Open Access Peer-Reviewed
Relatos de Caso

Large colloid drusen analyzed with structural en face optical coherence tomography

Análise de drusas grandes coloidais através de OCT en face estrutural

Nathália Corbelli Roberti1; João Rafael de Oliveira Dias2; Eduardo Amorim Novais2; Caio Saito Regatieri2; Rubens Belfort Jr.2

DOI: 10.5935/0004-2749.20170029

ABSTRACT

Drusen are extracellular deposits between the basal lamina of the retinal pigment epithelium (RPE) and the inner collagenous layer of Bruch's membrane. Large colloid drusen (LCD) are located below the RPE and are characterized by multiple, large, dome-shaped RPE detachments, with marked attenuation of the ellipsoid zone overlaying the drusen. This report presents the structural en face optical coherence tomography (OCT) findings of LCD and relates them to findings from fluorescein and indocyanine green angiography. We describe the case of a 55-year-old woman who presented with the chief complaint of a 5-year history of progressively worsening vision. Her best-corrected visual acuities were 20/40 and 20/400 in the right eye and the left eye, respectively. Fundus examination showed large bilateral, symmetrical, sub-retinal, yellowish lesions compatible with LCD. We describe the structural en face OCT characteristics and angiographic findings from this patient.

Keywords: Retinal drusen; Tomography, optical coherence/methods; Fluorescein angiography; Indocyanine green

RESUMO

Drusas são depósitos extracelulares localizados entre a lâmina basal do epitélio pig mentado da retina (RPE) e a camada colágena interna da membrana de Bruch. Drusas grandes coloidais (LCD) estão localizadas abaixo do EPR, e são caracterizadas por múltiplos descolamentos cupuliformes do EPR com atenuação da zona elipsoide sobrejacente às drusas. O objetivo deste relato é apresentar os achados de tomografia de coerência óptica (OCT en face estrutural em uma paciente com LCD, bem como correlacioná-los com angiografia fluoresceínica e angiografia com indocianina verde. Descrevemos o caso de uma paciente do sexo feminino, 55 anos, que referiu baixa acuidade visual em ambos os olhos há 5 anos. Sua acuidade visual corrigida era de 20/40 no olho direito e 20/400 no olho esquerdo. Ao exame fundoscópico a paciente apresentava lesões compatíveis com drusas grandes coloidais. As características tomográficas e angiográficas também são descritas neste relato de caso.

Descritores: Drusas retinianas; Tomografia de coerência óptica/métodos; Angiofluo resceinografia; Verde de indocianina

INTRODUCTION

Drusen are extracellular deposits between the basal lamina of the retinal pigment epithelium (RPE) and the inner collagenous layer of Bruch's membrane. Although drusen occur more frequently in people above 50 years of age, some drusen patterns, e.g., cuticular drusen, Malattia Leventinese (ML), and large colloid drusen (LCD) can occur earlier(1,2). LCD are large (200-300 microns) yellowish, bilateral lesions with hyperpigmented borders scattered throughout the posterior pole. The LCD are found outside of the RPE as is common with conventional drusen(3-5). Reticular pseudodrusen also occur in the sub-retinal rather than in the sub-RPE space(2,3).

Optical coherence tomography (OCT) is an important tool for diffe rentiating between various drusen patterns(6,7). In most cases, LCD appear on OCT B-scans as multiple convex or dome-shaped structures with medium and homogeneous internal reflectivity and marked attenuation of the ellipsoid zone overlaying the LCD(1,8). These drusen are homogenously hyperfluorescent in late-phase fluorescein an giography images. In late-phase indocyanine green angiography (ICGA) images, LCD are either hyperfluorescent or hypofluorescent and surrounded by a discreet hyperfluorescent halo(8).

This report presents structural en face OCT findings of LCD and correlations of these with findings with fluorescein angiography and ICGA.

CASE REPORT

A 55-year-old Caucasian woman from São Paulo, Brazil, presented with the chief complaint of a 5-year history of progressively worsening vision, particularly in the left eye. She had a 70-pack/year smoking history and a diagnosis of emphysema. She had not had any previous ocular surgeries, and there was no history of other familial diseases. Her best-corrected visual acuity levels were 20/40 in the right eye and 20/400 in the left eye. The pupillary reflexes were preserved and the anterior segment was normal. Indirect ophthalmoscopy revealed large sub-retinal yellowish lesions in the macular area and the mid periphery of the retina bilaterally. Fluorescein angiography showed early hyperfluorescence; ICGA showed that most drusen appeared hypofluorescent. En face OCT showed a hyper-reflective center surrounded by a hypo-reflective halo, which was bordered by hyper-reflective and hypo-reflective rings. In OCT B-scans, all drusen appeared convex with medium and homogenous internal reflectivity, marked attenuation of the ellipsoid zone overlaying the LCD, and RPE atrophy. Posterior segment findings can be seen in figure 1, while figure 2-4 display image findings. A conservative approach was adopted, and the patient was instructed to quit smoking and perform the Amsler Grid test routinely.

Figure 1 A fundus photograph showing large, bilateral, yellowish lesions in the macular area and retinal periphery. 

Figure 2 Optical coherence tomography (OCT) images obtained from a 55-year-old woman with large colloid drusen (LCD). A) Structural en face OCT with upper segmentation line located at the avascular outer retina and lower segmentation line placed at the sub-retinal pigment epithelium (RPE) space showing a hyper-reflective center surrounded by a hypo-reflective halo, bordered by hyper-reflective and hypo-reflective rings, similar to the donut effect. B) Corresponding OCT B-scan of (A) showing the convex contour of LCD with medium and homogeneous internal reflectivity under the RPE, as well as marked thinning of the outer nuclear and ellipsoid layers. A small area of RPE atrophy as seen under the horizontal foveal scan, identified as reverse shadowing (black arrow). No fluid accumulation is observed. C) Structural en face OCT on a choroid slab showing a hyper-reflective center surrounded by a hypo-reflective halo. D) Choroidal features on the OCT B-scan were not well defined due to signal blockage caused by the colloid drusen. 

Figure 3 Large colloid drusen in a late-phase indocyanine green angiography image with a hypofluorescent center surrounded by a hyperfluorescent halo. This halo is bordered by a hypofluorescent ring, referred to as the donut effect. 

Figure 4 Fluorescein angiography showing early hyperfluorescence of large colloid drusen. 

DISCUSSION

Large colloid drusen develop most often in women without a fa milial history of retinal problems. Drusen do not seem to be related to an increased risk of choroidal neovascularization or significant loss of mean visual acuity(3). The precise incidence and prevalence of cho roidal neovascularization in LCD is not well characterized, but most clinicians believe its incidence is significantly lower than in age-re lated macular degeneration(9).

The images obtained from this patient showed features of LCD. In the late-phase ICGA images, the larger drusen appeared hyperfluorescent with a hypofluorescent halo, traditionally described as the donut effect(3) (Figure 3). Drusen are lipid-rich, and the relative hydrophobicity of the commonly used angiographic dyes differs. A difference in the lipid composition between the core and the periphery of LCD has been reported, which might be responsible for the typical donut shape observed in the ICGA images(1).

The structural en face OCT images showed a hyper-reflective center surrounded by a hypo-reflective halo bordered by two rings, one of which was hyper-reflective and the other hypo-reflective, similar to the donut effect seen on the ICGA images (Figure 2). OCT is noninvasive and can help differentiate LCD from other early-onset drusen, such as Malattia Leventinese and cuticular drusen. In OCT images, LCD have been described as having a sawtooth pattern, with the height of each LCD approximately equal to its basal diameter. The neurosensory retina appears to be spared in the area overlaying the drusen, although the overlaying RPE is much thinner at the apex of each druse than between the drusen. In Malattia Leventinese, confluent sub-RPE accumulation on OCT has been reported. The smaller drusen of this condition have a radial distribution and a confluence of large drusen with sub-retinal fibrous plaque occurs. The typically pale drusen are adjacent to the optic disc(3). Furthermore, OCT allows observation of focal loss of cellular visibility, which has a mosaic pattern in patients presenting with drusen(6,7). The smallest LCD do not affect the ellipsoid zone(5). This imaging approach might serve as the foundation for valuable imaging-based biomarkers for detecting the earliest disease stages, tracking progression, and monitoring treatment response(9).

On fluorescein angiography images, drusen hyperfluorescence increased quickly, especially in the middle periphery. The areas of hy perfluorescent lesions did not vary among the capillary, venous, and washout angiography phases(4) (Figure 4). One study reported that large visible drusen in a group of adults with early-onset drusen were concentric to regions of hyperfluorescence, suggesting that drusen might have clinically detectable, substructural domains(9). Similarly, in another study, the measurements of the drusen areas on OCT were smaller than the measurements obtained from color fundus images(10).

These results led us to conclude that structural en face OCT is a useful noninvasive tool that facilitates better morphologic evaluation and quantification of structural changes in LCD on high-resolution images. While traditional OCT produces longitudinal cross-sectional images, en face OCT produces transverse images of the retinal and choroidal layers at any specified depth. This provides an extensive overview of the pathological structures in one image. Thus, combining dye-based angiographic images with structural en face OCT may provide a better understanding of this retinal entity.

Funding: No specific financial support was available for this study.

REFERENCES

1 Guigui B, Querques G, Leveziel N, Bouakkaz H, Massamba N, Coscas G, et al. Spectral domain optical coherence tomography of early onset large colloid drusen. Retina. 2013;33(7):1346-50.

2 De Bats F, Wolff B, Mauget-Faÿsse M, Meunier I, Denis P, Kodjikian L. Association of reticular pseudodrusen and early onset drusen. ISRN Ophthalmol. 2013; 273085.

3 Boon CJ, van de Ven JP, Hoyng CB, den Hollander AI, Klevering BJ. Cuticular drusen: stars in the sky. Prog Retin Eye Res. 2013;37:90-113.

4 Guigui B, Leveziel N, Martinet V, Massamba N, Sterkers M, Coscas G, et al. Angiography features of early onset drusen. Br J Ophthalmol. 2011;95(2)238-44.

5 Khan KN, Mahroo OA, Khan RS, Mohamed MD, McKibbin M, Bird A, et al. Differentiating drusen: drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processes. Prog Retin Eye Res. 2016;53:70-106.

6 Lamory B, NakashimaK, BenchabouneM, Ullern M, VuaillatE, Sahel JA, et al. In vivo microscopic imaging of drusen using adaptive optics. Invest Ophthalmol Vis Sci. 2011;52(14):4469.

7 Kozak I. Retinal imaging using adaptive optics technology. Saudi J Ophthalmol. 2014; 28(2):117-22.

8 Querques G, Massamba N, Guigui B, Lea Q, Lamory B, Soubrane G, et al. In vivo evalua tion of photoreceptor mosaic in early onset large colloid drusen using adaptive optics. Acta Ophthalmol. 2012;90(4):e327-8.

9 Russell SR, Gupta RR, Folk JC, Mullins RF, Hageman GS. Comparison of color to fluorescein angiographic images from patients with early-adult onset grouped drusen suggests drusen substructure. Am J Ophthalmol. 2004;137(5):924-930.

10 Gregori G, Yehoshua Z, Garcia Filho CA, Sadda SR, Portella Nunes R, Feuer WJ, et al. Change in drusen area over time compared using spectral-domain optical coherence tomography and color fundus imaging. Invest Ophthalmol Vis Sci. 2014;55(11):7662-8

Submitted for publication: October 13, 2016.
Accepted for publication: November 7, 2016.


Dimension

© 2024 - All rights reserved - Conselho Brasileiro de Oftalmologia