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首页> 外文期刊>Pediatric neurology >Atypical imaging evolution of Sturge-Weber syndrome without facial nevus
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Atypical imaging evolution of Sturge-Weber syndrome without facial nevus

机译：无面部痣的Sturge-Weber综合征的非典型成像演变

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摘要

We report a patient with Sturge-Weber syndrome without facial angioma, who presented with seizures and normal initial imaging results. The patient experienced several years without seizures before a sudden increase in seizure frequency, followed by an atypical evolution of imaging findings prompting biopsy to establish the diagnosis. This case highlights not only the rare presentation of isolated leptomeningeal angiomatosis, but also the potential for atypical evolution of imaging findings through the course of the disease. We detail the imaging findings of our case and review the potential pathophysiological basis for this appearance. Our experience suggests that repeat imaging is warranted in patients with suspected Sturge-Weber syndrome or those with intractable cryptogenic epilepsy, because some imaging features of Sturge-Weber syndrome may manifest over time.
机译：我们报告了一名无面部血管瘤的Sturge-Weber综合征患者，该患者出现癫痫发作且初始影像学检查结果正常。患者经历了数年的无癫痫发作，然后突然增加癫痫发作频率，随后影像学表现异常发展，提示进行活检以明确诊断。该病例不仅突显了罕见的孤立性脑膜脑膜血管瘤病表现，而且突显了整个疾病过程中影像学表现非典型性发展的可能性。我们详述了本例的影像学发现，并回顾了这种表现的潜在病理生理基础。我们的经验表明，对于疑似Sturge-Weber综合征或顽固性隐源性癫痫的患者，应进行重复成像，因为随着时间的推移，Sturge-Weber综合征的某些成像特征可能会出现。

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