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↑↑ ↑↑ ↑↑ !!
By
Ahmed Alsherbeny
MSc. Ophth , FICO , MRCSEd Ophth , FRCS Ophth (Glasg(
Upper
Capillary haemangioma  , most frequently
presents in the upper eyelid
Plexiform neurofibromas typically present in
childhood as a manifestation of neurofibromatosis
type 1 with a characteristic S-shaped deformity
of the upper eyelid
Nodular SGC presents as a discrete,
hard nodule, most commonly within the
upper tarsal plate
Merkel cell carcinoma    , A violaceous,
well-demarcated nodule with intact
overlying skin is seen, most frequently
involving the upper eyelid
Laser iridotomy, Many practitioners 
target a site under the upper eyelid
between 11 and 1 o’clock
High
A refractive
error of more
than −6 dioptres
constitutes a
common definition
of high myopia,
in which axial
length is usually
greater than 26
mm
In choroidal neavus,
Ultrasonography shows a localized
flat or slightly elevated lesion with
high internal acoustic reflectivity
Superior
Nerves passing through superior orbital
fissure
 
Live Free To See No Insult At All
Lacrimal nerve
Frontal nerve
Trochlear nerve
Superior division of 3rd nerve
Nasociliary nerve
Inferior division of 3rd nerve
Abducens nerve
Superior eye muscles (superior rectus &
superior oblique) are supplied by
conralateral nucleus
Temporal Lobe Lesions
Visual field defect consists of a
contralateral superior homonymous
quadrantanopia (‘pie in the sky’) because the
inferior fibres of the radiations
Oculomotor nerve
Superior division innervates the levator and
superior rectus muscles. 
Marfan’s syndrome; Bilateral ectopia
lentis (80%); subluxation is most
frequently superotemporal. The zonule
is frequently intact so that
accommodation is retained
A superficial orbital dermoid cyst
presents in infancy with a painless
nodule, most commonly located in the
superotemporal and occasionally the
superonasal part of the orbit. 
Rhabdomyosarcoma; The tumour is most commonly
superonasal or superior, but may arise anywhere in
the orbit, including inferiorly
Lattice is most commonly bilateral,
temporal and superior.
an acutely symptomatic RD should be operatively
repaired urgently, particularly if the macula is as yet
uninvolved. Other factors that may increase the urgency
of intervention include the presence of a superior or
large break, from which SRF is likely to spread more
rapidly, and advanced syneresis as in myopia
Lower nasal optic nerve fibres traverse the chiasm
inferiorly and anteriorly, hence the upper temporal
quadrants of both visual fields are affected first
by most expanding pituitary lesions, giving a
bitemporal superior quadrantanopia progressing to
the classic chiasmal visual field lesion, a
bitemporal hemianopia
Up
Upbeat nystagmus is a vertical nystagmus with the fast phase beating
upwards in all positions; causes include posterior fossa lesions, drugs
and Wernicke encephalopathy.
Hyper
Hypertelorism
in which there
is wide bony
separation of
the orbit
Type I : Spring catarrh
Type II : Cicatricial Pemphegoid
Type III : Steven Johnson Syndrome
Type IV : Phlycten
Hypersensetivity reactions in ophthalmology
Hypermetropia associated diseases
- AMD
- Leber’s congenital amaurosis
- Angle closure glaucoma
- Retinoschesis
Trabecular hyperpigmentation
PIGMENT
Pseudoexfoliation & Pigment dispersion syndrome
Iritis
Glaucoma (Post angle closure Glaucoma)
Melanosis of angle (oculodermal melanosis)
Endocrine (Diabetes & Addison’s Syndrome)
Naevus (Cogan-reese syndrome)
Trauma
Hyperchromia
Macro
Retinal artery macroaneurysm
localized dilatation of a retinal
arteriole; it has a predilection for
older hypertensive (75%) women.
Macropsia (increase in image size) is
due to crowding together of foveal
cones
Retinal  macrovessel
This is an aberrant blood vessel, often larger than
normal and usually a vein, located in the posterior
pole; it may cross the fovea and horizontal raphe.
Areas of capillary non-perfusion and foveal cysts
may be seen. The anomaly is non-progressive and is
usually associated with good vision.
Thank You

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↑ ↑ ↑ !

  • 1. ↑↑ ↑↑ ↑↑ !! By Ahmed Alsherbeny MSc. Ophth , FICO , MRCSEd Ophth , FRCS Ophth (Glasg(
  • 3. Capillary haemangioma  , most frequently presents in the upper eyelid
  • 4. Plexiform neurofibromas typically present in childhood as a manifestation of neurofibromatosis type 1 with a characteristic S-shaped deformity of the upper eyelid
  • 5. Nodular SGC presents as a discrete, hard nodule, most commonly within the upper tarsal plate
  • 6. Merkel cell carcinoma    , A violaceous, well-demarcated nodule with intact overlying skin is seen, most frequently involving the upper eyelid
  • 7. Laser iridotomy, Many practitioners  target a site under the upper eyelid between 11 and 1 o’clock
  • 9. A refractive error of more than −6 dioptres constitutes a common definition of high myopia, in which axial length is usually greater than 26 mm
  • 10. In choroidal neavus, Ultrasonography shows a localized flat or slightly elevated lesion with high internal acoustic reflectivity
  • 12. Nerves passing through superior orbital fissure   Live Free To See No Insult At All Lacrimal nerve Frontal nerve Trochlear nerve Superior division of 3rd nerve Nasociliary nerve Inferior division of 3rd nerve Abducens nerve
  • 13. Superior eye muscles (superior rectus & superior oblique) are supplied by conralateral nucleus
  • 14. Temporal Lobe Lesions Visual field defect consists of a contralateral superior homonymous quadrantanopia (‘pie in the sky’) because the inferior fibres of the radiations
  • 15. Oculomotor nerve Superior division innervates the levator and superior rectus muscles. 
  • 16. Marfan’s syndrome; Bilateral ectopia lentis (80%); subluxation is most frequently superotemporal. The zonule is frequently intact so that accommodation is retained
  • 17. A superficial orbital dermoid cyst presents in infancy with a painless nodule, most commonly located in the superotemporal and occasionally the superonasal part of the orbit. 
  • 18. Rhabdomyosarcoma; The tumour is most commonly superonasal or superior, but may arise anywhere in the orbit, including inferiorly
  • 19. Lattice is most commonly bilateral, temporal and superior.
  • 20. an acutely symptomatic RD should be operatively repaired urgently, particularly if the macula is as yet uninvolved. Other factors that may increase the urgency of intervention include the presence of a superior or large break, from which SRF is likely to spread more rapidly, and advanced syneresis as in myopia
  • 21. Lower nasal optic nerve fibres traverse the chiasm inferiorly and anteriorly, hence the upper temporal quadrants of both visual fields are affected first by most expanding pituitary lesions, giving a bitemporal superior quadrantanopia progressing to the classic chiasmal visual field lesion, a bitemporal hemianopia
  • 22. Up
  • 23. Upbeat nystagmus is a vertical nystagmus with the fast phase beating upwards in all positions; causes include posterior fossa lesions, drugs and Wernicke encephalopathy.
  • 24. Hyper
  • 25. Hypertelorism in which there is wide bony separation of the orbit
  • 26. Type I : Spring catarrh Type II : Cicatricial Pemphegoid Type III : Steven Johnson Syndrome Type IV : Phlycten Hypersensetivity reactions in ophthalmology
  • 27. Hypermetropia associated diseases - AMD - Leber’s congenital amaurosis - Angle closure glaucoma - Retinoschesis
  • 28. Trabecular hyperpigmentation PIGMENT Pseudoexfoliation & Pigment dispersion syndrome Iritis Glaucoma (Post angle closure Glaucoma) Melanosis of angle (oculodermal melanosis) Endocrine (Diabetes & Addison’s Syndrome) Naevus (Cogan-reese syndrome) Trauma
  • 30. Macro
  • 31. Retinal artery macroaneurysm localized dilatation of a retinal arteriole; it has a predilection for older hypertensive (75%) women.
  • 32. Macropsia (increase in image size) is due to crowding together of foveal cones
  • 33. Retinal  macrovessel This is an aberrant blood vessel, often larger than normal and usually a vein, located in the posterior pole; it may cross the fovea and horizontal raphe. Areas of capillary non-perfusion and foveal cysts may be seen. The anomaly is non-progressive and is usually associated with good vision.