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25 Cards in this Set

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Refers to the formation of an area of confluent tiny vesicles within the peripheral retina, such that it looks thickened or LESS transparent.
- Always extends from ora serrata posteriorly and circumferentially
- Does NOT by itself lead to RD
Microcystoid Degeneration
What's the management of Microcystoid Degeneration?
1. Does NOT require tx or referral
2. Recognize as a generally benign condition
3. Document & monitor for progression to retinoschisis
4. Discuss symptoms of RD with patient, but reassure unlikely to occur.
Refers to patches of chorioretinal atrophy aligned in a row parallel to the ora serrata.
- Represents thinned INTACT retina & choroid overlying visible sclera
- Does NOT lead to RD!
- occurs in roughly 1/4 of normal eyes
Pavingstone Degeneration
What's the management for Pavingstone Degeneration?
1. Recognize as NOT due to other pathology
2. NO need for tx or referral.
3. Merely document & educate the patient
4. Understand that there is NO "break" in the thinned, degenerative retinal tissue
Refers to peripheral perivascular pigmentation which may extend posteriorly to the equator.

- Occurs mostly in older patients
- It's NOT associated with pathology, decreased visual function or RD
Reticular Pigmentary Degeneration

aka:

Peripheral Senile Pigmentary Degeneration

Tapetochoroidal Degeneration
What's the management for Reticular Pigmentary Degeneration?
1. Recognize as a benign age-related change and NOT pathological.
2. Differentiate from similar appearing conditions which are pathological (RP, etc)
3. Document, but probably NO need to explain this relatively normal finding to patient.
Refers to the appearance of drusen OUTSIDE the macular region.

- Commonly observed in older pts
- NOT associated with AMD
- Does NOT lead to RD or any other problems
Peripheral Drusen
What's the management for Peripheral Drusen?
1. Differentiate between this benign manifestation of drusen and that associated with progressive macular changes (AMD)

2. Clearly communicate findings to patient with reassurance that they are NOT at increased risk for AMD.

3. Monitor regularly (AMD, etc. not prevented)
An elongated area of thinned (atrophic) retina beneath a pocket of liquefied vitreous which is surrounded by strong vitreal attachments at the margins of the lesion.

- Very common especially in myopes
- Pathogenesis is uncertain
- Present is up to nearly half of eyes with RD!
Lattice Degeneration
What's the clinical SIGNS for Lattice Degeneration?
1. Bilateral
2. Seen in the superiotemporal quadrant
3. Develop early (teen's and 20's)
4. White lines, "snowflakes," pigmentation and/or small holes often found within lesion.
What's the management for Lattice Degeneration?
1. Lattice Degeneration without retinal breaks does NOT require treatment or referral
2. Prophylactic laser may be considered in specific limited circumstances
3. All patients should be monitored regularly
4. All patients should be advised of symptoms of RD and need for immediate care if such occur
Should patients with Lattice Degeneration be worried about retinal detachment (RD)?
a) Most patients with Lattice Degeneration (LD) do NOT develop RD.

b) RD may develop in patients with LD:
1. following flap tear formation during PVD
2. from tears at posterior margin of lesion
3. from holes within lesion (rarely)
A peripheral retinal degeneration similar to LD:
- characterized by elongated patches of "frosted" looking retina in the periphery
- usually LONGER than those seen in lattice
- overlying vitreous liquefaction (like lattice), but without strong vitreoretinal attachments
- may exhibit "holes" within the lesions
Snailtrack Degeneration
What's the management for Snailtrack Degeneration?
1. Snailtrack Degeneration without retinal breaks does NOT require tx or referral.
2. Prophylactic laser may be considered in specific limited circumstances
3. All patients should be monitored regularly
4. All patients should be advised of symptoms of RD and need for immediate care if such occur

NOTE: Similar management/tx as Lattice Degeneration.
Describes the whitish opaque appearance of islands of peripheral retina that are attached more strongly to the cortical gel than normal.
White With & Without Pressure
What's a major difference between "White With Pressure" vs "White Without Pressure?"
1) White With Pressure
- it's only observed with scleral indentation

2) White Without Pressure
- constant
What's the management for White Without Pressure?
1. A common ancillary finding during routine DFE of asymptomatic patients
2. Rarely causes problems, but giant retinal tears have been known to occur at posterior border
3. Document and educate patient about symptoms of RD
A small area of retinal elevation occurring where focal vitreous traction "pulls up" the retina.
retinal tuft
What are some signs, symptoms, and tx in patients with retinal tuft?
1. Very common (mostly in adult eyes)
2. Seen as a small, light-colored, raised area of retina (may be pigmented at base)
3. Usually an incidental finding (NO symptoms)
4. Does NOT require tx!
This atrophic condition is often seen in the equatorial region of highly myopic eyes.
- Represents a thinning of choroid/retina
- Holes may form within the atrophied retina, leading to RD
- These holes are often difficult to see due to lack of contrast between retina and choroid
Diffuse Chorioretinal Atrophy
What 4 major conditions that occur more frequently in myopia?
The following conditions occur more frequently in myopia:

1. Lattice Degeneration
2. Snailtrack Degeneration
3. Diffuse Chorioretinal Atrophy
4. Macular Holes
What 3 major processes contribute to increased RD with myopia?
1. Vitreous Degeneration occurs with myopia
2. PVD occurs earlier with myopic individuals
3. Cataract tx is often more associated with RD in myopic patients
- CAT surgery with vitreous loss
- Laser posterior capsulotomy
Why should high myopic patients have periodic DFE check ups?
High myopic patients should have periodic DFE's to check for asymptomatic retinal breaks and detachments.
Which conditions do NOT lead to RD?
1. Microcystic Degeneration
2. Pavingstone Degeneration
3. Reticular Pigmentary Degeneration
4. Peripheral Drusen
Which conditions may LEAD to RD?
1. Lattice Degeneration
2. Snailtrack Degeneration
3. White With & Without Pressure
4. Diffuse Chorioretinal Atrophy