Recent Advances in Moyamoya Disease: Pathophysiology and Treatment

被引:68
作者
Kronenburg, Annick [1 ]
Braun, Kees P. J. [1 ]
van der Zwan, Albert [1 ]
Klijn, Catharina J. M. [1 ]
机构
[1] UMC Utrecht, Brain Ctr Rudolf Magnus, Dept Neurol & Neurosurg, NL-3508 GA Utrecht, Netherlands
关键词
Moyamoya; Latest advancements; Pathophysiology; Genetics; Revascularization; Direct bypass; Cerebral perfusion studies; Neuroimaging; Outcome; Cognition; ENDOTHELIAL PROGENITOR CELLS; CEREBRAL-ARTERY BYPASS; PEDIATRIC MOYAMOYA; REVASCULARIZATION SURGERY; SURGICAL-TREATMENT; CLINICAL-FEATURES; MATRIX METALLOPROTEINASES; SPONTANEOUS OCCLUSION; CHILDREN; ADULTS;
D O I
10.1007/s11910-013-0423-7
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Moyamoya disease is a progressive intracranial arteriopathy characterized by bilateral stenosis of the distal portion of the internal carotid artery and the proximal anterior and middle cerebral arteries, resulting in transient ischemic attacks or strokes. The pathogenesis of moyamoya disease remains unresolved, but recent advances have suggested exciting new insights into a genetic contribution as well as into other pathophysiological mechanisms. Treatment that may halt progression of the disease or even reverse the intracranial arteriopathy is yet to be found. There are strong indications that neurosurgical intervention, through direct, indirect, or combined revascularization surgery, can reduce the risk of ischemic stroke and possibly also cognitive dysfunction by improving cerebral perfusion, although randomized clinical trials have not been performed. Many questions regarding the indication for and timing of surgery remain unanswered. In this review, we discuss recent developments in the pathogenesis and treatment of moyamoya disease.
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页数:9
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