Govori Valbona, Gjikolli Bujar, Ajvazi Halil, Morina Nada
Neurology Clinic, University Clinical Center of Kosova, Prishtina, Republic of Kosova.
Cases J. 2009 Dec 23;2:9394. doi: 10.1186/1757-1626-2-9394.
Sturge-Weber syndrome sometimes referred to as encephalotrigeminal angiomatosis, is a rare congenital neurological and skin disorder.
This is case report of a 18-year-old mentally disabled boy, with long-standing seizures, with a port-wine nevi on the left side of the face along the distribution of trigeminal nerve. Interictal encephalogram showed bilateral slow activity, pronounced in the left hemisphere, with epileptogenic activity in the left temporo-parietal region. Skull radiograph, computerized tomography and magnetic resonance imaging showed intracranial calcifications and atrophy of the left brain hemisphere.
Professional counseling and support in addition to drug treatment can provide help to patients and their family to overcome their problems and improve the treatment outcome.
斯特奇-韦伯综合征有时也被称为脑三叉神经血管瘤病,是一种罕见的先天性神经和皮肤疾病。
这是一例关于一名18岁智障男孩的病例报告,他长期患有癫痫,左侧面部沿三叉神经分布有葡萄酒色斑痣。发作间期脑电图显示双侧慢波活动,以左半球明显,左颞顶区有癫痫样活动。颅骨X线片、计算机断层扫描和磁共振成像显示颅内钙化及左侧脑半球萎缩。
除药物治疗外,专业咨询和支持可为患者及其家庭提供帮助,以克服他们的问题并改善治疗效果。