Interactive Transcript
0:01
So when I start reading a pet ct,
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I usually follow the same systematic approach
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to make sure that I essentially don't forget anything
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and I review all the organs that need to be reviewed.
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I always start looking at the mip.
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MIP is uh, an image that gives you a lot
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of information about the study itself.
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In this case, what I go through my mind is, first,
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do I recognize the distribution
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and does this match
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with the intended tracer?
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And obviously this doesn't happen often,
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but sometimes there have been cases where
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the administer tracer is wrong.
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So in this case, I see that the distribution matches
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with FDG, which was the intended tracer.
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I also evaluate the distribution of the tracer
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if it's normal or abnormal
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like we have reviewed in other videos.
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And then I get a sense of where the abnormality are.
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Now, obviously this is only for cases
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where the uptake is greater than expected.
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In the meep I would be missing areas that are foric
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and so that's a caveat of that.
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But I, I like to start looking at this case with the meep
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and uh, see where the distribution
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of disease is, uh, grossly.
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And then I start with the hit.
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I manually change the contrast
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because the,
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the brain has physiologically intense trace
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uptake in the cortex.
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And in order to appreciate the differences, I have
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to change the color scale and now I can see the differences.
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So I scroll all the way from the top to the bottom
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of the brain and
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and see areas looking at the pit only areas
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that are normal versus abnormal uptake.
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After I have reviewed the pit, I will move on
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to the CT series.
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Some things are obvious on the CT
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but are not obvious on the pit,
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and you want to be able to provide an interpretation
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for both scenarios.
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Obviously in a pit viewer you can change the contrast
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the same way you would do on uh, regular ct.
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Once I have finished with the brain, I go back
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to my default uh, color scale on the pit,
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which is the zero to five.
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And then I will scroll through
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and try to identify on the pit images alone areas that are
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not physiologic uptake.
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Once I have done that, I move on again to the CT
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and if I identify something,
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I always use the fused images for anatomical correlation
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and triangulation of the findings.
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I don't read of the fused PET CT image
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because things overlap
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and if there's intense uptake in my obscure the CT findings.
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So it is very important that
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whenever you're reading at a pit ct,
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you look at the pit image only and then the CT image alone
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and then you can use your fusion
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for more correlation.
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Moving on to the chest, I would go through the same
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systematic approach of PET and ct.
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Here it is important
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to obviously not only look at the CT on a soft tissue
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window, but also will change to lung window as you go
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through your organ.
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I continue on the soft tissue window until the end
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and then I do lungs just to keep it consistent
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and not have to go back and forth.
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In this case, we see that there's an area
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of focal intense tracer uptake in the region
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of the upper mediastinum and we can triangulate better
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and see on the ct.
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And this corresponds to an adenopathy.
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You can scroll down
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and in this case we see
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that there's intense uptake in the posterior
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or middle mediastinum that localizes to the SFAs.
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Sometimes the axials are not enough
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and it's important to always go back
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and forth between your axial views
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and your sagittal and coronal views.
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Each viewer will have different options.
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For instance, in this case we see that the uptake is linear
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and it localizes to the esophagus
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and this was consistent with esophageal malignancy.
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The sagittal view allows us to see the extent
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of the FDG uptake along the esophagus
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better than we would appreciate on the axial images alone.
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So once we have gone through the mein structures
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and you know you have reviewed your medicinal organs,
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vascular and nonvascular, the adenopathy, I switch
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to lungs and again, I review the pit alone
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and then the CT separately.
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Same strategy is used for the remainder part
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of the body, the abdomen and pelvis.
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Always look at the pit first and then the CT
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and then correlate with your fusion.
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I personally do the bones at the end as then I can
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change my scale
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and just look at the entire skeleton on its
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own or the skeleton.
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I like to change my display
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and this is totally a personal choice,
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but I change it in a way that I'm able to see
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the most surface of the body that I can like this.
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For the spine, I like to see that the
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uptake is homogeneous throughout the vertebral body.
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I think this view helps me identify areas
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where the uptake might be focal
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and I can identify smaller lesions that go in
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from the top to the bottom.
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On axial view alone, obviously I use the meep
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to see specific areas of uptake that are abnormal, uh,
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like in the lesser counter on the right
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or the left femur.
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And once I have identified that you can change your view
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and for instance, in this case it correlates
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with a lytic lesion that is intensely VG Avid.
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Same on the other side.
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These were, these are ous metastatic lesions.
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So once I have reviewed the entire body, I have gone
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through all the organs
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and I've changed the windows respectively, I will go back
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to my MIP to make sure that
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I have reviewed everything.
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This is particularly important in cases where
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the disease is very extensive
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and we may have identified the majority
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of disease, but maybe we have not reviewed all of it.
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So the meep gives me another chance to make sure
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that I have discussed all the areas
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of abnormal trace uptake in the body.
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The other thing is to always look at the edges of the film.
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You know, these are like common areas where radiologists,
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uh, miss things and the me here helps me particularly
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on the edges
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and specifically on the extremities, you know,
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because if there was a lesion very distally on the leg,
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maybe I would have not scrolled all the way down
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on my axial view.
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But this meat image allows me to make sure
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that I review everything including those ages.
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So this is my personal approach.
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I'm sure that you will develop your own system
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and, uh, I hope this, uh, is useful for you
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and gives you ideas.