Cornea-Conjunctiva Flashcards

1
Q

Follicles vs Papillae

A

Follicles: blood vessels run around; lymphocytes; viral conj-chlamydial conj-perinaud oculoglandular syndrome-hypersensitivity to topical medications.

Papillae: vascular core; inflammatory cells; bacterial conj-allergic conj-chronic blepharitis-CL wear-superior limbic keratoconj-floppy eyelid syndrome.

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2
Q

Giant fornix syndrome

A

S.aureus

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3
Q

C.trachomatis serotipler

A

A-B-C: trachoma

D—K: other grnital, other systemic and ocular disease

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4
Q

Adenovirus serovars

A

PCF: 3-4-7
EKC: 8-19-37

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5
Q

Vernal keratoconjunctivitis lesions

A

Horner Trantas dots: transient limbal apically located white cellular collections.
Pseudogerontoxon: paralimbal band of superficial scarring resembling arcus senilis.

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6
Q

Acute haemmorrhagic conjunctivitis

A

Enterovirus

Coxsackievirus

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7
Q

Arlt line

A

Cicatricial trachoma

Broad confluent conjunctival scars

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8
Q

Horner Trantas dots

A

Vernal keratoconjunctivitis

Transient apically located white cellular collections

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9
Q

Pseudogerontoxon

A

Vernal keratoconjunctivitis

Paralimbal band of superficial scarring resembling arcus senilis

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10
Q

Dry eye investigation

A

BUT <10s is suspicious

Schirmer (after 5min):

  • with anaesthesia: <10mm is abnormal
  • without anaesthesia: <6mm is abnormal
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11
Q

Hertoghe sign

A

Atopic keratoconjunctivitis

Absence of the lateral portion of the eyebrows

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12
Q

Dennie-Morgan folds

A

Atopic keratoconjunctivitis

Lid skin folds caused by persistant rubbing

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13
Q

Cornea dimensions

A

Diameter: 11.5 mm vertical-12 mm horizontal
Thickness: 540 〽️m
Cell density: 3000 cells/mm2

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14
Q

Infectious scleritis-the most common cause

A

Herpes Zoster

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15
Q

Blue sclera

A

ROHEM:

Russell-Silver syndrome
Osteogenesis imperfecta
Hallermann-Streiff-François syndrome
Ehler-Danlos type 6
Marshall-Smith syndrome
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16
Q

Bacteria- able to penetrate a healthy corneal epithelium

A

CeHeNNem:

C.diphteriae
H.influenza
N.gonorrhae
N.meningitidis

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17
Q

Peripheral ulcerative keratitis PUK

A
RA-most common
Wegener
PAN
Relapsing polychondritis
SLE

Yes scleritis-distinguishing from Mooren ulcer
No clear zone btw the ulcer and the limbus-distinguishing from marginal keratitis and Terrien marginal degeneration

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18
Q

Fortified antibiotics shelf life

A

Cephalosporins=Fortum: 4 days (refrigerated), unless 24 hours

Gentamicin: 14 days (refrigerated)

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19
Q

Wessely immune ring

A

Disciform keratitis (HSV)

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20
Q

Hutchinson sign

A

Herpes Zoster-involvement of the skin supplied by the external nasal nerve

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21
Q

SSSyphilis-ocular features

A

Salt and pepper pigmentary retinopathy
Salmon patch
Argyll-Robertson pupils

22
Q

Acanthamoeba keratitis

A

Pain disproportionate to clinical signs
Perineural infiltrates-pathognomonic
Ring abcess

23
Q

Furrow degeneration

A

Mild peripheral corneal thinning in the elderly, usually benign

24
Q

Mooren ulcer

A

Autoimmune
Progressive circumferential peripheral stromal ulceration with later central spread
An undermined and infiltrated leading edge is characteristic
No scleritis-distinguishing from PUK
No clear zone btw the ulcer and the limbus-distinguishing from marginal keratitis and Terrien marginal degeneration

25
No clear zone
Mooren ulcer PUK Macular corneal dystrophy
26
Yes clear zone
``` Marginal keratitis Terrien Arcus senilis Vogt limbal girdle Band keratopathy ```
27
Infectious crystalline keratopathy
Streptococcus viridans
28
Bitot spots
Xerophthalmia
29
Keratoconus
``` Oil droplet red reflex Scissoring reflex in retinoscopy Vogt striae=deep stromal stress lines Fleisher ring=epithelial iron deposits Munson sign=bulging of the lower lid on downgaze ```
30
Epithelial dystrophies
``` Cogan Meesmann Lish Subepithelial mucinous Gelatinous drop-like ```
31
Bowman/anterior stromal dystrophies
Reis-Bucklers | Thiel-Behnke
32
Stromal dystrophies
``` Lattice Granular Macular Schnyder(crystalline) Francois Fleck Posterior amorphous ```
33
Descemet/endothelial dystrophies
Fuchs Posterior polymorphous Congenitalhereditary endothelial
34
Fuchs endothelial dystrophy
``` Women Mostly sporadic Open angle glaucoma risk Cornea guttata Beaten metal appearance ```
35
Microcornea
Diameter <10 mm (>2years) or <9 mm (newborn) Other dimensions are normal AD
36
Microphtalmus vs Nanopthalmus
Micro: short AL, entire eye is small; other features of dysgenesis; systemic abnormalities may be present Nan: entirely small but structurally normal eye, bilateral
37
Megalocornea
Diameter >13 mm | Bilateral
38
LASIK-refractive error correction
Hypermetropia 4D Astigmatism 5D Myopia 12D
39
PRK-refractive error correction
Hypermetropia low-moderate Astigmatism 3D Myopia 6D
40
Cataract in systemic disease
DM MD(myotonic dystrophy) AD(atopic dermatitis) NF
41
Suprachoroidal hemorrhage risk factors
``` Advanced age Glaucoma Increased AL Systemic cardiovascular disease Vitreous loss Conversion from phaco to ECCE ```
42
Acute postoperative endophthalmitis-risk factors
``` Posterior capsule rupture Prolonged procedure time Combined procedure Clear corneal sutureless incision Temporal incision Wound leak on the first day Delaying postop topical ab until the day after surgery Topical anesthesia Adnexal disease DM ```
43
Acute postoperative endophthalmitis-most common patogen
Staph epidermidis
44
Acute postoperative endophthalmitis-intravitreal treatment
Ceftazidime 2mg in 0.1 ml➡️gram➖ | Vancomycin 2mg in 0.1 ml➡️gram➕
45
Delayed onset postoperative endophyhalmitis-patogens
P.acnes (low virulans)
46
Congenital cataract
2/3 bilateral | AD inheritance is the most common etiological factor
47
Congenital cataract-associated metabolic disorders
Galactosemia Lowe syndrome Fabry disease Mannosidosis
48
Congenital cataract-treatment
<4 weeks:risk of glaucoma⚠️ Bilateral dense: surgery btw 4-10 weeks Bilateral partial: may not require surgery Unilateral dense: urgent❗️<6 weeks (4-6 weeks) Unilateral partial: observe
49
Alport syndrome
Posterior polymorphous dystrophy Anterior lenticonus Fleck retina
50
Frosted branch angiitis
CMV retinitis