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Vessel wall imaging in the diagnosis of antiphospholipid syndrome presenting as Moyamoya syndrome-A case report
被引:1
|作者:
Yang, David L.
[1
]
Thomas, Rachel
[2
]
Ford, Alice F.
[2
]
Cucchiara, Brett L.
[2
]
George, Donna K.
[2
]
Song, Jae W.
[3
]
机构:
[1] Univ Penn, Perelman Sch Med, Philadelphia, PA USA
[2] Univ Penn, Dept Neurol, Philadelphia, PA USA
[3] Univ Penn, Dept Radiol, 3400 Spruce St, Philadelphia, PA 19104 USA
来源:
关键词:
Anti-phospholipid syndrome;
vessel wall magnetic resonance imaging;
central nervous system vasculopathy;
proliferative vasculopathy;
moyamoya;
DISEASE;
D O I:
10.1177/19714009241247469
中图分类号:
R445 [影像诊断学];
学科分类号:
100207 ;
摘要:
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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页码:243 / 246
页数:4
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