Tobias chapter 28 – imaging of the neurologic system Flashcards

1
Q

What is T1W vs T2W good for? What is the exception?

A

T1W: anatomic detail
T2W: pathology

Exception: pathology involving fat or methemoglobin

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2
Q

What are each of these sequences good for?
T1 FLAIR
T2 FLAIR
STIR

A

T1 FLAIR: similar to T1 with better contrast to noise ratio
T2 FLAIR: help distinguish high protein fluid (edema) from normal fluid (CSF)
STIR: good contrast for fluid or fluid Rich tissues against fat background. Similar to T2. Should not be used with contrast.

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3
Q

What MRI sequence would you use to search for blood?

A

T1W

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4
Q

What MRI sequence would you use to look for edema or necrosis?

A

T2W

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5
Q

What contrast medium is used with CT? Why? What is the dose?

A

Iodine based contrast (metal)
400 to 800 mg of iodine/kilogram

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6
Q
A
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7
Q

What MRI sequence would you use to look for demyelination?

A

T2W

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8
Q
A
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9
Q

What contrast medium is used with MRI? What does it enhance in the CNS?

A

Gadolinium
Enhances meningitis, choroid plexus, pituitary gland

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10
Q

What does meningitis look like in a T1 weighted MRI image following gadolinium?

A

Hyper intense (increased perfusion)

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11
Q

Does contrast agent (gallium) penetrate the brain? Why?

A

No, the blood brain barrier prevents penetration, therefore only the meninges, chloride plexus and pituitary (highly vascular areas) will contrast enhance

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12
Q

What does vasogenic edema look like on noncontrast CT, T1 weighted MRI or T2 weighted MRI?

A

CT: hypoattenuating
T1: hypointense
T2: hyper intense (remember – T2 is great for protein, rich fluid).

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13
Q

Our brain tumors typically hypo or hyper attenuating on CT contrast? Why?

A

Typically, hypERattenuating due to breakage of the blood brain barrier

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14
Q

What is the typical appearance of an in fact on MRI ((T1 W) or CT contrast?

A

Ring appearance due to necrotic center [core hypoattenuating/hypo intense) with a ring of hyper attenuating/hyper intense tissue (perfused).

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15
Q

What are the three types of cerebral edema? How are they identified on MRI (features of each)

A

1) Vasogenic: causes hypointensity on T1W and a hypERintensity on T2W
2) Interstitial: transependymal migration of CSF into periventricular white matter
3) cytotoxic: results in ischemia

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16
Q

What are the three types of secondary hydrocephalus that can be observed on MRI? What are their causes?

A
  1. Non-communicating – obstruction of flow from ventricles to subarachnoid space.
  2. Communicating – reduced absorption by the arachnoid villi or increased production of CSF.
  3. Compensatory – from loss of cerebral parenchyma.
17
Q

Describe the four steps to classify CNS pathology. Include the meaning of the acronym MIIND.

A
  1. Intra-axial or extra-axial? (inside or outside the neuroparencha)
  2. Location
  3. Solitary, multifocal or diffuse.
    - if multifocal, classify symmetrical versus random, as symmetrical = neurodegenerative (metabolic or toxic disorder)
  4. Size, shape, margination, attenuation/intensity, contrast, enhancement pattern.
    MIIND: Malformations, inflammation, injury, neoplasia, degeneration