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儿童脑磁共振成像中多个T2高信号在1型神经纤维瘤病诊断中的临床敏感性和特异性:诊断准确性研究

Clinical sensitivity and specificity of multiple T2-hyperintensities on brain magnetic resonance imaging in diagnosis of neurofibromatosis type 1 in children: diagnostic accuracy study.

作者信息

Sabol Zlatko, Resić Biserka, Gjergja Juraski Romana, Sabol Filip, Kovac Sizgorić Matilda, Orsolić Kresimir, Ozretić David, Sepić-Grahovac Dubravka

机构信息

Sabol Outpatient Clinic for Sick Children, Zagreb, Croatia.

出版信息

Croat Med J. 2011 Aug 15;52(4):488-96. doi: 10.3325/cmj.2011.52.488.

Abstract

AIM

To determine the prevalence, number, and location of multiple (≥2) T2-hyperintensities on brain magnetic resonance imaging (MRI) in children with neurofibromatosis type 1 (NF1) and their correlation with age, and to establish their sensitivity, specificity, and accuracy for the diagnosis of NF1 in children, especially in the early age (2-7 years).

METHODS

We performed a cross-sectional study of 162 patients with NF1 from Croatian Neurofibromatosis Association Database and 163 control children between the ages of 2 and 18 years who underwent brain MRI between 1989 and 2009.

RESULTS

Multiple T2-hyperintensities were present in 74% of NF1 patients and 1.8% of controls. They were mainly located in the basal ganglia, brainstem, and cerebellum and were significantly decreased in prevalence and number in the older age. T2-hyperintensities had excellent diagnostic accuracy with the area under the receiver operating characteristic (ROC) curve of 0.849 and 95% confidence interval (CI) of 0.805-0.886. The diagnostic sensitivity, specificity, and accuracy rate of T2-hyperintensities for NF1 were highest in the youngest age (2-7 years): 81% (95% CI 71%-89.1%), 99% (95% CI 92.3%-100%), and 85.8 (95% CI 83.3-93.8), respectively.

CONCLUSION

This study strongly suggests the inclusion of T2-hyperintensities on brain MRI on the list of diagnostic criteria for NF1, especially in children of early age, when the clinical penetration of the NF1 gene has not yet been completely finished.

摘要

目的

确定1型神经纤维瘤病(NF1)患儿脑磁共振成像(MRI)上多发(≥2个)T2高信号的患病率、数量和位置及其与年龄的相关性,并确定其对儿童尤其是低龄(2 - 7岁)儿童NF1诊断的敏感性、特异性和准确性。

方法

我们对来自克罗地亚神经纤维瘤病协会数据库的162例NF1患者以及163例年龄在2至18岁之间、于1989年至2009年间接受脑MRI检查的对照儿童进行了横断面研究。

结果

74%的NF1患者存在多发T2高信号,而对照儿童中这一比例为1.8%。它们主要位于基底神经节、脑干和小脑,且患病率和数量在大龄儿童中显著降低。T2高信号具有出色的诊断准确性,受试者操作特征(ROC)曲线下面积为0.849,95%置信区间(CI)为0.805 - 0.886。T2高信号对NF1的诊断敏感性、特异性和准确率在最年幼年龄组(2 - 7岁)最高,分别为81%(95%CI 71% - 89.1%)、99%(95%CI 92.3% - 100%)和85.8(95%CI 83.3 - 93.8)。

结论

本研究强烈建议将脑MRI上的T2高信号纳入NF1的诊断标准清单,尤其是在NF1基因的临床外显尚未完全完成的低龄儿童中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4235/3160695/f8a4e408b08c/CroatMedJ_52_0488-F1.jpg

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