BCSC 8. External Disease and Cornea Flashcards

(46 cards)

1
Q

Cornea receives glucose from

A

Aqueous humor

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2
Q

Increased matrix metalloproteinase-9

A

DES

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3
Q

Initial treatment for neurotrophic ulcer

A

bandage contact lens

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4
Q

Shown to reduce postherpetic neuralgia (PHN)

A

Prior VZ vaccine reduces PHN by 66%

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5
Q

Broad activity against yeast and filamentous funghi

A

Topical amphotericin B 0.15%

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6
Q

Better for filamentous molds

A

Natamycin 5%

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7
Q

Treatment for repeated recurrence of HZ keratitis

A

maintenance dose of valacyclovir

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8
Q

Most common fungal corneal pathogen

A

Candida (yeast)

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9
Q

Radial perineuritis

A

Acanthamoebea keratitis

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10
Q

27 yo F s/p LASIK 6 wks ago noted to have infiltrate at interface with no improvement after 3 days of q1hr fluoroquinolone eyedrops. Next step

A

Lift flap; cx on blood, chocolate agar, Sabourad’s agar. Start Fortified vancoycin and gentamicin q1hr.

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11
Q

MC cause of late interface infections (after 2 weeks)

A

Slow-growing organisms - Candida or atypical mycobacteria. Require definitive identification of causative agent

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12
Q

Condition a/w keratinized epithelial cells (metaplastic epithelial change)

A

MUCOUS MEMBRANE PEMPHIGOID - associated conditions. SJS, TEN, GVHD (severe ocular surface dx)

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13
Q

Treatment for large corneal ulcer in nursing home patient

A

corneal scraping for culture and sensitivity testing, f/b fortified topical vancomycin and gentamicin

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14
Q

Tx for vision rehabilitation for severe ocular surface dx with SJS and TEN

A

OSTEO-ODONTO-KERATOPROSTHESIS and boston type II keratoprosthesis

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15
Q

Eosinophils in conjunctiva are less numerous and more often degranulated in ___ compared to ___.

A

Atopic keratoconjunctivitis c/t VKC

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16
Q

Percentage of patients with necrotizing scleritis that have detectable systemic disorder

A

66%

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17
Q

Percentage of patients with diffuse or nodular scleritis that have detectable systemic disorder

A

33%

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18
Q

central opacity of cornea with underlying ENDOTHELIAL DEFECT and IRIS ADHESIONS

A

Peters anomoly

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19
Q

Vertical ruptures in descemet membrane that can lead to corneal edema, permanent vertical striae in posterior cornea resulting in high astigmatism

A

Birth trauma injury

20
Q

Horizontal curvilinear breaks in the Descemet membrane associated with congenital glaucoma

21
Q

Opacities are accumulations of unesterified and esterified cholesterol and phospholipids

A

Schnyder corneal dystrophy

22
Q

X-linked recessive disorder of cornea

A

Hunter and Fabry

23
Q

Drug a/w cornea verticillata

24
Q

Produces lysosomal deposits in basal corneal epithelium creating whorl-like pattern

A

Amiodarone (similar pattern found in Fabry’s disease)

25
Inheritance of marfan syndrome
AD
26
AD disorder a/w defect in fibrillin gene, lens subluxation, scleral thinning (blue) and CORNEAL FLATTENING
Marfan syndrome
27
Corneal finding in Marfan
Corneal flattening
28
Thinning of peripheral cornea that is quiet, noninflammatory, slowly progressive.
Terrien marginal degeneration
29
Line of lipid deposits appears at leading edge of pannus
Terrien marginal degeneration
30
Lucid interval occurs between limbus and peripheral edge of keratopathy
Calcific band keratopathy
31
Fine, dustlike, basophilic deposits in bowman membrane
Band keratopathy
32
Always treat traumatic hyphema with these medicines
TOPICAL CORTICOSTEROIDS and CYCLOPLEGIC drugs - reduce inflammation and put pupil at rest to reduce incidence of rebleeding. +/- oral corticosteroids if severe inflammation. Topical anti-hypertensives mainstay (beta-bloackers and alpha agonists)
33
Clinical finding that best supports diagnosis of limbal stem cell failure
Absence of limbal palisades of Vogt, abnormal epithelium on cornea, vascularization
34
Corneal epithelium is highly differentiated cell type that is entirely regenerated approximately
every 7 days
35
Remove interrupted sutures s/p PK at this time interval
4 weeks
36
Tx for Fuchs CED
Endothelial keratoplasty (DSEK or DMEK)
37
POW3 s/p PKP p/w persistent epithelial defect
presume herpetic disease, trial of oral acyclovir 400 mg po QID. Giving topical corticosteroids is CONTRAINDICATED!!
38
DDx enlarged Corneal Nerves
``` MARKING "L" Cornea M: MEN II B (med Ca thyroid, pheo, neuroma) A: Acanthamoeba R: Refsum's disease (phytanic acid/Riley Day) K: Keratoconus I: Icthyosis N: Neurofibromatosis G: Grafts (failed) Glaucoma (infantile) L: Leprosy ```
39
D/Dx Ring infiltrate
``` the PATH to ring infiltrate P: Pseudomonas A: Acanthamoeba T: Topical anesthetic abuse H: Herpes simplex virus ```
40
MPS does NOT heavily involve cornea
Sam the Hunter must see to shoot S: Sanfilippo H: Hunter
41
MPS most heavily involves cornea
Hurler and Scheie's
42
Cloudy Corneas
``` STUMPED S: Sclerocornea T: Tears in descemet's (infantile glaucoma, birth trauma) U: Ulcers (HSV, bacterial, neutotrophic) M: Metabolic (mucopolysaccaridosis) P: Peter's anomaly E: Endothelial dystrophies (CHED, PPMD, CHSD D: Dermoid ```
43
Direct penetration of intact epithelium
``` "N & N Can Lyse Hole Skin" Neisseria gonorrhea N. meningidides Corynebacterium diptheriae Listeria Hemophilis Shigella ```
44
Derived from neuroectoderm
``` ROVINZ R: RPE/Pig CB epi O: Optic nerve/axons V: Vit (all) I: Iris sphincter/dilator N: Neurosensory ret/nonpig CB epithelium Z: Zonules ```
45
Derived from surface ectoderm
``` CCLLSZ C: Cilia C: Conj/Cornea epithelium L: Lids/Lacrimal gland and drainage L: Lens S: Skin Z: Zonules ```
46
Derived from mesoderm
``` MEETS M: Mesoderm E: EOM E - Endotherlial blood vessels T: Temporal sclera S: Schlem's canal ```