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Rapid Contralateral Progression of Focal Cerebral Arteriopathy Distinguished from RNF213-related moyamoya disease and fibromuscular dysplasia
http://hdl.handle.net/2237/27070
http://hdl.handle.net/2237/27070a09ec7dd-ac6f-4b70-8f64-c43cab24c4ef
名前 / ファイル | ライセンス | アクション |
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2017-11-07 | |||||
タイトル | ||||||
タイトル | Rapid Contralateral Progression of Focal Cerebral Arteriopathy Distinguished from RNF213-related moyamoya disease and fibromuscular dysplasia | |||||
言語 | en | |||||
著者 |
Yoshio, Araki
× Yoshio, Araki× Yasushi, Takagi× Yohei, Mineharu× Hatasu, Kobayashi× Susumu, Miyamoto× Toshihiko, Wakabayashi |
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アクセス権 | ||||||
アクセス権 | open access | |||||
アクセス権URI | http://purl.org/coar/access_right/c_abf2 | |||||
権利 | ||||||
言語 | en | |||||
権利情報 | The final publication is available at Springer via http://doi.org/10.1007/s00381-017-3451-9 | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Focal cerebral arteriopathy | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | RNF213 | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Moyamoya disease | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | Fibromuscular dysplasia | |||||
抄録 | ||||||
内容記述 | Background Focal cerebral arteriopathy includes unifocal or multifocal lesions that are unilateral or bilateral. Large- and/or medium-sized vessels are involved and can be visualized on angiography. Case report We report a case of cerebral infarction in a 9-yearold Japanese female who presented with a transient ischemic attack. Steno-occlusion involving the distal part of the internal carotid artery, proximal middle cerebral artery, and anterior cerebral artery was observed. Digital subtraction angiography demonstrated a beaded appearance in the cervical portion of the diseased internal carotid artery. Revascularization surgery was performed 45 days after the onset. A new infarction appeared on the other side of the anterior cerebral artery territory 7 months after the first onset. Antiplatelets and vasodilators were administered, and no progression was observed during 18 months of follow-up. Genetic analysis did not show ring finger protein 213 (RNF213)- related moyamoya disease, and pathological examination revealed no characteristics of fibromuscular dysplasia. Conclusion The radiological and genetic features coincided with focal cerebral arteriopathy, which is a distinct entity from fibromuscular dysplasia and RNF213-related moyamoya disease. | |||||
言語 | en | |||||
内容記述タイプ | Abstract | |||||
出版者 | ||||||
言語 | en | |||||
出版者 | Springer | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源タイプresource | http://purl.org/coar/resource_type/c_6501 | |||||
タイプ | journal article | |||||
出版タイプ | ||||||
出版タイプ | AM | |||||
出版タイプResource | http://purl.org/coar/version/c_ab4af688f83e57aa | |||||
DOI | ||||||
関連タイプ | isVersionOf | |||||
識別子タイプ | DOI | |||||
関連識別子 | https://doi.org/10.1007/s00381-017-3451-9 | |||||
ISSN | ||||||
収録物識別子タイプ | PISSN | |||||
収録物識別子 | 0256-7040 | |||||
書誌情報 |
en : Childs Nervous System 巻 33, 号 8, p. 1405-1409, 発行日 2017-08 |
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著者版フラグ | ||||||
値 | author | |||||
URI | ||||||
識別子 | http://doi.org/10.1007/s00381-017-3451-9 | |||||
識別子タイプ | DOI | |||||
URI | ||||||
識別子 | http://hdl.handle.net/2237/27070 | |||||
識別子タイプ | HDL |