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早期磁共振成像检测疑似 Sturge-Weber 综合征患儿的无症状性脑膜血管畸形。

Early magnetic resonance imaging to detect presymptomatic leptomeningeal angioma in children with suspected Sturge-Weber syndrome.

机构信息

Department of Paediatric Neurology, Hôpital Necker-Enfants Malades, Reference Centre for Rare Epilepsies, APHP, Bordeaux, France.

Imagine Institute UMR 1163, Paris, France.

出版信息

Dev Med Child Neurol. 2020 Feb;62(2):227-233. doi: 10.1111/dmcn.14253. Epub 2019 May 3.

Abstract

AIM

We aimed to evaluate the contribution of early magnetic resonance imaging (MRI) for the presymptomatic diagnosis of Sturge-Weber syndrome (SWS) in infants with a facial port-wine birthmark (PWB).

METHOD

Asymptomatic infants with a facial PWB who performed a first MRI scan before 3 months and a second MRI scan after 9 months were included in this study. Leptomeningeal enhancement on T1-weighted imaging and four indirect signs of leptomeningeal angioma (choroid plexus enlargement, cerebral atrophy, signal inversion of the white matter with T2 hyposignal, and T1 hypersignal) were screened on the first MRI scan and correlated with clinical and/or radiological diagnosis of SWS.

RESULTS

Thirteen of 30 included patients had SWS with leptomeningeal angioma. Eleven had a leptomeningeal enhancement on the first MRI scan and 10 had associated indirect signs. The presence of a direct or at least one indirect sign of leptomeningeal angioma on the first MRI scan confirmed the diagnosis of SWS with a sensitivity of 100 per cent (95% confidence interval 75-100%) and a specificity of 94 per cent (71-100%).

INTERPRETATION

Early diagnosis of SWS is possible on contrast-enhanced MRI performed in asymptomatic infants with a facial PWB before the age of 3 months. This early detection would help to select patients who may benefit from early neuroprotective intervention.

WHAT THIS PAPER ADDS

Specific magnetic resonance imaging markers provide early diagnosis of leptomeningeal angioma in Sturge-Weber syndrome (SWS). Presymptomatic diagnosis of SWS should help to select patients for early therapy intervention.

摘要

目的

我们旨在评估早期磁共振成像(MRI)对伴有面部葡萄酒色痣(PWB)的婴儿无症状性Sturge-Weber 综合征(SWS)的预测诊断价值。

方法

本研究纳入了 30 例无症状性伴有面部 PWB 的婴儿,他们在 3 个月前进行了首次 MRI 扫描,9 个月后进行了第二次 MRI 扫描。在首次 MRI 扫描上筛选脑膜强化(T1WI)和脑膜血管畸形的四个间接征象(脉络丛增大、脑萎缩、脑白质 T2 低信号伴 T1 高信号反转、T1 高信号),并与 SWS 的临床和/或放射学诊断相关联。

结果

30 例患者中有 13 例被诊断为伴有脑膜血管畸形的 SWS。11 例患者在首次 MRI 扫描上出现脑膜强化,10 例患者伴有间接征象。首次 MRI 扫描上存在脑膜血管畸形的直接或至少一个间接征象可确诊 SWS,其灵敏度为 100%(95%置信区间 75-100%),特异性为 94%(71-100%)。

解释

在 3 个月龄前无症状性伴有面部 PWB 的婴儿中进行增强 MRI 检查可早期诊断 SWS。早期发现有助于选择可能受益于早期神经保护干预的患者。

本文新内容

特定的磁共振成像标志物可提供脑膜血管畸形的早期诊断,从而有助于早期诊断 Sturge-Weber 综合征(SWS)。无症状性 SWS 的预测诊断有助于选择患者进行早期治疗干预。

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