Takayasu Arteritis presenting with stroke: A case of lateral medullary syndrome in a 29-year-old female

Chowdhury Adnan Sami , Mohammad Ferdous Ur Rahaman , Rafsana , Shohael Mahmud Arafat , Md Nazmul Hasan
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Abstract

Takayasu arteritis (TA) is a chronic large vessel vasculitis that typically targets the major vessels of our body, like the aorta and its branches. Infarction of the lateral medullatermed lateral medullary syndrome, is a rare presenting feature of TA. Our report presents a 29-year-old female who was diagnosed with TA, but her presentation was a rare early manifestation of TA, presenting with lateral medullary syndrome. She came to the hospital with gradually worsening vertigo, partial ptosis, dysphagia, contralateral sensory loss, and gait instability over a period of hours. On initial physical examination, her pulse and blood pressure were missing on the left upper limb. An Imaging test, which showed significant left vertebral artery stenosis and ischemic infarction in the lateral medulla. Further tests like erythrocyte sedimentation rate (ESR) and C-reactive protein (CRP) were raised, while the autoimmune panel and the coagulation panel results were negative. Diagnosis of TA was made, and treatment was started for TA with steroids and methotrexate and for stroke with aspirin and atorvastatin. Treatment showed significant improvement in symptoms within the two months of strict compliance. This case emphasizes the importance of early diagnosis and thorough treatment in young TA patients who present with rare ischemic events.
以中风为表现的高须动脉炎:一例29岁女性的外侧髓质综合征
高须动脉炎(TA)是一种慢性大血管炎,通常针对我们身体的主要血管,如主动脉及其分支。外侧延髓梗死是一种罕见的TA表现。我们报告了一位29岁的女性,她被诊断为TA,但她的表现是TA的罕见早期表现,表现为外侧髓质综合征。患者入院时出现眩晕、部分上睑下垂、吞咽困难、对侧感觉丧失、步态不稳等症状,持续数小时。在最初的体格检查中,她的左上肢脉搏和血压消失。影像学检查显示明显的左椎动脉狭窄和外侧髓质缺血性梗死。进一步的测试,如红细胞沉降率(ESR)和c反应蛋白(CRP)升高,而自身免疫小组和凝血小组结果为阴性。诊断为TA,并开始用类固醇和甲氨蝶呤治疗TA,用阿司匹林和阿托伐他汀治疗卒中。在严格依从治疗的两个月内,症状明显改善。这个病例强调了早期诊断和彻底治疗出现罕见缺血性事件的年轻TA患者的重要性。
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