Interactive Transcript
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If you've been following along with the course,
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you just saw a case of a patient who had multiple
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myeloma with a compression fracture
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of multiple vertebral bodies.
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The distinction between a malignant versus a benign
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osteoporotic compression fracture
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is one that has led to hundreds,
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if not thousands, of publications in the neuroradiology
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and Musculoskeletal radiology literature.
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Distinguishing between these two, in some
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cases when it's classic, is very easy,
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but in some cases is very difficult indeed.
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Let's talk about this problem.
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So here we have a patient who has two vertebral bodies
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that have abnormal signal intensity within them.
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The upper one,
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the L2 vertebral body is compressed and you see that
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there is decrease in the height as opposed to the
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L3 vertebral body. This is four, this is five.
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So are these metastases with compression fractures
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or are these on the basis of osteoporosis?
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This is the issue.
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Some people have advocated using diffusion-weighted
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imaging to identify whether or not a compression
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fracture is from metastatic disease or osteoporosis.
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The theory here is that if there is
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hypercellularity within the bone,
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it would suggest that this is secondary metastases.
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Hypercellularity would result in decreased ADC and
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brighter signal in diffusion-weighted imaging.
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Contrast that to osteoporotic fractures, which
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have less cellular vertebral bodies.
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And this would lead to more vasogenic edema
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and brighter signal intensity on the ADC map.
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So in this case, in particular,
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we have a patient who has a lesion,
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which is showing compression deformity on the
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T2-weighted scan. This is a T1-weighted scan.
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And here on your ADC map of the diffusion-weighted scan,
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we see that it's relatively bright.
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A brighter lesion would imply that
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this is on an osteoporotic basis.
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If it's darker on the ADC secondary to hypercellularity,
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it's going to lead to a diagnosis of metastatic disease.
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Here's another example of a compression fracture.
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This one shows vacuum phenomenon
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air within the vertebral body.
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Vacuum phenomenon air within the vertebral body is
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a marker for a benign compression fracture.
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Here we have a patient who has intermediate bright
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signal intensity in the vertebral body on the T1-weighted
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scan. This higher signal intensity on T1-weighted scan,
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as opposed to complete replacement of
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the T1 signal is a marker for a benign etiology.
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You notice that this patient has compression deformity
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of the superior endplate of the vertebral body,
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but we notice that it's brightened signal intensity.
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Again, brightened signal intensity means that there is normal
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bone marrow fat and therefore this is unlikely to be on
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a basis of neoplasm and is more likely to
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be on an osteoporotic reason.
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Similarly here, this wedged vertebral body has normal signal
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intensity and therefore is more likely
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to be benign osteoporotic in its etiology.
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Here's a diffusion-weighted scan showing that the high
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signal intensity in the vertebral body, on the diffusion
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weighted imaging, is associated with the compression
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deformity and when it's bright on
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DWI and bright on the ADC map,
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it's just that, indeed, the patient has a benign
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osteoporotic compression fracture.
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This is the follow-up on this patient, and this is the imaging
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finding that is most reliable in suggesting
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a benign compression fracture. That is,
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if the signal intensity of the compressed vertebra
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returns to a normal bone marrow,
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bright on T1-weighted scan,
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it suggests that this is a benign etiology since
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neoplastic infiltration would not return to bright.
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So once again,
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a reasonable approach is to do a follow up scan at two
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months in order to determine whether or not the bone
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marrow signal returns to normal,
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that is bright on T1-weighted scan, to suggest a benign etiology.
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That said,
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there are very few clinicians that I've run into,
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at least at Johns Hopkins, that are willing to wait to
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find out the diagnosis in a follow-up scan at
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six weeks to two months.
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And therefore, quite often, we are asked to do biopsies
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of these lesions to determine whether or not they're
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neoplastic or benign in their etiology.
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To summarize, what are the findings of a
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malignant compression fracture on MR? If you have
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convex posterior border of the vertebral body,
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suggesting that it's filled with neoplasm,
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more likely to be malignant.
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Abnormal signal intensity extending into the pedicle or
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the posterior element, or completely replacing the
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vertebral body, more likely to be malignant.
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An epidural mass or encasing epidural mass, or a focal
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paraspinal mass associated with the compression
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fracture, suggest a malignancy. If you see other lesions
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elsewhere in the spine or in the ribs,
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more likely to be metastatic disease. And if there is
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restricted diffusion, more likely to be malignancy.
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Benign features on MR, having low signal intensity linear
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bands, but the majority of the vertebral body
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being bright on T1 suggests benign.
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If you have spared normal bone marrow signal in the
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vertebral body, again, similarly to this linear band,
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that's more likely to be benign.
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If there are multiple compression fractures with high
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normal signal intensity on T1-weighted
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scan, more likely to be benign
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osteoporotic. Return of the normal signal intensity of
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the vertebral body on a follow-up
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scan at six to eight weeks,
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benign etiology. And/or fluid or the air that you saw,
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the vacuum phenomena within the fracture, is more
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likely to suggest benign etiology.
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