血管壁成像在诊断表现为莫亚莫亚综合征的抗磷脂综合征中的应用--病例报告。

David L Yang, Rachel Thomas, Alice F Ford, Brett L Cucchiara, Donna K George, Jae W. Song
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摘要

目的:我们描述了一例表现为莫亚莫亚综合征(MMS)的抗磷脂综合征(APLS)血管病变,并展示了相关的颅内血管壁磁共振成像(VWI)结果。研究方法一名 37 岁女性因急性发作性头晕和左侧肢体无力就诊。神经系统检查显示左侧面部下垂和左侧偏瘫。她接受了脑卒中综合实验室检查。神经影像学检查包括头部 CT、CT 血管造影、VWI 和数字减影血管造影。检查结果检查结果显示 APLS 抗体三项阳性。头部 CT 显示急性右侧基底节区梗死和右侧额叶蛛网膜下腔出血。CT 血管造影显示右侧颈内动脉末端严重狭窄,呈莫亚莫亚模式。颅内血管造影显示,狭窄的右侧颈内动脉末端、M1 大脑中动脉和 A1 大脑前动脉出现长段同心血管壁增厚、同质血管壁强化和 T2 超强血管壁水肿。她接受了华法林长期抗凝治疗和右侧颞浅动脉至大脑中动脉搭桥术。讨论:我们介绍了一名出现 MMS 的原发性 APLS 患者颅内血管壁病变的 VWI 特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vessel wall imaging in the diagnosis of antiphospholipid syndrome presenting as Moyamoya syndrome-A case report.
Objectives: We describe a case of anti-phospholipid syndrome (APLS) vasculopathy presenting with Moyamoya syndrome (MMS) and show the associated intracranial vessel wall MRI (VWI) findings. Methods: A 37-year-old-woman presented with acute onset dizziness and left-sided weakness. Neurologic exam revealed a left facial droop and left hemiparesis. She underwent a comprehensive laboratory work-up for stroke. Neuroimaging included a CT head, CT angiogram, VWI, and digital subtraction angiography. Results: Work-up revealed a triple-positive APLS antibody profile. CT of the head showed an acute right basal ganglia infarction and right frontal subarachnoid hemorrhage. CT angiogram revealed severe stenosis of the right internal carotid artery terminus in a Moyamoya pattern. Intracranial VWI showed long-segment concentric vessel wall thickening and homogeneous vessel wall enhancement and T2-hyperintense wall edema of the stenotic right ICA terminus, M1 middle cerebral artery, and A1 anterior cerebral artery. She was treated with long-term anticoagulation with warfarin and a right superficial temporal artery to middle cerebral artery bypass. Discussion: We present intracranial VWI features of vessel wall pathology in a patient with primary APLS presenting with MMS.
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