Ординатура / Офтальмология / Английские материалы / Ophthalmology A Short Textbook_Lang_2000
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7.4 Cataract 193
Secondary cataract.
Fig. 7.20 a Regenerative secondary cataracts lead to diminished visual acuity and increased glare. b Nd:YAG laser capsulotomy: the posterior capsulotomy removes the obstruction of the visual axis, and immediately improves vision.
Children with congenital cataract should undergo surgery as early as possible to avoid amblyopia.
The prognosis for successful surgery is less favorable for unilateral cataracts than for bilateral cataracts. This is because the amblyopia of the cataract eye puts it at an irreversible disadvantage in comparison with the fellow eye as the child learns how to see.
Plan for the future when performing surgery: After opening the extremely elastic anterior lens capsule, one can aspirate the soft infantile cortex and
194 7 Lens
Congenital cataract.
Fig. 7.21 One- and-one-half- year-old child with congenital cataract (leukocoria) and esotropia of the right eye.
nucleus. Secondary cataracts are frequent complications in infants. Therefore, the procedure should include a posterior capsulotomy with anterior vitrectomy to ensure an unobstructed visual axis. The operation preserves the equatorial portions of the capsule to permit subsequent implantation of a posterior chamber intraocular lens in later years.
Refraction changes constantly: The refractive power of the eye changes dramatically within a short period of time as the eye grows. The refraction in the eye of a newborn is 30–35 diopters and drops to 15–25 diopters within the first year of life. Refractive compensation for a unilateral cataract is achieved with a soft contact lens (Fig. 7.22). The use of soft contact lenses in infants is difficult and requires the parents’ intensive cooperation. Refractive correction of bilateral cataracts is achieved with cataract eyeglasses.
Refraction should be evaluated by retinoscopy (see Chapter 16) every two months during the first year of life and every three to four months during the second year, and contact lenses and eyeglasses should be changed accordingly.
Implantation of posterior chamber intraocular lenses for congenital cataract is not yet recommended in children under three years of age. This is because experience with the posterior chamber intraocular lens and present follow-up periods are significantly less than the life expectancy of the children. In addition, there is no way to adapt the refractive power of the lens to changing refraction of the eye as the child grows.
Orthoptic postoperative therapy is required: Unilateral cataracts in particular require orthoptic postoperative therapy in the operated eye to close the
7.5 Lens Dislocation 195
Refractive compensation with soft contact lens.
Fig. 7.22 In a unilateral cataract, a contact lens provide refractive compensation (the arrows indicate the edge of the contact lens).
gap with respect to the normal fellow eye. Regular evaluation of retinal fixation is indicated, as is amblyopia treatment (see patching).
7.5Lens Dislocation
Definition
Subluxation (partial dislocation): The suspension of the lens (the zonule fibers) is slackened, and the lens is only partially within the hyaloid fossa (Fig. 7.23).
Luxation (complete dislocation): The lens is torn completely free and has migrated into the vitreous body or, less frequently, into the anterior chamber.
Etiology: There are several causes of lens dislocation (Table 7.5). Most frequently, it is due to trauma (see contusion of the eyeball). Later in life, pseudoexfoliation may also lead to subluxation or luxation of the lens.
Hereditary causes and metabolic disease produce lens displacement early yet on the whole are rare. Additional rare causes include hyperlysinemia (characterized by retarded mental development and seizures) and sulfite oxidase deficiency (which leads to mental retardation and excretion of cysteine in the urine).
The most frequent atraumatic causes of lens dislocation are Marfan’s syndrome, homocystinuria, and Weill-Marchesani syndrome.
196 7 Lens
Table 7.5 Etiology of lens displacement
Causes |
Lens displacement |
|
|
Hereditary causes (rare)
–Ectopia lentis: isolated and monosymptomatic.
–Marfan’s syndrome: characterized by arachnodactyly, long limbs, and laxness of joints.
–Weill-Marchesani syndrome: symptoms include short stature and brachydactyly.
–Homocystinuria (metabolic disease): characterized by oligophrenia, osteoporosis, and skeletal deformities.
Acquired causes
–Trauma (probably the most frequent cause).
–Pseudoexfoliation (in advanced age).
–Ciliary body tumor (rare).
–Large eyes with severe myopia and buphthalmos (rare).
–Complete or partial displacement of the lens (for example, into the anterior chamber).
–Lens is abnormally round; lens displacement is usually superior and temporal; zonule fibers are elongated but frequently intact.
–Lens is abnormally round and often too small; lens is usually eccentric and displaced inferiorly.
–Lens displacement is usually medial and inferior; torn zonule fibers appear as a “permanent wave” on the lens.
–Zonule defects due to deformation can cause subluxation or luxation of the lens.
–Zonule weakness due to loosening of the insertion of the fibers on the lens can cause lens displacement.
–Lens is displaced by tumor.
–Zonule defects due to excessive longitudinal growth can cause lens displacement.
Symptoms: Slight displacement may be of no functional significance to the patient. More pronounced displacement produces severe optical distortion with loss of visual acuity.
Diagnostic considerations: Cardinal symptoms include tremulous motion of the iris and lens when the eye moves (iridodonesis and phacodonesis). These symptoms are detectable under slit-lamp examination.
Treatment: Optical considerations (see symptoms) and the risk of secondary angle closure glaucoma from protrusion of the iris and dislocation of the lens into the anterior chamber are indications for removal of the lens.
7.5 Lens Dislocation 197
Subluxation of the lens in Marfan’s syndrome.
Fig. 7.23 The lens is displaced superiorly and medially. As the zonule fibers are intact, a certain measure of accommodation is still possible.
199
8Uveal Tract
(Vascular pigmented layer)
Gabriele E. Lang and Gerhard K. Lang
8.1Basic Knowledge
Structure: The uveal tract (also known as the vascular pigmented layer, vascular tunic, and uvea) takes its name from the Latin uva (grape) because the dark pigmentation and shape of the structure are reminiscent of a grape. The uveal tract consists of the following structures:
Iris,
Ciliary body,
Choroid.
Position: The uveal tract lies between the sclera and retina.
Neurovascular supply: Arterial supply to the uveal tract is provided by the ophthalmic artery.
The short posterior ciliary arteries enter the eyeball with the optic nerve and supply the choroid.
The long posterior ciliary arteries course along the interior surface of the sclera to the ciliary body and the iris. They form the major arterial circle at the root of the iris and the minor arterial circle in the collarette of the iris.
The anterior ciliary arteries originate from the vessels of the rectus muscles and communicate with the posterior ciliary vessels.
Venous blood drains through four to eight vorticose or vortex veins that penetrate the sclera posterior to the equator and join the superior and inferior ophthalmic veins (Fig. 8.1). Sensory supply is provided by the long and short ciliary nerves.
8.1.1Iris
Structure and function: The iris consists of two layers:
The anterior mesodermal stromal layer.
The posterior ectodermal pigmented epithelial layer.
The posterior layer is opaque and protects the eye against excessive incident light. The anterior surface of the lens and the pigmented layer are so close together near the pupil that they can easily form adhesions in inflammation.
200 8 Uveal Tract (Vascular pigmented layer)
Vascular supply to the uveal tract.
Minor arterial circle of the iris (collarette of the iris)
Major arterial circle of the iris
Anterior ciliary artery
Long posterior ciliary artery
Vorticose vein
Short posterior ciliary artery
Fig. 8.1 See discussion in text.
The collarette of the iris covering the minor arterial circle of the iris divides the stroma into pupillary and ciliary portions. The pupillary portion contains the sphincter muscle, which is supplied by parasympathetic nerve fibers, and the dilator pupillae muscle, supplied by sympathetic nerve fibers. These muscles regulate the contraction and dilation of the pupil so that the iris may be regarded as the aperture of the optical system of the eye.
Pupil dilation is sometimes sluggish in preterm infants and the newborn because the dilator pupillae muscle develops relatively late.
Surface: The normal iris has a richly textured surface structure with crypts (tissue gaps) and interlinked trabeculae. A faded surface structure can be a sign of inflammation (see iridocyclitis).
8.2 Examination Methods 201
Color: The color of the iris varies in the individual according to the melanin content of the melanocytes (pigment cells) in the stroma and epithelial layer.
Eyes with a high melanin content are dark brown, whereas eyes with less melanin are grayish-blue. Caucasians at birth always have a grayish-blue iris as the pigmented layer only develops gradually during the first year of life. Even in albinos (see impaired melanin synthesis), the eyes have a grayishblue iris because of the melanin deficiency. Under slit lamp retroillumination they appear reddish due to the fundus reflex.
8.1.2Ciliary Body
Position and structure: The ciliary body extends from the root of the iris to the ora serrata, where it joins the choroid. It consists of anterior pars plicata and the posterior pars plana, which lies 3.5 mm posterior to the limbus. Numerous ciliary processes extend into the posterior chamber of the eye. The suspensory ligament, the zonule, extends from the pars plana and the intervals between the ciliary processes to the lens capsule.
Function: The ciliary muscle is responsible for accommodation. The doublelayered epithelium covering the ciliary body produces the aqueous humor.
8.1.3Choroid
Position and structure: The choroid is the middle tunic of the eyeball. It is bounded on the interior by Bruch’s membrane. The choroid is highly vascularized, containing a vessel layer with large blood vessels and a capillary layer. The blood flow through the choroid is the highest in the entire body.
Function: The choroid regulates temperature and supplies nourishment to the outer layers of the retina.
8.2Examination Methods
The slit lamp is used to examine the surface of the iris under a focused beam of light. Normally no vessels will be visible.
Iris vessels are only visible in atrophy of the iris, inflammation, or as neovascularization in rubeosis iridis (see Fig. 8.12).
Where vessels are present, they can be visualized by iris angiography after intravenous injection of fluorescein sodium dye.
Defects in the pigmented layer of the iris appear red under retroillumination with a slit lamp (see Fig. 8.6). Slit lamp biomicroscopy visualizes individual cells such as melanin cells at 40-power magnification.
The anterior chamber is normally transparent. Inflammation can increase the permeability of the vessels of the iris and compromise the barrier
202 8 Uveal Tract (Vascular pigmented layer)
between blood and aqueous humor. Opacification of the aqueous humor by proteins may be observed with the aid of a slit lamp when the eye is illuminated with a lateral focal beam of light (Tyndall effect). This method can also be used to diagnose cells in the anterior chamber in the presence of inflammation.
Direct inspection of the root of the iris is not possible because it does not lie within the line of sight. However, it can be indirectly visualized by gonioscopy. Inspection of the posterior portion of the pars plana requires a threemirror lens. The globe is also indented with a metal rod to permit visualization of this part of the ciliary body (for example in the presence of a suspected malignant melanoma of the ciliary body).
The pigmented epithelium of the retina permits only limited evaluation of the choroid by ophthalmoscopy and fluorescein angiography or indocyanine green angiography. Changes in the choroid such as tumors or hemangiomas can be visualized by ultrasound examination. Where a tumor is suspected, transillumination of the eye is indicated. After administration of topical anesthesia, a fiberoptic light source is placed on the eyeball to visualize the shadow of the tumor on the red of the fundus.
8.3Developmental Anomalies
8.3.1Aniridia
Aniridia is the absence of the iris. This generally bilateral condition is transmitted as an autosomal dominant trait or occurs sporadically. Aniridia may also be traumatic and can result from penetrating injuries. However, peripheral remnants of the iris are usually still present so that ciliary villi and zonule fibers will be visualized under slit-lamp examination (Fig. 8.2).
In sporadic aniridia, a Wilms’ tumor of the kidney should be excluded.
Vision is severely compromised as a result of the foveal hypoplasia. The disorder is frequently associated with nystagmus, amblyopia, buphthalmos, and cataract.
Visual acuity will generally be reduced in the presence of nystagmus.
