Clinical and pathologic features of Sturge-Weber syndrome in patients with refractory epilepsy.
Zejun DuanKe XuMingguo XieXiaolin TianXiongfei WangJing FengYuguang GuanJian ZhouGuo-Ming LuanXueling QiDehong LuPublished in: American journal of clinical pathology (2024)
Calcification of leptomeningeal arteries, focal cortical dysplasia, and GNAQ alteration are common features in SWS pathology. Patients with refractory epilepsy caused by SWS can achieve satisfactory seizure control after surgery, but seizure control was compromised in patients with comorbid HS.