Barreau Pauline, Prust Morgan J, Crane Jeremy, Loewenstein Johanna, Kadom Nadja, Vanderver Adeline
Faculté UFR de Médecine, Paris, France.
J Child Neurol. 2011 Nov;26(11):1422-4. doi: 10.1177/0883073811405381. Epub 2011 May 13.
Alexander disease is a neurodegenerative disorder of the central white matter caused by dominant mutations in GFAP, the gene encoding glial fibrillary acidic protein. Magnetic resonance imaging pattern recognition studies have established characteristic radiologic phenotypes for this disorder. In some cases, however, genetically confirmed cases do not express these features, and several reports have identified "atypical" radiologic findings in Alexander disease patients. Here, the authors report 3 genetically confirmed Alexander disease cases with focal central white matter lesions that, upon longitudinal clinical and radiologic evaluation, appear to reflect an atypical Alexander disease magnetic resonance imaging phenotype and not another pathophysiologic process such as encephalitis, infarction, or neoplasm.
亚历山大病是一种中枢白质神经退行性疾病,由编码胶质纤维酸性蛋白(GFAP)的基因显性突变引起。磁共振成像模式识别研究已经确定了该疾病的特征性放射学表型。然而,在某些情况下,基因确诊的病例并未表现出这些特征,并且有几份报告指出亚历山大病患者存在“非典型”放射学表现。在此,作者报告了3例基因确诊的亚历山大病病例,这些病例有局灶性中枢白质病变,经纵向临床和放射学评估,似乎反映了一种非典型的亚历山大病磁共振成像表型,而非其他病理生理过程,如脑炎、梗死或肿瘤。