DeBella K, Poskitt K, Szudek J, Friedman J M
Department of Medical Genetics, The University of British Columbia, Vancouver, British Columbia, Canada.
Neurology. 2000 Apr 25;54(8):1646-51. doi: 10.1212/wnl.54.8.1646.
"Unidentified bright objects" (UBOs) have been observed as areas of increased T2-weighted signal intensity on MRI in 43% to 93% of children with neurofibromatosis 1 (NF1). Because of this high frequency and the fact that the NIH diagnostic criteria often do not permit diagnosis of NF1 in early childhood, UBOs have been proposed as an additional diagnostic criterion.
The authors examined the sensitivity and specificity of UBOs for NF1 in 19 affected children and 19 age-matched controls. Eleven of the control patients had CNS pathology that might be classified as UBOs on MRI scan. The authors measured the agreement in recognition of UBOs between two pediatric neuroradiologists who independently examined the MRI studies of these patients. They also assessed the effect of adding UBOs to the NIH diagnostic criteria on ability to diagnose NF1 in young patients.
Sensitivity and specificity of UBOs for NF1 averaged 97% and 79%, respectively. Agreement between the two radiologists was 84% overall, but varied greatly from one brain region to another. Adding UBOs as a diagnostic criterion permitted the diagnosis of 30% of young patients with NF1 mutations who do not meet the existing NIH diagnostic criteria for NF1. The value of including UBOs is less in older patients because a larger proportion of them meet the existing diagnostic criteria.
UBOs are difficult to identify with certainty and occur in children with suspected CNS disorders who do not have NF1, but they tend to occur in different brain regions. UBOs may be more useful for diagnosis of NF1 in young children if they can be defined precisely and if only the cerebellum, brainstem, and basal ganglia are considered.
在1型神经纤维瘤病(NF1)患儿中,43%至93%的患儿在磁共振成像(MRI)的T2加权像上可见“不明亮物体”(UBO),表现为信号强度增加区域。鉴于其出现频率高,且美国国立卫生研究院(NIH)的诊断标准往往不允许在幼儿期诊断NF1,因此有人提议将UBO作为一项额外的诊断标准。
作者对19例患病儿童和19例年龄匹配的对照儿童进行了研究,以检测UBO对NF1的敏感性和特异性。11例对照患者患有中枢神经系统(CNS)病变,在MRI扫描上可能被归类为UBO。作者测量了两位独立检查这些患者MRI研究的儿科神经放射科医生在识别UBO方面的一致性。他们还评估了将UBO纳入NIH诊断标准对诊断年轻患者NF1能力的影响。
UBO对NF1的敏感性和特异性平均分别为97%和79%。两位放射科医生之间的总体一致性为84%,但在不同脑区差异很大。将UBO作为诊断标准可使30%不符合现有NIH NF1诊断标准的NF1突变年轻患者得到诊断。在年龄较大的患者中纳入UBO的价值较小,因为他们中较大比例的人符合现有诊断标准。
UBO难以确切识别,且在没有NF1的疑似CNS疾病儿童中也会出现,但它们往往出现在不同脑区。如果能精确界定UBO,并且仅考虑小脑、脑干和基底神经节,那么UBO可能对幼儿NF1的诊断更有用。