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PRINCIPLES OF MRI BRAIN
BY : DR. MANOJ SEERVI & DR. SURESH CHOUDHARY
INCHARGE: DR. ACHAL SHARMA
FACUILTY: DR. J S SHEKHAWAT
DR. GAURAV JAIN
DR. NAVNEET AGARWAL
HISTORICAL ASPECT
• 1940s –Felix Bloch &E. Purcell: discovered just after world
war II & named Nuclear Magnetic Resonance (noble prize
1952)
• 1973: Paul Lauterbur published the first nuclear magnetic
resonance image and the first cross-sectional image of a living
mouse in January 1974
• 1977 – Mansfield: first image of human anatomy, first echo
planar image
• 1990s - Discovery that MRI can be used to distinguish
oxygenated blood from deoxygenated blood ,it leads to
Functional Magnetic Resonance imaging (fMRI)
• Paul Lauterbur and Peter Mansfield won the Nobel Prize in
Physiology/Medicine (2003) for their pioneering work in
MRI
The first Human MRI scan was performed on 3rd july 1977 by Raymond
Damadian, Minkoff and Goldsmith.
Describing Radiological Terms
• USG(ultrasonography)- ECHOGENICITY
• CT(Computed tomography) scan- DENSITY
• MRI(magnetic resonance imaging)- INTENSITY
• Hyper- white/ bright
• Hypo- black/ dark
MRI is based on the principle of nuclear magnetic resonance
(NMR)
• Two basic principles of NMR
1. Atoms with an odd number of protons have spin
2. A moving electric charge, be it positive or negative,
produces a magnetic field
• Body has many such atoms that can act as good MR nuclei (1H,
13C, 19F, 23Na)
• MRI utilizes this magnetic spin property of protons of
hydrogen to produce images.
• In our natural state Hydrogen ions in body are spinning in a
haphazard fashion, and cancel all the magnetism. When an
external magnetic field is applied protons in the body align in
one direction.
BASIC PRINCIPLES OF MRI
Why Hydrogen ions are used in MRI?
1. Hydrogen nucleus has an unpaired proton which
is positively charged
2. Every hydrogen nucleus is a tiny magnet which
produces small but noticeable magnetic field
3. Hydrogen is abundant in the body in the form
of water and fat
4. Essentially all MRI is hydrogen (proton) imaging
• TE (Echo Time) : the time between the delivery of the RF
pulse and the receipt of the echo signal
• TR (Repetition Time) : The time between two excitations
is called repetition time.
TR & TE
• By varying the TR and TE one can obtain T1WI and T2WI.
• In general a short TR (<1000ms) and short TE (<45 ms) scan
is T1WI.
• Long TR (>2000ms) and long TE (>45ms) scan is T2WI.
BASIC MR BRAIN SEQUENCES
• ROUTINE SEQUENCES
– T1 – for anatomy
– T2- for pathological details
– FLAIR – suppress fluid
• SPECIAL SEQUENCES
– DWI – for infarcts, abscess , tumour detection
– ADC – for differentiation of different age of infarcts
– MRA – for arterial details
– MRV – for venous details
– MRS – spectroscopy for chemical compositions of the lesion
– GRE
– FIESTA(FAST IMAGING EMPLOYING STEADY STATE ACQUISITION)
/CISS(CONSTRUCTIVE INTERFERENCE STEADY STATE),
– STIR
– SWI
• SHORT TE
• SHORT TR
• BETTER ANATOMICAL DETAILS
• FLUID : DARK/CSF BLACK
• GRAY MATTER : GRAY
• WHITE MATTER: WHITE
T1 W IMAGES
• Most of pathologies are DARK/ HYPOINTENSE
on T1
• BRIGHT ON T1
– Fat
– Sub acute H’age (Methaemoglobin)
– Melanin
– High Protein Contents
– Posterior Pituitary appears bright on T1
(Neurosecretory granules)
– Gadolinium contrast
– Cholesterol
• LONGTE
• LONG TR
• BETTER PATHOLOGICAL DETAILS
• FLUID: BRIGHT/Hyperintense
• GRAY MATTER : RELATIVELY BRIGHT
• WHITE MATTER: DARK
T2 W IMAGES
T1 W IMAGES
T1W AND T2 W IMAGES
• LONG TE
• LONG TR
• SIMILAR TO T2 EXCEPT FREE WATER SUPRESSION
(INVERSION RECOVERY)
• CSF : DARK
• GRAY MATTER : RELATIVELY BRIGHT
• WHITE MATTER: DARK
• Most pathology is BRIGHT
• Hydrocephalous: Periventricular hyperintensity(CSF
ooze)
• Especially good for lesions near ventricles or sulci or
CSF containing spaces (eg Multilpe Sclerosis)
FLAIR (Fluid Attenuated Inversion Recovery Sequences)
Same as T2
with CSF
suppression
CT
FLAIR
T2
T1
Multiple sclerosis:
periventricular
demyelinating process
(white arrows) and
white matter
inflammatory changes
around the
perimedullary veins,
known as Dawson
Fingers (red arrows)
Clinical Applications of FLAIR sequences:
• Used to evaluate diseases affecting the brain parenchyma neighboring
the CSF-containing spaces for
eg: MS & other demyelinating disorders.
• Unfortunately, less sensitive for lesions involving the brainstem &
cerebellum, owing to CSF pulsation artifacts
• Mesial temporal sclerosis (MTS) (thin section coronal FLAIR)
• Tuberous Sclerosis – for detection of Hamartomatous lesions.
• Helpful in evaluation of neonates with perinatal HIE.
T1W T2W FLAIR(T2)
TR SHORT LONG LONG
TE SHORT LONG LONG
CSF LOW HIGH LOW
FAT HIGH HIGH MEDIUM
GREY MATTER LOW HIGH HIGH
WHITE MATTER HIGH LOW LOW
EDEMA LOW HIGH HIGH
GRADATION OF INTENSITY
IMAGING
CT SCAN CSF Edema White
Matter
Gray
Matter
Blood Bone
MRI T1 CSF Edema Gray
Matter
White
Matter
Cartilage Fat
MRI T2 Cartilage Fat White
Matter
Gray
Matter
Edema CSF
MRI T2 Flair CSF Cartilage Fat White
Matter
Gray
Matter
Edema
MRI BRAIN :AXIAL SECTIONS
MRI BRAIN :SAGITTAL SECTIONS
White Matter
Cerebellum
Parietal Lobe
Frontal Lobe
Lateral Sulcus
Grey Matter
Occipital Lobe
Temporal Lobe
Gyri of cerebral
cortex
Sulci of cerebral
Cortex
Cerebellum
Frontal Lobe
Temporal
Lobe
Frontal Lobe
Temporal
Lobe
Parietal Lobe
Occipital
Lobe
Cerebellum
Frontal Lobe
Parietal Lobe
Orbit
Occipital Lobe
Transverse sinus
Cerebellar
Hemisphere
Optic Nerve
Precentral Sulcus
Lateral Ventricle
Occipital Lobe
Maxillary sinus
Caudate
Nucleus
Corpus callosum
Thalamus
Tongue
Tentorium
Cerebell
Pons
Splenium of
Corpus callosum
Pons
Ethmoid air
Cells
Inferior nasal
Concha
Midbrain
Fourth Ventricle
Genu of Corpus
Callosum
Hypophysis
Thalamus
Splenium of
Corpus
callosum
Genu of corpus
callosum
Pons
Superior
Colliculus
Inferior
Colliculus
Nasal Septuml
Medulla
Body of corpus
callosum
Thalamus
Cingulate Gyrus
Genu of corpus
callosum
Ethmoid
air cells
Oral cavity
Splenium of
Corpus
callosum
Fourth Ventricle
Frontal
Lobe
Maxillary
Sinus
Parietal Lobe
Occipital Lobe
Corpus Callosum
Thalamus
Cerebellum
Frontal Lobe
Temporal
Lobe
Parietal Lobe
Lateral Ventricle
Occipital Lobe
Cerebellum
Frontal Lobe
Parietal Lobe
Superior Temporal
Gyrus
Lateral Sulcus
Inferior Temporal
Gyrus
Middle Temporal Gyrus
External Auditory
Meatus
. Bone
Inferior sagittal sinus
Corpus callosum
Internal cerebral vein
Superior sagittal sinus
Parietal lobe
Vein of Galen
Occipital lobe
Straight sinus
. Vermis
. IV ventricle
Cerebellar tonsil
Mass intermedia
of thalamus
Sphenoid Sinus
MRI BRAIN :CORONAL SECTIONS
Longitudinal
Fissure
Straight Sinus
Superior Sagittal Sinus
Sigmoid Sinus
Vermis
Arachnoid Villi
Great Cerebral
Vein
Tentorium
Cerebelli
Falx Cerebri
Lateral Ventricle
Vermis of
Cerebellum
Cerebellum
Splenium of
Corpus callosum
Posterior
Cerebral
Artery
Superior
Cerebellar
Artery
Foramen
Magnum
Lateral Ventricle
Internal Cerebral
Vein
Tentorium
Cerebelli
Fourth Ventricle
Cingulate Gyrus
Choroid Plexus
Superior Colliculus
Cerebral Aqueduct
Corpus Callosum
Thalamus
Pineal Gland
Vertebral Artery
Insula
Lateral Sulcus
Cerebral Peduncle
Olive
Crus of Fornix
Middle Cerebellar
Peduncle
Caudate Nucleus
Third Ventricle
Hippocampus
Pons
Corpus Callosum
Thalamus
Cerebral
Peduncle
Parahippocampal
gyrus
Lateral Ventricle
Temporal Horn of
Lateral Ventricle
Uncus of Temporal
Lobe
Body of Fornix
Third Ventricle
Hippocampus
Internal Capsule
Caudate Nucleus
Optic Tract
Insula
Parotid Gland
Amygdala
Lentiform
Nucleus
Hypothalamus
Internal Capsule
Cingulate Gyrus
Optic Nerve
Nasopharynx
Caudate
Nucleusa
Lentiform
Nucleus
Internal
Carottid Artery
Longitudinal
Fissure
Superior Sagittal
Sinus
Lateral Sulcus
Parotid Gland
Genu Of
Corpus
Callosum
Temporal Lobe
Frontal Lobe
Nasal
Turbinate
Massetor
Ethmoid Sinus
Nasal Septum
Nasal Cavity
Tongue
Frontal Lobe
Medial Rectus
Lateral Rectus
Inferior Turbinate
Superior Rectus
Inferior Rectus
Maxillary Sinus
Tooth
Grey Matter
Superior Sagittal Sinus
White Matter
Eye Ball
Maxillary Sinus
Tongue
Coronal Section of the Brain at the level of Pituitary gland
Post Contrast Coronal T1 Weighted MRI
sp
np
Frontal lobe
Corpus callosum
Frontal horn
III
Pituitary stalk
Pituitary gland Caudate nucleus
Optic nerve
Internal carotid artery
Cavernous sinus
CENTRAL SULCUS
•Upper T sign : the superior frontal sulcus intersects the precentral sulcus in a
"T" junction. The central sulcus is the next posterior sulcus.
•L sign: the superior frontal gyrus intersects precentral gyrus in an "L"
junction. The central sulcus is immediately posterior.
•Lower T sign: the inferior frontal sulcus terminates posteriorly in the
precentral sulcus in a "T" junction. The central sulcus is the next posterior
sulcus.
•M sign: the inferior frontal gyrus has a characteristic "M" configuration and
terminates posteriorly in the precentral gyrus. The central sulcus is
immediately posterior.
 Bracket sign: the marginal sulcus is visible immediately posterior to the
central sulcus, and is easily identifiable of sagittal paramedian images as the
continuation of the cingulate sulcus
sigmoidal hook (handknob, omega) sign: the precentral gyrus bulges
posteriorly at the hand motor area
bifid postcentral gyrus sign: the postcentral gyrus is split medially by the pars
marginalis of the cingulate sulcus
 U sign: the most inferolateral extent of the central sulcus is capped by a U-
shaped gyrus – the subcentral gyrus – which abuts the lateral fissure
• Free water diffusion in the images is Dark (Normal)
• Acute stroke, cytotoxic edema causes decreased rate of water
diffusion within the tissue i.e. Restricted Diffusion (due to
inactivation of Na K Pump )
• Increased intracellular water causes cell swelling
• Areas of restricted diffusion are BRIGHT.
• Restricted diffusion occurs in
– Cytotoxic edema
– Ischemia (within minutes)
– Abscess
DIFFUSION WEIGHTED IMAGES (DWI)
Other Causes of Positive DWI
• Bacterial abscess, Epidermoid ,Acute demyelination,
Acute Encephalitis, CJD(Creutzfeldt-Jakob disease)
• T2 shine through ( High ADC)
• To confirm true restricted diffusion - 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.
• In contrast, in cases of T2 shine-through, the ADC will be
normal or high signal.
• Calculated by the software.
• Areas of restricted diffusion are dark
• Negative of DWI
– i.e. Restricted diffusion is bright on DWI,
dark on ADC
NON-ISCHEMIC CAUSES of low ADC :
• Abscess
• Lymphoma and other tumors
• Multiple sclerosis
• Seizures
• Metabolic (Canavans Disease)
APPARENT DIFFUSION COEFFICIENT Sequences
(ADC MAP)
• TheADC may be useful for estimating the lesion age and
distinguishing acute from subacute DWI lesions.
• Acute ischemic lesions can be divided into Hyperacute
lesions (lowADC and DWI-positive) and Subacute
lesions (normalizedADC, T2 shine through effect).
• Chronic lesions can be differentiated from acute lesions by
normalization ofADC and DWI.
ADC Sequence
65 year male-Acute Rt ACA Infarct
DWI Sequence
STIR: Short T1 (Short Tau) inversion recovery
sequence
• In STIR sequences, an inversion-recovery pulse is used to
null the signal from fat (180° RF Pulse).
• STIR sequences provide excellent depiction of bone
marrow edema which may be the only indication of an
occult fracture.
• STIR images are highly water-sensitive and the timing of the
pulse sequence used acts to suppress signal coming from fatty
tissues – so ONLY WATER is bright
• A combination of standard T1 images and STIR images can
be compared to determine the amount of fat or water within a
body part
• Abnormal low signal on the T1 image and abnormal high
signal on the STIR image – indicates abnormal fluid
• TWO TYPES OF MR ANGIOGRAPHY
– CE (contrast-enhanced) MRA
– Non-Contrast Enhanced MRA
• TOF (time-of-flight) MRA
• PC (phase contrast) MRA
MR ANGIOGRAPHY
CE (CONTRAST ENHANCED) MRA
 T1-shortening agent, Gadolinium, injected iv as contrast
 Gadolinium reduces T1 relaxation time
 When TR<<T1, minimal signal from background tissues
 Result is increased signal from Gd containing structures
 Faster gradients allow imaging in a single breathhold
 CAN BE USED FOR MRA, MRV
 FASTER (WITHIN SECONDS)
TOF (TIME OF FLIGHT) MRA
 These techniques derive contrast between stationary
tissues and flowing blood by manipulating the magnitude
of the magnetization
 The magnitude of magnetization from the moving spins is
very large as compared to the magnetization from the
stationary spins which are relatively small. This leads to a
large signal from moving blood spins and a diminished
signal from stationary tissue spins. Blood vessels usually
appear bright on TOF image
 2D TOF- SENSITIVE TO SLOW FLOW – VENOGRAPHY
 3D TOF- SENSITIVE TO HIGH FLOW – MR ANGIOGRAPHY
PHASE CONTRAST (PC) MRA
• It derive contrast between stationary tissues and flowing blood by
manipulating the phase of the magnetization.
• The phase of the magnetization from the stationary spins is zero and the phase
of the magnetization from the moving spins is non-zero.
• In phase difference images, the signal is linearly proportional to the velocity
of the spins. Fast moving spins give rise to a larger signal and spins moving in
one direction are assigned a bright signal and appear white in the scan ,
• whereas spins moving in the opposite direction are assigned a dark signal and
appear black on the scan.
Vertebral Artery
Middle Cerebral
Artery
Internal Carotid
Artery
Basilar Artery
Anterior Cerebral
Artery
Posterior Cerebral
Artery
Posterior Inferior
Cerebellar Artery
Superior
Cerebellar Artery
Anterior Inferior
Cerebellar Artery
Vertebral Artery
Posterior Cerebral
Artery
Anterior Cerebral
Artery
Middle Cerebral
Artery
Internal Carotid
Artery
Basilar Artery
MR VENOGRAPHY
Oblique view
• Form of T2-weighted image which is susceptible
to iron, calcium or blood.
• Blood, bone, calcium appear dark
• Areas of blood often appears much larger than
reality (BLOOMING)
• Useful for:
– Identification of haemorrhage / calcification
Look for: DARK only
GRE Sequences (GRADIENT RECALLED
ECHO/T2 *)
 Perfusion is the process of nutritive delivery of arterial
blood to a capillary bed in the biological tissue
means that the tissue is not getting
enough blood with oxygen and nutritive elements
(ischemia)
means neoangiogenesis – increased
capillary formation (e.g. tumor activity)
PERFUSION STUDIES
⚫ Stroke
Detection and
assessment of
ischemic stroke
(Lower perfusion )
 Tumors
Diagnosis, staging, assessment of
tumour grade and prognosis
Treatment response
Post treatment evaluation
Prognosis of therapy effectiveness
(Higher perfusion)
APPLICATIONS OF PERFUSION IMAGING
CISS OR FIESTA
• FIESTA (Fast Imaging Employing Steady-state
Acquisition) is the GE name for a balanced steady-state
gradient echo sequence. Philips calls balanced-FFE
(Fast Field Echo). The equivalent Siemens product is
called CISS (Constructive Interference Steady State).
• CISS sequence uses a strong T2-weighted 3D gradient echo
technique which produces high resolution isotropic images.
• Two consecutive runs of 3D balanced steady-state free
precession with different excitation levels are performed
internally and subsequently combined. Image contrast in CISS is
determined by the T2/T1 ratio of the tissue.
• Tissues with both long T2 and short T1 relaxation
times have high signal intensity on CISS images.
• Due to high T2/T1 ratio, water and fat have high
signal on this sequence.
• The CISS sequence provides excellent contrast
between cerebrospinal fluid (CSF) and other
structures in the brain.
• For these reasons, CISS sequence is very useful for
evaluating structures surrounded by CSF (e.g.
cranial nerves).
CN I
CN II
CN III
CN IV
CN V
CN V
CN V
CN V
Trigeminal neuralgia
CN VI
CN VII
CN VII
CN VIII
CN VIII
CN IX
CN X
CN XI
CN XII
Cisterns
Cisterns
Oculomotor cistern
THANK YOU

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PRICIPLES OF MRI BRAIN FINAL COPY.pptx

  • 1. PRINCIPLES OF MRI BRAIN BY : DR. MANOJ SEERVI & DR. SURESH CHOUDHARY INCHARGE: DR. ACHAL SHARMA FACUILTY: DR. J S SHEKHAWAT DR. GAURAV JAIN DR. NAVNEET AGARWAL
  • 2. HISTORICAL ASPECT • 1940s –Felix Bloch &E. Purcell: discovered just after world war II & named Nuclear Magnetic Resonance (noble prize 1952) • 1973: Paul Lauterbur published the first nuclear magnetic resonance image and the first cross-sectional image of a living mouse in January 1974 • 1977 – Mansfield: first image of human anatomy, first echo planar image • 1990s - Discovery that MRI can be used to distinguish oxygenated blood from deoxygenated blood ,it leads to Functional Magnetic Resonance imaging (fMRI) • Paul Lauterbur and Peter Mansfield won the Nobel Prize in Physiology/Medicine (2003) for their pioneering work in MRI
  • 3. The first Human MRI scan was performed on 3rd july 1977 by Raymond Damadian, Minkoff and Goldsmith.
  • 4. Describing Radiological Terms • USG(ultrasonography)- ECHOGENICITY • CT(Computed tomography) scan- DENSITY • MRI(magnetic resonance imaging)- INTENSITY • Hyper- white/ bright • Hypo- black/ dark
  • 5. MRI is based on the principle of nuclear magnetic resonance (NMR) • Two basic principles of NMR 1. Atoms with an odd number of protons have spin 2. A moving electric charge, be it positive or negative, produces a magnetic field • Body has many such atoms that can act as good MR nuclei (1H, 13C, 19F, 23Na) • MRI utilizes this magnetic spin property of protons of hydrogen to produce images. • In our natural state Hydrogen ions in body are spinning in a haphazard fashion, and cancel all the magnetism. When an external magnetic field is applied protons in the body align in one direction. BASIC PRINCIPLES OF MRI
  • 6. Why Hydrogen ions are used in MRI? 1. Hydrogen nucleus has an unpaired proton which is positively charged 2. Every hydrogen nucleus is a tiny magnet which produces small but noticeable magnetic field 3. Hydrogen is abundant in the body in the form of water and fat 4. Essentially all MRI is hydrogen (proton) imaging
  • 7. • TE (Echo Time) : the time between the delivery of the RF pulse and the receipt of the echo signal • TR (Repetition Time) : The time between two excitations is called repetition time. TR & TE
  • 8. • By varying the TR and TE one can obtain T1WI and T2WI. • In general a short TR (<1000ms) and short TE (<45 ms) scan is T1WI. • Long TR (>2000ms) and long TE (>45ms) scan is T2WI.
  • 9. BASIC MR BRAIN SEQUENCES • ROUTINE SEQUENCES – T1 – for anatomy – T2- for pathological details – FLAIR – suppress fluid • SPECIAL SEQUENCES – DWI – for infarcts, abscess , tumour detection – ADC – for differentiation of different age of infarcts – MRA – for arterial details – MRV – for venous details – MRS – spectroscopy for chemical compositions of the lesion – GRE – FIESTA(FAST IMAGING EMPLOYING STEADY STATE ACQUISITION) /CISS(CONSTRUCTIVE INTERFERENCE STEADY STATE), – STIR – SWI
  • 10. • SHORT TE • SHORT TR • BETTER ANATOMICAL DETAILS • FLUID : DARK/CSF BLACK • GRAY MATTER : GRAY • WHITE MATTER: WHITE T1 W IMAGES
  • 11. • Most of pathologies are DARK/ HYPOINTENSE on T1 • BRIGHT ON T1 – Fat – Sub acute H’age (Methaemoglobin) – Melanin – High Protein Contents – Posterior Pituitary appears bright on T1 (Neurosecretory granules) – Gadolinium contrast – Cholesterol
  • 12. • LONGTE • LONG TR • BETTER PATHOLOGICAL DETAILS • FLUID: BRIGHT/Hyperintense • GRAY MATTER : RELATIVELY BRIGHT • WHITE MATTER: DARK T2 W IMAGES
  • 14. T1W AND T2 W IMAGES
  • 15. • LONG TE • LONG TR • SIMILAR TO T2 EXCEPT FREE WATER SUPRESSION (INVERSION RECOVERY) • CSF : DARK • GRAY MATTER : RELATIVELY BRIGHT • WHITE MATTER: DARK • Most pathology is BRIGHT • Hydrocephalous: Periventricular hyperintensity(CSF ooze) • Especially good for lesions near ventricles or sulci or CSF containing spaces (eg Multilpe Sclerosis) FLAIR (Fluid Attenuated Inversion Recovery Sequences) Same as T2 with CSF suppression
  • 17.
  • 18. Multiple sclerosis: periventricular demyelinating process (white arrows) and white matter inflammatory changes around the perimedullary veins, known as Dawson Fingers (red arrows)
  • 19. Clinical Applications of FLAIR sequences: • Used to evaluate diseases affecting the brain parenchyma neighboring the CSF-containing spaces for eg: MS & other demyelinating disorders. • Unfortunately, less sensitive for lesions involving the brainstem & cerebellum, owing to CSF pulsation artifacts • Mesial temporal sclerosis (MTS) (thin section coronal FLAIR) • Tuberous Sclerosis – for detection of Hamartomatous lesions. • Helpful in evaluation of neonates with perinatal HIE.
  • 20. T1W T2W FLAIR(T2) TR SHORT LONG LONG TE SHORT LONG LONG CSF LOW HIGH LOW FAT HIGH HIGH MEDIUM GREY MATTER LOW HIGH HIGH WHITE MATTER HIGH LOW LOW EDEMA LOW HIGH HIGH
  • 21. GRADATION OF INTENSITY IMAGING CT SCAN CSF Edema White Matter Gray Matter Blood Bone MRI T1 CSF Edema Gray Matter White Matter Cartilage Fat MRI T2 Cartilage Fat White Matter Gray Matter Edema CSF MRI T2 Flair CSF Cartilage Fat White Matter Gray Matter Edema
  • 22. MRI BRAIN :AXIAL SECTIONS
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  • 48. White Matter Cerebellum Parietal Lobe Frontal Lobe Lateral Sulcus Grey Matter Occipital Lobe Temporal Lobe
  • 49. Gyri of cerebral cortex Sulci of cerebral Cortex Cerebellum Frontal Lobe Temporal Lobe
  • 51. Frontal Lobe Parietal Lobe Orbit Occipital Lobe Transverse sinus Cerebellar Hemisphere
  • 52. Optic Nerve Precentral Sulcus Lateral Ventricle Occipital Lobe Maxillary sinus
  • 54. Splenium of Corpus callosum Pons Ethmoid air Cells Inferior nasal Concha Midbrain Fourth Ventricle Genu of Corpus Callosum Hypophysis Thalamus
  • 55. Splenium of Corpus callosum Genu of corpus callosum Pons Superior Colliculus Inferior Colliculus Nasal Septuml Medulla Body of corpus callosum Thalamus
  • 56. Cingulate Gyrus Genu of corpus callosum Ethmoid air cells Oral cavity Splenium of Corpus callosum Fourth Ventricle
  • 58. Frontal Lobe Temporal Lobe Parietal Lobe Lateral Ventricle Occipital Lobe Cerebellum
  • 59. Frontal Lobe Parietal Lobe Superior Temporal Gyrus Lateral Sulcus Inferior Temporal Gyrus Middle Temporal Gyrus External Auditory Meatus
  • 60. . Bone Inferior sagittal sinus Corpus callosum Internal cerebral vein Superior sagittal sinus Parietal lobe Vein of Galen Occipital lobe Straight sinus . Vermis . IV ventricle Cerebellar tonsil Mass intermedia of thalamus Sphenoid Sinus
  • 61. MRI BRAIN :CORONAL SECTIONS
  • 63. Arachnoid Villi Great Cerebral Vein Tentorium Cerebelli Falx Cerebri Lateral Ventricle Vermis of Cerebellum Cerebellum
  • 64. Splenium of Corpus callosum Posterior Cerebral Artery Superior Cerebellar Artery Foramen Magnum Lateral Ventricle Internal Cerebral Vein Tentorium Cerebelli Fourth Ventricle
  • 65. Cingulate Gyrus Choroid Plexus Superior Colliculus Cerebral Aqueduct Corpus Callosum Thalamus Pineal Gland Vertebral Artery
  • 66. Insula Lateral Sulcus Cerebral Peduncle Olive Crus of Fornix Middle Cerebellar Peduncle
  • 67. Caudate Nucleus Third Ventricle Hippocampus Pons Corpus Callosum Thalamus Cerebral Peduncle Parahippocampal gyrus
  • 68. Lateral Ventricle Temporal Horn of Lateral Ventricle Uncus of Temporal Lobe Body of Fornix Third Ventricle Hippocampus
  • 69. Internal Capsule Caudate Nucleus Optic Tract Insula Parotid Gland Amygdala Lentiform Nucleus Hypothalamus
  • 70. Internal Capsule Cingulate Gyrus Optic Nerve Nasopharynx Caudate Nucleusa Lentiform Nucleus Internal Carottid Artery
  • 71. Longitudinal Fissure Superior Sagittal Sinus Lateral Sulcus Parotid Gland Genu Of Corpus Callosum Temporal Lobe
  • 73. Frontal Lobe Medial Rectus Lateral Rectus Inferior Turbinate Superior Rectus Inferior Rectus Maxillary Sinus Tooth
  • 74. Grey Matter Superior Sagittal Sinus White Matter Eye Ball Maxillary Sinus Tongue
  • 75. Coronal Section of the Brain at the level of Pituitary gland Post Contrast Coronal T1 Weighted MRI sp np Frontal lobe Corpus callosum Frontal horn III Pituitary stalk Pituitary gland Caudate nucleus Optic nerve Internal carotid artery Cavernous sinus
  • 76. CENTRAL SULCUS •Upper T sign : the superior frontal sulcus intersects the precentral sulcus in a "T" junction. The central sulcus is the next posterior sulcus. •L sign: the superior frontal gyrus intersects precentral gyrus in an "L" junction. The central sulcus is immediately posterior. •Lower T sign: the inferior frontal sulcus terminates posteriorly in the precentral sulcus in a "T" junction. The central sulcus is the next posterior sulcus. •M sign: the inferior frontal gyrus has a characteristic "M" configuration and terminates posteriorly in the precentral gyrus. The central sulcus is immediately posterior.
  • 77.
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  • 82.  Bracket sign: the marginal sulcus is visible immediately posterior to the central sulcus, and is easily identifiable of sagittal paramedian images as the continuation of the cingulate sulcus sigmoidal hook (handknob, omega) sign: the precentral gyrus bulges posteriorly at the hand motor area bifid postcentral gyrus sign: the postcentral gyrus is split medially by the pars marginalis of the cingulate sulcus  U sign: the most inferolateral extent of the central sulcus is capped by a U- shaped gyrus – the subcentral gyrus – which abuts the lateral fissure
  • 83. • Free water diffusion in the images is Dark (Normal) • Acute stroke, cytotoxic edema causes decreased rate of water diffusion within the tissue i.e. Restricted Diffusion (due to inactivation of Na K Pump ) • Increased intracellular water causes cell swelling • Areas of restricted diffusion are BRIGHT. • Restricted diffusion occurs in – Cytotoxic edema – Ischemia (within minutes) – Abscess DIFFUSION WEIGHTED IMAGES (DWI)
  • 84. Other Causes of Positive DWI • Bacterial abscess, Epidermoid ,Acute demyelination, Acute Encephalitis, CJD(Creutzfeldt-Jakob disease) • T2 shine through ( High ADC) • To confirm true restricted diffusion - 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. • In contrast, in cases of T2 shine-through, the ADC will be normal or high signal.
  • 85. • Calculated by the software. • Areas of restricted diffusion are dark • Negative of DWI – i.e. Restricted diffusion is bright on DWI, dark on ADC NON-ISCHEMIC CAUSES of low ADC : • Abscess • Lymphoma and other tumors • Multiple sclerosis • Seizures • Metabolic (Canavans Disease) APPARENT DIFFUSION COEFFICIENT Sequences (ADC MAP)
  • 86.
  • 87. • TheADC may be useful for estimating the lesion age and distinguishing acute from subacute DWI lesions. • Acute ischemic lesions can be divided into Hyperacute lesions (lowADC and DWI-positive) and Subacute lesions (normalizedADC, T2 shine through effect). • Chronic lesions can be differentiated from acute lesions by normalization ofADC and DWI.
  • 88. ADC Sequence 65 year male-Acute Rt ACA Infarct DWI Sequence
  • 89. STIR: Short T1 (Short Tau) inversion recovery sequence • In STIR sequences, an inversion-recovery pulse is used to null the signal from fat (180° RF Pulse). • STIR sequences provide excellent depiction of bone marrow edema which may be the only indication of an occult fracture.
  • 90. • STIR images are highly water-sensitive and the timing of the pulse sequence used acts to suppress signal coming from fatty tissues – so ONLY WATER is bright • A combination of standard T1 images and STIR images can be compared to determine the amount of fat or water within a body part • Abnormal low signal on the T1 image and abnormal high signal on the STIR image – indicates abnormal fluid
  • 91. • TWO TYPES OF MR ANGIOGRAPHY – CE (contrast-enhanced) MRA – Non-Contrast Enhanced MRA • TOF (time-of-flight) MRA • PC (phase contrast) MRA MR ANGIOGRAPHY
  • 92. CE (CONTRAST ENHANCED) MRA  T1-shortening agent, Gadolinium, injected iv as contrast  Gadolinium reduces T1 relaxation time  When TR<<T1, minimal signal from background tissues  Result is increased signal from Gd containing structures  Faster gradients allow imaging in a single breathhold  CAN BE USED FOR MRA, MRV  FASTER (WITHIN SECONDS)
  • 93. TOF (TIME OF FLIGHT) MRA  These techniques derive contrast between stationary tissues and flowing blood by manipulating the magnitude of the magnetization  The magnitude of magnetization from the moving spins is very large as compared to the magnetization from the stationary spins which are relatively small. This leads to a large signal from moving blood spins and a diminished signal from stationary tissue spins. Blood vessels usually appear bright on TOF image  2D TOF- SENSITIVE TO SLOW FLOW – VENOGRAPHY  3D TOF- SENSITIVE TO HIGH FLOW – MR ANGIOGRAPHY
  • 94. PHASE CONTRAST (PC) MRA • It derive contrast between stationary tissues and flowing blood by manipulating the phase of the magnetization. • The phase of the magnetization from the stationary spins is zero and the phase of the magnetization from the moving spins is non-zero. • In phase difference images, the signal is linearly proportional to the velocity of the spins. Fast moving spins give rise to a larger signal and spins moving in one direction are assigned a bright signal and appear white in the scan , • whereas spins moving in the opposite direction are assigned a dark signal and appear black on the scan.
  • 95. Vertebral Artery Middle Cerebral Artery Internal Carotid Artery Basilar Artery Anterior Cerebral Artery Posterior Cerebral Artery Posterior Inferior Cerebellar Artery Superior Cerebellar Artery Anterior Inferior Cerebellar Artery
  • 96. Vertebral Artery Posterior Cerebral Artery Anterior Cerebral Artery Middle Cerebral Artery Internal Carotid Artery Basilar Artery
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  • 102. • Form of T2-weighted image which is susceptible to iron, calcium or blood. • Blood, bone, calcium appear dark • Areas of blood often appears much larger than reality (BLOOMING) • Useful for: – Identification of haemorrhage / calcification Look for: DARK only GRE Sequences (GRADIENT RECALLED ECHO/T2 *)
  • 103.
  • 104.  Perfusion is the process of nutritive delivery of arterial blood to a capillary bed in the biological tissue means that the tissue is not getting enough blood with oxygen and nutritive elements (ischemia) means neoangiogenesis – increased capillary formation (e.g. tumor activity) PERFUSION STUDIES
  • 105. ⚫ Stroke Detection and assessment of ischemic stroke (Lower perfusion )  Tumors Diagnosis, staging, assessment of tumour grade and prognosis Treatment response Post treatment evaluation Prognosis of therapy effectiveness (Higher perfusion) APPLICATIONS OF PERFUSION IMAGING
  • 106. CISS OR FIESTA • FIESTA (Fast Imaging Employing Steady-state Acquisition) is the GE name for a balanced steady-state gradient echo sequence. Philips calls balanced-FFE (Fast Field Echo). The equivalent Siemens product is called CISS (Constructive Interference Steady State). • CISS sequence uses a strong T2-weighted 3D gradient echo technique which produces high resolution isotropic images. • Two consecutive runs of 3D balanced steady-state free precession with different excitation levels are performed internally and subsequently combined. Image contrast in CISS is determined by the T2/T1 ratio of the tissue.
  • 107. • Tissues with both long T2 and short T1 relaxation times have high signal intensity on CISS images. • Due to high T2/T1 ratio, water and fat have high signal on this sequence. • The CISS sequence provides excellent contrast between cerebrospinal fluid (CSF) and other structures in the brain. • For these reasons, CISS sequence is very useful for evaluating structures surrounded by CSF (e.g. cranial nerves).
  • 108. CN I
  • 109.
  • 110. CN II
  • 111. CN III
  • 112. CN IV
  • 113. CN V
  • 114. CN V
  • 115. CN V
  • 116. CN V
  • 118. CN VI
  • 119. CN VII
  • 120. CN VII
  • 123. CN IX
  • 124. CN X
  • 125. CN XI
  • 126. CN XII
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