Tanriverdi Sema, Terek Demet, Koroglu Ozge Altun, Yalaz Mehmet, Tekgul Hasan, Kultursay Nilgun
Faculty of Medicine, Department of Pediatrics, Division of Neonatology, Ege University, Izmir, Turkey.
Brain Dev. 2013 Apr;35(4):367-71. doi: 10.1016/j.braindev.2012.06.005. Epub 2012 Jul 16.
Sturge-Weber syndrome is a rare, sporadic, congenital neurocutaneous syndrome characterized by facial cutaneous vascular malformation, leptomeningeal angioma and eye abnormalities. Seizures develop during the first year of life, may become refractory to multiple anticonvulsants and status epilepticus may develop. A rare subtype of Sturge-Weber syndrome with bilateral facial vascular malformation, unilateral cerebral involvement and neonatal status epilepticus is reported here. Neonatal status epilepticus was successfully controlled with intravenous levetiracetam infusion.
斯特奇-韦伯综合征是一种罕见的、散发性的先天性神经皮肤综合征，其特征为面部皮肤血管畸形、软脑膜血管瘤和眼部异常。癫痫发作在出生后第一年出现，可能对多种抗惊厥药物产生耐药，且可能发展为癫痫持续状态。本文报道了斯特奇-韦伯综合征的一种罕见亚型，其具有双侧面部血管畸形、单侧脑部受累及新生儿癫痫持续状态。静脉输注左乙拉西坦成功控制了新生儿癫痫持续状态。
