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Japanese

Neurofibromatosis with Occlusion of Internal Carotid Artery:Case report Naoya KUWAYAMA 1 , Shin-ichiro TAKAHASHI 1 , Makoto SONOBE 1 , Shigeki KAGAWA 1 , Hidetoshi IKEDA 1 1Division of Neurosurgery, Mito National Hospital Keyword: Neurofibromatosis , von Recklinghausen’s disease , Cerebrovascular disease , Moya-moya disease pp.743-747
Published Date 1985/7/10
DOI https://doi.org/10.11477/mf.1436202041
  • Abstract
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Vascular lesions of the central nervous system in neurofibromatosis (NF) are uncommon. Cerebral arterial occlusive diseases in NF have been documented in only 29 patients. This paper reports a case of a 16-year-old male having occlusion of the right internal carotid artery with NF. He was admitted with an episode of clonic convulsion and left hemi-paresis at the age of five years. On admission, he bad multiple café-au-lait spots, depigmentation and fibroma molle throughout his body.


Copyright © 1985, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1251 印刷版ISSN 0301-2603 医学書院

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