脊髓动静脉异长综合征(SAMS)中硬膜外高流量血管畸形的自发消退:一个独特的病例报告。

Q3 Medicine
Prasert Iampreechakul, Songpol Chuntaroj, Yodkhwan Wattanasen, Sunisa Hangsapruek, Punjama Lertbutsayanukul, Somkiet Siriwimonmas
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引用次数: 0

摘要

背景:脊髓动静脉异聚综合征(SAMS)是一种罕见的非遗传性遗传性血管疾病,涉及同一异聚水平的多层组织。SAMS自发性消退在医学文献中从未报道过。病例描述:一名42岁女性,间歇性腰痛6个月。胸腰椎的磁共振成像偶然发现了脊髓、椎体、硬膜外间隙和棘旁肌肉的血管畸形。没有静脉充血的迹象。磁共振血管造影和脊髓血管造影显示硬膜内脊髓动静脉畸形(SCAVM)在T10-11水平和硬膜外高流量骨性动静脉瘘。由于无症状的SAMS和治疗期间脊柱前动脉损伤的高风险,我们考虑保守治疗。首次血管造影后8年的脊髓血管造影显示SAMS的硬膜外成分明显消退,硬膜内SCAVM稳定。结论:我们描述了一个独特的SAMS病例,在长期观察期间,硬膜外成分自发消退。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Spontaneous regression of extradural high-flow vascular malformation in spinal arteriovenous metameric syndrome (SAMS): A unique case report.

Spontaneous regression of extradural high-flow vascular malformation in spinal arteriovenous metameric syndrome (SAMS): A unique case report.

Spontaneous regression of extradural high-flow vascular malformation in spinal arteriovenous metameric syndrome (SAMS): A unique case report.

Spontaneous regression of extradural high-flow vascular malformation in spinal arteriovenous metameric syndrome (SAMS): A unique case report.

Background: Spinal arteriovenous metameric syndrome (SAMS) is a rare nonhereditary genetic vascular disorder, involving multiple layers of tissues in the same metameric level. Spontaneous regression of SAMS has never been reported in the medical literature.

Case description: A 42-year-old woman presented with intermittent low back pain for 6 months. Magnetic resonance imaging of the thoracolumbar spine incidentally found clusters of spinal vascular malformations involving spinal cord, vertebral bodies, epidural space, and paraspinal muscles. There was no sign of venous congestion. Magnetic resonance angiography and spinal angiography revealed intradural spinal cord arteriovenous malformation (SCAVM) at the level of T10-11 and extradural high-flow osseous arteriovenous fistula. Due to asymptomatic SAMS and a high risk of anterior spinal arterial compromise during treatment, conservative treatment was considered in our patient. Spinal angiography obtained 8 years after initial angiography demonstrated significant regression of extradural component of SAMS and stable intradural SCAVM.

Conclusion: We describe a unique case of SAMS with spontaneous regression of extradural component during a long-term observation period.

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