Episclera and Sclera Collagen (1)

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  • 8/13/2019 Episclera and Sclera Collagen (1)

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    EPISCLERA and SCLERA

    EPISCLERA SCLERA

    characteristics

    - above sclera

    - Loose vascular complex between conj and sclerawithin Tenons capsule

    - Superficial and deep plexus derived from anterior and posterior ciliary

    arteries

    Superficial = radial arranement! larer in

    caliber than conjunct vessels! "oins with

    conjun vessels at limbus #eep plexus = $%T scleral vessels! closely

    applied to sclera! irreular nonradial

    confiuration!-

    - collaen with small amt of proteolycans arraned

    in criss cross pattern- thic&ness varies from '()-'(*+ mm near optic nerve

    and thins anteriorly- thinnest immediately behind insertion of ,%S

    - ./.S01L.2

    - .nteriorly continuous with cornea3 division is atlimbus

    - 4ave endothelial pumps- 5osteriorly continous with dura sheath coverin

    optic nerve

    Functions - .cts as synovial membrane for smooth movementof eye

    - Supplies nutrition to ./.S01L.2 sclera

    - protective coverin- bloc&s extraneous liht from enterin lobe

    - site of insertion of ,% 6resists lobal chaneswith eye movement7

    -

    Things to remember - 0.$ 6do and will7 have an episcleritis 89T4%1T

    a scleritis- 0.$$%T have an scleritis 89T4%1T an

    episcleritis- ,piscleritis is very common red eye seen in

    clinical practice

    - ./.S01L.2

    - 0an be ruptured with direct trauma- .ny inflammation is due to autoimmune d: and d:

    processes of collaen fibers- 8ith ae3 increased thic&ness and riidity and

    increased fat deposition 6appears yellow7- "aundice can also cause yellowin of sclera

    -

    Inflammation

    ,pidemioloy

    Episcleritis- ;enin3 self-limitin inflammation of episclera

    6superficial plexus7! usually resolves in

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    0auses

    5athophysioloy

    - Stress3 hormones 6why f?m7 simple episcleritis

    intermittent boults of moderate to severe

    inflammation recur at '-* month intervals episode lasts B-') days

    most resolve after ?

    - C-Dthdecades with pea& incidence in + thdecade

    6reported in patients from ''-@B yrs of ae7- ;ilateral

    - 4ih association with systemic d:

    - 0an be presentin manifestation of collaenvascular disorder and preceded additional

    symptoms by ' to several months

    - ? +)A are associated with underlyin systemic d:- CA annual rate of developin systemic d: in

    patients w( initially dx idiopathic scleritis

    - 529.2E inflammation of sclera

    - .utoimmune in nature

    - ? +)A demonstrate systemic d: associations

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    Types 1. Simple or iffuse !"#$ of cases%- ,ntire anterior sement 6*)A7

    - Section 6B)A7- 0ornea not involved

    - $% dischare&. 'odule !$%

    - 0entral pale nodule accumulation of inflammatory cells

    6sectoral episcleritis wF build up of non-

    ranulomatous material results in centralpale nodule7

    mobile 6move with touch7

    does not undero necrosis 6if it does3 thin&

    scleritis7

    - 2esolution is usually slower than simple episcleritis- Tender but not painful

    1. Anterior iffuse

    - 5resentation can be sectoral or diffuse

    - 'F* have underlyin systemic conditions&. Anterior 'odular

    - 5resents much li&e nodular episcleritis- $odule immobile and /,2E tender G painful to

    touch

    (. 'ecroti)ing Anterior- 0an be 89T4 or 89T4%1T inflammation

    - Tissue meltin away- Scleromalacia perforans 6scleral thinnin7 w(o

    inflammation! indicative of lon-standin severe2.

    - ajority of underlyin cause

    - 0haracteri:ed by avasculararea of scleral necrosisand profound inflammation of surroundin sclera

    - /enulitis leads to vaso-occlusion and later to vaso-

    obliteration*. Posterior

    - 9nvolves sclera enclosed by orbital tissue

    - 2are3 accounts for '-+A of scleritis cases- 1sually unilateral! >? H! all aes

    - $o underlyin cause found

    - Non specificpresentation! difficult or oftendelayed dx

    - 5ain 6persistant3 worsen with eye movements73

    reduced acuity3 diplopia3 ,% restrictions

    - 5resentin features may include choroidal mass3 wFor wFo effusion3 choroidal folds3 cystoid macularedema or exudative retinal detachment

    - Tenderness3 proptosis3 vision loss and restricted

    motility- Testin

    Iuantitative .-Scan( Ultrasonographyisusually dianostic

    #emonstratin thic&enin of affected sclera

    ;-scans can be used to follow tx sucess

    - 2esponds best to oral corticosteroid3 prednisone

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    +hat brings patient

    in,

    - relatively asymptomatic acute onset of redness in

    one or both eyes

    - mild discomfort 6>; sensation7! not painful- waterin but $% dischare

    - radual3 insidious onset of pain and redness

    - bilateral or unilateral

    - associated with photophobia3 tearin3 decreasedacuity

    -o is / made, - 0linical presentation

    - 4J systemic d:H! onset 6sudden and unilateral7!pain level 6minimal discomfort or irritation7

    - 5rove its $%T episcleritis

    - 5.9$ 6severe3 borin pain that radiates( #efinitepain with palpation7

    - 5hotophobia- #ecreased vision

    0I E2amination - 1nilateral 6most of the time7 or bilateral 6if it isbilateral3 thin& systemic d:7

    - 2edness 6usually wede or sector! can be diffuse7- obile nodule or not

    - #efinitely no dischare KKKK

    - /essels will blanch with instillation of larex

    - #examethasone- Lotemax

    - .t least I9# 6 up to M

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    - 5atient education about recurrence

    - >or severe cases that do not respond well to tx

    ormore than three recurrences refer for med eval

    handled by an Oit is ophthalmoloist specialist

    orFand rheumatroloist

    ifferential /3

    complications

    ##J- Scleritis

    - 0onjunctival abrasion or >;- Superior limbic &eratoconjunctivitis of Theodore

    - 5hlyctenular &eratoconjunctivitis- 5inueculitis- .cute anle closure laucoma

    - 9ntraocular tumors with overlyin lobe injection-

    0omplications- 5eripheral ulcerative &eratitis

    - 5erforation- Secondary laucoma

    - Scleral meltin- 5erforation- ,xudative retinal detachment

    Prognosis - ,xcellentN

    - $o seMuelae

    - 2arely any underlyin d: process ever found 6otherthan alleriesP7

    - $ot reat3 not even ood

    - uarded at best

    - 'CA lose sinificant /. wFin ' yr of dx- *)A lose sinificant /. in * yrs

    - Sinif percentae of patients w( concurrent scleritis

    and collaen vascular d: die wFin + yrs

    Sclero7eratitis

    - 042%$90 process mar&ed by area of %5.09>9,# and/.S01L.29Q,# cornea3 which proresses toward visual

    axis- .ssociated with peripheral and paracentral 1L0,2.T9/,

    &eratitis3 mar&ed by juxtalimbal or central corneal thinnin

    0lue Sclera

    - bluish discoloration secondary to thinned sclera

    - $eonates and .. children normal variation- .cMuired Oassociation with arfans syndrome and other

    systemic d:

    - /ery uncommon

    Scleral -8aline pla9ues

    - small round translucent to rayish areas

    - calcium deposition in area of scleral thinnin associated wF reorani:ation of scleral fibers due to ae- ;enin $o TJ

    Sclera Ectasia

    - stretchin of sclera

    - conenital abnormality around nerve head or macula- may follow inflammation or trauma

    - may result from proloned 9%5 elevation in infancy

    - may occur with hih 6proressive7 myopia

    Staph8loma

    - wea&ened sclera allows for bulin of uvea- anterior-eMuatorial posterior

    - causes decreased /.