Nemoc moyamoya Moyamoya disease

被引:0
作者
Priban, V [1 ,2 ]
Dostal, J. [1 ,2 ]
Mracek, J. [1 ,2 ]
Baxa, J. [2 ,3 ]
Duras, P. [2 ,3 ]
机构
[1] LF UK, Neurochirurg Klin, E Benese 1128, Plzen 30100, Czech Republic
[2] FN Plzen, E Benese 1128, Plzen 30100, Czech Republic
[3] LF UK, Klin Zobrazovacich Metod, Plzen, Czech Republic
关键词
moyamoya disease; etiology; extra-intracranial bypass; zation techniques; revascularization techniques; FOLLOW-UP; SURGICAL-TREATMENT; SURGERY; FEATURES; CHILDREN; BYPASS; RNF213;
D O I
10.48095/cccsnn2021116
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Moyamoya disease is bilateral progressive steno-occlusive impairment of the distal internal carotid artery accompanied by the formation of basal collaterals and finally by the exclusive collateralization from the territory of the external carotid artery. Suzuki angiographic classification describes progression of moyamoya disease. Aetiology is not known, but it is probably a combination of inherited and autoimmune factors. Asian population is mostly aff ected. Ischemic symptoms are typical in a pediatric population, and in adults, haemorrhage is a frequent symptom. Prognosis is poor. Therapy is exclusively surgical, either direct extra-intracranial bypass or indirect revascularization. Indirect techniques utilize potential of neoangiogenesis of vascularized tissue in the proximity of the brain. Combination of direct and indirect revascularization represents optimal treatment of symptomatic patients.
引用
收藏
页码:116 / 125
页数:10
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