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2  Histopathological lesions and clinical classification  251




                  SD-OCT images show the absence of the ONL, ELM, and the ellipsoid layer, and
                  either absence or marked attenuation of the RPE and Bruch’s membrane complex.
                  Due to the absence of these layers there is enhanced choroidal reflectivity [33]. On
                  fluorescein angiography, GA appears as well demarcated areas of hyperfluorescence
                  that appear during the transit phase of the angiogram, sometimes with visualization
                  of the choroidal vessels. A rim of blocked fluorescence from pigment may surround
                  the edge. In late-phase, the hyperfluorescence decreases in intensity; some staining
                  may persist.


                  2.3  Lesions of neovascular AMD

                  Neovascular AMD refers to the proliferation of new vessels either under the RPE,
                  breaking through the RPE, or within the retina layers. Exudation of fluid, lipids and
                  blood leads to the death of photoreceptors and subsequently fibrosis. Untreated pro-
                  gression may be rapid resulting in permanent legal blindness. Choroidal neovascular
                  membrane (CNV) may appear as a gray-green elevation of tissue deep to the retina
                  with overlying detachment of the neurosensory retina. Other signs visible on biomi-
                  croscopy and color photography are lipid exudates and blood (which may be subreti-
                  nal, intraretinal or pre-retinal). CNV can be classified by anatomical location. Type 1
                  membranes are beneath the RPE (usually proliferating within the inner aspect of an
                  abnormally thickened Bruch’s membrane). Type 2 membranes are located between
                  the RPE and the photoreceptors. Retinal angiomatous proliferation (RAP or type 3
                  membranes) are characterized by intraretinal neovascularization. RPE tears (rip or
                  dehiscence) are a recognized complication associated with CNV, particularly when
                  fibrovascular PED. Tears occur at the junction of attached and detached RPE. The
                  free edge of the RPE retracts and rolls toward the fibrovascular tissue.
                     CNV may also be classified on the basis of stereoscopic fluorescein angiography
                  (FA) imaging (see Fig. 5). FA can determine the pattern of fluorescence (classic or
                  occult and the proportions of each), boundaries (well defined or poorly defined) and
                  location of the neovascular lesions with respect to the center of the foveal avascular
                  zone (FAZ). The fluorescein angiographic appearance of classic CNV is an area of
                  hyperfluorescence identified in the early phase of the angiogram that progressively
                  intensifies throughout the transit phase, with leakage of dye obscuring the boundaries
                  of this area by the late phases of the angiogram [34]. Two types of occult CNV are
                  described. Fibrovascular PED is characterized by irregular elevation (best seen with
                  stereoscopic view) of the RPE with stippled or granular irregular fluorescence first seen
                  early in the angiogram, usually by 1–2 min (see Fig. 6). There is progressive leakage
                  from these regions, with a stippled hyperfluorescent pattern. Late leakage of undeter-
                  mined origin is characterized by regions of fluorescence at the level of the RPE that are
                  best appreciated in the late phases of an angiogram; they do not correspond to classic
                  CNV or to areas of irregular elevation of the RPE during the early or mid-phases of the
                  angiogram [34]. Angiographic features of RAP lesions include a retinal vessel directed
                  into the lesion and retinal-retinal anastomosis. ICG imaging is essential for identify-
                  ing polypoidal choroidopathy. Video ICG may demonstrate pulsatile choroidal polyps.
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