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未诊断的斯-韦综合征作为癫痫发作和大脑深部静脉系统扩张的鉴别诊断:一例报告

Undiagnosed Sturge-Weber Syndrome as a Differential Diagnosis of Seizures and Deep Cerebral Venous System Dilation: A Case Report.

作者信息

Bertani Raphael, Garret Bruno, Perret Caio M, Batista Sávio, Koester Stefan W, Azeredo Rodrigo, Guimarães Cavalcante Carlos de Carvalho Tamires, Almeida José A

机构信息

Neurosurgery, Hospital Municipal Miguel Couto, Rio de Janeiro, BRA.

Neuroscience, Federal University of Rio de Janeiro, Rio de Janeiro, BRA.

出版信息

Cureus. 2021 Oct 29;13(10):e19111. doi: 10.7759/cureus.19111. eCollection 2021 Oct.

Abstract

Sturge-Weber syndrome (SWS) is a capillary-venous malformation affecting the brain, the eye, and the adjacent trigeminal dermatomes of the skin. This illness is usually diagnosed during the first years of life. If left undiagnosed (and consequently untreated), the condition could develop into severe refractory seizures, ischemic strokes, visual loss, and early cognitive impairment. We report a case of a 23-year-old female patient with a port-wine facial stain, presenting her first convulsive episode in adulthood, associated with a moderate dilation of the deep venous system in the angiography, which raised the diagnostic of Sturge-Weber syndrome.

摘要

斯特奇-韦伯综合征(SWS)是一种影响大脑、眼睛及相邻三叉神经皮肤节段的毛细血管-静脉畸形。这种疾病通常在生命的最初几年被诊断出来。如果未被诊断(进而未得到治疗),病情可能发展为严重的难治性癫痫、缺血性中风、视力丧失和早期认知障碍。我们报告一例23岁女性患者,其面部有葡萄酒色斑,成年后首次出现惊厥发作,血管造影显示深部静脉系统中度扩张,这提示了斯特奇-韦伯综合征的诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cf4/8627585/17487f453d97/cureus-0013-00000019111-i01.jpg

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