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Neuro-
Ophthalmology
Neuro-Ophthalmology
• Eyes
– intimately related to the brain
• Give diagnostic clues to CNS disorders
• IC Disease - visual disturbance
 CN III, IV, VI – EOM
 CN V, VII – also associated with ocular
function
Anatomy of the Optic
Nerve
• Trunk consisting of about 1 million axons
arising from the ganglion cells of the
retina
 Ganglion Cells axons nerve
fiber layer of the retina OPTIC
NERVE
• Portions:
 Orbital Portion: 25-30 mm long within the
muscle cone
 Intraosseous Portion: 4-9 mm
 Intracranial Portion: 10 mm
 Diameter: 1.5 mm (within the sclera)
3 mm (within the orbit)
 80%: visual fibers
 20%: pupillary fibers
Anatomy of the Optic Nerve
Optic Nerve
Sheaths of the Optic Nerve
• PIA
– fibrous tissue with numerous small blood
vessel
– divides the nerve into bundles
– continues to the sclera
Continous with the meninges
• ARACHNOID
– from the IC end of optic foramen to sclera
– diaphanous connective tissue membrane
with many septate connections with PIA
Sheaths of the Optic Nerve
Continous with the meninges
• DURA
– splits into 2: periorbita (lining the orbital
cavity) and outer dural covering of the optic
nerve
– continous with outer 2/3 of sclera
Sheaths of the Optic Nerve
Continous with the meninges
• SPACES
–Subdural
–Subarachnoid
Sheaths of the Optic Nerve
Continous with the meninges
Sheaths of the Optic Nerve
Visual Pathway
• CN II – pathway for special sense of vision
– at the chiasm, more than half of the fibers
decussate; join uncrossed temporal fibers of
the opposite side optic tract
– all impulses from RVF projected to left
cerebrum and vice versa
Visual Pathway
• 80% of fibers to lateral geniculate body
and 20% to pretectal area and superior
colliculi
geniculocalcarine tract
optic radiation
occipital cortex
Visual Pathway
• Lesions:
– anterior to chiasm – unilateral VF defect
– posterior to chiasm – contralateral
homonymous defect
– chiasmal – bitemporal defect
– more congrous homonomous defect – farther
posterior lesion with macular sparing
(maintenance of good visual acuity)
Visual
Pathway
Lesions
Pupillary Pathways
A. Light Reflex
– Entirely subcortical
– Affrent pupillary fibers within the optic nerve go
to pretectal area of midbrain
Edinger-Westphal nucleus
– Efferent pathway is via CN III to the ciliary
ganglion within the muscle cone
short ciliary nerves sphincter muscle
of the iris
Pupillary Pathways
B. Near Reflex
– 3 Reactions:
• Accommodation
• Convergence
• Constriction of the pupil
– Final common pathway – CN III
– Marcus-Gunn Pupil
• Relative Afferent Pupillary Defect (RAPD)
–Swinging flashlight test
Pupillary
Pathways
• Normal pupillary diameter: 3-4 mm
– smaller in infancy
– larger in childhood
– progressively smaller with advancing age
• Physiologic Anisocoria
– seen in 20-40% of normal patients
– Difference in pupil size is about 0.5mm
• Argyll-Robertson Pupil
– Usually bilateral
– <3mm in diameter
– No response to light but responds to neural
stimulus
– Dilate poorly with mydriatics
– Suggestive of: CNS syphillis
Optic Neuritis
• Inflammation, degeneration, demyelinization of
optic nerve
• Retrobulbar Neuritis
Clinical Features:
• visual loss is subacute
• impaired color vision and
contrast sensitivity
• pain in the region of the
eye in 90% of cases
• 50% exacerbated by eye
movement
• sluggish pupillary-light
reflex
• central scotoma
• hyperemic optic disc w/
blurring of disc margin
• distension of large veins
Treatment
• Steroid therapy
• Methylprednisolone by IV, 1g/day for 3
days
OR
• Oral prednisolone, 1mg/kilo/day tapered
over 10-21 days
Optic Disc Edema
• Papilledema/Choked Disk
– non-inflammatory congestion of optic disk
associated with increased ICP (due to
cerebral tumors, abscesses, subdural
hematoma, hydrocephalous, malignant
hypertension)
– Mechanism: obstruction of venous flow
caused by pressure on the Central Retinal
Vein where it leaves the optic nerve
Clinical Findings
• enlarged blind spot
• normal VA and
normal VF
• Fundus Findings:
hyperemia of the disk,
blurring of the
margins, distention of
retinal veins, absence
of pulsation of CRV,
disk swelling to 6-10
D, hemorrhages
Papilledema
• Takes 24-48 hrs for early papilledema to
occur, 1 wk to develop fully
• Takes 6-8 wks to resolve following
adequate treatment
Papilledema
• Foster Kennedy’s syndrome
– papilledema on one side w/ optic atrophy on
the other eye
Papilledema
• Can be mimicked by buried drusen of the
optic nerve, small hyperopic disc,
myelinated nerve fibers
Course and Prognosis
• May or may not affect vision permanently
• Papilledema of more than 5D, extensive
retinal hemorrhages, macular stars – poor
prognosis
Multiple Sclerosis
• Demyelinating disorder of the CNS of
unknown cause, chronic, relapsing, onset
young adult
• Involves the optic nerve, chiasm, brain
stem, cerebellar peduncles, and spinal
cord
• Degeneration of myelin sheaths, glial
tissue overgrowth, and complete nerve
fiber destruction
MS in the Retinal Nerve Fiber Layer
MS
• Retrobulbar/Optic Neuritis
– blurring of vision, central scotoma, dilated
pupil
– diplopia due to EOM involvement from
internuclear ophthalmoplegia
– weakness of one rectus muscle/ptosis
– nystagmus may become permanent (70%)
– VER (visual evoked response) – abnormal in
80% of definite, 43% of probable, and 22% of
suspected cases of MS
Anterior Ischemic Optic Neuropathy
• characterized by pallid disc swelling with
acute loss of vision
• due to infarction of the optic nerve from
occlusion or decreased perfusion of the
short posterior ciliary arteries
• occurs in 6th
or 7th
decade of age
• associated with arteriosclerosis
Nutritional & Toxic Optic
Neuropathies
• Clinical Features:
– Subacute progressive symmetrical visual loss
w/ central visual field defects
– Poor color vision and temporal disc pallor
Nutritional & Toxic Optic
Neuropathies
• Causes:
– Vitamin B Complex deficiency
– Tobacco-Alcohol Amblyopia
– Heavy metal poisoning
– Chemical-induced optic neuropathy
• methanol poisoning (used in photocopier
machines)
– Drug-induced optic neuropathy
• ethambutol, quinine
Optic Nerve Trauma
• Indirect Optic Nerve Trauma:
– Optic nerve damage secondary to distant
skull injury
– Occurs in 1% of all head injuries
– Due to transmission of shock waves through
the orbital apex
– Optic nerve avulsion usually results from an
abrupt rotational injury to the globe
Optic Nerve Trauma
• Direct Optic Nerve Trauma
– Penetrating orbital trauma
– e.g. fractures involving the optic canal
Optic Chiasm
• Lesions of the chiasm cause bitemporal
hemianopsia
• Pituitary gland tumor
Internuclear Ophthalmoplegia
• Conjugate horizontal eye movements are
disrupted due to failure of coordination
between the abducens nerve nucleus in
the pons and the oculomotor nucleus in
the midbrain
• Results in slowing of saccades in the
adducting eye producing transient diplopia
on lateral gaze
Internuclear Ophthalmoplegia
• Causes
– Multiple sclerosis in young adults
– Brain stem infarction in older patients
– Tumors at arteriovenous malformations
– Encephalitis
Syndromes Affecting CN III, IV, VI
• Superior Orbital Fissure Syndrome
– All extraocular peripheral nerves pass through
the superior orbital fissure and can be
involved by trauma or by tumor encroaching
on the fissure
Syndromes Affecting CN III, IV, VI
• Orbital Apex Syndrome
• Similar to the superior orbital fissure
syndrome with the addition of optic nerve
signs and greater proptosis and less pain
• Caused by orbital tumor, inflammation,
trauma that damages the optic and
extraocular nerves
Syndromes Affecting CN III, IV, VI
• Complete Ophthalmoplegia (Sudden)
– Can be due to brainstem vascular disease,
pituitary apoplexy, myasthenia gravis,
arteriosclerotic basilar aneurysm
Myasthenia Gravis
• Abnormal fatigability of striated muscles
after repetitive contraction
• Improves after rest
• Often is first manifested by weakness of
the extraocular muscles
• Diplopia is often an early symptom
Chronic Progressive External
Ophthalmoplegia
• Slowly progressive inability to move the
eyes
• Severe early ptosis
• Normal pupillary reactions and
accommodation
• A form of mitochondrial myopathy
Color VisionColor Vision
Electromagnetic SpectrumElectromagnetic Spectrum
• Photons are classified according to their
wavelength
• Longest wavelength: radio and television
waves
• Shortest wavelength: gamma rays
• Middle of the spectrum: visible light
Rods and ConesRods and Cones
• Retinal photoreceptors that contain
pigments that preferentially absorb
photons with wavelengths 400-700 nm
• Shortest wavelength: blue and green
• Longer wavelengths: yellow, orange, red
Visual PigmentsVisual Pigments
• Four visual pigments:
– Rhodopsin: present in rods
– 3 cone pigments
• Erythrolabe (R cones): red, 570 nm
• Cyanolabe (B cones): blue, 440 nm
• Chlorolabe (G cones): green, 540 nm
3 Attributes of Color3 Attributes of Color
• Hue
– “color”
– Attribute of color perception denoted by blue,
red, purple, etc
– Depends largely on what the eye and brain
perceive to be the predominant wavelength
present in the incoming light
3 Attributes of Color3 Attributes of Color
• Saturation
– “chroma”
– purity or richness of a color
– When all the light seen by the eye is the same
wavelength, the color is fully saturated
– e.g. pink is a desaturated red
3 Attributes of Color3 Attributes of Color
• Brightness
– Luminance, value
– Quantity of light coming from an object (the
number of photons striking the eye)
Primary ColorsPrimary Colors
• Red
• Green
• Blue
Relative Luminosity CurvesRelative Luminosity Curves
• Illustrate the eye’s sensitivity to different
wavelengths of light
• Cones’ peak sensitivity: 555 nm
• Rods’ peak sensitivity: 505 nm (blue)
TrichromatsTrichromats
• 92% of the population who have “normal”
color vision
• Have all 3 different kinds of cones, normal
concentration of cone pigments, normal
retinal wiring
Congenital DichromatismCongenital Dichromatism
• Cones themselves are normal, but one of
the 3 contains the wrong pigment
• Deutranopes:
– Lack green pigment
• Protanopes
– Lack red pigment
• Tritanopes
– Lack blue pigment
Congenital DichromatismCongenital Dichromatism
• Mode of inheritance: sex-linked recessive
– Men almost exclusively manifest the disorder
– Women are carriers
.thank you..thank you.

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7344134 ophtha-neuro-ophthalmology

  • 2. Neuro-Ophthalmology • Eyes – intimately related to the brain • Give diagnostic clues to CNS disorders • IC Disease - visual disturbance  CN III, IV, VI – EOM  CN V, VII – also associated with ocular function
  • 3. Anatomy of the Optic Nerve • Trunk consisting of about 1 million axons arising from the ganglion cells of the retina  Ganglion Cells axons nerve fiber layer of the retina OPTIC NERVE
  • 4. • Portions:  Orbital Portion: 25-30 mm long within the muscle cone  Intraosseous Portion: 4-9 mm  Intracranial Portion: 10 mm  Diameter: 1.5 mm (within the sclera) 3 mm (within the orbit)  80%: visual fibers  20%: pupillary fibers Anatomy of the Optic Nerve
  • 6. Sheaths of the Optic Nerve • PIA – fibrous tissue with numerous small blood vessel – divides the nerve into bundles – continues to the sclera Continous with the meninges
  • 7. • ARACHNOID – from the IC end of optic foramen to sclera – diaphanous connective tissue membrane with many septate connections with PIA Sheaths of the Optic Nerve Continous with the meninges
  • 8. • DURA – splits into 2: periorbita (lining the orbital cavity) and outer dural covering of the optic nerve – continous with outer 2/3 of sclera Sheaths of the Optic Nerve Continous with the meninges
  • 9. • SPACES –Subdural –Subarachnoid Sheaths of the Optic Nerve Continous with the meninges
  • 10. Sheaths of the Optic Nerve
  • 11. Visual Pathway • CN II – pathway for special sense of vision – at the chiasm, more than half of the fibers decussate; join uncrossed temporal fibers of the opposite side optic tract – all impulses from RVF projected to left cerebrum and vice versa
  • 12. Visual Pathway • 80% of fibers to lateral geniculate body and 20% to pretectal area and superior colliculi geniculocalcarine tract optic radiation occipital cortex
  • 13. Visual Pathway • Lesions: – anterior to chiasm – unilateral VF defect – posterior to chiasm – contralateral homonymous defect – chiasmal – bitemporal defect – more congrous homonomous defect – farther posterior lesion with macular sparing (maintenance of good visual acuity)
  • 16. Pupillary Pathways A. Light Reflex – Entirely subcortical – Affrent pupillary fibers within the optic nerve go to pretectal area of midbrain Edinger-Westphal nucleus – Efferent pathway is via CN III to the ciliary ganglion within the muscle cone short ciliary nerves sphincter muscle of the iris
  • 17. Pupillary Pathways B. Near Reflex – 3 Reactions: • Accommodation • Convergence • Constriction of the pupil – Final common pathway – CN III – Marcus-Gunn Pupil • Relative Afferent Pupillary Defect (RAPD) –Swinging flashlight test
  • 19. • Normal pupillary diameter: 3-4 mm – smaller in infancy – larger in childhood – progressively smaller with advancing age
  • 20. • Physiologic Anisocoria – seen in 20-40% of normal patients – Difference in pupil size is about 0.5mm
  • 21. • Argyll-Robertson Pupil – Usually bilateral – <3mm in diameter – No response to light but responds to neural stimulus – Dilate poorly with mydriatics – Suggestive of: CNS syphillis
  • 22. Optic Neuritis • Inflammation, degeneration, demyelinization of optic nerve • Retrobulbar Neuritis
  • 23. Clinical Features: • visual loss is subacute • impaired color vision and contrast sensitivity • pain in the region of the eye in 90% of cases • 50% exacerbated by eye movement • sluggish pupillary-light reflex • central scotoma • hyperemic optic disc w/ blurring of disc margin • distension of large veins
  • 24. Treatment • Steroid therapy • Methylprednisolone by IV, 1g/day for 3 days OR • Oral prednisolone, 1mg/kilo/day tapered over 10-21 days
  • 25. Optic Disc Edema • Papilledema/Choked Disk – non-inflammatory congestion of optic disk associated with increased ICP (due to cerebral tumors, abscesses, subdural hematoma, hydrocephalous, malignant hypertension) – Mechanism: obstruction of venous flow caused by pressure on the Central Retinal Vein where it leaves the optic nerve
  • 26. Clinical Findings • enlarged blind spot • normal VA and normal VF • Fundus Findings: hyperemia of the disk, blurring of the margins, distention of retinal veins, absence of pulsation of CRV, disk swelling to 6-10 D, hemorrhages
  • 27. Papilledema • Takes 24-48 hrs for early papilledema to occur, 1 wk to develop fully • Takes 6-8 wks to resolve following adequate treatment
  • 28. Papilledema • Foster Kennedy’s syndrome – papilledema on one side w/ optic atrophy on the other eye
  • 29. Papilledema • Can be mimicked by buried drusen of the optic nerve, small hyperopic disc, myelinated nerve fibers
  • 30. Course and Prognosis • May or may not affect vision permanently • Papilledema of more than 5D, extensive retinal hemorrhages, macular stars – poor prognosis
  • 31. Multiple Sclerosis • Demyelinating disorder of the CNS of unknown cause, chronic, relapsing, onset young adult • Involves the optic nerve, chiasm, brain stem, cerebellar peduncles, and spinal cord • Degeneration of myelin sheaths, glial tissue overgrowth, and complete nerve fiber destruction
  • 32. MS in the Retinal Nerve Fiber Layer
  • 33. MS • Retrobulbar/Optic Neuritis – blurring of vision, central scotoma, dilated pupil – diplopia due to EOM involvement from internuclear ophthalmoplegia – weakness of one rectus muscle/ptosis – nystagmus may become permanent (70%) – VER (visual evoked response) – abnormal in 80% of definite, 43% of probable, and 22% of suspected cases of MS
  • 34. Anterior Ischemic Optic Neuropathy • characterized by pallid disc swelling with acute loss of vision • due to infarction of the optic nerve from occlusion or decreased perfusion of the short posterior ciliary arteries • occurs in 6th or 7th decade of age • associated with arteriosclerosis
  • 35. Nutritional & Toxic Optic Neuropathies • Clinical Features: – Subacute progressive symmetrical visual loss w/ central visual field defects – Poor color vision and temporal disc pallor
  • 36. Nutritional & Toxic Optic Neuropathies • Causes: – Vitamin B Complex deficiency – Tobacco-Alcohol Amblyopia – Heavy metal poisoning – Chemical-induced optic neuropathy • methanol poisoning (used in photocopier machines) – Drug-induced optic neuropathy • ethambutol, quinine
  • 37. Optic Nerve Trauma • Indirect Optic Nerve Trauma: – Optic nerve damage secondary to distant skull injury – Occurs in 1% of all head injuries – Due to transmission of shock waves through the orbital apex – Optic nerve avulsion usually results from an abrupt rotational injury to the globe
  • 38. Optic Nerve Trauma • Direct Optic Nerve Trauma – Penetrating orbital trauma – e.g. fractures involving the optic canal
  • 39. Optic Chiasm • Lesions of the chiasm cause bitemporal hemianopsia • Pituitary gland tumor
  • 40. Internuclear Ophthalmoplegia • Conjugate horizontal eye movements are disrupted due to failure of coordination between the abducens nerve nucleus in the pons and the oculomotor nucleus in the midbrain • Results in slowing of saccades in the adducting eye producing transient diplopia on lateral gaze
  • 41. Internuclear Ophthalmoplegia • Causes – Multiple sclerosis in young adults – Brain stem infarction in older patients – Tumors at arteriovenous malformations – Encephalitis
  • 42. Syndromes Affecting CN III, IV, VI • Superior Orbital Fissure Syndrome – All extraocular peripheral nerves pass through the superior orbital fissure and can be involved by trauma or by tumor encroaching on the fissure
  • 43. Syndromes Affecting CN III, IV, VI • Orbital Apex Syndrome • Similar to the superior orbital fissure syndrome with the addition of optic nerve signs and greater proptosis and less pain • Caused by orbital tumor, inflammation, trauma that damages the optic and extraocular nerves
  • 44. Syndromes Affecting CN III, IV, VI • Complete Ophthalmoplegia (Sudden) – Can be due to brainstem vascular disease, pituitary apoplexy, myasthenia gravis, arteriosclerotic basilar aneurysm
  • 45. Myasthenia Gravis • Abnormal fatigability of striated muscles after repetitive contraction • Improves after rest • Often is first manifested by weakness of the extraocular muscles • Diplopia is often an early symptom
  • 46. Chronic Progressive External Ophthalmoplegia • Slowly progressive inability to move the eyes • Severe early ptosis • Normal pupillary reactions and accommodation • A form of mitochondrial myopathy
  • 48. Electromagnetic SpectrumElectromagnetic Spectrum • Photons are classified according to their wavelength • Longest wavelength: radio and television waves • Shortest wavelength: gamma rays • Middle of the spectrum: visible light
  • 49. Rods and ConesRods and Cones • Retinal photoreceptors that contain pigments that preferentially absorb photons with wavelengths 400-700 nm • Shortest wavelength: blue and green • Longer wavelengths: yellow, orange, red
  • 50. Visual PigmentsVisual Pigments • Four visual pigments: – Rhodopsin: present in rods – 3 cone pigments • Erythrolabe (R cones): red, 570 nm • Cyanolabe (B cones): blue, 440 nm • Chlorolabe (G cones): green, 540 nm
  • 51. 3 Attributes of Color3 Attributes of Color • Hue – “color” – Attribute of color perception denoted by blue, red, purple, etc – Depends largely on what the eye and brain perceive to be the predominant wavelength present in the incoming light
  • 52. 3 Attributes of Color3 Attributes of Color • Saturation – “chroma” – purity or richness of a color – When all the light seen by the eye is the same wavelength, the color is fully saturated – e.g. pink is a desaturated red
  • 53. 3 Attributes of Color3 Attributes of Color • Brightness – Luminance, value – Quantity of light coming from an object (the number of photons striking the eye)
  • 54. Primary ColorsPrimary Colors • Red • Green • Blue
  • 55. Relative Luminosity CurvesRelative Luminosity Curves • Illustrate the eye’s sensitivity to different wavelengths of light • Cones’ peak sensitivity: 555 nm • Rods’ peak sensitivity: 505 nm (blue)
  • 56. TrichromatsTrichromats • 92% of the population who have “normal” color vision • Have all 3 different kinds of cones, normal concentration of cone pigments, normal retinal wiring
  • 57. Congenital DichromatismCongenital Dichromatism • Cones themselves are normal, but one of the 3 contains the wrong pigment • Deutranopes: – Lack green pigment • Protanopes – Lack red pigment • Tritanopes – Lack blue pigment
  • 58. Congenital DichromatismCongenital Dichromatism • Mode of inheritance: sex-linked recessive – Men almost exclusively manifest the disorder – Women are carriers