Blue 1-2 Flashcards

(31 cards)

1
Q

What is treatment for HZO

A

PO aciclovir 800mg 5x/day for 7-10 days

No benefit of topical aciclovir

Starting PO aciclovir within 72 hours of rash onset reuces the risk of post-herpetic nerualgia and ocular complications but still consider if later.

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2
Q

What are Karchmer’s spots? Khodadoust line?

A

subepithelial opacities in graft suggesting rejection.

Endothelial line in endothelial graft rejection

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3
Q

Corneal arcus
Where does it start
Which layer?
Association?
What occurs with it?
Ipsilateral

A

Starts at 12 and 6 o clock

Lipid deposits in peripheral stroma but can be in DM/Bowman’s layer

Associated with peripheral corneal thinning - senile furrow degeneration

Unilateral arcus - contralateral carotid artery disease
Ipsilateral ocular hypotony

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4
Q

Which layer is Wilson’s disease

A

Copper deposition in Descemet’s membrnae

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5
Q

Wilson’s disease inheritance?
Gene? Signs?

A

Autosomal recessive
ATP7B gene - regulates copper transport protein

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6
Q

What is treatment for Wilson’s disease

A

D-penicillamine promotes unirary secretion of copper - may disappear Keyser Fleischer ring

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7
Q

What is Meesmann dystrophy?

A

Autosomal dominant
Epithelial

Irregular thickening of the epithelial basement membrane and intraepithelial cysts

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8
Q

What is Reis Buckler Dystrophy?

A

Autosomal dominant
Bowman’s layer

REplacement of Bowman’s layer and epithelial basement memvrnae with fibrous tissuesW

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9
Q

hat is Thiel BEnke dystrophy

A

Curly fibres in Bowman layer

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10
Q

What is Schnyder dystrophy

A

AD
Abnormal metabolism of lipid
Central crystalline dystrophy
Deposition of cholesterol and phospholipids in stroma

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11
Q

What are Vogt striae

A

Vertical lines in storma which may disappear on pressure (in keratoconus)

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12
Q

What is Fleischer ring

A

IRon deposition at base of cone in keratoconusW

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13
Q

What is Munson’s sign

A

Conical distortion of the lwoer lid on down gaze

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14
Q

What is Rizutti’s sign

A

Abdnormal fobussing of beam orientated obliquely across the cone from the temporal side

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15
Q

What is seen on histopathology in keratoconus

A

Breaks in Bowman’s layer

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16
Q

What is acute hydrops?

A

Descemet’s membrane rupture resulting in acute corneal oedema

Treat with topical steorids lubrication and cycloplegia

Intracamers air injection or gas can be used to tamponade Descemet’s break

17
Q

Which corneal curvture affected in keratoconus?

A

Both anterior and posterior

18
Q

What is Belin AMbroso Enhance Ectasia tdisplay

A

Analytic tool in pentacam to detect early keratoconus
Displays anterior and posterior elvation data relative to best fit sphere

19
Q

What is posterior keratoconus

A

Abnormal steepening of the posterior cornea in presence of normal anterior corneal surface.

Isolated unilateral congenital finding

20
Q

What is Peter’s anomaly

A

Congenital central corneal opacity (leukoma) associated with posterior corneal defect (posterior stromal, DM, endothelium)

May be associated with anterior iris strands, lens corneal strands and glaucoma (50-70%)
Sporadic

Associated with Anairida (PAX6), PIT2X and FOXC1 (Axenfel Riegler)

May be associated with cardian and CNS anomalies (peter plus sydnrome)

21
Q

What are features sugestive of conjunctival naevus

A

Unilaterality
Focal lesion
Chornicity
PResence of cysts

22
Q

What are features suggestive of conjunctival melanoma

A

Elevation
Immobility
Vascularity

23
Q

What is conjunctival melanosis?

A

Excessive melanin production and retention of melanin by epithelial melanocytes
Does not elevate surface of conjunctiva and not associated with cystic changes.

May be associated with periocular skin changes called naevus of Ota (oculodermal melanocytosis)

24
Q

What is Mooren’s ulcer

A

Idiopathic peripheral ulcerative keratitis with absence of systemic disorder

Painful and progressive
Starts from peripheral cornea and progresses circumferentially and centrally.

Ulcer is concentric to limbus and leading edge is undermined, infiltrated and de-epithelialised

Creates overhanding edge at central borderW

25
What are associations of Mooren's ulcer
Hepatits C Hookworm
26
What happen sin bilateral Mooren ulcer
More painful, more aggressive, poor response to treatment
27
Beaten bronze corneal endothelium, iris atrophy and peripehral anterior synechiae
Iridocorneal Endothelial sydnrome Hgih peirpheral anterior synechiae extending above Schwalbe's line Women > men 20-50 years
28
What are variants of ICE syndrome?
Iris naevus/Cogan-Reese syndrome Changler syndrome - corneal eodema with less iris findings Essential iris atrophy - greater extent of iris atrophy with polycoria, ectropion uveae, correctopia
29
What is primary acquired melanosis? Most common location? Risk?
Melanocytic lesion that affects mostly bulbar conjunctiva Mostly affects white people Risk of progression to melanoma in severe atypia
30
What i pellucid marginal degeneration
Diopathic corneal ectatic disorder affecting peripheral cornea SUually in inferior quadrant More commonly affects men Against the rule astigmatism Crab-claw or kissing dove appearance on topography Steepest area of cornea superior to thinned areas.
31