Diseases


Fig. 3.1

Anatomical schematic diagram of the macula



The macular diseases mainly involve congenital anomaly (congenital macular coloboma), central serous chorioretinopathy, vitreomacular traction syndrome, vitreous hemorrhage beneath the inner limiting membrane, macular edema, macular hole, macular atrophy and proliferative diseases of the macula, such as retinal angiomatous proliferation (RAP), choroidal neovascularization (CNV), and polypoidal choroidal vasculopathy (PCV).


Stereoscopic photography plays an important role in macular diseases [13]. In the past, stereoscopic slide film photography of the retina is the standard with which other imaging modalities have been compared when identifying age-related macular degeneration (AMD). The Age-Related Eye Disease Study, a multicenter prospective cohort study of 4757 participants designed to access the clinical course, prognosis, and risk factor for age-related macular degeneration and cataract, uses stereoscopic color fundus photographs in a standardized fashion by certified photographers [4, 5]. In ETDRS, besides the grading diabetic retinopathy severity by stereoscopic retinal photography, the clinically significant macular edema (CSME), which is one of the key factors affecting the visual acuity, is also diagnosed correctly by stereoscopic digital fundus photography. The kappa (ƙ) values among contact lens biomicroscopy (CLBM), slit-lamp biomicroscopy with 90D/78D or by stereoscopic pairs are more than 0.6. So, in most cases, the stereoscopic photography can be used as a diagnosis tool, especially for screening and telemedicine [46].


Abnormalities in macular diseases are various [3, 7, 8]. Drusen are yellow-white deposits within Bruch’s membrane underlying the RPE and vary greatly in appearance, ranging from small round, flat spots in size and shape to large deposits even confluent with adjacent drusen. Geographic atrophy may show a sharply demarcated, usually circular zone of partial or complete depigmentation of RPE and exposure of underlying large choroidal blood vessels. The three kinds of choroidal neovascularization (type I, II, and III), which are correspondent with occult CNV, classic CNV, and retinal angiomatous proliferation (RAP), are more vividly and comprehensively shown on stereoscopic pairs than monoscopic and even OCT scans. The retina will be dome-shaped with intra-retinal exudates and cyst, accompanying by intra-retinal, sub-retinal and sub-RPE hemorrhages, sub-retinal and sub-RPE neovascularies, etc. The anastomosis between retina and choroid will be shown clearly on stereoscopic FFA pairs [7]. Macular holes are well-defined defects in the middle of the macula in various sizes. Sometimes, there is a thin membrane above the posterior retina called epi-retinal membrane (ERM).


Generally speaking, with the combination of stereoscopic photography and other high-tech tools such as OCT, more and more macular signs and characteristics will be explored.



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Fig. 3.2

Central serous chorioretinopathy


I. The central reflex was disappeared


II. The apex of sensory retinal detachment


III. Fold of ILM



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Fig. 3.3

Central serous chorioretinopathy


I. Leakage from venules inferior-nasal to the macula


II. The area of sensory retinal detachment



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Fig. 3.4

Sensory retinal detachment


I. Apex of detachment


II. Fold of epiretinal tissue (ILM)


III. Intermediate retinal exudates


IV. Vessels located in the depressed area, which was lower than the area I



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Fig. 3.5

Central serous chorioretinopathy


I. Retinal detachment in the posterior pole


II. One of the apexes of detachment


III. Bottom of detachment


IV. The other one of apexes of detachment


V. Retinal fold



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Fig. 3.6

Pouch-shaped retinal pigment epithelium detachment


I. The area of RPE detachment, which was larger in the color photograph than in the fluorescein angiography


II. Apex of detachment


III. Sub-RPE fluid


IV. Blocked fluorescence by hemorrhage and intermediate hyperfluorescence



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Fig. 3.7

Idiopathic macular hole


I. Full thickness macular hole


II. Shallow retinal detachment in the adjacent area



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Fig. 3.8

Secondary macular hole


I. Full thickness macular hole


II. Proliferative membrane in the vitreous


III. Retinal detachment


IV. Ghost vessels


V. Segmented sheath in the retinal arteries


VI.   Artery-Vein crossing of the superficial retinal artery and deep retinal vein


VII. ILM fold



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Fig. 3.9

Macular hole secondary to optic disc pit


I. Full thickness macular hole


II. Shallow retinal detachment in the adjacent area


III. Fold of posterior hyaloids and ILM, the retinal vessels were obscure


IV. Choroidal coloboma


V. Optic disc pit



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Fig. 3.10

Retinal detachment secondary to macular hole


I. Full thickness macular hole, approximately 1/4 PD in diameter


II. Retinal detachment and fold


III. Proliferation under the retina like a streak


IV. Peripapillary atrophy



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Fig. 3.11

Retinal detachment secondary to juxta foveal hole


I. Suspected para-macular hole, approximately 1/4 PD in diameter, which was confirmed by OCT


II. Detached macula


III. Vitreous band


IV. Peripapillary atrophy



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Fig. 3.12

Dry age-related macular degeneration


I. Diffused hard drusen


II. Confused soft drusen


III. Macula uninvolved



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Fig. 3.13

Juxtafoveal choroidal neovascularization


I. Juxtafoveal choroidal neovascularization


II. RPE detachment and exudates


III. The area of sensory retinal detachment


IV. Macular edema



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Fig. 3.14

Choroidal neovascularization


I. Subfoveal CNV


II. Superficial retinal exudates


III. Exudates in the inner retina


IV. Deep retinal hemorrhage


V. Suspected area of CNV



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Fig. 3.15

Choroidal neovascularization


I. Subfoveal choroidal neovascularization


II. Intra-retinal hemorrhage around the lesion

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Mar 22, 2020 | Posted by in OPHTHALMOLOGY | Comments Off on Diseases

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