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Spontaneous cervical intradural disc herniation

机译:自发性颈硬脑膜间盘突出症

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摘要

Cervical intradural disc herniation (IDH) is a rare condition with very few case reports in the literature. We report a 64-year-old man who presented with sudden onset neck pain and rapidly progressing weakness in the left upper and lower limb. There was no history of trauma. MRI of the cervical spine showed a C6-C7 disc prolapse, for which he underwent a C6-C7 discectomy and fusion with bone graft through an anterior cervical approach. To our knowledge, all patients with a cervical IDH reported in the literature have a traumatic etiology. To the best of our knowledge, we report the first patient with a spontaneous cervical IDH.
机译:颈硬脑膜间盘突出症(IDH)是一种罕见病,文献报道很少。我们报告了一个64岁的男性,他突然出现颈部疼痛,左上肢和下肢迅速发展无力。没有外伤史。颈椎MRI显示C6-C7椎间盘脱垂,为此,他接受了C6-C7椎间盘切除术并通过颈椎前路入路与植骨融合。据我们所知,文献中报道的所有患有颈部IDH的患者都有外伤性病因。据我们所知,我们报告了首例自发性颈椎IDH的患者。

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