following posterior fossa decompression. METHODS: The authors reviewed 34 consecutive cases involving symptomatic children with achondroplasia undergoing cervicomedullary decompression performed by a single surgeon over 11 years. Of these patients, 29 had undergone preoperative dynamic MRI of the cervicomedullary junction with cine (cinema) CSF flow studies; 13 of these patients underwent postoperative dynamic MRI studies. Clinical outcomes included changes in polysomnography, head circumference percentile, and fontanel characteristics. Radiographic outcomes included changes in dynamic spinal cord diameter, improvement in CSF flow at the foramen magnum, and change in the Evans ratio. RESULTS: Patients were predominantly female, with a mean age at presentation of 6.6 years and mean follow-up of 3.7 years (range 1-10 years). All patients had moderate to excellent improvement in postoperative polysomnography, slight decrease in average head circumference percentile (from 46.9th percentile to 45.7th percentile), and no subjective worsening of fontanel characteristics. The Evans ratio decreased by 2%, spinal cord diameter increased an average of 3.1 mm, 5.2 mm, and 0.2 mm in the neutral, flexed, and extended positions, respectively, and CSF flow improved qualitatively in all 3 positions. There were no postoperative infections, CSF leaks, or other major complications. None of the patients undergoing initial foramen magnum decompression performed at our medical center required reoperation. CONCLUSIONS: Patients with achondroplasia and symptomatic cervicomedullary compression have increased risk of dynamic stenosis at the foramen magnum evident upon dynamic cine MRI. Operative decompression may be offered with low risk of complications or need for reoperation.

摘要

目的:软骨发育不全可能与颈髓交界处受压有关。确定哪些患者发生颈髓受压神经并发症的风险最高可能具有挑战性。在本研究中,作者回顾了他们的记录,以确定动态颈髓狭窄和脑脊液流动梗阻的发生率及临床意义,以及后颅窝减压术后的手术效果。 方法:作者回顾了11年间由同一位外科医生为34例有症状的软骨发育不全儿童行颈髓减压术的连续病例。其中29例患者术前行颈髓交界处动态磁共振成像(MRI)及电影(动态)脑脊液流动研究;其中13例患者术后行动态MRI研究。临床结果包括多导睡眠图、头围百分位数和囟门特征的变化。影像学结果包括动态脊髓直径的变化、枕骨大孔处脑脊液流动的改善以及埃文斯比率的变化。 结果:患者以女性为主,就诊时平均年龄为6.6岁,平均随访3.7年(范围1 - 10年)。所有患者术后多导睡眠图均有中度至显著改善,平均头围百分位数略有下降(从第46.9百分位数降至第45.7百分位数),囟门特征无主观恶化。埃文斯比率下降2%,脊髓直径在中立位、屈曲位和伸展位分别平均增加3.1 mm、5.2 mm和0.2 mm,脑脊液流动在所有3个位置均有定性改善。术后无感染、脑脊液漏或其他重大并发症。在我们医疗中心接受初次枕骨大孔减压术的患者均无需再次手术。 结论:软骨发育不全且有症状性颈髓受压的患者在动态电影MRI上显示枕骨大孔处动态狭窄风险增加。手术减压并发症风险低或无需再次手术。

相似文献

[1]
Dynamic cervicomedullary cord compression and alterations in cerebrospinal fluid dynamics in children with achondroplasia: review of an 11-year surgical case series.

J Neurosurg Pediatr. 2014-9

[2]
Improvement in ventriculomegaly following cervicomedullary decompressive surgery in children with achondroplasia and foramen magnum stenosis.

Am J Med Genet A. 2020-8

[3]
Polysomnography as an indicator for cervicomedullary decompression to treat foramen magnum stenosis in achondroplasia.

Childs Nerv Syst. 2018-11

[4]
Dynamic cervicomedullary cord compression and alterations in cerebrospinal fluid dynamics in children with achondroplasia. Report of four cases.

J Neurosurg. 2007-12

[5]
Surgical management of cervicomedullary compression in achondroplasia.

Childs Nerv Syst. 1996-12

[6]
Cervicomedullary compression in achondroplasia.

J Neurosurg. 1994-7

[7]
Cervicomedullary decompression for foramen magnum stenosis in achondroplasia.

J Neurosurg. 2006-3

[8]
Is there a correlation between sleep disordered breathing and foramen magnum stenosis in children with achondroplasia?

Am J Med Genet A. 2016-1

[9]
Achondroplasia and cervicomedullary compression: prospective evaluation and surgical treatment.

Pediatr Neurosurg. 1999-8

[10]
Surgical treatment for cervicomedullary compression among infants with achondroplasia.

Childs Nerv Syst. 2015-5

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Childs Nerv Syst. 2025-2-25

[2]
Jugular foramen stenosis in external hydrocephalus in infants.

Childs Nerv Syst. 2024-7

[3]
Alteration of major venous drainage routes in a patient with achondroplasia after ventriculoperitoneal shunt placement.

Childs Nerv Syst. 2024-3

[4]
Recommendations for neuroradiological examinations in children living with achondroplasia: a European Society of Pediatric Radiology and European Society of Neuroradiology opinion paper.

Pediatr Radiol. 2023-11

[5]
Interventions for improving clinical outcomes and health-related quality-of-life for people living with skeletal dysplasias: an evidence gap map.

Qual Life Res. 2023-10

[6]
The (extended) achondroplasia foramen magnum score has good observer reliability.

Pediatr Radiol. 2022-7

[7]
Functional and morphological changes in hypoplasic posterior fossa.

Childs Nerv Syst. 2021-10

[8]
Identification of clinical and radiographic predictors of central nervous system injury in genetic skeletal disorders.

Sci Rep. 2021-5-31

[9]
Apparently benign craniocervical signs in achondroplasia: "neurologic leftovers" identified through a retrospective dataset.

Orphanet J Rare Dis. 2020-10-23

[10]
Achondroplasia: a comprehensive clinical review.

Orphanet J Rare Dis. 2019-1-3

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