Verrips A, Nijeholt G J, Barkhof F, Van Engelen B G, Wesseling P, Luyten J A, Wevers R A, Stam J, Wokke J H, van den Heuvel L P, Keyser A, Gabreëls F J
Departments of Neurology, Pathology and Laboratory of Pediatrics and Neurology, University Hospital Nijmegen, Utrecht, The Netherlands.
Brain. 1999 Aug;122 ( Pt 8):1589-95. doi: 10.1093/brain/122.8.1589.
We describe seven Dutch patients from six families with a slowly progressive, mainly spinal cord syndrome that remained for many years the sole expression of cerebrotendinous xanthomatosis (CTX). MRI demonstrated white matter abnormalities in the lateral and dorsal columns of the spinal cord. Post-mortem examination of one of the patients showed extensive myelin loss in these columns. An array of genotypes was found in these patients. We conclude that 'spinal xanthomatosis' is a clinical and radiological separate entity of CTX that should be included in the differential diagnosis of 'chronic myelopathy'.
我们描述了来自六个家庭的七名荷兰患者,他们患有缓慢进展的、主要为脊髓综合征,多年来一直是脑腱黄瘤病(CTX)的唯一表现形式。MRI显示脊髓侧柱和后柱有白质异常。对其中一名患者的尸检显示这些柱中有广泛的髓鞘丢失。在这些患者中发现了一系列基因型。我们得出结论,“脊髓黄瘤病”是CTX的一种临床和放射学上独立的实体,应纳入“慢性脊髓病”的鉴别诊断中。