Juvenile Vogt-Koyanagi-Harada Disease in Which Good Visual Prognosis Was Derived from Swift and Definitive Diagnosis
Joint Authors
Yoshida, Atsushi
Kawashima, Hidetoshi
Tominaga, Satoko
Source
Case Reports in Ophthalmological Medicine
Issue
Vol. 2016, Issue 2016 (31 Dec. 2016), pp.1-3, 3 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2016-03-27
Country of Publication
Egypt
No. of Pages
3
Main Subjects
Abstract EN
We report an 8-year-old girl who manifested Vogt-Koyanagi-Harada (VKH) disease.
At the first visit, conjunctival hyperemia, inflammation in the anterior chamber, serous retinal detachment, and papillitis were observed in both eyes.
Fluorescein angiography (FA) revealed bilateral subretinal fluid and papillitis.
Ocular computed tomography (OCT) showed subretinal fluid and choroidal hypertrophy underneath macula in both eyes.
Cerebrospinal fluid examination indicated aseptic meningitis.
Systemic data did not suggest the other systemic diseases.
Therefore, she was diagnosed with incomplete VKH disease.
After corticosteroid pulse therapy, oral prednisolone was administered for seven months.
Eighteen days after the induction of the treatments, inflammation in the anterior chamber and serous retinal detachment of both eyes disappeared completely.
For seven months after the induction of the treatments, she had no relapses of any symptoms.
Cerebrospinal fluid examination and FA for children are difficult to conduct, since it is difficult to get informed consent of these examinations from their parents.
However, those thorough examinations enable us to make a swift and definitive diagnosis of VKH disease, thus assuring good visual prognosis.
We have to bear in mind that juvenile VKH disease is very rare, yet when it occurs, ophthalmologic examinations help us diagnose and treat it.
American Psychological Association (APA)
Yoshida, Atsushi& Tominaga, Satoko& Kawashima, Hidetoshi. 2016. Juvenile Vogt-Koyanagi-Harada Disease in Which Good Visual Prognosis Was Derived from Swift and Definitive Diagnosis. Case Reports in Ophthalmological Medicine،Vol. 2016, no. 2016, pp.1-3.
https://search.emarefa.net/detail/BIM-1101851
Modern Language Association (MLA)
Yoshida, Atsushi…[et al.]. Juvenile Vogt-Koyanagi-Harada Disease in Which Good Visual Prognosis Was Derived from Swift and Definitive Diagnosis. Case Reports in Ophthalmological Medicine No. 2016 (2016), pp.1-3.
https://search.emarefa.net/detail/BIM-1101851
American Medical Association (AMA)
Yoshida, Atsushi& Tominaga, Satoko& Kawashima, Hidetoshi. Juvenile Vogt-Koyanagi-Harada Disease in Which Good Visual Prognosis Was Derived from Swift and Definitive Diagnosis. Case Reports in Ophthalmological Medicine. 2016. Vol. 2016, no. 2016, pp.1-3.
https://search.emarefa.net/detail/BIM-1101851
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1101851