Cornea
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| Cornea | |
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| Schematic diagram of the human eye. (Cornea labeled at center top.) | |
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| Vertical section of human cornea from near the margin. (Waldeyer.) Magnified. 1. Epithelium. 2. Anterior elastic lamina. 3. substantia propria. 4. Posterior elastic lamina. 5. Endothelium of the anterior chamber. a. Oblique fibers in the anterior layer of the substantia propria. b. Lamellæ the fibers of which are cut across, producing a dotted appearance. c. Corneal corpuscles appearing fusiform in section. d. Lamellæ the fibers of which are cut longitudinally. e. Transition to the sclera, with more distinct fibrillation, and surmounted by a thicker epithelium. f. Small bloodvessels cut across near the margin of the cornea. | |
| Gray's | subject #225 1006 |
| Dorlands/Elsevier | c_55/12259559 |
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WikiDoc Resources for Cornea | |
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Ongoing Trials on Cornea at Clinical Trials.gov Clinical Trials on Cornea at Google
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US National Guidelines Clearinghouse on Cornea
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Directions to Hospitals Treating Cornea Risk calculators and risk factors for Cornea
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The cornea is the transparent front part of the eye that covers the iris, pupil, and anterior chamber, providing most of an eye's optical power.[1] Together with the lens, the cornea refracts light, and as a result helps the eye to focus, accounting for approximately 80% of its production to 20% of the lens focusing power.[1] The cornea contributes more to the total refraction than the lens does, but, whereas the curvature of the lens can be adjusted to "tune" the focus depending upon the object's distance, the curvature of the cornea is fixed.
The cornea has unmyelinated nerve endings sensitive to touch, temperature and chemicals; a touch of the cornea causes an involuntary reflex to close the eyelid. Because transparency is of prime importance the cornea does not have blood vessels; it receives nutrients via diffusion from the tear fluid at the outside and the aqueous humour at the inside and also from neurotrophins supplied by nerve fibres that innervate it. In humans, the cornea has a diameter of about 11.5 mm and a thickness of 0.5 mm - 0.6 mm in the center and 0.6 mm - 0.8 mm at the periphery. Transparency, avascularity, and immunologic privilege makes the cornea a very special tissue.
In humans, the refractive power of the cornea is approximately 43 dioptres, roughly two-thirds of the eye's total refractive power.[1]
Medical terms related to the cornea often start with the prefix "kerat-".
Layers
The human cornea, like that of other primates, has five layers. The corneas of cats, dogs, and other carnivores have only four.[1] From the anterior to posterior they are:
- Corneal epithelium: a thin epithelial multicellular layer of fast-growing and easily-regenerated cells, kept moist with tears. Irregularity or edema of the corneal epithelium disrupts the smoothness of the air-tear film interface, the most significant component of the total refractive power of the eye, thereby reducing visual acuity.
- Bowman's layer (also erroneously known as the anterior limiting membrane, when in fact it is not a membrane but a condensed layer of collagen): a tough layer that protects the corneal stroma, consisting of irregularly-arranged collagen fibers. This layer is absent in carnivores.[1]
- Corneal stroma (also substantia propria): a thick, transparent middle layer, consisting of regularly-arranged collagen fibers along with sparsely populated keratocytes. The corneal stroma consists of approximately 200 layers of type I collagen fibrils. There are 2 theories of how transparency in the cornea comes about:
- The lattice arrangements of the collagen fibrils in the stroma. The light scatter by individual fibrils is cancelled by destructive interference from the scattered light from other individual fibrils.(Maurice)
- The spacing of the neighbouring collagen fibrils in the stroma must be < 200 nm for there to be transparency. (Goldman and Benedek)
- Descemet's membrane (also posterior limiting membrane): a thin acellular layer that serves as the modified basement membrane of the corneal endothelium.
- Corneal endothelium: a simple squamous or low cuboidal monolayer of mitochondria-rich cells responsible for regulating fluid and solute transport between the aqueous and corneal stromal compartments. (The term endothelium is a misnomer here. The corneal endothelium is bathed by aqueous humour, not by blood or lymph, and has a very different origin, function, and appearance from vascular endothelia.)
Innervation
The cornea is one of the most sensitive tissues of the body, it is densely innervated with sensory nerve fibres via the ophthalmic division of the trigeminal nerve by way of 70 - 80 long ciliary nerves and short ciliary nerves.
The nerves enter the cornea via three levels, scleral, episcleral and conjunctival. Most of the bundles give rise by subdivision to a network in the stroma, from which fibres supply the different regions. The three networks are midstromal, subepithelial/Bowman's layer, and epithelium. The receptive fields of each nerve ending are very large, and may overlap.
Corneal nerves have been observed to terminate in a logarithmic spiral pattern.[1]
Diseases and disorders
Treatment and management of corneal diseases and disorders
Surgical procedures involving the cornea
Various refractive eye surgery techniques change the shape of the cornea in order to reduce the need for corrective lenses or otherwise improve the refractive state of the eye. In many of the techniques used today, reshaping of the cornea is performed by photoablation using the excimer laser.
If the corneal stroma develops visually significant opacity, irregularity, or edema, a cornea of a deceased donor can be transplanted. Because there are no blood vessels in the cornea, there are also few problems with rejection of the new cornea.
There are also synthetic corneas (keratoprostheses) in development. Most are merely plastic inserts, but there are also composed of biocompatible synthetic materials that encourage tissue ingrowth into the synthetic cornea, thereby promoting biointegration.
Non-surgical procedures involving the cornea
Orthokeratology is a method using specialized hard or rigid gas-permeable contact lenses to transiently reshape the cornea in order to improve the refractive state of the eye or reduce the need for eyeglasses and contact lenses.
References
- Daxer A, Misof K, Grabner B, Ettl A, Fratzl P. "Collagen fibrils in the human corneal stroma: structure and aging." Invest Ophthalmol Vis Sci. 1998 Mar;39(3):644-8. PMID 9501878.
- Daxer A, Fratzl P. "Collagen fibril orientation in the human corneal stroma and its implication in keratoconus." Invest Ophthalmol Vis Sci. 1997 Jan;38(1):121-9. PMID 9008637.
- Fratzl P, Daxer A. "Structural transformation of collagen fibrils in corneal stroma during drying. An x-ray scattering study." Biophys J. 1993 Apr;64(4):1210-4. PMID 8494978.
See also
External links
- Atlas of anatomy at UMich eye_1 - "Sagittal Section Through the Eyeball"
- Facts About The Cornea and Corneal Disease National Eye Institute (NEI)
- Keratoconus (Irregular Astigmatism), Patient Support
Sensory system - Visual system - Eye | |
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| Fibrous tunic (outer) | Conjunctiva • Sclera • Schlemm's canal • Trabecular meshwork • Limbus Cornea (Epithelium, Bowman's, Stroma, Descemet's, Endothelium) |
| Uvea (middle) | Choroid (Ciliary processes, Choriocapillaris, Bruch's membrane) • Iris (Stroma) • Pupil • Ciliary body |
| Retina (inner) | Macula • Fovea • Optic disc |
| Anterior segment | Anterior chamber • Aqueous humour • Posterior chamber • Lens |
| Posterior segment | Vitreous humour • Zonule of Zinn |
| Intraocular muscles | parasympathetic (Ciliary muscle, Iris sphincter muscle) • sympathetic (Iris dilator muscle) |
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .
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