Sturge-Weber syndrome involved frontoparietal region without facial Nevus

被引:26
作者
Dilber, C [1 ]
Tasdemir, HA
Dagdemir, A
Incesu, L
Odaci, E
机构
[1] Ondokuz Mayis Univ, Fac Med, Dept Pediat, TR-55139 Samsun, Turkey
[2] Ondokuz Mayis Univ, Fac Med, Dept Radiol, TR-55139 Samsun, Turkey
[3] Ondokuz Mayis Univ, Fac Med, Dept Histol & Embryol, TR-55139 Samsun, Turkey
关键词
D O I
10.1016/S0887-8994(01)00412-X
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Classic Sturge-Weber syndrome is characterized by a facial nevus and hamartomatous lesion in the brain. Hamartomatous lesions are usually located in the ipsilateral occipital region of the facial nevus. The other lobes may be involved. A few cases of Sturge-Weber syndrome without facial nevus have been reported. A 9-month-old male was admitted with the complaint of afebrile seizures two times. We observed the third seizure, which was complex partial, in the clinic. There was no facial hemangioma. On computed tomography and magnetic resonance imaging of the brain we observed findings concordant with the angioma in the right frontoparietal region, although the occipital region was intact. This patient appears to be the first with Sturge-Weber syndrome without facial nevus, and with involvement of the frontoparietal region but not the occipital region. We do not know the embryologic basis of this association. (C) 2002 by Elsevier Science Inc. All rights reserved.
引用
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页码:387 / 390
页数:4
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