Sturge-Weber syndrome without facial nevus

被引：33

作者：

Aydin, A

Çakmakçi, H

Kovanlikaya, A

Dirik, E

机构：

[1] Dokuz Eylul Univ, Fac Med, Dept Pediat Neurol, Izmir, Turkey

[2] Dokuz Eylul Univ, Fac Med, Dept Radiol, Izmir, Turkey

来源：

PEDIATRIC NEUROLOGY | 2000年 / 22卷 / 05期

关键词：

D O I：

10.1016/S0887-8994(00)00127-2

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

An 11-month-old patient with Sturge-Weber syndrome with the absence of facial angioma and normal mental development is presented. Noncontrast computed tomography revealed left parieto-occipital atrophy with heavy gyriform calcifications, Axial T-2-weighed magnetic resonance imaging confirmed the presence of low-signal areas corresponding to the gyral calcifications evident on computed tomography, Contrast-enhanced T-1-weighted axial and coronal images exhibited high signals in the left parieto-occipital cortical and subcortical areas, representing angiomatous malformations, The clinical appearance and pathologic features of the reported patient were compared with those of similar patients described in published reports. (C) 2000 by Elsevier Science Inc. All rights reserved.

引用

页码：400 / 402

页数：3

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