{"title":"右侧大脑中动脉区域缺血性中风并发的斯约格伦综合征--病例报告","authors":"Muhammad Mubashir, Imaan Jauhar, Saba Zaidi","doi":"10.1016/j.glmedi.2024.100104","DOIUrl":null,"url":null,"abstract":"<div><p>Sjögren's syndrome (SS) is a chronic autoimmune condition characterized by lymphoplasmacytic infiltration into salivary and lacrimal glands, leading to sicca syndrome and systemic symptoms. While pulmonary, musculoskeletal, dermatological, and renal manifestations are well-documented, reports of central nervous system (CNS) involvement, particularly stroke, remain rare. We present a case report of a 30-year-old female whose initial manifestation of vasculitis associated with Sjögren's syndrome was an ischemic stroke. Laboratory findings revealed a positive ANA profile and radiological investigations showed an infarct in the right middle cerebral artery (MCA). The patient was then managed using steroids, antiplatelets, hydroxychloroquine, and physiotherapy. Although small-vessel vasculitis is commonly implicated in CNS involvement, major cerebral vessel involvement in Sjögren's syndrome is infrequently reported, with only three cases documented in the literature. This case highlights the importance of recognizing stroke as a potential manifestation of Sjögren-related vasculitis and expands the understanding of CNS complications in this autoimmune disorder. Increased awareness of this rare presentation may aid in prompt diagnosis and appropriate management of vasculitic complications in Sjögren's syndrome patients. Further research is needed to elucidate the underlying mechanisms and explore optimal treatment strategies for this subset of patients.</p></div>","PeriodicalId":100804,"journal":{"name":"Journal of Medicine, Surgery, and Public Health","volume":"3 ","pages":"Article 100104"},"PeriodicalIF":0.0000,"publicationDate":"2024-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2949916X24000574/pdfft?md5=49b88ff4a391f053a77f0495aa1e66f8&pid=1-s2.0-S2949916X24000574-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Sjögren’s syndrome complicated by ischemic stroke in the right middle cerebral artery territory – A case report\",\"authors\":\"Muhammad Mubashir, Imaan Jauhar, Saba Zaidi\",\"doi\":\"10.1016/j.glmedi.2024.100104\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Sjögren's syndrome (SS) is a chronic autoimmune condition characterized by lymphoplasmacytic infiltration into salivary and lacrimal glands, leading to sicca syndrome and systemic symptoms. While pulmonary, musculoskeletal, dermatological, and renal manifestations are well-documented, reports of central nervous system (CNS) involvement, particularly stroke, remain rare. We present a case report of a 30-year-old female whose initial manifestation of vasculitis associated with Sjögren's syndrome was an ischemic stroke. Laboratory findings revealed a positive ANA profile and radiological investigations showed an infarct in the right middle cerebral artery (MCA). The patient was then managed using steroids, antiplatelets, hydroxychloroquine, and physiotherapy. Although small-vessel vasculitis is commonly implicated in CNS involvement, major cerebral vessel involvement in Sjögren's syndrome is infrequently reported, with only three cases documented in the literature. This case highlights the importance of recognizing stroke as a potential manifestation of Sjögren-related vasculitis and expands the understanding of CNS complications in this autoimmune disorder. Increased awareness of this rare presentation may aid in prompt diagnosis and appropriate management of vasculitic complications in Sjögren's syndrome patients. Further research is needed to elucidate the underlying mechanisms and explore optimal treatment strategies for this subset of patients.</p></div>\",\"PeriodicalId\":100804,\"journal\":{\"name\":\"Journal of Medicine, Surgery, and Public Health\",\"volume\":\"3 \",\"pages\":\"Article 100104\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-04-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2949916X24000574/pdfft?md5=49b88ff4a391f053a77f0495aa1e66f8&pid=1-s2.0-S2949916X24000574-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Medicine, Surgery, and Public Health\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2949916X24000574\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Medicine, Surgery, and Public Health","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949916X24000574","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
斯约格伦综合征(SS)是一种慢性自身免疫性疾病,其特征是唾液腺和泪腺的淋巴浆细胞浸润,导致疱疹综合征和全身症状。虽然肺部、肌肉骨骼、皮肤和肾脏表现已得到充分证实,但中枢神经系统(CNS)受累,尤其是中风的报道仍然罕见。我们报告了一例 30 岁女性的病例,她最初表现为与斯约格伦综合征相关的血管炎,后来发生了缺血性中风。实验室检查结果显示 ANA 阳性,放射学检查显示右侧大脑中动脉 (MCA) 梗死。患者随后接受了类固醇、抗血小板、羟氯喹和物理治疗。虽然中枢神经系统受累通常与小血管炎有关,但斯约恩综合征的主要脑血管受累却鲜有报道,文献中仅记载了三例。本病例强调了认识中风作为斯约格伦相关血管炎潜在表现的重要性,并拓展了对这种自身免疫性疾病中枢神经系统并发症的认识。提高对这种罕见表现的认识有助于及时诊断和适当处理斯约格伦综合征患者的血管炎并发症。我们还需要进一步研究,以阐明其潜在机制,并探索针对这一亚群患者的最佳治疗策略。
Sjögren’s syndrome complicated by ischemic stroke in the right middle cerebral artery territory – A case report
Sjögren's syndrome (SS) is a chronic autoimmune condition characterized by lymphoplasmacytic infiltration into salivary and lacrimal glands, leading to sicca syndrome and systemic symptoms. While pulmonary, musculoskeletal, dermatological, and renal manifestations are well-documented, reports of central nervous system (CNS) involvement, particularly stroke, remain rare. We present a case report of a 30-year-old female whose initial manifestation of vasculitis associated with Sjögren's syndrome was an ischemic stroke. Laboratory findings revealed a positive ANA profile and radiological investigations showed an infarct in the right middle cerebral artery (MCA). The patient was then managed using steroids, antiplatelets, hydroxychloroquine, and physiotherapy. Although small-vessel vasculitis is commonly implicated in CNS involvement, major cerebral vessel involvement in Sjögren's syndrome is infrequently reported, with only three cases documented in the literature. This case highlights the importance of recognizing stroke as a potential manifestation of Sjögren-related vasculitis and expands the understanding of CNS complications in this autoimmune disorder. Increased awareness of this rare presentation may aid in prompt diagnosis and appropriate management of vasculitic complications in Sjögren's syndrome patients. Further research is needed to elucidate the underlying mechanisms and explore optimal treatment strategies for this subset of patients.