• 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

伴有颈内动脉和大脑中动脉血管炎及狭窄的神经囊尾蚴病

Neurocysticercosis With Internal Carotid Artery and Middle Cerebral Artery Vasculitis and Stenosis.

作者信息

Kumar Pradeep, Prasad Arun, Kumar Subhash

机构信息

Pediatrics, All India Institute of Medical Sciences, Patna, IND.

Radiodiagnosis, All India Institute of Medical Sciences, Patna, IND.

出版信息

Cureus. 2022 Jul 28;14(7):e27407. doi: 10.7759/cureus.27407. eCollection 2022 Jul.

DOI:10.7759/cureus.27407
PMID:36046302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9419848/
Abstract

A seven-year-old female child presented with sub-acute onset headache, vomiting, and aphasia with right-sided upper motor neuron (UMN) type hemiparesis and ipsilateral UMN type facial nerve weakness. Her coagulation profile and thrombotic profile were normal. MRI brain with magnetic resonance angiography (MRA) detected neurocysticercosis causing secondary vasculitis and narrowing of supraclinoid left internal carotid artery (ICA) and middle cerebral artery (MCA). The patient was given aspirin along with steroids and albendazole. She improved gradually, and her hemiparesis and facial nerve palsy improved completely by three months and aphasia by four months.

摘要

一名七岁女童出现亚急性起病的头痛、呕吐、失语,伴有右侧上运动神经元(UMN)型偏瘫及同侧UMN型面神经无力。她的凝血指标和血栓形成指标均正常。头颅磁共振成像(MRI)及磁共振血管造影(MRA)检查发现神经囊尾蚴病导致继发性血管炎,以及左侧颈内动脉床突上段(ICA)和大脑中动脉(MCA)狭窄。该患者接受了阿司匹林、类固醇及阿苯达唑治疗。她逐渐好转,三个月时偏瘫和面神经麻痹完全改善,四个月时失语改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fe/9419848/13a15ef016a2/cureus-0014-00000027407-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fe/9419848/13a15ef016a2/cureus-0014-00000027407-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89fe/9419848/13a15ef016a2/cureus-0014-00000027407-i01.jpg

相似文献

1
Neurocysticercosis With Internal Carotid Artery and Middle Cerebral Artery Vasculitis and Stenosis.伴有颈内动脉和大脑中动脉血管炎及狭窄的神经囊尾蚴病
Cureus. 2022 Jul 28;14(7):e27407. doi: 10.7759/cureus.27407. eCollection 2022 Jul.
2
Internal Carotid Artery Agenesis with an Intercavernous Anastomosis: A Rare Case.伴有海绵窦间吻合的颈内动脉缺如:1例罕见病例
J Stroke Cerebrovasc Dis. 2017 Oct;26(10):2442-2445. doi: 10.1016/j.jstrokecerebrovasdis.2017.06.055. Epub 2017 Aug 3.
3
Acute progressive stroke with middle cerebral artery occlusion caused by idiopathic hypereosinophilic syndrome: a case report.特发性嗜酸性粒细胞增多综合征致大脑中动脉闭塞性急性进展性脑卒中 1 例报告
BMC Neurol. 2020 Oct 1;20(1):361. doi: 10.1186/s12883-020-01941-8.
4
Crohns disease with central nervous system vasculitis causing subarachnoid hemorrhage due to aneurysm and cerebral ischemic stroke.克罗恩病合并中枢神经系统血管炎,因动脉瘤导致蛛网膜下腔出血及脑缺血性中风。
Ann Indian Acad Neurol. 2014 Oct;17(4):444-7. doi: 10.4103/0972-2327.144035.
5
Spontaneous intracranial internal carotid artery dissection treated by intra-arterial thrombolysis and superficial temporal artery-middle cerebral artery anastomosis in the acute stage--case report--.急性期经动脉内溶栓和颞浅动脉-大脑中动脉吻合术治疗自发性颅内颈内动脉夹层——病例报告——
Neurol Med Chir (Tokyo). 2005 Mar;45(3):148-51. doi: 10.2176/nmc.45.148.
6
Internal carotid artery dissection heralded by an oculomotor nerve palsy: case report and literature review.以动眼神经麻痹为先兆的颈内动脉夹层:病例报告及文献综述
Neurologist. 2011 Nov;17(6):333-7. doi: 10.1097/NRL.0b013e318218030a.
7
Traumatic retroclival epidural hematoma associated with reversible ipsilateral internal carotid artery stenosis.与可逆性同侧颈内动脉狭窄相关的创伤性斜坡后硬膜外血肿。
Childs Nerv Syst. 2022 Feb;38(2):485-489. doi: 10.1007/s00381-021-05276-8. Epub 2021 Nov 27.
8
Acute Ischemic Stroke due to Internal Carotid Artery Dissection in a 10-Year-Old Child.一名10岁儿童因颈内动脉夹层导致的急性缺血性卒中
Asian J Neurosurg. 2020 Aug 28;15(3):716-718. doi: 10.4103/ajns.AJNS_146_20. eCollection 2020 Jul-Sep.
9
[Spontaneous intracranial internal carotid artery dissection: 6 case reports and a review of 39 cases in the literature].[自发性颅内颈内动脉夹层:6例报告及文献中39例病例回顾]
Rinsho Shinkeigaku. 2003 Jun;43(6):313-21.
10
Spontaneous carotid dissection presenting lower cranial nerve palsies.自发性颈动脉夹层伴下颅神经麻痹。
J Neurol Sci. 2001 Mar 1;184(2):203-7. doi: 10.1016/s0022-510x(01)00440-3.

引用本文的文献

1
Calcified Neurocysticercosis: Understanding Dead (Not Necessarily Inactive) Parasites.钙化性神经囊尾蚴病:了解死亡(不一定无活性)的寄生虫
Am J Trop Med Hyg. 2025 Mar 18;112(6):1187-1192. doi: 10.4269/ajtmh.24-0446. Print 2025 Jun 4.

本文引用的文献

1
Cortical Blindness Due to Neurocysticercosis in an Adolescent Patient.一名青少年患者因神经囊尾蚴病导致皮质盲
Trop Med Infect Dis. 2022 Jun 8;7(6):96. doi: 10.3390/tropicalmed7060096.
2
Subarachnoid neurocysticercosis and an intracranial infectious aneurysm: case report.脑底蛛网膜囊虫病伴颅内感染性动脉瘤:病例报告。
Neurosurg Focus. 2019 Aug 1;47(2):E16. doi: 10.3171/2019.5.FOCUS19280.
3
Pediatric Neurocysticercosis.小儿神经囊尾蚴病。
Indian J Pediatr. 2019 Jan;86(1):76-82. doi: 10.1007/s12098-017-2460-8. Epub 2017 Sep 20.
4
Clinical management of infectious cerebral vasculitides.感染性脑动脉炎的临床管理
Expert Rev Neurother. 2016;16(2):205-21. doi: 10.1586/14737175.2015.1134321. Epub 2016 Jan 19.
5
Department of Paediatrics, Nalanda Medical College, Patna.巴特那那烂陀医学院儿科学系
J Indian Med Assoc. 2004 Jun;102(6):317-8, 320, 322 passim.
6
Granuloma formation and parasite disintegration in porcine cysticercosis: comparison with human neurocysticercosis.猪囊尾蚴病中的肉芽肿形成和寄生虫解体:与人类神经囊尾蚴病的比较。
J Comp Pathol. 2002 Aug-Oct;127(2-3):186-93. doi: 10.1053/jcpa.2002.0579.
7
Neurocysticercosis presenting as stroke.表现为中风的神经囊尾蚴病。
Neurol India. 2000 Dec;48(4):391-4.
8
Clinical spectrum of 500 children with neurocysticercosis and response to albendazole therapy.500例儿童神经囊尾蚴病的临床谱及对阿苯达唑治疗的反应
J Child Neurol. 2000 Apr;15(4):207-13. doi: 10.1177/088307380001500401.
9
Neurocysticercosis.神经囊尾蚴病
Postgrad Med J. 1998 Jun;74(872):321-6. doi: 10.1136/pgmj.74.872.321.
10
Cerebral cysticercotic arteritis: detection and follow-up by transcranial Doppler.
Cerebrovasc Dis. 1998 Jan-Feb;8(1):2-7. doi: 10.1159/000015808.