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Wk 3, Case 1 - Review

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0:04

Let's start with the first case.

0:05

It's a multiple myeloma patient.

0:07

You already saw the cases, so there's nothing blinded

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Or anything.

0:10

Um, this is, um, this was a multiple myeloma patient

0:13

coming for, um, initial staging.

0:16

Um, as you see here in this patient, um, I,

0:19

as I always tell my, um,

0:21

and again, I'm not gonna go through my search pattern today.

0:25

Um, we're just going through the findings.

0:27

Uh, so I'm not gonna go systematically,

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although I always go systematically when I, when

0:31

I look at my cases, um, as you see here,

0:35

we starting there is finding here for collectivity

0:39

and, um, I'll put it in a, in a bone window.

0:43

There's a litic lesion here in the skull.

0:48

And if I put it in a soft tissue window,

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you can obviously see that there is a soft tissue component

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that is extending out to thecal,

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but also it has, um, an extra axial

1:00

and intercranial, extra AAL extension.

1:03

I will put it in a brain window.

1:08

It's not the best brain window you can have.

1:11

'cause the CT here is like a one kernel ct.

1:15

So it's not the best CT for the brain, right?

1:19

It's trying to manually make it there.

1:21

It's not helping much. This is the best I can show you.

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But see there is here a soft tissue component

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that is extending intracranial,

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but I think it's, look, it's obviously extra axial, right?

1:35

So there's a soft tissue component of that lytic lesion,

1:38

which, which is typical for multiple myeloma, right?

1:41

This is the first one,

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and I can show you the, let's put the volume of interest

1:47

here, right?

1:54

Like I told you before, for clinical use,

1:56

you wanna make your volume of interest the biggest you can,

2:00

but make sure that you're not including something

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that might be hotter than your lesion.

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Because we report the max UV, right? The SUV max.

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So I'm gonna take it away from the cortex

2:08

because the cortex might be hotter than my

2:10

lesion, although I don't think so.

2:11

But see, I'm scrolling up

2:13

and down, making sure that I'm not touching the cortex

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and oh, I always can go corona

2:19

and to make sure that I'm out.

2:21

It's kind of 7.9 near the max SUV, right?

2:25

You, you notice that I have in mind I can display more.

2:28

I have the peak, the means and the vision.

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I have others, but we report in the clinical report,

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the max, the SUV max, right?

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I'll go down more in the axi.

2:39

You always have to look at the brain.

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Like I said, I'm not gonna go systematically,

2:43

but quickly through

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the pet only image, which I always depend on a lot,

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all you see is basically

2:59

skeletal findings.

3:01

See here and this rep, right?

3:07

Yeah. So you guys can see it.

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I, I know that you guys went through these cases.

3:12

These were last weak cases.

3:15

Again, it's a,

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it's a bone lesion with a soft tissue component.

3:23

Ative, some areas it's a,

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it's an obvious litic destructive lesion

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of the soft tissue component.

3:29

In other areas, it's more of permi, right?

3:32

This most eaten how you describe it.

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See here, you have to zoom in to be able

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to see the abnormality, the bone abnormality you see here,

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it's not the obvious litic destructive,

3:43

but it's obvious that the bone is abnormal, right?

3:46

So really this is a bone lesion

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with a soft tissue component.

3:49

It's not a subpleural or pleura based, um, lesion.

3:53

It's not a long lesion. Let me put it in a long window here.

3:57

So look here. See, it's not a long nodule. It is not.

4:02

It is actually a bone lesion with soft tissue component.

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And this is important to determine in a multiple myeloma.

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Why? Because multiple myeloma lesions are either middle

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or extramedullary lesion.

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And it's important to decide on this patient,

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are all these lesions gonna be middle only or there is mid

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and extra medullary?

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This is important in their staging.

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And it's, so Im important to emphasize this

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and I, I always tell that to my president

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'cause they always do this mistake.

4:34

They still use primary

4:36

and metastatic terms in, um,

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myeloma and in lymphoma.

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And these are the two that we see a lot.

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We don't see leukemia a lot in our, uh, pet suite

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because leukemia is considered low grade for us.

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So re rarely we would see them coming through our suite.

4:53

Um, so what is the point I'm making here?

4:56

I'm making the point that

4:59

primary metastatic disease are not valid terms

5:02

in lymphoma and myeloma.

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And you have to think about it for a second.

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If you think about myeloma, what is the primary site?

5:10

And if you tell me, well,

5:12

bone marrow is the primary site, okay?

5:14

Bone marrow is the primary site.

5:15

What is the metastatic site? In the myeloma disease?

5:20

There's no metastatic, right?

5:21

Because hematologic malignancies are different than

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the rest of malignancies.

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There's no primary metastatic.

5:27

So they have, we, we have our own terms when we talk about

5:31

hematologic cancers.

5:32

So we need to use their terms, right?

5:35

So the terms we use here in myeloma is medullary, intary,

5:40

and extramedullary, right?

5:41

Or medullary and extramedullary patients.

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Um, in lymphoma we use nodal and extra nodal disease, right?

5:47

So just use their terms in your reports.

5:51

Never say primary metastatic disease.

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When you talk about, um, a myeloma patient,

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a lymphoma patients, even if it's a negative scan,

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don't say, okay, there is no f dg avid primary metastatic

6:02

disease in the myeloma or lymphoma patients.

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It just doesn't look right

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and it makes you look like you

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don't understand what you're talking about.

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This is my advice, okay? So coming back to the patients.

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So in, in a, in a lesion like this, it's easy

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for you when you're looking like on, on, um,

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on the point in the long window

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or the soft tissue window to say, okay,

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is this a pleural based nodule?

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Don't look carefully

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because this will put it in an extra medullary lesion

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category and this will stage the patient differently.

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So make sure, and in this lesion too, make sure that,

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is this a bone lesion or is this really a long lesion?

6:41

Okay? Again, this is another

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litic lesion, right?

6:49

And like I said

6:50

before, you already went through this whole patient,

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the whole case,

6:55

and you just figured out that all these lesions are

7:00

just here.

7:02

Look how here, put this one here. TIC lesion here.

7:05

That is ly active. This is the uter.

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You have to make sure it is the uter. Just follow it up.

7:16

This there, right? So this isn't, there's no problem.

7:19

It's not a lymph, it's just David.

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So all the lesions in these patients are,

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um, bone lesions, right?

7:31

I'm looking at bladder

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and there's nothing suspicious here.

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It's just like some, um, bladder neck funneling

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that we sometimes see or there's maybe, I don't remember.

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There's something in this.

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I'll just go slowly and make sure what are we seeing?

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Because there's some budding here

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and the, it's just how the most probably it's how the

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bowel is sitting on the semi empty bladder.

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Just put it in a different orientation and go there.

8:16

I'm sorry it's a little bit slow

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because I have like four cases open.

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So single here is gonna be slower than normal.

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See how, how it is looking in the sagittal, see this

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here, the in the bowel is sitting on the bladder,

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making the bladder look kind of concave, right?

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This one, this is why when you look axial,

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it looks like there's focal connectivity here,

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but it's not focal connectivity, it's just

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the bladder, right?

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You just confirm that this is what it's, okay.

8:47

So this lesion, this patient has numerous metabolically

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active medullary,

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but plate lesions with soft tissue,

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some are some which is the larger,

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larger ones have soft tissue components.

8:57

All this has been lower disease, right?

9:01

And then some incidental findings, right?

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And I'm not gonna go over the incidental findings.

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You know how to report incidental CT findings

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and we do report the CT findings, of course.

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Um, the important other point I always make in these cases

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is that there's no evidence

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of metabolically active extramedullary disease.

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This is it because this is important in the stage.

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That's it for this multiple myeloma patient

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because this was an interest staging, um, patient.

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And of course if you look here at the map,

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although there is diffuse in this patient,

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there is diffuse bone marrow activation as you see here.

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There's diffuse homogenous bone marrow activation,

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but it's obvious that is in the, there's a background

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of bone marrow activation, but there's also disease, right?

9:48

It's obvious. This is what we always say.

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We can tell when there is a bone marrow involvement on top

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of the bone marrow activation, right?

9:59

So there's a difference between the look of involvement

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or infiltration and activation.

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There's a difference. And we can tell when there is

10:07

both in the same patient.

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And you can see here how there is bone marrow activation

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and infiltration in the same time, right?

10:15

It's obvious in this patient, right? It's beautiful, right?

10:20

I don't think there's anything else in this patient that is,

10:22

um, significant.

Report

Please note: Items with dashed lines (--) are information withheld as it is not relevant for you to arrive at the correct findings and impression for the report and/or it was withheld for privacy information. The items were left in to show you the typical information documented in a PET report.

Clinical Indication:
---year-old male recently diagnosed with IgG kappa multiple myeloma, presenting for initial staging.

Technique:
Preparation: Last oral intake (except water) on --at --.
Diabetic: --.
Blood glucose at time of FDG administration: --- mg/dL.
Radiopharmaceutical: -- mCi of F-18 FDG administered IV at -- at --.
Incubation interval: -- minutes.
Oral contrast: --.
Positioning: --.
PET/CT scanner: ---.
PET/CT acquisition: Vertex-to-feet.
PET reconstruction method: ---
Standardized uptake value (SUV): Corrected for body weight only.
CT: Low-dose, non-breath-hold, without intravenous contrast.
TOTAL DLP (Dose Length Product): -- mGy cm.

Comparison/Correlation:
--

Findings:
Technical quality: Diagnostic.
Measurements: Unless otherwise specified, all SUVs refer to maximum value in the target (mSUV) and all CT linear measurements are performed on axial images.


Head and Neck:
Intensely hypermetabolic lytic lesion involving both the inner and outer tables of the left parietal bone/vertex with a large soft tissue component showing dural extension measuring 2.9 x 2.4 cm with maximum SUV 9.0.
No suspicious hypermetabolic cervical lymphadenopathy.
The thyroid is unremarkable.


Chest:
No suspicious hypermetabolic lesions within the chest.
Physiologic FDG avidity involving the left ventricular myocardium.
There is no pericardial effusion.
There are no suspicious hypermetabolic or pathologically enlarged mediastinal, hilar or axillary lymph nodes.
No suspicious hypermetabolic pulmonary masses, nodules or airspace consolidations.
Multiple calcified lung granulomas.
Right IJ Port-A-Cath with tip in the cavoatrial junction.
Calcified mediastinal and perihilar granulomas.
Small right pleural effusion, likely reactive.


Abdomen:
No suspicious hypermetabolic lesions within the abdomen and pelvis.
Physiologic FDG avidity in the liver, spleen, adrenal glands and pancreas. The spleen is normal in size, measuring 12.7 cm in maximum craniocaudal dimension.
Tubular, physiologic FDG avidity throughout normal caliber loops of small bowel. There is no ascites.
There are no suspicious hypermetabolic or pathologically enlarged mesenteric, retroperitoneal, pelvic or inguinal lymph nodes.
Symmetric, physiologic excretion of the radiotracer from both kidneys.


Musculoskeletal:
Diffuse intensely hypermetabolic lytic lesions, many of them with soft tissue components, involving the axial and appendicular skeleton. Index lesions are:

Intense focal FDG activity fusing to a permeative lesion of the right 5th rib anteriorly with associated hypermetabolic subpleural soft tissue thickening, maximum SUV 12.4.
Intensely hypermetabolic lytic lesion involving the left pedicle and the left the transverse process of T9: maximum SUV 12.4.
Intensely hypermetabolic right iliac crest lytic lesion: maximum SUV 7.5.

Impression:
1. Diffuse intensely hypermetabolic lytic lesions, many of which have soft tissue components, involving the axial and appendicular skeleton, including a left vertical parietal lesion with soft tissue component on both sides of the calvarium, consistent with biopsy proven multiple myeloma.
2. No evidence of hypermetabolic extramedullary disease.

Case Discussion

Faculty

Riham El Khouli, MD

Associate Professor of Radiology, Chief, Division of Nuclear Medicine/Molecular Imaging & Radiotheranostics

University of Kentucky

Michael F. Shriver, MD

Director of Nuclear Medicine

Proscan-NCH Imaging

Tags

PET/CT FDG

PET

Nuclear Medicine

Hematologic

CT