Lopes Ferraz Filho José Roberto, Munis Marcos Pontes, Soares Souza Antonio, Sanches Rafael Angelo, Goloni-Bertollo Eni Maria, Pavarino-Bertelli Erika Cristina
Imaging Department, Medical School in São José do Rio Preto, Av. Brigadeiro Faria Lima 5544, São Pedro, São José do Rio Preto, São Paulo 15090000, Brazil.
Pediatr Radiol. 2008 Mar;38(3):305-10. doi: 10.1007/s00247-007-0712-x. Epub 2008 Jan 30.
Lesions of the brain denominated as unidentified bright objects (UBOs), which are not included in the diagnostic criteria for neurofibromatosis type 1 (NF1) established by the National Institutes of Health (NIH), have been detected by MRI.
The purpose of this study was to investigate the possibility of including the presence of UBOs as a diagnostic criterion for NF1 in children.
The study included 88 children between the ages of 2 and 18 years. The case group consisted of 40 children diagnosed with sporadic or familial NF1 according to the criteria established by the NIH. A control group consisted of 48 individuals referred for routine MRI of the brain for other complaints not related to NF1.
UBOs were identified in 70% of the NF1 patients and in none of the control group. The sensitivity of the presence of UBOs for the diagnosis of NF1 was 70% (CI 53-83%), with a false-negative rate of 30% (CI 27-47%), a specificity of 100% (CI 86-100%) and a false-positive rate of 0% (CI 0-14%).
Faced with the difficulties in diagnosing NF1 in children and the high frequency and specificity of the presence UBOs identified by MRI in our series, we recommend the inclusion of the presence UBOs as a diagnostic criterion for NF1 in children.
磁共振成像(MRI)检测到大脑中存在一些被称为不明亮物体(UBOs)的病变,而这些病变未被美国国立卫生研究院(NIH)制定的1型神经纤维瘤病(NF1)诊断标准所涵盖。
本研究旨在探讨将UBOs的存在纳入儿童NF1诊断标准的可能性。
该研究纳入了88名年龄在2至18岁之间的儿童。病例组由40名根据NIH标准诊断为散发性或家族性NF1的儿童组成。对照组由48名因与NF1无关的其他主诉而接受脑部常规MRI检查的个体组成。
70%的NF1患者中发现了UBOs,而对照组中无一例发现。UBOs存在对NF1诊断的敏感性为70%(可信区间53 - 83%),假阴性率为30%(可信区间27 - 47%),特异性为100%(可信区间86 - 100%),假阳性率为0%(可信区间0 - 14%)。
鉴于儿童NF1诊断存在困难,且在我们的系列研究中MRI检测到的UBOs存在频率较高且具有特异性,我们建议将UBOs的存在纳入儿童NF1的诊断标准。