Zhu Juehua, Dong Qiang, Cao Zhipeng, Xu Yi, Zhang Shufan, Fang Qi, Cai Xiuying, Han Xiang, Yang Shilin
Department of Neurology, The First Affiliated Hospital of Soochow University, Suzhou, China.
Department of Neurology, Huashan Hospital, Fudan University, Shanghai, China.
Heliyon. 2024 Jul 6;10(14):e34225. doi: 10.1016/j.heliyon.2024.e34225. eCollection 2024 Jul 30.
Primary Sjögren's syndrome (PSS) is a systemic autoimmune disease that mainly affects exocrine glands. Little is known about PSS associated cervical and intracranial cerebral large-vessel vasculitis outside of individual case reports.
We present 5 cases of ischemic stroke or transient ischemic stroke (TIA) caused by PSS associated cervical and intracranial large-vessel vasculitis. Literature review was performed to summarize and identify the demographic, clinical features, treatment, and prognosis of this condition.
The review resulted in 8 included articles with 8 patients, plus our 5 new patients, leading to a total of 13 subjects included in the analysis. The median age was 43 (range, 17-69) years old, among which 69.2 % (9/13) were female, and 92.3 % (12/13) came from Asia. Among them, 84.6 % (11/13) presented with cerebral infarction and 70.0 % (7/10) with watershed infarction. Middle cerebral artery (MCA) (6/13, 46.2 %) and internal carotid artery (ICA) (6/13, 46.2 %) were the most frequently involved arteries. Remarkable vessel wall concentric thickening and enhancement was observed in 57.1 % (4/7) patients and intravascular thrombi was identified in 28.6 % (2/7) patients. Glucocorticoid combined with non-glucocorticoid immunosuppressants (8/12, 66.7 %) were the most often chosen medication therapy and 4 patients received surgical intervention.
Asian females are the most vulnerable population to ischemic stroke or TIA due to PSS associated cervical and intracranial large-vessel vasculitis. Cerebral infarctions were characterized by recurrence and watershed pattern. Magnetic resonance vessel wall imaging (MR-VWI) helps to identify the inflammatory pathology of large vessel lesion in PSS.
原发性干燥综合征(PSS)是一种主要累及外分泌腺的系统性自身免疫性疾病。除个别病例报告外,关于PSS相关的颈内和颅内大脑大血管血管炎知之甚少。
我们报告5例由PSS相关的颈内和颅内大血管血管炎引起的缺血性卒中或短暂性脑缺血发作(TIA)。进行文献综述以总结和确定该疾病的人口统计学、临床特征、治疗和预后。
综述纳入8篇文章共8例患者,加上我们新报告的5例患者,分析共纳入13例受试者。中位年龄为43岁(范围17 - 69岁),其中69.2%(9/13)为女性,92.3%(12/13)来自亚洲。其中,84.6%(11/13)表现为脑梗死,70.0%(7/10)为分水岭梗死。大脑中动脉(MCA)(6/13,46.2%)和颈内动脉(ICA)(6/13,46.2%)是最常受累的动脉。57.1%(4/7)的患者观察到明显的血管壁同心性增厚和强化,28.6%(2/7)的患者发现血管内血栓形成。糖皮质激素联合非糖皮质激素免疫抑制剂(8/12,66.7%)是最常选择的药物治疗方法,4例患者接受了手术干预。
亚洲女性是因PSS相关的颈内和颅内大血管血管炎导致缺血性卒中或TIA的最易感人群。脑梗死的特征是复发和分水岭模式。磁共振血管壁成像(MR-VWI)有助于识别PSS中大血管病变的炎症病理。