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Technique for Salivary Gland Imaging – Summary

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Well, we're about an hour into this course and all

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we've done is go through the anatomy.

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But this is a mastery course after all.

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So you've learned quite a bit of the anatomy of the

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major salivary glands, those including the parotid,

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the submandibular and the sublingual glands,

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as well as the minor salivary gland tissue.

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Let's talk very briefly about scan sequences

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and how we actually image it.

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I've pointed out a few of these cases thus far

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in which we've looked at the technique.

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Now, at my institution at Johns Hopkins,

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we collect and display all of the thin

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section images of multidetector CT.

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So in our analysis of the head and neck region

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or the salivary gland region,

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we will obtain 0.6 millimeter thick slices,

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and we get the whole body of the anatomy at

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0.6 millimeter slices available to us.

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That usually runs about 700 images.

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However, the technologists then reconstruct those images

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in 3 millimeter bytes that we can

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look at for a quick overview.

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So if the 3 millimeters are not of sufficient

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detail, we go to those thin section raw data,

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0.6 millimeter thick slices.

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With those 0.6 millimeter slices,

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obviously, we can create beautiful coronal

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and sagittal reconstructions ourselves.

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However, the technologist provide to us multiplanar

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reconstructions in the coronal and sagittal plane

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at the 3 millimeter thick reconstructions.

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So you get the axial, coronal and sagittal.

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When do we need contrast?

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So if the question is about calcifications

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and calculi,

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you really don't need contrast-enhanced images.

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We can just use non-contrast CT scans to identify

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calcifications and calculi.

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However, if we're looking at whether or not

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the gland is inflamed,

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it's useful to have post-contrast scans that can be

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compared with the pre-contrast scans and can be

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compared side to side to see whether the gland is

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enhancing more on the one side, the pathologic side

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versus the non-pathologic side to suggest that there

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is indeed inflammation of the gland.

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When we are looking for neoplasms,

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however, with CT scan,

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we are obviously giving contrast

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enhancement and in that situation

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we do not do pre-contrast,

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non-contrast imaging.

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We go straight to the contrast-enhanced CT scan

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with the typical sort of venous phase imaging,

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which allows both the

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anatomy of the arteries and the

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veins to be identified,

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as well as to see whether the neoplasm

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imbibes any contrast itself.

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And that also is helpful for inflammatory lesions

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where we're looking for abscesses,

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for example.

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I showed an example of CT sialography.

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I'll do a mea culpa.

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I haven't done sialography in probably 10 years

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because the CT and the MRI scans usually

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solve the questions themselves.

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So we don't do CT sialography except

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in exceptional cases nowadays.

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Let's move to MR of the salivary glands.

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Well,

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since we are doing such thin sections with CT scan,

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there has become a competition, if you will,

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for higher resolution on our MR studies.

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So, you probably are doing 3-5 millimeter

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thick sections for your neck MRI studies routinely.

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However, at Johns Hopkins,

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we will often include thin

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section 0.6 millimetre MR images.

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Why? Because we have to compete with CT, right?

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We want to have as good a resolution as with CT.

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In order to achieve those 0.6 mm thick sections,

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you have to do thin section

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CISS or VIBE imaging.

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These are Siemens terms

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for the constructive interference in the steady state.

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And I've forgotten VIBE,

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but it's T1-weighted sequences,

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and these are also called FIESTA on

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some of the other manufacturers,

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and MP RAGE or MP GSBR for the VIBE option.

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So that allows us to get submillimeter thick sections.

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Routinely, these are your images,

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3 mm thick T1-weighted.

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You need good quality fat-suppressed

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T2-weighted imaging.

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That usually requires inversion recovery sequences,

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either fast spin-echo or STIR sequences with good fat

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suppression and post-gad, T1-weighted scans.

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These may also be inversion recovery.

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Some people do in-phase,

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out-of-phase, Dixon type, post-gad scans

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with 3 mm thick sections.

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You can just do pre-imposed VIBE and

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get thin section images.

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Again, the value of the VIBE imaging and the CISS imaging is

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that you could do reconstructions in the sagittal and

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coronal planes that are very high-quality.

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MR sialography does not require

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contrast injection. In this situation,

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it's a very highly T2-weighted scan,

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very much like a CISS sequence with suppression of

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the tissue around, in which case you can see

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the ductal system very nicely.

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MR sialography has been stolen, if you will, from MR

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cholangiopancreatography.

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So this is basically the same pulse sequence

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that you do for your MRCP.

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You're going to apply to the salivary glands

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in order to see ductal pathology.

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It's pretty uncommon that we do MR sialography.

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That's usually for patients who have chronic sialadenitis ,

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often patients who have, for example,

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Sjogren's syndrome or whatnot.

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So not a frequently utilized application for MRI.

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We have embraced diffusion-weighted

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imaging in the salivary glands.

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Low ADC,

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manifested as bright signal in the DWI sequence,

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is commonly associated with parotid malignancies.

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There is some overlap with Warthin's tumor, however,

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but we routinely now do DWI.

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It also sometimes will be helpful for

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you in looking at lymphadenopathy.

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If we see lymph nodes who have...

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which have reduced ADC,

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we're more likely to suggest that they are metastatic

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lymph nodes than those who have high ADC and are,

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and are more likely to be inflammatory.

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Perfusion-weighted imaging has been advocated in

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academic circles also to distinguish benign versus

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malignant neoplasms in the parotid gland,

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predominantly or inflammatory lesions

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from neoplastic lesions.

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And I'll demonstrate some of the

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findings on that as well.

Report

Description

Faculty

David M Yousem, MD, MBA

Professor of Radiology, Vice Chairman and Associate Dean

Johns Hopkins University

Tags

Salivary Glands

Non-infectious Inflammatory

Neuroradiology

Neoplastic

Metabolic

MRI

Infectious

Head and Neck

CT

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