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首页> 外文期刊>European spine journal >Brown-Sequard syndrome revealing intradural thoracic disc herniation
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Brown-Sequard syndrome revealing intradural thoracic disc herniation

机译:Brown-Sequard综合征显示硬膜内胸椎间盘突出

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Brown-Sequard syndrome (BSS) is a rare form of severe myelopathy characterised by a clinical picture reflecting hemisection of the spinal cord. This syndrome is mostly due to a penetrating injury to the spine but many other non-traumatic causes have been described. Intradural thoracic disc herniation (TDH) is one of the rare aetiologies of this syndrome. Despite progress in imaging techniques, diagnosis and treatment remain difficult. We retrospectively reviewed one of the largest reported series of six patients with BSS revealing intradural TDH between 2003 and 2007. There was a marked female predominance and the mean age was 44?years. Before surgery, half of the patients had a severe neurological deficit. The mean duration of symptoms until surgery was 8.5?months (range 0.5–24?months). Spine magnetic resonance imaging (MRI) or spine computer tomography scan showed calcified TDH between T5–T6 and T9–T10. The intradural location of the thoracic herniation was strongly suspected from the clinical data. All the patients underwent posterolateral transpedicular surgery with an operative microscope to open the dura mater. The intradural location of the herniation was overlooked in one case and the patient underwent a second procedure. The dura mater was carefully closed. Two patients’ condition worsened immediately after the surgery before slowly improving. All the other patients improved their neurological status immediately after the surgery and at 12?months follow-up. BSS with TDH on the spine MRI scan may be a warning symptom of the intradural location of the herniated disc. In such cases, spine surgeons are advised to use an operative magnification and to open the dura mater to avoid missing this potentially curable cause of severe myelopathy...
机译:Brown-Sequard综合征(BSS)是一种严重的脊髓病的罕见形式,其特征是反映脊髓半切的临床图像。该综合征主要是由于脊椎的穿透性损伤,但是已经描述了许多其他非创伤性原因。硬膜内胸椎间盘突出症(TDH)是该综合征的罕见病因之一。尽管成像技术取得了进步,但是诊断和治疗仍然很困难。我们回顾性分析了2003年至2007年间报告的最大的6例BSS揭示硬膜内TDH的患者之一。女性占优势,平均年龄为44岁。手术前,一半的患者患有严重的神经功能缺损。直到手术的平均症状持续时间为8.5个月(0.5到24个月)。脊柱磁共振成像(MRI)或脊柱计算机断层扫描显示T5–T6和T9–T10之间钙化的TDH。从临床数据强烈怀疑胸膜疝的硬膜内位置。所有患者均接受后外侧经蒂手术,并用手术显微镜打开硬脑膜。在一种情况下,忽略了硬膜外突出的硬膜外位置,并且对患者进行了第二次手术。硬脑膜被仔细关闭。两名患者的状况在手术后立即恶化,然后逐渐好转。所有其他患者在手术后和随访12个月后均改善了神经系统状态。脊柱MRI扫描上带有TDH的BSS可能是椎间盘突出症硬膜内位置的警告症状。在这种情况下,建议脊柱外科医生使用手术放大倍数并打开硬脑膜以避免遗漏这种可能治愈的严重脊髓病原因。

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