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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。

A rare case of Collet-Sicard syndrome caused by diffuse large B-cell lymphoma.

作者信息

Jakubik Karol, Szewczyk Anna K, Jeżak Mikołaj, Staśkiewicz Grzegorz, Rejdak Konrad

机构信息

Department of Human Anatomy, Medical University of Lublin, Poland.

Department of Neurology, Medical University of Lublin, Poland.

出版信息

Postep Psychiatr Neurol. 2025 Sep;34(3):216-219. doi: 10.5114/ppn.2025.151809. Epub 2025 Aug 21.

DOI:10.5114/ppn.2025.151809
PMID:40959685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12435555/
Abstract

PURPOSE

Collet-Sicard syndrome (CSS) is a neurological condition secondary to various neoplastic and non-neoplastic lesions, manifesting as palsy of the lower cranial nerves. This article aims to disseminate knowledge and share insights into this disorder.

CASE DESCRIPTION

A 58-year-old male presented with a four-month history of progressive dysphagia and dysphonia. Neurological examination revealed cranial nerve IX, X, XI and XII palsy. Imaging demonstrated a focal lesion situated between the internal carotid artery and the jugular vein, ultimately diagnosed as diffuse large B-cell lymphoma. The patient was referred for hematological treatment.

COMMENT

A constellation of symptoms such as dysphagia, hoarseness or dysphonia, and tongue weakness should alert clinicians to the possibility of CSS. Awareness of the characteristic symptoms of CSS is essential for identifying the underlying cause and reducing delays in diagnosis and treatment.

摘要

目的

科莱-西卡尔综合征(CSS)是一种继发于各种肿瘤性和非肿瘤性病变的神经系统疾病,表现为下组颅神经麻痹。本文旨在传播关于这种疾病的知识并分享见解。

病例描述

一名58岁男性,有四个月进行性吞咽困难和发音困难病史。神经系统检查显示第IX、X、XI和XII颅神经麻痹。影像学检查显示在颈内动脉和颈静脉之间有一个局灶性病变,最终诊断为弥漫性大B细胞淋巴瘤。该患者被转诊接受血液学治疗。

评论

吞咽困难、声音嘶哑或发音困难以及舌肌无力等一系列症状应提醒临床医生注意CSS的可能性。了解CSS的特征性症状对于确定潜在病因以及减少诊断和治疗延迟至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34cb/12435555/5652f77e2658/PPN-34-56207-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34cb/12435555/5652f77e2658/PPN-34-56207-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34cb/12435555/5652f77e2658/PPN-34-56207-g001.jpg

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本文引用的文献

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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.
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Collet-Sicard syndrome: prelude to a systematic review and meta-analysis.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.
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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.
4
Internal Carotid Artery Aneurysm Presenting as Lower Cranial Nerve Palsies.表现为下颅神经麻痹的颈内动脉瘤
World Neurosurg. 2023 May;173:23-24. doi: 10.1016/j.wneu.2023.02.055. Epub 2023 Feb 18.
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Case report: A complicated course of Collet-Sicard syndrome after internal carotid artery dissection and lenticulo-striatal artery infarction.病例报告:颈内动脉夹层和豆纹动脉梗死后出现的复杂的科莱-西卡尔综合征病程。
Front Neurol. 2022 Oct 20;13:939236. doi: 10.3389/fneur.2022.939236. eCollection 2022.
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Be careful of Collet-Sicard syndrome: A rare result of carotid artery dissection.警惕科莱-西卡尔综合征:一种罕见的颈动脉夹层结果。
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