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 [1–3]. 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 [4–6].
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.

Central serous chorioretinopathy
I. The central reflex was disappeared
II. The apex of sensory retinal detachment
III. Fold of ILM

Central serous chorioretinopathy
I. Leakage from venules inferior-nasal to the macula
II. The area of sensory retinal detachment

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

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


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

Idiopathic macular hole
I. Full thickness macular hole
II. Shallow retinal detachment in the adjacent area

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

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

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

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

Dry age-related macular degeneration
I. Diffused hard drusen
II. Confused soft drusen
III. Macula uninvolved


Juxtafoveal choroidal neovascularization
I. Juxtafoveal choroidal neovascularization
II. RPE detachment and exudates
III. The area of sensory retinal detachment
IV. Macular edema

Choroidal neovascularization
I. Subfoveal CNV
II. Superficial retinal exudates
III. Exudates in the inner retina
IV. Deep retinal hemorrhage
V. Suspected area of CNV

Choroidal neovascularization
I. Subfoveal choroidal neovascularization
II. Intra-retinal hemorrhage around the lesion

Stay updated, free articles. Join our Telegram channel

Full access? Get Clinical Tree

