Raila F A, Zimmerman J, Azordegan P, Fratkin J, Parent A D
Department of Radiology, University of Mississippi Medical Center, Jackson 39216-4505, USA.
J Neuroimaging. 1997 Jan;7(1):48-50. doi: 10.1111/jon19977148.
An asymptomatic patient with a family history of von Hippel-Lindau disease carried the abnormal gene for this disease. An imaging survey that consisted of computed tomography, magnetic resonance imaging, and cerebral angiography revealed an optic nerve hemangioblastoma. The potential for visual loss in the future was the indication for microsurgical intervention. This was the first asymptomatic optic nerve hemangioblastoma to be imaged and the first to be successfully removed without any permanent neurological deficits or vision loss.
一名有冯·希佩尔-林道病家族史的无症状患者携带了该疾病的异常基因。一项包括计算机断层扫描、磁共振成像和脑血管造影的影像学检查发现了一例视神经成血管细胞瘤。未来存在视力丧失的可能性是进行显微手术干预的指征。这是首例进行影像学检查的无症状视神经成血管细胞瘤,也是首例成功切除且未出现任何永久性神经功能缺损或视力丧失的病例。