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Shreeji Shrestha
Rete = net
Thin, delicate, transparent multilayered
sheet of neural tissue lining innermost
aspect of eyeball (photochemical
transduction occurs where nerve impulse
are created and transmitted by visual
pathway to brain)
Extends from optic disc to ora serrata
Area = 266mm2
Thickest near optic disc (0.56mm)
Equator (0.18mm)
Ora serrata (0.10mm)
Retina extends more anteriorly on medial
side so, ora serrata lies closer to limbus on
medial side
Its landmark externally is insertion of
medial rectus in medially and lateral recuts
in laterally
Inner layer of neuroectodermal cells
Differentiation of cells begins within
1month producing 3-4 compat cells
At 7th week, Nuclei segregate in outer 2/3rd
of primodial retina = outer primitive zone
Nuclei absent in inner 1/3rd = inner
marginal zone
Differentition of neuroepthelialcells begins
from center to periphery
2 layers:- a) inner neuroblastic layer
Ganglion cells, muller cells, amacrine cells
b) outer neuroblastic layer
Rods, cones, bipolar cells, horizontal cells
Separated by tangled cell processes =
transient nerve fiber layer of Chievtz
(inner plexiform layer)
 Starts around 6 weeks
 Origin= Pseudostratified columnar epithelial
cells of outer wall of cup
 Adjacent cells are joined by zonulae
occludentes and zonulae adherentes
 6th week = melanogenesis begins
 Differentiation starts from posterior to anterior
& by 8th week = single layer of hexagonal
columnar cells
 After birth = enlargement and expansion of
individual cells
As retina matures from center to periphery,
disproportiante amount of expansion
occurs in periphery,
hence, ganglion cell = lower density
 Pale-pink, well defined circular, 1.5mm in
diameter
 Comparatively pale due to: absence of
vascular choroid and lamina cribosa with medullated
nerve fibers behind it.
 No rods and cones (insensitive to light)–blind spot
 Centrally – depression = physiological cup: =
a)centre retinal vessels
b)varies in size, shape, position, depth
Sometimes, disc is more pink, scarcely any cup, seen
when central retinal vessels divide before they come
to surface
Optic disc unlike surrounding retina
doesnot have cells of muller; these cells
hold nerve fiber together hence optic disc
easily swells up in papilloedema.
Sometimes retina doesn’t reach edge of
disc leaving crescent of pigmented choriod
visible on ophthalmoscope
5.5mm
0.35mm
1.5mm
150micm
 location- posterior fundus, temporal to optic
disc, between temporal vascular arcade
 Corresponds to 15 degree of visual field
 Functions :- photopic vision and color vision
 Yellow color in cadaver eye :- carotenoid
pigment ( zeaxanthin and lutein) in ganglion
and bipolar cells
 L:Z ratio: central area – 1:2.4
peripheral – 2:1
corresponds to rods:cone ratio
Lutein more in rods
Clivus 22
Thickness – 0.13mm
4mm temporal, 0.8mm inferior to optic disc
Photoreceptor layers made up of cones
Area of highest VA
Center of foveola is umbo
Correspond 1 degree of Visual field
Color of fovea persist and even
accentuated = called as cherry red spot
when surrounding retina become cloudy
due to ischemia eg CRAO and in
metabolic Storage disease
 Located inside fovea and outside foveola
 Important landmark in treatment of
subretinal neovascular membrane by
laser photocoagulation
 Parafovea = 0.5mm in width surrounds
fovea
GCL, INL, OPL are thickest
 Perifovea = 1.5mm
Retina around equator = equatorial retina
Divided into 4 regions:
1. Near periphery: 1.5mm around area
centralis
2. Mid periphery: 3mm around near
periphery
3. Far periphery: extend from equator to ora
serrata
4. Ora Serrata: area of retina and pars plana
 Peripheral margin of retina which consists of
dentate fringe (denotes termination of retina)
 Ora is 2.1 mm temporally and 0.7-0.8mm
wide nasally
 Watershed zone between anterior and posterior
vascular system hence retinal degeneration is
relatively common at periphery
Photoreceptors are malformed and
overlying retina frequently appears
cystic in parafin section
Monolayer of hexagonal cells containing
pigments merges with pigmented
epithelium of ciliary body
Unequal pigmentation of cells leads
granular appearance of fundus
Firmly attached to bruch membrane
Loosely attached to photoreceptor (between
= Subretinal space)
RD = separation between RPE and sensory
retina
1. Vitamin A metabolism
2. Maintenance of outer retina-blood barrier
3. Phagocytosis of photoreceptor outer
segments
4. Absorption of light
5. Heat exchange
6. Formation of basal lamina
7. Active transport of material in and out of RPE
8. Production of mucopolysachharide matrix
surrounding outer segment
Apices of RPE has multiple villous process
that engage with photoreceptor outer
segments embedded in
mucopolysaccharide matrix (chondroitin-6-
sulfate, sialic acid, hyaluronic acid)
Lack of laminin and
Fibronectin in matrix,
Junctional complex between
Microvilli (prone for RD)
Contiguous RPE cells are firmly attached
By junctional complex.
Zonulae occludentes and adherentes
provide structural stability and maintain
outer retinal barrier
Number – 4.2 to 6.1 million
RPE cells in fovea are taller and thinner
and contain more and larger melanosome
Hence decreased transmission of choroidal
fluorescence during FFA
 contains multiple round and ovoid pigment
granules :- 1)melanosomes (apex)
This melanin absorb stray light and
minimize scatter
2) Lipofuscin granules :- arise from outer
segment of photoreceptor, represent
residual bodies from phagosomal activity
Aka wear and tear pigment
3) Phagosome = membrane enclosed
packets of disc outer segments engulfed
by RPE
4) Mitochondria = aerobic metabolism
5) RER
6) Golgi apparatus
Incompletely digested residual bodies,
lipofusin, phagosome = drusen
Located between basement membrane of
RPE cells and inner collagenous zone of
bruch membrane
in ocular albinism-loss of melanin in RPE
and uvea. O/E once can see through
iris(transillumination of iris) and visualize
ciliary process and pupil is red
In older age, melanin combine with
lysosome – breakdown – hence, fundus
appears less pigmented.
PDGF- cell growth and healing
VEGF- stimulate normal or pathologic
neovascular growth
TGF- moderates inflammation
PEDF- neuroprotectant
Composed of
neuronal,
glial
vascular elements
Photoreceptor layer - Rods and cones
Average 92 million rods and 4.6 million
cones
Consist- outer and inner segment
Outer segments, surrounded by
mucopolysaccharide matrix and make
contact with RPE
Highest density of cones is at fovea
Number of cones falls off rapidly outside
fovea
Cones are greater on nasal and inferior
Rods are absent at fovea but present in
large number in ring-shaped zone 5-6mm
from fovea
 Rod outersegment – cylindrical, multiple laminated
disc (600-1000) resembling stack of coin and cilium
(connects outer and inner segments)
 Microtubules of cilium have 9 plus 0 cross-sectional
configuration (nonmotile)
 Inner segment – a) outer eosinopilic ellipsoid –
mitochondria
b) inner basophilic myoid-
glycogen and ribosome (protein synthesis)
 Inner portion of cell consist of spherule formed by
single invagination accommodating 2 horizontal cell
process and 1 or more central bipolar process
Outer segments have different morphology
depending on location on retina
Extrafoveal cone have short conical
ellipsoids and myoids and nucleus tends to
be closer to ELM
Foveal cone have longer cylindrical inner
segments
Cones outersegment have more disc (1000-
1200) & attached to each other
Intradisc and interdisc space are wider
Cone inner segments: at fovea are long
and tapered but at periphery are conical
Ellipsoid part - more mitochondria (200-
300 per cells)
Unlike rod inner segment is directly
continuous with its nucleus
Cone pedicle synapse with other rods,
cones, horizontal and bipolar cells
process.
3 classes of cones: red, green, blue
(sensitive at 560, 530 and 430nm)
Gene for cone is in X chromosome.
Color blindess more common in males
Bipolar cells are oriented vertically, axons
synapse with rods and cones forming outer
plexiform layer and with axons of
ganglionc cells and amacrine cell forming
inner plexiform layer
Form 1st order neuron
Rod- connect rod to ganglion cell
Flat- many cones with many ganglion
Midget- single cone with single ganglion
 Axons of ganglion cells bend to become
parallel to retina forming nerve fiber layer.
 Ganglion cell forms second order
neuron(nerve cells of LGB -3rd order)
 Nerve fiber from temporal retina follow
arcuate around macula entering sup and inf
pole of optic disc
 Visibility of nerve fiber is enhanced using
green illumination
Unna orcein polychrome stain
a) rods- colourless
b) cones- deep blue
Mallory trichome stain and fixation with
zenker fluid
a) rods – blue
b) cones – red
In foveola all photorecepter stain red,
indicates- absence of rods
 Muller cells – extend vertically from ELM to
ILM
 Nuclei located in INL
Fx :- a)structural support, nutrition to retina
b)insulin and GF produced by muller
cells helps in metabolism of sensory retina
c) degradation of glutamate and GABA
d)mRNA for CA II – buffering CO2
liberated into extracellular space by
neurosensory retina
 Contains :- retinaldehyde binding protein,
glutamine, taurine
Astrocytes
Microglia
Oligodendrocytes
Outer 4 layers- choriocapillaris
Inner 6 layers – central retinal artery
Outer plexiform layer supplied by both
Macula - superior and inferior temporal
branches of central retinal artery
30% - cilioretinal artery, branch of ciliary
circulation supplies inner retina
Retinal vessels are end arteries but
anastomosis occur bet retinal and ciliary
system with vessel which enter Optic nerve
head from arterial circle of zinn.
Retinal blood vessels forms Blood-retina
barrier fromed by
single layer of nonfenestrated
endothelial cells with tight junction
(presence of barrier is confirmed by absence
of fluorescein leak from capillary)
Basal lamina covers outer surface of
endothelium.
Contains an interrupted layer of pericytes (
mural cells)
 Pericytes are also surrounded by a layer of
basement membrane.
 Pericytes contain contactile protein so contract
in response to angiotensin and relax to CO2
and nitric oxide
 Young:- endothelial cell : pericytes = 1:1
 In DM relative decrease in pericytes
 With inc age gradual decrease in endothelial
cells
 Retinal blood vessels lack internal elastic
lamina and smooth muscle cell
 When venules and arterioles cross they share
common basement membrane. Hence venous
occlusive disorder are common at AV crossing
First branch of ophthalmic artery
Arises near optic foramen and course as
follows:
Outside optic nerve: runs a wavy course
forward below optic nerve, inferomedial
aspect of nerve it bends upwards to pierce
dura and arachnoid.
In subarachnoid space: it bends upwards
and invaginates pia reaching centre of
nerve (surrounded by sympathetic nerve-
nerve of Tiedemann)
In centre of optic nerve: bends forwards
and with vein lie in temporal side, pierces
lamina cribosa and appear in eye
In optic nerve head: lies superficial nasal
of cup and divides into 2 branches superior
and inferior which subdivides into temporal
and nasal branch near margin
In retina: 4 branches superior nasal,
superior temporal, inferior nasal, inferior
temporal divide dichotomously and
proceed towards ora serrata
Accompanies retinal artery
Diameter 1/3rd larger than artery
Artery tends to lie superficial to vein thus
tend to cross superficial to the vein
Drains to cavernous sinus or superior
ophthalmic vein
1. ELM- outermost layer, not a true
membrane, formed by attachment sites of
adjacent photoreceptors and muller cells,
highly fenestrated
2. ONL- nuclei of cones and rods
(cones>rods).
Nasal to disc: 8-9 layers of nuclei
Temporal to disc: 4 rows
Fovea: 10 rows
Rest of retina except ora: 1 cone nucleiand 4
rods
3. OPL-synapse between rod
spherules,cone pedicles with dendrite of
bipolar and horizontal cells. Thickest at
macula and contains more fibers and more
oblique as they deviate from fovea (henle
fiber layer)
4. INL- nuclei of Bipolar, muller, horizontal,
amacrine cells
5. IPL- axons of bipolar and amacrine cells
and dendrites of ganglion cells
absent at foveola
6.GCL- cell bodies of ganglion cells
Single row except at macula 6-8 layered
In glaucoma, defect is in GCL, Inc IOP leads to
anoxia, reduced axonal transport and excess
glutamate (excitatory damage)- apoptosis of
GCL
7. NFL- formed of axons of ganglion cells,
unmyelinated, 0.5-2micm, converge at optic
nerve head, pass through lamina cribrosa.
It also contains: Centrifugal nerve fiber
Muller processes, Neuroglial cells
In some case ganglion nerve fiber sheath
are myelinated usually seen around optic
disc; such area are nonseeing and
produce a blind spot
Arterial branch run in NFL close to ILM.
ILM is extremely thin and transparent,
hence retinal blood vessels are easily seen
in ophthaloscope
SR
F
IRF
Superior Arcuate fiber
Inferior arcuate fiber
thinnestthickest
Papilloedema: first appear in nasal fibers
Rise in CSF pressure in meningeal sheath
that surrounds optic nerve impedes axon
flow and cause disc to bulge into eyeball
Arcuate nerve fibers – most sensitive to
glaucomatous changes
Macular fibers lateral quadrant most
resistant to glaucomatous damage.
ILM- formed by footplate of muller cells
and attachments to basal lamina.
Cells and process are oriented
perpendicular to RPE in middle and outer
layers but, parallel in inner layers.
Hence, deposits of blood or exudates tend
to form round blot in outer layers and flame
shaped in nerve fiber layer
At fovea,outer layer parallel to surface so
star shaped patterns arise when exudate
collects
Fundamentals and principles of
ophthalmology- AAO
Clinical anatomy of eye –snells
Wolf’s anatomy
Retina and vitreous- AAO section 12

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anatomy of retina

  • 2. Rete = net Thin, delicate, transparent multilayered sheet of neural tissue lining innermost aspect of eyeball (photochemical transduction occurs where nerve impulse are created and transmitted by visual pathway to brain) Extends from optic disc to ora serrata Area = 266mm2 Thickest near optic disc (0.56mm) Equator (0.18mm) Ora serrata (0.10mm)
  • 3. Retina extends more anteriorly on medial side so, ora serrata lies closer to limbus on medial side Its landmark externally is insertion of medial rectus in medially and lateral recuts in laterally
  • 4.
  • 5. Inner layer of neuroectodermal cells Differentiation of cells begins within 1month producing 3-4 compat cells At 7th week, Nuclei segregate in outer 2/3rd of primodial retina = outer primitive zone Nuclei absent in inner 1/3rd = inner marginal zone
  • 6. Differentition of neuroepthelialcells begins from center to periphery 2 layers:- a) inner neuroblastic layer Ganglion cells, muller cells, amacrine cells b) outer neuroblastic layer Rods, cones, bipolar cells, horizontal cells Separated by tangled cell processes = transient nerve fiber layer of Chievtz (inner plexiform layer)
  • 7.  Starts around 6 weeks  Origin= Pseudostratified columnar epithelial cells of outer wall of cup  Adjacent cells are joined by zonulae occludentes and zonulae adherentes  6th week = melanogenesis begins  Differentiation starts from posterior to anterior & by 8th week = single layer of hexagonal columnar cells  After birth = enlargement and expansion of individual cells
  • 8. As retina matures from center to periphery, disproportiante amount of expansion occurs in periphery, hence, ganglion cell = lower density
  • 9.  Pale-pink, well defined circular, 1.5mm in diameter  Comparatively pale due to: absence of vascular choroid and lamina cribosa with medullated nerve fibers behind it.  No rods and cones (insensitive to light)–blind spot  Centrally – depression = physiological cup: = a)centre retinal vessels b)varies in size, shape, position, depth Sometimes, disc is more pink, scarcely any cup, seen when central retinal vessels divide before they come to surface
  • 10. Optic disc unlike surrounding retina doesnot have cells of muller; these cells hold nerve fiber together hence optic disc easily swells up in papilloedema. Sometimes retina doesn’t reach edge of disc leaving crescent of pigmented choriod visible on ophthalmoscope
  • 12.
  • 13.  location- posterior fundus, temporal to optic disc, between temporal vascular arcade  Corresponds to 15 degree of visual field  Functions :- photopic vision and color vision  Yellow color in cadaver eye :- carotenoid pigment ( zeaxanthin and lutein) in ganglion and bipolar cells  L:Z ratio: central area – 1:2.4 peripheral – 2:1 corresponds to rods:cone ratio Lutein more in rods
  • 15. Thickness – 0.13mm 4mm temporal, 0.8mm inferior to optic disc Photoreceptor layers made up of cones Area of highest VA Center of foveola is umbo Correspond 1 degree of Visual field
  • 16. Color of fovea persist and even accentuated = called as cherry red spot when surrounding retina become cloudy due to ischemia eg CRAO and in metabolic Storage disease
  • 17.  Located inside fovea and outside foveola  Important landmark in treatment of subretinal neovascular membrane by laser photocoagulation  Parafovea = 0.5mm in width surrounds fovea GCL, INL, OPL are thickest  Perifovea = 1.5mm
  • 18. Retina around equator = equatorial retina Divided into 4 regions: 1. Near periphery: 1.5mm around area centralis 2. Mid periphery: 3mm around near periphery 3. Far periphery: extend from equator to ora serrata 4. Ora Serrata: area of retina and pars plana
  • 19.  Peripheral margin of retina which consists of dentate fringe (denotes termination of retina)  Ora is 2.1 mm temporally and 0.7-0.8mm wide nasally  Watershed zone between anterior and posterior vascular system hence retinal degeneration is relatively common at periphery
  • 20. Photoreceptors are malformed and overlying retina frequently appears cystic in parafin section
  • 21.
  • 22. Monolayer of hexagonal cells containing pigments merges with pigmented epithelium of ciliary body Unequal pigmentation of cells leads granular appearance of fundus Firmly attached to bruch membrane Loosely attached to photoreceptor (between = Subretinal space) RD = separation between RPE and sensory retina
  • 23.
  • 24. 1. Vitamin A metabolism 2. Maintenance of outer retina-blood barrier 3. Phagocytosis of photoreceptor outer segments 4. Absorption of light 5. Heat exchange 6. Formation of basal lamina 7. Active transport of material in and out of RPE 8. Production of mucopolysachharide matrix surrounding outer segment
  • 25. Apices of RPE has multiple villous process that engage with photoreceptor outer segments embedded in mucopolysaccharide matrix (chondroitin-6- sulfate, sialic acid, hyaluronic acid) Lack of laminin and Fibronectin in matrix, Junctional complex between Microvilli (prone for RD)
  • 26. Contiguous RPE cells are firmly attached By junctional complex. Zonulae occludentes and adherentes provide structural stability and maintain outer retinal barrier Number – 4.2 to 6.1 million RPE cells in fovea are taller and thinner and contain more and larger melanosome Hence decreased transmission of choroidal fluorescence during FFA
  • 27.  contains multiple round and ovoid pigment granules :- 1)melanosomes (apex) This melanin absorb stray light and minimize scatter 2) Lipofuscin granules :- arise from outer segment of photoreceptor, represent residual bodies from phagosomal activity Aka wear and tear pigment
  • 28. 3) Phagosome = membrane enclosed packets of disc outer segments engulfed by RPE 4) Mitochondria = aerobic metabolism 5) RER 6) Golgi apparatus
  • 29. Incompletely digested residual bodies, lipofusin, phagosome = drusen Located between basement membrane of RPE cells and inner collagenous zone of bruch membrane in ocular albinism-loss of melanin in RPE and uvea. O/E once can see through iris(transillumination of iris) and visualize ciliary process and pupil is red In older age, melanin combine with lysosome – breakdown – hence, fundus appears less pigmented.
  • 30. PDGF- cell growth and healing VEGF- stimulate normal or pathologic neovascular growth TGF- moderates inflammation PEDF- neuroprotectant
  • 32. Photoreceptor layer - Rods and cones Average 92 million rods and 4.6 million cones Consist- outer and inner segment Outer segments, surrounded by mucopolysaccharide matrix and make contact with RPE
  • 33. Highest density of cones is at fovea Number of cones falls off rapidly outside fovea Cones are greater on nasal and inferior Rods are absent at fovea but present in large number in ring-shaped zone 5-6mm from fovea
  • 34.
  • 35.
  • 36.  Rod outersegment – cylindrical, multiple laminated disc (600-1000) resembling stack of coin and cilium (connects outer and inner segments)  Microtubules of cilium have 9 plus 0 cross-sectional configuration (nonmotile)  Inner segment – a) outer eosinopilic ellipsoid – mitochondria b) inner basophilic myoid- glycogen and ribosome (protein synthesis)  Inner portion of cell consist of spherule formed by single invagination accommodating 2 horizontal cell process and 1 or more central bipolar process
  • 37.
  • 38. Outer segments have different morphology depending on location on retina Extrafoveal cone have short conical ellipsoids and myoids and nucleus tends to be closer to ELM Foveal cone have longer cylindrical inner segments Cones outersegment have more disc (1000- 1200) & attached to each other Intradisc and interdisc space are wider
  • 39.
  • 40. Cone inner segments: at fovea are long and tapered but at periphery are conical Ellipsoid part - more mitochondria (200- 300 per cells) Unlike rod inner segment is directly continuous with its nucleus Cone pedicle synapse with other rods, cones, horizontal and bipolar cells process.
  • 41.
  • 42. 3 classes of cones: red, green, blue (sensitive at 560, 530 and 430nm) Gene for cone is in X chromosome. Color blindess more common in males
  • 43. Bipolar cells are oriented vertically, axons synapse with rods and cones forming outer plexiform layer and with axons of ganglionc cells and amacrine cell forming inner plexiform layer Form 1st order neuron
  • 44. Rod- connect rod to ganglion cell Flat- many cones with many ganglion Midget- single cone with single ganglion
  • 45.  Axons of ganglion cells bend to become parallel to retina forming nerve fiber layer.  Ganglion cell forms second order neuron(nerve cells of LGB -3rd order)  Nerve fiber from temporal retina follow arcuate around macula entering sup and inf pole of optic disc  Visibility of nerve fiber is enhanced using green illumination
  • 46. Unna orcein polychrome stain a) rods- colourless b) cones- deep blue Mallory trichome stain and fixation with zenker fluid a) rods – blue b) cones – red In foveola all photorecepter stain red, indicates- absence of rods
  • 47.  Muller cells – extend vertically from ELM to ILM  Nuclei located in INL Fx :- a)structural support, nutrition to retina b)insulin and GF produced by muller cells helps in metabolism of sensory retina c) degradation of glutamate and GABA d)mRNA for CA II – buffering CO2 liberated into extracellular space by neurosensory retina  Contains :- retinaldehyde binding protein, glutamine, taurine
  • 49. Outer 4 layers- choriocapillaris Inner 6 layers – central retinal artery Outer plexiform layer supplied by both Macula - superior and inferior temporal branches of central retinal artery 30% - cilioretinal artery, branch of ciliary circulation supplies inner retina Retinal vessels are end arteries but anastomosis occur bet retinal and ciliary system with vessel which enter Optic nerve head from arterial circle of zinn.
  • 50. Retinal blood vessels forms Blood-retina barrier fromed by single layer of nonfenestrated endothelial cells with tight junction (presence of barrier is confirmed by absence of fluorescein leak from capillary) Basal lamina covers outer surface of endothelium. Contains an interrupted layer of pericytes ( mural cells)
  • 51.  Pericytes are also surrounded by a layer of basement membrane.  Pericytes contain contactile protein so contract in response to angiotensin and relax to CO2 and nitric oxide  Young:- endothelial cell : pericytes = 1:1  In DM relative decrease in pericytes  With inc age gradual decrease in endothelial cells  Retinal blood vessels lack internal elastic lamina and smooth muscle cell  When venules and arterioles cross they share common basement membrane. Hence venous occlusive disorder are common at AV crossing
  • 52.
  • 53. First branch of ophthalmic artery Arises near optic foramen and course as follows: Outside optic nerve: runs a wavy course forward below optic nerve, inferomedial aspect of nerve it bends upwards to pierce dura and arachnoid. In subarachnoid space: it bends upwards and invaginates pia reaching centre of nerve (surrounded by sympathetic nerve- nerve of Tiedemann)
  • 54. In centre of optic nerve: bends forwards and with vein lie in temporal side, pierces lamina cribosa and appear in eye In optic nerve head: lies superficial nasal of cup and divides into 2 branches superior and inferior which subdivides into temporal and nasal branch near margin
  • 55. In retina: 4 branches superior nasal, superior temporal, inferior nasal, inferior temporal divide dichotomously and proceed towards ora serrata
  • 56. Accompanies retinal artery Diameter 1/3rd larger than artery Artery tends to lie superficial to vein thus tend to cross superficial to the vein Drains to cavernous sinus or superior ophthalmic vein
  • 57. 1. ELM- outermost layer, not a true membrane, formed by attachment sites of adjacent photoreceptors and muller cells, highly fenestrated 2. ONL- nuclei of cones and rods (cones>rods). Nasal to disc: 8-9 layers of nuclei Temporal to disc: 4 rows Fovea: 10 rows Rest of retina except ora: 1 cone nucleiand 4 rods
  • 58. 3. OPL-synapse between rod spherules,cone pedicles with dendrite of bipolar and horizontal cells. Thickest at macula and contains more fibers and more oblique as they deviate from fovea (henle fiber layer) 4. INL- nuclei of Bipolar, muller, horizontal, amacrine cells
  • 59. 5. IPL- axons of bipolar and amacrine cells and dendrites of ganglion cells absent at foveola 6.GCL- cell bodies of ganglion cells Single row except at macula 6-8 layered In glaucoma, defect is in GCL, Inc IOP leads to anoxia, reduced axonal transport and excess glutamate (excitatory damage)- apoptosis of GCL 7. NFL- formed of axons of ganglion cells, unmyelinated, 0.5-2micm, converge at optic nerve head, pass through lamina cribrosa. It also contains: Centrifugal nerve fiber Muller processes, Neuroglial cells
  • 60.
  • 61. In some case ganglion nerve fiber sheath are myelinated usually seen around optic disc; such area are nonseeing and produce a blind spot Arterial branch run in NFL close to ILM. ILM is extremely thin and transparent, hence retinal blood vessels are easily seen in ophthaloscope
  • 62. SR F IRF Superior Arcuate fiber Inferior arcuate fiber thinnestthickest
  • 63. Papilloedema: first appear in nasal fibers Rise in CSF pressure in meningeal sheath that surrounds optic nerve impedes axon flow and cause disc to bulge into eyeball Arcuate nerve fibers – most sensitive to glaucomatous changes Macular fibers lateral quadrant most resistant to glaucomatous damage.
  • 64. ILM- formed by footplate of muller cells and attachments to basal lamina. Cells and process are oriented perpendicular to RPE in middle and outer layers but, parallel in inner layers. Hence, deposits of blood or exudates tend to form round blot in outer layers and flame shaped in nerve fiber layer At fovea,outer layer parallel to surface so star shaped patterns arise when exudate collects
  • 65. Fundamentals and principles of ophthalmology- AAO Clinical anatomy of eye –snells Wolf’s anatomy Retina and vitreous- AAO section 12