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ALLERGIC
CONJUNCTIVITIS
Types of Allergic Conjunctivitis
• Acute allergic conjunctivitis.
• Seasonal allergic conjunctivitis.
• Perennial allergic conjunctivitis.
• Phlyctenular Keratoconjunctivitis.
• Vernal keratoconjunctivitis.
• Atopic keratoconjunctivitis.
• Others ( Eosinophilic , Contact allergic , Giant papillary)
Acute allergic conjunctivitis.
Etiology :
Acute reaction(type 1) to environmental allergen (pollen)
Typical picture (children playing outside in spring/summer)
Especially patients with Asthma , Hay fever , Atopy
Clinical picture :
Acute itching, watering, lid swelling, Hyperemia and the hall mark is
CHEMOSIS
Mild
Severe
Acute allergic conjunctivitis.
Treatment :
First remove cause if known
Not usually required , Resolves in hours
In cases of severe chemosis :
1- Cool compresses.
2- Vasoconstrictor of 0.1 adrenaline.
3- Steroids & Anti- allergics.
Seasonal / perennial allergic conjunctivitis.
Etiology :
Subacute & common conditions cc by timing of exacerbation.
Seasonal
(hay fever eyes) Perennial
Worsen in spring and
summer.
Worsen in autumn.
Plants allergens. House dust mites,Animal &
Fungal allergens.
Seasonal / perennial allergic conjunctivitis.
Clinical picture :
Similar to acute allergic conjunctivitis, but occurs in transient
Attacks Which is less severe, subacute & accompanied by
Sneezing and nasal discharge.
Treatment :
Similar to acute allergic conjunctivitis.
Phlyctenular Keratoconjunctivitis.
Pathogenesis :
• Chronic allergic inflammation due to endogenous toxins.
• Incidence mainly in malnourished children.
• Type IV hypersensitivity reaction in following cases :
a- Septic focus .
b- Staphylococcus blepharo-conjunctivitis.
c- T.B
d- Toxins of intestinal parasites.
Symptoms :
• Diffuse pain ( Burning no Itching )
• Red eye .
• Watery mucoid discharge.
2ry
Bacterial
infection
Muco-
purulent
discharge
Corneal ulcer Reflex
Lacrimation
Photophobia
blepharospasm
Phlyctenular Keratoconjunctivitis.
Signs : A- Conjunctiva PHLYCTEN
• Grey nodule.
• Surrounded by hyperemia.
• Size : 1-3 mm.
• At limbus.
• One or multiple and may ulcerate leading to 2ry infection.
Phlyctenular Keratoconjunctivitis.
B- Cornea :
Corneal phlycten
Vascularize Ulcerate
Pannus Ulcer
Deep vascularization
INF cell infiltration
Marginal
limbal
Ring
Fascicular
(Serpiginous)
Phlyctenular Keratoconjunctivitis.
Complications :
• M.P.C (2ry bacterial infection).
• Corneal opacity.
• Recurrence
Treatment :
• Treat cause ( Anti-biotics & good nutrition ) .
• Steroids ( drops & ointments )
• Treatment of complications
• Infection ( Anti-biotics ).
• Corneal ulcer ( Atropine + Dark glasses ).
• Fascicular ulcer ( Topical steroids + Cautery ).
Vernal keratoconjunctivitis.
Pathogenesis :
• Recurrent bilateral disorder.
• IgE and cell mediated immune response are involved.
• Primarily affects boys from the age of 5 years onwards.
• There is remission by the late teens in 95% of cases.
• Common in warm dry climate such as Africa and Middle East.
• Occurs on a seasonal basis (late spring and summer).
Classification
Palpebral Limbal Mixed
Vernal keratoconjunctivitis.
Clinical picture :
1- Symptoms:
Intense itching , Photophobia , Lacrimation , Burning
Increased blinking and thick mucous discharge (Ropy) .
2-Signs
Conjunctiva
Palpebral Limbal
Cornea Eyelid
Vernal keratoconjunctivitis.
Conjunctiva Palpebral type :
1. Conjunctival hyperemia & Diffuse velvety hypertrophy on STP.
2. Macro papillae with flat-topped polygonal appearance (COBBLESTONES).
3. Whitish inflammatory infiltrates.
1 2 3
Vernal keratoconjunctivitis.
Conjunctiva Palpebral type :
4. Giant papillae.
5. Mucous deposition between giant papillae.
6. Decreased disease activity is characterized by milder
conjunctival injection and decreased mucus production.
4 5 6
Vernal keratoconjunctivitis.
Conjunctiva B- Limbal type :
1. Gelatinous limbal conjunctival papillae (Horner–Trantas dots)
2. In tropical regions, limbal disease may be severe.
Vernal keratoconjunctivitis.
Keratopathy :
1. Superior punctate epithelial erosions.
2. Epithelial macroerosions.(caused by inflammatory toxins and mechanical erosion by papillae)
Vernal keratoconjunctivitis.
Keratopathy :
3. Plaques & SHIELD ulcer :
May develop in palpebral or mixed disease when the exposed bowman membrane
becomes coated with mucus and calcium phosphate, leading to inadequate witting
and delayed re-epithelialization. This development is serious and requires urgent
attention to prevent 2ry bacterial infection.
4. Sub epithelial scars.
Vernal keratoconjunctivitis.
Keratopathy :
5. Pseudogerontoxon :
In recurrent limbal disease cc by paralimbal band of superficial scarring
resembling arcus senilis .
6. Vascularization (especially superiorly) .
Vernal keratoconjunctivitis.
Keratopathy :
7. Corneal ectasia (Keratoconus).
8. Herpes simplex keratitis (Dendritic ulcer).
8
Atopic Keratoconjunctivitis
Pathogenesis :
• Bilateral rare disease.
• Develops in adulthood (30-50 years).
• Follows long history of Eczema & Asthma which is common in these patients.
• No gender preponderance.
• Chronic , unremitting and with low expectation of eventual resolution.
• Associated with significant visual morbidity.
• Patients are sensitive to wide range of airborne allergens.
• Perennial disease which is worse in winter.
VKCAKC
ChildhoodAdults
SeasonalPerennial
SpringWinter
Atopic Keratoconjunctivitis
Clinical picture :
1- Symptoms :
Similar to VKC but more severe and unremitting
2-Signs
Eye lid Conjunctiva Keratopathy Cataract
Retinal
Detachment
Atopic Keratoconjunctivitis
A- Eye lid :
1. Skin changes (Eczema , Erythema , Dryness ).
2. Lower lid Ectropion & Epiphora due to facial skin tightening.
3. Ptosis not uncommon.
Important note :
Differentiation between AKC&VKC
is essentially clinical ,but eosinophils
is less in conjunctival scraping in
AKC.
Atopic Keratoconjunctivitis
B- Conjunctiva :
1. Watery discharge& Hyperemia& Chemosis.
2. Papillae which is initially smaller than VKC.
3. Whitish , Featureless appearance.
4. Cicatricial changes leading to :
a- Moderate symblepharon b- Forniceal shortening c- Caruncle Keratinization
5. Limbal involvement Horner-Trantas dots .
Atopic Keratoconjunctivitis
C- Keratopathy :
1. Punctate erosions over lower 1/3.
2.
Persistent
epithelial
defects
Corneal
thinning
Descematocele
Atopic Keratoconjunctivitis
3. Plaque formation.
4. Peripheral vascularization & Stromal scarring.
5. Keratoconus ( about 15% )
6. Predisposition to Fungal , Bacterial & HS Keratitis.
Atopic Keratoconjunctivitis
D- Cataract :
1. Pre-senile shield-like ant or post sub-capsular cataract.
2. Because of high lid margin carriage of S.aureus , Cataract surgery
carries an increased risk of endophthalmitis.
ANT POST
Atopic Keratoconjunctivitis
E- Retinal Detachment :
More common than in the general population, and there is a particular risk
following cataract surgery.
Management of VKC and AKC
Management
General
Measures
Local
Treatment
General
Treatment
Surgery
Management of VKC and AKC
1- General Measures :
Allergen Avoidance, Cold Compresses, Lid Hygiene, BCL
2- Local Treatment :
• Mast cells stabilizers.
• Topical Anti-Histamines ( not for long term ).
• Anti-Histamines + Vasoconstrictors.
• Anti-Histamines + Mast cells stabilizers.
• NSAIDs ( replacement for Anti-Histamines ).
• Topical steroids
- For Keratopathy and severe conjunctivitis .
- Short intensive term ( 2 hours initially )
- Monitor IOP as there is a minimal risk of steroid induced glaucoma
except with prednisolone 1% which is high.
• Steroid ointment.
• Antibiotics.
Management of VKC and AKC
• Acetylcysteine.
• Immune modulators.
- If steroids ineffective , inadequate , poorly tolerated .
- Calcineurin inhibitors ( Tacrolimus )
Shows great promises in AKC treatment as steroid alternative.
• Supratarsal steroid injection
- In severe disease or non-compliant patients.
3- Systemic Treatment :
• Oral Anti-Histamines.
• Antibiotics.
• Immuno-suppressive agents.
Management of VKC and AKC
4- Surgery :
• Superficial Keratectomy :
- Required to remove plaques or debride shield ulcers.
- Excimer laser phototherapeutic keratectomy is an alternative.
• Restoration Surgery :
- Amniotic membrane overlay grafting or lamellar keratoplasty.
- Eyelid procedures for severe persistent epithelial defects or ulceration.
- Gluing may be appropriate for focal corneal perforations.
Non-allergic eosinophilic conjunctivitis
• Recently proposed chronic non-atopic condition.
• Occur predominantly in middle-aged women in whom dry eye is also common.
• Thought to be of similar pathogenesis to non-allergic eosinophilic rhinitis.
• Conjunctival eosinophilia is present without significant IgE levels in the serum or
tear film.
• Symptoms are similar to those of allergic conjunctivitis.
• Treatment is with a 1–2 week course of
topical steroid.
Contact allergic blepharoconjunctivitis
• Analogous to contact dermatitis.
• Acute or sub acute T-cell-mediated delayed hypersensitivity reaction.
• Seen most commonly by ophthalmologists as a reaction to eye drop constituents
and by optometrists as a reaction to contact lens solutions.
• Signs predominantly involve the eyelid skin: erythema, thickening, induration and
sometimes fissuring.
• Treatment is by removal or discontinuation of the precipitant, sometimes with a
mild topical steroid ointment.
Giant papillary conjunctivitis
Pathogenesis :
• Secondary to a variety of mechanical stimuli of the tarsal conjunctiva.
• Most frequently encountered with contact lens (CL) wear.
• The risk is increased by the build-up of proteinaceous deposits and cellular
debris on contact lens surface.
Symptoms :
• Foreign body sensation, redness, itching.
• Increased mucus production.
• Blurring and loss of CL tolerance.
• Symptoms may be worse after lens removal.
• Patients should be questioned about CL cleaning and maintenance.
Giant papillary conjunctivitis
Signs :
• Variable mucous discharge.
• Substantial CL protein deposits.
• Excessive CL mobility due to upper lid capture.
• Superior tarsal hyperemia and papillae.
• Focal apical ulceration and whitish scarring.
• Ptosis may occur.
Giant papillary conjunctivitis
Treatment :
• Removal of the stimulus.
• Ensure effective cleaning of CL or prosthesis.
• Topical
1. Mast cell stabilizers.
2. Antihistamines.
3. NSAIDs.
4. Topical steroids.
References
• Kanski's Clinical Ophthalmology 8th edition.
• Tanta Ophthalmology department textbook.
• Ramadology 6th edition

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Allergic conjuctivitis

  • 2. Types of Allergic Conjunctivitis • Acute allergic conjunctivitis. • Seasonal allergic conjunctivitis. • Perennial allergic conjunctivitis. • Phlyctenular Keratoconjunctivitis. • Vernal keratoconjunctivitis. • Atopic keratoconjunctivitis. • Others ( Eosinophilic , Contact allergic , Giant papillary)
  • 3. Acute allergic conjunctivitis. Etiology : Acute reaction(type 1) to environmental allergen (pollen) Typical picture (children playing outside in spring/summer) Especially patients with Asthma , Hay fever , Atopy Clinical picture : Acute itching, watering, lid swelling, Hyperemia and the hall mark is CHEMOSIS Mild Severe
  • 4. Acute allergic conjunctivitis. Treatment : First remove cause if known Not usually required , Resolves in hours In cases of severe chemosis : 1- Cool compresses. 2- Vasoconstrictor of 0.1 adrenaline. 3- Steroids & Anti- allergics.
  • 5. Seasonal / perennial allergic conjunctivitis. Etiology : Subacute & common conditions cc by timing of exacerbation. Seasonal (hay fever eyes) Perennial Worsen in spring and summer. Worsen in autumn. Plants allergens. House dust mites,Animal & Fungal allergens.
  • 6. Seasonal / perennial allergic conjunctivitis. Clinical picture : Similar to acute allergic conjunctivitis, but occurs in transient Attacks Which is less severe, subacute & accompanied by Sneezing and nasal discharge. Treatment : Similar to acute allergic conjunctivitis.
  • 7. Phlyctenular Keratoconjunctivitis. Pathogenesis : • Chronic allergic inflammation due to endogenous toxins. • Incidence mainly in malnourished children. • Type IV hypersensitivity reaction in following cases : a- Septic focus . b- Staphylococcus blepharo-conjunctivitis. c- T.B d- Toxins of intestinal parasites. Symptoms : • Diffuse pain ( Burning no Itching ) • Red eye . • Watery mucoid discharge. 2ry Bacterial infection Muco- purulent discharge Corneal ulcer Reflex Lacrimation Photophobia blepharospasm
  • 8. Phlyctenular Keratoconjunctivitis. Signs : A- Conjunctiva PHLYCTEN • Grey nodule. • Surrounded by hyperemia. • Size : 1-3 mm. • At limbus. • One or multiple and may ulcerate leading to 2ry infection.
  • 9. Phlyctenular Keratoconjunctivitis. B- Cornea : Corneal phlycten Vascularize Ulcerate Pannus Ulcer Deep vascularization INF cell infiltration Marginal limbal Ring Fascicular (Serpiginous)
  • 10. Phlyctenular Keratoconjunctivitis. Complications : • M.P.C (2ry bacterial infection). • Corneal opacity. • Recurrence Treatment : • Treat cause ( Anti-biotics & good nutrition ) . • Steroids ( drops & ointments ) • Treatment of complications • Infection ( Anti-biotics ). • Corneal ulcer ( Atropine + Dark glasses ). • Fascicular ulcer ( Topical steroids + Cautery ).
  • 11. Vernal keratoconjunctivitis. Pathogenesis : • Recurrent bilateral disorder. • IgE and cell mediated immune response are involved. • Primarily affects boys from the age of 5 years onwards. • There is remission by the late teens in 95% of cases. • Common in warm dry climate such as Africa and Middle East. • Occurs on a seasonal basis (late spring and summer). Classification Palpebral Limbal Mixed
  • 12. Vernal keratoconjunctivitis. Clinical picture : 1- Symptoms: Intense itching , Photophobia , Lacrimation , Burning Increased blinking and thick mucous discharge (Ropy) . 2-Signs Conjunctiva Palpebral Limbal Cornea Eyelid
  • 13. Vernal keratoconjunctivitis. Conjunctiva Palpebral type : 1. Conjunctival hyperemia & Diffuse velvety hypertrophy on STP. 2. Macro papillae with flat-topped polygonal appearance (COBBLESTONES). 3. Whitish inflammatory infiltrates. 1 2 3
  • 14. Vernal keratoconjunctivitis. Conjunctiva Palpebral type : 4. Giant papillae. 5. Mucous deposition between giant papillae. 6. Decreased disease activity is characterized by milder conjunctival injection and decreased mucus production. 4 5 6
  • 15. Vernal keratoconjunctivitis. Conjunctiva B- Limbal type : 1. Gelatinous limbal conjunctival papillae (Horner–Trantas dots) 2. In tropical regions, limbal disease may be severe.
  • 16. Vernal keratoconjunctivitis. Keratopathy : 1. Superior punctate epithelial erosions. 2. Epithelial macroerosions.(caused by inflammatory toxins and mechanical erosion by papillae)
  • 17. Vernal keratoconjunctivitis. Keratopathy : 3. Plaques & SHIELD ulcer : May develop in palpebral or mixed disease when the exposed bowman membrane becomes coated with mucus and calcium phosphate, leading to inadequate witting and delayed re-epithelialization. This development is serious and requires urgent attention to prevent 2ry bacterial infection. 4. Sub epithelial scars.
  • 18. Vernal keratoconjunctivitis. Keratopathy : 5. Pseudogerontoxon : In recurrent limbal disease cc by paralimbal band of superficial scarring resembling arcus senilis . 6. Vascularization (especially superiorly) .
  • 19. Vernal keratoconjunctivitis. Keratopathy : 7. Corneal ectasia (Keratoconus). 8. Herpes simplex keratitis (Dendritic ulcer). 8
  • 20. Atopic Keratoconjunctivitis Pathogenesis : • Bilateral rare disease. • Develops in adulthood (30-50 years). • Follows long history of Eczema & Asthma which is common in these patients. • No gender preponderance. • Chronic , unremitting and with low expectation of eventual resolution. • Associated with significant visual morbidity. • Patients are sensitive to wide range of airborne allergens. • Perennial disease which is worse in winter. VKCAKC ChildhoodAdults SeasonalPerennial SpringWinter
  • 21. Atopic Keratoconjunctivitis Clinical picture : 1- Symptoms : Similar to VKC but more severe and unremitting 2-Signs Eye lid Conjunctiva Keratopathy Cataract Retinal Detachment
  • 22. Atopic Keratoconjunctivitis A- Eye lid : 1. Skin changes (Eczema , Erythema , Dryness ). 2. Lower lid Ectropion & Epiphora due to facial skin tightening. 3. Ptosis not uncommon. Important note : Differentiation between AKC&VKC is essentially clinical ,but eosinophils is less in conjunctival scraping in AKC.
  • 23. Atopic Keratoconjunctivitis B- Conjunctiva : 1. Watery discharge& Hyperemia& Chemosis. 2. Papillae which is initially smaller than VKC. 3. Whitish , Featureless appearance. 4. Cicatricial changes leading to : a- Moderate symblepharon b- Forniceal shortening c- Caruncle Keratinization 5. Limbal involvement Horner-Trantas dots .
  • 24. Atopic Keratoconjunctivitis C- Keratopathy : 1. Punctate erosions over lower 1/3. 2. Persistent epithelial defects Corneal thinning Descematocele
  • 25. Atopic Keratoconjunctivitis 3. Plaque formation. 4. Peripheral vascularization & Stromal scarring. 5. Keratoconus ( about 15% ) 6. Predisposition to Fungal , Bacterial & HS Keratitis.
  • 26. Atopic Keratoconjunctivitis D- Cataract : 1. Pre-senile shield-like ant or post sub-capsular cataract. 2. Because of high lid margin carriage of S.aureus , Cataract surgery carries an increased risk of endophthalmitis. ANT POST
  • 27. Atopic Keratoconjunctivitis E- Retinal Detachment : More common than in the general population, and there is a particular risk following cataract surgery.
  • 28. Management of VKC and AKC Management General Measures Local Treatment General Treatment Surgery
  • 29. Management of VKC and AKC 1- General Measures : Allergen Avoidance, Cold Compresses, Lid Hygiene, BCL 2- Local Treatment : • Mast cells stabilizers. • Topical Anti-Histamines ( not for long term ). • Anti-Histamines + Vasoconstrictors. • Anti-Histamines + Mast cells stabilizers. • NSAIDs ( replacement for Anti-Histamines ). • Topical steroids - For Keratopathy and severe conjunctivitis . - Short intensive term ( 2 hours initially ) - Monitor IOP as there is a minimal risk of steroid induced glaucoma except with prednisolone 1% which is high. • Steroid ointment. • Antibiotics.
  • 30. Management of VKC and AKC • Acetylcysteine. • Immune modulators. - If steroids ineffective , inadequate , poorly tolerated . - Calcineurin inhibitors ( Tacrolimus ) Shows great promises in AKC treatment as steroid alternative. • Supratarsal steroid injection - In severe disease or non-compliant patients. 3- Systemic Treatment : • Oral Anti-Histamines. • Antibiotics. • Immuno-suppressive agents.
  • 31. Management of VKC and AKC 4- Surgery : • Superficial Keratectomy : - Required to remove plaques or debride shield ulcers. - Excimer laser phototherapeutic keratectomy is an alternative. • Restoration Surgery : - Amniotic membrane overlay grafting or lamellar keratoplasty. - Eyelid procedures for severe persistent epithelial defects or ulceration. - Gluing may be appropriate for focal corneal perforations.
  • 32. Non-allergic eosinophilic conjunctivitis • Recently proposed chronic non-atopic condition. • Occur predominantly in middle-aged women in whom dry eye is also common. • Thought to be of similar pathogenesis to non-allergic eosinophilic rhinitis. • Conjunctival eosinophilia is present without significant IgE levels in the serum or tear film. • Symptoms are similar to those of allergic conjunctivitis. • Treatment is with a 1–2 week course of topical steroid.
  • 33. Contact allergic blepharoconjunctivitis • Analogous to contact dermatitis. • Acute or sub acute T-cell-mediated delayed hypersensitivity reaction. • Seen most commonly by ophthalmologists as a reaction to eye drop constituents and by optometrists as a reaction to contact lens solutions. • Signs predominantly involve the eyelid skin: erythema, thickening, induration and sometimes fissuring. • Treatment is by removal or discontinuation of the precipitant, sometimes with a mild topical steroid ointment.
  • 34. Giant papillary conjunctivitis Pathogenesis : • Secondary to a variety of mechanical stimuli of the tarsal conjunctiva. • Most frequently encountered with contact lens (CL) wear. • The risk is increased by the build-up of proteinaceous deposits and cellular debris on contact lens surface. Symptoms : • Foreign body sensation, redness, itching. • Increased mucus production. • Blurring and loss of CL tolerance. • Symptoms may be worse after lens removal. • Patients should be questioned about CL cleaning and maintenance.
  • 35. Giant papillary conjunctivitis Signs : • Variable mucous discharge. • Substantial CL protein deposits. • Excessive CL mobility due to upper lid capture. • Superior tarsal hyperemia and papillae. • Focal apical ulceration and whitish scarring. • Ptosis may occur.
  • 36. Giant papillary conjunctivitis Treatment : • Removal of the stimulus. • Ensure effective cleaning of CL or prosthesis. • Topical 1. Mast cell stabilizers. 2. Antihistamines. 3. NSAIDs. 4. Topical steroids.
  • 37. References • Kanski's Clinical Ophthalmology 8th edition. • Tanta Ophthalmology department textbook. • Ramadology 6th edition