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Clinical-radiological improvement following low-tech surgical treatment of an extensive cervical-medullary idiopathic syringomyelia in a low-resource African neurosurgical practice.在资源匮乏的非洲神经外科实践中,对广泛型颈髓性特发性脊髓空洞症进行低技术手术治疗后的临床影像学改善。
Neurosurg Rev. 2015 Jul;38(3):579-83; discussion 583. doi: 10.1007/s10143-015-0618-2. Epub 2015 Feb 21.
2
Syringomyelia associated with spinal arachnoiditis treated by partial arachnoid dissection and syrinx-far distal subarachnoid shunt.采用部分蛛网膜剥离术和脊髓空洞远侧蛛网膜下腔分流术治疗的脊髓空洞症合并脊髓蛛网膜炎。
Clin Med Insights Case Rep. 2014 Sep 4;7:107-10. doi: 10.4137/CCRep.S14895. eCollection 2014.
3
A painless burn due to lack of painkillers.因缺乏止痛药导致的无痛烧伤。
JAMA Neurol. 2014 Feb;71(2):240-1. doi: 10.1001/jamaneurol.2013.2192.
4
Basilar invagination, Chiari malformation, syringomyelia: a review.基底凹陷症、 Chiari 畸形、脊髓空洞症:综述
Neurol India. 2009 May-Jun;57(3):235-46. doi: 10.4103/0028-3886.53260.
5
Syringomyelia: current concepts in pathogenesis, diagnosis, and treatment.脊髓空洞症:发病机制、诊断及治疗的当前概念
J Vet Intern Med. 2006 May-Jun;20(3):469-79. doi: 10.1892/0891-6640(2006)20[469:sccipd]2.0.co;2.
6
Is syringomyelia pathology or a natural protective phenomenon?脊髓空洞症是一种病理状态还是一种自然保护现象?
J Postgrad Med. 2001 Apr-Jun;47(2):87-8.
7
Surgical management of syringomyelia-Chiari complex.脊髓空洞症- Chiari复合体的外科治疗
Eur Spine J. 2000 Dec;9(6):553-7. doi: 10.1007/s005860000157.
8
Surgical technique for cranio-cervical decompression in syringomyelia associated with Chiari type I malformation.与I型Chiari畸形相关的脊髓空洞症的颅颈减压手术技术
Acta Neurochir (Wien). 1997;139(6):529-39; discussion 539-40. doi: 10.1007/BF02750996.
9
Post-traumatic syringomyelia: a review of the literature.创伤后脊髓空洞症:文献综述
Paraplegia. 1994 Nov;32(11):723-31. doi: 10.1038/sc.1994.117.
10
Review article: post-spinal cord injury syringomyelia.综述文章:脊髓损伤后空洞症
Paraplegia. 1991 May;29(4):219-21. doi: 10.1038/sc.1991.32.

尼日利亚患者脊髓空洞症的概况及外科治疗

THE PROFILE AND SURGICAL TREATMENT OF SYRINGOMYELIA IN NIGERIAN PATIENTS.

作者信息

Ukachukwu Aek, Shokunbi M T, Tiamiyu L O, Adeolu A A, Malomo A O

机构信息

Department of Neurological Surgery, University College Hospital, Ibadan, Nigeria.

Department of Surgery, College of Medicine, University of Ibadan, Ibadan, Nigeria. Department of Neurological Surgery, University College Hospital, Ibadan, Nigeria.

出版信息

J West Afr Coll Surg. 2018 Apr-Jun;8(2):76-90.

PMID:32551318
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7276219/
Abstract

BACKGROUND

Syringomyelia is an often progressive disorder of the spinal cord. There is a dearth of reports in the African population.

AIMS AND OBJECTIVES

This study describes the profile and the outcome of treatment in our population of patients.

DESIGN OF THE STUDY

A retrospective review of patients surgically treated for syringomyelia over a ten year period.

SETTING

Department of Neurological Surgery, University College Hospital, Ibadan, Nigeria.

MATERIALS AND METHODS

Eight patients were surgically treated for Syringomyelia over the period 2004-2014. We extracted data on their gender, age, aetiology, syrinx location, diagnosis, operative procedure and outcome. Simple statistical analysis was done.

RESULTS

There were five males and three females. The mean age was 31.6(SD15.3) years (median: 32.5 years). The causes of the syrinx were: Chiari malformation (3), intramedullary spinal tumour (2), foramen magnum tumour (1), post-traumatic (1), and iatrogenic chemical arachnoiditis (1). The syrinx location was: cervical region (4), cervicothoracic region (2) and multi-level (2). The operative procedures were posterior fossa decompression (2), sub-occipital craniectomy with laminectomy and tumour excision (2), laminectomy and syringomyelotomy (2), laminectomy and tumour excision (1), and ventriculoperitoneal shunting (1). The duration of follow up was 2 weeks to 35 months. Outcome was satisfactory in six patients. A child who had initial ventriculoperitoneal shunting died at home before definitive surgery, and an adult male died of respiratory insufficiency post operatively.

CONCLUSION

Syringomyelia is rare in our population. It affects young patients, typically in the cervico-thoracic region. The aetiologies are similar to those from previous reports. The outcome of surgical treatment in our small group of patients is satisfactory.

摘要

背景

脊髓空洞症是一种常呈进行性发展的脊髓疾病。非洲人群中关于该病的报道较少。

目的

本研究描述了我们所治疗患者群体的概况及治疗结果。

研究设计

对10年间接受脊髓空洞症手术治疗的患者进行回顾性研究。

研究地点

尼日利亚伊巴丹大学学院医院神经外科。

材料与方法

2004年至2014年期间,8例患者接受了脊髓空洞症手术治疗。我们提取了他们的性别、年龄、病因、空洞位置、诊断、手术方式及治疗结果等数据,并进行了简单的统计学分析。

结果

男性5例,女性3例。平均年龄为31.6(标准差15.3)岁(中位数:32.5岁)。空洞形成的原因有:Chiari畸形(3例)、髓内脊髓肿瘤(2例)、枕骨大孔肿瘤(1例)、创伤后(1例)和医源性化学性蛛网膜炎(1例)。空洞位置为:颈部(4例)、颈胸段(2例)和多节段(2例)。手术方式包括后颅窝减压术(2例)、枕下颅骨切除术联合椎板切除术及肿瘤切除术(2例)、椎板切除术及脊髓空洞切开术(2例)、椎板切除术及肿瘤切除术(1例)和脑室腹腔分流术(1例)。随访时间为2周至35个月。6例患者的治疗结果满意。1例最初接受脑室腹腔分流术的儿童在确定性手术前在家中死亡,1例成年男性术后死于呼吸功能不全。

结论

脊髓空洞症在我们的患者群体中较为罕见。它影响年轻患者,典型部位为颈胸段。病因与既往报道相似。我们这一小群患者的手术治疗结果令人满意。