Matsushima Y, Aoyagi M, Masaoka H, Suzuki R, Ohno K
Department of Neurosurgery, Tokyo Medical and Dental University, Japan.
Childs Nerv Syst. 1990 Dec;6(8):440-3. doi: 10.1007/BF00302089.
The mental prognosis of children with moyamoya disease, in whom the onset was when they were younger than 5 years of age, has been reported to be very poor. We studied the mental outcome of these patients after encephaloduroarteriosynangiosis (EDAS) in relation to the age at the onset of the disease and the age at operation. For patients in whom the onset of moyamoya disease occurs when they are younger than 2 years of age, the prognosis is very poor with regard to mental abilities even if they have an operation within a year after the onset. Slight hope remains if the operation is within 3 months of the onset. For patients in whom the disease begins when they are 2-5 years of age, EDAS performed before the age of 9 years may result in a good outcome with regard to mental ability, as well as resolution of the paroxysmal symptoms and cerebral revascularization.
据报道,发病年龄小于5岁的烟雾病患儿的智力预后非常差。我们研究了这些患者在脑硬脑膜动脉血管融合术(EDAS)后的智力转归,以及发病年龄和手术年龄之间的关系。对于发病年龄小于2岁的烟雾病患者,即便在发病后1年内接受手术,其智力预后仍非常差。若在发病后3个月内进行手术,则仍有一线希望。对于发病年龄在2至5岁之间的患者,9岁前进行EDAS可能会在智力方面带来良好的转归,同时还能缓解阵发性症状并实现脑血运重建。