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以脑桥梗死和椎动脉夹层动脉瘤为首发表现的白塞病:一例报告

Pontine Infarction and Vertebral Artery Dissecting Aneurysm as the First Presentation of Behçet's Disease: A Case Report.

作者信息

Jalali Kafaf S, Alhazzaa Mohammed Ahmed, Alqahtani Sultan, Alattas Mahmood Yassin

机构信息

Internal Medicine, Prince Mohammed Bin Abdulaziz Hospital/Saudi Commission for Health Specialties, Medina, SAU.

Neurology, King Fahad Hospital, Hofuf, SAU.

出版信息

Cureus. 2022 Sep 15;14(9):e29204. doi: 10.7759/cureus.29204. eCollection 2022 Sep.

Abstract

Behçet's disease (BD) is a systemic disease of inflammatory origin that appears most often in the third or fourth decade of life. Behçet's disease is hallmarked predominantly by mucocutaneous lesions and ocular involvement. Vertebral artery dissection and neurological manifestations are rare complications in Behçet's disease. We examine the case of a medically free 33-year-old male who was admitted to the emergency department complaining of sudden-onset dizziness, vomiting, and tinnitus. Neurological examination revealed fluctuating consciousness, multiple gaze nystagmus, motor deficit in the upper and lower limbs, bilateral Babinski sign, and truncal ataxia. Magnetic resonance imaging (MRI) showed a right pontine hyperintense lesion on T2-weighted images (T2WI). A right vertebral angiogram four months after the incident showed a dissection in the mid-cervical third of an anomalous duplicated origin arm of the right vertebral artery. This case describes an uncommon form of initial presentation of Behçet's disease via a pontine infarction triggered by a dissecting aneurysm in an anatomically rare variant of the vertebral artery.

摘要

白塞病(BD)是一种炎症性起源的全身性疾病,最常出现在人生的第三个或第四个十年。白塞病的主要特征是皮肤黏膜病变和眼部受累。椎动脉夹层和神经表现是白塞病罕见的并发症。我们检查了一名33岁无病史男性的病例,他因突发头晕、呕吐和耳鸣被送往急诊科。神经系统检查发现意识波动、多向性眼球震颤、上下肢运动障碍、双侧巴宾斯基征和躯干共济失调。磁共振成像(MRI)在T2加权图像(T2WI)上显示右侧脑桥高信号病变。事件发生四个月后进行的右侧椎动脉血管造影显示,右侧椎动脉异常重复起源臂的颈段中部三分之一处有夹层。本病例描述了白塞病一种不常见的初始表现形式,即由椎动脉解剖学上罕见变异中的夹层动脉瘤引发的脑桥梗死。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5db9/9572958/d87dea40e075/cureus-0014-00000029204-i01.jpg

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