Curless R G, Siatkowski M, Glaser J S, Shatz N J
Department of Neurology, Bascom Palmer Eye Institute, University of Miami School of Medicine, Florida, USA.
Pediatr Neurol. 1998 Mar;18(3):269-71. doi: 10.1016/s0887-8994(97)00189-6.
Three of ten children with optic gliomas satisfy the 1987 National Institutes of Health consensus criteria for neurofibromatosis type 1 (NF-1). The diagnosis in these cases is based on the presence of café-au-lait skin lesions in addition to the optic glioma. Two children without skin lesions have typical findings on magnetic resonance imaging (MRI) that also suggest a diagnosis of NF-1. A review of 281 NF-1 children with brain MRI results demonstrates the presence of these abnormalities in 57% of the cases. It is suggested that this MRI abnormality is sufficiently specific to add this feature to the list of diagnostic criteria. When MRI findings are present in a child with optic glioma and without skin lesions, counseling should be given for NF-1. It is noteworthy that these typical MRI findings in NF-1 are less common in adulthood, apparently because of spontaneous resolution.
10名患有视神经胶质瘤的儿童中,有3名符合1987年美国国立卫生研究院关于1型神经纤维瘤病(NF-1)的共识标准。这些病例的诊断除了基于视神经胶质瘤外,还依据咖啡斑样皮肤损害的存在。2名没有皮肤损害的儿童在磁共振成像(MRI)上有典型表现,这也提示诊断为NF-1。对281名有脑部MRI结果的NF-1儿童进行回顾显示,57%的病例存在这些异常。有人认为这种MRI异常具有足够的特异性,应将此特征添加到诊断标准列表中。当患有视神经胶质瘤且无皮肤损害的儿童出现MRI表现时,应就NF-1进行咨询。值得注意的是,NF-1中这些典型的MRI表现在成年期不太常见,显然是由于自发消退。