| Item type |
学術雑誌論文 / Journal Article_02(1) |
| 公開日 |
2008-04-04 |
| タイトル |
|
|
タイトル |
網脈絡膜で発生する白点症候群 |
|
言語 |
ja |
| 言語 |
|
|
言語 |
jpn |
| 資源タイプ |
|
|
資源タイプ |
journal article |
| 著者 |
福井, 勝彦
花田, 一臣
吉田, 晃敏
|
| 著者 ローマ字 |
|
|
|
Fukui, Katsuhiko |
| 著者 ローマ字 |
|
|
|
en |
|
|
Hanada, Kazuomi |
| 著者 ローマ字 |
|
|
|
en |
|
|
Yoshida, Akitoshi |
| 著者 ローマ字 |
|
|
|
en |
| 書誌情報 |
眼科写真
巻 24,
p. 6-17,
発行日 2008-01-01
|
| 抄録 |
|
|
内容記述タイプ |
Abstract |
|
内容記述 |
White dot syndrome refers to a group of diseases characterized by appearance of white patchy exudate in the deep layer of the retina to the inner layer of the choroid. Although there has been a case report in which viral infection was considered as the cause, the etiology was unknown and no histopathological investigation was conducted. White dot syndrome is called by many other names depending on the clinical picture in terms of the exudate size, intensity, and presence or absence of associated residual symptoms such as scar or fibrous proliferation. Since many features are common between diseases in this syndrome, definite differentiation of a condition from others is difficult. White dot syndrome includes Acute Posterior Multifocal Placoid Epitheliopathy (APMPPE), Multiple Evanescent White Dot Syndrome(MEWDS), Acute Retinal Pigment Epithelitis (ARPE), Multifocal Choroiditis with Panuveitis(MFC with panuveitis), Punctate Inner Choroidopathy(PIC), Multifocal Choroiditis with subretinal fibrosis. In this repot , fundus findings and FA and IA findings allowed determination of these diseases, and we describes the characteristics of these disease. |
|
言語 |
en |
| 注記 |
|
|
内容記述タイプ |
Other |
|
注記 |
出版社版 |
| 資源タイプ |
|
|
内容記述タイプ |
Other |
|
資源タイプ |
text |
| 著者版フラグ |
|
|
出版タイプ |
VoR |
| フォーマット |
|
|
内容記述タイプ |
Other |
|
内容記述 |
application/pdf |
| ID(XooNIps) |
|
|
|
24-2008 |
| 閲覧数(XooNIps) |
|
| ダウンロード数(XooNIps) |
|
|
|
14485 |
924.pdf (6.7 MB)
