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JR-3 MS ophthalmology
RNTMC Udaipur
HIstopathology showing homogeneous eosinophilic
deposits lying between the renal pigment epithelium
(RPE and the inner conagenous layer or Bruch
membrane:
OCT showing
drusen (arrows): C
initial image: (D
same eye 4 years
after showing an
increase in number
and size of drusen:
(E) drusen with
associated
pigmentary
abnormalities
Age-related macular
degeneration without
neovascularization. (A)
Druse and mild
pigmentary changes; b
same eye as [A) 4
years later with
moderate retinal
atrophy and
pigmentary
abnormalities; (C)
geographic atrophy;
(D) late FA of eye in
(C);
; (E) substantial geographic atrophy and pigmentary
abnormalities; (F) OCT showing outer retinal
tubulations
Occult (Type 1)
choroidal
neovascularization. (A)
Specks of blood at the
fovea; (B–D) FA
showing diffuse
hyperfluorescence but
the limits of the
membrane cannot be
defined; (E) OCT
showing a PED with
variable internal
reflectivity and
subretinal fluid
Classic (Type 2) subfoveal
choroidal neovascularization.
(A) Colour image showing
grey–green area and small
haemorrhage; (B) early FA
showing ‘lacy’
hyperfluorescent pattern and
an area of hypofluorescence
secondary to the haemorrhage;
(C) late venous phase – more
intense hyperfluorescence with
leakage and staining; (D)
persistent staining at 10
minutes; (E) OCT showing
subretinal hyper-reflective
material (arrow)
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Maina copy.pptx

  • 2.
  • 3.
  • 4.
  • 5.
  • 6.
  • 7.
  • 8.
  • 9.
  • 10.
  • 11.
  • 12.
  • 13.
  • 14.
  • 15. HIstopathology showing homogeneous eosinophilic deposits lying between the renal pigment epithelium (RPE and the inner conagenous layer or Bruch membrane:
  • 16. OCT showing drusen (arrows): C initial image: (D same eye 4 years after showing an increase in number and size of drusen: (E) drusen with associated pigmentary abnormalities
  • 17.
  • 18.
  • 19.
  • 20.
  • 21.
  • 22.
  • 23.
  • 24. Age-related macular degeneration without neovascularization. (A) Druse and mild pigmentary changes; b same eye as [A) 4 years later with moderate retinal atrophy and pigmentary abnormalities; (C) geographic atrophy; (D) late FA of eye in (C);
  • 25.
  • 26. ; (E) substantial geographic atrophy and pigmentary abnormalities; (F) OCT showing outer retinal tubulations
  • 27.
  • 28.
  • 29.
  • 30.
  • 31.
  • 32.
  • 33.
  • 34.
  • 35.
  • 36.
  • 37. Occult (Type 1) choroidal neovascularization. (A) Specks of blood at the fovea; (B–D) FA showing diffuse hyperfluorescence but the limits of the membrane cannot be defined; (E) OCT showing a PED with variable internal reflectivity and subretinal fluid
  • 38. Classic (Type 2) subfoveal choroidal neovascularization. (A) Colour image showing grey–green area and small haemorrhage; (B) early FA showing ‘lacy’ hyperfluorescent pattern and an area of hypofluorescence secondary to the haemorrhage; (C) late venous phase – more intense hyperfluorescence with leakage and staining; (D) persistent staining at 10 minutes; (E) OCT showing subretinal hyper-reflective material (arrow)