This presentation describes all a clinical aspects of noninfectious corneal ulcers
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Added: Jul 27, 2020
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Non Infectious Corneal Ulcers
Corneal Ulcers Def : Corneal ulcers are defects in the corneal epithelium with or without stromal infiltration. Types: A) Infectious ulcerative keratitis B) Non infectious ulcerative keratitis
Bacteria and Fungi Viruses Acanthamoeba Systemic Autoimmune/ Inflammatory Local Toxic Infectious Non infectious Etiology
Non Infectious Ulcerative Keratitis Causes: Local causes: Punctate marginal keratitis: Staphylococci, Streptococci, hypersensitivity to medications Peripheral keratitis associated with blepharitis : Systemic causes: Generally manifestation of systemic, immune-mediated disease Most common: Rheumatoid arthritis, Wegener’s granulomatosis and polyarteritis nodosa
Non INFECTIOUS INFECTIOUS No pain Pain No discharge Discharge AC reaction: absent AC reaction: present Peripheral Central Trauma: ------- Trauma : ++++
Important Types - Marginal keratitis - Mooren ulcer - Terrien marginal degeneration - Associated with systemic autoimmune diseases - Dellen Other types: Phlyctenulosis
Marginal keratitis
Marginal Keratitis • Caused by hypersensitivity reaction against Staphylococcal exotoxin and cell wall proteins with deposition of Ag- Ab complex in peripheral cornea • Lesions are culture negative but S. aureus can be isolated from lid margin
Signs and symptoms • Chronic Blepheritis • Subepithelial marginal infiltrates seperated from limbus by a clear zone • Conjunctival Injection • Coalescence and circumferential spread • Little or no AC reaction • Resolution usually occurs in 1-4 wks , occasionally there is residual superficial scarring
Treatment • Weak topical steroid • May be combined with a topical antibiotic • Tetracycline orally • For children , breastfeeding and pregnancy erythromycin • Treatment of blepheritis
Mooren's Ulcer • Rare autoimmune disease • Characterized by – Progressive , – Peripheral,with Limbitis – Circumferential , stromal corneal ulceration Vascularization involving the bed of the ulcer up to its leading edge but not beyond – Later central spread Risk factors for Mooren's ulcer include corneal surgery, previous trauma, and infection.
Circumferential Healing
Complications • Severe astigmatism due to extensive vascularization & fibrosis • Perforation following minor trauma • Secondary bacterial infection
Management • Topical – Steroids – Cyclosporin (weeks to show significant effect) – Artificial tears – Collagenase inhibitors ( acetylcystine ) • bandage contact lenses • Conjunctival resection • Immunosuppression • Systemic collagenase inhibitors such as doxycycline Lamellar keratoplasty, keratoepithelioplasty and conjunctival flap and patch grafts
Terrien marginal degeneration • Idiopathic thinning of the peripheral cornea • Young adult to elderly patients • Uncommon • 75% males • Usually bilateral
Symptoms • Asymptomatic • Gradual visual deterioration can occur due to astigmatism • A few patients experience episodic pain and inflammation
Signs It causes a slowly progressive non-inflammatory, unilateral or asymmetrically bilateral peripheral corneal thinning and is associated with corneal neovascularization, Opacification and lipid deposition
- Perforation is rare but may be spontaneous or follow blunt trauma - Pseudopterygia sometimes develop
Management • Safety spectacles if thinning is significant • Contact lenses for astigmatism. Scleral or soft lenses with rigid gas permeable • Surgery :- Cresentric excision of the gutter with lamellar or full-thickness corneoscleral patch grafts transplantation
Peripheral Ulcerative Keratitis Associated With Systemic Autoimmune Disease
Destructive inflammation of the peripheral cornea associated with corneal epithelial sloughing and Keratolysis The mechanism includes immune complex deposition in peripheral cornea, episcleral and conjunctival capillary occlusion with secondary cytokine release and inflammatory cell recruitment, the upregulation of collagenases and reduced activity of their inhibitor s
Systemic associations • Rheumatoid arthritis (most common) – PUK is bilateral in 30% and tends to occur in advanced RA • Wegener granulomatosis (2nd most common) – In contrast to RA ocular complications are the initial presentation in 50% • Other conditions include polyarteritis nodosa , relapsing polychondritis ,SLE , Churg – Strauss ,Microscopic Polyangiitis , Inflammatory Bowel Disease
Peripheral corneal involvement in rheumatoid arthritis Chronic and asymptomatic Circumferential thinning with intact epithelium (‘contact lens cornea’) Acute and painful Circumferential ulceration and infiltration Without inflammation With inflammation
Management Principally with systemic immunosuppression in collaboration with a rheumatologist Topical Artificial tears (preservative-free) Antibiotics as prophylaxis Steroids may worsen thinning so are generally avoided Systemic Steroids (via pulsed IV administration) are used to control acute disease, with immunosuppressive therapy and biological blockers for longer-term management Tetracycline for its anticollagenase effect
Dellen Localized corneal disturbance associated with drying of a focal area Usually associated with an adjacent elevated lesion as pinguecula or large subconjunctival haemorrhage that impairs physiological lubrication
Treatment by lubricants and elimination of cause
Phlyctenulosis Uncommon, unilateral - typically affects children Severe photophobia, lacrimation and blepharospasm Delayed hypersensitivity reaction to staphylococcal antigen. In developing countries, the majority are associated with tuberculosis or helminthic infestation
Small pinkish-white nodule near limbus Usually transient and resolves spontaneously Starts astride limbus Resolves spontaneously or extends onto cornea Conjunctival phlycten Treatment - Topical steroids Corneal phlycten