Stoll G, Reiners K, Schwartz A, Kaup F G, Althaus C, Freund H J
Department of Neurology, Heinrich-Heine Universität, Düsseldorf, Germany.
J Neurol Neurosurg Psychiatry. 1991 Jan;54(1):77-9. doi: 10.1136/jnnp.54.1.77.
In a patient with angiographically proven cerebral vasculitis five months after acute posterior multifocal placoid pigment epitheliopathy (APMPPE) neurological symptoms promptly responded to steroid treatment. Cerebrospinal fluid (CSF) showed a lymphocytic pleocytosis. Magnetic resonance imaging (MRI) revealed multifocal white matter lesions in the hemispheres and the brain stem suggesting a diffuse subcortical vasculitis.
一名急性后极部多灶性鳞状色素上皮病变（APMPPE）五个月后经血管造影证实患有脑血管炎的患者，其神经症状对类固醇治疗迅速产生反应。脑脊液（CSF）显示淋巴细胞增多。磁共振成像（MRI）显示大脑半球和脑干有多灶性白质病变，提示弥漫性皮质下血管炎。
