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F R O N T I E R University
Lect 12. Eye and Ear
Disorder:
Dr: Ayub Abdulkadir Abdi
26/12/2021
Arcus senilis:
• Most often occurs in elderly Gray-opaque ring at
the corneal margin (periphery of cornea}
• Cholesterol deposits in corneal stroma; may
indicate hypercholesterolemia if the patient is <50
years old and a smoker.
Ophthalmia neonatorum:
• Conjunctivitis in newbom.
• Pathogens: Neisseria gonorrhoeae (first week; 2-4
days), Chlamydia trachomatis (second week; 3-10
days).
• Treatment:
• N gonorrhea: ceftriaxone.
• Chlamydia trachomatis: erythromycin.
• Erythromycin eye drops (chemical irritation)
Bacterial conjunctivitis:
• Purulent conjunctivitis; pain but no Blurry vision
• Pathogens: Staphylococcus aureus (most common),
pneumoniae, Haemophilus infivenzae
(Haemophilus aegyotius, pinkeye).
• Treatment: gatifloxacin ophthalmic solution.
Viral conjunctivitis:
• Watery exudates.
• Adenovirus: viral cause of pinkeye, painful preauricular
lymphadenopathy.
• No treatment.
• HSV-1: keratoconjunctivitis with dendritic ulcers noted
with fluorescein staining.
• Treatment: trifluridine ophthalmic.
Allergic conjunctivitis:
• Seasonal itching of eyes.
• Treatment antihistamine ophthalmic solutions;
olopatadine (mast cell stabilizer).
Acanthamoeia infection:
• Severe keratoconjunctivitis in patients who do not
clean their contact lenses properly.
• Treatment:
• Propamidine + polymyxin/neomycin/gramicidin
ophthalmic.
Stye:
• Infection of the eyelid.
• Most commonly due to S. aureus.
• Treatment:
• Hot packs + dicloxacillin.
Chalazion:
• Granulomatous inflammation involving the
meibomian gland in the eyelid; usually disappear
on their own within 2 months.
• Treatment:
• They do not disappear,
• Use an intralesional corticosteroid Injection.
• Remove it surgically.
Orbita cellulitis:
• Pentorbital redness and swelling that is often
secondary to sinusitis (e.g., ethmoiditis in children).
• Pathogens: S. pneumonia, H. influenza.
• Clinical feature: Fever, proptosis (eye bulges out),
periorbital swelling, ophthalmoplegia (eye
movement impaired).
• Normal retinal examination.
• Treatment:
• Naftcillin + ceftriaxone + metronidazole.
Orbital fracture:
• Most often associated with blunt trauma to the
eye that produces an orbital floor fracture.
• Often associated with edema and ecchymoses of
the eyelids and periorbital region ("RACCAON"
EYES).
• Clinical feature: Vertical diplopia, prolapse of
orbital contents into the maxillary sinus (sunken
eye), damage to infraorbital nerve may occur in
severe fractures.
• Treatment:
• Varies according to degree of severity.
Pterygium:
• Raised, triangular encroachment of thickened
conjunctiva on the nasal side of the conjunctiva;
may grow onto the cornea.
• Due to excessive exposure to wind, sun, and sand.
• Treatment:
• Surgical removal.
Pinguecula:
• Yellow-white conjunctival degeneration at the
junction of cornea and sclera on the temporal side
of the conjunctiva.
• Does not grow onto the cornea like a pterygium
does.
• Usually requires no treatment.
Optic neuritis:
• Inflammation of optic nerve.
• Causes: multiple sclerosis (most common),
methanol poisoning.
• Clinical feature: Blurry vision or loss of vision, may
cause optic atrophy.
• Treatment:
• Corticosteroids
Central retinal artery occlusion:
• Causes: embolization of plaque material from
ipsilateral carotid or ophthalmic artery; giant cell
temporal arteritis involving the ophthalmic artery.
• 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.
• Treatment:
1. Acetazolamide to lower intraocular pressure.
2. Carbogen (CO, dilates + O2).
3. Hyperbaric 0, therapy.
Central retinal vein occlusion:
• Causes: hypercoagulable state (e.g. polythemia
vera).
• Clinical feature: Sudden, painless, unilateral loss of
vision, swelling of optic disk, and engorged retinal
veins with hemorrhage ("blood and thunder"
appearance).
• Treatment:
1. Intravitreal injections.
2. Laser photocoagulation.
Glaucoma:
• Increased intraccular pressure.
• Chronic open-angle type:
• Decreased rate of aqueous outflow into the canal
of Schlemm.
• 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.
• Treatment:
• Drugs_
1st: B-blockers (e.g., timolol; decrease rate of flow into eye).
2nd: prostaglandins, α-adrenergic agonists, pilocarpine,
carbonic anhydrase inhibitors.
• Laser trabeculoplasty if the drugs fail.
• Acute angle-closure type:
• Narrowing of anterior chamber angle; medical
emergency; precipitated by mydriatic agent,
• 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.
• Treatment:
• Pilocarpine + systemic carbonic anhydrase inhibitor
to lower pressure to allow for laser surgery.
Optic nerve atrophy:
• Pale optic disk.
• Most commonly due to optic neuritis or glaucoma.
• No effective treatment
Uveitis:
• Inflammation of the uveal tract (iris, ciliary body,
choroid).
• Causes: sarcoidosis, ulcerative colitis, ankylosing
spondylitis.
• Clinical feature: Pain with Blurry vision, miotic pupil,
circumcorneal ciliary body vascular congestion, normal
intraocular pressure, adhesions between iris and
anterior lens capsule.
• Treatment:
1. Corticosteroids (oral or topical).
2. Atropine.
Macular degeneration:
• Most common cause of permanent visual loss in the
elderly.
• Disruption of Bruch membrane in the retina.
• Dry type: thinning of the retina and formation of
yellowish white deposits called drusen.
• Wet type: extension of the dry type; vessels under the
retina hemorrhage causing retinal cells to die, creating
blind spot or distorted central vision.
• Treatment:
• Antioudants may decrease risk.
• Antiangiogenics (drugs that block vascular growth
factors).
• Insertion of special intraocular lens.
Cytomegalovirus ‘CMV’ retinitis:
• Most common cause of blindness in AIDS; usually
occurs when the CD4 T helper cell count is <50µl
usually painless.
• But in case of varicella/zoster virus retinitis is
usually painful.
• Cotton-wool exudates and retinal hemorrhages .
• Treatment:
• Oral, IV intraocular ganciclovir or foscarnet.
Cataracts:
• Opacity in the lens.
• Causes: advanced age (most common), diabetes
mellitus (osmotic damage), infection (e.g., rubella),
corticosteroids.
• Common in congenital infections (e.g. CMV, rubella).
• Treatment:
• Cataract extraction.
Malignant tumors:
• Retinoblastoma in children ("white eye reflex).
• Malignant melanoma in adults.
• Treatment:
• Enucleation.
•Retinoblastoma:
• It is an uncommon neoplasm.
• Incidence in the United Kingdom of around 1 per
20 000 live births.
• 5-10% of cases are familial.
• It demonstrates homozygous deletion of the Rb
gene (located on chromosome 13 at band q14).
• The tumor is the prototype of the “two-hit”
hypothesis of Knudson:
• 1st germ line and 2nd somatic mutation.
• Both deletions are required for tumor
development.
Meniere disease:
• Increased endolymph in inner ear and boss of
cochlear hairs.
• Clinical feature: Dizziness, vertigo, tinnitus,
sensorineural hearing loss.
• Treatment:
1. Hydrochlorothiazide + triamterene.
2. Surgery in resistant cases.
Sensonneural defect:
• Weber test:
• Lateralizes to normal ear (contralateral ear is
affected).
Conduction defect:
• Weber test:
• Lateralizes to affected ear.
• Due to degeneration of cochlear hairs.
• Treatment:
1. Amplification devices.
2. Cochlear implants.
Otosclerosis:
• Most common cause of conduction deafness in elderly.
• Due to fusion of middle ear ossicles.
• Other causes of conduction defects:
a) Impacted cerumen in outer ear canal.
b) Otitis media.
• Treatment:
1. Amplification devices.
2. Surgery.
Otitis media:
• Most common cause of conduction deafness in
children.
• Usually due to Streptococcus pneumonia.
• Other causes: Haemophilus influenzae, Moraxeila
catarrhalis.
• Treatment:
• Antipyrine and benzocaine ear drops for pain.
• Controversy regarding antibiotics; those that use
antibiotics most frequently use amoxicillin-clavulanate
External otitis:
• Inflammation of outer ear canal
• "Swimmer's ear”: due to Pseudomonas aeruginosa,
Staphylococcus aureus, Aspergilius species.
• Treatment:
• Ear drops-polymyxin B + neomycin + hydrocortisone +
selenium sulfide shampoo.
• Malignant external otitis: severe infection of outer ear
canal in patients with diabetes mellitus; Pseudomonas
aeruginosa most common cause.
• Treatment:
• Imipenem-cilastatin.
EYE AND EAR DISORDERS

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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: • Most often occurs in elderly Gray-opaque ring at the corneal margin (periphery of cornea} • Cholesterol deposits in corneal stroma; may indicate hypercholesterolemia if the patient is <50 years old and a smoker.
  • 4. Ophthalmia neonatorum: • Conjunctivitis in newbom. • Pathogens: Neisseria gonorrhoeae (first week; 2-4 days), Chlamydia trachomatis (second week; 3-10 days). • Treatment: • N gonorrhea: ceftriaxone. • Chlamydia trachomatis: erythromycin. • Erythromycin eye drops (chemical irritation)
  • 5.
  • 6. Bacterial conjunctivitis: • Purulent conjunctivitis; pain but no Blurry vision • Pathogens: Staphylococcus aureus (most common), pneumoniae, Haemophilus infivenzae (Haemophilus aegyotius, pinkeye). • Treatment: gatifloxacin ophthalmic solution.
  • 7.
  • 8. Viral conjunctivitis: • Watery exudates. • Adenovirus: viral cause of pinkeye, painful preauricular lymphadenopathy. • No treatment. • HSV-1: keratoconjunctivitis with dendritic ulcers noted with fluorescein staining. • Treatment: trifluridine ophthalmic.
  • 9.
  • 10. Allergic conjunctivitis: • Seasonal itching of eyes. • Treatment antihistamine ophthalmic solutions; olopatadine (mast cell stabilizer).
  • 11. Acanthamoeia infection: • Severe keratoconjunctivitis in patients who do not clean their contact lenses properly. • Treatment: • Propamidine + polymyxin/neomycin/gramicidin ophthalmic.
  • 12. Stye: • Infection of the eyelid. • Most commonly due to S. aureus. • Treatment: • Hot packs + dicloxacillin.
  • 13. Chalazion: • Granulomatous inflammation involving the meibomian gland in the eyelid; usually disappear on their own within 2 months. • Treatment: • They do not disappear, • Use an intralesional corticosteroid Injection. • Remove it surgically.
  • 14.
  • 15.
  • 16. Orbita cellulitis: • Pentorbital redness and swelling that is often secondary to sinusitis (e.g., ethmoiditis in children). • Pathogens: S. pneumonia, H. influenza. • Clinical feature: Fever, proptosis (eye bulges out), periorbital swelling, ophthalmoplegia (eye movement impaired). • Normal retinal examination. • Treatment: • Naftcillin + ceftriaxone + metronidazole.
  • 17.
  • 18. Orbital fracture: • Most often associated with blunt trauma to the eye that produces an orbital floor fracture. • Often associated with edema and ecchymoses of the eyelids and periorbital region ("RACCAON" EYES). • Clinical feature: Vertical diplopia, prolapse of orbital contents into the maxillary sinus (sunken eye), damage to infraorbital nerve may occur in severe fractures. • Treatment: • Varies according to degree of severity.
  • 19.
  • 20. Pterygium: • Raised, triangular encroachment of thickened conjunctiva on the nasal side of the conjunctiva; may grow onto the cornea. • Due to excessive exposure to wind, sun, and sand. • Treatment: • Surgical removal.
  • 21. Pinguecula: • Yellow-white conjunctival degeneration at the junction of cornea and sclera on the temporal side of the conjunctiva. • Does not grow onto the cornea like a pterygium does. • Usually requires no treatment.
  • 22. Optic neuritis: • Inflammation of optic nerve. • Causes: multiple sclerosis (most common), methanol poisoning. • Clinical feature: Blurry vision or loss of vision, may cause optic atrophy. • Treatment: • Corticosteroids
  • 23.
  • 24. Central retinal artery occlusion: • Causes: embolization of plaque material from ipsilateral carotid or ophthalmic artery; giant cell temporal arteritis involving the ophthalmic artery. • 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. • Treatment: 1. Acetazolamide to lower intraocular pressure. 2. Carbogen (CO, dilates + O2). 3. Hyperbaric 0, therapy.
  • 25.
  • 26.
  • 27. Central retinal vein occlusion: • Causes: hypercoagulable state (e.g. polythemia vera). • Clinical feature: Sudden, painless, unilateral loss of vision, swelling of optic disk, and engorged retinal veins with hemorrhage ("blood and thunder" appearance). • Treatment: 1. Intravitreal injections. 2. Laser photocoagulation.
  • 28.
  • 29. Glaucoma: • Increased intraccular pressure. • Chronic open-angle type: • Decreased rate of aqueous outflow into the canal of Schlemm. • 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. • Treatment: • Drugs_ 1st: B-blockers (e.g., timolol; decrease rate of flow into eye). 2nd: prostaglandins, α-adrenergic agonists, pilocarpine, carbonic anhydrase inhibitors. • Laser trabeculoplasty if the drugs fail.
  • 31. • Acute angle-closure type: • Narrowing of anterior chamber angle; medical emergency; precipitated by mydriatic agent, • 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. • Treatment: • Pilocarpine + systemic carbonic anhydrase inhibitor to lower pressure to allow for laser surgery.
  • 32. Optic nerve atrophy: • Pale optic disk. • Most commonly due to optic neuritis or glaucoma. • No effective treatment
  • 33. Uveitis: • Inflammation of the uveal tract (iris, ciliary body, choroid). • Causes: sarcoidosis, ulcerative colitis, ankylosing spondylitis. • Clinical feature: Pain with Blurry vision, miotic pupil, circumcorneal ciliary body vascular congestion, normal intraocular pressure, adhesions between iris and anterior lens capsule. • Treatment: 1. Corticosteroids (oral or topical). 2. Atropine.
  • 34.
  • 35. Macular degeneration: • Most common cause of permanent visual loss in the elderly. • Disruption of Bruch membrane in the retina. • Dry type: thinning of the retina and formation of yellowish white deposits called drusen. • Wet type: extension of the dry type; vessels under the retina hemorrhage causing retinal cells to die, creating blind spot or distorted central vision. • Treatment: • Antioudants may decrease risk. • Antiangiogenics (drugs that block vascular growth factors). • Insertion of special intraocular lens.
  • 36.
  • 37.
  • 38. Cytomegalovirus ‘CMV’ retinitis: • Most common cause of blindness in AIDS; usually occurs when the CD4 T helper cell count is <50µl usually painless. • But in case of varicella/zoster virus retinitis is usually painful. • Cotton-wool exudates and retinal hemorrhages . • Treatment: • Oral, IV intraocular ganciclovir or foscarnet.
  • 39.
  • 40. Cataracts: • Opacity in the lens. • Causes: advanced age (most common), diabetes mellitus (osmotic damage), infection (e.g., rubella), corticosteroids. • Common in congenital infections (e.g. CMV, rubella). • Treatment: • Cataract extraction.
  • 41. Malignant tumors: • Retinoblastoma in children ("white eye reflex). • Malignant melanoma in adults. • Treatment: • Enucleation.
  • 42. •Retinoblastoma: • It is an uncommon neoplasm. • Incidence in the United Kingdom of around 1 per 20 000 live births. • 5-10% of cases are familial. • It demonstrates homozygous deletion of the Rb gene (located on chromosome 13 at band q14). • The tumor is the prototype of the “two-hit” hypothesis of Knudson: • 1st germ line and 2nd somatic mutation. • Both deletions are required for tumor development.
  • 43.
  • 44.
  • 45. Meniere disease: • Increased endolymph in inner ear and boss of cochlear hairs. • Clinical feature: Dizziness, vertigo, tinnitus, sensorineural hearing loss. • Treatment: 1. Hydrochlorothiazide + triamterene. 2. Surgery in resistant cases.
  • 46.
  • 47.
  • 48.
  • 49. Sensonneural defect: • Weber test: • Lateralizes to normal ear (contralateral ear is affected).
  • 50. Conduction defect: • Weber test: • Lateralizes to affected ear. • Due to degeneration of cochlear hairs. • Treatment: 1. Amplification devices. 2. Cochlear implants.
  • 51. Otosclerosis: • Most common cause of conduction deafness in elderly. • Due to fusion of middle ear ossicles. • Other causes of conduction defects: a) Impacted cerumen in outer ear canal. b) Otitis media. • Treatment: 1. Amplification devices. 2. Surgery.
  • 52. Otitis media: • Most common cause of conduction deafness in children. • Usually due to Streptococcus pneumonia. • Other causes: Haemophilus influenzae, Moraxeila catarrhalis. • Treatment: • Antipyrine and benzocaine ear drops for pain. • Controversy regarding antibiotics; those that use antibiotics most frequently use amoxicillin-clavulanate
  • 53.
  • 54. External otitis: • Inflammation of outer ear canal • "Swimmer's ear”: due to Pseudomonas aeruginosa, Staphylococcus aureus, Aspergilius species. • Treatment: • Ear drops-polymyxin B + neomycin + hydrocortisone + selenium sulfide shampoo. • Malignant external otitis: severe infection of outer ear canal in patients with diabetes mellitus; Pseudomonas aeruginosa most common cause. • Treatment: • Imipenem-cilastatin.