| Item type |
[ELS]学術雑誌論文 / Journal Article(1) |
| 公開日 |
2017-01-23 |
| タイトル |
|
|
タイトル |
Harada's Disease (Vogt-Koyanagi-Harada Syndrome; VKH Syndrome) |
|
言語 |
en |
| 言語 |
|
|
言語 |
eng |
| 資源タイプ |
|
|
資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
|
資源タイプ |
journal article |
| 著者 |
FUJIWARA, Hisako
SUZUKI, Takashi
KAMEDA, Hiroshi
TAKIGAWA, Yasushi
KATAYAMA, Toshio
OHGA, Hitomi
EGI, Kuniaki
MURAMATSU, Norifumi
|
| 著者所属(英) |
|
|
|
en |
|
|
Department of Ophthalmology, Kawasaki Medical School |
| 著者所属(英) |
|
|
|
en |
|
|
Department of Ophthalmology, Kawasaki Medical School |
| 著者所属(英) |
|
|
|
en |
|
|
Department of Ophthalmology, Kawasaki Medical School |
| 著者所属(英) |
|
|
|
en |
|
|
Department of Ophthalmology, Kawasaki Medical School |
| 著者所属(英) |
|
|
|
en |
|
|
Department of Ophthalmology, Kawasaki Medical School |
| 著者所属(英) |
|
|
|
en |
|
|
Department of Ophthalmology, Kawasaki Medical School |
| 著者所属(英) |
|
|
|
en |
|
|
Department of Ophthalmology, Kawasaki Medical School |
| 著者所属(英) |
|
|
|
en |
|
|
Department of Ophthalmology, Kawasaki Medical School |
| キーワード |
|
|
言語 |
en |
|
主題Scheme |
Other |
|
主題 |
Harada's disease |
| キーワード |
|
|
言語 |
en |
|
主題Scheme |
Other |
|
主題 |
Clinical picture |
| キーワード |
|
|
言語 |
en |
|
主題Scheme |
Other |
|
主題 |
Treatment |
| キーワード |
|
|
言語 |
en |
|
主題Scheme |
Other |
|
主題 |
Complications |
| 記事種別(英) |
|
|
内容記述タイプ |
Other |
|
内容記述 |
Original Article |
|
言語 |
en |
| 抄録(英) |
|
|
|
en |
|
|
We studied the course and outcome of 44 patients with Harada's disease (17 males and 27 females) who were treated in the Department of Ophthalmology of Kawasaki Hospital, an affiliated hospital of Kawasaki Medical School, between April 1980 and March 1990. The age at onset ranged from 14 to 77 years with the mean age±SD being 46.5 ± 15.6 years. Thus the disease was frequent among the elderly. The posterior and optic types of the disease were most frequently found in our patients. As extraocular symptoms, perceptive deafness and an increase in the cell count of the cerebrospinal fluid were frequently observed, and these were important factors in the diagnosis of the disease. Systemic administration of steroids was the main treatment, with immunosuppressive agents being administereted to patiens with the delayed type of the disease. As for the visual prognosis, the final corrected visual acuity was 1.0 in 79% of the patients. As eye complications, cataracts and glaucoma were frequently noted, and various other lesions of the fundus were also observed with increasing age. Patients with the delayed type of the disease accounted for 34.1% of the patients studied. |
| 書誌情報 |
en : Kawasaki medical journal
巻 16,
号 1,
p. 43-47,
発行日 1990
|
| URL |
|
|
識別子 |
http://igakkai.kms-igakkai.com/wp/wp-content/uploads/1990en/16(1)43-47.1990.pdf |
|
識別子タイプ |
URI |
| DOI |
|
|
|
識別子タイプ |
DOI |
|
|
関連識別子 |
https://doi.org/10.11482/KMJ-E16(1)43 |
| ISSN |
|
|
収録物識別子タイプ |
PISSN |
|
収録物識別子 |
0385-0234 |
| ISSN |
|
|
収録物識別子タイプ |
EISSN |
|
収録物識別子 |
2434-3404 |
| 雑誌書誌ID |
|
|
収録物識別子タイプ |
NCID |
|
収録物識別子 |
AA00710169 |
| 雑誌書誌ID |
|
|
収録物識別子タイプ |
NCID |
|
収録物識別子 |
AA12029005 |
| 著者版フラグ |
|
|
出版タイプ |
VoR |
KJ00010211419.pdf (404.2 kB)
