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  1. C100 医学部/医学系研究科
  2. C100a 雑誌掲載論文
  3. 学術雑誌

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/2237/27070
a09ec7dd-ac6f-4b70-8f64-c43cab24c4ef
名前 / ファイル ライセンス アクション
manuscript_for_child_nervous_system_version.pdf manuscript_for_child_nervous_system_version.pdf ファイル公開日:2018/08/01 (4.0 MB)
Item type 学術雑誌論文 / Journal Article(1)
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

WEKO 73906

en Yoshio, Araki

Search repository
Yasushi, Takagi

× Yasushi, Takagi

WEKO 73907

en Yasushi, Takagi

Search repository
Yohei, Mineharu

× Yohei, Mineharu

WEKO 73908

en Yohei, Mineharu

Search repository
Hatasu, Kobayashi

× Hatasu, Kobayashi

WEKO 73909

en Hatasu, Kobayashi

Search repository
Susumu, Miyamoto

× Susumu, Miyamoto

WEKO 73910

en Susumu, Miyamoto

Search repository
Toshihiko, Wakabayashi

× Toshihiko, Wakabayashi

WEKO 73911

en Toshihiko, Wakabayashi

Search repository
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
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
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