Retina and Optic Nerve Flashcards

1
Q

What causes Retinal Dysplasia?

A
  • Usually inherited
    • can be associated with multiple ocular anomalies
  • Other causes:
    • maternal viral infections
      • canine herpes and parvo viruses
      • feline panleukopenia
    • Vit A deficiency
    • X-ray irradiation
    • Drug toxicities
    • Intrauterine trauma
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2
Q

What are the features of Retinal dysplasia?

A
  • Retinal folds
    • dots, linear, or V/Y shaped
    • dull grey streaks in tapetum
    • depigmented or white in non-tapetal
  • Geographic retinal dysplasia
    • larger, irregular often horseshoe-shaped hyperreflective lesion in tapetal fundus
  • Retinal detachment - most severe form
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3
Q

What is Hereditary Oculoskeletal dysplasia

A
  • Retinal dysplasia in Labrador Retrievers
  • Incomplete dominant ocular abnormalities
    • cataracts, vitreous strands, persistent hyaloid remnants, retinal folds, retinal dysplasia, rhegmatogenous retinal detachments
  • Recessive-skeletal abnormalities
    • Short forelimbs and abnormal radius and ulna, hip dysplasia, hypoplasia of anconeal and coronoid processes
  • Similar condition in Samoyeds
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4
Q

What is Collie Eye Anomaly (CEA)?

A
  • Collies
    • High prevalence
      • reduction due to selective breeding
    • Other breeds: shetland sheepdogs, australian shepherds, Border collies
  • Simple autosomal recessive suspected - but condition may be polygenic
  • Abnormal mesodermal differentiation
    • Choroidal hypoplasia
      • Hallmark sign
      • Incidentally found (no clinical signs)
  • Optic nerve coloboma
    • More severe signs
    • Retinal detachment
    • hyphema
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5
Q

What are the clinical signs of progressive retinal atrophy?

A
  • Bilateral - progressive loss of vision - blindness
  • Decreased night vision (nyctalopia) usually first sign
  • Progressive decrease in PLR
  • Larger than normal resting pupil size
    • Owner will sometimes report increase in “eye shine”
  • Cataract formation in very late stages
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6
Q

What is Sudden Acquired Retinal Degeneration Syndrome (SARDS)

A
  • Acute photoreceptor death
  • Usually middle aged to older dogs
    • females overreptresented
  • All breed affected
  • Associated clinical signs
    • may have ‘Cushing’s-like’ signs for weeks or months prior to vision loss
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7
Q

What are the clinical signs of SARDS?

A
  • Acute vision loss
  • Variable PLR
    • Chromatic PLR
    • Red light negative
    • Blue light positive
  • Fundic exam
    • Normal initially
    • Chronic cases
      • retinal degeneration
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8
Q

How is SARDS diagnosed?

A
  • Electroretinogram (ERG)
  • May have elevated ALP, or other Cushing’s like changes on blood work
    • less commonly diagnosed with Cushing’s via traditional screeding tests
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9
Q

What is the treatment for SARDS

A
  • No proven treatment
  • Permanent blindness
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10
Q

What are the effects of Retinal detachments on vision?

A
  • Small detachments - no deficit
  • large detachments - visual deficit/blindness
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11
Q

What is Rhegmatogenous retinal detachment

A
  • Retinal tear present which allows liquified vitreous to enter sub-retinal space
  • Primary ocular disorder (previous cataract surgery, inherited vitreal degeneration, etc)
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12
Q

What is Non-rhegmatogenous retinal detachment

A
  • Remains attached at ora ciliaris retinae & optic disc
  • Serous sub-retinal fluid-bullous retinal detachment
  • Exudative retinal detachments-inflammatory or exudative sub-retinal fluid
  • Systemic disease
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13
Q

What are the differentials for Non-rhegmatogenous Retinal detachment?

A
  • Depends on type of sub-retinal fluid/material
  • Exudate (cloudy or discolored, yellow)
    • same as chorioretinitis (i.e. posterior uveitis) ⇢ suspect systemic infection
  • Transudate (clear)
    • Aka Bullous
    • Hypertension
    • Hypoproteinemia
    • Idiopathic (steroid responsive)
      • dog specific
  • Always perform systemic work-up
    • CBC/chemistry panel/UA
    • Blood pressure
    • CHest radiographs
    • Titers/antigen tests
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14
Q

How is Retinal detachments repaired?

A
  • Only appropriate for rhegmatogenous detachments
  • Laser retinopexy
    • 2 rows of burns around detachment to create adhesions
    • Prophylactic vs. barrier
  • Retinal reattachment
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15
Q

What are the possible etiologies for Retinal hemorrhages?

A
  • Anemia
  • COagulopathy
  • Systemic hypertension
  • Hyperviscosity
  • Systemic infections that cause vasculitis
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16
Q

What is the diagnostic approach to retinal hemorrhages

A
  • Thorough PE
  • CBC, Chemistry, UA
  • Blood pressure
  • Clotting times
  • BMBT
  • Chest radiographs
  • Titers/antigen testing if any suspicion of infectious cause
17
Q

What is Optic neuritis?

A
  • Optic nerve inflammation
  • Unilateral or bilateral
  • Can involve any segment of optic nerve (intraocular vs retrobulbar)
  • Associated with sudden blindness, fixed and dilated pupils
  • Intraocular involvement:
    • disc appears swollen, elevated, and hyperemic, with indistinct margins = papillitis
  • Retrobulbar involvement:
    • optic disc will appear normal
    • need ERG to distinguish from SARDS
18
Q

What are the differentials for Optic Neuritis?

A
  • Infectious
    • Fungal
    • Tick-borne encephalitis or ehrlichiosis
    • Protozoal - toxoplasmosis
  • Neoplasia
    • lymphoma
    • orbital/retrobulbar neoplasia
  • GME
  • Immune mediated
  • Idiopathic
  • Other:
    • Orbital abscess/cellulitis
    • Trauma
    • Toxins
    • Vitamin A deficiency
19
Q

What is the diagnostic approach to Optic Neuritis?

A
  • CBC, chemistry panel, USA
  • titers/antigen tests for infectious organisms
  • Chest radiographs
  • MRI or CT scan
  • CSG Tap
  • Thick of Optic neuritis as a neurologic disease
20
Q

What is the treatment for optic neuritis

A
  • Treat primary cause
  • Systemic steroids (immunosuppressive dose)
  • Oral antibiotics (empiric)
  • Prognosis for vision = poor
21
Q

What are the hallmark fundoscopic signs of Progressive Retinal Atrophy?

A
  • Tapetal hyper-reflectivity
  • Retinal attenuation of blood vessels
  • Optic disk pallor