• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

儿童脑海绵状血管畸形手术后的功能结果。

Functional outcome after pediatric cerebral cavernous malformation surgery.

机构信息

Department of Neurosurgery and Spine Surgery, University Hospital Essen, Essen, Germany.

Center for Translational Neuro- and Behavioral Sciences, C-TNBS, University Duisburg Essen, Essen, Germany.

出版信息

Sci Rep. 2023 Feb 9;13(1):2286. doi: 10.1038/s41598-023-29472-5.

DOI:10.1038/s41598-023-29472-5
PMID:36759693
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9911771/
Abstract

The purpose of this study was to investigate the functional outcome following surgical resection of cerebral cavernous malformations (CCM) in pediatric patients. We screened our institutional database of CCM patients treated between 2003 and 2021. Inclusion regarded individuals younger or equal than 18 years of age with complete clinical baseline characteristics, magnetic resonance imaging dataset, and postoperative follow-up time of at least three months. Functional outcome was quantified using the modified Rankin Scale (mRS) score and assessed at admission, discharge, and last follow-up examination. The primary endpoint was the postoperative functional outcome. As a secondary endpoint, predictors of postoperative functional deterioration were assessed. A total of 49 pediatric patients with a mean age of 11.3 ± 5.7 years were included for subsequent analyses. Twenty individuals (40.8%) were female. Complete resection of the lesion was achieved in 44 patients (89.8%), and two patients with incomplete resection were referred for successive remnant removal. The mean follow-up time after surgery was 44 months (IQR: 13 - 131). The mean mRS score was 1.6 on admission, 1.7 at discharge, and 0.9 at the latest follow-up. Logistic regression analysis adjusted to age and sex identified brainstem localization (aOR = 53.45 [95%CI = 2.26 - 1261.81], p = .014) as a predictor of postoperative deterioration. This study indicates that CCM removal in children can be regarded as safe and favorable for the majority of patients, depending on lesion localization. Brainstem localization implies a high risk of postoperative morbidity and indication for surgery should be balanced carefully. Minor evidence indicates that second-look surgery for CCM remnants might be safe and favorable.

摘要

本研究旨在探讨儿童脑动静脉畸形(CAVM)手术切除后的功能预后。我们筛选了 2003 年至 2021 年间在我院接受治疗的 CAVM 患者的机构数据库。纳入标准为年龄小于或等于 18 岁,具有完整的临床基线特征、磁共振成像数据集和至少 3 个月的术后随访时间。采用改良 Rankin 量表(mRS)评分评估功能预后,并在入院时、出院时和最后一次随访时进行评估。主要终点为术后功能结局。次要终点为评估术后功能恶化的预测因素。共纳入 49 例平均年龄为 11.3±5.7 岁的儿科患者进行后续分析。20 例(40.8%)为女性。44 例患者(89.8%)实现了病变的完全切除,2 例不完全切除的患者接受了进一步的残腔切除术。术后平均随访时间为 44 个月(IQR:13-131)。入院时 mRS 评分的平均值为 1.6,出院时为 1.7,最后一次随访时为 0.9。经年龄和性别调整的逻辑回归分析确定脑干定位(优势比[aOR]=53.45[95%CI=2.26-1261.81],p=0.014)为术后恶化的预测因素。本研究表明,对于大多数患者而言,儿童 CAVM 的切除是安全且有利的,但取决于病变的定位。脑干定位提示术后发病率高,手术指征应仔细权衡。有少量证据表明,CAVM 残腔的二次探查手术可能是安全且有利的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1528/9911771/051e834e3ad2/41598_2023_29472_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1528/9911771/051e834e3ad2/41598_2023_29472_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1528/9911771/051e834e3ad2/41598_2023_29472_Fig1_HTML.jpg

相似文献

1
Functional outcome after pediatric cerebral cavernous malformation surgery.儿童脑海绵状血管畸形手术后的功能结果。
Sci Rep. 2023 Feb 9;13(1):2286. doi: 10.1038/s41598-023-29472-5.
2
Surgical management of pediatric brainstem cavernous malformations.小儿脑干海绵状血管畸形的外科治疗
J Neurosurg Pediatr. 2014 May;13(5):484-502. doi: 10.3171/2014.2.PEDS13536. Epub 2014 Mar 28.
3
Natural Course of Cerebral Cavernous Malformations in Children: A Five-Year Follow-Up Study.儿童脑海绵状血管畸形的自然病程:一项为期五年的随访研究。
Stroke. 2022 Mar;53(3):817-824. doi: 10.1161/STROKEAHA.121.035338. Epub 2021 Oct 28.
4
The utility of preoperative diffusion tensor imaging in the surgical management of brainstem cavernous malformations.术前弥散张量成像在脑干海绵状血管畸形手术治疗中的应用
J Neurosurg. 2015 Mar;122(3):653-62. doi: 10.3171/2014.11.JNS13680. Epub 2015 Jan 9.
5
Reliable? The Value of Early Postoperative Magnetic Resonance Imaging after Cerebral Cavernous Malformation Surgery.可靠吗?脑海绵状血管畸形手术后早期磁共振成像的价值。
World Neurosurg. 2017 Jul;103:138-144. doi: 10.1016/j.wneu.2017.03.135. Epub 2017 Apr 5.
6
Hemorrhage risk, surgical management, and functional outcome of brainstem cavernous malformations.脑干海绵状血管畸形的出血风险、手术治疗和功能预后。
J Neurosurg. 2013 Oct;119(4):996-1008. doi: 10.3171/2013.7.JNS13462. Epub 2013 Aug 16.
7
Functional outcome after initial and multiple intracerebral hemorrhages in children with cerebral cavernous malformations.患有脑海绵状血管畸形的儿童首次及多次脑出血后的功能转归
Eur J Neurol. 2023 May;30(5):1364-1370. doi: 10.1111/ene.15749. Epub 2023 Mar 3.
8
Long-term outcomes after surgery for brainstem cavernous malformations: analysis of 46 consecutive cases.脑干海绵状血管畸形手术后的长期结果:46 例连续病例分析。
J Neurosurg. 2022 Sep 9;138(4):900-909. doi: 10.3171/2022.7.JNS22314. Print 2023 Apr 1.
9
Cerebellar cavernous malformation in pediatric patients: defining clinical, neuroimaging, and therapeutic characteristics.小儿患者的小脑海绵状血管畸形:界定临床、神经影像学及治疗特征
J Neurosurg Pediatr. 2015 Sep;16(3):256-66. doi: 10.3171/2015.1.PEDS14366. Epub 2015 May 22.
10
Central nervous system cavernous malformations: cross-sectional study assessing rebleeding risk after a second haemorrhage.中枢神经系统海绵状血管畸形:评估第二次出血后再出血风险的横断面研究
Eur J Neurol. 2023 Jan;30(1):144-149. doi: 10.1111/ene.15574. Epub 2022 Oct 13.

引用本文的文献

1
A rare cause of persistent hiccups: familial cerebral cavernous malformations associated with mutation of the KRIT1 gene.持续性呃逆的罕见病因:与KRIT1基因突变相关的家族性脑海绵状血管畸形。
Acta Neurol Belg. 2025 Jun 2. doi: 10.1007/s13760-025-02817-9.
2
Magnetic resonance-guided laser interstitial thermal therapy (MRgLITT) for paediatric intracranial cavernous malformations: case series and review of the literature.磁共振引导激光间质热疗(MRgLITT)治疗小儿颅内海绵状畸形:病例系列及文献综述
Childs Nerv Syst. 2025 May 17;41(1):183. doi: 10.1007/s00381-025-06839-9.
3
Outcomes after surgical and nonsurgical treatment of pediatric cerebral cavernous malformation.

本文引用的文献

1
A systematic review and meta-analysis of surgeries performed for cerebral cavernous malformation-related epilepsy in pediatric patients.小儿脑海绵状血管畸形相关癫痫手术的系统评价与荟萃分析。
Front Pediatr. 2022 Sep 6;10:892456. doi: 10.3389/fped.2022.892456. eCollection 2022.
2
Natural Course of Cerebral Cavernous Malformations in Children: A Five-Year Follow-Up Study.儿童脑海绵状血管畸形的自然病程:一项为期五年的随访研究。
Stroke. 2022 Mar;53(3):817-824. doi: 10.1161/STROKEAHA.121.035338. Epub 2021 Oct 28.
3
Surgical treatment of brainstem cavernous malformations: an international Delphi consensus.
小儿脑海绵状血管畸形手术及非手术治疗后的结果
Pediatr Investig. 2024 Jun 11;8(2):126-134. doi: 10.1002/ped4.12435. eCollection 2024 Jun.
4
Focused Ultrasound Blood-Brain Barrier Opening Arrests the Growth and Formation of Cerebral Cavernous Malformations.聚焦超声打开血脑屏障可抑制脑海绵状血管畸形的生长和形成。
bioRxiv. 2024 Feb 4:2024.01.31.577810. doi: 10.1101/2024.01.31.577810.
脑干海绵状血管畸形的外科治疗:一项国际德尔菲共识
J Neurosurg. 2021 Oct 1;136(5):1220-1230. doi: 10.3171/2021.3.JNS2156. Print 2022 May 1.
4
Assessment and validation of proposed classification tools for brainstem cavernous malformations.脑干海绵状血管畸形拟用分类工具的评估与验证
J Neurosurg. 2020 Oct 16;135(2):410-416. doi: 10.3171/2020.6.JNS201585. Print 2021 Aug 1.
5
Cerebral cavernous malformation presenting in childhood: a single-centered surgical experience of 29 cases.儿童期脑内海绵状血管畸形:单中心 29 例手术经验。
Clin Neurol Neurosurg. 2020 Jul;194:105830. doi: 10.1016/j.clineuro.2020.105830. Epub 2020 Apr 10.
6
Natural history of brainstem cavernous malformations: prospective hemorrhage rate and adverse factors in a consecutive prospective cohort.脑干海绵状血管畸形的自然史:连续前瞻性队列中的前瞻性出血率和不良因素。
J Neurosurg. 2020 Mar 13;134(3):917-928. doi: 10.3171/2019.12.JNS192856. Print 2021 Mar 1.
7
Frontal Lobe Cavernous Malformations in Pediatric Patients: Clinical Features and Surgical Outcomes.小儿额叶海绵状血管畸形:临床特征与手术结果
J Child Neurol. 2018 Jul;33(8):512-518. doi: 10.1177/0883073818768156. Epub 2018 Apr 26.
8
Cavernous malformations of central nervous system in pediatric patients: our single-centered experience in 50 patients and review of literature.小儿中枢神经系统海绵状畸形:我们对50例患者的单中心经验及文献回顾
Childs Nerv Syst. 2017 Sep;33(9):1525-1538. doi: 10.1007/s00381-017-3429-7. Epub 2017 Jun 20.
9
Synopsis of Guidelines for the Clinical Management of Cerebral Cavernous Malformations: Consensus Recommendations Based on Systematic Literature Review by the Angioma Alliance Scientific Advisory Board Clinical Experts Panel.脑海绵状血管畸形临床管理指南概要:基于血管瘤联盟科学咨询委员会临床专家小组系统文献综述的共识建议
Neurosurgery. 2017 May 1;80(5):665-680. doi: 10.1093/neuros/nyx091.
10
Correlation of the venous angioarchitecture of multiple cerebral cavernous malformations with familial or sporadic disease: a susceptibility-weighted imaging study with 7-Tesla MRI.多发性脑海绵状血管畸形的静脉血管构筑与家族性或散发性疾病的相关性:7 特斯拉 MRI 下的磁敏感加权成像研究。
J Neurosurg. 2017 Feb;126(2):570-577. doi: 10.3171/2016.2.JNS152322. Epub 2016 May 6.