Becker D H, Silverberg G D, Nelson D H, Hanbery J W
Neurosurgery. 1978 Jan-Feb;2(1):1-7. doi: 10.1227/00006123-197801000-00001.
A case of intracranial saccular aneurysm occurring in early childhood and presenting with sudden dysphasia and hemiplegia is reported. A review of the literature emphasizes the rarity of this lesion. Despite a significant preoperative neurological deficit, the patient tolerated aneurysm clipping and recovered well. The majority of reported cases involve males under 2 years old. Aneurysms in infants have a distribution different from that seen in adults. Microscopic examination of these lesions fails to show any evidence of inflammation or atherosclerosis. The data suggest that the pathogenesis of these rare childhool lesions differs from that of adult saccular aneurysms.
报告了一例发生于幼儿期的颅内囊状动脉瘤,表现为突发言语困难和偏瘫。文献回顾强调了该病变的罕见性。尽管术前存在明显的神经功能缺损,但患者耐受了动脉瘤夹闭术且恢复良好。大多数报道的病例涉及2岁以下男性。婴儿期的动脉瘤分布与成人不同。对这些病变的显微镜检查未发现任何炎症或动脉粥样硬化的证据。数据表明,这些罕见的儿童期病变的发病机制与成人囊状动脉瘤不同。