- •Preface
- •Acknowledgments
- •Anatomic Features
- •Anatomic Directions and Planes
- •Refractive Conditions
- •Epithelial Tissue
- •Glandular Epithelium
- •Connective Tissue
- •Muscle Tissue
- •Nerve Tissue
- •Intercellular Junctions
- •References
- •Cornea
- •Corneal Dimensions
- •Corneal Histologic Features
- •Epithelium
- •Epithelial Replacement
- •Bowman’s Layer
- •Stroma or Substantia Propria
- •Descemet’s Membrane
- •Endothelium
- •Corneal Function
- •Corneal Hydration
- •Aquaporins
- •Corneal Metabolism
- •Corneal Repair: Wound Healing
- •Epithelium
- •Bowman’s
- •Stroma
- •Descemet’s
- •Endothelium
- •Absorption of Ultraviolet Radiation (UVR)
- •Corneal Innervation
- •Corneal Blood Supply
- •Sclera
- •Scleral Histologic Features
- •Episclera
- •Sclera
- •Physiology of Scleral Changes in Myopia
- •Scleral Spur
- •Scleral Opacity
- •Scleral Color
- •Scleral Foramina And Canals
- •Scleral Blood Supply
- •Scleral Innervation
- •Limbal Histologic Features
- •Palisades of Vogt
- •References
- •IRIS
- •Histologic Features of Iris
- •Anterior Border Layer
- •Iris Stroma and Sphincter Muscle
- •Anterior Epithelium and Dilator Muscle
- •Posterior Epithelium
- •Anterior Iris Surface
- •Posterior Iris Surface
- •Iris Color
- •CILIARY BODY
- •Supraciliaris (Supraciliary Lamina)
- •Ciliary Muscle
- •Ciliary Stroma
- •Ciliary Epithelium
- •Choroid
- •Suprachoroid Lamina (Lamina Fusca)
- •Choroidal Stroma
- •Choriocapillaris
- •Functions of Iris
- •Functions of Ciliary Body
- •Aqueous Production
- •Function and Rate of Production
- •Vitreous Production
- •Blood-Aqueous Barrier
- •Functions of Choroid
- •Iris
- •Ciliary Body
- •Choroid
- •References
- •Retinal Pigment Epithelium
- •Photoreceptor Cells
- •Composition of Rods and Cones
- •Outer Segment
- •Cilium
- •Inner Segment
- •Outer Fiber, Cell Body, and Inner Fiber
- •Rod and Cone Morphology
- •Rods
- •Cones
- •Bipolar Cells
- •Ganglion Cells
- •Horizontal Cells
- •Amacrine Cells
- •Interplexiform Neurons
- •Neuroglial Cells
- •Müller Cells
- •Microglial Cells and Astrocytes
- •Retinal Pigment Epithelium
- •Photoreceptor Layer
- •External Limiting Membrane
- •Outer Nuclear Layer
- •Outer Plexiform Layer
- •Inner Nuclear Layer
- •Inner Plexiform Layer
- •Ganglion Cell Layer
- •Nerve Fiber Layer
- •Internal Limiting Membrane
- •Physiology of the rpe
- •Scotopic and Photopic Vision
- •Neural Signals
- •Number and Distribution of Neural Cells
- •Physiology of the neural retina
- •Retinal Synapses
- •Neurotransmitters
- •Phototransduction
- •Information Processing
- •Receptive Fields
- •Light and Dark Adaptation
- •Circadian Rhythm
- •Retinal Metabolism
- •Central Retina
- •Macula Lutea
- •Fovea (Fovea Centralis)
- •Foveola
- •Parafoveal and Perifoveal Areas
- •Peripheral Retina
- •Optic Disc
- •Blood-Retinal Barrier
- •References
- •Lens Capsule
- •Lens Epithelium
- •Lens Fibers
- •Epithelium-Fiber Interface
- •Lens Capsule
- •LENS Fibers
- •Fiber Components
- •Formation of Lens Fibers
- •Fiber Junctions
- •Lens Metabolism
- •Ionic Current
- •Regulation of Fluid Volume
- •Oxidative Stress
- •Cataracts
- •The Physiology of Cataract Formation
- •Age-Related Cortical Cataract
- •Age-Related Nuclear Cataract
- •Posterior Subcapsular Cataract (PSC)
- •Steroid-Induced Cataract
- •References
- •Scleral Spur
- •Trabecular Meshwork
- •Canal of Schlemm
- •Juxtacanalicular Connective Tissue
- •Function of the Filtration Apparatus
- •Posterior Chamber
- •FACTORS AFFECTING Intraocular Pressure
- •Drugs that Effect IOP
- •Vitreous Chamber
- •Vitreal Attachments
- •Vitreous Zones
- •Vitreous Cortex
- •Intermediate Zone
- •Cloquet’s Canal
- •Composition of Vitreous
- •Collagen
- •Hyaluronic Acid (hyaluronan)
- •Hyalocytes
- •Vitreal Function
- •Age-Related Vitreal Changes
- •References
- •Optic Pits
- •Optic Cup, Lens, and hyaloid vessels
- •Optic Cup
- •Lens
- •Hyaloid Arterial System
- •Retinal Pigment Epithelium
- •Neural Retina
- •Retinal Vessels
- •Cornea
- •Sclera
- •UVEA
- •Choroid
- •Ciliary Body
- •Iris
- •Pupillary Membrane
- •Anterior Chamber
- •Vitreous
- •Optic Nerve
- •Eyelids
- •Orbit
- •Extraocular Muscles
- •Nasolacrimal System
- •References
- •Orbital Walls
- •Roof
- •Floor
- •Medial Wall
- •Lateral Wall
- •Orbital Margins
- •Orbital Foramina and Fissures
- •Paranasal Sinuses
- •ORBITAL CONNECTIVE TISSUE
- •Periorbita
- •Orbital Septum
- •Tenon’s Capsule
- •Suspensory Ligament (of Lockwood)
- •Orbital Muscle of Müller
- •Orbital Septal System
- •Orbital Fat
- •Aging Changes in the Orbit
- •References
- •Palpebral Fissure
- •Eyelid Topography
- •Eyelid Margin
- •Eyelid Structures
- •Orbicularis Oculi Muscle
- •Palpebral Portion
- •Orbital Portion
- •Orbicularis Action
- •Superior Palpebral Levator Muscle
- •Levator Aponeurosis
- •Levator Action
- •Retractor of Lower Eyelid
- •Tarsal Muscle (of Müller)
- •Tarsal Plate
- •Palpebral Ligaments
- •Glands of the Lids
- •Histologic Features
- •Skin
- •Muscles
- •Tarsal Plates
- •Palpebral Conjunctiva
- •Glands
- •Innervation of Eyelids
- •Blood Supply of Eyelids
- •Conjunctiva
- •Plica Semilunaris
- •Caruncle
- •Conjunctival Blood Vessels
- •Conjunctival Lymphatics
- •Conjunctival Innervation
- •Lacrimal Secretory System
- •Tear Film Distribution
- •Nasolacrimal Drainage System
- •Puncta and Canaliculi
- •Lacrimal Sac and Nasolacrimal Duct
- •Tear Drainage
- •References
- •Sliding Ratchet Model of Muscle Contraction
- •Structure of the Extraocular Muscles
- •Fick’s Axes
- •Ductions
- •Vergences and Versions
- •Positions of Gaze
- •Origin of the Rectus Muscles
- •Insertions of the Rectus Muscles: Spiral of Tillaux
- •Medial Rectus Muscle
- •Lateral Rectus Muscle
- •Superior Rectus Muscle
- •Inferior Rectus Muscle
- •Superior Oblique Muscle
- •Inferior Oblique Muscle
- •FIBERS OF THE Extraocular muscleS
- •ORBITAL CONNECTIVE TISSUE STRUCTURES
- •Horizontal Rectus Muscles
- •Vertical Rectus Muscles
- •Oblique Muscles
- •Movements From Secondary Positions
- •Vertical Rectus Muscles
- •Oblique Muscles
- •Yoke Muscles
- •Innervation
- •Blood Supply
- •References
- •Ophthalmic Artery
- •Central Retinal Artery
- •Lacrimal Artery
- •Posterior Ciliary Arteries
- •Ethmoid Arteries
- •Supraorbital Artery
- •Muscular Arteries
- •Anterior Ciliary Arteries
- •Medial Palpebral Arteries
- •Supratrochlear Artery
- •Dorsonasal Artery
- •Facial Artery
- •Superficial Temporal Artery
- •Maxillary Artery
- •Superior Ophthalmic Vein
- •Central Retinal Vein
- •Vortex Veins
- •Inferior Ophthalmic Vein
- •Anterior Ciliary Veins
- •Infraorbital Vein
- •Cavernous Sinus
- •References
- •Trigeminal Nerve
- •Ophthalmic Division of Trigeminal Nerve
- •Nasociliary Nerve
- •Frontal Nerve
- •Lacrimal Nerve
- •Ophthalmic Nerve Formation
- •Maxillary Division of Trigeminal Nerve
- •Infraorbital Nerve
- •Zygomatic Nerve
- •Maxillary Nerve Formation
- •Trigeminal Nerve Formation
- •Oculomotor Nerve: Cranial Nerve III
- •Oculomotor Nucleus
- •Oculomotor Nerve Pathway
- •Trochlear Nerve: Cranial Nerve IV
- •Trochlear Nucleus
- •Trochlear Nerve Pathway
- •Abducens Nucleus
- •Abducens Nerve Pathway
- •Superior Orbital Fissure
- •Control of Eye Movements
- •Facial Nerve: Cranial Nerve VII
- •Facial Nucleus
- •Facial Nerve Pathway
- •References
- •Optic Nerve
- •Optic Chiasm
- •Optic Tract
- •Lateral Geniculate Nucleus
- •Optic Radiations (Geniculocalcarine Tract)
- •Primary Visual Cortex (Striate Cortex)
- •Retina
- •Optic Disc
- •Optic Nerve
- •Optic Chiasm
- •Optic Tract
- •Lateral Geniculate Nucleus
- •Optic Radiations
- •Striate Cortex
- •Striate Cortex Maps
- •Macular Sparing
- •References
- •Sympathetic Pathway to Ocular Structures
- •Parasympathetic Pathway to Ocular Structures
- •Neurotransmitters
- •Ophthalmic Agonist Agents
- •Ophthalmic Antagonist Agents
- •Disruption in the Afferent Pathway
- •Disruption within the Central Nervous System
- •Disruption in the Efferent Pathway
- •Disruption in the Sympathetic Pathway
- •References
- •Index
176 Clinical Anatomy of the Visual System
FIGURE 9-25
Pterygium. (From Krachmer JH, Palay DA: Cornea color atlas, St Louis, 1995, Mosby.)
The collagen fibrils that form Tenon’s capsule are arranged in a three-dimensional network of longitudinal, horizontal, and oblique groups.83 In young people, Tenon’s capsule contains collagen fibrils of uniform shape and diameters of 70 to 110 nm; in older individuals there is greater variation in fibril shape, and diameters vary from 30 to 160 nm.83,84 Few fibroblasts and some elastic fibers are present, but in a very small ratio compared with the number of collagen fibrils.84
T E A R F I L M
The tear film, which covers the anterior surface of the globe, has several functions: (1) keeps the surface moist and serves as a lubricant between the globe and eyelids;
(2) traps debris and helps remove sloughed epithelial cells and debris; (3) is the primary source of atmospheric oxygen for the cornea; (4) provides a smooth refractive surface necessary for optimum optical function85; (5) contains antibacterial substances (lysozyme, beta-lysin, lactoferrin, immunoglobulins) to help protect against infection86; (6) helps to maintain corneal hydration by changes in tonicity that occur with evaporation87; and
(7) contains various growth factors and peptides that can regulate ocular surface wound repair.58
The tear film is composed of three layers (Figure 9-26). The outermost is a lipid layer containing waxy esters, cholesterol, and free fatty acids, primarily produced by the meibomian glands. The lipid layer retards evaporation and provides lubrication for smooth eyelid movement. The middle or aqueous layer contains inorganic salts, glucose, urea, enzymes, proteins, glycoproteins, and most of the antibacterial substances.2 It is secreted by the main and accessory lacrimal glands. The innermost or mucous layer acts as an interface that
Lipid layer
Aqueous layer
Mucin layer
Epithelium – glycolcalyx
FIGURE 9-26
Schematic representation of tear film.
facilitates adhesion of the aqueous layer of the tears to the ocular surface.88,89 It is composed of the glycocalyx secretion from the surface epithelia and mucin produced and secreted by the conjunctival goblet cells. Mucins can also bind and entrap bacteria and viruses blocking binding sites on microbes and preventing them from penetrating the ocular surface.58
According to some sources, the tear film is 7 to 10 μm thick, with the aqueous layer accounting for 90% of the thickness.9,90 However, measurements using laser interferometry suggest that the full thickness of the mucous layer was not recognized using conventional measuring methods. Some have estimated tear layer thickness in the range of 34 to 45 μm, with the mucous layer the thickest.91-93 The mucous and aqueous portions are not static and may not remain as separate and distinct layers but may form a sort of gradient hampering accurate measurements.58
LACRIMAL SECRETORY SYSTEM
The secretory system includes the main lacrimal gland, the accessory lacrimal glands, meibomian glands, and the conjunctival goblet cells. The main lacrimal gland is located in a fossa on the temporal side of the orbital plate of the frontal bone, just posterior to the superior orbital margin.
The lacrimal gland is divided into two portions, palpebral and orbital, by the aponeurosis of the levator muscle (see Figure 9-9). The superior orbital portion is larger and almond shaped. The superior surface lies against the periorbita of the lacrimal fossa, the inferior surface rests against the aponeurosis, the medial edge lies against the levator, and the lateral edge lies on the lateral rectus muscle. The palpebral lobe is one third to one half the size of the orbital lobe and is subdivided into two or three sections.38 If the upper lid is everted, the lacrimal gland can be seen above the edge of the upper tarsal plate. Ducts from both portions of the gland exit through the palpebral lobe.
The lacrimal gland consists of lobules made up of numerous acini. Each acinus is an irregular arrangement of secretory cells around a central lumen surrounded by an incomplete layer of myoepithelial cells.94 (Histologically, the main lacrimal gland is identical to the accessory
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CHAPTER 9 t Ocular Adnexa and Lacrimal System |
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lacrimal glands.) A network of ducts connects the acini and drains into one of the main excretory ducts. There are approximately 12 of these ducts, which empty into the conjunctival sac in the superior fornix.49 The secretion is composed of water, electrolytes, and antibacterial agents including lysozyme, lactoferrin, and immunoglobulins. The accessory glands are located in the subconjunctival tissue from the fornix area to near the tarsal plate. Basic secretion maintains the normal volume of the aqueous portion of the tears, and reflex secretion increases the volume in response to a stimulus. Both main and accessory glands play a role in basic and reflex secretion.
The lacrimal gland is supplied by the lacrimal artery, a branch of the ophthalmic artery. Sensory innervation is through the lacrimal nerve, a branch of the ophthalmic division of the trigeminal nerve. The gland receives vasomotor sympathetic innervation and secretomotor parasympathetic innervation.95 Reflex tearing occurs with stimulation of branches of the ophthalmic nerve or in response to external stimuli, such as intense light; the afferent pathway is through the trigeminal nerve, and the parasympathetic pathway is through the facial nerve.
Disagreement still exists regarding the relative contributions of the main and accessory lacrimal glands. In the traditional view, accessory glands provide basic secretion, and the main lacrimal gland is primarily active during reflex or psychogenic stimulation.95 A more recent view holds that all lacrimal glands produce the aqueous layer and that production is stimulus driven, with the rate of production ranging from low levels in sleep to high levels under conditions of stimulation.58,96
Clinical Comment: Tear Film
Assessment
Various clinical tests are used to assess the extent of tear abnormalities, although no single test is thought to be diagnostically effective.97 The Schirmer test is a clinical measure of the adequacy of the aqueous portion of
the tears. A special piece of filter paper is inserted over the inferior eyelid margin. Normally the strip should be moistened by at least 5 mm after 5 minutes.86,98 This test can be done with or without topical anesthesia; the test without topical anesthetic measures both reflex and basic
secretion, and the test with anesthetic measures only basic secretion. The phenol red thread test, which uses a thread treated with a pH indicator, may be used in place of the Schirmer strips.
In another clinical assessment method, fluorescein dye is instilled into the lower cul-de-sac and it spreads throughout the tear film. After a blink the thin lipid upper layer begins to break down, and dry spots appear. The time between the completion of the blink and the first appearance of a dry spot is termed the tear film breakup time (TBUT) and gives an indirect measure of the evaporative rate. Normally the TBUT is greater than 10 seconds and longer than
the time between blinks.2,98-100 A short TBUT can occur if
irregularities or disturbances in the corneal surface prevent complete tear film adherence or if abnormalities exist in the lipid layer causing increased evaporation.101
Clinical Comment: Dry Eye
Alteration in any of the layers of the tear film or in normal lid anatomy and closure can result in depletion of the tear film and cause dry eye, one of the most common disorders seen in clinical eye care practice. Dry eye syndrome has a complex etiology and may be caused by a deficiency or alteration
of any of the layers of the tear film or by an abnormal interaction between the layers.102 Aqueous deficiencies are common, and normal aging can cause a decrease of
aqueous tear production. Patients with rheumatoid arthritis often develop Sjögren syndrome, an autoimmune disease that affects the lacrimal gland, causing a deficiency in the aqueous layer. This can cause an uncomfortable gritty, sandy feeling.103,104 Inflammation of the meibomian glands, meibomianitis, can modify the composition of
the secretion producing a more viscous meibum that does not flow as easily through the pores.105,106 Loss of lipid secretion can lead to alterations in the lipid layer,
allowing increased evaporation of the tear film and leading to dry eye symptoms of irritation and corneal epithelial compromise .36,67 Conditions with deficient secretion of mucus are associated with reduced goblet cell populations, such as chemical burns, Stevens-Johnson syndrome, and ocular pemphigoid.99,107 Complaints associated with dry eye include scratchy and foreign body sensations.
The diagnosis of dry eye is not usually based on a single definitive finding. The instillation of dye (fluorescein, lissamine green, or rose Bengal) can indicate tissue damage that occurs because of a defective tear film but does not indicate the reason.97 The tear film can be augmented by the application of ocular lubricants, consisting of artificial tears during the day and ointments at night. More serious dry eye problems can be treated with procedures that decrease tear drainage; punctual plugs are a temporary solution, and electrocautery can produce permanent closure of the punctum. Recent clinical studies suggest that a subclinical inflammatory condition contributing to dry eye may be successfully treated with topical antiinflammatory agents such as cyclosporin A.108-111
TEAR FILM DISTRIBUTION
The lacrimal gland fluid is secreted into the lateral part of the upper fornix and descends across the anterior surface of the globe. Contraction of the orbicularis forces meibum out of the pores and lid motion can spread the thin lipid layer across the surface. Each blink reforms the tear film, spreading it over the ocular surface.
At the posterior edge of both upper and lower eyelid margins, there is a meniscus of tear fluid. The meniscus at the lower lid is more easily seen. The upper tear meniscus is continuous with the lower meniscus at the lateral canthus, whereas at the medial canthus the tear menisci lead directly to the puncta and drain into them.112 The
