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Imaging/Nuclear medicine
In magnet
Loosely bound
hydrogen atoms,
the stronger the
excitation, the
more intense the
recovered signal-
lighter the recovered
image.
Proton/Spin Density- Indicates the distribution of protons in the tissues. Increase in protons,
increase in transverse image thereby increased intensity of the recovered signal-brighter the MR
image
• The patient’s hydrogen protons which normally
spin on an axis behave like small “magnets” to
produce the net magnetization vector which
aligns itself readily to the long axis of the
magnetic field-longitudinal magnetic
force/moment.
• The RF pulses cause the excitation of the
protons;
• a) from longitudinal magnetic moment they
become transverse magnetic moment
• b) The spins synchronize, spinning like tops in
phase with each other
Spin-
up,
spin
down
Radiofrequency
Magnetic Resonance Imaging (MR)
Once RF pulse is turned off, energy
released by hydrogen nuclei and return to Different tissues
original spin state (relaxation)- recorded by have different T1
coils in the scanner. and T2
Relaxation results in: relaxation times
•transfer of energy to a state of equilibrium. Time
constant required to do this is called T1 relaxation
time
NB: Variance in T1
•Along with loss of transverse magnetization,
there is dephasing of the hydrogen proton. Time and T2 between
constant describing this rate of loss is the T2 tissues is higher
relaxation time than differences in
x-ray absorption
Magnetic Resonance Imaging (MR): optimising
image appearance
T1 weighted images: short
RF pulse repetition time
[TR] and short signal
recovery(echo) time [TE]:
‘fat image’ (e.g red
marrow)- high
signal/bright on image
High anatomic detail
Magnetic Resonance Imaging (MR): optimising
image appearance
T2 weighted images: long RF
pulse repetition time [TR] and
long signal recovery time [TE]:
‘water image’ (e.g CSF, TMJ
fluid) high signal/bright on
image
Generally, abnormal tissues are
brighter on T2 images (good for
pathology)
• Techniques such as turbo spin echo and gradient
echo, allow images to be captured rapidly.
•salivary glands
•implant planning? No ionizing radiation
Contra-indications:
. replace anything ferromagnetic (gold is considered
ferromagnetic??susuk??)
•cardiac pacemakers; cerebral aneurysm clips
•Claustrophobia
•1st trimester of pregnancy
•• Electronically operated stapedial implants
Stainless steel brackets, bands, and fixed
retainers should be checked to ensure secure
attachment, and may be left in place if secure,
unless they interfere with the region of the
image being examined.
Nuclear Medicine
• Radionuclide (radioisotope) imaging relies upon
altering the patient by making the tissues
radioactive and the patient becoming the source
of ionization radiation. This is done by injecting
certain radioactive compounds into the patient
that have affinity for particular tissues-so called
target tissues.
• Gamma radiation
The main emissions used in imaging are gamma ray and beta + (positron) particles.
Alpha particles are banned from use in nuclear medicine and beta – (electron) particles have very
limited use in diagnostic imaging.
Nuclear Medicine (for imaging)
Many radioisotopes
used, e.g:
131
Iodine
67
Gallium
74
Selenium Salivary gland imaging:
99m
Technetium 99m
technetium pertechnetate
Bone scanning:
Technetium methylene
99m
diphosphonate (MDP)
Nuclear Medicine (Non-Imaging)
• Iodine-131 with a half-life of 8 days – Used for thyroid function
and with beta emission also provided a therapeutic potential for
treatment of hyperthyroidism (Graves disorder, multinodular
toxic goitre, toxic solitary nodule or adenoma) and thyroid
carcinoma with local and distal metastases.
• Thallium-201 with a half-life of 3.1days – for myocardial
visualization.
• Xenon-133 and Krypton – 81m for determining lung ventilation.
• For other therapeutic purposes, yttrium-90 is used for acromegaly
and bone tumours.
• cobalt -90 for external radiotherapy and phosphorus -32 for
polycythaemia rubra .
Nuclear Medicine
Uses ionising radiation, mainly
gamma rays, from radioactive
sources
Radioactive gamma emitter
introduced into body attached to a
pharmaceutical or in a form that will
concentrate in the tissue/ organ/ cell
of choice
Gamma rays detected by gamma
camera
Images really relate to physiological
activity rather than anatomy
Nuclear Medicine
• The gamma camera which is most commonly used now is the
Anger scintillation camera. It was invented by Hal Anger of
Donner Laboratory, University of California, at Berkeley,
United States of America in the late 1950s . The principle of
the instrument lies in the ability of a large sodium iodide
crystal, contained within the detector head, to respond to the
gamma rays emitted from the radioisotope by the emission of
tiny scintillations of light (or flourescence). These
scintillations are magnified by a photomultiplier tube and
altered electronically into electric signals. From the positions
of the scintillations which occur within the crystals, the
picture of the isotope distribution in the organ is built up. The
use of a scintillation crystal for the acquisition of the data for
image formation has led to the labelling of this technique as
scintigraphy and the images scintigrams.
Nuclear Medicine
• However, nuclear medicine techniques are
known for their sensitivity to changes of function
induced by disease but not for the specificity in
determining the nature of the disease process.
Nuclear Medicine
• Radionuclide images are obtained by injecting radionuclide
intravenously into a patient, waiting about two hours for it to be
taken up in the target tissue, and assessing its uptake in that tissue
by measuring the gamma radiation given off by means of the
gamma camera.
Submandibular
Thyroid
Nuclear Medicine
99m
Technetium
According to Maisey (1980)the advantages of 99mTc are:
• During this decay it emits only gamma photons and not beta particles
(which are responsible for the larger radiation dose incurred by other
radionuclides such as Iodine-131).
• The relative ease with which it can be attached to many varied chemical
compounds. It may be used to perform scans of virtually every organ of
Nuclear Medicine
Bone scanning:
99m
Technetium methylene diphosphonate
i.v injection. Imaging after 3 hours
Uses:
•Detecting bony metastases in malignancy
•Bone dysplasias/fibroosseous lesions to assess activity
•Paget’s disease to identify sites
•TMJ: condylar hyperplasia
•Osteid osteoma- skeletal pain not detected for years.
Nuclear Medicine-bone scanning
• The radionuclide may be taken up in areas where there is increased
blood flow (hyperemia) because of increased metabolic activity
within the bone (e.g. tumour growth) or rate of production of new
hydroxyapatite crystals (osteogenesis) - especially reaction of the
bone at the margins of the tumour. Decreased activity is associated
with metabolically inactive bone, a lack of osteogenesis, or an absent
vascular supply. Areas of increased uptake are referred to as “hot
spots”, whereas zones of diminished or absent activity are called
“cold spots”.
• At the present time the use of PET is somewhat limited because of high cost.
PET facilities cost US$ two million and require more space, electricity and
air-conditioning than conventional nuclear units. Additionally, PET
requires an on-site cyclotron because of the short half-life of positron
emitting radionuclides (for example the half-life of 150 is 124 seconds).
Cyclotron cost a minimum of US$ one million and are quite expensive to
install and operate.
Nuclear Medicine
•Hofer and colleagues stated that although the combination of scintigraphic
and radiologic investigations does not facilitate differential diagnosis, the two
modalities support each other in offering valuable information on the rate of
growth of jaw lesions. Furthermore they concluded the following:-
•Although the radiographic assessment is more specific, the nuclear bone scan
is more sensitive.
•Scans are especially useful in determining surgical margins. This is because the
bone scans were more accurate than radiologic examination in delineating the
true limits of a lesions.
•Radiographs alone are adequate for the study of cysts and benign tumours.