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Published byAllan Pearson Modified over 8 years ago
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1.OUTER COAT 2.MIDDLE COAT 3.INNER COAT
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Tough Fibrous Coat Post 5/6 th of Globe White & Opaque Sclera Radius---12mm
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Tough Fibrous Coat Ant 1/6th of Globe Transparent Cornea Radius---8mm
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Junction of Cornea and Sclera Contains 1.Trabecular Meshwork 2.Canal of Schlemn
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Verticle-------10.6 mm Horizontal---11.7 mm Thickness Central portion----0.52 mm Peripheral portion----1 mm
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Three Layers 1. Epithelium & its Basement 2. Stroma & its ant condensation ( Bowman Zone) 3.Endothelium & its Basement (Descemet Membrane)
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From Anterior to Posterior 1. Epithelium 2. Bowman Zone 3. Stroma 4. Descemet Membrane 5. Endothelium
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* 50-60 µm thick * Covers the stroma anteriorly * Continuous with epithelium of conjunctiva * Life of epithelial cells is 7 days * Prevent aqueous solutions to penetrate
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* Surface cell layer * Wing cell layer * Basal cell layer * Basement membrane
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90% of the corneal thickness * Bowman Zone * Lamellar Stroma Once deformed its typical structure is not restored
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* Descemet membrane (Regenerates) * Endothelium Single layer of cells Cells are tightly bound together Responsible for dehydration Never regenerates
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* Central cornea is avascular * Corneoscleral limbus is generously supplied by anterior conjuntival branches of the anterior ciliary arteries * Aqueous humor and tear film provides nutrients
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* Branches of the ophthalmic division of trigeminal nerve and are solely sensory * Most are concentrated in the anterior stroma beneath the Bowman zone and send branches forward into epithelium * Descemet membrane and endothelium are not innervated
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* The microvilli of the anterior surface of the squamous cell layer are wet by the mucin of tear film * These cells are joined by tight junctions that exclude water soluble substances
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* Tight junctions of the epithelial cells * Endothelial pump mechanism * Absence of blood vessels * Absence of pigments * Scarcity of cell nuclei in stroma * Regular structure of stroma
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Superficial 1.Punctate epithelial erosions Tiny,slightly depressed, epithelial defects which stain with flourescein but not with rose Bengal PEE are non specific and may develop in a wide variety of keratopathies
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Superficial 2.Punctate epithelial keratitis It is the hallmark of viral infections. * Swollen epithelial cells * Visible unstained * Stains with rose bengal
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Superficial 3.Epithelial Oedema Sign of * Endothelial decompensation * Severe acute elevation of IOP
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Superficial 4.Filaments Small coma shaped mucus strands lined with epithelium. One end attached with epithelium
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Superficial 5.Pannus Inflammatory or degenerative ingrowth of fibro vascular tissue from limbus
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Stromal Lesions 1.Infiltrates Focal areas of active stromal inflammation 2. Oedema Increased corneal thickness Decreased transparency 3. Vascularization
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Lesions of Descemet Membrane 1. Breaks Corneal enlargement Keratoconus Birth trauma 2. Folds (Striate Keratopathy) Surgical trauma Ocular hypotony Stromal oedema
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* Control of infection * Control of inflammation * Promotion of re-epithelialization – lubrication – lid closure – bandage soft contact lens * Prevention of perforation – tissue adhesive glue – conjunctival flap – systemic immunosuppressive agents * Corneal grafting
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* Ocular surface disease: Trauma, post-herpetic corneal disease, bullous keratopathy, corneal exposure, dry eye and diminished corneal sensation. * Contact lens wear
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Pathogens which can produce corneal infection in intact epithelium. * 1.Neisseria gonorrhoeae * 2.Corynebacterium diphtheriae * 3.Listeria * 4.Haemophilus
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* Oval, yellow-white, densely opaque stromal suppuration surrounded by relatively clear cornea
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* Thick mucopurulent exudate, diffuse liquefactive necrosis and semi-opaque ground glass appearance of adjacent stroma
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* Shallow ulceration, grey-white pleomorphic suppuration and diffuse stromal opalescence. Endotoxins may induce ring-shaped corneal infilterates
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* History * Clinical examination (including staining and sensitivity) * Hospitalization * Corneal scrapping * Treatment
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* Topical antibiotics – combination therapy with fortified amino glycoside and fortified cephalosporin or monotherapy with fluoroquinolone. Initial instillation at hourly intervals. * Subconjunctival injections * Systemic ciprofloxacin 750mg BD
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* Cycloplegics * Steroid therapy (controversial) * Corneal biopsy or excisional keratoplasty
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* Wrong diagnosis * Wrong treatment * Drug toxicity
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* Filamentous fungal keratitis –Aspergillus - Fusarium
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* Greyish-white ulcer with indistinct margins * Surrounded by feathery infilterates * Ring infilterate * Endothelial plaque * Hypopyon
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* Usually develops in pre-existing corneal disease or immunocompromised patient * Yellow-white ulcer * Dense suppuration
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* Suppurative bacterial keratitis * Herpetic stromal necrotic keratitis
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* Culture * Biopsy * Antifungal therapy – Initially broad- spectrum econazole 1% topically – Then depending upon sensitivity natamycin or imidazole for 6 weeks * Systemic ketoconazole * Therapeutic penetrating keratoplasty
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* Protozoan – active (trophozoite) – dormant (cystic) * Common in swimmers and CL wearers
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* Blurred vision and disproportionate pain * Patchy anterior stromal infilterates * Perineural infilterates (radial keratoneuritis) * Infilterates coalesce –ring abcess, ulceration and hypopyon * White satellite lesions
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* Corneal scrappings stained with calcoflour white * Corneal biopsy * Treatment with chlorhexidine, polyhexamethylenebiguanide drops, dipropamidine and propamidine. * Therapeutic penetrating keratoplasty
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Primary ocular herpes: - Blepharoconjunctivitis - Keatitis (punctate epithelial)
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* Opaque cells arranged in a course punctate or stellate pattern * Central desquamation leads to a linear branching ulcer. –Fluorescein stain – Rose Bengal stain –Diminished corneal sensitivity * Anterior stromal infilterates * Geographical or amoeboid ulcer
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* Herpes zoster keratitis * Healing corneal abrasion * Pseudodendrites due to soft contact lens * Acanthamoeba keratitis * Drug toxicity
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* Antiviral therapy – Acycloguanosine 3% ointment – Trifluorothymidine 1% drops – Adenine arabinoside 3% ointment, 0.1% drops – Idoxuridine * Debridement (with sterile cotton- tipped bud 2mm beyond the edge of ulcer)
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* Stromal necrotic keratitis * Disciform keratitis
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* Predominantly affects children * Etiology – Tuberculosis – Delayed hypersensitivity reaction to staphylococcal or other bacterial antigen
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* Photophobia, lacrimation and blepharospasm.
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* Conjunctival: Pinkish-white nodule surrounded by hyperaemia * Corneal: May resolve spontaneously or extend radially to the cornea. May cause severe ulceration or perforation.
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* Short course of topical steroids * Topical antibiotics
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* Onset at puberty * Central or paracentral stromal thinning * Apical protrusion * Irregular astigmatism * Autosomal dominant transmission with incomplete penetrance proposed
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* By keratometry: - Mild ( 54 D) * By morphology: - Nipple cones – Oval cones – Globus cones
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* Ophthalmoscopy: Oil droplet reflex * Retinoscopy: Irregular scissor reflex * Keratometry: Irregular astigmatism (principal meridians no longer 90 degree apart and mires cannot be superimposed) * Placido disc: Irregular reflected ring * Slit-lamp: Very fine deep stromal striae (Vogt lines).
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* Decreased visual acuity * Munson sign * Fleischer ring * Corneal scarring * Acute hydrops
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* Spectacle correction * Contact lenses * Penetrating keratoplasty
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