Neurovascular manifestations of connective-tissue diseases: A review

被引:54
|
作者
Kim, Sarasa T. [1 ]
Brinjikji, Waleed [2 ]
Lanzino, Giuseppe [3 ]
Kallmes, David F. [2 ]
机构
[1] Mayo Clin, Mayo Med Sch, Rochester, MN USA
[2] Mayo Clin, Dept Radiol, 200 1st St SW, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Neurol Surg, Rochester, MN USA
关键词
Ehlers-Danlos syndrome; Marfan syndrome; neurofibromatosis type 1 (NF1); Loeys-Dietz syndrome; intracranial aneurysm; dissection; EHLERS-DANLOS-SYNDROME; CAROTID-CAVERNOUS FISTULA; SYNDROME TYPE-IV; VERTEBRAL ARTERIOVENOUS-FISTULA; CERVICAL ARTERY DISSECTION; LOEYS-DIETZ SYNDROME; NEUROFIBROMATOSIS TYPE-I; TERM-FOLLOW-UP; MOYAMOYA SYNDROME; INTRACRANIAL ANEURYSMS;
D O I
10.1177/1591019916659262
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Patients with connective tissue diseases are thought to be at a higher risk for a number of cerebrovascular diseases such as intracranial aneurysms, dissections, and acute ischemic strokes. In this report, we aim to understand the prevalence and occurrences of such neurovascular manifestations in four heritable connective tissue disorders: Marfan syndrome, EhlersDanlos syndrome, Neurofibromatosis Type 1, and LoeysDietz syndrome. We discuss the fact that although there are various case studies reporting neurovascular findings in these connective tissue diseases, there is a general lack of case-control and prospective studies investigating the true prevalence of these findings in these patient populations. Furthermore, the differences observed in the manifestations and histology of such disease pathologies encourages future multi-center registries and studies in better characterizing the pathophysiology, prevalence, and ideal treatment options of neurovascular lesions in patents with connective tissue diseases.
引用
收藏
页码:624 / 637
页数:14
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