Isolated granulomatous angiitis with eosinophilia in the central nervous system

Shirai, Shinichi; Yabe, Ichiro; Sakushima, Ken et al.

Neurology and Clinical Neuroscience, 2013, 1(3), 119-121

Permalink : https://hdl.handle.net/2115/56893

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アクセス権
open access
URI
https://hdl.handle.net/2115/56893
タイトル
Isolated granulomatous angiitis with eosinophilia in the central nervous system
著者
Shirai, Shinichi ; Yabe, Ichiro ; Sakushima, Ken ; Hiromi, Kanno ; Uwatoko, Hisashi ; Hirotani, Makoto ; Kano, Takahiro ; Kamoshima, Yuuta ; Tanaka, Shinya ; Sasaki, Hidenao
著者名
Shirai, Shinichi
e-Rad_Researcher
60372273
著者名
Yabe, Ichiro
著者名
Sakushima, Ken
著者名
Hiromi, Kanno
著者名
Uwatoko, Hisashi
e-Rad_Researcher
60399920
著者名
Hirotani, Makoto
著者名
Kano, Takahiro
著者名
Kamoshima, Yuuta
e-Rad_Researcher
70261287
著者名
Tanaka, Shinya
e-Rad_Researcher
80281806
著者名
Sasaki, Hidenao
言語
英語
キーワード
eosinophilic granulomatosis with polyangiitis
EGPA
Primary angiitis of the central nervous system
発行日
2013-05
出版者
Wiley
収録物名
Neurology and Clinical Neuroscience
巻(号)
1(3)
ページ
119-121
抄録
A 73-year-old man was admitted for epileptic seizures. Diffuse white matter lesions were observed in the bilateral occipital lobes, and the left occipital lobe biopsy showed eosinophils and giant cells in the walls of medium to small blood vessels, fibrinoid necrosis, occluded blood vessels, and glia degeneration. Allergic granulomatous angiitis was pathologically diagnosed. No eosinophilic granulomatosis with polyangiitis findings were observed in other organs, and isolated granulomatous angiitis with eosinophilia in the central nervous system was clinically diagnosed. Prednisolone combined with immunosuppressant therapies improved his symptoms markedly.
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/j.2049-4173.2013.00027.x