|LETTER TO THE EDITOR
|Year : 2013 | Volume
| Issue : 1 | Page : 38-39
Ultra-wide-field green (532 nm) and red (633 nm) reflectance imaging of the "sunset glow" fundus in chronic Vogt-Koyanagi-Harada disease
Soh-Eun Ahn, Seong-Woo Kim, Jaeryung Oh, Kuhl Huh
Department of Ophthalmology, Korea University College of Medicine, Seoul, Korea
|Date of Web Publication||26-Dec-2012|
Department of Ophthalmology, Korea University Ansan Hospital, 516, Gojan 1-dong, Danwon-gu, Ansan-si, Kyunggi-do, 425-707
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Ahn SE, Kim SW, Oh J, Huh K. Ultra-wide-field green (532 nm) and red (633 nm) reflectance imaging of the "sunset glow" fundus in chronic Vogt-Koyanagi-Harada disease. Indian J Ophthalmol 2013;61:38-9
|How to cite this URL:|
Ahn SE, Kim SW, Oh J, Huh K. Ultra-wide-field green (532 nm) and red (633 nm) reflectance imaging of the "sunset glow" fundus in chronic Vogt-Koyanagi-Harada disease. Indian J Ophthalmol [serial online] 2013 [cited 2020 May 28];61:38-9. Available from: http://www.ijo.in/text.asp?2013/61/1/38/105054
A 55-year-old man complaining of recurring obscured vision in both eyes presented to our clinic during his second episode of Vogt-Koyanagi-Harada (VKH) disease [Figure 1]a. At 2 months after recurrence, a "sunset glow" change of the fundus was observed [Figure 1]c. Upon fundus autofluorescence (FAF) imaging taken 3 months after recurrence, short wavelength FAF (SW-FAF) images revealed normal background autofluorescence (AF) with multiple focal granular hyper-AF signals [Figure 1]e, while near infrared FAF (NI-FAF) images demonstrated decreased background AF with multiple focal granular hyper-AF signals [Figure 1]f. Most of the hyper-AF lesions were similar between FAF images, except in the macular area. Numerous hypo-AF dots surrounded by a relatively hyper-AF halo were also observed on both FAF images, which suggested corresponding swollen retinal pigmented epithelium (RPE) cells resembling a target (target sign).  On FAF images taken 5 months after recurrence, several previous hyper-AF signals on both images had become weak or had disappeared [Figure 1]h,i. Composite fundus imaging with the ultra-wide-field Optomap® 200Dx system (Optos, Dunfermline, Scotland, UK) at 1 year after recurrence revealed a characteristic "sunset glow" fundus with a clearly visible array of choroidal vessels [Figure 2]a. In green (523 nm) laser separation imaging, retinal and choroidal vessels, including vortex veins, were clearly observed [Figure 2]b. The red (633 nm) separation view appeared to penetrate deeper and demonstrated zones of sclera, but the choroidal vessels were obscured [Figure 2]c.
|Figure 1: Color fundus image and a HRA2 cSLO fundus autofluorescence (FAF) image of the left eye. Multiple serous retinal detachments are observed after recurrence (a), A "sunset glow" sign is not observed 1 month after recurrence (b), "Sunset glow" sign begins to appear 2 months after recurrence (c), At 3 months (d-f) and 5 months (g-i) after recurrence, short wavelength FAF (SW-FAF) image (e, h) shows normal background AF with multiple focal granular hyper-AF, and near infrared FAF (NI-FAF) image (f, i) shows decreased background AF with multiple, focal granular hyper-AF signals|
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|Figure 2: Optomap® composite images of the left eye at 1 year after recurrence showing a lightly pigmented fundus with obvious choroidal vessels (a), In a green separation image, a green laser penetrates to the choroid and captures choroidal vessels, including the vortex vein (b), In a red separation image, the red laser penetrates deeper than usual and demonstrates zones of the sclera, while choroidal vessels are obscured (c)|
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The "sunset glow" appearance of the fundus, which reflects depigmentation occurring at the RPE or choroid level, is commonly seen in eyes with chronic VKH disease that has persisted for months.  VKH disease is thought to be caused by autoimmune reactions against proteins related to stromal choroidal melanocytes. The initial inflammatory events occur in the choroidal stroma, and adjacent structures, such as the RPE and the retina, are secondarily involved.  SW-FAF and NI-FAF originate from two different fluorophores (lipofuscin and melanin). Lipofuscin does not demonstrate properties of NI-FAF that are known to be associated with melanin in RPE and the choroid.  Decreased background NI-FAF images of the eye may be due to the depigmented RPE and choroid. Regarding the correspondences of hyper-AF lesions between the 2 FAF images, it is not unusual that some fundus lesions may exhibit similar and dual AF patterns.  The exact mechanism underlying dual AF behavior is not known, but melanolipofuscin, oxidized melanin, or other inflammatory remnant fluorophores are potential causes.
The Optomap® 200Dx imaging system is a scanning laser ophthalmoscope that uses dual frequency lasers (523 nm green laser and 633 nm red laser), and simultaneously obtains both green and red separation views. Unlike the longer red laser wavelength, green lasers cannot penetrate significantly deeper than the RPE.  For this reason, in healthy normal eyes, observation of the choroidal vessels or nevus posterior to the RPE with the green separation view is not possible. The choroidal vessels are better visualized on the red separation view. However, if the RPE and choroid are depigmented during the convalescent and chronic stages of VKH, the green laser may penetrate the depigmented RPE to the choroid and capture the choroidal vessels. These changes also enhance the penetration of the red (633 nm) laser, resulting in severe blurring of the choroidal vessels due to increased reflectance from the inner sclera. Therefore, if choroidal vessels begin to appear in the green separation view after initial treatment, subclinical choroidal inflammation may persist, resulting in RPE and choroidal depigmentation.
| References|| |
Ayata A, Dogru S, Senol MG, Unal M, Ersanli D, Bilge AH. Autofluorescence findings in Vogt-Koyanagi-Harada disease. Eur J Ophthalmol 2009;19:1094-7.
Keino H, Goto H, Usui M. Sunset glow fundus in Vogt-Koyanagi-Harada disease with or without chronic ocular inflammation. Graefes Arch Clin Exp Ophthalmol 2002;240:878-82.
Sugita S, Takase H, Taguchi C, Imai Y, Kamoi K, Kawaguchi T, et al
. Ocular infiltrating CD4+ T cells from patients with Vogt-Koyanagi-Harada disease recognize human melanocyte antigens. Invest Ophthalmol Vis Sci 2006;47:2547-54.
Keilhauer CN, Delori FC. Near-infrared autofluorescence imaging of the fundus: Visualization of ocular melanin. Invest Ophthalmol Vis Sci 2006;47:3556-64.
Ayata A., Tatlipinar S, Kar T, Unal M, Ersanli D, Bilge AH. Near-infrared and short-wavelength autofluorescence imaging in central serous chorioretinopathy. Br J Ophthalmol 2009;93:79-82.
Sherman J, Karamchandani G, Jones W, Nath S, Yannuzzi L. Panoramic Ophthalmoscopy: Optomap Images and Interpretation. 1 st
ed. New Jersey: Slack Incorporated; 2007.
[Figure 1], [Figure 2]