This presentation talks about abnormal fluorescein angiograph
The causes of hypo flourescence and hyper fluorescence are dealth with in this presentation.
Each condition is illustrated with appropriate images of the FFA.
2. What is abnormal FFA?
If we do not find
• Normal amount of dye at the expected level
of time
• Normal amount of dye at the expected level
of tissue
THEN WE SAY THAT THERE IS ABNORMAL
FLUORESCENCE
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3. How to read FFA
•Always keep color fundus photograph
for interpretation
•IVF is a dynamic process-so one
frame may not tell the whole story
•Serial Frames should be examined to
determine the pathology
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4. Abnormal Fluorescence
Two types
I) Hypo-fluorescence-less than normal
fl
II) Hyper-fluorescence –more than
normal fl
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5. I) Hypo-Fluorescence
There are two reasons for hypo fluorescence
Either something blocks the fl that is present normally so we
don’t see it
A- Blocked Fl
Blocking material can be pigments (Hb, melanin,
xanthophyll), exudates, edema, flecks or FB
Or
B- Filling defect
there is no fluorescein in the tissues where it must be
present -- due to loss of vessels -
Filling defect—closure of retinal or choroidal vessels
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7. Hypo-fluorescence –Blocked fluorescence
• Which circulation is blocked by the blocking
material?
• Retinal or choroidal or both?
• Blocking depends upon the location of the
blocking material
• It is important to read a color photograph or red-
free photograph to correlate area of blocked fl
with the material blocking the fl
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8. Blocked Fl due to pigment-HB
Which circulation is not seen here (blocked here)?
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9. Blocked fl due to -----blood -hb
Which circulation is not seen here (blocked here)?
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10. Blocked Fl due to subretinal material
which circulation is blocked here?
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11. Blocked Fl-Hard exudate- mainly the
choroidal circulation is blocked
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15. Hypo fluorescence -Filling defect
• Delay or Occlusion of blood flow
• Retinal- Artery, vein or capillaries
• Choroidal tissue- loss of choroidal tissue – dystrophy or
degeneration
Important to rule out blocked fl in the area of hypo fl that
there is no material blocking the fl and it is due to filling
defect
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16. Filling defect –retinal artery
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34. Hyper-Fluorescence
Excess fluorescein seen than expected
Leakage
Increased transmission of Fl-window defect
Abnormal vessels- Retinal, Sub-retinal and tumors
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36. Hyper-fluorescence
• Leakage
Pooling in a space-
Retinal –CME –flower petal appearance
Sub-retinal –CSR,RPE detachment
Staining of a tissue-
Retinal –non cystoid edema or fibrovascular staining
Sub-retinal ----drusens , sclera, scars
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37. Pooling in a space-Retinal –CME
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39. Pooling in a space Sub-retinal
• Serous RD
• RPE detachment
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40. Pooling in a space-Subretinal CSR
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41. Pooling in a space-subretinal-CSR
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43. Pooling in a space-Subretinal-RPE
detachment
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RPE detachment
• Because of firm adhesion
of RPE the detachment
has sharp borders unlike
serous RD
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45. RPE detachment
• The area fluoresces in Choroidal phase
• The size remains same
• The intensity increases gradually as more
fluorescein molecules accumulate
• It has sharp borders
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47. Hyperfluorescence- Staining of a tissue
•Retinal – perivascular staining
•Subretinal-drusen, scars sclera
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48. STAINING OF VEINS -VASCULITIS
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57. Transmission Defect –RPE Window
defect
• Atrophic RPE revealing the choroidal circulation brightly –
RPE Window defect
• RPE atrophy may be due to several causes –drusen,
inflammation, hereditary diseases, trauma etc
• Hyperfl in choroidal phase in the area of atrophy
• Gradually increases in intensity
• Later the fl decreases in intensity as the dye exits the
circulation
• Some staining of the sclera is seen in late phases and
leakage from choriocapillaris at the edge of the lesion
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63. Hyper-fluorescence-abnormal vessels
• Retinal- telengiectasia, NVE,NVD, Macroanuerysms etc
{They leak because of lack of inner BRB}
• Subretinal- CNV, Scars with vessels
• Tumors- Retinoblastoma, melanoma, hemangiomas,
secondaries
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67. Hyperfl due to microaneurysms
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