• 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

一例罕见复杂病例报告:双侧先天性颈内动脉发育不全伴左侧真性后交通动脉瘤破裂

A Rare Complex Case Report: Bilateral Congenital Internal Carotid Artery Hypoplasia Associated with Ruptured Left True Posterior Communicating Artery Aneurysm.

作者信息

Soni Tushar V, Patel Shreyansh, Shah Varshesh, Deo Manas Ranjan, Kotadiya Kuldeep

机构信息

Department of Neurosurgery, Smt. NHL Municipal Medical College and Sardar Vallabhbhai Patel Institute of Medical Sciences & Research, Ahmedabad, Gujarat, India.

出版信息

Asian J Neurosurg. 2024 Jun 24;19(3):567-571. doi: 10.1055/s-0044-1787861. eCollection 2024 Sep.

DOI:10.1055/s-0044-1787861
PMID:39205880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11349397/
Abstract

Congenital internal carotid artery hypoplasia is a rare condition characterized by underdevelopment or reduced caliber of the internal carotid artery during embryonic development. This anomaly presents significant challenges in management, particularly in neurosurgical interventions for cerebrovascular events. We present a case report of a 67-year-old male who presented with subarachnoid hemorrhage and intraparenchymal hemorrhage extending as intraventricular hemorrhage due to a ruptured left true posterior communicating artery aneurysm, associated with intraoperative findings of left internal carotid artery aneurysm, accompanied by incidental findings of bilateral congenital hypoplasia of the internal carotid artery on computed tomography angiography. Surgical intervention involved a left frontotemporal craniotomy, during which both aneurysms were successfully clipped. This case underscores the critical importance of meticulous preoperative evaluation, utilizing advanced neuroimaging modalities to identify such anomalies, particularly in patients with acute cerebrovascular events. Furthermore, it emphasizes the necessity for meticulous surgical planning and intraoperative vigilance to effectively manage associated vascular pathologies.

摘要

先天性颈内动脉发育不全是一种罕见的病症,其特征是在胚胎发育过程中颈内动脉发育不良或管径变细。这种异常在治疗中带来了重大挑战,尤其是在针对脑血管事件的神经外科干预中。我们报告一例67岁男性病例,该患者因左侧真性后交通动脉瘤破裂出现蛛网膜下腔出血和脑实质内出血并扩展至脑室内出血,术中发现左侧颈内动脉瘤,同时计算机断层血管造影偶然发现双侧颈内动脉先天性发育不全。手术干预采用左侧额颞开颅术,术中成功夹闭了两个动脉瘤。该病例强调了术前细致评估的至关重要性,利用先进的神经影像学手段识别此类异常,特别是在急性脑血管事件患者中。此外,它还强调了精心的手术规划和术中警惕性对于有效处理相关血管病变的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c1/11349397/55914a75ab98/10-1055-s-0044-1787861-i2430028-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c1/11349397/7c83bd5da1eb/10-1055-s-0044-1787861-i2430028-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c1/11349397/019ac47d2946/10-1055-s-0044-1787861-i2430028-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c1/11349397/32642cee21ad/10-1055-s-0044-1787861-i2430028-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c1/11349397/c60344ea6004/10-1055-s-0044-1787861-i2430028-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c1/11349397/fb6440736145/10-1055-s-0044-1787861-i2430028-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c1/11349397/55914a75ab98/10-1055-s-0044-1787861-i2430028-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c1/11349397/7c83bd5da1eb/10-1055-s-0044-1787861-i2430028-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c1/11349397/019ac47d2946/10-1055-s-0044-1787861-i2430028-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c1/11349397/32642cee21ad/10-1055-s-0044-1787861-i2430028-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c1/11349397/c60344ea6004/10-1055-s-0044-1787861-i2430028-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c1/11349397/fb6440736145/10-1055-s-0044-1787861-i2430028-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5c1/11349397/55914a75ab98/10-1055-s-0044-1787861-i2430028-6.jpg

相似文献

1
A Rare Complex Case Report: Bilateral Congenital Internal Carotid Artery Hypoplasia Associated with Ruptured Left True Posterior Communicating Artery Aneurysm.一例罕见复杂病例报告:双侧先天性颈内动脉发育不全伴左侧真性后交通动脉瘤破裂
Asian J Neurosurg. 2024 Jun 24;19(3):567-571. doi: 10.1055/s-0044-1787861. eCollection 2024 Sep.
2
Bilateral hypoplasia of the internal carotid artery, presenting as a subarachnoid hemorrhage secondary to intracranial aneurysmal formation: a case report.双侧颈内动脉发育不全,表现为颅内动脉瘤形成继发蛛网膜下腔出血:一例报告
J Med Case Rep. 2012 Jan 30;6:45. doi: 10.1186/1752-1947-6-45.
3
Bilateral internal carotid artery hypoplasia and multiple posterior circulation aneurysms. Importance of 3DCTA for the diagnosis.双侧颈内动脉发育不全与多发后循环动脉瘤。三维CT血管造影术在诊断中的重要性。
Turk Neurosurg. 2009 Apr;19(2):168-71.
4
"True" aneurysm of the posterior communicating artery as a possible effect of collateral circulation in a patient with occlusion of the internal carotid artery. A case study and literature review.后交通动脉“真性”动脉瘤作为颈内动脉闭塞患者侧支循环的一种可能影响。病例研究及文献综述。
Minim Invasive Neurosurg. 2002 Dec;45(4):240-4. doi: 10.1055/s-2002-36194.
5
An unruptured posterior communicating artery aneurysm ruptured during angiography: A case report.一例未破裂的后交通动脉瘤在血管造影术中破裂:病例报告。
Medicine (Baltimore). 2019 Nov;98(44):e17785. doi: 10.1097/MD.0000000000017785.
6
[Ruptured internal carotid -posterior communicating artery aneurysm associated with an anomalous hyperplastic anterior choroidal artery and aneurysm: case report].[破裂的颈内动脉 - 后交通动脉瘤伴异常增生的脉络膜前动脉及动脉瘤:病例报告]
No Shinkei Geka. 2005 Feb;33(2):155-62.
7
[A case of ruptured true posterior communicating artery aneurysm thirteen years after surgical occlusion of the ipsilateral cervical internal carotid artery].[同侧颈内动脉手术闭塞十三年后发生的真性后交通动脉瘤破裂一例]
No Shinkei Geka. 1995 Apr;23(4):359-63.
8
Ruptured pial-pial collateral aneurysm associated with left internal carotid artery occlusion: nuances of surgical management. Illustrative case.与左颈内动脉闭塞相关的软膜-软膜侧支动脉瘤破裂:手术治疗的细微差别。病例说明
J Neurosurg Case Lessons. 2024 Mar 18;7(12). doi: 10.3171/CASE2454.
9
Unilateral rete mirabile in multiple intracranial arteries with ipsilateral agenesis of the internal carotid artery: a case report.单侧颅内动脉多发网状异常合并同侧颈内动脉发育不全 1 例报告。
J Med Case Rep. 2023 Jun 29;17(1):268. doi: 10.1186/s13256-023-04013-w.
10
Bilateral Internal Carotid Artery Hypoplasia with Craniofacial Anomalies: A Case of Suspected Treacher Collins Syndrome.双侧颈内动脉发育不全伴颅面畸形:一例疑似特雷彻·柯林斯综合征病例
NMC Case Rep J. 2023 Mar 15;10:55-60. doi: 10.2176/jns-nmc.2022-0267. eCollection 2023.

本文引用的文献

1
Radiologic exploration of the morphometric and morphological features of the carotid canal.颈动脉管形态测量和形态学特征的放射学研究。
J Taibah Univ Med Sci. 2022 May 13;17(6):936-942. doi: 10.1016/j.jtumed.2022.04.013. eCollection 2022 Dec.
2
Congenital aural atresia associated with agenesis of internal carotid artery in a girl with a FOXI3 deletion.一名患有FOXI3基因缺失的女孩,先天性耳道闭锁合并颈内动脉发育不全。
Am J Med Genet A. 2015 Mar;167A(3):537-44. doi: 10.1002/ajmg.a.36895. Epub 2015 Feb 5.
3
Absence of both internal carotid arteries.
双侧颈内动脉缺如。
Clin Proc. 1945;4(10):588-94.
4
A case of congenitally absent left internal carotid artery: vascular malformations in 22q11.2 deletion syndrome.一例先天性左侧颈内动脉缺如:22q11.2缺失综合征中的血管畸形
Cleft Palate Craniofac J. 2010 May;47(3):314-7. doi: 10.1597/09-061.1.
5
Radiological findings in a case with absence of the left internal carotid artery and compression of several cranial nerve roots in the posterior fossa by the basilar artery.一例左侧颈内动脉缺如且基底动脉在后颅窝压迫多条颅神经根的放射学表现。
Med Contemp. 1954 Dec;72(12):601-9.
6
Bilateral "hypoplasia" of the internal carotid arteries.双侧颈内动脉“发育不全”。
Neurology. 1968 Dec;18(12):1149-56. doi: 10.1212/wnl.18.12.1149.
7
Cerebral hemiatrophy, hypoplasia of internal carotid artery, and intracranial aneurysm. A rare association occurring in an infant.大脑半球萎缩、颈内动脉发育不全与颅内动脉瘤。一种发生于婴儿的罕见关联情况。
Arch Neurol. 1987 Feb;44(2):232-5. doi: 10.1001/archneur.1987.00520140090024.
8
The absence of the internal carotid artery: report of two cases.颈内动脉缺如:两例报告。
Aust N Z J Surg. 1986 Jan;56(1):85-8. doi: 10.1111/j.1445-2197.1986.tb01827.x.
9
Congenital absence of the cervical and petrous internal carotid artery with intercavernous anastomosis.先天性颈内动脉和岩骨段颈内动脉缺如伴海绵窦间吻合。
AJNR Am J Neuroradiol. 1989 Mar-Apr;10(2):435-9.
10
Intrasellar carotid anastomosis simulating pituitary microadenoma.鞍内颈动脉吻合模拟垂体微腺瘤。
Radiology. 1979 Aug;132(2):381-3. doi: 10.1148/132.2.381.