Is deformity correction essential in a "Myelopathic Cord"? - A case series.

IF 0.7 Q4 CLINICAL NEUROLOGY
Rajat Mahajan, Ganesh Kumar
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Abstract

Introduction: The incidence of preoperative neurological deficits in pediatric patients with complex deformities ranges from 15% to 23%. Furthermore, the likelihood of a postoperative neurological deficit can be considerably increased to 83.3% in the presence of a preoperative neurological deficit. Hence, the management of pediatric spinal deformities with neurological deficits is a challenge for every spine surgeon. Here, we describe four consecutive cases of pediatric spinal deformity with myelopathic cord, all of which were managed with decompressive surgery and stabilization without any attempts to correct the deformity. All the patients recovered well neurologically, without any progression of deformity.

Case presentation: The authors obtained the informed written consent from the patient and their parents for the print and electronic publication of the case. All four patients had clinical myelopathy with a progressive, worsening neurological deficit. The pathology was in the thoracic region in all the patients. Of the four cases, two were post-tubercular deformities, and two were congenital deformities. The treatment strategy for all patients was circumferential decompression of the spinal cord with posterior pedicle screw instrumentation. Although all patients had significant neurological deficits (Nurick grade 4 or 5) preoperatively, we used intraoperative neuromonitoring to prevent the worsening of the deficit during the procedure. None of the patients experienced intraoperative signal changes. All patients had significant neurological recovery (Nurick grade 0 to 2) and showed no worsening of deformity at their latest follow-up, up to 4 years. All showed good improvement in all domains of the SRS22r questionnaire.

Discussion: It is challenging for spine surgeons to manage complex spinal abnormalities in pediatric patients with myelopathic cords. Even a minimal manipulation of the cord during surgery might result in severe long-term morbidity. The primary objective in managing such patients should be neurological recovery rather than deformity correction-"First do no harm," and if necessary, the deformity can be corrected at a later stage under neuromonitoring.

Abstract Image

髓鞘病性脊柱炎 "患者是否必须进行畸形矫正?- 一个病例系列。
简介儿科复杂畸形患者术前神经功能缺损的发生率为 15%至 23%。此外,如果术前存在神经功能缺损,术后出现神经功能缺损的可能性会大大增加,达到 83.3%。因此,小儿脊柱畸形伴神经功能缺损的治疗对每一位脊柱外科医生来说都是一项挑战。在此,我们连续描述了四例伴有脊髓病性脊柱畸形的小儿脊柱畸形病例,所有病例均采用减压手术和稳定术进行治疗,未试图矫正畸形。所有患者的神经系统均恢复良好,畸形没有任何进展:作者获得了患者及其父母的知情同意书,并将病例以印刷版和电子版形式发表。四名患者均患有临床脊髓病,神经功能缺损呈进行性恶化。所有患者的病变均位于胸椎部位。在这四例病例中,两例为结核病后畸形,两例为先天性畸形。所有患者的治疗策略都是通过后椎弓根螺钉器械对脊髓进行环绕减压。虽然所有患者术前都有明显的神经功能缺损(Nurick 4级或5级),但我们在术中使用了神经监测仪,以防止缺损在术中恶化。没有一名患者在术中出现信号变化。所有患者的神经功能都得到了明显恢复(Nurick 分级 0 至 2),并且在最近 4 年的随访中畸形没有恶化。所有患者在SRS22r问卷调查的所有方面都有良好的改善:讨论:脊柱外科医生在处理脊髓病索小儿患者的复杂脊柱畸形时面临挑战。即使在手术过程中对脊髓进行最小程度的操作,也可能导致严重的长期发病率。处理这类患者的首要目标应该是神经功能的恢复,而不是畸形矫正--"首先不要伤害",如有必要,可在神经监测的后期阶段矫正畸形。
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来源期刊
Spinal Cord Series and Cases
Spinal Cord Series and Cases Medicine-Neurology (clinical)
CiteScore
2.20
自引率
8.30%
发文量
92
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