Conjunctiva Flashcards

(80 cards)

1
Q

Which arteries supply the conjunctiva

A

anterior ciliary
palpebral arteries

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2
Q

What are the types of conjunctiva?

A

palpebral
forniceal
bulbar

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3
Q

What is the anatomy of the conjunctiva

A

Epithelium- non keratinizing 5 cell layers deep. Basal cuboidal layers evolve into polyhedral cells.
Stroma- richly vascular loose connective tissue. Glands of wolfring and krause located deep in the stroma.
CALT- Critical ocular surface immune response. Lymphocytes within epithelial layers, follicular aggregates

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4
Q

Symptoms of conjunctival inflammation

A

lacrimation
grittiness
stinging
burning
itching is the hallmark of allergic disease but can occur in dry eye/blepharitis

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5
Q

Chemosis causes

A

Local: TED, Chronic allergic conjunctivitis, ocular/ eyelid surgery/ trauma
Increased systemic vascular permeability eg allergic conditions/ infections like meningitis/ vasculitis
Increased venous pressure: SVC syndrome/ right sided heart failure
Nephrotic syndrome

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6
Q

Difference between pseudomembrane and true membranes and causes

A

can peel pseudomembrane no issue
true membranes involve superficial layers of conj epithelium so removal leads to tearing. Both can leave scarring

Causes: severe Adenoviral Conjunctivitis, gonococcal, strep/corneybacterium, ligneous, SJS

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7
Q

Causes of subconjunctival cicatrization

A

trachoma
severe scarring due to loss of goblet cells/ accessory lacrimal glands, cicatricial entropion can result

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8
Q

Causes of conj follicles

A

blood vessels run around rather than within lesions.
Causes: viral/ chlamydial conjunctivitis, parinaud oculoglandular syndrome, hypersensitivity to topical medications.

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9
Q

What does histology of a conj follicle show

A

Subepithelial lymphoid germinal centre with central immature lymphocytes and mature cells peripherally

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10
Q

What is a conj papillae

A

vascular core present. Micropapillae form mosaic like pattern elevated red dots. Macropapillae <1mm and Giant papillae >1mm. Apical infiltrate/ stain with NaFl or mucous can be present with marked activity.

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11
Q

What does histology of a conj papillae show

A

folds of hyperplastic conjunctival epithelium with fibrovascular core and subepithelial stromal infiltration with inflammatory cells. Late changes show superficial stromal hyalinization, scarring and crypts containing goblet cells

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12
Q

Causes of lymphadenopathy and conjunctivitis

A

viral
chlamydial
severe bacterial infection (gonococcal)
Parinaud oculoglandular syndrome (preauricular site)

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13
Q

Bugs causing acute bacterial conjuncitivitis

A

S pneumonia
s aureus
h influenze
moraxella catarrhalis

N. gonorrhoea- invades intact epithelium
N meningitides affects children

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14
Q

What does meningogococcal infection show on gram stain

A

gram negative kidney shaped intracellular diplococci

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15
Q

What culture grows N. gonorrhoea

A

Thayer Martin/ chocolate agar.

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16
Q

How to treat bacterial conjunctivitis

A

60% resolve within 5 days with treatment.
CPL ointment
Aminoglycosidees
Quinolones
Macrolides
Polymyxin B
Fusidic acid
Bacitracin

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17
Q

How to manage gonococccal or meningococcal conjunctivitis

A

Topical 1-2 hourly quinolone and systemic therapy. Involve GUM.
Systemic: third generation cephalosporin like ceftriaxone, quinolones, macrolids.
H influenza in children- oral Co-Amoxiclav. 25% risk of developing otitis media.
Meningococcal conjunctivitis- children- systemic prophylaxis may be lifesaving. 30% may develop systemic disease. IM benpen/ceftriaxone/oral cipro

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18
Q

What is Giant fornix syndrome and how to treat it

A

uncommon entity causing chronic relapsing pseudomembranous purulent conjunctivitis. Due to retained debris in large upper fornix acting as a focus for persistent bacterial colonization.

Treat: sweep upper fornix with cotton tip- topical and systemic abx. intense steroid drops. surgical reconstruction of fornix last resort

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19
Q

What are the 2 forms of Chlamydia trachomitis

A

robust infective extracellular elementary body
fragile intracellular replicating reticular body

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20
Q

Which serotypes of chlamydia cause conjunctivitis

A

D-K of chlamydia trachomitis affecting 5-20% of sexually active young adults in western countries. Incubation is 1 week

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21
Q

Which serotypes of chlamydia cause trachoma

A

A,B,C

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22
Q

Signs of chlamydial conjunctivitis

A

watery/ mucopurullent discharge
tender preauricular lymphadenopathy
large follicles in inferior fornix. SPK common.. Chronic cases prominent follicles. mild conj scarring superior corneal pannus

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23
Q

How to investigate suspected chlamydial conjunctivitis

A

Tarsal conj scrapings, PCR, Giemsa staning for basophilic intracytoplasmic bodies
Direct immunofluorescence detecting free elementary bodies with 90% sens+ spec
McCoy culture highly specific

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24
Q

How to treat chlamydial conjunctivitis

A

Refer to GUM specialist
Systemic treatment: Azithromycin 1gram repeated after 1 week. But can be STAT
Doxycycline 100mg PO BD for 10 days
Erythromycin, Amoxicillin, Ciprofloxacin alternatives

Advised no intercourse for 1 week after PO completion of abx
Retest after 6-12 weeks

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25
What is the world leading cause of preventable irreversible blindness
trachoma
26
How does trachoma happen?
recurrent infection elicits a chronic immune response consisting of a cell-mediated delayed hypersensitivity (Type IV) reaction to the intermittent presence of chlamydial antigen and can lead to loss of sight
27
There exists the active and cicatricial chronic stage of trachoma. What are the features of each
Active: pre school children with mixed follicular/papillary conjunctivitis, mucopurulent discharge. Children <2 papillary component dominates, epithelial keratitis + pannus Cicatricial trachoma: middle age. Linear or stellate conj scars in mild/ broader confluent scars. Arlt line in severe disease. Upper tarsal plate most commonly involved.Superior limbal follicles Herbert pits. Trichiasis/ distichiasis/ CoNV, cicatricial entropion, Dry eye from goblet cell loss + lacrimal gland loss
28
What is the WHO grading for trachoma
TF- Trachoma inflammation follicular 5 or more follicles >0.5mm, on superior tarsal plate TI- Trachoma inflammation intense diffuse involvement of tarsal conj obscuring 50% or more of normal deep tarsal vessels TS- Trachoma conj scarring: easily visible fibrous white tarsal bands TT- Trachoma trichiasis at least one lash touching globe CO- Corneal opacity blur details of pupil margin
29
Management of trahcoma
SAFE: Surgery for trichiasis (relieve entropion/ trichiasis/ bilamellar tarsal rotation) Abx for active disease (single dose Azithromycin) Facial hygiene Environmental improvement
30
Define ophthalmia neonatorum
conjunctival inflammation developing within the first month of life. Occurs in upto 10% of neonates. Often result of infection transmitted from mother to infant during delivery
31
What are the causes of ophthalmia neonatorum
Acquired organisms during vaginal delivery. C trachomitis/ N gonorrhoea. HSV2. C trachomitis most common cause for moderate- severe conjunctivitis Staph mild conjunctivitis. Strep/H influenza/ Gram neg organisms Congenital NLDO
32
What is the timeline for the various bugs causing Ophthalmia Neonatorum
Chemical irritation: first few days Gonococcal first week Staph other bacteria: end of the first week HSV 1-2 weeks Chlamydia 1-3 weeks
33
What important differential can masquerade as conjunctivitis
Congenital glaucoma
34
How to investigate ophthalmia neonatorum
Parental prenatal STI testing results Conj scrapings for NAAT/ PCR chlamydia HSV Conj scrapings on glass slide for gram/ giemsa stain. Multi nucleated giant cells seen on gram stain in HSV Conj swabs for standard bacterial culture/ chocolate agar/ thayer martin for gonorrhoea
35
How to treat Ophthalmia Neonatorum
Prophylaxis routinely performed but no standard protocol. Single instillation of povidone iodine 2.5% effective. Erythromycin 0.5% or tetracycline 1% ointment. Silver nitrate 1% agglutinates gonococci + IM Benpen Chlamydia- oral erythromycin for 2 weeks. Longer course may be needed Gonococcal- third generation cephalosporin + topical treatment. Co- treat for chlamydia HSV- High dose intravenous aciclovir +/- LP if encephalitis GUM/ paeds involvement
36
What is the most common cause of viral conjunctivitis
Adenoviral (90%) non enveloped double stranded DNA virus
37
What are the spectrum of viral conjunctivitis presentations
Non specific acute follicular conjunctivitis Pharyngoconjunctival fever (PCF)- adenovirus serovasrs 3,4,7 Epidemic Keratoconjunctivitis (EKC)- Adenovirus serovars 8, 19, 37 Acute haemorrhagic conjunctivitis Chronic/relapsing adenoviral conjunctivitis Herpes simplex virus Systemic viral infections Molluscum contagiosum (human specific ds DNA pox virus) SARS Cov2 virus
38
What are some signs of viral conjunctivitis
eyelid oedema lymphadenopathy conj hyperaemia + follicles severe inflammation associated with haemorrhages petechial in adenoviral/ pseudomembranes. Membranes rare Keratitis (Adenoviral) epithelial microcysts, Punctate epithelial keratitis , focal white subepithelial anterior stromal infiltrates Mild AAU Mollluscum- pale waxy unbilicated nodule on lid margin + follicular conjunctivitis
39
How to investigate viral conjunctivitis
Giemsa stain- mononuclear cells in adenoviral conjunctivitis + multinucleated cells in herpetic infection NAAT- PC R test Viral culture Point of care immunochromatography Serology for IgG/IgM
40
Treatment of viral conjunctivitis
Spontaneous resolution 2-3 weeks adenoviral Handwashing Molluscum- self limiting but removal often necessary to address secondary conjunctivitis/cosmetic reasons. Topical steroids- pred 0.5% qds, for severe (pseudo) membranous conjunctivitis Lubricants Povidone iodine 5%
41
What type of reaction is allergic conjunctivitis
IgE T1 hypersensitivity reaction
42
What is seasonal vs perennial allergic conjunctivitis
differ in timings of exacerbations seasonal- hay fever eyes worse in spring and summer perennial- symptoms throughout the year worse in autumn when exposed to house dust mites/animal dander/ fungal allergens.
43
How to treat seasonal and perennial allergic conjuncitvitis
artificial tears for mild symptoms Mast cell stabilisers (sodium cromoglicate) Antihistamines for symptomatic exacerbations Dual action antihistamine and mast cell stabilisers (ketotifen, olopatadine) act rapidly combined antihistamine and vasconstrictor (antazoline +xylometazoline) NSAID like diclofenac Topical steroids eefective PO Antihistamine
44
What is VKC
Recurrent bilateral disorder both IgE and cell mediated immune mechanisms play a role. Affects boys from 5 onwards. Remission in teenage years in 95% cases.
45
How can VKC be classified
Palpebral VKC- upper tarsal conj. Significant corneal disease Limbal disease- black and asian patients Mixed VKC- both palpebral and limbal disease
46
What are the signs/symptoms of VKC
Palpebral: early conj hyperaemia, macropapillae <1mm cobblestone/diffuse. Progression to giant papillae >1mm. Mucus deposition, decreased disease activity by mild conj injection Limbal: Gelatnous limbal conj papillae with white cellular collections (horner trantas dots). Keratopathy: SPK, Shield Ulcers, subepithelial scars, pseudogerontoxon in recurrent limbal disease, keratoconus, HSK
47
What is AKC (atopic Keratoconjunctivitis)
rare bilateral disease developing in adulthood peak incidence 30-50 years after a history of eczema. Asthma common in these patients. Chronic and unremitting low expectation of eventual resolution. VKC more seasonal AKC- perennial worse in winter.
48
How can AKC be differentiated from VKC on conj scrapings
Eosinophils less common on AKC conj scrapings compared to VKC
49
Differences between AKC and VKC
AKC more symptomatic than vkc Skin changes more prominent in AKC than VKC eczematoid, erythema, dryness, scaling, thickening, associated chronic blepharitis, keratinization, Hertoghe sign, Dennie morgaan folds, tightening of facial skin Conj involvement inferior palpebral in AKC vs Superior in VKC Keratopathy: PEEs over inferior 1/3 cornea marked, persistent ED's, plaque formation Cataract: presnile shield like anterior/ posterior subcapsular cataracts. High risk of endoph due to s. aureus
50
How to treat AKC and VKC
Same for seasonal/ perennial allergic disease + steroid ointment, antibiotics to prevent bacterial infection, NAC for mucus filaments, immunomodulators ciclosporin, calcineurin inhibitors,(tacrolimus 0.1% ointment), supratarsal steroid injections for severe palpebral disease. Systemic: PO antihistamines promote sleep/ reduce eye rubbing. Antibiotics like doxycycline, steroids, ciclosporin, tacrolimus, azathioprine. short course of high dose steroids Surgery: Superficial keratectomy remove plaques/ debride shield ulcers. Excimer laser Amniotic membrane overlay graft, botox to induce ptosis for persistent E
51
What is Giant (mechanically induced) papillary conjunctivitis
GPC occurs secondary to a variety of mechanical stimuli of tarsal conjunctiva. Encountered with CL wear.Related to mucus fishing syndrome
52
What are the signs/ symptoms of GPC
FB sensation, redness, itching, mucus production. Signs are substantial CL protein deposits, excessive CL mobility due to upper lid capture, superior tarsal hyperaemia/ papillae. Focal apical ulceration and whitish scarring, keratopathy rare, ptosis
53
How to treat GPC
Removal of CL discontinued for several weeks, replace lenses. Reduce CL wear time. Removal of other causes like exposed sutures or scleral buckle. Assess the fit of ocular prosthesis Filtering bleb partial excision/ revision. Change CL solution brand. switch to monthly then daily disposable lenses Rigid lenses reduced risk of GPC (5%) Regular use of CL protein removal tablets, regular prosthesis polishing and cleaning. Topcial mast cell stabilisers, antihistamines, topical steroids
54
What is MMP or OCP (ocular cicatricial pempigoid)
group of chronic immune mucocutaneous blistering diseases. Unknown trigger leads to T2 hypersensitivity reaction. Antibodies binding to basement membrane zone (BMZ). Complement activation and recruitment of inflammatory cells with separation of epidermis from dermis leads to scarring. OCP involves the conjunctiva progressive cicatrization. Other causes are SJS/ trachoma/ drug induced/ trauma/ severe/ chronic conjunctivitis.
55
What HLA subtypes are associated with MMP/ OCP
HLA DR4 HLA DQB1
56
How tis the diagnosis of OCP / MMP made
Clinical but: biopsy of mucus membrane shows linear antibody and complement BMZ deposition Michel's transport medium when taking a specimen for direct immunofluorescence and immnoelectron microscopy
57
How is progression of OCP measured
Foster's classification system: Stage 1= early, chronic conjunctivitis, tear dysfunction ,subepithelial fibrosis Stage 2= forniceal shortening, inferiorly Stage 3= symblepharon formation Stage 4= surface keratinization and cicatricial ankyloblepharon Mondino's classification (based on inferior forniceal depth loss) Stage 1= upto 25% Stage 2= 25-50% Stage 3= 50-75% Stage 4= greater than 75%
58
What are the symptoms of OCP/ MMP
Conj: papillary conjunctivitis, diffuse hyperaemia, oedema, subtle fibrosis, fine lines of subconj fibrosis, shortening of inferior fornices, symblepharon adhesion between bulbar and palpebral conjunctiva, necrosis, flattening of plica and keratinization of caruncle, dry eye loss of goblet cells, monitor by forniceal depth. Eyelids: aberrant lashes, chronic blepharitis, keratinization of lid margin cornea: epithelial defects, infiltration and peripheral vascularization, corneal keratinization. End stage total symblepharon.
59
What is the treatment for OCP/ MMP
Systemic: Dapsone- 70% response. Contraindicated in G6PD deficiency. Sulfasalazine better tolerated sometimes Antimetabolites: azathioprine methotrexate, MMF for mild- mod disease. Cyclophosphamide for severe disease Steorids- pred 1-1.5mg/kg. effective for rapid control. Long term IOP monitoring needed. Other measures are IV IG and rituximab Topical: lubricants/ steroids/ ciclosporin/ tacrolimus/ retinoic acid to reduce keratinization/ abx/ lid hygiene Subconj MMC +/- steroid injection. CL worn with caution protect cornea
60
What are some surgical treatment options for MMP/ OCP
Reconstructive surgery for: aberrant eyelashes punctal occlusion to aid tear retention Lateral tarsorrhaphy, botox induced ptosis Entropion repair Cataract surgery Mucous membrane autografting. Amniotic membrane transplant Limbal stem cell transfer Keratoplasty high risk failure. Boston keratoprosthesis for end stage disease
61
What is SJS
TEN is a variant of SJS. Cell mediated delayed hypersensitivity reaction usually related to drug exposure. Medications like sulfonamides/trimethoprim, paracetamol, nevirapine. cold remedies and anticonvulsants.Infections due to mycoplasma pneumonia HSV some cancers.
62
What are the ocular features of SJS
Redness/ grittiness/ photophobia/ watering and blurring. haemorrhagic crusting of lid margins, papillary conjunctivitis, keratopathy, conj membranes/ pseudomembranes.iritis not infrequent Late signs: conj cicatrization forniceal shortening and symblepharon formation. Keratinization of conjunctiva and lid margin, eyelid cicatricial entropion + ectropion, trichasis, keratopathy scarring/ vascularization, keratinization. fibrosis of lacrimal puncta watery eye.
63
What are the systemic features of SJS
Flu like symptoms lasting upto 14 days before lesion appearance. systemic mucosal involvement nasal pain/ discharge/ pain on micturition, diarrhoea, cough, SOB, pain on eating/ drinking signs: blistering/ haemorrhagic crusting of lips. Purpuric vesicular haemorrhagic/ necrotic skin lesions involving face/ extremites/ trunk. Target lesions more classic for erythema multiforme rather than SJS/TEN
64
How to treat SJS/TEN
Removal of precipitant discontinue drugs adequate hydration/ electrolyte balance/ nutrition/ protein replacement. systemic steroids controversial. Ciclosporin/ azathioprine/ cyclophosphamide, IVIG Systemic abx- prophylaxis against skin infections Ocular: acute disease lubricants/ prevent corneal exposrure/ topical steroids iritis + conj inflammation, cycloplegia comfort, lysis of developing symblephara with glass rod, pseudomembrane peeling, treat bacterial keratitis, conj swabs for culture, IOP monitoring. Chronic disease lubrication/ punctal occlusion, topical transretinoic acid 0.01%, treat aberrant lashes, BCL, mucous membrane graft, corneal rehab STK, lamella graft, amniotic membrane graft, LSCC, keratoprosthesis
65
What is SLK
uncommon disease of superior limbus/ superior bulbar and tarsal conj. affects 1/ both eyes of middle aged woman 50% have abnormal thyroid function. 3% TED patients have SLK. Condition believed to be linked to blink related trauma between upper lid and superior bulbar conj. precipitated by tear insufficiency, excess lax of conj tissue.
66
Symptoms and signs of SLK
FB sensation/ burning / photophobia/ mucoid discharge. similar to GPC. Conj: hyperaemia of radial band of superior bulbar conj staining with rose bengal/ limbal papillary hypertrophy. Papillary hypertrophy of tarsal plate. Petechial haemorrhages. Keratinization. Cornea: superior SPK, superior filamentary keratitis 1/3rd cases. Mild superior pannus. KCS 50%.
67
How to investigate SLK
Thyroid function biopsy/impression cytology reveal keratinization of superior bulbar conjunctiva
68
How to treat SLK
Lubricants to reduce friction, NAC break down filaments, mast cell stabilisers, steroids, topical rebampide ciclosporin .05%BD, Retinoic acid retard keratinization, autologous serum 20%. Soft CL can help/ supratarsal steroid injection/ superior/inferior punctal occlusion, resection of superior limbal conj. conj ablation, treat thyroid dysfunction.
69
What is ligneous conjunctivitis
rare potentially sight and life threatening disorder with recurrent bilateral fibrin rich pseudomembranous lesion of wood like consistency on tarsal conj. death can occur from pulmonary involvement.
70
How is ligneous conjunctivitis diagnosed
Histopathology: amorphous subepithelial deposits of eosinophilic material consisting of fibrin Presentation with non specific conjnctivitis in childhood 5 years median age. conj lesion noted by parents. enlarging red white lobular conj masses covered by thick yellow white mucoid discharge. corneal scarring/ vascularization/ infection/ melting.
71
How is Ligneous conjunctivitis treated?
surgical removal with meticulous diathermy. Discontinue antifibrinolytic drugs. After membrane removal- hourly heparin and steroids, continue until wound re-epithelialized and taper over several weeks until all inflammation resolves. IV/ topical plasminogen amniotic membrane transplant prophylactic heparin
72
What is factitious conjunctivitis
self injury but occur inadvertently. damage result of mechanical trauma/ instillation of irritant from household substances like soap. Over instillation of ocular meds can be responsible.
73
What are the signs/ symptoms of factitious conjunctivitis
inferior conj injection/ stain with rose bengal with quiet superior bulbar conj. linear corneal abrasions, persistent ED, secondary infection with candida spp, sterile ring infiltrate and hypopyon, corneal scarring
74
How to manage factitious conjunctivitis
exclude other diagnoses close observation confrontation leads to failure to return for review psychiatric opinion may be appropriate
75
What is pingeculae
innocuous but extremely common asymptomatic elasstotic degeneration of conj stroma. Yellow white mound or aggregation of smaller mounds seen on bulbar conj adjacent to limbus more frequently located at nasal than temporal limbus. Can be calficied. Due to actinic damage
76
How to treat pingecula
irritation- topical lubricants pingueculitis- short course topical steroid excision for cosmesis/ irritation. recurrence low. thermal laser ablation effective. Gentian violet maring necessary
77
What is pterygium
triangular fibrovascular subepithelial ingrowth of degenerative bulbar conj tissue over limbus onto cornea. Excess UV exposure risk factor, runs in families. histologically similar to pingecula show elastotic degeneration in vascular subepithelial stromal collagen. pterygia enroach onto cornea invade bowman layer in contrast to pingecula which doesnt.
78
Symptoms/signs of pterygium
three parts to it: cap (avascular halo like zone at advancing edge), head and body. Linear iron depostion stocker line seen anterior to head of pterygium on corneal epithelium). pseudopterygium: distinguished as location far from horizontal and firm attachment t ocornea only at apex (head)
79
How is pterygium treated
surgery: bare sclera simple excision results in recurrence 80%. conj autografting donor patch harvested from superior edge/ upper temporal paralimbal region. graft sutured into position 10-0 nylon. graft can be secured with TISSEEEL glue rather than sutures. Adjunctive treatment with MMC can be used. Peripheral lamellar keratoplasty for deep lesions
80