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20 Cards in this Set
- Front
- Back
Levator (LPS)
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-CN III
-Fxn: raises upper eyelid, works w/ orbicularis in involunatry blinking & forced lid closure |
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Dysfxn of LPS causes
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PTOSIS! (more than 3mm)
1. Mechanical: heavy lid, from lid mass (chalazion) 2. Myogenic: aging changes or inherited levator deterioration 3. Neurogenic: CN III lesion, stroke/aneurysms |
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Mueller's muscle
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-Sympathetic NS
-Fxn: maintain tonus of elevated upper lid and opened lower lid |
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Dysfxn of Mueller's causes
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-Slight ptosis (1-3mm)
-Inverse ptosis |
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Orbicularis
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-CN VII
-Fxn: involuntary & forced blinking, maintains apposition of lacrimal puncta to globe |
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Components of orbicularis
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1. Palpebral (lid only): involuntary blinking
2. Orbital (forehead, temples, cheeks): forced lid closure |
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Dysfxn of orbicularis
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1. Lesion of CN VII can cause paresis or paralysis
a. Bell's Palsy: unilateral, viral, decreased tonus on affected side b. Lagophthalmos: 1-3mm opening of the eye that leads to dessication problems 2. Epiphora (over tearing): puncta not in good apposition to globe b/c of loss of tonus 3. Entropion (eyelid rolls inward fr forced lid closure): esp in lower eyelid |
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Lymphatics fr ____ drains into the pre-auricular lymph nodes.
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Lateral 2/3 of top
Lateral 1/3 of bottom |
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Lymphatics fr ____ drains into the submandibular lymph nodes.
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Medial 1/3 of top
Medial 2/3 of bottom *Note: check lymph nodes in red eyes |
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Most common bacteria in pts
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S. epidermidis
(2nd most common is combination of S. epidermidis, S. aureus and diphtheroids) |
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Least common bacteria in pts
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Diphtheroids
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Most common anaerobe
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Propionibacterium acnes
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Congenital ptosis (background)
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-Onset: @ birth or before 6 months old
-Exam includes: ~~Hx (when parents first noticed it) ~~FAT scans (old photos) ~~Superior lid sulcus is absent (KEY SIGN in non-asians) -Not usually accompanied by neurological dz (except neonatal myasthenia gravis pts who are too sick to see us) |
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Significance of congenital ptosis
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1. Occlusion amblyopia
-Get surgical consult w/ pediatric ophthalmologist |
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Types of congenital ptosis
1. Autosomal dominant |
-70%
-Check family members -Look for other congenital anomalies |
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Types of congenital ptosis
2. SR palsy w/ LPS palsy |
-Isolated SR palsy congenital is very RARE
-Look for vertical tropia in primary position w/ ptosis |
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Types of congenital ptosis
3. Paradoxical CN III innervation |
-Marcus Gunn jaw winking: CN II misconnected to levator & jaw (pterygoid) muscle --> eyelids pop open when open mouth to sing/chew/etc
-Amblyopia secondary to ptosis in 20% of cases -Surgery for ptosis = impt -Acquired --> pseudo von Graefe sign (no thyroid dz, when pt looks down lid doesn't follow at same rate) |
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Types of congenital ptosis
4. Congenital Horners syndrome |
-Heterochromia irides (suggests onset before age 2)
-Iris color = different tones w/in same eye |
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Types of congenital ptosis
5. Birth trauma 6. Neonatal myasthenia gravis |
5. Not common b/c don't use plungers/calipers anymore
6. Very sick pts, not at our service |
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Ankyloblepharon (background)
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-Adhesion b/n upper and lower eyelids along the lid margin (usually lateral canthus)
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