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A rare presentation of spontaneous internal carotid artery dissection with Horner's syndrome, VIIth, Xth and XIIth nerve palsies.一例罕见的自发性颈内动脉夹层伴霍纳综合征、第七、第十和第十二脑神经麻痹。
Oxf Med Case Reports. 2016 Oct 1;2016(10):omw078. doi: 10.1093/omcr/omw078. eCollection 2016 Oct.
2
Cervical Artery Dissection: A Review of the Epidemiology, Pathophysiology, Treatment, and Outcome.颈动脉夹层:流行病学、病理生理学、治疗及预后综述
Arch Neurosci. 2015 Oct;2(4). doi: 10.5812/archneurosci.26670. Epub 2015 Oct 17.
3
Collet-Sicard syndrome.科莱-西卡德综合征
Neurologia. 2015 Mar;30(2):130-2. doi: 10.1016/j.nrl.2013.04.002. Epub 2013 Jun 22.
4
Coughing into the darkness.对着黑暗咳嗽。
Lancet. 2011 May 14;377(9778):1718. doi: 10.1016/S0140-6736(11)60206-7.
5
Collet-sicard syndrome from thrombosis of the sigmoid-jugular complex: a case report and review of the literature.乙状窦-颈静脉复合体血栓形成所致科莱-西卡尔综合征:一例报告并文献复习
Int J Otolaryngol. 2010;2010. doi: 10.1155/2010/203587. Epub 2010 Jul 25.
6
Spontaneous dissection of internal carotid artery masquerading as angioedema.伪装成血管性水肿的颈内动脉自发性夹层。
J Gen Intern Med. 2009 Jan;24(1):126-8. doi: 10.1007/s11606-008-0813-8. Epub 2008 Oct 3.
7
Carotid artery dissection as a possible severe complication of pertussis in an adult: clinical case report and review.成人百日咳可能的严重并发症——颈动脉夹层:临床病例报告及文献复习
Clin Infect Dis. 2003 Jan 1;36(1):e1-4. doi: 10.1086/344776. Epub 2002 Dec 16.

吞咽困难、声音嘶哑和舌偏斜:诊断 Collet-Sicard 综合征。

Dysphagia, dysphonia and a deviated tongue: diagnosing Collet-Sicard syndrome.

机构信息

Neurology, University of Colorado - Anschutz Medical Campus, Aurora, Colorado, USA

Neurology, The Johns Hopkins Hospital, Baltimore, Maryland, USA.

出版信息

BMJ Case Rep. 2021 May 21;14(5):e243154. doi: 10.1136/bcr-2021-243154.

DOI:10.1136/bcr-2021-243154
PMID:34020993
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8144025/
Abstract

A healthy middle-aged man presents with symptoms of dysphagia and dysphonia following an upper respiratory infection, and is diagnosed and treated for complications of pharyngitis. He presents for evaluation at a tertiary care hospital after symptoms fail to resolve, with the final diagnosis being a carotid artery dissection with compressing pseudoaneurysm. This patient's constellation of symptoms and physical examination findings are consistent with Collet-Sicard syndrome, a rare disorder caused by cranial nerve compression at the skull base. Understanding the morbidity of missing, or delaying, a diagnosis of carotid artery pathology, such as Collet-Sicard syndrome, underscores the importance of an accurate diagnosis. A review of cranial nerve anatomy, surrounding structures and potential mechanism of injury to the carotid artery are emphasised as key learning points.

摘要

一位健康的中年男性,在上呼吸道感染后出现吞咽困难和声音嘶哑的症状,并被诊断和治疗为咽炎的并发症。他在症状未缓解后到三级保健医院就诊,最终诊断为颈动脉夹层伴压迫假性动脉瘤。该患者的症状和体格检查结果与 Collet-Sicard 综合征一致,这是一种罕见的疾病,由颅底颅神经受压引起。了解漏诊或延迟诊断颈动脉病变(如 Collet-Sicard 综合征)的发病率,强调了准确诊断的重要性。重点介绍了颅神经解剖、周围结构和颈动脉损伤的潜在机制的复习,作为关键的学习要点。