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小儿患者Chiari畸形的综合治疗方法。

Comprehensive approach to Chiari malformation in pediatric patients.

作者信息

Greenlee Jeremy, Garell P Charles, Stence Nicholas, Menezes Arnold H

出版信息

Neurosurg Focus. 1999 Jun 15;6(6):E6. doi: 10.3171/foc.1999.6.6.7.

DOI:10.3171/foc.1999.6.6.7
PMID:16972750
Abstract

Chiari malformation is a developmental disorder that is often associated with other abnormalities of the cerebrospinal axis. Despite widespread recognition of this association, there is relatively little information on the treatment of these coexisting disorders in the setting of cerebellar tonsillar ectopia. In an effort to improve the care provided to pediatric patients with Chiari malformations the authors reviewed their management practices over the last 20 years. Specifically, they recorded presenting symptoms, radiological studies, comorbidities, and management (surgical and nonsurgical) of 112 patients (all < 20 years of age) with Chiari malformation without myelodysplasia. They found an associated syrinx in 29% of patients, basilar invagination in 17%, and scoliosis in 14%. The basal angle varied from 120 to 190 degrees and Boogard's angle varied from 120 to 220 degrees ; both angles were larger than those measured in normal controls. The vertical height of the posterior fossa was shortened and the volume decreased as compared with normal controls. The surgical management of this group of patients included posterior decompressive (44%), combined transoral and posterior decompressive (31%), combined posterior decompressive and posterior fusion (8%), and multiple posterior decompressive procedures in the same patient (5%). The authors conclude that pediatric patients with a Chiari malformation should be specifically examined for evidence of additional craniovertebral malformations so that procedures are directed at correcting both the comorbidities and the herniation of the cerebellar tonsils through the foramen.

摘要

Chiari畸形是一种发育障碍,常与其他脑脊轴异常相关。尽管人们普遍认识到这种关联,但关于小脑扁桃体下疝情况下这些共存疾病的治疗信息相对较少。为了改善对患有Chiari畸形的儿科患者的护理,作者回顾了他们过去20年的管理实践。具体而言,他们记录了112例(均小于20岁)无脊髓发育异常的Chiari畸形患者的症状表现、影像学检查、合并症以及治疗情况(手术和非手术)。他们发现29%的患者伴有脊髓空洞症,17%伴有基底凹陷,14%伴有脊柱侧弯。基底角在120度至190度之间变化,Boogard角在120度至220度之间变化;这两个角度均大于正常对照组测量值。与正常对照组相比,后颅窝的垂直高度缩短,体积减小。该组患者的手术治疗包括后颅窝减压术(44%)、经口和后颅窝联合减压术(31%)、后颅窝减压和后路融合联合术(8%)以及同一患者多次后颅窝减压术(5%)。作者得出结论,患有Chiari畸形的儿科患者应接受专门检查,以寻找额外颅颈畸形的证据,以便针对合并症以及小脑扁桃体通过枕骨大孔的疝出进行治疗。

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Comprehensive approach to Chiari malformation in pediatric patients.小儿患者Chiari畸形的综合治疗方法。
Neurosurg Focus. 1999 Jun 15;6(6):E6. doi: 10.3171/foc.1999.6.6.7.
2
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引用本文的文献

1
Occipital-Cervical Fusion and Ventral Decompression in the Surgical Management of Chiari-1 Malformation and Syringomyelia: Analysis of Data From the Park-Reeves Syringomyelia Research Consortium.颅颈融合术和腹侧减压术在 Chiari-1 畸形伴脊髓空洞症的外科治疗中的应用:来自 Park-Reeves 脊髓空洞症研究联合会的数据分析。
Neurosurgery. 2021 Jan 13;88(2):332-341. doi: 10.1093/neuros/nyaa460.
2
Opinion for different centers: surgical experience with Chiari malformation type I in children at Xuanwu Hospital, China.不同中心观点:中国宣武医院小儿I型Chiari畸形的手术经验
Childs Nerv Syst. 2019 Oct;35(10):1915-1919. doi: 10.1007/s00381-019-04230-z. Epub 2019 Jun 18.
3
Transnasal endoscopic removal of malformation of the odontoid process in a patient with type I Arnold-Chiari malformation: a case report.
经鼻内镜切除 I 型 Arnold-Chiari 畸形患者齿状突畸形:病例报告。
Acta Otorhinolaryngol Ital. 2011 Aug;31(4):248-52.
4
Chiari type I malformation in a pediatric population.小儿人群中的 Chiari I 型畸形。
Pediatr Neurol. 2009 Jun;40(6):449-54. doi: 10.1016/j.pediatrneurol.2009.01.003.