Neuro -- Spinal Tumors
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- We are ignoring osseous metastatic disease compressing the cord in this module. It is easy to recognize and don't need to spend much time on it.
- ok
- What is the first thing to do when seeing a lesion within the spinal cord?
- Determine what space you are in
- What are the choices?
-
Intramedullary
Intradural extramedullary
Extradural - Why do it this way?
- You only have to know three entities for each of those areas, simplifying your ddx greatly!
- What if you still aren't sure whether you have covered the full ddx for a given lesion?
- Just throw in Sarcoid and Lymphoma, and you are DONE!
- What are non-neoplastic categories that can cause intramedullary masses?
-
Demyelinating dz
Inflammatory
Vascular lesions
Developmental lesions
Trauma - What sequences are used for the cord?
- T1, T1 post, T2, proton density, STIR (or other fat suppressed fluid sens)
- Where in the cord are demyelinating lesions located?
- Posterior cord, since that is where the bulk of the white matter tracts is
- What is the hallmark of spinal neoplasm?
- Cord enlargement
- What are other features seen in spinal tumors?
-
1) Hemorrhage
2) Cystic components
3) Enhancement - How many different types of cysts are seen with cord tumors?
- 2
- What are they?
-
Intratumoral cysts -- part of the tumor itself
Tumor associated cysts - Where are tumor associated cysts?
- They cap the lesion above and below
- What sequence is always done whenever cord tumor is suspected?
- T1 Postgado. Must evaluate enhancement
- How many intramedullary tumors do we need to remember for adults?
- 3
- Which ones?
-
1) Hemangioblastoma
2) Astrocytoma
3) Ependymoma - When does hemangioblastoma present?
- 20s -- 40s
- What other lesions are seen in patients with cord hemangioblastomas?
-
RCCA
Pancreatic cysts
Retinal angiomas - Why?
- Because hemangioblastoma is assd with VHL, just like when it is seen in posterior fossa.
- What percent of patients with cord hemangioblastoma will have VHL?
- 30%
- What is their general appearance?
- Variable, just like they are in posterior fossa.
- What are the variations?
-
Can be large, can be small
Can be totally solid, can be primarily cystic with mural nodule.
And anything in between - What are the CONSTANT findings in hemangioblastoma?
-
1) LIGHT BULB enhancement of its cystic portions
2) Flow voids from large vessels feeding tumor
3) Edema within adjacent cord - What does the edema do to the cord?
- It causes cord expansion itself.
- Before giving contrast, how do you differentiate hemangioblastoma for holocord astrocytoma?
- You really cant. But when you give contrast, BAM, you see very well defined super-bright cord lesion, which is significantly smaller than the whole region of distortion that it creates
- When you treat it surgically, what part of cord do you remove?
- Just the enhancing tumor nidus (and any associated cyst). Not the edematous cord.
- What does edema look like in the cord?
- Looks flame-shaped on T2, extending up or down the central part of the cord, sparing the periphery of the cord
- What type of edema is this?
- Vasogenic edema, of course. It does not involve the cord periphery (i.e. where the gray matter is). The flame-shape is the cord equivalent of vasogenic edema.
- What is a more typical appearance of hemangioblastoma in VHL?
- They get multiple small hemangioblastoma nodules, which are up against the pial surface, not so much central in the cord.
- Does hemangioblastoma have tumor associated cysts?
- Yes. The tumor assd cysts are just collections of edema. They are not sensitive or specific
- What is age dist'n of cord astrocytoma?
- Mainly 20s to 40s, but also occur in kiddies.
- What is true of size of astrocytomas?
- Fusiform expansion, usually greater than 2 segments.
- How big are demyelinating plaques in the cord?
- Small. 2 segments or less!
- What percent of astrocytomas enhance?
- For my purposes all do. Only 10% dont
- What do they look like?
- Basically just like they would in brain. They enhance. They can have central areas of necrosis. Nothing really specific about em.
- Where do astrocytomas not occur?
- Filum
- What is the most common primary cord tumor?
- Ependymoma
- What tumor feature is suggestive of ependymoma?
- Certain locations
- What tumor locations make ependymoma much more likely?
- Lower cord, conus, and filum
- What is another feature of ependymoma that is somewhat specific?
- Hemorrhage
- How does this manifest?
- Dark hemosiderin cap above and below lesion
- What is another very typical finding of ependymoma?
- Tumor associated cysts above and below lesion
- How do you differentiate tumor associated cysts with intratumoral cysts?
- No enhancement on outer sides of tumor assd cysts
- What does ependymoma do to bones?
- Remodels vertebrae
- Why is this important to know?
- Because you cant just assume that something remodeling the spine is benign. It is not always so. It is a slow growing tumor though.
- What percent of ependymomas enhance?
- For my purposes, all cord tumors will enhance. But if you must know, 80% of ependymomas do enhance.
- What if you see a cord tumor which is extensive, involving many segments, but which demostrates lots of areas of dark signal?
- C/W hemosiderin deposition, which represents old hemorrhage, as is suspicious for ependymoma.
- What is classic appearance of cord mets?
- Lots of separate foci of enhancement throughout the cord in patient with known primary
- What are the 4 most common mets to cord?
-
Lung
Breast
Melanoma
RCCA - What are vascular malformations of cord?
-
Cavernous hemangioma
AV Malformation - What does cord cavernoma look like?
- Look up. Looks same as brain I guess. But I don't know that either!
- What is the classic presentation for a particular vascular malformation of the cord?
- Young patient presenting with subarachnoid hemorrhage
- What malformation is this a classic presentation for?
- AVM of the cord
- What does ill defined cord enhancement in an expanded segment of cord suggest?
- Cord infection
- What should you consider in all cases that look atypical (poor enhancement, multiple segments, indistinct margins of enhancement)?
-
Sarcoid
Lymphoma - What is the differential for intradural extramedullary lesions?
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1) Schwannoma
2) Meningioma
3) Mets - What are the characteristics of intradural extramedullary lesions?
-
Displace cord
AND
Widen adjacent CSF space - What is a classic characteristic of meningioma on MRI (nice when you see it to clinch diagnosis, but don't always see)
- Dark on T2
- What is the appearance of schwannoma?
- Enhancing with unenhancing cystic component. May be mostly cystic with just peripheral enhancement.
- What is the most classic finding of schwannoma?
- Dumbell lesion extending through and expanding the neural foramen
- What patients get dural dysplasia?
- NF-1
- What patients get frequent spinal tumors.
- NF-2
- What spinal tumors do they get in NF-2?
-
Meningiomas
Schwannomas (can have schwannomas at multiple levels, classic appearance)
Ependymomas - What type of metastatic disease is intradural extramedullary?
- Drop mets
- What tumors give drop mets?
-
Medulloblastoma
Ependymoma
Oligodendroglioma
Pinealoma
Astrocytoma - What other type of tumor can give drop mets?
-
Metastatic disease near CSF:
Breast
Lun
Melanoma