5 - Ant Seg Eyelids Flashcards

1
Q

Telecanthus

A

> normal distance b/w inner canthi

Seen in many syndromes

Dist b/w orbital walls is normal (i.e. orbits are not displaced)

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2
Q

Hypertelorism

A

Large dist b/w medial orbital walls bc of lateralization of the orbits

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3
Q

Epicanthus

A

Crescent-shaped vertical skin folds overlying medial canthi

Seen in prominent epicanthal folds

From immature facial bones

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4
Q

Cryptophthalmos

A

Rare

Due to failed differentiation of lid and anterior eye structures

Skin fused over eye, blends into anomalous cornea

Basically no eye
Usually occurs in kids with systemic problems with short lifespans

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5
Q

Eyelid coloboma

A
Congential
Fairly common
Usually cleft/notching of upper lid
Eyelid can fuse to the globe
Unrelated to other colobomas, which are inferior
Concerns = exposure keratopathy
Goldenhar syndrome = smaller ear, cleft palate, lid coloboma
Surgerically closed
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6
Q

Congentical ectropion

A

Eversion of margin, usually lower lid

Lateral tarshorrhaphy could be indicated
-dump a lot of artif tears, suture lids together

Skin flap/graft in more severe cases

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7
Q

Congential entropion

A

Eyelid inversion at birth

Rare

Surgery if concerns for corneal integrity
-scarring, amblyopia, strab, etc.

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8
Q

Ankyloblepharon

A

Partial/complete eyelid fusion

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9
Q

Epiblepharon

A
Common, esp in Asians
Congenital redundant fold of skin at lid margin
-epiblepharon due to extra fold of skin
-entropion due to eyelid folded inwards
Commonly lower lid
Lashes turn inward, onto cornea
-cornea tolerates better than entropion
Could resolve spontaneously
Lubricants 
Repair if chronic K irritation
-if severe, sx to release fold
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10
Q

Distichiasis

A

Partial/complete extra row of lashes at/posterior to MGs

Thinner, shorterm less pigmented

Tx if irritation (K integrity)

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11
Q

Blepharophimosis/congenital eyelid syndrome

A

Palpebral fissure is tight, shortened horiz and vert
-so tight, looks light eyes are being pushed back in

Spordic or AD

Poor levator function - difficulty looking in upgaze

Treatment

  • delay in repair bc epicanthus and telecanthus can improve with age
  • ptosis repair (frontalis suspension)
  • repair to allow bridge to develop fully
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12
Q

Congenital ptosis

A

Blepharoptosis = eyelid droop

Poor levator func

Can run in families

Anisometropic amblyopia and strab can develop

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13
Q

Ptosis evaluation

  • assess (4)
  • measure (2)
A

Upper lid crease, VF, tear function, corneal sensitivity

Palpebral fissure height
Magin reflex distance (MRD) = dist from upper lid margin to corneal reflex in primary

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14
Q

Ptosis evaluation

-levator function

A
Hold brow (block frontalis action) and measure dist upper lid can move when pt looks from up to downgaze
-e.g. ~18mm in good eye, ~12mm in ptotic
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15
Q

Ptosis evaluation

  • bell’s phenomenon
  • globe assessment
A

Poor

Determine if microphthalmic or hypertropia is present that could be a pseudoptosis

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16
Q

Ptosis management

  • mild/mod
  • severe
  • procedures (3)
A

Repair can be delayed several years - esp if have chin up position

Early correction required to prevent deprivation amblyopia

Levator resection
Levator tuck
Frontalis suspension

17
Q

Marcus Gunn jaw winking

A

Congenital synkinesis of the jaw and levator muscles

Ptotic lid elevates with opening of mouth or jaw movement

Seen with infants suck bottle/pacifier

Tx: ptosis repair, combo of surgery with frontalis suspension

18
Q

Chalazion

A

Blocked meibomian gland

Evolved from hordeolum

Hardened, painless

19
Q

Hordeolum

A

Block meibomian gland

Acute, painful

20
Q

Treatment for chalazion/hordeolum

A

Wam compress, blepharitis management, surgery for large/painful/chronic

Concerned if infant, eye is covered (amblyogenic)

21
Q

Pyogenic granuloma

A

Pink growth of granulation tissue rapidly from conj over a chalazion or site of trauma

Nothing was ever done about the chalazion

Lumpy/bumpy appearance

Moves when touched

Snipped off

22
Q

Molluscum contagiosum

A

Caused by DNA poxvirus
Shiny, dome-shaped, waxy, umbilicated skin papule
At/near lid margin
Can release viral particles onto conj -> follicular conj-itis
Most resolve spontaneously
-up to months/years

23
Q

Neoplasms, other non-infectious lid lesions

  • more common in what pop
  • in less likely pop, when is it found
A

Adults&raquo_space;> children

Neoplasms in children more likely with systemic disorders (e.g. xeroderma pigmentosum)

  • easily bruise, bleed
  • follow with dermatology
  • cornea also scars up
24
Q

Capillary malformation

A

Aka port-wine stain

Congenital malformation
Flat red/pink cutaneous lesion
Could fade, but more likely to darken
More nodular/hardened with time
Assoc with sturge-weber (vascular syndrome)
Glaucoma could occur
25
Q

Congenital nevus of skin

A

Could cause depriv amblyopia or have malignant transformation
-transf risk incr with size = importance of adequate measurements, referal to derm

Observe small/moderate lesions

  • small <1.5mm
  • mod <20mm
26
Q

Trichotillomania

A

Pulling of one’s own hair

Assoc with OCD

Psych eval indicated