Neuroradiology Flashcards

1
Q

A patient with severe renal failure but not on dialysis required CT angiogram. In addition to keeping the patient well hydrated, what may be given to the patient to minimize contrast nephropathy?
a. Hydrocortisone
b. Magnesium sulfate
c. N-Acetylcysteine
d. Ramipril
e. Sodium bicarbonate

A

c. N-Acetylcysteine

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2
Q

Early subacute subdural hematoma (4-7 days old) is most likely to display which one of the following characteristics on MRI?
a. T1 hypointense, T2 hypointense
b. T1 hypointense, T2 isointense
c. T1 hypointense, T2 hyperintense
d. T1 isointense, T2 hypointense
e. T1 isointense, T2 hyperintense
f. T1 hyperintense, T2 hypointense
g. T1 hyperintense, T2 isointense
h. T1 hyperintense, T2 hyperintens

A

f. T1 hyperintense, T2 hypointense

The table below describes the appearance of subdural blood clots on MRI as they ag

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3
Q

True diffusion restriction is best assessed by looking at which one of the following MR sequences?
a. Diffusion tensor imaging
b. Diffusion weighted image and apparent
diffusion coefficient map
c. Fractional anisotropy map
d. T2 gradient echo
e. T1 with gadolinium

A

b. Diffusion weighted image and apparent

Diffusion restriction is assessed with a diffusion
weighted imaging protocol which includes a T2
weighted sequence (low b¼0), diffusion weighted
sequence (high b¼1000) and apparent diffusion
coefficient map. The b-value parameter identifies
the measurement’s sensitivity to diffusion and
determines the strength and duration of the diffusion gradients. A b value of 0 produces a T2
weighted image for anatomical reference. In the
range of clinically relevant b values (i.e. up to
1000) the greater the b value the stronger the diffusion weighting and the higher the contrast in
pathogenic regions. A minimum of two b-values
must be acquired for an apparent diffusion coefficient map, which is a measure of the strength of
diffusion in tissue after eliminating any overlying
T2 shine through/contrast effects. T2 shinethrough refers to high signal on DWI images that
is not due to restricted diffusion, but rather to high
T2 signal which “shines through” to the DWI
image. T2 shine through occurs because of long
T2 decay time in some normal tissue. This is most
often seen with subacute infarctions due to vasogenic edema but can be seen in other pathologic
abnormalities e.g. epidermoid cyst. To confirm true
restricted diffusion one should always compare the
DWI image to the ADC. In cases of true restricted
diffusion, the region of increased DWI signal will
demonstrate low signal on ADC. ADC is a value
that measures the effect of diffusion independent
of the influence of T2 shine-through. ADC maps
thus portray restricted diffusion, such as in ischemic
injury, as hypointense lesions relative to normal
brain. In contrast, in cases of T2 shine-through,
the ADC will be normal or high signal.

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4
Q

A ring-enhancing lesion on contrast CT has the below appearance on DWI (C- DWI, D- ADC map) sequence. Which one of the following is of most concern?
a. Cerebral abscess
b. Encephalitis
c. Glioblastoma multiforme
d. Metastasis
e. Radiation necrosis

A

a. Cerebral abscess

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5
Q

Which one of the following combinations of findings on perfusion weighted MR suggests early infarction
a. Bright on DWI, low rCBF, long rMTT,
low CBV
b. Bright on DWI, high rCBF, long rMTT,
low CBV
c. Bright on DWI, low rCBF, short rMTT,
low CBV
d. Bright on DWI, low rCBF, long rMTT,
high CBV
e. Dark on DWI, low rCBF, long rMTT,
low CBV

A

a. Bright on DWI, low rCBF, long rMTT,
low CBV

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6
Q

Which one of the following tracts is most likely depicted in the figure below?
a. Cingulum
b. Corona radiata
c. Corpus callosum
d. U fibers
e. Vertical occipital fasciculus

A

c. Corpus callosum

The corpus callosum facilitates interhemispheric interactions for communicating and
integrating perceptual, cognitive, learned,
and volitional information. It is important for
the performance of visual and tactile tasks that
require transfer of sensory information
between the cerebral hemispheres. Commissural fibers crossing through the anterior portion and body of the corpus callosum are
essential to perform temporally independent bimanual finger movements. Commissural
fibers passing through the posterior corpus callosum play an important role in visual and
visuospatial integration. Callosal fibers are also
important for higher-order cognition, including normal social, attentional, and emotional
function.

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7
Q

Which one of the following tracts is most likely depicted in the figures below?
a. Anterior commissure
b. Extreme capsule
c. Fornix
d. Posterior commissure
e. Posterior limb of internal capsule

A

c. Fornix

The fornix is part of the dorsal limbic system and
the Papez circuit. It participates in high-level
mental processes relevant to episodic memory
and emotion. It also provides the main cholinergic input to the hippocampus.

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8
Q

Which one of the following tracts is most likely depicted in the figure below?
a. Corpus callosum
b. Corona radiata
c. Corticospinal tract
d. Inferior frontooccipital fasciculus
e. Superior frontooccipital fasciculus

A

b. Corona radiata

The fibers of the corona radiata interconnect the
cerebral cortex with the thalamus and brainstem
in both directions. From anterior to posterior,
they include (1) the thalamic connections to
the frontal lobes and the frontopontine motor
fibers that pass through the anterior limb of the
internal capsule; (2) the thalamic connections to
the anterior parietal lobe and the corticonuclear
motor projections that pass through the genu;
and (3) the thalamic connections to the central
parietal and occipitotemporal lobes and corticospinal, corticopontine, and corticotegmental motor
fibers that pass through the posterior limb of the
internal capsule. The thalamic radiations to and
from the cortex are grouped into four thalamic
peduncles.

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9
Q

Which one of the following tracts is most likely depicted in the figure below?
a. Corona radiata
b. Corticospinal tract
c. Medial longitudinal fasciculus
d. Reticulospinal tract
e. Spinothalamic tract

A

b. Corticospinal tract

The corticospinal tract is the predominant
pathway for the relay of impulses for voluntary
skilled movements of the upper extremities,
trunk, and lower extremities. It connects pyramidal Giant cells of Betz in layer V of primary
motor cortex to alpha motor neurons, decussating in the medulla.

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10
Q

Which one of the following tracts is most likely depicted in the figure below?
a. Arcuate fasciculus
b. Cingulum bundle
c. Corona radiata
d. Corticospinal tract
e. SFOF

A

b. Cingulum bundle

The cingulum bundle is the major component of
the dorsal limbic pathway. It is involved in a wide
range of motivational and emotional aspects of
behavior and participates in spatial working
memory. It interconnects the hippocampus and
parahippocampal gyrus (critical for memory) with
the (1) prefrontal areas (important for manipulating information, monitoring behavior and working memory) and (2) rostral cingulate gyrus
(involved in motivation and drive). It can be
lesioned or stimulated to treat pain, obsessive
compulsive disorder or depression. The limbic
system is also important for high-level mental
processes relevant to memory and emotion. It is
part of the Papez circuit that links the hippocampus, parahippocampal gyrus, mammillary bodies,
thalamus, and cingulate gyrus. Other structures
subsequently integrated into the limbic system
include the amygdala, septal region, and olfactory
bulb. These structures have been implicated in
dementia, epilepsy, and schizophrenia.

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11
Q

Which one of the following tracts is most likely depicted in the figure below?
a. Inferior fronto-occipital fasciculus
b. Inferior longitudinal fasciculus
c. Fornix
d. Superiorlongitudinal fasciculus (II and III)
e. U-fibers

A

d. Superiorlongitudinal fasciculus (II and III)

The SLF is significant for initiation of motor
activity and higher-order control of bodycentered action. It connects the superior parietal
lobule (important for limb and trunk location in
body-centered space) with premotor areas
(engaged in higher aspects of motor behavior).
The SLF is also significant for spatial attention,
because it connects the inferior parietal lobule
(concerned with visual spatial information) with
the posterior prefrontal cortex (important for
perception and awareness). Furthermore, the
SLF is relevant to gestural components of language and orofacial working memory, because
it connects the supramarginal gyrus (concerned
with higher order somatosensory information)
with the ventral premotor area (containing mirror
neurons for action imitation).

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12
Q

Which one of the following tracts is most likely depicted in the figure below?
a. Arcuate fasciculus
b. Cingulum bundle
c. Fornix
d. Inferior longitudinal fasciculus
e. Superior longitudinal fasciculus

A

a. Arcuate fasciculus

The classical (direct) arcuate fasciculus interconnects Wernicke’s receptive, auditory word processing area in the superior temporal lobe with Broca’s
speech production area in the inferior frontal lobe.
This connection provides for the ability to recognize language and respond to it appropriately. Individuals with more symmetric patterns of connection perform better overall on word tasks of semantic association. It has been considered by some to be the fourth portion of SLF.

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13
Q

Which one of the following tracts is most likely depicted in the figure below?
a. Cingulum
b. Posterior commissure
c. Superior fronto-orbital fasciculus
d. Superior longitudinal fasciculus
e. U association fiber

A

c. Superior fronto-orbital fasciculus

The SFOF is significant for peripheral vision,
visual perception of motion, and visual spatial processing. The SFOF connects the superior parietal
gyrus (parastriate areas important for peripheral
vision and visual appreciation of motion) with
the dorsolateral prefrontal cortex of the middle
and inferior frontal gyri (necessary for attention)

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14
Q

Which one of the following tracts is most likely depicted in the figure below?
a. Arcuate fasciculus
b. External capsule
c. Fornix
d. Inferior fronto orbital fasciculus
e. Inferior longitudinal fasciculus

A

e. Inferior longitudinal fasciculus

The inferior longitudinal fasciculus has a role in
the ventral visual stream for object recognition,
discrimination, and memory. It appears to mediate the fast transfer of visual signals to anterior
temporal regions and neuromodulatory backprojections from the amygdala to early visual
areas. It likely plays a role in linking object representations to their lexical labels. Face recognition
probably depends on the ILF, because disruption
of the tract has been implicated in associative
visual agnosia, prosopagnosia, visual amnesia,
and visual hypoemotionality.

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15
Q

Which one of the following tracts is most likely depicted in the figure below?
a. Commissure of Probst
b. Corona radiata
c. Inferior fronto orbital fasciculus
d. Inferior longitudinal fasciculs
e. Internal capsule

A

c. Inferior fronto orbital fasciculus

This fascicle may be a major component of the
ventral subcortical “what” pathway important
for object recognition and discrimination. The
IFOF most likely also has a significant role in
semantic processing, because it interconnects
the occipital associative extrastriate cortex with
the temporobasal region, two areas important
to semantic processing. The IFOF also functions
in visuospatial processing and enables the interaction between emotion and cognition

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16
Q

Which one of the following tracts is most likely depicted in the figure below?
a. Anterior commissure
b. Anterior region of the corona radiata
c. Fornix
d. Optic tract
e. Uncinate fasciculus

A

e. Uncinate fasciculus

The uncinate fasciculus is a ventral limbic
pathway that is critical for processing novel
information, for positive/negative valuations
of the emotional aspects of data, and for
self-regulation. The fibers of the uncinate
fasciculus link the rostral superior temporal
gyrus (important for sound recognition),
the rostral inferior temporal gyrus (important for object recognition), and the medial
temporal area (important for recognition
memory) with the orbital, medial, and prefrontal cortices (involved in emotion, inhibition, and self-regulation). The uncinate
fasciculus may also be critical in visual
learning.

17
Q

In MR Spectroscopy, Hunter’s angle is best described as which one of the following?
a. The rough angle formed with the x axis
when a line is drawn between choline
and creatine peaks
b. The rough angle formed with the x axis
when a line is drawn between NAA and
creatine peaks
c. The rough angle formed with the x axis when a line is drawn between choline, creatine and NAA peaks
d. The rough angle formed with the x axis
when a line is drawn between lactate and
lipid peaks
e. The rough angle formed with the x axis when a line is drawn between choline and lactate peaks

A

c. The rough angle formed with the x axis when a line is drawn between choline, creatine and NAA peaks

The rough angle formed with the x axis
when a line is drawn between choline, creatine
and NAA peaks. Hunter’s angle is the formed
by a line approximately joining the ascending
peaks of the metabolites in MR spectroscopy
and is roughly 45°. Myoinositol, Choline,
Creatine and N-Acetyl aspartate peaks are
ascending in normal spectrum, any alteration
in the ascending nature of the peaks means
spectrum is abnormal.

18
Q
  1. Pathway important for recognition of language and appropriate response

Tractography:
a. Anterior commissure
b. Anterior region of the corona radiata
c. Arcuate fasciculus
d. Corticobulbar tract
e. Corticospinal tract
f. Cingulum
g. Cerebral peduncle
h. Fornix
i. Inferior fronto-occipital fasciculus
j. Inferior longitudinal fasciculus
k. Optic tract
l. Superior fronto-occipital fasciculus
m. Superior longitudinal fasciculus
n. Uncinate fasciculus
o. Vertical occipital fasciculus

A

c. Arcuate fasciculus

19
Q
  1. Pathway important for object recognition
    and discrimination, semantic processing
    and visuospatial processing.

Tractography:
a. Anterior commissure
b. Anterior region of the corona radiata
c. Arcuate fasciculus
d. Corticobulbar tract
e. Corticospinal tract
f. Cingulum
g. Cerebral peduncle
h. Fornix
i. Inferior fronto-occipital fasciculus
j. Inferior longitudinal fasciculus
k. Optic tract
l. Superior fronto-occipital fasciculus
m. Superior longitudinal fasciculus
n. Uncinate fasciculus
o. Vertical occipital fasciculus

A

i. Inferior fronto-occipital fasciculus

20
Q
  1. Pathway with role in linking object representations to their lexical labels and face recognition.

Tractography:
a. Anterior commissure
b. Anterior region of the corona radiata
c. Arcuate fasciculus
d. Corticobulbar tract
e. Corticospinal tract
f. Cingulum
g. Cerebral peduncle
h. Fornix
i. Inferior fronto-occipital fasciculus
j. Inferior longitudinal fasciculus
k. Optic tract
l. Superior fronto-occipital fasciculus
m. Superior longitudinal fasciculus
n. Uncinate fasciculus
o. Vertical occipital fasciculus

A

j. Inferior longitudinal fasciculus

21
Q
  1. Pathway with role in peripheral vision, visual perception of motion, and visual spatial processing

Tractography:
a. Anterior commissure
b. Anterior region of the corona radiata
c. Arcuate fasciculus
d. Corticobulbar tract
e. Corticospinal tract
f. Cingulum
g. Cerebral peduncle
h. Fornix
i. Inferior fronto-occipital fasciculus
j. Inferior longitudinal fasciculus
k. Optic tract
l. Superior fronto-occipital fasciculus
m. Superior longitudinal fasciculus
n. Uncinate fasciculus
o. Vertical occipital fasciculus

A

l. Superior fronto-occipital fasciculus

22
Q
  1. Pathway with role in initiation of motor activity and higher-order control of body-centered
    action, spatial attention and gestural components of language and orofacial working
    memory.

Tractography:
a. Anterior commissure
b. Anterior region of the corona radiata
c. Arcuate fasciculus
d. Corticobulbar tract
e. Corticospinal tract
f. Cingulum
g. Cerebral peduncle
h. Fornix
i. Inferior fronto-occipital fasciculus
j. Inferior longitudinal fasciculus
k. Optic tract
l. Superior fronto-occipital fasciculus
m. Superior longitudinal fasciculus
n. Uncinate fasciculus
o. Vertical occipital fasciculus

A

m. Superior longitudinal fasciculus

23
Q
  1. CSF flow studies

MRI Sequences:
a. BOLD Functional MRI
b. Diffusion tensor imaging
c. Diffusion weighted imaging (Echo planar)
d. Fast spin echo
e. FIESTA
f. FLAIR CSF suppression
g. Gradient echo
h. MR Spectroscopy
i. Phase-contrast
j. STIR fat suppression
k. Susceptibility weighted imaging
l. T1
m. T1 with gadolinium
n. T2
o. Time of flight

A

i. Phase-contrast

24
Q
  1. Cavernous malformations

MRI Sequences:
a. BOLD Functional MRI
b. Diffusion tensor imaging
c. Diffusion weighted imaging (Echo planar)
d. Fast spin echo
e. FIESTA
f. FLAIR CSF suppression
g. Gradient echo
h. MR Spectroscopy
i. Phase-contrast
j. STIR fat suppression
k. Susceptibility weighted imaging
l. T1
m. T1 with gadolinium
n. T2
o. Time of flight

A

k. Susceptibility weighted imaging

25
Q
  1. Resection of an eloquent temporal glioma in an intact patient presenting with headache

MRI Sequences:
a. BOLD Functional MRI
b. Diffusion tensor imaging
c. Diffusion weighted imaging (Echo planar)
d. Fast spin echo
e. FIESTA
f. FLAIR CSF suppression
g. Gradient echo
h. MR Spectroscopy
i. Phase-contrast
j. STIR fat suppression
k. Susceptibility weighted imaging
l. T1
m. T1 with gadolinium
n. T2
o. Time of flight

A

a. BOLD Functional MRI

26
Q
  1. Consideration of microvascular decompression for trigeminal neuralgia

MRI Sequences:
a. BOLD Functional MRI
b. Diffusion tensor imaging
c. Diffusion weighted imaging (Echo planar)
d. Fast spin echo
e. FIESTA
f. FLAIR CSF suppression
g. Gradient echo
h. MR Spectroscopy
i. Phase-contrast
j. STIR fat suppression
k. Susceptibility weighted imaging
l. T1
m. T1 with gadolinium
n. T2
o. Time of flight

A

e. FIESTA

27
Q
  1. Postoperatively to distinguish between
    tumor recurrence and radiation necrosis

Imaging Modalities:
a. B-mode Ultrasound
b. CT intracranial angiogram
c. CT myelogram
d. CT venogram cerebral
e. DAT scan
f. Doppler ultrasound
g. FDG-PET CT
h. Indium-11 Diethylenepentaacetic acid
study
i. MIBG scan
j. MR perfusion
k. Somatostatin-PET CT
l. SPECT
m. Xenon-133 CT

A

g. FDG-PET CT

28
Q
  1. Cisternography

Imaging Modalities:
a. B-mode Ultrasound
b. CT intracranial angiogram
c. CT myelogram
d. CT venogram cerebral
e. DAT scan
f. Doppler ultrasound
g. FDG-PET CT
h. Indium-11 Diethylenepentaacetic acid study
i. MIBG scan
j. MR perfusion
k. Somatostatin-PET CT
l. SPECT
m. Xenon-133 CT

A

h. Indium-11 Diethylenepentaacetic acid study

29
Q
  1. Intraoperative localization of spinal cord tumor

Imaging Modalities:
a. B-mode Ultrasound
b. CT intracranial angiogram
c. CT myelogram
d. CT venogram cerebral
e. DAT scan
f. Doppler ultrasound
g. FDG-PET CT
h. Indium-11 Diethylenepentaacetic acid
study
i. MIBG scan
j. MR perfusion
k. Somatostatin-PET CT
l. SPECT
m. Xenon-133 CT

A

a. B-mode Ultrasound

30
Q
  1. Reference metabolite in MR spectroscopy

MR Spectroscopy:
a. Alanine
b. Choline
c. Citrate peak
d. Creatine/phosphocreatine
e. Gamma-aminobutyric acid
f. Glucose
g. Glutamate (Glu)/Glutamine peak
h. Lactate
i. Myo-inositol (ml)
j. N-acetyl aspartate

A

d. Creatine/phosphocreatine

In order to interpret MRS, one needs to understand the function of the different molecules being measured. NAA is synthesized in the mitochondria of neurons, and its function is unknown. Clinically, NAA serves as a marker
for the presence of neurons, including neuronal
axons in white matter. Creatine (Cr) is used
clinically as a marker for energy metabolism.
Low levels of creatine suggest that the area of
interest is highly metabolically active. Creatine
is also often assumed to be stable and is used
for calculating metabolite ratios (e.g., Cho:Cr
and NAA:Cr). Choline (Cho) is found in the
cell membrane. It serves as a marker for the cellular turnover of a lesion. Choline is elevated
both in the setting of increased cellular production, such as in a tumor, and in the setting of cellular breakdown, such as in leukodystrophy and
multiple sclerosis. Lactate is a marker for
anaerobic metabolism. Normally, lactate levels
in the brain are so low that they cannot be measured by spectroscopy. Increased anaerobic
metabolism, such as with ischemia or tumor
necrosis, results in lactate peaks. Myoinositol
is a sugar. It is absent from neurons but present in glial cells. It is used as a marker for glial proliferation or an increase in glial size. Lipids are markers for fat, as is seen in the subcutaneous tissues or in the diploic space of the calvarium. Description of Common Spectroscopy Molecules: Their Chemical Shifts, Main Functions, and Classic Associations

31
Q
  1. Marker for cellular turnover

MR Spectroscopy:
a. Alanine
b. Choline
c. Citrate peak
d. Creatine/phosphocreatine
e. Gamma-aminobutyric acid
f. Glucose
g. Glutamate (Glu)/Glutamine peak
h. Lactate
i. Myo-inositol (ml)
j. N-acetyl aspartate

A

b. Choline

In order to interpret MRS, one needs to understand the function of the different molecules being measured. NAA is synthesized in the mitochondria of neurons, and its function is unknown. Clinically, NAA serves as a marker
for the presence of neurons, including neuronal
axons in white matter. Creatine (Cr) is used
clinically as a marker for energy metabolism.
Low levels of creatine suggest that the area of
interest is highly metabolically active. Creatine
is also often assumed to be stable and is used
for calculating metabolite ratios (e.g., Cho:Cr
and NAA:Cr). Choline (Cho) is found in the
cell membrane. It serves as a marker for the cellular turnover of a lesion. Choline is elevated
both in the setting of increased cellular production, such as in a tumor, and in the setting of cellular breakdown, such as in leukodystrophy and
multiple sclerosis. Lactate is a marker for
anaerobic metabolism. Normally, lactate levels
in the brain are so low that they cannot be measured by spectroscopy. Increased anaerobic
metabolism, such as with ischemia or tumor
necrosis, results in lactate peaks. Myoinositol
is a sugar. It is absent from neurons but present in glial cells. It is used as a marker for glial proliferation or an increase in glial size. Lipids are markers for fat, as is seen in the subcutaneous tissues or in the diploic space of the calvarium. Description of Common Spectroscopy Molecules: Their Chemical Shifts, Main Functions, and Classic Associations

32
Q
  1. Marker for ischaemia and necrosis

MR Spectroscopy:
a. Alanine
b. Choline
c. Citrate peak
d. Creatine/phosphocreatine
e. Gamma-aminobutyric acid
f. Glucose
g. Glutamate (Glu)/Glutamine peak
h. Lactate
i. Myo-inositol (ml)
j. N-acetyl aspartate

A

h. Lactate

In order to interpret MRS, one needs to understand the function of the different molecules being measured. NAA is synthesized in the mitochondria of neurons, and its function is unknown. Clinically, NAA serves as a marker
for the presence of neurons, including neuronal
axons in white matter. Creatine (Cr) is used
clinically as a marker for energy metabolism.
Low levels of creatine suggest that the area of
interest is highly metabolically active. Creatine
is also often assumed to be stable and is used
for calculating metabolite ratios (e.g., Cho:Cr
and NAA:Cr). Choline (Cho) is found in the
cell membrane. It serves as a marker for the cellular turnover of a lesion. Choline is elevated
both in the setting of increased cellular production, such as in a tumor, and in the setting of cellular breakdown, such as in leukodystrophy and
multiple sclerosis. Lactate is a marker for
anaerobic metabolism. Normally, lactate levels
in the brain are so low that they cannot be measured by spectroscopy. Increased anaerobic
metabolism, such as with ischemia or tumor
necrosis, results in lactate peaks. Myoinositol
is a sugar. It is absent from neurons but present in glial cells. It is used as a marker for glial proliferation or an increase in glial size. Lipids are markers for fat, as is seen in the subcutaneous tissues or in the diploic space of the calvarium. Description of Common Spectroscopy Molecules: Their Chemical Shifts, Main Functions, and Classic Associations

33
Q
  1. Epidermoid

Diffusion weighted imaging:
a. T2 low signal, DWI low signal, ADC low
signal
b. T2 low signal, DWI isointense or low
signal, ADC low signal
c. T2 low signal, DWI isointense or high
signal, ADC low signal
d. T2 low signal, DWI high signal in border
and low within lesion, ADC low signal
e. T2 low signal, DWI high signal, ADC
high signal
f. T2 isointense signal, DWI low signal,
ADC low signal
g. T2 isointense signal, DWI isointense or
low signal, ADC low signal
h. T2 isointense signal, DWI isointense or
high signal, ADC low signal
i. T2 isointense signal, DWI high, ADC
low signal
j. T2 isointense signal, DWI high signal in
border and low within lesion, ADC high
signal
k. T2 high signal, DWI low signal, ADC
high signal
l. T2 high signal, DWI isointense or low
signal, ADC low signal
m. T2 high signal, DWI high signal in border and low within lesion, ADC low
signal
n. T2 high signal, DWI high, ADC isointense signal
o. T2 high signal, DWI high signal, ADC
low signal

A

n. T2 high signal, DWI high, ADC isointense signal

Epidermoids are usually an expansive lesion in
the left aspect of the posterior fossa, and despite being solid they demonstrate similar signal intensity to CSF on T2WI, but demonstrate diffusion restriction on diffusion-weighted imaging (high signal DWI, isointense ADC). In contrast, arachnoid cysts may also be seen as a lesion in the posterior fossa demonstrating similar signal intensity to CSF but do not show restricted diffusion (low DWI, high ADC). Cerebral abscess must be considered when a ring enhancing necrotic lesion (usually surrounded by vasogenic edema) demonstrates restricted diffusion (bright DWI, dark ADC). An expansive ring enhancing cystic/necrotic lesion, surrounded by vasogenic edema/infiltrative lesion, demonstrating restricted diffusion and high perfusion in its borders but unrestricted diffusion within the lesion is more
consistent with glioblastoma or metastasis. Other highly cellular brain tumors demonstrating restricted diffusion on DWI include lymphoma, medulloblastoma and anaplastic astrocytoma.

34
Q
  1. Arachnoid cyst

Diffusion weighted imaging:
a. T2 low signal, DWI low signal, ADC low
signal
b. T2 low signal, DWI isointense or low
signal, ADC low signal
c. T2 low signal, DWI isointense or high
signal, ADC low signal
d. T2 low signal, DWI high signal in border
and low within lesion, ADC low signal
e. T2 low signal, DWI high signal, ADC
high signal
f. T2 isointense signal, DWI low signal,
ADC low signal
g. T2 isointense signal, DWI isointense or
low signal, ADC low signal
h. T2 isointense signal, DWI isointense or
high signal, ADC low signal
i. T2 isointense signal, DWI high, ADC
low signal
j. T2 isointense signal, DWI high signal in
border and low within lesion, ADC high
signal
k. T2 high signal, DWI low signal, ADC
high signal
l. T2 high signal, DWI isointense or low
signal, ADC low signal
m. T2 high signal, DWI high signal in border and low within lesion, ADC low
signal
n. T2 high signal, DWI high, ADC isointense signal
o. T2 high signal, DWI high signal, ADC
low signal

A

k. T2 high signal, DWI low signal, ADC
high signal

Epidermoids are usually an expansive lesion in
the left aspect of the posterior fossa, and despite being solid they demonstrate similar signal intensity to CSF on T2WI, but demonstrate diffusion restriction on diffusion-weighted imaging (high signal DWI, isointense ADC). In contrast, arachnoid cysts may also be seen as a lesion in the posterior fossa demonstrating similar signal intensity to CSF but do not show restricted diffusion (low DWI, high ADC). Cerebral abscess must be considered when a ring enhancing necrotic lesion (usually surrounded by vasogenic edema) demonstrates restricted diffusion (bright DWI, dark ADC). An expansive ring enhancing cystic/necrotic lesion, surrounded by vasogenic edema/infiltrative lesion, demonstrating restricted diffusion and high perfusion in its borders but unrestricted diffusion within the lesion is more
consistent with glioblastoma or metastasis. Other highly cellular brain tumors demonstrating restricted diffusion on DWI include lymphoma, medulloblastoma and anaplastic astrocytoma.

35
Q
  1. Ring-enhancing cerebral abscess

Diffusion weighted imaging:
a. T2 low signal, DWI low signal, ADC low
signal
b. T2 low signal, DWI isointense or low
signal, ADC low signal
c. T2 low signal, DWI isointense or high
signal, ADC low signal
d. T2 low signal, DWI high signal in border
and low within lesion, ADC low signal
e. T2 low signal, DWI high signal, ADC
high signal
f. T2 isointense signal, DWI low signal,
ADC low signal
g. T2 isointense signal, DWI isointense or
low signal, ADC low signal
h. T2 isointense signal, DWI isointense or
high signal, ADC low signal
i. T2 isointense signal, DWI high, ADC
low signal
j. T2 isointense signal, DWI high signal in
border and low within lesion, ADC high
signal
k. T2 high signal, DWI low signal, ADC
high signal
l. T2 high signal, DWI isointense or low
signal, ADC low signal
m. T2 high signal, DWI high signal in border and low within lesion, ADC low
signal
n. T2 high signal, DWI high, ADC isointense signal
o. T2 high signal, DWI high signal, ADC
low signal

A

o. T2 high signal, DWI high signal, ADC
low signal

Epidermoids are usually an expansive lesion in
the left aspect of the posterior fossa, and despite being solid they demonstrate similar signal intensity to CSF on T2WI, but demonstrate diffusion restriction on diffusion-weighted imaging (high signal DWI, isointense ADC). In contrast, arachnoid cysts may also be seen as a lesion in the posterior fossa demonstrating similar signal intensity to CSF but do not show restricted diffusion (low DWI, high ADC). Cerebral abscess must be considered when a ring enhancing necrotic lesion (usually surrounded by vasogenic edema) demonstrates restricted diffusion (bright DWI, dark ADC). An expansive ring enhancing cystic/necrotic lesion, surrounded by vasogenic edema/infiltrative lesion, demonstrating restricted diffusion and high perfusion in its borders but unrestricted diffusion within the lesion is more
consistent with glioblastoma or metastasis. Other highly cellular brain tumors demonstrating restricted diffusion on DWI include lymphoma, medulloblastoma and anaplastic astrocytoma.

36
Q
  1. Ring-enhancing glioblastoma multiforme

Diffusion weighted imaging:
a. T2 low signal, DWI low signal, ADC low
signal
b. T2 low signal, DWI isointense or low
signal, ADC low signal
c. T2 low signal, DWI isointense or high
signal, ADC low signal
d. T2 low signal, DWI high signal in border
and low within lesion, ADC low signal
e. T2 low signal, DWI high signal, ADC
high signal
f. T2 isointense signal, DWI low signal,
ADC low signal
g. T2 isointense signal, DWI isointense or
low signal, ADC low signal
h. T2 isointense signal, DWI isointense or
high signal, ADC low signal
i. T2 isointense signal, DWI high, ADC
low signal
j. T2 isointense signal, DWI high signal in
border and low within lesion, ADC high
signal
k. T2 high signal, DWI low signal, ADC
high signal
l. T2 high signal, DWI isointense or low
signal, ADC low signal
m. T2 high signal, DWI high signal in border and low within lesion, ADC low
signal
n. T2 high signal, DWI high, ADC isointense signal
o. T2 high signal, DWI high signal, ADC
low signal

A

j. T2 isointense signal, DWI high signal in
border and low within lesion, ADC high
signal

Epidermoids are usually an expansive lesion in
the left aspect of the posterior fossa, and despite being solid they demonstrate similar signal intensity to CSF on T2WI, but demonstrate diffusion restriction on diffusion-weighted imaging (high signal DWI, isointense ADC). In contrast, arachnoid cysts may also be seen as a lesion in the posterior fossa demonstrating similar signal intensity to CSF but do not show restricted diffusion (low DWI, high ADC). Cerebral abscess must be considered when a ring enhancing necrotic lesion (usually surrounded by vasogenic edema) demonstrates restricted diffusion (bright DWI, dark ADC). An expansive ring enhancing cystic/necrotic lesion, surrounded by vasogenic edema/infiltrative lesion, demonstrating restricted diffusion and high perfusion in its borders but unrestricted diffusion within the lesion is more
consistent with glioblastoma or metastasis. Other highly cellular brain tumors demonstrating restricted diffusion on DWI include lymphoma, medulloblastoma and anaplastic astrocytoma.