Interactive Transcript
1:59
Um, but we will see plenty of, uh, great cases,
2:04
uh, of both Crohn's disease, ulcerative colitis.
2:06
Small and large bowel tumors.
2:08
All the indications, uh, CT and
2:11
MR, MR enterography are used for.
2:13
Um, and also we will spend a few minutes just
2:18
looking over the structured, standardized, uh,
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reporting systems suggested for CTE's and MRE's.
2:25
And again, coming back to, let's start with CTE.
2:28
Um, of course, inflammatory bowel disease
2:31
remains the number one indication for CTE.
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Uh, we also, um, suggest our, the
2:38
referring providers also request this for
2:40
evaluation of small bowel neoplasms and.
2:44
These are also wonderful for, uh, detecting
2:47
GI bleeding, and in fact, these are the, these
2:50
are the optimum imaging studies for detecting
2:53
GI bleeding and also for mesenteric ischemia with
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just a slight modification in the protocol.
2:59
So.
3:00
Now for in general for CT enterography prep,
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um, usually we advise fasting for six hours.
3:06
Some institutions use laxatives.
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We don't use it in our institution, it's optional.
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Um, in cases like this with large colonic stool
3:14
volumes, sometimes laxatives are very helpful.
3:17
Uh, these can compress on the
3:19
edges in small bowel loops.
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Uh, also on MR, the large amount of
3:23
stool can sometimes cause artifacts.
3:25
So some laxatives can be useful.
3:28
Um, this is the protocol followed by our institution.
3:32
We don't do a pre-contrast image.
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We are trying to reduce radiation as much as possible.
3:39
Uh, we have found that just the venous phase,
3:42
uh, done in axial and with reconstruction,
3:46
sagittal and coronal reconstruction suffice,
3:49
giving us all the information we need.
3:51
Uh, we also image from dome of liver to pubis.
3:58
Just a couple of minutes compared to MR
4:00
enterography, which takes much longer.
4:03
Uh, so we are able to cover large
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areas in a short amount of time.
4:07
Now we do give PIC to the patients.
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These may or may not be used in other institutions.
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Um.
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This was a policy in place before
4:16
I started here as a faculty.
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Uh, I guess because of better
4:20
safety, renal safety profile of PIC.
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It is slightly expensive, so may
4:24
not be feasible in all institutions.
4:26
Uh, contrast is given at a rate of four ccs.
4:29
The scan delay for, of 60 to 17.
4:32
Second, this is the typical
4:33
venous phase, oral contrast.
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We give what is called, uh, the, uh, it's
4:39
called Bria, which is a flavored beverage.
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Now let's take a step back and
4:43
talk about oral contrast agent.
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Um, so the number one goal of oral
4:48
contrast agent is to identify bowel from
4:51
non-bowel structures in the abdomen.
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Um.
4:54
This is also important for accurate assessment of
4:58
bowel wall thickness because, as you know, collapsed
5:00
bowel falsely gives us, um, increased thicken—thicken.
5:05
It gives the appearance of increased thickness,
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and so we need to optimally distend it
5:09
before measuring the bowel thickness. And also,
5:13
especially with inflammatory bowel disease
5:16
and any enteritis as such, we absolutely need
5:19
to appreciate the mucosal, lip enhancement.
5:23
So, in general, there are like three types of
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contrast: negative contrast, which is air—
5:27
It is
5:28
black. It outlines the wall.
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Uh, positive contrast is the contrast which is used
5:34
in the normal outpatient, uh, inpatient settings.
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It is bright. Contrast has barium or iodine
5:40
in it. And then we use neutral contrast.
5:43
So this is an image, is an example
5:45
of how positive contrast is
5:47
being—we are able to differentiate these
5:49
large lymph nodes, uh, in this patient with
5:52
non-Hodgkin's lymphoma from the actual bowel,
5:55
which are opacified with the contrast.
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Again, this can be barium-based or iodine-based.
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Um, if we are thinking of an, you know, in an ED
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setting or, uh, where we—the patient may get
6:06
operated on, there is concern for perforation,
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it's best to avoid barium to avoid the peritonitis.
6:12
Another example where these were actually the ovarian
6:16
in the pelvis in a patient with, uh,
6:18
ovarian hyperstimulation syndrome, you
6:20
can see some pleural effusion still.
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Um, in this, we were able to effectively differentiate
6:25
these structures in the pelvis from the actual bowel.
6:30
Now, neutral contrast agent.
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This is the contrast agent used
6:34
for CT and MR enterography.
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We want the bowel to be not bright, so that we
6:41
can appre—appreciate this mucosal enhancement.
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Um, and also the other goal for—to give
6:47
this large amount of fluid is to displace.
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All the air in the bowel, uh, that
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way it's kind of optimally distended,
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doesn't create a lot of artifacts.
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We typically give about 1,350 mL over 60 minutes.
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Not all patients are able to drink this amount.
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Uh, there are patients with large
7:03
bowel redundancy who may require more.
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Um, the last 200 mL is given just 10
7:08
minutes before the study to—and the stomach
7:10
and di—di—the commercially available agents.
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Um, Volumen—it's called Lumox now—and Bracco.
7:20
So Volumen has an extra component, which
7:23
is, um, uh, barium sulfate suspension,
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but it is very, very low amount of barium.
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The purpose—why barium is used for contrast agent is
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it slightly increases the osmolality of the fluid,
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and it keeps the bowel distended for several minutes,
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giving us the time to image these
7:42
patients while the bowel is distended.
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Now, Bracco does not have that component.
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Um, it has other components which kind
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of increase the slight thickness of
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the, uh, fluid—like sorbitol, citric acid.
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Um, but it is—theoretically it wouldn't
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distend the bowel as much as Volumen does.
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However, Bracco tastes like soda.
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It has—
8:07
better, um, taste.
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It has better, uh, flavor characteristics.
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So it is, uh, kind of accepted by patients more.
8:15
In fact, there have been several
8:17
studies comparing these two agents.
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Uh, there was one published in Radiology in
8:21
2018, which was a randomized control study of
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66 pediatric patients, and they concluded
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that the neutral oral contrast material,
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uh, Bracco, uh, they provide similar small bowel
8:34
distension, and the patients tended—tended to
8:38
drink the entire volume of, uh, Bracco compared to
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Volumen, where they were—Volumen—and where they were
8:45
not able to tolerate more than one or two bottles.
8:48
Now with imaging studies,
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especially a long study such as MR
8:52
Enterography, patient cooperation
8:54
is extremely important.
8:56
So if you would ask me, I would rather
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give the patient something which
9:00
they like, makes them comfortable.
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And also, I would rather make them drink
9:06
a lot of fluid just than their bowel,
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uh, than give something, uh, which, um.
9:12
Makes them, uh, creates discomfort.
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There was another study in pediatric population,
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uh, in which they said, uh, the Briza was more
9:20
palatable than Volin, and they also suggested
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that, you know, you could try Volin. If the
9:25
patient doesn't like it, give them Briza.
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So, use combination of both.
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And so, what is a perfect, uh, CT Enterography?
9:35
Obviously, the bowel should be well distended.
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Uh, most importantly, it should also have
9:40
an appropriate, uh, IV contrast phase.
9:44
And I have recently started loving
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the multiplanar reconstructions.
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These are really good to localize the mass or
9:53
inflammation, or they just exaggerate the abnormality.
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Uh, they also show this, um, the prominent vasa
10:02
which you see in IBD really well.
10:05
And let's see, a few cases, uh.
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Patient with, um, you know, really long
10:14
segment thickening of duodenum.
10:17
There is mucosal hyperenhancement.
10:20
Um, there is prominent vasa recta.
10:23
There were no fistulas or other abnormalities.
10:26
Um, in the cecal loops, you may have
10:28
noticed some enlarged lymph nodes.
10:30
And also, um, there was also a
10:35
perianal abscess as well.
10:37
All these findings were seen really well
10:39
on the enterography image in this patient
10:41
with active inflammatory bowel disease.
10:44
Another case, this case you could actually see
10:48
there is upstream, uh, dilatation of the bowel.
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So, we could call this segment a stricture.
10:54
For you to call something stricture,
10:55
there should be a very obvious upstream dilatation.
10:59
Uh, also, the bowel was dilated
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more than three or 3.5 centimeters.
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This patient also had a perianal abscess.
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All these features were seen on the CT Enterography.
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Another example of, uh, a perianal abscess
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as well as a fistula, um, which
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was well visualized on this study.
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And this is a case of a young woman with,
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um, rectovaginal fistula, and you
11:29
can actually follow the tract pretty well.
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Uh, this is coronal reconstruction.
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You can see the fistula.
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Um, so I do think that with experience and,
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um, um, these can be picked up on CT as well.
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Although MRI is considered the gold
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standard for penetrating disease.
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Um, very tiny fistulas are
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kind of harder to see on CT.
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Uh, this is the MR on the same patient.
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Uh.
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This was done a few months later and, uh, she's
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pregnant on this MR. You can actually see.
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And the non-contrast MRI was performed.
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Um, you can actually see the fistula
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tract pretty well on the MRI.
12:11
Again, the tract extending from ECT temp to...
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So there are benefits to both techniques.
12:19
Um, another case, soft tissue mass in a
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patient with biliary ductal dilatation
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in the duodenum right at the ampulla.
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So that was a case of ampullary
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adenoma, um, again seen on enterography.
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Um, so this would be a question slide.
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So could we load question one?
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Uh, for these images please?
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Jaw, actually.
12:47
Oh yes, there it is.
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Okay, so this — these windows can actually move to
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the side if you still wanna look at the images.
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These are the CT images of the pelvis.
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What is your diagnosis?
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Do you see a colon malignancy, colonic,
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diverticulitis, aortitis, chronic
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bleeding, or ulcerative colitis?
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I love this combination of answers.
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Thank you for participating.
13:14
So, looks like colonic
13:16
diverticulitis has the most words.
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And to be honest, I'm from Missouri.
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I see this like literally every day.
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Uh, but in this case, there is diverticulosis,
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there are tons of diverticula.
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There is no inflammation around the colon.
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There is no diverticulitis.
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But you do see this.
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So this is a non-contrast CT on the top and
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then you start seeing the bright stuff inside
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the colon, which tends to enlarge over time.
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So this was a case of colonic bleeding,
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and we were able to appreciate this bleeding
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because of the enterography template.
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Now, for GI—suspected GI bleeding,
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we do get a non-contrast CT.
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Uh, we also get an arterial and venous phase.
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Um.
14:06
I am trying to get to the next slide.
14:08
Okay, there it is.
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So this was, uh, the diagnosis
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was actually colonic bleeding.
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Um, and we ended up getting a
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really delayed phase for the CT.
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I don't know why, but then now the
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colon's filled up with all the contrast.
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You can see it in multiplanar reconstructions.
14:26
Case six.
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So there's no question with this case, but I'll
14:29
give you guys a moment to spot that abnormality.
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It's kind of an eye test.
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I thought it was a cool case.
14:37
Okay, I think that moment's done.
14:40
Uh, so there is this fatty lesion in the ileal wall.
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So this was a case of lipoma in the wall of the ileum.
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This would be question two.
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I could launch the poll.
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I'll just move this to the side.
15:02
Uh, what is your diagnosis?
15:04
Is it small bowel lymphoma?
15:07
Small bowel hematoma? Crohn's disease?
15:10
I'm referring to the segment, uh, of proximal
15:13
small bowel—or small bowel adenocarcinoma.
15:19
That is great.
15:20
Yes, this is indeed small bowel lymphoma.
15:23
You all have very keen eyes.
15:26
Uh, so do you see this classic aneurysmal thickening
15:30
of the small bowel extending over a long segment?
15:34
So this came back as non-Hodgkin's
15:36
lymphoma of the small bowel.
15:41
Okay, so that was small bowel lymphoma.
15:44
I have a few example cases. I'll try
15:46
to get through as many as possible.
15:48
This was a case of small bowel to colonic fistula.
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There were multiple tracts
15:56
in a patient with Crohn's disease.
15:58
Um, case nine, uh, there was—
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uh, wait. Is this a question?
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Yes.
16:06
So this is question number three.
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What is the diagnosis?
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Is this cecal adenocarcinoma?
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Ccal angio ectasia, lower GI bleeding, or both B and
16:20
C. Which would be SL angio and lower GI bleeding.
16:26
Very well done.
16:28
So, yes.
16:29
So this was indeed.
16:31
So these hyper-enhancing dots, areas that you see
16:35
was actually a vascular abnormality in the SSL wall.
16:39
This is SL angioectasia, but you also see a blush.
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Something which doesn't conform to the wall.
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And it was confirmed on, um, angio.
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So there was bleeding from this angio.
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I have few more example cases.
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Um, so this was both BMC, which is
17:00
SL angio with bleeding.
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Uh, so there are abnormally dilated, uh, submucosal
17:08
veins, and right colon is the most common location.
17:13
Also, you can see there are exam—
17:15
These are the examples of arteriovenous
17:16
malformation where there are giant dilated
17:19
veins, uh, extending to the sigmoid colon.
17:23
Another case of a, uh, AV malformation in the jejunum.
17:31
This is, um, let me try to pronounce this.
17:37
Dieulafoy, sorry, I, I am, uh, not even gonna try it.
17:41
It's like, I think it's called like the Dieulafoy lesion.
17:44
Uh, I may be wrong.
17:45
So this is actually rare.
17:47
Um, it is seen, it's a large caliber arterial
17:51
in the bowel wall, and that sometimes erodes
17:54
and bleeds and can lead to GI bleeding.
17:58
A few other cases.
18:00
Uh, this is a case of, uh, mesenteric hematoma.
18:05
And these bright stuff, which you see
18:08
was actually just blood products, as there
18:10
was no active bleeding seen on, um, uh,
18:14
subtraction images, a case of adrenal hematoma.
18:19
And this was a case of, um, ileal adenocarcinoma,
18:25
again, seen on— okay, this would be a question four.
18:36
I would say this is the highlight of today's doc.
18:40
What is your diagnosis?
18:43
Is this a small bowel obstruction secondary
18:46
to adhesions, small bowel obstruction,
18:48
secondary to closed loop, uh, obstruction,
18:52
or a small bowel obstruction from internal
18:54
hernia, or a small bowel obstruction from B.
18:59
Yes, this indeed was a small bowel obstruction
19:04
secondary to— this was a giant hairball.
19:09
This was a baby hairball in the kind of—
19:13
Well, the report said distal jejunum, proximal
19:17
ileal region causing upstream dilatation.
19:21
And I have to apologize in advance.
19:26
I will be showing you some unpleasant images.
19:29
So this was actually endoscopy images.
19:31
You can see gastric rugae.
19:33
This was the hairball in the stomach.
19:36
Hairball in the jejunum.
19:37
You can see all mucosal part there.
19:40
Uh, so that was also spotted on enterography.
19:45
Um, I think this is the last case for CT enterography.
19:48
This was a case of obstruction secondary to adhesions.
19:52
Oh, and this was a case from last week.
19:55
I couldn't stop myself from, uh, posting this.
19:57
This was a case of small bowel wall, and because there
20:01
was no oral contrast present, uh, to create confusion,
20:06
you can actually see the segments which are
20:09
enhancing and the segments that were not enhancing.
20:12
There was extensive ischemia in
20:13
this patient from twisting cent.
20:16
At this point, you can see the beak there.
20:21
And, uh, this is a case of colon to duodenal
20:24
fistula, a small—this case shows how
20:29
important it is for the small bowel to be distended.
20:32
Okay, let's talk about MR enterography.
20:35
MR enterography, it's becoming the preferred
20:37
imaging modality to assess disease activity.
20:41
The GI docs are like more familiar with
20:44
this technique, and they've been requesting
20:46
more and more of MR enterography.
20:48
Uh, the advantages are there is no radiation
20:51
exposure, so this is extremely helpful, especially in
20:55
pediatric population, in children with inflammatory
20:57
bowel disease, who will get follow-up studies
20:59
all their life. Uh, because these radiation doses can
21:03
accumulate over time to cancer-forming doses, it's
21:06
important that we image wisely in this population.
21:10
And also, this is extreme.
21:12
This gives us high diagnostic confidence in evaluating
21:15
inflammatory, stricturing, and penetrating disease.
21:18
Um, prep, again, similar to CT—fast for six hours.
21:22
Laxative optional. Oral contrast is
21:25
given one hour before the procedure.
21:26
Again, Breather versus Volumen, things still stay.
21:29
Okay.
21:30
Just one point about Volumen: although it has barium
21:32
sulfate, which technically, uh, should
21:36
make, uh, this, um, the bowel dark, uh, because of
21:40
barium, but it's such minimal amount of barium
21:43
that this really doesn't signal intensity.
21:47
The sequence we perform are—
21:51
A regular T2-weighted sequence
21:53
in coronal and axial planes.
21:55
This gives us, the purpose of this is for anatomy,
21:58
to localize the lesion where it is present.
22:00
And this sequence is pretty robust for motion.
22:04
So even if there is peristalsis, kind of, it's, it
22:07
doesn't appear as, um, uh, you know, with peristalsis,
22:12
the, the motion is not reflected on the images.
22:15
Um, T2 fat saturation.
22:16
This is extremely important.
22:19
And also imaging,
22:20
the perianal region is really
22:21
important in all IBD patients.
22:23
That's part of our protocol, whether
22:25
the providers request it or not.
22:27
And with these T2 fat sat images,
22:29
the abscesses and fistulas just become
22:32
more conspicuous, and they stand out.
22:34
Um, another sequence, which is my
22:36
favorite is, um, the steady-state fast
22:40
precision sequence, which is slightly T
22:42
2-weighted so that the wa— the lumen,
22:44
the fluid within the lumen appears bright.
22:46
Uh, this kind of, uh, marks the bowel segment
22:50
and also this is pretty robust to motion.
22:52
Uh, so if you wanna evaluate, um, any
22:55
narrowing, uh, this, this is a good
22:58
sequence for thick wall thickening and—
23:01
Actually, this is my favorite sequence.
23:03
It's the cine, uh, steady-
23:05
state fast precision sequence.
23:07
Unfortunately, because we are trying
23:08
to make our MR shorter and shorter, uh,
23:12
we don't do this, um, sequence anymore.
23:16
Uh, but this gives us such a good idea about
23:19
the motility of the bowel, um, kind of,
23:23
um, is able to point us or lead us towards—
23:27
the actual segments which are narrow or strictured.
23:32
And, uh, of course, the— I say my, um,
23:36
my mentor used to call this the money shot,
23:38
which is the post-contrast sequences.
23:41
Um, these— it's so important to have as
23:45
less motion because these are gradient
23:48
sequences, and they are susceptible to motion
23:51
artifacts and to— wide or decrease the—
23:56
Glucagon is usually given, uh, just before
23:59
imaging, getting the post-contrast images. Now,
24:04
there are several different
24:05
protocols suggested for glucagon.
24:07
Uh, it can be given both IM or IV.
24:10
IM has a more unpredictable, uh, response.
24:13
IV has a more predictable response, but it causes
24:16
nausea, so it has to be injected very slowly, and it
24:20
has given— uh, some institutions recommend giving
24:23
it both before the pre-contrast sequences and also
24:27
just before administering contrast administration.
24:31
Um, unfortunately, because of the
24:32
nausea and the patient discomfort, we
24:35
don't give this in our institution.
24:37
Um, but, uh, this definitely
24:41
increases, um, that it, it stops the
24:44
peristalsis of the bowel and really helps, uh.
24:48
Decrease the amount of artifacts.
24:51
Uh, this is contraindicated in patients with
24:53
insulinoma, pheochromocytoma, glucagon.
24:56
Now, glucagon and imaging, again, this
24:59
is a little controversial, just like,
25:01
uh, volume and Brisac, um, controversy.
25:04
So there is—the evidence for its efficacy is lacking.
25:08
Um.
25:08
So there was this article in 1999, uh,
25:12
by EJ and group. Uh, they did not find
25:15
any improvement in colonic distension.
25:18
They—and then there was a publication by Dhan,
25:21
uh, which, uh—the publication said the IV
25:24
glucagon improved bowel visualization in pediatric MR
25:28
enterography, decreases examination length,
25:31
but however, it causes nausea, uh, commonly.
25:35
And, uh, in my experience,
25:39
patients have tolerated this.
25:40
Okay?
25:41
And some patients have crawled out of the scanner
25:44
because this just makes them extremely uncomfortable.
25:48
Uh, so there is wide variation in
25:50
how people react to glucagon and, uh.
25:53
There is this article in which, uh, Dhan concluded
25:57
that they tolerated hyoscine butylbromide—
26:00
it's also called Buscopan—better.
26:03
This could be a good alternative, um,
26:05
especially in developing countries where,
26:07
because hyoscine is, uh, cheaper than glucagon.
26:10
Uh, and this—but however, in this article, they
26:13
said that the distension with glucagon was better.
26:15
So there are two options.
26:17
Glucagon now.
26:19
Diffusion-weighted images.
26:21
These—
26:22
I feel are critical for diagnosis
26:25
of, um, especially in IBD.
26:27
Also, if there are any small and large bowel
26:30
tumors, these sequences make them more conspicuous.
26:34
Diffusion-weighted images are
26:35
also helpful, uh, to look for
26:38
any extraintestinal manifestations, for example.
26:42
Um, if there is cholangitis associated
26:44
with primary sclerosing cholangitis or if
26:47
there are metastases in the liver, um, we,
26:49
these sequences make it more conspicuous.
26:53
Um, now interpretation.
26:56
I would strongly recommend to refer to these articles.
26:59
I have referred to them and I continue
27:02
to refer to them while reporting.
27:04
Um, I think it's important for us to follow
27:06
the consensus recommendations and kind of
27:09
have, we do have structured reporting for CT
27:11
Enterography, and the structured reporting is
27:14
really helpful just to consistently communicate
27:17
the findings, uh, with the referring providers.
27:20
Uh, all the next few slides are
27:22
heavily based on these articles.
27:24
Let's start with this case.
27:26
This was an example of, um, you know, routine MR
27:30
uh, in which you could see in a patient with IBD.
27:33
There is a long segment inflammation.
27:36
Um, it's highlighted well on this steady
27:39
state free precession, uh, sequence.
27:42
Seen well on T2 and the diffusion-weighted image
27:46
is especially being able to highlight that portion
27:50
of mucosal, uh, enhancement or mucosal, uh, activity,
27:54
disease activity, which is shown as restriction.
27:59
So the important, uh, description and why MRI is
28:03
also useful and consistently shows these features
28:06
is, uh, segmental mural hyperenhancement.
28:09
Uh, this is increased signal
28:11
on contrast-enhanced, uh, MRI.
28:14
This could be asymmetric, it
28:17
could be bi- or tri-laminar.
28:19
For example, the mucosa and muscularis
28:22
propria enhanced, uh, with mucosa in between.
28:25
Or they could be homogeneous.
28:29
So this brings us to question number five.
28:33
Don't have image with this.
28:35
Which one of the following is considered a
28:38
highly specific feature of Crohn's disease?
28:42
Is it asymmetric bowel wall thickening?
28:44
Is it intramural edema, stricturing, or ulceration?
28:52
Yes, I am.
28:53
I'm glad it's kind of, uh, divided between asymmetric
28:57
bowel wall thickening and stricturing actually until,
29:01
um, the recent publications by Braining et al.
29:05
I was under the impression too that
29:07
stricturing is highly specific.
29:10
Um, so I think I should have, like,
29:12
reworded this a little bit better.
29:14
Structuring can be seen in several etiology.
29:17
We have to remember that it is
29:18
seen with radiation enteritis.
29:20
It is actually commonly seen
29:22
with NSAIDs intake for pain.
29:26
So that having said, asymmetric bowel wall thickening
29:29
is actually considered a highly specific feature.
29:33
Um, especially in active Crohn's disease and,
29:38
uh, this asymmetric thickening, um, is actually,
29:41
once this information came out, or I have been
29:44
like seeing this in a lot of, um, enterography,
29:48
a lot of active disease cases where the mucosal
29:52
border seems to be more affected than the—
29:57
It is thickened.
29:58
Uh, and what, what is meant
30:00
by this asymmetric thickening?
30:01
And they described in that article, uh, by Broering
30:05
that it could be asymmetric pattern of hyper
30:09
enhancement, or it could be asymmetric wall
30:12
thickening, or it could be asymmetric stratification.
30:15
Any of these three constitutes as
30:18
asymmetric thickening as seen in this case.
30:22
And wall thickening should only be measured in
30:25
the bowel that is well distended by, uh,
30:28
contrast, and it can be graded as mild, moderate,
30:31
and severe based on the amount of thickness.
30:33
Mild would be 3 to 5 millimeter thickness,
30:36
moderate would be 5 to 9 millimeter thickness,
30:39
and if it's more than 10 millimeter
30:40
thickness, it's considered severe disease.
30:44
And if it is way more than one centimeter—
30:48
if it's like almost 1.5 centimeters—then you
30:50
should start getting concerned about malignancy.
30:53
And also another point, uh, if there is
30:57
concern for malignancy, like in that, um,
31:00
uh, small bowel carcinoma case that we
31:03
saw today, the wall was really thickened.
31:06
Uh, mass and malignancy can also grow into—
31:09
organs. They kind of start growing
31:11
outside their serosal border.
31:13
So that could be another tip too.
31:15
So if there is significant thickening,
31:17
don't ignore that as just IBD.
31:20
Um, also, you should be concerned for malignancy.
31:23
Next point: we'll discuss intramural edema.
31:26
This is really well seen on the
31:27
T2 fat images, and if you see—
31:32
uh, hyperintense signal on fat-sat images,
31:35
as well as restriction on diffusion-weighted
31:37
images—that confirms, uh, severe inflammation.
31:43
Now, um, luminal stricture.
31:46
So I actually, I know we are speaking about the MR
31:48
portion, but I brought up the CT image because this
31:50
shows the definition of stricture really, really well.
31:54
Uh, for you to call something a
31:55
stricture, there should be unequivocal
31:58
upstream dilatation and the lumen.
32:00
Upstream dilatation should be
32:02
at least three centimeters.
32:04
And, uh, we should describe
32:06
the length of the stricture.
32:07
This will be helpful for
32:08
surgical endoscopic evaluation.
32:10
And also, as I was mentioning, strictures can
32:13
also be seen with NSAIDs and radiation pathy.
32:16
Um, so this, these are few other examples
32:19
of strictures with, like, upstream dilatation.
32:22
This is a long segment stricture.
32:25
And ulcerations, we actually see them,
32:27
especially if the study is done really well.
32:29
Um, these are, uh, kind of small focal
32:33
breaks in the surface of the bowel wall.
32:36
We can also see them on these T2 FSE images,
32:39
and in the article, um, they, uh, suggest that
32:44
avoid the term penetrating ulcer so that it is not
32:47
confused with penetrating disease such as fistula.
32:52
We can also sometimes see micro
32:54
abscesses in the wall, and also there
32:58
is a terminology called pseudopolyps. The border
33:03
shows asymmetric thickening and strictures.
33:06
The wall can also stricture asymmetrically.
33:09
So sometimes you see these
33:10
projections along the mesenteric border.
33:13
This is the mesenteric border.
33:14
It's just that the baby is flipped.
33:16
Um, these are called pseudosacculations.
33:19
They indicate more, uh, chronic, uh, disease and
33:23
there is diminished motility, which you see as well.
33:26
In this case, there is, um...
33:29
Fistula, and these few segments are moving
33:33
less than the other non-affected segments.
33:36
Now let's talk about penetrating
33:38
disease, uh, because the highlight of MR
33:40
enterography is the ability to
33:44
identify and describe these lesions. So,
33:47
fistulas can be defined as simple.
33:49
So penetrating disease can be
33:51
fistulas, abscesses, sinus tracts.
33:54
So, simple fistula.
33:56
Again, the definition is from the article.
33:58
Again, I cannot emphasize how often this article is.
34:01
Um, so simple fistula can arise from a
34:04
segment of active inflammation or stricture.
34:07
It can connect.
34:08
Bowel to bowel when it is tract,
34:10
fistula to adjacent organs.
34:12
Uh, for example, vagina or bladder, or
34:15
to the skin when it's called a cutaneous.
34:17
Complex fistula is kind of, you cannot
34:21
really, uh, have a start and endpoint to it.
34:24
Multiple bowel just come and they converge, uh,
34:27
usually around an abscess or an inflammatory centric
34:30
mass, and they form what is called a star sign.
34:34
Sinus tract is kind of a blind-ended tract.
34:37
It extends outside the, but
34:39
it doesn't really extend to
34:42
organ, soft skin.
34:44
And then, yes, we always image the perianal
34:47
region and, uh, uh, so there could be many
34:52
patients who present at the time of initial
34:54
diagnosis with the penetrating disease.
34:56
Uh, so this unfortunately brings me to this case,
35:00
uh, of a young man with Crohn's disease who had
35:04
all types of fistulas, sinuses,
35:06
and all, and abscesses.
35:08
Um, there were several perianal
35:12
draining, uh, fistulas extending to the skin.
35:15
In fact, the fistulas were crossing over.
35:18
There were a few transsphincteric, uh, fistulas.
35:23
And this is, uh, an enterocutaneous fistula,
35:27
draining both posteriorly and anteriorly.
35:31
This is the star sign, where all the bowel kind
35:34
of confluence around this, uh, area of scarring.
35:41
And this patient, the ureter also got caught up
35:44
in the clover sign or the star sign, a complex
35:47
fistula tract, and there was debris within
35:49
the ureter, which end upstream dilatation.
35:53
The patient also had myositis, uh, the inflammation
35:56
extended to the muscle, and also, it's not included
35:59
in the image, but the coccyx was inflamed, uh, coccyx,
36:02
and the patient also had osteomyelitis.
36:07
So, last question for the day.
36:10
Identify the structure indicated by the arrow.
36:14
It's the same patient.
36:18
All right, so.
36:21
This was actually this patient's undescended testicle.
36:27
And I will be honest, it took me a few minutes
36:30
to figure this out, and that's why I have
36:33
this companion image of the left groin, where
36:36
you kind of see this on the left side too.
36:38
It was undescended.
36:40
Um.
36:41
But it was not completely
36:43
descended into the scrotal sac.
36:44
It was kind of in the inguinal canal, but on the
36:47
right side it was actually along the pelvic sidewall
36:51
and it was caught up in all this inflammation.
36:55
And, uh, so there was no testicle present
36:57
in the right groin or right scrotal sac.
37:01
And it has, the appearance of it has, it's T
37:03
2 intermediate, uh, does not hyperenhance.
37:07
Uh, so, um.
37:10
So for those of you unstatistical,
37:12
that, that's the right answer.
37:18
Okay.
37:20
This is another case of trans
37:22
fistula, different patient.
37:24
Uh, it starts from a small abscess, but
37:27
then you can see, um, let me control this.
37:31
So it kind of extends.
37:34
Along, uh, the external and internal sphincters.
37:39
Uh, it's also shown based on the coronal
37:42
images, uh, the dark signal with the
37:46
fistula because of the presence of air.
37:50
And, uh, this extraordinarily good resolution,
37:54
um, is seen on T2 fat-saturated images.
37:58
Um.
37:59
Also the other entities we should know with.
38:02
Um, uh.
38:04
Inflammatory bowel disease is, um, the inflammatory
38:07
mass, which we can see shows restriction
38:10
of diffusion and heterogeneous enhancement.
38:12
There is fibro-fatty proliferation, which
38:15
is, which we have seen in all these examples.
38:17
Uh, some of the sequelae of IBD could also be centric
38:21
vein thrombosis, and we almost always see adenopathy.
38:25
Um.
38:26
With MR enterography, we can
38:27
also see extraintestinal findings.
38:30
For example, in this patient with ulcerative
38:32
colitis who also had primary sclerosing
38:35
cholangitis, and we were able to see
38:38
multiple areas of strictures in the liver.
38:43
So reporting-wise to kind of, um, we
38:47
did see all the interpretation portions.
38:49
Uh, so what do the GI docs want?
38:51
They want to know if there is Crohn's.
38:53
First of all, they wanna know if there is IBD or not.
38:56
And then we should, uh, report the number of
38:59
involved bowel segments, approximate location,
39:02
length, and degree of upstream dilatation, and, um.
39:06
When describing the bowel loops, having
39:08
Crohn's stricture, it's important for us
39:11
to say if there is active disease or not,
39:14
because you can still see strictures, fistulas,
39:17
in patients who do not have active disease.
39:21
Uh, so the, uh, the article in Radiology
39:24
has given us, um, suggestions on how we can
39:27
structure our imaging findings and impression.
39:30
Uh, for example, if there is just
39:32
segment hyperenhancement, um.
39:35
Or, uh, you know, if there is no
39:38
known diagnosis of Crohn's disease.
39:40
You can call the impression of non-specific small
39:43
bowel inflammation until it is diagnosed, um,
39:47
by colonoscopy or other tests, and if there is
39:51
asymmetric wall thickening, hyperenhancement, edema.
39:55
Um.
39:56
You could say, uh, and if in a patient with high
39:59
suspicion for Crohn's disease in the impression,
40:01
you could include it as active inflammatory,
40:03
small bowel Crohn's disease, and, uh, whether
40:06
you can also include in the impression without
40:08
luminal narrowing or with luminal narrowing.
40:11
Um, and then in a patient with known Crohn's disease,
40:16
uh, if there are no imaging findings of inflammation.
40:20
You could include in your impression as
40:22
Crohn's disease with no imaging signs of
40:25
active inflammation, and if there is persistent
40:29
luminal narrowing with upstream dilatation,
40:32
that's when you're gonna call it a stricture.
40:34
And if there is, uh, there is upstream dilatation.
40:38
You can also call it a small bowel obstruction.
40:40
And you need to see active inflammation—
40:42
that is, mucosal hyperenhancement—
40:45
uh, to call this, um, stricture with
40:48
imaging findings of active inflammation.
40:51
If there is fistula, sinus tract, or abscesses,
40:55
you could include penetrating Crohn's disease in
40:57
your, uh, disease, and depending on the location,
40:59
you can call it perianal Crohn's disease.
41:02
Now, creeping fat, you know, this is—
41:06
no longer an entity, entity, which is
41:08
ignored, uh, because, um, it is, it is becoming—
41:12
they're becoming more and more aware of the
41:14
fact that visceral and mesenteric fat can become,
41:17
is to become a therapeutic target in IBD.
41:20
And, uh, people are coming up with various imaging,
41:23
uh, techniques to actually assess the changes
41:26
in, um, fat around the inflamed segment or the
41:29
creeping fat to assist the response to treatment.
41:32
Um.
41:34
Few examples of MR enterography.
41:36
Uh, this is a patient with ulcerative colitis.
41:39
You see a long segment of descending colon, which
41:43
is, uh, starting from rectum, then sigmoid colon,
41:49
and then you see descending colon, splenic flexure,
41:54
portion of transverse colon are all a RA.
41:57
It's interesting how you can actually
41:59
see the transition to normal RA and
42:02
the transverse level of transverse colon
42:07
right over here.
42:10
Uh, this is T2-weighted images, which also shows
42:14
that haustral nature of the colon pretty well.
42:18
Uh, so this mainly affects the mucosa, submucosa.
42:21
So stricture is really rare.
42:23
If you do see a stricture in the colon in
42:26
a patient with ulcerative colitis, there, you
42:28
should start getting concerned about cancer.
42:31
You can also see pseudopolyps.
42:33
Um, this, because of the stricture, because of
42:36
the inflammation, it can shorten the colon.
42:39
Now, CT versus MR. There’s always this debate—
42:44
Which one's best?
42:45
There are several articles which said both
42:47
have similar sensitivity in detecting the—
42:50
uh, active disease or chronic changes.
42:53
I think for inpatient and ER settings, CT
42:57
enterography, which can be done rapidly, is optimal.
43:01
I'm yet to see a single, uh, inpatient MR
43:04
enterography which has come out perfectly.
43:06
These patients cannot hold— like,
43:08
they cannot really cooperate.
43:09
They cannot hold the breath.
43:10
They have other comorbidities.
43:12
So I think doing a rapid test,
43:14
such as CT, is better with them.
43:16
Enterography needs more, uh, patients
43:19
who can cooperate a little better.
43:21
Um, CT—
43:22
Great for initial diagnosis and then for
43:25
follow-up studies to assess response to treatment.
43:27
MR enterography would be—
43:29
optimal in pediatric patients.
43:31
I strongly recommend MR enterography
43:34
because there is no radiation risk.
43:36
MR enterography can also be utilized in
43:38
pregnancy or in incidences, uh, in and other
43:41
examples where you want to do a non-contrast
43:44
MRI, um.
43:46
But if there are contraindications to MRI,
43:49
uh, pacemaker or other contraindications, CT
43:52
Enterography would be the default technique to do.
43:55
Again, if there's iodine dye
43:57
allergy, we can consider MR
43:59
Enterography for penetrating Crohn's disease.
44:02
MR Enterography is optimal at the end of all this.
44:06
I think, um, the.
44:08
It completely depends on local
44:10
image access and expertise.
44:12
Um, and also the preferences of
44:14
referring providers sometimes.
44:15
And also we should follow the ACR and
44:18
other, um, GI guidelines while, uh,
44:21
performing and ordering these studies.
44:24
A couple more examples.
44:26
Um, so this was a patient who had a
44:29
centric mass, also had a mass in the cecum.
44:33
Right at the level of ileocecal junction, there
44:36
were some calcifications seen within the mass.
44:40
An octreotide scan — it lit up.
44:43
In addition, there were two lesions
44:45
also seen in the right liver.
44:47
So this was a neuroendocrine tumor,
44:50
um, for carcinoid tumor possibly.
44:53
And, um, so.
44:55
We did do an MR Enterography on this patient in
44:58
which you can see the mass, which is lobulated,
45:02
and on MRI you will not be able to appreciate
45:04
the calcifications, and we were able to see
45:08
really well the liver lesions. The, it, it has
45:12
T2 intermediate intensity, enhances as well.
45:16
Uh, restrict and diffusion in addition, but we
45:19
saw numerous spots of restriction of diffusion.
45:22
So these were all neuroendocrine
45:24
metastases, which were not seen on the CT.
45:27
So with this case, I would like to say
45:29
that sometimes CT and MR Enterography
45:31
are complementary to each other, so we
45:33
may not have to decide one over the other.
45:36
Um, you know, if you don't see penetrating
45:38
diseases well, or if you want to work
45:40
up, the metastases can come in handy.
45:45
This is another case, uh, which was
45:46
actually seen initially on CT and
45:48
then an Enterography was performed.
45:51
There is a mass in the duodenum, restrict on
45:55
diffusion, and, uh, you can actually see it on
45:59
T2, seen well on, uh, coronal images as well.
46:03
And that was an adenoma.
46:05
And this is another case of, um, really this
46:09
is a T2-bright lesion in the colon, which.
46:13
Shows nodular enhancement with gradual fill-in.
46:17
Does it ring a bell?
46:18
This is how hemangiomas enhance, right?
46:20
In liver or in the colon.
46:22
So this was a great example of hemangioma.
46:26
So to summarize, CT Enterography and MRI
46:30
are both excellent imaging options, uh, for
46:33
evaluation of IBD and other bowel tumors.
46:36
Uh, CT is excellent for initial diagnosis.
46:38
MRE could be used for follow-up and for evaluation
46:41
of the penetrating disease, and it's important for
46:44
us to use a consistent, standardized terminology.
46:47
Again, going back to the article by Brainey,
46:50
I would recommend that, um, to accurately
46:53
describe radiology findings, and also
46:57
this ensures the comprehensive evaluation
47:01
and facilitates the compatibility of the reports.
47:05
Thank you.
47:05
Um, you can email me with any questions,
47:07
but I guess we have a few minutes
47:09
to discuss your question as well.
47:15
If you, uh, look in the bottom right-hand
47:17
corner, or actually it should be at the
47:18
top because you're sharing your screen.
47:20
Oh yeah.
47:21
There should be a Q&A section you can click
47:23
on, and you'll be able to see all the questions.
47:25
Yeah, I think I was able to pull it up,
47:27
but just let me know if I missed any questions.
47:30
So the first question I see is,
47:32
can water act as neutral agent?
47:35
Absolutely.
47:36
Water is a neutral agent.
47:38
Uh, the only issue with
47:40
using water for CT and MR Enterography is they—it
47:44
gets absorbed really fast, which is kind of okay for
47:49
CT Enterography too, but you know, it's more rapid.
47:53
You need something which has slightly higher osmolality
47:56
and distends the bowel, at least for a few minutes.
47:59
Uh, water absolutely doesn't
48:01
work for MR Enterography.
48:03
You need the bowel to be distended,
48:04
at least for 20 to 30 minutes.
48:06
So you need to use other agents which have sorbitol,
48:09
gum, and you know, barium sulfate in volume, and
48:13
other agents which can kind of increase the
48:16
osmolality of the water to keep the bowel extended.
48:19
Um, next question is, can we give neutral
48:23
contrast in case of subacute obstruction?
48:26
You know what?
48:27
I, at the, for obstruction, any contrast is great.
48:32
Any contrast which is safe is great because you
48:36
want to extend the, to find a transition point.
48:40
For subacute obstruction, I would personally give a,
48:43
um, bright contrast agent or a positive contrast agent,
48:47
just so that I can definitively say if the contrast
48:51
has transitioned beyond the transition point. I will
48:55
not be able to say that with neutral contrast agent.
48:58
So for subacute obstruction, my personal
49:00
preference would be a positive contrast agent.
49:03
The next question is, do you give
49:04
medications for bowel paresis?
49:07
You know what? I, personally, I think giving
49:11
medications for bowel paresis is very helpful.
49:14
Um, glucagon and Buscopan are both
49:17
agents, which I discussed in this—
49:19
Um.
49:19
—presentation. We don't give them at our
49:22
institutions because it was just
49:25
really hard to kind of, um, coordinate.
49:28
And then, um, it's just, many
49:31
patients—we have only used glucagon.
49:34
We have not used Buscopan, so I cannot, um,
49:37
really speak about our experience with
49:39
that medication, but with glucagon,
49:41
many patients were uncomfortable.
49:43
So the nurses have to be trained, or the
49:45
technologist, to inject this really, really slowly.
49:49
And we, as a fellow—I, um, I actually injected
49:53
it myself really slowly, but you know, the
49:56
workflow—things have become so much busier.
49:58
So it's kind of harder for us to get involved.
50:01
Yes.
50:02
So if you are able to do it, then
50:04
I think medications really help.
50:06
Uh, we don't do it in our institutions.
50:10
So are these videos available for watching later?
50:12
I think this is a question for Joe.
50:14
They, they are available as replays, right?
50:17
Yes.
50:18
It'll be available on the website later this evening.
50:21
Okay.
50:24
Yes.
50:25
And, uh, thank you, Joe.
50:27
And they said, can we have structured
50:29
reporting format available?
50:32
You know what, um, I will be
50:33
happy to share it with you.
50:35
Uh, we have a very well-functioning, uh,
50:37
structured, structured reporting format.
50:40
I can send it to Ashley and Joe, or you could
50:42
like email me, uh, on this email on the
50:45
screen, and I'll be happy to share it with you.
50:49
Um.
50:50
For underdeveloped countries, what
50:51
alternative preparation we can use if we
50:53
don't have Briza and Volumen really available?
50:56
You know what, that's a very good question.
50:59
I have been thinking about this, and I, I have
51:04
tasted Briza, so you know what, I, I don't, I'm
51:07
sure, like the companies have better reasoning.
51:10
These are safer, well-tested on people.
51:13
Um, so.
51:16
I would just give water or soda or other
51:19
preparations, which, um, could, uh, so
51:22
fizzy water, basically, um, soda, can they
51:26
say, um, can, uh, keep the bowel distended?
51:31
I don't have personal experience with this,
51:33
so I'm not really endorsing the technique.
51:35
But, um, that is something I've thought of.
51:37
And, uh, I would, I would like to know if any of you
51:41
have used anything other than this, which is, um.
51:45
Kind of less expensive alternatives, but I would,
51:48
I would think soda or, uh, you know, just sparkling
51:51
water should do that, you know, should help.
51:54
Although I have no experience with this.
51:56
Um, can patients with difficult bowel prep
51:59
for endoscopy can be, uh, so can people
52:06
with difficult bowel prep for endoscopy
52:08
can be an indication for CT enteroscopy?
52:13
You know what, I don't think so, because
52:16
large amount of stool in the colon
52:20
really creates a lot of artifacts.
52:23
So I think a good, uh, that is not really
52:26
an indication, but if the patient cannot
52:29
get an endoscopy for any reason, we
52:31
could definitely try CT enterography.
52:33
I think it'll still give you information,
52:36
but you shouldn't be referring the patient
52:38
just because the bowel prep is not good.
52:41
Maybe repeat endoscopy with the stronger
52:43
regimen would be a good option, uh, because.
52:47
Excessive amount of stool just
52:49
does, just degrades the images.
52:51
But if there are no other choices,
52:53
definitely CT enterography.
52:56
Now, 1.5 was the 3T magnet for abdominal MRIs.
53:00
I think a lot of, um, they, they're, you
53:04
know, it's improving now, right?
53:06
They're bringing in all these newer
53:09
sequences which are more robust to motion.
53:12
I personally do like 1.5 Tesla, especially
53:16
uh, imaging structures which have, you know,
53:21
techniques or imaging studies which are
53:23
prone to artifact, which is the best example,
53:26
is the post-contrast images of, uh, MR
53:28
enterography.
53:30
The bowel is peristalsing.
53:31
So if you have not given glucagon, if there
53:33
is no adequate, uh, distension, I think
53:36
1.5 would be more robust for the artifacts.
53:40
But, um, 3T, uh, is also fine, uh,
53:45
with the newer sequences.
53:46
But if I had to choose, I would choose 1.5.
53:51
Any clues for finding bowel-to-bowel
53:53
fistulas? There are times they are difficult to find.
53:56
Um, thank you for your compliment.
53:58
Um, so, uh, they said, "Thanks
54:02
for the wonderful lecture anyway."
54:04
So any clues for finding bowel-to-bowel fistula?
54:08
You know what?
54:09
Adequate distension always helps.
54:12
And for me, like for the CT study in which there
54:16
was this perianal fistula, that was a hard one.
54:20
For the CT especially, windowing really helps.
54:23
I actually
54:24
window it down to the liver window
54:27
and then slightly adjust it.
54:29
And that kind of makes, especially in the
54:31
perianal region, it makes it more conspicuous.
54:35
Um, so for the CT, windowing definitely helps.
54:39
Bowel distension is a must.
54:41
And, uh—
54:42
For MRI, it's important for us
54:45
to have larger field of view.
54:47
And again, for MRI T2, fat sat is the key.
54:51
There are also, like, STIR images, which
54:53
are inversion recovery images, which also
54:55
are very sensitive to show the fistulas.
54:58
So spend more time on the T2 fat sat images.
55:02
Can 2% mannitol be used as a neutral contrast agent?
55:06
I did read an article on this
55:07
while doing research for this.
55:09
I don't have experience on this.
55:11
I think I would refer
55:12
you to do independent search.
55:14
I, I absolutely don't have experience on Mannitol.
55:18
Can we use pineapple juice as oral contrast?
55:20
You know what?
55:22
I was, I read an article on milk being used as oral
55:26
contrast, pineapple juice being used as oral contrast.
55:29
I do, you know what?
55:30
Technically, pineapple juice does
55:32
have all the sugary osmolal stuff.
55:34
So again, I don't know.
55:36
I do feel these are alternatives,
55:38
which is completely worth the try.
55:41
Um, as long as they're safe and your patients
55:43
are okay with that, try it on your patients.
55:45
Do a couple of MRs and see if
55:47
you're able to achieve this.
55:50
Technically, I feel anything
55:52
other than water should be good.
55:53
Uh, so, but I think if you, if you have
55:56
some experience with this, please share with
55:58
me how to know by CT and MRI, the cause of
56:01
stricture is more due to Crohn's or cancer.
56:04
Very good question.
56:06
Sometimes in early cancer, it's impossible to know.
56:10
Um, so that's why we ask for follow-up.
56:13
If the thickness of the wall is more than
56:16
one, one centimeter or 1.5 centimeters,
56:20
I am really concerned about malignancy.
56:23
Malignancy also restricts. Uh, so I would get a
56:26
short interval, but if it's between one to 1.5,
56:30
there is, and also in malignancy, you don't see much
56:32
inflammation around it. In Crohn's disease and MRI,
56:36
there is bowel wall thickening and there is
56:38
extensive restriction or prominent vasa recta, or like
56:42
all other features of inflammation around it.
56:45
With cancer, you can have a little bit of
56:47
inflammation, but not a lot of inflammation.
56:50
So if it is more than 1.5 centimeters
56:53
thickness in a well-standard bowel wall,
56:56
if without much inflammation around it,
56:58
I would be more concerned for malignancy.
57:01
But if it is between one to 1.5, you're
57:04
not sure, get a short interval follow-
57:06
up and, uh, see if this mass has grown.
57:10
And I would suggest like in short interval
57:12
follow-up in three months, we are—
57:15
Um, lactose mixed with water and
57:17
diluted Mannitol prescription.
57:19
That is good to know.
57:21
Um, so because that could be an alternative
57:24
for the previous questions, uh, which are
57:26
asked. Uh, I don't have experience, but
57:28
thank you for sharing water and Mannitol.
57:31
Can it be a good combination?
57:32
You know what, I need to really look into Mannitol.
57:34
I have no experience.
57:36
It could be. We have to look at the
57:38
literature for this post-treatment appearance.
57:42
Um.
57:44
Particularly biologicals.
57:45
You know what, I would like to—maybe as a
57:48
follow-up lecture, I could actually bring
57:51
cases post-treatment, but I think it's
57:53
like beyond the scope of this discussion.
57:55
But that's, that's a good question.
57:57
Um, thank you for your comments.
58:00
I think I've, uh, I think I've
58:02
like answered all the questions.
58:03
What do you think, Jill?
58:07
You do?
58:07
I think we're done.
58:08
Yes.
58:09
Yeah, as we bring this to a close, I want to thank you,
58:11
Dr. Tepa, for giving this lecture, and thanks to all
58:14
you guys for participating in our noon conference.
58:16
A quick reminder that this conference will
58:18
be available on demand on MRIonline.com,
58:21
in addition to all the previous noon conferences.
58:25
Tomorrow we're gonna be joined by Dr.
58:26
Maher Mehta for a replay lecture on
58:28
imaging of the gallbladder and bile ducts.
58:31
You can register for that at MRIonline.com, and
58:33
follow us on social media at MRI Online for
58:36
updates and reminders on upcoming noon conferences.
58:38
Thanks again and have a great day.
58:41
Thank you, Joe.
58:42
Thank you, guys.
58:43
Bye.
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