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I型脊髓纵裂畸形新的临床放射学分类方案:25例前瞻性研究

Proposal for a new clinicoradiological classification of type I split-cord malformations: a prospective study of 25 cases.

作者信息

Gupta Deepak Kumar, Mahapatra Ashok Kumar

机构信息

Department of Neurosurgery, All India Institute of Medical Sciences, New Delhi, India.

出版信息

Pediatr Neurosurg. 2006;42(6):341-6. doi: 10.1159/000095563.

DOI:10.1159/000095563
PMID:17047413
Abstract

BACKGROUND AND METHODS

Split-cord malformations (SCMs) are rare malformations of the spinal cord. A new classification is proposed based on intraoperative findings in 25 cases of type I SCMs (with bony spur). Patients' demographic profile, radiological and surgical details, complications and outcome were noted.

FINDINGS

All patients had type I SCMs. The mean age of the patients was 6.2 years (female:male ratio 1.2:1). Asymmetric lower-limb and sphincter weakness were present in 17/25 (68%) and 5/25 (20%) cases, respectively. Of the symptomatic cases, 29.4% (5/17) showed improvement in motor power and sensory improvement was recorded in 33.3% (4/12) of patients while 40% (2/5) regained continence. No patient in the asymptomatic group (0/8) showed postoperative neurological deterioration. A new subclassification of type I SCM is proposed based on the location of the bony spur responsible for the split, which can affect surgical dissection and outcome.

CONCLUSIONS

In SCM patients, the risk of developing neurological deficits increases with age, hence all SCM patients should undergo prophylactic surgery, even if they are asymptomatic. Our new classification is easy to use and takes into account intraoperative findings that may affect surgical outcome.

摘要

背景与方法

脊髓纵裂畸形(SCMs)是一种罕见的脊髓畸形。基于25例I型SCMs(伴有骨嵴)的术中发现提出了一种新的分类方法。记录了患者的人口统计学资料、影像学和手术细节、并发症及预后情况。

研究结果

所有患者均为I型SCMs。患者的平均年龄为6.2岁(女性与男性比例为1.2:1)。17/25(68%)的病例存在不对称下肢无力,5/25(20%)的病例存在括约肌无力。在有症状的病例中,29.4%(5/17)的患者运动能力有所改善,33.3%(4/12)的患者感觉有所改善,40%(2/5)的患者恢复了控尿功能。无症状组患者(0/8)术后均未出现神经功能恶化。根据导致脊髓纵裂的骨嵴位置提出了I型SCM的一种新的亚分类方法,该位置可能影响手术分离及预后。

结论

在SCM患者中,出现神经功能缺损的风险随年龄增长而增加,因此所有SCM患者均应接受预防性手术,即使他们无症状。我们的新分类方法易于使用,并考虑到了可能影响手术预后的术中发现。

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Proposal for a new clinicoradiological classification of type I split-cord malformations: a prospective study of 25 cases.I型脊髓纵裂畸形新的临床放射学分类方案:25例前瞻性研究
Pediatr Neurosurg. 2006;42(6):341-6. doi: 10.1159/000095563.
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Split cord malformations: a clinical study of 254 patients and a proposal for a new clinical-imaging classification.脊髓纵裂畸形:254例患者的临床研究及一种新的临床影像学分类建议
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Pol J Radiol. 2025 Jan 30;90:e46-e54. doi: 10.5114/pjr/199683. eCollection 2025.
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Split cord malformation types I and II: a personal series of 131 patients.I型和II型脊髓纵裂畸形:131例患者的个人病例系列
Childs Nerv Syst. 2013 Sep;29(9):1515-26. doi: 10.1007/s00381-013-2115-7. Epub 2013 Sep 7.
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Split cord malformation - A study of 300 cases at AIIMS 1990-2006.脊髓纵裂畸形——全印度医学科学研究所1990年至2006年300例病例研究
J Pediatr Neurosci. 2011 Oct;6(Suppl 1):S41-5. doi: 10.4103/1817-1745.85708.
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An unusual case of 4 level spinal dysraphism: Multiple composite type 1 and type 2 split cord malformation, dorsal myelocystocele and hydrocephalous.一例罕见的四级脊柱裂病例:多发性复合型1型和2型脊髓纵裂畸形、背侧脊髓脊膜膨出和脑积水。
J Pediatr Neurosci. 2011 Jan;6(1):58-61. doi: 10.4103/1817-1745.84411.