Interactive Transcript
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Within our mnemonic of vitamin C and D,
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that is vascular, infectious, traumatic, acquired,
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metabolic, idiopathic, neoplastic,
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congenital, and drugs.
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We are now under the C of vitamin C and D
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for congenital lesions.
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And I've just shown a case of hydromyelia
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associated with Chiari 1 malformation.
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Here's another example of a patient who has the
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classic pegging of the cerebellar tonsils
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through the foramen magnum.
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This shape is what we mean by pegging.
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And again,
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we would draw the line from the basion to the
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episthenon and then measure the degree
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of cerebellar tonsillar descent.
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That number has been set at 5 mm or greater
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for representing Chiari 1 malformation.
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That said, we do see patients who have
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greater than 5 mm of descent
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where there is no crowding and the patient asymptomatic.
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And we have patients who have 3 or 4 mm of descent
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and the patient is symptomatic and
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has a syrinx associated with it.
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So these numbers are not necessarily absolute.
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What we do see, in this case, is the expansion of the
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spinal cord with the hydromyelia of
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Chiari 1 malformation.
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Again, this is because it's dilatation of the
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central canal of the spinal cord,
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which is the classic description of the
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etiology of the cavity,
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that is increase in the pressure in the spinal canal being
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transmitted along the perivascular spaces
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and decompressing into the central canal.
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Chiari malformations are more common in women.
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They occur in young adults and they have a multitude
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of different potential symptoms that are associated
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with them, including most commonly headaches,
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dizziness,
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tinnitus, or dysphasia, or odynophagia,
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or other lower cranial nerve symptomatology.
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Here is another example of the same.
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Here you have a T1-weighted,
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T2-weighted, and axial T2-weighted scan
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where you just see on this post-gadolinium-enhanced
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T1-weighted image, no evidence of enhancement.
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You see a central syrinx in the spinal cord.
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It's relatively short in this example.
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And you see the tonsillar herniation.
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On the axial T2-weighted scan,
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enlargement of the spinal cord
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with the central hydromyelic cavity of
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Chiari 1 malformation. As I mentioned,
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with the central canal nature of the hydromyelia,
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you will get the central cord symptomatology of
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muscular weakness, usually affecting the upper
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extremities greater than the lower extremities,
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impaired position sense, and impaired fine motor function.
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If you have an equivocal case of a Chiari 1 malformation,
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maybe at 4 mm, but it seems a little tight,
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or maybe at 6 mm, but it doesn't seem tight,
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it's helpful to perform the phase
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contrast CSF pulsation study.
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Here we have a patient who has a pretty classic
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Chiari 1 malformation with an associated syrinx.
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This is well demonstrated on the T1-weighted scan
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with both the tonsillar pegging, as well as the
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hydromyelic cavity or syringohydromyelia.
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When one performs the CSF pulsation study,
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you should be seeing bright signal intensity
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and then dark signal intensity,
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as you see here around the spinal cord that
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would be present also at the skull base.
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In this case, we are not seeing that normal CSF
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pulsation because of the obstruction of normal
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pulsation by the cerebellar tonsils within the
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foramen magnum.
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Contrast that with this case.
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So here we have a patient,
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the same patient who has undergone decompression.
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So with the decompression, as I stated earlier,
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you have the suboccipital decompression procedure.
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You have the posterior arch of C1,
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which has been removed, and you have the duraplasty,
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which is the expansion of the dura to allow more CSF
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to bathe the cerebellar tonsils.
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Upon the performance
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of the suboccipital decompression,
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C1 posterior arch removal, and duroplasty,
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you note that the patient's hydromyelic
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cavity has decreased in size.
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And now, we have a more normal appearance to the
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pulsation posteriorly around the tonsils,
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as well as anteriorly in front of the brainstem.
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So let me just go back and show that slide
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one more time of the previous example.
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Here we have the size of the syrinx.
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As you see, post-decompression
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and the more normal appearance to the CSF pulsations.
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If we go back to the pre-op examination, abnormal CSF
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pulsation and abnormal enlarged hydromyelic cavity,
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which subsequently is treated.
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The hydromyelic cavity has been
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described by Milhorat,
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who is a neurosurgeon from approximately the 1970s.
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Let me actually get the reference here.
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Milhorat from 1999,
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who looked at over 300 patients with Chiari 1 and
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described the presence of
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syringohydromyelia in 60% of cases.
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I've since looked at the Johns Hopkins experience,
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and our number is closer to about 36%.
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And I think that's because we've gotten more comfortable
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with calling asymptomatic Chiari 1 malformations.
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You can get syrinx cavities within the spinal cord
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without an associated Chiari 1 malformation.
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Here's a patient who has normal cerebellar tonsils
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which are above the foramen magnum.
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Let me just draw that in.
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So here's our basion to opisthion,
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and you see that the tonsils are above that level,
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and yet the patient has a cavity within the
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spinal cord, which looks pretty clean.
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If you see this on your degenerative disc
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disease or post-trauma cases,
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it behooves the radiologist to recommend
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a post-contrast scan.
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We just want to make sure we don't
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see a tiny little nodule
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that might suggest that this is a
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hemangioblastoma, which can be relatively subtle.
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So, if you see an isolated cord syrinx,
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recommend post-contrast enhanced scan to see
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whether there's any peripheral nodular enhancement
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that would indicate that this represents
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hemangioblastoma instead.
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Quite often,
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you won't see any enhancement and you'll just
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have an asymptomatic cord syrinx.
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Now, is this due to a previous traumatic event?
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Is it just a congenital rest that has been
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with the patient all their life?
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Or is it the residual from a previous myelitis?
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Many of these patients are totally asymptomatic,
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so we presume that they are just a congenital cyst,
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similar, if you will,
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to an arachnoid cyst intracranially,
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but obviously within the spinal cord.
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So I mentioned that the cord lipoma was the second
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most bizarre case that I've ever seen.
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This is the number one.
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This is an amazing case.
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Here we have a patient with a T1-weighted
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and a T2-weighted scan, and we have a lesion
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which spans all three spaces.
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You notice that there is a little meniscus here
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posteriorly, identifying this as
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intradural extramedullary.
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You see there is widening of the CSF space,
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identifying this as intradural extramedullary lesion.
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However, when we look at the inferior most portion,
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the lesion clearly is within the spinal
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cord and therefore is intradural intramedullary.
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Except that, in addition,
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there is another component of this same lesion,
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with a cyst, in the extradural compartment.
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So we have all three spaces of the spinal cord and
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the spinal canal that are involved:
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intradural extramedullary,
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intradural intramedullary, and extradural.
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Not only that,
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but this patient also has
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abnormality in the vertebral bodies.
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And you can see that there is a segmentation
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abnormality that there are fused vertebrae.
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In fact, this patient had butterfly vertebrae as well.
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Put it all together. What do you got?
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This is a neuroenteric cyst.
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A neuroenteric cyst is something that occurs in
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association with a segment of the spine where
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there is abnormality in development,
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which is usually the synchondrosis of the sine qua non
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anomaly in the vertebral bodies.
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But you may have intradural extramedullary,
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intradural intramedullary, or extradural components.
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This is the enteric component of the neuroenteric cyst.
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And these parts are the neural component of the
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neurenteric cyst.
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The most bizarre spine case I've ever seen,
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and I wanted to share it with you.
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This is obviously a congenital anomaly.
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