The vitreous and fundus Flashcards

1
Q

What is the vitreous

A

The vitreous is an elastic hydrogel that occupies the posterior segment of the globe
- it is composed of 99% of water with the remaining 1% largely mage up of collagen fibers, hyalocytes and hyaluronic acid

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2
Q

What are the role of the vitreous

A

The vitreous is transparent to enable transmission of light and it provides support to the globe and intraocular tissues
- the anterior vitreous supports the lens
- the posterior vitreous helps maintain close contact of the neurosensory retina with the retinal pigment epithelium

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3
Q

What is the fundus

A

The fundus can be defined as the posterior region of the eye that is viewed via the pupil during ophtalmoscopy

It always includes:
- the retina
- optic nerve
- choroid

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4
Q

What is the anatomy of the retina

A

The retina is composed of ten layers and is divided into the inner, sensory retina and the outer, nonsensory retina

The inner retina is composed of nine layers with the photoreceptors (rods and cones) located outermost

The retinal pigment epithelium is the outermost layer of the retina, is nonsensory and is immediately adjacent to the choroid

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5
Q

What is the role of cones

A

Cones are responsible for visual acuity and color detection

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6
Q

What are the main causes for retinal dysplasia

A

Retinal dysplasia is uncommon but can have a number of causes

The most commonly cited cause in cats is intrauterine infection with feline leukemia virus or feline panleukopenia virus

Inherited retinal dysplasia is not well characterized in cats but is seen occasionally
- a rod-cone photoreceptor dysplasia leading to retinal degeneration has been documented in the Abyssinian
- optic disc hypoplasia and optic disc aplasia are uncommon

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7
Q

What are the earliest clinical signs detectable on fundoscopy indicating hypertensive retionpathy

A

The earliest detectable signs of hypertension on fundoscopy are tortuosity of the retinal arterioles and retinal edema with focal bullae

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8
Q

What fundic modification accompanies severe hypertensive retinopathy

A

More severe disease is associated with hemorrhage and, depending on which vessels are involved, focal hemorrhages may be:
- subretinal
- intraretinal
- preretinal

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9
Q

What is the typical presentation of a cat with hypertensive retinopathy

A

Acute blindness associated with total retinal detachment with varying extents of anterior and posterior segment hemorrhage

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10
Q

What is the prognosis for retinal detachment

A

If treatment is instigated early, then even very large retinal detachments can resolve and vision be restored, but this does depend on the extent of the initial damage to the retina

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11
Q

What are the characteristics of diabetic and megestrol acetate retinopathy

A

Diabetic retinopathy is not well characterized in the cat

The ophtalmoscopic signs are identical to those of hypertensive retinopathy and thus are more likely explained by systemic hypertension rather than glycemic status per se

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12
Q

What are the characteristic of anemic retinopathy

A

In its mildest form, anemic retinopathy appears as a relative pallor of the retinal vessels

Profound anemia, with hematocrit less than 10% and hemoglobin concentrations less than 5g/dL, is associated with retinal hemorrhages
- it is thought that anemia leads to hypoxic damage of the vascular endothelium with resultant fragility of the vascular walls

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13
Q

What are the fundoscopic signs of active chorioretinitis

A

Fundoscopic signs of active chorioretinitis include:
- edema
- exudates
- cellular infiltrate
- hemorrhages
- when inflammation is severe, retinal detachment often ensues

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14
Q

What are the documented causes of feline retinal degeneration

A

Documented causes of feline retinal degeneration include:
- inherited dysplasias and dystrophies
- nutritional imbalances
- drug toxicities
- inflammation

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15
Q

What are the key features for photoreceptor dysplasia

A

An inherited abnormality of rod and cone development which leads to their degeneration prior to maturation has been reported in the Abyssinian
- this cone-rod dysplasia is inherited in an autosomal dominant fashion
- it is caused by a single base pair deletion in the CRX gene

The disease is very early in onset and the cones appear to be affected before the rods
- the tapetum appears dull with lack of detail from approximately eight weeks of age
- more advanced signs of retinal degeneration progress rapidly
- tapetal hyperreflectivity
- nontapetal depigmentation
- vascular attenuation

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16
Q

What is photoreceptor degeneration

A

This is a later onset photoreceptor degeneration which is inherited in an autosomal recessive fashion in the Abyssinian
the disease is also described in Somalis, Persian and Siamese

Disease onset occurs from around 18 months of age
- typical signs of advanced degeneration are usually present by 4-6 years of age