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Malignant versus Benign Compression Fractures

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0:01

If you've been following along with the course,

0:03

you just saw a case of a patient who had multiple

0:06

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.

Report

Description

Faculty

David M Yousem, MD, MBA

Professor of Radiology, Vice Chairman and Associate Dean

Johns Hopkins University

Tags

Spine

Neuroradiology

Neoplastic

Musculoskeletal (MSK)

MRI

CT

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