Spontaneous Anterior Thoracic Spinal Cord Herniation through Dura Defect: A Case Report.

Korean Journal of Spine Pub Date : 2016-06-01 Epub Date: 2016-06-30 DOI:10.14245/kjs.2016.13.2.77
Kyung-Ho Jeong, Hyun-Woo Lee, Young-Min Kwon
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引用次数: 4

Abstract

Thoracic spinal cord herniation is a rare disease cause of progressive myelopathy. Magnetic resonance image is a useful tool to diagnose preoperatively. Operation is a treatment of option. Sixty-six-year-old female visited Dong-A University Medical Center for progressive gait disturbance with falling tendency to right side. She had radiating pain and tingling sense on both leg. Sense of touch and temperature was decreased below T6 level. Both hip and knee motor power were grade IV. Magnetic resonance imaging scan showed anterior displacement of the spinal cord at T4-T5 vertebral level. Under the diagnosis of thoracic spinal cord herniation with dura defect, operation was performed for the patient with intraoperative neuromonitoring. Laminectomy at T4 and T5 level was done, and intradural exploration of the spinal cord revealed dura defect about 25mm×8mm in size. Spinal cord was released under microscope and dura defect was repaired with Lyoplant. The patient's symptom improved after the surgical procedure, but touch and temperature sense under T6 level had unchanged.

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自发性胸前段脊髓硬脑膜缺损疝1例。
胸段脊髓突出症是一种罕见的进行性脊髓病的病因。磁共振成像是术前诊断的有用工具。手术是一种治疗的选择。66岁(女)因有右侧跌倒倾向的进行性步态障碍来到东亚大学医院。她两条腿都有放射状的疼痛和刺痛感。触觉和体温下降至T6以下。髋关节和膝关节运动功率均为IV级。磁共振成像扫描显示T4-T5椎体水平脊髓前移位。在诊断为胸段脊髓疝合并硬脑膜缺损的情况下,对患者行术中神经监测。在T4和T5水平行椎板切除术,硬膜内探查脊髓发现硬脑膜缺损,大小约25mm×8mm。显微镜下释放脊髓,用Lyoplant修复硬脑膜缺损。手术后患者症状有所改善,但T6水平下触觉和体温感觉无变化。
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