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脊柱罕见的骨内动静脉畸形。

A rare intraosseous arteriovenous malformation of the spine.

机构信息

Department of Neurological Surgery, University of Virginia Health System, Charlottesville, Virginia 22903, USA.

出版信息

J Neurosurg Spine. 2011 Sep;15(3):336-9. doi: 10.3171/2011.5.SPINE10872. Epub 2011 Jun 10.

Abstract

The authors report the case of a patient with an intraosseous spinal arteriovenous malformation (AVM) presenting as an epidural mass lesion that was causing spinal cord compression. The 59-year-old woman had bilateral numbness, weakness, and hyperreflexia of both legs. Magnetic resonance imaging revealed intermediate T1 signal and hyperintense T2 signal involving the right transverse process, bilateral pedicles, and T-5 spinous process; the lesion's epidural extension was causing severe canal compromise and cord displacement. Coil embolization was performed, and the patient underwent resection, after which preoperative symptoms improved. Histopathological analysis revealed a benign vascular proliferation consistent with an intraosseous spinal AVM. On review of the literature, the authors found this case to be the second intraosseous spinal AVM, and the first in a patient whose clinical presentation was consistent with that of a mass lesion of the bone.

摘要

作者报告了一例椎管内骨内动静脉畸形(AVM)患者,表现为硬膜外肿块病变导致脊髓受压。这名 59 岁女性出现双侧腿部麻木、无力和反射亢进。磁共振成像显示 T1 信号中等强度和 T2 信号高信号累及右侧横突、双侧椎弓根和 T-5 棘突;病变的硬膜外延伸导致严重的椎管狭窄和脊髓移位。进行了线圈栓塞,随后进行了切除,术前症状改善。组织病理学分析显示良性血管增生,符合骨内脊髓 AVM。文献复习发现,这是第二例骨内脊髓 AVM,也是首例临床表现与骨内肿块病变一致的患者。

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