弥漫性大b细胞淋巴瘤致Collet-Sicard综合征1例。

Postepy psychiatrii neurologii Pub Date : 2025-09-01 Epub Date: 2025-08-21 DOI:10.5114/ppn.2025.151809
Karol Jakubik, Anna K Szewczyk, Mikołaj Jeżak, Grzegorz Staśkiewicz, Konrad Rejdak
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引用次数: 0

摘要

目的:Collet-Sicard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,表现为下颅神经麻痹。本文旨在传播知识并分享对这种疾病的见解。病例描述:一名58岁男性,有4个月进行性吞咽困难和发音困难病史。神经学检查显示颅九、十、十一、十二神经麻痹。影像学显示局灶性病变位于颈内动脉和颈静脉之间,最终诊断为弥漫性大b细胞淋巴瘤。病人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、舌头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的特征症状对于确定其根本原因和减少诊断和治疗延误至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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.

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