• 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

科雷尔-西卡德综合征:范围综述。

Collet-Sicard syndrome: a scoping review.

机构信息

Center for Research and Training in Neurosurgery (CIEN), Bogotá, Colombia.

Neurosurgery Department, Hospital Universitario Samaritana, Bogotá, Colombia.

出版信息

Neurosurg Rev. 2023 Sep 14;46(1):244. doi: 10.1007/s10143-023-02145-7.

DOI:10.1007/s10143-023-02145-7
PMID:37707587
Abstract

Collet-Sicard syndrome (CSS) is the unilateral palsy of the cranial nerves (CN) IX, X, XI, and XII. To our knowledge, no review describes the characteristics of patients diagnosed with CSS. Therefore, this review aims to collect and describe all cases in the literature labeled as CSS. We performed a scoping review of the literature and conducted a database search in Embase and PubMed. We included articles and abstracts with case reports or case series of patients with CSS diagnosis. We classified the cases into two groups: "CSS", referring to patients presenting exclusively with IX-XII nerve involvement, and "CSS-plus", which corresponds to cases with CSS and other neurological impairments. We included 135 patients from 126 articles, of which 84 (67.7%) were male. The most common clinical manifestations reported were dysphagia and dysphonia. The most common etiology was tumoral in 53 cases (39.6%) and vascular in 37 cases (27.6%). The majority of patients showed partial or total improvement, with just over half receiving conservative treatment. The most frequent anatomic space was the jugular foramen (44.4%) and the parapharyngeal retrostyloid space (28.9%). Approximately 21% of the patients had other CN impairments, with the seventh and eighth CN most frequently compromised. We conclude that although there is a need for greater rigor in CSS reporting, the syndrome has a clear utility in identifying the localization of jugular foramen and parapharyngeal retrostyloid space pathology.

摘要

科利特-西卡德综合征(CSS)是颅神经(CN)IX、X、XI 和 XII 的单侧麻痹。据我们所知,尚无文献综述描述 CSS 患者的特征。因此,本综述旨在收集和描述文献中所有标记为 CSS 的病例。我们对文献进行了范围综述,并在 Embase 和 PubMed 中进行了数据库检索。我们纳入了有 CSS 诊断的病例报告或病例系列的文章和摘要。我们将病例分为两组:“CSS”,指仅存在 IX-XII 神经受累的患者,“CSS-plus”,指 CSS 合并其他神经损伤的病例。我们共纳入了 126 篇文章中的 135 例患者,其中 84 例(67.7%)为男性。最常见的临床表现为吞咽困难和声音嘶哑。最常见的病因是肿瘤 53 例(39.6%)和血管 37 例(27.6%)。大多数患者表现出部分或完全改善,超过一半接受保守治疗。最常见的解剖部位是颈静脉孔(44.4%)和咽旁茎突后间隙(28.9%)。约 21%的患者存在其他 CN 损伤,第七和第八对 CN 最常受损。我们的结论是,尽管 CSS 报告需要更加严格,但该综合征在确定颈静脉孔和咽旁茎突后间隙病变的定位方面具有明确的作用。

相似文献

1
Collet-Sicard syndrome: a scoping review.科雷尔-西卡德综合征:范围综述。
Neurosurg Rev. 2023 Sep 14;46(1):244. doi: 10.1007/s10143-023-02145-7.
2
Combined Deficit of the Four Lower Cranial Nerves also Known as the Syndrome of Collet-Sicard: A Systematic Review and Meta-analysis.下四对颅神经联合缺损(又称科莱-西卡尔综合征):一项系统评价和荟萃分析
Asian J Neurosurg. 2024 May 13;19(2):112-125. doi: 10.1055/s-0044-1787050. eCollection 2024 Jun.
3
[A case of Collet-Sicard syndrome caused by skull base metastasis of prostate carcinoma].[1例由前列腺癌颅底转移引起的Collet-Sicard综合征]
Nihon Hinyokika Gakkai Zasshi. 2000 Jun;91(6):562-4. doi: 10.5980/jpnjurol1989.91.562.
4
Collet-Sicard syndrome caused by a paraganglioma in the region of the jugular foramen on one side: A case report and review.一侧颈静脉孔区副神经节瘤所致科莱-西卡尔综合征:病例报告及文献复习
SAGE Open Med Case Rep. 2024 May 9;12:2050313X241249613. doi: 10.1177/2050313X241249613. eCollection 2024.
5
Collet-Sicard Syndrome Attributable to Extramedullary Plasmacytoma of the Jugular Foramen.颈静脉孔髓外浆细胞瘤所致的科莱-西卡尔综合征
World Neurosurg. 2018 Feb;110:386-390. doi: 10.1016/j.wneu.2017.11.130. Epub 2017 Nov 28.
6
[Schwannoma of the hypoglossal nerve presenting as a syndrome of Collet-Sicard].表现为科莱-西卡尔综合征的舌下神经鞘瘤
Neurologia. 2005 Jul-Aug;20(6):311-3.
7
Skull Base Squamous Cell Carcinoma Presenting as Collet-Sicard Syndrome: A Rare Cause of Multicranial Nerve Dysfunction.以科莱-西卡尔综合征为表现的颅底鳞状细胞癌:多组颅神经功能障碍的罕见病因
Cureus. 2025 Jan 30;17(1):e78237. doi: 10.7759/cureus.78237. eCollection 2025 Jan.
8
Skull Base Osteomyelitis from Otitis Media Presenting as the Collet-Sicard Syndrome.中耳炎导致的颅底骨髓炎表现为科莱-西卡尔综合征。
Case Rep Otolaryngol. 2018 Mar 18;2018:1407417. doi: 10.1155/2018/1407417. eCollection 2018.
9
Developmental abnormalities of the craniocervical junction resulting in Collet-Sicard syndrome.导致科莱-西卡尔综合征的颅颈交界区发育异常。
Spine J. 2016 Sep;16(9):e635-9. doi: 10.1016/j.spinee.2016.04.022. Epub 2016 May 6.
10
A Case of Collet-Sicard Syndrome Caused by Otitis Externa.1例由外耳道炎引起的科莱-西卡尔综合征
Cureus. 2022 Jul 25;14(7):e27218. doi: 10.7759/cureus.27218. eCollection 2022 Jul.

引用本文的文献

1
A rare case of Collet-Sicard syndrome caused by diffuse large B-cell lymphoma.一例由弥漫性大B细胞淋巴瘤引起的科莱-西卡尔综合征罕见病例。
Postep Psychiatr Neurol. 2025 Sep;34(3):216-219. doi: 10.5114/ppn.2025.151809. Epub 2025 Aug 21.
2
Clival Fracture With Multiple Cranial Nerve Palsy Treated With a Halo Device: A Case Report and Literature Review.采用头环装置治疗的斜坡骨折伴多发颅神经麻痹:病例报告及文献综述
Cureus. 2024 Sep 10;16(9):e69120. doi: 10.7759/cureus.69120. eCollection 2024 Sep.
3
Collet-Sicard syndrome: prelude to a systematic review and meta-analysis.

本文引用的文献

1
[A Case of Rectal Cancer with Collet-Sicard Syndrome].[一例直肠癌合并科莱-西卡尔综合征的病例]
Gan To Kagaku Ryoho. 2020 Dec;47(13):2225-2226.
2
The diagnosis process of Collet-Sicard syndrome caused by skull base fracture: A case report.
Neurologia (Engl Ed). 2020 Dec 9. doi: 10.1016/j.nrl.2020.11.004.
3
Collet-Sicard Syndrome Secondary to Internal Carotid Artery Dissection: A Firing Link.继发于颈内动脉夹层的科莱-西卡尔综合征:一个触发环节。
Neurohospitalist. 2020 Oct;10(4):322-323. doi: 10.1177/1941874420916377. Epub 2020 Apr 6.
科莱-西卡尔综合征:系统评价与荟萃分析的前奏。
Neurosurg Rev. 2024 Jan 20;47(1):57. doi: 10.1007/s10143-024-02298-z.
4
Tapia Syndrome and Severe Pain Induced by Occipital Bone Metastasis of Prostate Cancer.塔皮亚综合征与前列腺癌枕骨转移所致的剧痛
Cureus. 2023 Nov 24;15(11):e49327. doi: 10.7759/cureus.49327. eCollection 2023 Nov.
4
Collet-Sicard Syndrome as the Presentation of Malignant Pheochromocytoma.以科莱-西卡尔综合征为表现的恶性嗜铬细胞瘤
Neurohospitalist. 2020 Oct;10(4):320-321. doi: 10.1177/1941874420916302. Epub 2020 Apr 6.
5
Teaching NeuroImages: Collet-Sicard syndrome and hearing loss with glomus jugulotympanicum.教学神经影像:科莱-西卡尔综合征与颈静脉鼓室球瘤所致听力损失
Neurology. 2019 Oct 1;93(14):e1408-e1409. doi: 10.1212/WNL.0000000000008205.
6
Jugular Paraganglioma Presenting With Collet-Sicard Syndrome.
Mayo Clin Proc. 2019 Sep;94(9):1832-1833. doi: 10.1016/j.mayocp.2019.04.014.
7
Metastatic Adenocarcinoma of Temporal Bone with Collet-Sicard Syndrome.颞骨转移性腺癌伴科列特-西卡尔综合征
Iran J Otorhinolaryngol. 2018 Nov;30(101):361-364.
8
A long styloid process and Collet-Sicard syndrome.
Acta Otorrinolaringol Esp (Engl Ed). 2019 Sep-Oct;70(5):310-311. doi: 10.1016/j.otorri.2018.06.004. Epub 2018 Aug 4.
9
A Collet-Sicard syndrome due to internal carotid artery dissection associated with cerebral amyloid angiopathy-related inflammation.一例由颈内动脉夹层伴脑淀粉样血管病相关炎症引起的科莱-西卡尔综合征。
SAGE Open Med Case Rep. 2018 May 21;6:2050313X18777176. doi: 10.1177/2050313X18777176. eCollection 2018.
10
Severe localised granulomatosis with polyangiitis (Wegener's granulomatosis) manifesting with extensive cranial nerve palsies and cranial diabetes insipidus: a case report and literature review.以广泛颅神经麻痹和颅性尿崩症为表现的严重局限性肉芽肿性多血管炎(韦格纳肉芽肿):一例报告及文献综述
BMC Neurol. 2018 May 1;18(1):59. doi: 10.1186/s12883-018-1058-8.