Arias M, Osorio Xr, Dapena D, Arias-Rivas S, Vázquez F
Department of Neurology, Complexo Hospitalario, Universitario, Santiago de Compostela, Spain.
Mult Scler. 2008 Sep;14(8):1139-41. doi: 10.1177/1352458508094642.
Diagnosis of primary angiitis of the central nervous system (PACNS) is difficult in relation to variability in its clinical manifestations and absence of specific signs in neuroimaging. A young patient presented with a recurrent encephalopathic clinical course. T2 and fluid-attenuated inversion recovery-magnetic resonance imaging (FLAIR-MRI) showed hyperintense lesions in the cerebral white matter suggesting demyelination. Those lesions decreased or even disappeared after treatment with steroids and immunoglobulins. In echo gradient MRI (T2*-MRI), there were permanent cortical-subcortical petechial hypointense lesions (microhemorrhages). Definite diagnosis was established after cerebral biopsy. Intravenous cyclophosphamide was administrated with no new relapses in more than 18 months of follow-up. In a compatible clinical course, the finding of petechial hemorrhages in T2*-WI could play an important role in early diagnosis of PACNS.
由于中枢神经系统原发性血管炎(PACNS)临床表现的变异性以及神经影像学缺乏特异性征象,其诊断较为困难。一名年轻患者呈现出复发性脑病的临床病程。T2加权像和液体衰减反转恢复序列磁共振成像(FLAIR-MRI)显示脑白质高信号病变,提示脱髓鞘。经类固醇和免疫球蛋白治疗后,这些病变减轻甚至消失。在回波梯度MRI(T2加权像)上,可见永久性皮质-皮质下瘀点状低信号病变(微出血)。经脑活检后确诊。给予静脉环磷酰胺治疗,随访18个月以上无新的复发。在符合临床病程的情况下,T2加权像上瘀点状出血的发现可能对PACNS的早期诊断具有重要作用。