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Fat is only in the located in the ___ portion of th eyelid skin
orbital
Horner's muscle
Deep palpebral fibers that wrap around the lacrimal canaliculi
move tears
Riolan's muscle
at lid margin around both sides of each meibomian gland openings
maintains lif globe congruity
espress meibum
Gray line
Gray line
divides lid into aterior and posterior
Superior Levator Muscle
retract upper eyelids
1. Ligaments
form sleeve around SPL and changes its direction to superoinferior
superior transverse ligament (Whitenall's)
Intermusclar transver ligament
2. Levator Aponeurosis
fan like tendinous expansion of the SPL
pierces the orbital septum and attaches to superior tarsal plate
attachment to skin and orbicularis = upper lid crease
3. Tarsal Muscle of Muller
posterior inferior expasion of the SPL
smooth muscle with sympathetic autonomic innervation
Inferior Rectus Muscle
1. Capsulopalpebral Fascia (lower lid aponerousis)
extension of the inferior rectus muscle sheath and inferior suspensory ligaments
retract the lower lid
(like aponerosis)
2. Inferior tarsal muscle
Extension of inferior rectus muscle sheath inserting into lower palpebral conjunctiva and lower tarsal plate
smooth muscle with sympathetic autonomic innervation
(like muller muscle)
orbital septum
barrier
separates the anterior and posterior extend of the orbit
continuous with periorbital and periosteum of the orbital rim bones
Zeis glands
sebaceous glands
coats lash follicles with sebum
Moll glands
sweat (apocrine) glands
Meibomian glands
sebaceous glands
embedded in tarsal palte
secrete meibum which forms lipid ayer of tear film
Accessory lacrimal glands
Sectrtions contribute to aqueous layer of the tear film
Wolfring Glands
Kruse glands (fornix)
Look at blood supply
Hordeolum Symptoms
Tender
painful
warm
red
swollen
acute onset
Hordeolum signs
Visible palpable, well defined subcutaneous nodule
may be one or multiple
Hordeolum Etiology
inflammation of the sebaceous glands due to bacterial infection
95% due to staph. aureus
Staphylcoccus epidermidis
both gram (+)
Hordeolum Epidemiology
common
affects every age and demographic
30-50
females>males
Hordeoulm risk factors
blepharitis
ocular rosacea
meibomian gland dysfunction
immunocompromised states
poor eyelid hygiene (excessive makeup)
External hordeolum
infection of glands of zeis and moll
Internal hordeolum
infection of meibomian gland
Differential of Hordeoulum
Chalazion (painless)
Orbital cellulitis (proptosis, double vision)
preseptal cellulitis (entire periorbital region)
sebaceous cell carcinoma (recurrent chalazion, eyelid thicking, loss of lashes, non acute)
Hordeolum treatment
warm compress with digital massage 10 min session x4/day
internal hordeolum treatment
Oral abibiotic
follow up 7-10 days
External hordeolum treatment
topical antibiotic
or topical antiobiotic steroid combo
follow up 7-10 days
Hordeolum Antibiotic treatment
Cephalexin (Keflex) 500 mg
take 1 capsule BID by mouth for 7-10 days
Augmentin 500 mg take 1 capsule BID by mouth for 7-10 days
Doxycycline 100 mg take 1 capsule BID by mouth for 7-10 days
Cephalexin (Keflex)
Bactericidal
Gram (+)
Contra: Warfarin
ADR:
Steven Johnson Syndrome
X-sensitivity with penicillin
Augementin
Bactericidal
Gram (+) and some (-)
ADR:
Steven Johnsons
Z-sensitivity with Cephalosporin
Doxycycline
Bacteriostatic
Gram (+)(-)
Contra: children less than 8 and pregnancy
bone rgowth and tooth discolotation
ADR: Photosensitivity
Psuedotumor cerebri
Topical Antibiotic
Erythromycin 0.5% ophthalmic ointment apply over lesion BID for 2 weeks
Tobradex 0.3-0.1% apply over lesion BID x2 weeks
Erythromycin
Bacteriostatic
gram (+)
Very safe
Tobradex (tobramycin/dexamethasone)
bactericidal
Gram + and -
contra: Glaucoma
ADR: Delayed corneal healing
IOP spike
post. subcapsular cataract
Chalazion Symptoms
painless
bump
few moths
Chalazion signs
palpable solid bump
mildly red
non tender !!!
not warm
Chalazion etiology
obstruction of the sebaceous gland with resultant lipogranuloma formation
seconday to hordeolum
Chalazion epidemiolgy
common
affects every age
30-50
Females=males
Chalazion risk factors
blepharitis
ocular rosacea
meibomian gland dysfunction
use of Velcade for multiple myeloma
Chalazion differentials
Hordeolum ( acute, focal pain)
Orbital cellulitis (proptosis, diplopia, pain)
Preseptal (redness of entire lid)
sebaceous cell carinoma (recurrent chalazion, eyelid thickning, loss of lashes)
Chalazion: Treatment (Conservative)
Warm compress with digital massage 10 min session x4day
Chalazion: Treatment pharmaceuticals
Doxycycline 20 mg BID Po x 4 weeks FU Few weeks
Tobradex 0.3-0.1% apply over lesion BID x2 weeks FU few weeks
Chalazion treatment (invasive)
no improvement with conservative mangement or large and chronic
1. intralesional steroid injetion
2. incision and curettage
Preseptal Cellulitis symptoms
Painful
red
swollen
"i had____"
insect bite
stye
sinus infection
cut to skin
Preseptal Cellulitis signs
eyelid red
warm ad tender to touch
Possibly swollen shut
Preseptal Cellulitus etiology
inflammation of the periorbtial tissue anterior to the orbital septum
bacterial infection (S. aureus)
from another adjacent infection such as hordeoulm, sinitis, or injury
Preseptal Celllulitis epidemiology
more common in youn adults and children
more common than orbital cellulitis
no specific race or gender
Preseptal Celllulitis Risk factors
hordeolum
dacrocystitis
upper respiratory tract infection/sinitis
trauma
Preseptal Celllulitis Differentials
Hordeoulm (acute, painful, nodule)
Orbital cellulitis (proptosis, double vision, and pain)
contact dermitis (nontender, itchy, alelrgic reaction)
sebaceous cell carcinoma ( recurrent chalazion, thickineing, loss of lashes)
Pre-septal Cellulitis: treatment
oral antibiotic
Augementin 875mg take 1 capsule BID by mouth for 7-10days (higher dosing than hordeolum)
Sulfamethoxazole/Trimethoprim (Bactrim) 800 mg/160mg take 1 capsule BID by mouth for 7-10 days
(if alelrgic to penicillin or exposure to MRSA)
Sulfamethoxazole/Trimethoprim (Bactrim) contraindicaitons
sulfa allergy
pregnancy
Preseptal Cellulitis follow up
daily
Preseptal Cellulitis : no improvement or worsening of s+s
admit to hospital for orbtial CT scan and switch to IV antibiotics
Ocular Rosacea: signs and symptoms
eyelid/facial telangectasia
ttearing
FB senstion
irritation
burning
Flares on and off with
alcohol
spciy foods
caffeine
hot weather
sunlight
Ocular Rosacea etiology
auto immune mediated chronic inflammatory disorder
blood vessel dilaiton
leakage of inflammatory substances into the skin
Ocular Rosacea Epidemiology
Northern European ancestoery
2-3x more common in females
20% have ocular rosaces without cutaneous rosacea
Ocular Rosacea risk factors
associated triggers: alcohol, spicy food , heat, sunlight, caffeine
Possible correlation with Demodex Folliculorum or H pylori
Ocular Rosacea Slit lamp examination
- Telangiectatic vessels at lid margin
- associated Meibomian gland dysfunction and demodex blepharitis
- Corneal disease (Keratitis, pannus)
Ocular Rosacea Gross examination
May have rhinophyma
- associated with cutaneous rosacea
- more seen in men
Ocular Rosacea differetials
Preseptal cellulitis (pain, entire eyelid)
Lupus Erythmatosis ( malar rash, multiorgan dysfunction)
Contact dermititis (nontender, itchy, allergic)
Atopic Dermatitis (scaly, pathcy, and discolration of skin)
Ocular rosacea treatment
Educate on avoiding triggers
Eyelid Hygiene (treat secondary demadox belph)
Oral Antibiotic
Intense Pulse Therapy (IPL)
Oral Antibiotic for ocular Rosacea Low Maintenance Dose
Low Maintenance Dose
Doxycycline 20 mg take 1 capsule BID by mouth for 3-4 months
anti inflammatory action
decrease MMP
Anti-angiogenic
Oral Antibiotic for ocular Rosacea Acute Dose
Doxycycline 100 mg take 1 capsule BID by mouth 3-4 weeks
Intense Pulsed Light Therapy (IPL)
- non-laser high intensity light
Light absorbed by tissue is converteed to heat destroying telangiectiasia but not surrounding tissues
Intense Pulsed Light Therapy (IPL) contraindications
darker skin tones at higher risk of complications (Fitzpatrick skin type scale)
Photosensitivizing medications (Doxy) *******
Allergic Contact Dermatitis signs and symptoms
Eyelids are
puffy
red
ithcy
tearig
FB sensation
Came in contact with ____ a few days ago
Erythema, flaking, crusting rash, edema
ocular surface involvement: conjunctival chemosis
Allergic contact dermatitis etiology
acute inflammation caused by an immunologic hypersensitivity to an allergic stimulus
Common ingredients
Ophthalmic drops
Airborne and aerosolized ingredients
Plan and animal protein
Allergic contact dermatitis Epidemiology
higher in females (jewlry, makeup, fragrances)
affects all demographics but may be higher in fairer skin
Allergic contact dermatitis risk factors
age (infants, elderly)
occupation (exposer to allergens)
history of atropic dematitis (more breaks in skin)
Allergic contact dermatitis pathophysiology
delayed/cell mediated type 4 hypersensitivity reaction
48-72 hours after exposure
T cells must be sensitized first
Allergic Contact Dermatitis Differentials
- Herpes zoster ( painful, unilateral)
Preseptal Cellulitis (pain,s welling entire lid)
Ocular Rosacea (telectasia of eyelid margin)
Atopic dermatis (chronic, scaly patches)
Allergic contact dermatitis Treatment
Identify ad remove inciting agent
cold compresses, several times daily
Allergic contact dermatitis Treatment IF crusted/weeping lesions
Prophylaxis antiobiotic
Erythromycin 0.5% ung QHS OU along eyelids for 1 week
Contact dermatitis treatment
FML 0.1 BID 7-10dats Taper to QD for 1-2 weeks
Corticosteroid
OR
Tacrolimus 0.03% -0.1% BID to affected area 7-10 days
FML contraindicaitons
IOP pressure spike
post. subcapsular cataract
Tacrolimus contraindications
Macrolide allergy
Children <2
Pregnancy
Immunocompromised
BBW: Cancer
Atopic Dermatitis signs and symptoms
Acute: red crusting blisters
Chronic: Diffuse dry, sclay, itchy pacthes of skin
Discoloration
Leathery and lichenified
Dennie Morgan Folds and allergic shiners
remission and relapse
"on and off"
" flares up"
Atopic Dermatitis Etiology
Genetic and environmental factors
Atopic triad: atopic dermatitis, allergic rhinitiis, asthma
Atopic Dermatitis epidemiology
starts in ifacncy
80% affected before age 6
REmission periods with relpase in adult hood
40% have concurrent atopic keratoconjunctivitis
Atopic Dermatitis Risk factors
Family history
genetic mutation that predisopes for imapired skin barrier
enviormental exposures
Atopic Dermatitis Pathophysiology
defect skin battier
over expression of Type 2 Hel[er cells and IgE
Atopic Dermatitis Differntials
Seborrheic Anterior Belph ( scaling of eyelid margin only)
Psoriasis (well defined patches)
Ocular Rosacea (teliectasia)
Allergic Contact dermititis (acute, purely allergic reaction)
Atopic dermatitis treatment
Treat ocular complications as needed
consult dermatology for non-ocular AD
consider treating periorbital AD
Atopic Dermatitis if crusting and weaping lesions
Erythromycin 0.5% ung QHS OU along eyelids for 1 week
FML 0.1 BID 7-10dats Taper to QD for 1-2 weeks
OR
Tacrolimus 0.03% -0.1% BID long term but not to exceed 6 weeks
Blepharochalasis signs and symptoms
acute phase: painless edema of the upper eyelid margins
Chronic phase: wrinkled redundant, thinned eyelid skin
relapsing and remitting edema
3-4x year
Blepharochalasis etiology
idiopathic recurrent episodes of painless edema of upper eyelids with and without redness/ithcing
may be part of larger syndrome or disease
related to hormonal changes during puberty
Blepharochalasis Epidemiology
Rare
Females>males
Onset before 30
Blepharochalasis Risk factors
hormonal changes
genetic predisoption
Blepharochalasis pathophysiology
unclear inflammaotry mediated etiology
IgA deposits noted within periorbital tissue with increased elastolysis actovity
Blepharochalasis Differentials
Dermatochalasis (age related, increased laxity)
Preseptal cellulitys (painful, swelling, redness of entire lid)
Hordeolum (acute, focal, painful
Allergic Contact dermitis ( allergic rxn, ithcy)
Blepharochalasis treatment: acute phase
FML 0.1% BID OU for 7-10 days
Taper to QD OU for 1-2 weeks
Follow up 2-4 weeks
Repeat when reactivates
Blepharochalasis treatment: chronic phase
surgical blepharoplasty once quiescent for at least 2 years
Vitiligo
absence of melanin in skin
Poliosis
absence of melanin in hair follicles of eyelashes and eyebrows
Associated conditions
- Vogt-Koyanagi- Hardara Syndrome (VKH)
- Tuberous sclerosis complex
- Waardenburg's syndrome