MRI provides detailed images of the brain without exposing patients to radiation. It is useful for evaluating conditions like tumors, strokes, and multiple sclerosis. The document describes the MRI procedure for brain imaging including patient preparation, head coils, sequences, and protocols. Key sequences discussed are T1-weighted, T2-weighted, FLAIR, diffusion weighted, MR angiography, and MR venography.

1. MRI Procedure of Brain
By: Sudil Paudyal
BSc. MIT Final year
Roll no. 51

2. Introduction
• Brain is the most frequently imaged organ by MR imaging.
• Technological developments in computer design and processing
speeds as well as hardware developments have enabled significant
growth in MR brain imaging.
• Beyond simple anatomical imaging of the brain, advanced
techniques now include functional MRI (fMRI), such as blood
oxygen-level dependent (BOLD) imaging and 3D proton
spectroscopy, diffusion tensor imaging (DTI), perfusion imaging, and
volumetric measurements.
• However, basic techniques remain the foundation for all MR brain
imaging.
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3. Advantages of MRI over CT in brain imaging
• MRI does not use ionizing radiation, and is thus preferred over CT in
children and patients requiring multiple imaging examinations.
• MRI has a much greater range of available soft tissue contrast, depicts
anatomy in greater detail, and is more sensitive and specific for
abnormalities within the brain itself.
• MRI scanning can be performed in any imaging plane without having to
physically move the patient.
• MRI contrast agents have a considerably smaller risk of causing potentially
lethal allergic reaction.
• MRI allows the evaluation of structures that may be obscured by artifacts
from bone in CT images.
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4. Indications
• Multiple Sclerosis (MS)
• Primary Tumor Assessment and / or Metastatic disease.
• AIDS (toxoplasmosis)
• Infarction [ Cerebral Vascular Accident (CVA) vs. transient
Ischaemic Attack (TIA) ]
• Hemorrhage
• Hearing Loss
• Visual Disturbances
• Infection trauma
• Unexplained Neurological Symptoms or deficit
• Mapping of brain function
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5. Equipment
• Head Coils:
– Surface coils for brain imaging usually consist of two types:
Single-channel transmit/receive coils
High-channel phased array coils.
• Immobilization pads and straps
• Ear plugs
• High performance gradients for EPI (Eco planer
Imaging), diffusion and perfusion imaging.
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6. Head Coils:
• Single channel transmit/ receive coils:
A whole volume “bird-cage” design
Surround the entire head to below the level of C2 or C3.
A quadrature design to further boost SNR
Serve as both a transmit and receive antennae.
Provides adequate SNR for most general brain applications
when small detail is not required.
However, to visualize very small pathology such as small
MS lesions or pituitary micro-adenomas, scan times can
become unacceptably long in order to attain the required
SNR.
The development of phased array technology has
addressed this issue.
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7. • High-Channel Phased Array
Coils:
Addressed both SNR issues
and concerns about
anatomical coverage.
Higher SNR provided by these
coils allows for imaging with
higher spatial resolution —
smaller voxels, thinner slice
acquisitions, and small fields-
of-view for greater detection
of small pathology and small-
vessel stenoses.
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8. Patient preparation
• Before preparation, complete history should be checked. If
indication is unclear, the referring physician should be contacted.
• All metallic objects should be removed from pts body to ensure that
artifacts are not created during scanning.
• Disposable ear plugs should be provided to the patient to devoid
the patients from repeated noises during scanning.
• The patient should be instructed to avoid coughing, wriggling or
producing other large motion during or in between the scans.
• Ensure the IV line prior to the precontrast acquistion preferably
with 20 or 22 gauge IV canula.
• Pts who present with claustrophobic features may require sedation
with diazepam/ alprazolam/ midazolam.
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9. Contrast Media
• Gadolinium-based contrast enhancement is useful in brain imaging.
• Physicians often believe that administration of contrast is indicated for all
lesions.
• Three conditions must be met in order for contrast enhancement to occur:
– 1. An adequate blood supply to the lesion must exist
– 2. Blood-brain barrier breakdown must be present
– 3. Sufficient extracellular space must be available for the contrast agent to
localize after it has leaked out of the vasculature
• In cases in which lesions do not enhance, the lack of enhancement in and
of itself provides useful clinical information
• IV Gadolinium: 0.1-0.2 mmol/kg body weight
– given as a bolus at the rate of 1 ml/sec or
– as a slow infusion at the rate of 1 ml/6 sec.
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10. Patient Positioning
• Supine with head placed within the coil.
• Arms beside the trunk.
• Interpupillary line parallel to the couch and the head should
be straight.
• Longitudinal alignment line in the midline.
• Horizontal alignment line through the nasion.
• Straps and foam pads for immobilization.
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11. Tips & Tricks:
 Symmetric positioning of the patient: use the bridge of the
nose as reference point
 Place cushions behind the knees
 In patients with increased kyphosis, place cushion under the
pelvis as well; in those with neck problems it may be necessary
to raise the head somewhat and cushion it.
 A mirror mounted on the head coil reduces claustrophobia.
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12. Protocols
• Protocols used in MRI are not written in stone.
• Each facility decides on the best method for imaging the brain
based on their MRI system configuration, patient and
referring physician needs, and prevailing academic literature.
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13. Routine Brain Protocol
• Sequences:
– Scout : 3 plane localiser
– T2 FSE in axial plane
– T2 FLAIR in axial plane
– T1 SE in sagittal and coronal plane
– DW EPI based in axial plane
– Post contrast T1 SE in the axial and coronal
plane.
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15. Axial sequence:
• Plot on sagittal plane,
• Parallel to line through
anterior and posterior
commissure ,
• From the foramen
magnum to vertex .
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16. Parameters
• FOV: 220-240 mm
• Slice thickness : 5-6 mm
• Slice gap : 20% of the slice
thickness ( 1-1.2 mm)
• Saturation slab : parallel to
slices , inferior to most
caudal slice 10 mm and
thickness 50-80 mm
• Matrix: 512 x 512
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17. T2 weighted
TR: 4500
TE : 100
Freq.# : 256
Phase# : 192
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18. T1 weighted
TR : 364 ms
TE : 15 ms
Or Proton-density
weighted:
TR: 2000-3500 ms
TE: 15 ms
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19. FLAIR
• TR : 10717 ms
• TE : 100 ms
• TI : 2000 ms
• Pathology appears hyperintense due to the
optimization of TI required to null the signal of water.
• FLAIR vs PD:
 CSF appears low intensity on FLAIR which has two
advantages:
 First, periventricular lesions are better differentiated
from CSF
 Second , infectious exudates may replace CSF in the
sulci to appear hyperintense on FLAIR images but may
be difficult to detect on conventional proton density
spin echo images.
 For this reason, FLAIR imaging has largely replaced
PDWI for many indications.
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20. Fig. 1.1 Post Contrast Axial MR Image of the brain
1
2
3
4
5
Post Contrast sagittal T1 Weighted
M.R.I.
Section at the level of Foramen
Magnum
1. Cisterna Magna
2. Cervical Cord
3. Nasopharynx
4. Mandible
5. Maxillary Sinus
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21. Fig. 1.2 Post Contrast Axial MR Image of the brain
7
6
Post Contrast sagittal T1 Wtd M.R.I.
Section at the level of medulla
6. Medulla
7. Sigmoid Sinus
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22. Fig. 1.3 Post Contrast Axial MR Image of the brain
15
8
9
10
11
12
13
14
16
17
Post Contrast sagittal T1 Wtd M.R.I.
Section at the level of Pons
8. Cerebellar
Hemisphere
9. Vermis
10. 4th Ventricle
11. Pons
12. Basilar Artery
13. Internal Carotid
Artery
14. Cavernous Sinus
15. Middle Cerebellar
Peduncle
16. Internal Auditory
Canal
17. Temporal Lobe
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23. Fig. 1.4 Post Contrast Axial MR Image of the brain
18
19
20
21
22
Post Contrast sagittal T1 Wtd M.R.I.
Section at the level of Mid Brain
18. Aqueduct of Sylvius
19. Midbrain
20. Orbits
21. Posterior Cerebral Artery
22. Middle Cerebral Artery
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24. Fig. 1.5 Post Contrast Axial MR Image of the brain
23
24
25
26
27
Post Contrast sagittal T1 Wtd M.R.I.
Section at the level of the 3rd
Ventricle
23. Occipital Lobe
24. 3rd Ventricle
25. Frontal Lobe
26. Temporal Lobe
27. Sylvian Fissure
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25. Fig. 1.6 Post Contrast Axial MR Image of the brain
28
29
30
31
32
38
33
34
36
35
37
Post Contrast sagittal T1 Wtd M.R.I.
Section at the level of Thalamus
28. Superior Sagittal
Sinus
29. Occipital Lobe
30. Choroid Plexus
within the occipital
horn
31. Internal Cerebral
Vein
32. Frontal Horn
33. Thalamus
34. Temporal Lobe
35. Internal Capsule
36. Putamen
37. Caudate Nucleus
38. Frontal Lobe
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26. Fig. 1.7 Post Contrast Axial MR Image of the brain
39
40
41
Post Contrast sagittal T1 Wtd M.R.I.
Section at the level of Corpus
Callosum
39. Splenium of corpus callosum
40. Choroid plexus within the
body of lateral ventricle
41. Genu of corpus callosum
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27. Fig. 1.8 Post Contrast Axial MR Image of the brain
42
43
44
Post Contrast sagittal T1 Wtd M.R.I.
Section at the level of Body of Corpus
Callosum
42. Parietal Lobe
43. Body of the Corpus
Callosum
44. Frontal Lobe
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28. Fig. 1.9 Post Contrast Axial MR Image of the brain
45
46
Post Contrast sagittal T1 Wtd M.R.I.
Section above the Corpus Callosum
45. Parietal Lobe
46. Frontal Lobe
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29. Sagittal sequence:
 Sagittal plot on coronal and axial localizer .
 Same slice thickness , gap and saturation
slab .
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30. • Sagittal images are essential in the evaluation of sellar and
parasellar lesions, posterior fossa lesions, and intraventricular
lesions as well as for evaluation of the vascular anatomy.
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31. Coronal sequence:
• Plot on sagittal localizer
• Plane perpendicular to
axial plane
• Parallel to posterior
surface of brain stem
• Coverage from anterior
cranial vault to
posterior cranial vault.
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33. MR Angiography (MRA)
• Time-of-flight (TOF) or Inflow
angiography, uses a short echo time
and flow compensation to make
flowing blood much brighter than
stationary tissue.
• As flowing blood enters the area
being imaged it has seen a limited
number of excitation pulses so it is
not saturated, this gives it a much
higher signal than the saturated
stationary tissue.
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34. • Indications :
– Evaluation of cerebral arteries in cases of stroke,
subarachnoid and intracerebral hemorrhage,
trauma, AVM, suspected or known aneurysm etc.
• Sequence:
– 3D TOF for circle of willis in the axial plane
– 3D TOF for vertebrobasilar system in axial plane
– For AVM, additional sequences needed are
– 3D TOF through region of interest
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35. • Parameters:
– FOV : 160 ms
– TR : 42.8 ms
– TE : 7.1
– FA : 330
– Thickness : 1.2 mm
– Multislab: 12
• Contrast is administered if one has to
differentiate between tumor and unusual
cavernous malformation or to look for adjacent
venous malformation.
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37. MR Venography (MRV)
• Indications:
–Evaluation of intracerebral veins and
intradural venous sinuses for thrombosis
• Sequences
– Routine brain protocol
– PC images in the sagittal plane (for superior sagittal
sinus) and in the axial plane (for transverse sinus).
– 2D TOF in the sagittal and coronal plane through whole
head.
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38. • Parameters:
– FOV : 220
– TR : 35 ms
– TE : 8 ms
– FA : 60 0
– Thickness : 3.3
– Interval : 2.2
– Multislice : 80
• The coronal sequence must include the confluence of
sinuses in posterior part of the head.
• The coronal TOF acquisition can lead to artefactual loss of
signal in transverse sinuses due to in plane flow. An oblique
transverse scan obtained in plane of transverse sinus help
evaluate such an artifact.
• For evaluation of patient suspected of having venous
thrombosis, MRV is done along with stroke protocol.
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40. Diffusion Weighted Sequence:
• Images the random motion of water molecules as they diffuse
through the extra-cellular space
• A typical diffusion-weighted pulse sequence is constructed by
the addition of a pair of diffusion-sensitizing gradients, also
known as motion-probing gradients, applied along the same
directional axis before and after the 180°refocusing pulse of a
spin-echo sequence.
• Diffusion thus results in loss of signal due to incomplete
rephasing of spins that change position between and during
the applications of the 2 diffusion-sensitizing gradients.
• Regions of high mobility “rapid diffusion”  dark
• Regions of low mobility “slow diffusion”  bright
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41. • Postprocessing ’Diffusion’
package to calculate
parametric maps (e.g.
ADC-, eADC-, FA-map).
• FiberTrak package to
track fibers for diffusion
tensor data with at least
6 diffusion directions.
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42. Multiple Sclerosis (MS)
• An autoimmune condition in which the immune system attacks the
CNS (principally the white matter in the brain and spinal cord ),
leading to demyelination.
• Protocol:
– Best with sagittal FLAIR
– Administration of contrast .
– Sequences:
- Routine protocol
- Sagittal FLAIR FSE/TSE
- Axial T1 FS + contrast
- Axial FLAIR + contrast
- Coronal T1 FS + contrast
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43. FLAIR and Post Gd T1WI showing lesion at roof of fourth ventricle.
 MS and stroke lesions can have similar appearance on
conventional sequences but only acute stroke lesions will have
restricted diffusion.
 Therefore a diffusion sequence should be done for suspected
but unconfirmed MS.
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44. Trauma
• Indications:
– For old trauma to the head and brain when CT
findings are discrepant.
– Diffuse axonal injury or nonaccidental trauma
suspected and posterior fossa lesions where CT is
limited because of beam hardening artifacts.
• Sequences
– Routine protocol
– MPRAGE with sagittal and axial reformats (5 mm).
– Axial GRE
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45. Hemorrhage
• Hyperacute ( < 24 hrs old )
• Acute ( 1-3 days ),
• Subacute ( 4-14 days ),
• Chronic (> 14 days )
• Sequences
- Routine protocol
- Ax GRE
- Ax T1 FS + contrast
- FLAIR + contrast
- Coronal T1 FS + contrast
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46. Stroke
• Indications:- TIA, vertebro-basilar infarct
• Sequences :-
– T1 SE in axial and sagittal plane
– T2 FSE in axial plane
– T2 FLAIR with fat suppression in axial and coronal plane
– DW EPI based in axial plane
– Post Gd T1 SE in axial and coronal plane
• For suspected hyperacute stroke:
– DW in the coronal plane
– 3D- TOF for MRA of circle of willis
– Perfusion imaging in axial plane.
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47. Magnetic resonance imaging in acute stroke. Left: Diffusion-weighted
MRI in acute ischemic stroke performed 35 minutes after symptom
onset. Right: Apparent diffusion coefficient (ADC) map obtained from
the same patient at the same time.
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48. ICSOLs
• Indications:
• Evaluation of the intraparenchymal space occupying
lesions as tumors, metastases, abscesses etc.
• For localization, complication and management,
meningeal disease and post op follow up of these
cases.
• Sequences
- Routine protocol
- Axial and coronal T1 FS + contrast
- Axial FLAIR + contrast
- Sagittal T1 Fat Sat +contrast
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49. • All pt.s with neoplasms should be evaluated by MRS.
• For melanoma and hemorrhagic metastases, axial MPGR
susceptibility sequences should be added.
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Post contrast axial T1WI shows a glioma extending
across corpus callosum

50. Cranial nerve
• Indications : For optimal demonstration of cranial
nerve anatomy along their entire course to detect any
pathology, injury, infection, tumor and any clinical
condition related to possible dysfunction of the nerve.
• Sequences:
– Routine protocol
– 3D CISS (3D BASG) in the axial plane from midbrain to
formen magnum
– Post contrast T1 SE with fat sat. in axial and coronal plane
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51. • Although all cranial nerves can be identified in this protocol,
certain cranial nerves such as II, VII and VIII are best evaluated
with separate protocols.
• Cranial nerve 2 is evaluated in the orbit protocol.
• Cranial nerve 7 and 8 are evaluated in IAC protocol.
• In coronal plane images, make sure to include the inferior tip
of mandible to demonstrate course of mandibular division of
trigeminal nerve.
• The 3D CISS is a very high resolution, heavily T2W, 3D
sequence. It allows evaluation of CP angle and fluid structures
of IAC and inner ear.
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52. Acoustic schwannoma
T1 Axial T1 axial with Gad.
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53. IAC
• Indications : Evaluation of temporal bone for
inflammatory, vascular and neoplastic disorders of soft
tissues for eg those related to otic capsule, carotid
sheath, jugular bulb etc.
• Sequences:
– Routine protocol
– 3D CISS in th axial plane through the temporal bone region
– Pre/post Gd, HR T1 in axial plane 3mm through temporal
bone
– Post Gd, HR T1 in coronal plane 3mm through temporal
bone
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Fig : Coronal ultra thin slice T1 WI demonstrates
both internal auditory canals

55. Temporal lobe
• Indications:
– Evaluation of pt.s with
epilepsy, esp. complex
partial seizures which have
not responded to
medication
– Pre op evalutation for
planning in cases of partial
or full temporal lobectomy,
suspected mesial temporal
lobe sclerosis and short
term memory loss.
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56. • Sequences :-
– Routine protocol ( in sagittal use
MPRAGE isotropic T1)
– Coronal and Axial T1 post
contrast
– Axial FLAIR post contrast
– 3D SPGR through whole brain
– Post contrast T1 sag if any SOL
detected in midline or occipital
lobes.
Coronal sequence
• Plot on sagittal perpendicular
to line of hippocamaple grey
matter.
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57. Pituitary fossa
• Indications:
– To detect sellar and parasellar lesions, to delineate intrusion into
surrounding structures.
– Hormonal disturbances(amenorhea, hyperprolactinemia,
acromegaly),
– Suspected or known microadenoma or macroadenoma,
– Pituitary apoplexy and sudden visual loss.
• Sequences :
– Routine protocol
– Coronal T1SE through the sella
– Post contrast T1SE with fat sat. in Sagittal and coronal plane
through the sella
– Post contrast T1SE with fat sat in the axial plane through the
whole brain.
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58. Brain MRI protocol (Pituitary)
• Coronal sequence
• Plot on mediosagittal
localizer superior to
sella.
• Slice thickness: 2mm
• Slice Interval : 0-20% of
thickness
• 2 sat. slab
• Small FOV
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60. Dynamic study of sella
• Performed to evaluate cavernous sinus invasion by macroadenoma
• Standard pituitary exam should be performed before the dynamic study.
• FSE T1 coronal series of images is taken with a fast injecion of half dose
contrast.
• The injection is rapidly given at the start of the 2nd measurement. There is
a 10 second pause between the first scan and the start of continuous
string of post contrast measurements to prepare the injector and give a
countdown.
• Consists of four 3mm slices to cover sella in coronal plane.
• Five sets of images are obtained at 25 sec interval, with first set before
contrast and the other 4 sets after contrast.
• Main aim is to look for differential contrast enhancement between tumor(
slow enhancement) and gland (fast enhancement).
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61. Orbit MRI protocol
• Indications:
– Detection and staging of ocular tumors as melanoma
and metastases
– Evaluation of extraocular orbital infection, tumor,
myopathy, neuropathy and vascular diseases
– Lacrimal gland pathology
• Sequences:
– Routine brain protocol
– Pre/post Gd, high resolution T1SE with fat sat in axial
and coronal plane through the orbit
– Parasagittal T2 through the orbit
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62. Orbit MRI protocol
• Coronal
• Plot on axial localizer
• 3mm slice thickness
• Gap 20%
• Axial plot on coronal
localizer
• 3mm slice thickness
• Gap 20%
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63. Orbit MRI protocol
• Parasagittal :
• Plot on axial along with
optic nerve
• 3mm slice thickness
• Gap 20%
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64. Perfusion imaging
 Perfusion imaging tracks the
transient passage of a Gd-
based contrast agent bolus by
means of a fast dynamic scan.
 Contrast agent will be
injected as a bolus: double
dose Gd, power injected at
rate of 5ml/sec with a 10 sec
delay.
 Simultaneously, a fast
dynamic scan will be started.
 This dynamic scan will be
evaluated with post-
processing packages.
Perfusion image with
pathology in left
parietal area
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 Above color maps are from MRI Dynamic Susceptibility Contrast
Perfusion (DSCP) study
 What we see are the color maps representing:
TTP (Time To Peak) - that shows the regional distribution of
arrival time of the bolus in the tissue
CBF (Cerebral Blood Flow)
CBV (Cerebral Blood Volume)
MTT (Mean Transit Time)

66. Magnetic Resonance Spectroscopy (MRS)
• The use of magnetic resonance in quantification of various
metabolites (chemical composition) and the study of their
distribution in different tissues.
• Rather than displaying MRI proton signals on a gray scale as
an image depending on its relative signal strength, MRS
displays the quantities as a spectrum.
• The resonance frequency of each metabolite is represented
on a graph and is expressed as parts per million (ppm).
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67.  Using MRS, the more metabolite that is present, the taller
the peak or greater the area under the peak. Specific
metabolites can be located along an x-axis.
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68. Functional MRI (fMRI)
• fMRI detects the blood oxygen level–dependent (BOLD) changes in
the MRI signal that arise when changes in neuronal activity occur
following a change in brain state.
• An increase in neural activity in a region of cortex stimulates an
increase in the local blood flow in order to meet the larger demand
for oxygen and other substrates.
• The change in blood flow actually exceeds more than needed so
that, at the capillary level, there is a net increase in the balance of
oxygenated arterial blood to deoxygenated venous blood.
• Essentially, the change in tissue perfusion exceeds the additional
metabolic demand, so the concentration of deoxyhemoglobin
within tissues decreases. This decrease has a direct effect on the
signals used to produce magnetic resonance images.
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69. • While blood that contains oxyhemoglobin is not very
different, in terms of its magnetic susceptibility, from
other tissues or water, deoxyhemoglobin is significantly
paramagnetic (like the agents used for MRI contrast
materials, such as gadolinium), and thus deoxygenated
blood differs substantially in its magnetic properties
from surrounding tissues
• The result of having lower levels of deoxyhemoglobin
present in blood in a region of brain tissue is therefore
that the MRI signal from that region decays less rapidly
and so is stronger when it is recorded in a typical
magnetic resonance image acquisition.
• This small signal increase is the BOLD signal recorded in
fMRI.
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70.  During a typical functional imaging series, nearly 30 images are
acquired in a 90 sec run where the first and last 10 images
represent the baseline scans and the middle 10 scans are
acquired during the task.
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71. fMRI
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72. References
• Hand Book of MRI Technique by Catherine
Westbrook
• CT & MRI Protocol by Satish k Bhargava
• MRI parameters and positioning by Torsten B.
Moeller
• CT and MRI of the whole body by John. R.
Haaga
• Various research articles and ppts.
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HUMAN BRAIN :- REALLY A MAZE !!!!!!
  