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表现为局灶性运动功能缺损的Chiari畸形。两例报告。

Chiari malformation presenting as a focal motor deficit. Report of two cases.

作者信息

Laufer Ilya, Engel Murray, Feldstein Neil, Souweidane Mark M

机构信息

Department of Neurological Surgery, Weill Cornell Medical College, New York Presbyterian Hospital, New York, New York 10021, USA.

出版信息

J Neurosurg Pediatr. 2008 May;1(5):392-5. doi: 10.3171/PED/2008/1/5/392.

Abstract

Chiari malformations may present with a wide range of symptoms and signs. Nevertheless, focal foot weakness as a presentation of a Chiari malformation has not been described in the pediatric neurosurgical literature. Two children with Chiari malformations and holocord syringomyelia presented with manifestations of a supposed isolated lumbar radiculopathy. Neurological deficits completely resolved after decompressive suboccipital craniectomy and cervical laminectomy. These cases emphasize the importance of imaging the entire craniospinal axis and avoidance of therapeutic intervention specifically aimed at a radiculopathic process when initial imaging fails to show a structural abnormality at the spinal level of deficit. The possible pathophysiological origins for this unusual presentation are discussed. Based on the experience gained with these patients, recommendations are made regarding the diagnostic workup and management of this entity in children presenting with focal deficits that are not supported by imaging of the affected root levels. Chiari malformations may rarely masquerade as lower motor and sensory deficits, and appropriate treatment may result in excellent recovery of function.

摘要

Chiari畸形可能表现出广泛的症状和体征。然而,小儿神经外科文献中尚未描述以局灶性足部无力作为Chiari畸形的表现。两名患有Chiari畸形和全脊髓空洞症的儿童表现出疑似孤立性腰神经根病的症状。枕下减压颅骨切除术和颈椎椎板切除术后神经功能缺损完全消失。这些病例强调了对整个颅脊柱轴进行成像的重要性,以及当初始成像未能在缺损的脊髓水平显示结构异常时,避免专门针对神经根病过程进行治疗干预。本文讨论了这种不寻常表现的可能病理生理起源。基于对这些患者的经验,针对在受影响神经根水平成像未支持的局灶性缺损患儿中该疾病的诊断检查和管理提出了建议。Chiari畸形可能很少伪装为下运动和感觉功能缺损,适当的治疗可能会导致功能的极佳恢复。

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