已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

Quantitative Analysis of Intracranial Vertebrobasilar Dissecting Aneurysm with Intramural Hematoma After Endovascular Treatment Using 3-T High-Resolution Magnetic Resonance Imaging

医学 磁共振成像 放射科 动脉瘤 血肿 血管内治疗
作者
Zhongbin Tian,Junfan Chen,Yisen Zhang,Jian Liu,Yang Wang,Binbin Sui,Xinjian Yang
出处
期刊:World Neurosurgery [Elsevier BV]
卷期号:108: 236-243 被引量:5
标识
DOI:10.1016/j.wneu.2017.08.161
摘要

Quantitative measurements of intracranial vessel walls are reliable in 3-T high-resolution magnetic resonance imaging (HR-MRI). However, few reports have assessed the arterial wall after endovascular treatment (EVT) by 3-T HR-MRI. This study aimed to quantitatively analyze vessel walls in vertebrobasilar artery dissecting aneurysms after EVT.From May 2012 to December 2015, a total of 21 patients with 21 intracranial vertebrobasilar dissecting aneurysms (VBDAs) were enrolled in this consecutive study. All the VBDAs were characterized by intramural hematomas (IMHs ≥5 mm) and treated with reconstructive EVT. Images of preoperative and follow-up 3-T HR-MRI were used to evaluate the arterial wall. The relative signal intensity (RSI) of IMHs was quantified on T1-weighted imaging (T1WI) and magnetization-prepared rapid acquisition gradient-echo (MPRAGE).Angiographic follow-up was performed for a mean of 9.19 ± 3.22 months. According to angiographic results at follow-up, 21 patients were divided into 2 groups (progressive group, n = 6; stable group, n = 15). In the progressive group, RSI of IMHs was significantly increased on MPRAGE of follow-up 3-T HR-MRI compared with that before treatment (P < 0.05), and the difference was not significant on T1WI. However, in the stable group, RSI of IMHs was significantly reduced after treatment (P < 0.05).Persistent high signal intensity of IMHs in VBDAs after reconstructive EVT may be associated with the progression of VBDAs. It may also indicate an unsteady state of the aneurysm, which suggests that reconstruction of the parent artery is not satisfactory.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
小小完成签到 ,获得积分10
1秒前
大力的图图应助小明月采纳,获得10
1秒前
FashionBoy应助科研通管家采纳,获得10
2秒前
小二郎应助科研通管家采纳,获得10
2秒前
彭于晏应助科研通管家采纳,获得10
2秒前
酷波er应助科研通管家采纳,获得10
2秒前
科目三应助科研通管家采纳,获得10
2秒前
2秒前
晨晨发布了新的文献求助10
6秒前
小枣完成签到 ,获得积分10
8秒前
9秒前
Lucas应助pink采纳,获得10
10秒前
六六发布了新的文献求助10
12秒前
小明月完成签到,获得积分10
15秒前
壳聚糖完成签到 ,获得积分10
17秒前
思源应助LLL采纳,获得10
18秒前
拟闲发布了新的文献求助10
19秒前
传奇3应助卡卡卡采纳,获得10
20秒前
GingerF应助Zbw采纳,获得50
20秒前
妩媚完成签到,获得积分10
22秒前
27秒前
Lucas应助妩媚采纳,获得10
27秒前
无敌大鸡腿完成签到,获得积分10
28秒前
28秒前
Muncy完成签到 ,获得积分10
30秒前
Viiigo完成签到,获得积分10
36秒前
活力的招牌完成签到 ,获得积分10
37秒前
Cc完成签到 ,获得积分10
40秒前
Zbw给Zbw的求助进行了留言
40秒前
小蘑菇应助LiTianHao采纳,获得10
42秒前
42秒前
luster完成签到 ,获得积分10
43秒前
CMUSK完成签到 ,获得积分10
44秒前
49秒前
jzfbx发布了新的文献求助20
50秒前
CLZ完成签到 ,获得积分10
50秒前
50秒前
53秒前
肉松发布了新的文献求助10
54秒前
优雅枫叶完成签到 ,获得积分10
55秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
HANDBOOK OF CHEMISTRY AND PHYSICS 106th edition 1000
ASPEN Adult Nutrition Support Core Curriculum, Fourth Edition 1000
AnnualResearch andConsultation Report of Panorama survey and Investment strategy onChinaIndustry 1000
Continuing Syntax 1000
Signals, Systems, and Signal Processing 610
Decentring Leadership 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6277260
求助须知:如何正确求助?哪些是违规求助? 8096857
关于积分的说明 16926547
捐赠科研通 5346365
什么是DOI,文献DOI怎么找? 2842392
邀请新用户注册赠送积分活动 1819644
关于科研通互助平台的介绍 1676797