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EYE AND EAR DISORDERS
1. F R O N T I E R University
Lect 12. Eye and Ear
Disorder:
Dr: Ayub Abdulkadir Abdi
26/12/2021
2.
3. Arcus senilis:
ā¢ Most often occurs in elderly Gray-opaque ring at
the corneal margin (periphery of cornea}
ā¢ Cholesterol deposits in corneal stroma; may
indicate hypercholesterolemia if the patient is <50
years old and a smoker.
11. Acanthamoeia infection:
ā¢ Severe keratoconjunctivitis in patients who do not
clean their contact lenses properly.
ā¢ Treatment:
ā¢ Propamidine + polymyxin/neomycin/gramicidin
ophthalmic.
12. Stye:
ā¢ Infection of the eyelid.
ā¢ Most commonly due to S. aureus.
ā¢ Treatment:
ā¢ Hot packs + dicloxacillin.
13. Chalazion:
ā¢ Granulomatous inflammation involving the
meibomian gland in the eyelid; usually disappear
on their own within 2 months.
ā¢ Treatment:
ā¢ They do not disappear,
ā¢ Use an intralesional corticosteroid Injection.
ā¢ Remove it surgically.
14.
15.
16. Orbita cellulitis:
ā¢ Pentorbital redness and swelling that is often
secondary to sinusitis (e.g., ethmoiditis in children).
ā¢ Pathogens: S. pneumonia, H. influenza.
ā¢ Clinical feature: Fever, proptosis (eye bulges out),
periorbital swelling, ophthalmoplegia (eye
movement impaired).
ā¢ Normal retinal examination.
ā¢ Treatment:
ā¢ Naftcillin + ceftriaxone + metronidazole.
17.
18. Orbital fracture:
ā¢ Most often associated with blunt trauma to the
eye that produces an orbital floor fracture.
ā¢ Often associated with edema and ecchymoses of
the eyelids and periorbital region ("RACCAON"
EYES).
ā¢ Clinical feature: Vertical diplopia, prolapse of
orbital contents into the maxillary sinus (sunken
eye), damage to infraorbital nerve may occur in
severe fractures.
ā¢ Treatment:
ā¢ Varies according to degree of severity.
19.
20. Pterygium:
ā¢ Raised, triangular encroachment of thickened
conjunctiva on the nasal side of the conjunctiva;
may grow onto the cornea.
ā¢ Due to excessive exposure to wind, sun, and sand.
ā¢ Treatment:
ā¢ Surgical removal.
21. Pinguecula:
ā¢ Yellow-white conjunctival degeneration at the
junction of cornea and sclera on the temporal side
of the conjunctiva.
ā¢ Does not grow onto the cornea like a pterygium
does.
ā¢ Usually requires no treatment.
22. Optic neuritis:
ā¢ Inflammation of optic nerve.
ā¢ Causes: multiple sclerosis (most common),
methanol poisoning.
ā¢ Clinical feature: Blurry vision or loss of vision, may
cause optic atrophy.
ā¢ Treatment:
ā¢ Corticosteroids
23.
24. Central retinal artery occlusion:
ā¢ Causes: embolization of plaque material from
ipsilateral carotid or ophthalmic artery; giant cell
temporal arteritis involving the ophthalmic artery.
ā¢ Clinical feature: Sudden, painless, complete loss of
vision in one eye, pallor of optic disk due to narrowed
arteries, "boxcar" segmentation of Blood in retinal
veins, and cherry red macula.
ā¢ Treatment:
1. Acetazolamide to lower intraocular pressure.
2. Carbogen (CO, dilates + O2).
3. Hyperbaric 0, therapy.
25.
26.
27. Central retinal vein occlusion:
ā¢ Causes: hypercoagulable state (e.g. polythemia
vera).
ā¢ Clinical feature: Sudden, painless, unilateral loss of
vision, swelling of optic disk, and engorged retinal
veins with hemorrhage ("blood and thunder"
appearance).
ā¢ Treatment:
1. Intravitreal injections.
2. Laser photocoagulation.
28.
29. Glaucoma:
ā¢ Increased intraccular pressure.
ā¢ Chronic open-angle type:
ā¢ Decreased rate of aqueous outflow into the canal
of Schlemm.
ā¢ Common in persons with severe near-sightedness;
bilateral aching eyes; pathologic cupping of the
optic disks; night blindness and gradual loss of
peripheral vision leading to tunnel vision and
blindness.
30. ā¢ Treatment:
ā¢ Drugs_
1st: B-blockers (e.g., timolol; decrease rate of flow into eye).
2nd: prostaglandins, Ī±-adrenergic agonists, pilocarpine,
carbonic anhydrase inhibitors.
ā¢ Laser trabeculoplasty if the drugs fail.
31. ā¢ Acute angle-closure type:
ā¢ Narrowing of anterior chamber angle; medical
emergency; precipitated by mydriatic agent,
ā¢ Clinical feature: uveitis, lens dislocation; severe
pain associated with photophobia and blurry vision;
red eye with a steamy cornea; pupil fixed and
nonreactive to light.
ā¢ Treatment:
ā¢ Pilocarpine + systemic carbonic anhydrase inhibitor
to lower pressure to allow for laser surgery.
32. Optic nerve atrophy:
ā¢ Pale optic disk.
ā¢ Most commonly due to optic neuritis or glaucoma.
ā¢ No effective treatment
33. Uveitis:
ā¢ Inflammation of the uveal tract (iris, ciliary body,
choroid).
ā¢ Causes: sarcoidosis, ulcerative colitis, ankylosing
spondylitis.
ā¢ Clinical feature: Pain with Blurry vision, miotic pupil,
circumcorneal ciliary body vascular congestion, normal
intraocular pressure, adhesions between iris and
anterior lens capsule.
ā¢ Treatment:
1. Corticosteroids (oral or topical).
2. Atropine.
34.
35. Macular degeneration:
ā¢ Most common cause of permanent visual loss in the
elderly.
ā¢ Disruption of Bruch membrane in the retina.
ā¢ Dry type: thinning of the retina and formation of
yellowish white deposits called drusen.
ā¢ Wet type: extension of the dry type; vessels under the
retina hemorrhage causing retinal cells to die, creating
blind spot or distorted central vision.
ā¢ Treatment:
ā¢ Antioudants may decrease risk.
ā¢ Antiangiogenics (drugs that block vascular growth
factors).
ā¢ Insertion of special intraocular lens.
36.
37.
38. Cytomegalovirus āCMVā retinitis:
ā¢ Most common cause of blindness in AIDS; usually
occurs when the CD4 T helper cell count is <50Āµl
usually painless.
ā¢ But in case of varicella/zoster virus retinitis is
usually painful.
ā¢ Cotton-wool exudates and retinal hemorrhages .
ā¢ Treatment:
ā¢ Oral, IV intraocular ganciclovir or foscarnet.
39.
40. Cataracts:
ā¢ Opacity in the lens.
ā¢ Causes: advanced age (most common), diabetes
mellitus (osmotic damage), infection (e.g., rubella),
corticosteroids.
ā¢ Common in congenital infections (e.g. CMV, rubella).
ā¢ Treatment:
ā¢ Cataract extraction.
42. ā¢Retinoblastoma:
ā¢ It is an uncommon neoplasm.
ā¢ Incidence in the United Kingdom of around 1 per
20 000 live births.
ā¢ 5-10% of cases are familial.
ā¢ It demonstrates homozygous deletion of the Rb
gene (located on chromosome 13 at band q14).
ā¢ The tumor is the prototype of the ātwo-hitā
hypothesis of Knudson:
ā¢ 1st germ line and 2nd somatic mutation.
ā¢ Both deletions are required for tumor
development.
43.
44.
45. Meniere disease:
ā¢ Increased endolymph in inner ear and boss of
cochlear hairs.
ā¢ Clinical feature: Dizziness, vertigo, tinnitus,
sensorineural hearing loss.
ā¢ Treatment:
1. Hydrochlorothiazide + triamterene.
2. Surgery in resistant cases.
50. Conduction defect:
ā¢ Weber test:
ā¢ Lateralizes to affected ear.
ā¢ Due to degeneration of cochlear hairs.
ā¢ Treatment:
1. Amplification devices.
2. Cochlear implants.
51. Otosclerosis:
ā¢ Most common cause of conduction deafness in elderly.
ā¢ Due to fusion of middle ear ossicles.
ā¢ Other causes of conduction defects:
a) Impacted cerumen in outer ear canal.
b) Otitis media.
ā¢ Treatment:
1. Amplification devices.
2. Surgery.
52. Otitis media:
ā¢ Most common cause of conduction deafness in
children.
ā¢ Usually due to Streptococcus pneumonia.
ā¢ Other causes: Haemophilus influenzae, Moraxeila
catarrhalis.
ā¢ Treatment:
ā¢ Antipyrine and benzocaine ear drops for pain.
ā¢ Controversy regarding antibiotics; those that use
antibiotics most frequently use amoxicillin-clavulanate
53.
54. External otitis:
ā¢ Inflammation of outer ear canal
ā¢ "Swimmer's earā: due to Pseudomonas aeruginosa,
Staphylococcus aureus, Aspergilius species.
ā¢ Treatment:
ā¢ Ear drops-polymyxin B + neomycin + hydrocortisone +
selenium sulfide shampoo.
ā¢ Malignant external otitis: severe infection of outer ear
canal in patients with diabetes mellitus; Pseudomonas
aeruginosa most common cause.
ā¢ Treatment:
ā¢ Imipenem-cilastatin.