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脊髓动静脉畸形伴脊髓空洞症。

Spinal arteriovenous malformation associated with syringomyelia.

作者信息

Srivatanakul Kittipong, Songsaeng Dittapong, Ozanne Augustin, Toulgoat Frédérique, Lasjaunias Pierre

机构信息

Service de Neuroradiologie Diagnostique et Thérapeutique, Hôpital de Bicêtre, Paris, France.

出版信息

J Neurosurg Spine. 2009 May;10(5):436-42. doi: 10.3171/2009.2.SPINE08172.

Abstract

The authors describe 4 cases of syringomyelia-associated spinal cord arteriovenous malformation (AVM). All cases were managed with embolization of the AVM. Treatments were aimed to stabilize the AVM itself and not directed toward the syrinx. In 3 of the 4 cases the syringomyelia resolved after treatment. Reports concerning AVM as a cause of syringomyelia is very scarce and lacks posttreatment clinical information. In light of the clinical course and imaging findings, the authors propose a theory that venous hypertension in the spinal cord is the trigger for the development of syringomyelia, which may reverse after AVM treatment.

摘要

作者描述了4例与脊髓空洞症相关的脊髓动静脉畸形(AVM)病例。所有病例均采用AVM栓塞治疗。治疗旨在稳定AVM本身,而非针对脊髓空洞。4例中有3例在治疗后脊髓空洞症消失。关于AVM作为脊髓空洞症病因的报道非常稀少,且缺乏治疗后的临床信息。根据临床病程和影像学表现,作者提出一种理论,即脊髓静脉高压是脊髓空洞症发生发展的触发因素,在AVM治疗后可能逆转。

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