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Intradural Intramedullary Lesions - Conclusion

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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.

Report

Description

Faculty

David M Yousem, MD, MBA

Professor of Radiology, Vice Chairman and Associate Dean

Johns Hopkins University

Tags

Vascular

Trauma

Syndromes

Spine

Non-infectious Inflammatory

Neuroradiology

Neoplastic

Musculoskeletal (MSK)

Metabolic

MRI

Infectious

Idiopathic

Iatrogenic

Drug related

Congenital

Acquired/Developmental

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