Sturge-Weber syndrome involved frontoparietal region without facial Nevus

DİLBER C., TAŞDEMİR H. A., DAĞDEMİR A., İNCESU L., Odaci E.

PEDIATRIC NEUROLOGY, cilt.26, sa.5, ss.387-390, 2002 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 26 Sayı: 5
  • Basım Tarihi: 2002
  • Doi Numarası: 10.1016/s0887-8994(01)00412-x
  • Dergi Adı: PEDIATRIC NEUROLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.387-390
  • Karadeniz Teknik Üniversitesi Adresli: Hayır

Özet

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.