Neuromyelitis optica spectrum disorders accompanying subarachnoid hemorrhage and reversible white matter lesions

Shirai, Shinichi; Mito, Yasunori; Nojo, Tatsuru; Yaguchi, Hiroaki; Takahashi, Toshiyuki; Sato, Kazunori; Hirotani, Makoto; Kano, Takahiro; Yabe, Ichiro; Sasaki, Hidenao

Neuromyelitis optica spectrum disorders accompanying subarachnoid hemorrhage and reversible white matter lesions

Shirai, Shinichi; Mito, Yasunori; Nojo, Tatsuru et al.

Neurology and Clinical Neuroscience, 2014, 2(1), 10-12

Permalink : https://hdl.handle.net/2115/57873

このアイテムのアクセス数:1,538件（2026-08-13 19:20 集計）

閲覧可能ファイル

ファイル	フォーマット	サイズ	閲覧回数	説明
Neurol Clin Neurosci_2(1)_10-12	pdf	587 KB	1,148

論文情報

ファイル出力 EndNote Basic出力 Mendeley出力

アクセス権	open access
URI	https://hdl.handle.net/2115/57873
タイトル	Neuromyelitis optica spectrum disorders accompanying subarachnoid hemorrhage and reversible white matter lesions
著者	Shirai, Shinichi ; Mito, Yasunori ; Nojo, Tatsuru ; Yaguchi, Hiroaki ; Takahashi, Toshiyuki ; Sato, Kazunori ; Hirotani, Makoto ; Kano, Takahiro ; Yabe, Ichiro ; Sasaki, Hidenao
著者名 Shirai, Shinichi
著者名 Mito, Yasunori
著者名 Nojo, Tatsuru
著者名 Yaguchi, Hiroaki
著者名 Takahashi, Toshiyuki
著者名 Sato, Kazunori
e-Rad_Researcher 60399920 著者名 Hirotani, Makoto
著者名 Kano, Takahiro
e-Rad_Researcher 60372273 著者名 Yabe, Ichiro
e-Rad_Researcher 80281806 著者名 Sasaki, Hidenao
言語	英語
キーワード	Neuromyelitis optica
	subarachnoid hemorrhage
	posterior reversible encephalopathy syndrome
	anti-Aquaporin 4 antibody
発行日	2014-01
出版者	Wiley
収録物名	Neurology and Clinical Neuroscience
巻(号)	2(1)
ページ	10-12
抄録	A 48-year-old man was admitted to Tomakomai City Hospital, Tomakomai, Japan, because of intractable hiccups and nausea, and orthostatic hypotension. Brain magnetic resonance imaging findings showed a dorsal medullary lesion. Respiratory failure occurred, and he underwent tracheotomy and mechanical ventilation when magnetic resonance imaging showed subarachnoid hemorrhage in addition to enlarged medullary lesions. Serum anti-aquaporin-4 antibody was positive and the cerebrospinal fluid was bloody. We diagnosed meuromyelitis optica spectrum disorders complicating subarachnoid hemorrhage. He was treated with a steroid. Although extensive white matter lesions occurred transiently, the patient was discharged from the hospital when he became able to walk with the use of the walker on the 52nd day. We suggest that the subarachnoid hemorrhage and transient white matter lesions were associated with vascular damage associated with the meuromyelitis optica spectrum disorders.
資源タイプ	学術雑誌論文
出版タイプ	Submitted Manuscript Under Review
PISSN	2049-4173
関連情報 (isVersionOf)	出版社版DOI https://doi.org/10.1111/ncn3.68