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导致儿童椎动脉夹层的颈椎异常。

Cervical abnormalities causing vertebral artery dissection in children.

作者信息

Sedney Cara L, Rosen Charles L

机构信息

Department of Neurosurgery, West Virginia University, Morgantown, West Virginia 26506-9183, USA.

出版信息

J Neurosurg Pediatr. 2011 Mar;7(3):272-5. doi: 10.3171/2010.12.PEDS10106.

Abstract

Vertebral artery dissection (VAD) is rare in children but is increasingly recognized as a cause of stroke in the pediatric population. Traditionally, VAD was thought to be attributable to either trauma or spontaneous dissections. Recently, several underlying causes, such as bony cervical abnormalities, connective tissue diseases, and infection, have been determined to account for spontaneous VAD or those cases associated with only minor trauma. Two pediatric cases of VAD are presented, both caused by bony cervical abnormalities and each treated with different surgical procedures for symptom resolution. The first case required suboccipital decompression and endovascular sacrifice of the vertebral artery. The second case was treated with surgical decompression of the foramen transversarium at C-1 and C-2. The treatment of both of these patients required accurate diagnosis via cervical spine CT to define the bone anatomy and delineate a cause for what was originally theorized to be spontaneous VAD.

摘要

椎动脉夹层(VAD)在儿童中较为罕见,但越来越被认为是儿科人群中风的一个病因。传统上,VAD被认为要么归因于创伤,要么是自发性夹层。最近,一些潜在病因,如颈椎骨异常、结缔组织疾病和感染,已被确定可导致自发性VAD或那些仅与轻微创伤相关的病例。本文介绍了两例儿科VAD病例,均由颈椎骨异常引起,且每例均采用不同的外科手术来缓解症状。第一例需要枕下减压并对椎动脉进行血管内栓塞。第二例通过对C-1和C-2横突孔进行手术减压来治疗。这两名患者的治疗都需要通过颈椎CT进行准确诊断,以确定骨骼解剖结构并找出最初被认为是自发性VAD的病因。

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