A Brief Introduction To Medical Imaging: Outline
A Brief Introduction To Medical Imaging: Outline
Outline
• General Goals
• Linear Imaging Systems
• An Example, The Pin Hole Camera
• Radiations and Their Interactions with Matter
• Coherent vs. Incoherent Imaging
• Length Scales
• Contrasts
• Photon Intensity Tomography
• Magnetic Resonance Imaging
Imaging Definitions
a b
Notice, however, that the object function is also blurred due to the
finite width of the pin-hole.
a b
As the object becomes too large, the ray approaches the pin-hole too
steeply to make it through.
Distortions of a Pin-hole Camera 2
Also, as the object moves off the center line, the shadow on the
detector grows in area, (and the solid angle is decreased) so the image
intensity is reduced.
a b
Spatial Frequencies 2
source y r
Absorption imaging
s φ
φ
x
r
object detector
In absorption imaging, the integrated absorption along a column through the object is
measured. An array of detectors therefore measures a ‘shadow profile’.
Projection Imaging
Object
Projections
Central Slice Theorem
source y r
Absorption imaging
s φ
φ
x
r
object detector
In absorption imaging, the integrated absorption along a column through the object is
measured. An array of detectors therefore measures a ‘shadow profile’.
Coherent vs. Incoherent Imaging
In both cases the image is the result of the scattering of a field by the object.
Incoherent - measure only the intensity fluctuations of this scatter. Usually
frequencies are too high to permit convenient measures of the phase. Examples,
light 1014 Hz
X-rays 1018 Hz
γ-rays 1020 Hz
A photograph is an incoherent image.
Coherent - measure both the intensity and the phase of the scattered field. This is
usually measured as a temporal evolution of the scattered field. The frequency of
radiation is normally quite low to permit an accurate measure of the phase (such as
microwaves). MRI is an example of coherent imaging.
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Incoherent images are most readily measured by scanning a well collimated beam
across the sample and observing the attenuation of that beam (this may be
multiplexed with many detectors).
Coherent images permit the characterization of the entire sample at once and with
observation through a single detector element. A series of measurements are made
for fields of varying frequency or direction.
X-ray Attenuation Coefficients
µ/ρ
(cm2/g)
2.5
2
1.0
BONE
0.5
0.4 MUSCLE
0.3
FAT
0.2
0.15
PHOTON
0.1 ENERGY
10 20 30 40 50 100 150 200 300 500 (kev)
X-ray attenuation coefficients for muscle, fat, and bone, as a function of photon
energy.
Binding energy (KeV) Characteristic
Binding energy (KeV) X-ray
66 KeV
≈0
λ4 0.6 KeV (N→M)
≈0
Photoelectron
0.6 λ3 4.4 KeV (M→L)
0.6
100 KeV 5 5
λ2 29 KeV (L→K)
incident Total 34 KeV
photon 34 34
K K
λ1 L L
M M
N N
Valence electrons
K
L Compton
M Electron (Ee-)
Incident
photon
(E0)
θ Angle of deflection
λ1 λ2
λ1 < λ2 Scattered
Photon (Esc)
Attenuation Mechanisms
µ Dependence
Attenuation
(log plot)
total
Compton
Compton
photoelectric
simple scatter pair
The optimum photon energy is about 30 keV (tube voltage 80-100 kV) where the
photoelectric effect dominates. The Z3 dependence leads to good contrast:
Zfat 5.9
Zmuscles 7.4
Zbone 13.9
⇒ Photoelectric attenuation from bone is about 11x that due to soft tissue, which is
dominated by Compton scattering.
Photon Intensity Tomography
anatomical Yes No No
information
source y r
Absorption imaging
s φ
φ
x
r
object detector
In absorption imaging, the integrated absorption along a column through the object is
measured. An array of detectors therefore measures a ‘shadow profile’.
Photon Intensity Tomography 2
y r
Emission imaging
s φ
φ
x
r
object
detector
NMR-microscopy
1µm
1nm
°
1A
1µs 1ms 1s
Time
The Bloch Equations
d M
M x = ∆ω ⋅ M y − x
dt T2
d My
M y = −∆ω ⋅ M x + ω1 (t ) ⋅ M z −
dt T2
d M − M0
M z = −ω1 (t ) ⋅ M y − z
dt T1
u
u u
2π
k
Mx Mx Mx
My My My
This produces a grating as a linear phase ramp, since motions are torques.
Moire complex gratings are produced through a combination of RF and gradient
pulses. The spatial frequency distribution of these are describable by a distribution of
components, each at a given wave-number.
Mz(t)
My(t)
time
Mx(t)
spatial offset
precession 2t
angle
t
t=0
spatial offset
Mz(t)
My(t)
time
Mx(t)
Diagrams of the spin magnetization’s return to equilibrium after being aligned along
the x-axis. In both pictures the evolution of a single bulk magnetization vector is
being followed. The initial position is shown as the green vector at top, which spirals
into the z-axis, the red vector. In the figure on the right, the three individual
components of the magnetization are shown as a function of time. The NMR
experiment measures the two transverse components, Mx and My. There are three
motions, a precession about the z-axis, a decay of the transverse components and a
slower growth along z towards the static equilibrium value.
G = 1 G/cm
1.0
attenuation D = 3×10-5 cm2/s
0.8
T2 = 0.1 s
0.6
0.4
0.2
k
500 1000 1500 2000 2500
k
t=
γG
k t
− −
γGT2
attenuation T2 = e ; e T2
k 3D k 2 Dt
− −
3γG
attenuation D=e ; e 3