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A Case of Atypical Type of Sturge-Weber Syndrome Demonstrated Reversible Change by MRI FLAIR Method in Ictus and in Postictal State Masanori Sasaki 1 , Koji Igarashi 1 , Susumu Suzuki 1 , Koji Saito 2 1Department of Neurosurgery Hoshigaura Hospital 2Kushiro Neurosurgical Hospital Keyword: Sturge-Weber syndrome , MRI FLAIR , seizure pp.633-637
Published Date 1999/7/1
DOI https://doi.org/10.11477/mf.1406901466
  • Abstract
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We report a patient of atypical type of Sturge-We-ber syndrome who demonstrated a reversible change by MRI FLAIR method in ictus and postictal state.

A 5-year-old boy was admitted to our hospital be-cause of severe headache, vomiting and loss of con-sciousness with his eyes conjugated to left for a few minutes. He had no facial nevus and other abnormal findings in physical examination. CT scan showed two small calcifications in the right occipital lobe. Postcon-trast T 1-weighted image of MRI demonstrated a right parieto-occipital leptomeningeal enhancement. We di-agnosed this case as an atypical type of Sturge-Weber syndrome.


Copyright © 1999, Igaku-Shoin Ltd. All rights reserved.

基本情報

電子版ISSN 2185-405X 印刷版ISSN 0006-8969 医学書院

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