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Ординатура / Офтальмология / Английские материалы / Illustrated Tutorials in Ophthalmology Kanski, Bolton 2001

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Causes of hyperfluorescence (2)

Leakage of dye

Prolonged dye retention

( staining )

 

 

 

 

 

 

 

Into sensory retina

 

From new vessels

Associated with drusen

 

(cystoid macular oedema)

(choroidal neovascularization

 

 

 

 

 

 

 

 

 

 

 

Causes of hypofluorescence (1)

Blocked retinal or choroidal fluorescence

 

 

 

 

Blood under retinal pigment

Abnormal

Preretinal or intraretinal blood

epithelium

 

material

 

 

Increased

 

 

 

pigment

 

 

 

 

 

Causes of hypofluorescence (2)

Vascular occlusion

Loss of vascular tissue

Capillary non-perfusion

Choroideremia or high myopia

(venous occlusion)

 

General Principles of ICG Angiography

1.Binding

98% bound to proteins

Less leakage from choriocapillaris

2.Fluorescence

Much less than fluorescein

Excitation peak 800 nm

Emission at 835 nm

3.Filters

Infrared barrier and excitation

4. Safer than fluorescein

Phases of normal ICG angiogram (1)

Early (20 sec)

Early middle (3 min)

Disc hypofluorescence

Filling of watershed zone

Poor perfusion of vertical

 

 

 

(watershed) zone near disc

Fading of choroidal arterial filling

Prominent filling of choroidal arteries

 

Prominent filling of choroidal veins

Early filling of choroidal veins

 

 

Filling of retinal arteries but not veins

Filling of retinal arteries and veins

Phases of normal ICG angiogram (2)

Late middle (6 min)

Late (21 min)

Reduced filling of choroidal vessels

Large choroidal and retinal vessels are

 

 

Diffuse hyperfluorescence due to

 

empty

 

diffusion of dye from choriocapillaris

 

 

 

Persistent filling of retinal vessels

Diffuse background hyperfluorescence

 

 

AGE-RELATED MACULAR DEGENERATION (AMD)

1.Drusen

2.Drusen and AMD

3.Atrophic AMD

4.Exudative AMD

Pigment epithelial detachment (PED)

Choroidal neovascularization (CNV)

Drusen

Histopathology

 

Hard

 

Soft

 

 

 

 

 

 

 

 

Small well-defined

Larger, ill-defined spots

 

spots

May enlarge and coalesce

 

Usually innocuous

 

Increased risk of AMD

 

 

 

 

 

 

FA of drusen

``

Degree of hyperfluorescence depends on:

Extent of overlying RPE atrophy (window defect)

Amount of staining

Lipid content

Drusen and AMD - progression

Atrophic AMD

Exudative AMD

 

 

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