PDF(Pubmed)
Abstract：
Sturge-Weber syndrome is a rare, sporadic, progressive neurocutaneous condition that presents with congenital hamartomatous malformations, epilepsy, and a variety of facial symptoms. We discussed a rare case of an eighteen-year-old female child who came to our neurology department with status epilepticus, mental impairment, and a port-wine in the lateral left side of her face. We diagnosed Sturge-Weber syndrome after a thorough neurological and radiological evaluation. The purpose of presenting this case is to illustrate both the characteristic presentation and the complications associated with managing Sturge-Weber syndrome.
摘要：
Sturge-Weber综合征是一种罕见的,零星的,进行性神经皮肤疾病表现为先天性错构瘤畸形，癫痫,和各种面部症状。我们讨论了一个罕见的病例，一个18岁的女性儿童因癫痫持续状态来到我们的神经科，精神障碍,在她左边的脸上有一瓶葡萄酒.经过全面的神经和放射学评估，我们诊断为Sturge-Weber综合征。介绍此病例的目的是说明与管理Sturge-Weber综合征相关的特征性表现和并发症。
