Interactive Transcript
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I'd like to summarize what we've learned in.
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This series of sessions on intradural
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intramedullary cord lesions.
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So let's start with our Mnemonic.
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On the V side of things,
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we emphasize that the most common vascular.
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malformation in the spinal.
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cord is the cavernoma.
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There are numerous vascular malformations.
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that can be evaluated and this sometimes.
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requires dynamic MRA. For best evaluation,
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we talked about cord infarcts and usually.
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in the setting of aortic disease either.
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treatment thereof or dissections.
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of the aorta or its branches.
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From the standpoint of infectious.
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inflammatory lesions we emphasize that viral.
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etiologies for myelitis are the most common.
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and there are a whole wealth of infectious.
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etiologies that we consider.
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in patients who have AIDS.
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Of the noninfectious inflammatory lesions,
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sarcoidosis will predominate but we do have.
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all of those other collagen vascular.
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diseases including lupus.
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Trauma to the spinal cord is unusual when it.
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occurs in association with hemorrhage.
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The patient's prognosis is quite poor.
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Particularly when you have a long segment.
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Hematomyelia, in which case the patient's.
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Unlikely to have complete recovery.
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Of their neurologic deficits.
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From the standpoint of acquired and.
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Metabolic, we think about vitamin B12.
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Folate and copper deficiency as potential causes.
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Of subacute combined degeneration affecting the posterior.
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Columns with the eye.
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We're usually thinking about idiopathic.
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Disorders, and for that is where we put our.
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Demyelinating disorders, be it adem.
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Multiple sclerosis, neuromyelitis.
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Optica in alphabetical order.
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Those etiologies may have multifocal lesions.
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They may have brain lesions as well, and we.
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Usually say to make sure that you.
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Scan the entire neuroaxis.
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When we're considering patients with.
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Multiple sclerosis, neuromyelitis.
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The end of neoplasm is usually separated.
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Depending upon whether we're dealing with.
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Children and cervical spine, in which case.
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We favor astrocytoma, and adults.
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And the lumbosacral spine.
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Where we're usually favoring ependymoma.
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That said,
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there are other potential etiologies of
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neoplasms, including hemangioblastomas, in the
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setting of von Hippolindal disease, and
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metastases in patients who generally
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have breast or lung cancer.
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Of the congenital lesions,
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we focused on Chiari I malformation that
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is cerebellar tonsillar descent
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through the foramen magnum.
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And magnum in association with
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hydromyelia, that is,
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dilatation of the central canal of the
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spinal cord, which occurs in about one third
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of cases who have Chiari I malformation.
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I also showed that bizarre norenteric
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cyst case where you can have both
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intradural extramedullary and intradural
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intramedullary manifestations
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of norenteric cysts.
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Within this category,
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I would probably also include the
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neurodegenerative disorders of the spinal
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cerebellar ataxia, which may be transmitted
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in a genetic fashion. Finally,
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we have drugs, and the drug that I mentioned
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was nitrous oxide toxicity that can occur
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in both recreational use or occasionally
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iatrogenic overdose of nitrous
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oxide used as an anesthetic.
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This too will influence the posterior
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columns of the spinal cord.
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So clinical history is very important.
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This is the opportunity for you to make the
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optimal use of the review of the
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electronic medical record.
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Remember that not all enlarged
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cords are neoplasms.
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We saw cases of inflammatory lesions,
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rare demyelinating lesions, including
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transverse myelitis.
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The acute setting of spinal cord strokes
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and some of these may also show faint
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enhancement like neoplasm.
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So some of your myelidities,
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infectious and noninfectious myelidities,
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may simulate neoplasm in this instance.
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Again,
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refer to the electronic medical record or
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recommend specific CSF or blood laboratory
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tests that might point to
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a correct diagnosis.
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So search for corroborative findings
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elsewhere on the scans or in scans
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of the entire CNS axis.
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By that, I mean if you're looking at a
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patient who has a neoplasm in
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the thoracic lumbar region,
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look for renal cell carcinoma or cysts or
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other regions that might suggest
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von Hippolindal disease.
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Look in the paraspinal location or in the
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neural pharamina in order to potentially
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make the diagnosis of neurofibromatosis type
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one or neurofibromatosis type two.
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Remember that neurofibromatosis type 1 may
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lead to dural ectasias and posterior
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scalloping of the bone, and that might be
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useful in identifying the etiology for a
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cord mass that would be an astrocytoma
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associated with NF one.
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Similarly,
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if you find lesions in the spinal cord,
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look at the brain.
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This is useful for the demyelinating
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disorders of multiple sclerosis, but
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also for the fake comatoses,
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including von Hippolindal disease
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and neurofibromatosis type.
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One or type two and for the presence of
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Menostatic disease if there are multiple
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lesions. On that basis,
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clearly, the intraduro intermediary
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evaluation of the spinal canal is replete
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with multiple fascinating lesions.
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And I hope you enjoyed this session.
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Thank you very much for your attention.
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