DSpace university logo mark
Japanese | English 

NAOSITE : Nagasaki University's Academic Output SITE > 130 病院 > 130 学術雑誌論文 >

Clinical Features and Long-Term Follow-Up of Quasi-Moyamoya Disease in Children.

ファイル 記述 サイズフォーマット
PedNeu_Hayashi.pdf496.47 kBAdobe PDF本文ファイル

タイトル: Clinical Features and Long-Term Follow-Up of Quasi-Moyamoya Disease in Children.
著者: Hayashi, Kentaro / Horie, Nobutaka / Suyama, Kazuhiko / Nagata, Izumi
発行日: 2011年 9月
出版者: Karger
引用: Pediatric Neurosurgery, 47(1), pp.15-21; 2011
抄録: Background: Inherited or acquired disorders and conditions may present in conjunction with moyamoya disease. This condition is known as quasi-moyamoya disease. Methods: A retrospective review of 69 moyamoya disease patients treated for the past 20 years identified 7 patients with quasi-moyamoya disease and 5 of them were pediatric patients. Results: The mean age at initial diagnosis was 6.4 years (range 5-9). Associated disorders were: craniosynostosis, dwarfism with coarctation of aorta, Proteus syndrome, and cranial irradiation for brain tumor. Their clinical type included cerebral ischemia in 3 patients, cerebral bleeding with ischemia in 1 and epilepsy in 1. The 3 patients with cerebral ischemia underwent bypass surgery and their ischemia was improved. One patient died of brain tumor recurrence and the activities of daily living in the remaining patients were affected by mental retardation. Conclusions: The clinical course and radiological finding of quasi-moyamoya disease are diverse because of associated disorders, distinguishing definite moyamoya disease.
キーワード: ischemic stroke / moyamoya disease / brain tumor / radiation therapy
URI: http://hdl.handle.net/10069/25474
ISSN: 10162291
DOI: 10.1159/000324912
PubMed ID: 21576916
権利: Copyright © 2011 S. Karger AG, Basel.
資料タイプ: Journal Article
原稿種類: publisher
出現コレクション:130 学術雑誌論文

引用URI : http://hdl.handle.net/10069/25474



Valid XHTML 1.0! Copyright © 2006-2015 長崎大学附属図書館 - お問い合わせ Powerd by DSpace