Skip to main content

Drusen in non-neovascular ARMD and subtypes

Drusen deposit extracellular yellow material between retinal pigment epithelium (RPE) and Bruch's membrane, consisting of lipids and fatty proteins, mainly oxidized and apolipoproteins. Also, zinc may play a role in blocking complement cascade factor H.


Drusen can be classified by size as hard drusen (small with defined edges), and when they enlarge in size or coalesce, forming soft drusen has blurred edges.


Fundus image showing hard drusen
Fundus image showing hard drusen

Fundus image showing soft drusen
Fundus image showing soft drusen




Drusen can be different in content as there are homogenous drusen and heterogeneous. The latter indicates transforming (regressing) drusen, a prognostic factor of developing atrophic (Advanced) ARMD.


Fundus image showing regressing drusen
Fundus image showing regressing drusen


Drusen can come in different shapes, such as reticular pseudodrusen, implying developing advanced or wet ARMD, and drusenoid RPE detachment. It takes years to induce choroidal neovascularization membrane (CNVm) or advanced ARMD.

Fundus image showing drusnoid RPE detachment
Fundus image showing drusnoid RPE detachment


Drusen can be different in the location where it can be located in the optic disc forming optic disc drusen, macula, or periphery.


In clinical practice, hard drusen is a sign of early non-neovascular ARMD when combined with intermediate drusen and can be benign without disturbing the ellipsoid zone or causing pigment migration. However, on OCT, hyperreflectivity can be found next to hard drusen as altered Henle fiber layer (HFL). When hard drusen coalesce and enlarge in size can form soft drusen, which becomes more homogenous. Indeed, it can cause disturbed ellipsoid zone and pigment migration, which can be found as hyperreflectivity in OCT's outer retinal tissues. 


OCT cross-section showing drusen
OCT cross-section showing drusen

OCT cross-section showing soft drusen
OCT cross-section showing soft drusen


Soft drusen are the hallmark of intermediate non-neovascular ARMD, which can come with reduced vision and risk of developing advanced or wet ARMD. Therefore,  a close follow-up should be done along with systemic supplements if the other eye suffered from wet/advanced ARMD.


Other types of drusen, such as transforming (Regressing) drusen that features heterogeneous martial on OCT, can be a prognostic factor for atrophy or CNVm formation, the same as for reticular drusen. However, drusenoid RPE detachment needs years to lead to CNVm or an advanced stage of degeneration.

OCT cross-section shows regressing drusen
OCT cross-section shows regressing drusen

OCT cross-section shows drusnoid RPE detachment
OCT cross-section shows drusnoid RPE detachment

Please check Clinical guidelines for ARMD and course of clinical changes in RPE



Comments

Popular posts from this blog

Cellophane maculopathy

Caused by an epiretinal membrane, clinically, it appears as a sheen abnormal foveal reflex which features epiretinal membrane, due to inflammatory mediators and proliferation of glial cells secondary to a partial separation of posterior cortical vitreous. Fundus image shows cellophane maculopathy OCT features a hyperreflective band covering the inner retinal layers, causing minimal disturbance of inner retinal tissues. OCT cross-section shows epiretinal membrane  Cellophane maculopathy itself in individuals with good visual acuity may not need any interventions, but it is warranted to do a detailed peripheral retinal exam to rule out retinal tear or hole However, an epiretinal membrane may proliferate further and cause additional tangential traction. Thus, it may induce macular pucker or lamellar/pseudo hole and increase disturbance of inner retinal tissues, macular thickness, and reduction of vision. These patients may require pars plana vitrectomy to remove the epiretinal membrane an

RPE tear, and it's OCT features in a nutshell

RPE tear can occur in vascularized PEDs due to a complication of intravitreal AntiVEGF treatment, which causes a rapid contraction of CNVm, inducing traction on the RPE surface and shrinking of RPE surface. On OCT, the RPE rip will indent the retina with increased hyperreflectivity in contracted RPE with underlying shadowing hinders choroidal view in contrast to the area where RPE where it ripped of which only Bruch's membrane is visible and increasing the visibility of the underlying choroid. RPE tear Thus two opposite forces, the regression of CNVm and remaining attached RPE, other causes such as laser or spontaneous can occur. However, the AntiVEGF treatment continued despite the RPE tear. Please check  Clinical guidelines for ARMD  and  course of clinical changes in RPE

Diabetic macular edema with ischemic changes associated with very severe NPDR

A 51 years old male known to be diabetic for ten years with excellent glycemic control profile along with normal blood pressure presented with BCVA 20/100 in his left eye; he had a better vision of 20/30 in the same eye one year ago when he used to be on intravitreal injections of aflibercept, but he decided to discontinue intravitreal injection as been advised by another physician. Fundus image His fundus image shows cystic formation at the fovea with a sign of intraretinal dot and blots hemorrhages in the mid periphery with cotton wool spots and IRMA (Intra Retinal Microvascular Abnormalities). Fundus image showing macular edema with intraretinal hemorrhage and cotton wool spots Optical coherence tomography His OCT scan shows thickened central macular tissues with disorganization of inner retinal layers and non-empty cystic formation as it is classic findings of diabetic macular edema with some empty cystic formation; however, the ellipsoid zone looks intact. OCT cross-section for ce