Medical Imaging
◉ Medicalimaging is a type of diagnostic testing.
◉ Non-invasive techniques and approaches used to create visual
representations of the internal organs and tissues of the human
body.
◉ Medical imaging is widely used to examine and visualize different
parts of the body, including bones, muscles, organs, blood vessels,
and other internal structures.
3
4.
Medical Imaging
Medical imagingis used to visualize body parts in different anatomical
planes.
4
*=
ray Ct bruin
details
show MRI-CSEshows
-Space
btur
vertebreas
(disc
Shows
clearly
5.
Medical Imaging
Medical imagingis used to visualize body parts in different anatomical
planes.
5
X-ray Ct CT MRI
-
> brain
details,
bones are
notbright
6.
Medical Imaging
Medical imagingis used to visualize body parts in different anatomical
planes.
6
MRI+
p
ul luyers show
↳ Skull Shows
white more details -
> ventricles
parts are
in cancer dye would
contrast/dye-Oralsprea more, or it blood
Vessel blocked,youcan
see
dye stopped
7.
Medical Imaging
Medical imagingis used to visualize body parts in different anatomical
planes.
7
4th pic page(axial) first pic is ct,( abdomen) and you can’t really see csf,
2nd pic is mri( white part which is first layer in mri is always fat) ct
however shows bone clearly as white
↓
w , contrast
Imaging Modalities
◉ Eachmodality has its own principles, indications and limitations.
◉ Understanding the principles of each modality is essential for
interpreting images accurately and providing effective patient care.
9
·
Tomo
=
Slice or section
ComputedTomography (CT Scan)
58
Graph
=
To write or to describe
From Ancient Greek
Computed tomography (CT) is a powerful
imaging technique that utilizes X-Rays to
create detailed cross-sectional images of
the human body.
16.
◉ Unlike traditionalX-Rays that provide a flat
2D image, CT scans offer a much more
comprehensive view, by capturing X-Ray
data from multiple angles.
◉ A sophisticated computerized method is
used to obtain data and transform them
into cross-sectional slices of the human
body.
◉ Advanced computer processing is utilized
to reconstruct highly detailed 3D images of
internal organs, bones, and soft tissues.
59
CT Scan
◉ All CTexaminations are performed by obtaining data for a series of
slices through a designated area of interest.
◉ The structures in a CT image are represented by varying shades of
gray. The creation of these shades of gray is based on basic X-
radiation principles.
◉ Hounsfield Units can be defined as the quantification of the degree
that a structure attenuates an X-Ray beam.
◉ These units are also referred to as CT numbers, or density values.
61
CT Scan
◉ CT contrastmedia, also known as CT contrast
dye or contrast agent, is a substance that is used
to improve the visibility of certain organs,
tissues, and blood vessels during a CT scan.
◉ They are chemically designed to be radiopaque.
◉ Iodine-based contrast is the most common
type. It may be ingested (orally) or injected
intravenously (IV) by a contrast injector
(automatically) or manually.
70
CT Contrast Media
Contrast Injector
◉ Limited softtissue visualization
○ CT scans are not as good as MRI scans for visualizing certain soft tissues,
such as the brain and muscles.
◉ Radiation exposure
○ CT scans use ionizing radiation, which carries a risk of harm to the patient.
○ CT scan generally is not recommended for pregnant patients.
◉ Contrast media
○ Some CT scans require the use of contrast media, which may cause allergic
reactions and may be harmful to patients with kidney problems.
77
Limitations of CT Scan
◉ Nuclear medicineutilizes radioactive materials called
radiopharmaceuticals.
◉ These radiopharmaceuticals are radioactive drugs used
for diagnosis or therapy in trace quantities.
◉ Once injected or ingested, the radiopharmaceuticals
accumulate in the target areas, emitting energy in the
form of gamma rays or positrons, which can be
detected by special imaging equipment.
79
Nuclear Medicine
Beta-Plus ẞ+ Decay(Positron Emission)
◉ Unstable atomic nucleus (a proton-rich
nucleus) undergoes a transformation.
◉ A proton inside the nucleus is transformed
into a neutron, resulting in emission of a
positron (e+) and neutrino (ve).
81
Radionuclides
39.
Commonly used radionuclidesin nuclear medicine:
Technetium-99m (Tc-99m) → Half-life of 6 hours
Fluorine-18 (F-18) → Half-life of 109.7 minutes
Iodine-131 (I-131) → Half-life of 8 days
Thallium-201 (Tl-201) → Half-life of 73.1 hours
Gallium-67 (Ga-67) → Half-life of 3.26 days
And others …
82
Radionuclides
The first Tc-99m generator, 1958
40.
Imaging Techniques:
There areseveral different imaging
techniques used in nuclear medicine,
including:
◉ Single-photon emission computed
tomography (SPECT): this technique
uses a gamma camera that rotate
around the patient to create 3D
images of the distribution of
radioactivity in the body.
83
Nuclear Medicine
41.
Imaging Techniques:
◉ Positronemission tomography (PET):
this technique uses a PET scanner to
detect positrons that are emitted by
certain radiopharmaceuticals, creating
a 3D image of the distribution of
radioactivity in body, which reflects
the level of cellular activity in different
tissues.
84
Nuclear Medicine
Safe Handling ofRadioactive Materials
◉ Personal Protective Equipment (PPE): lab
coat, gloves, eye protection, thyroid shield
and shoe covers.
◉ Healthcare professional should work in
designated areas with proper ventilation.
◉ Radioactive waste is disposed in designated
containers according to regulations.
◉ Typically, radioactive waste should be
stored for at least 10 half-lives.
87
Safety First: A Crucial Aspect of Nuclear Medicine
45.
◉ Presenting cellularfunction.
◉ Cancer detection.
◉ Monitoring treatment.
◉ Other uses → diagnose and assess heart disease, brain disorders,
and other conditions.
88
Clinical Applications of Nuclear Medicine
46.
◉ Nuclear medicineimages primarily reveal function, not detailed
anatomy. Sometimes, additional imaging tests like CT or MRI
might be needed for a complete picture.
◉ Pregnant and breastfeeding women often require special
considerations due to radiation exposure risks to the fetus or
infant.
89
Limitations of Nuclear Medicine
The primary atomused in MR imaging is Hydrogen (1H).
Due to:
◉ Abundance in the human body, primarily found in
water and fat, making up around 70% of the body.
◉ Its nucleus has a single proton, which has a
significant magnetic moment → produces a strong
signal.
92
Basic Principle
What happens, whenwe put a patient into
the magnet of MR machine?
◉ Proton inside the nucleus of (H) atom
has a positive electrical charge which
possesses a spin (rotates around its
own axis).
◉ A moving of electrical charge (electrical
current) is accompanied by a magnetic
field.
◉ The proton has its own magnetic field.
94
Basic Principle
52.
What happens, whenwe put a patient into the
magnet of MR machine?
◉ The protons -being a little magnets- in the
human body align themselves in the external
magnetic field.
◉ Radiofrequency (RF) pulses are sent from the
RF coils to the human body.
◉ Protons pick up some energy from those radio
waves (RF pulses) → Resonance phenomenon.
95
Basic Principle
53.
What happens, whenwe put a patient into the
magnet of MR machine?
◉ When the RF pulse is switched off, protons
start to relax, and release the absorbed
energy (relaxation).
◉ The rate at which the protons relax back to
their original state depends on the type of
tissue they are in.
◉ Different tissues have different relaxation
times, aiding in tissue differentiation.
96
Basic Principle
54.
Signal Detection
◉ TheMRI scanner detects the radio
signals emitted by the relaxing protons.
◉ By analyzing these signals, the MRI
scanner can create a map of the
different tissues in the body.
97
Basic Principle
55.
Magnetic Field Strength:Measured in Tesla (T), a stronger magnetic field
generally produces higher quality images with better resolution.
98
MR Magnet
The commonly encounteredfield strengths:
◉ 0.2T to 1.5T: This is the most common range for clinical MRI scanners.
○ 1.5T: This is the current workhorse of MRI, offering a good balance
between image quality, patient comfort, and cost.
○ 0.2T to 1.0T: these scanners might be used in specific situations like
imaging or for patients who experience claustrophobia.
◉ 3T: This is considered a high-field strength and offers improved image
quality and advanced techniques.
◉ 7T and above: These are considered ultra-high-field strengths and are
primarily used in research settings.
100
MR Magnet
58.
MRI encompasses avariety of techniques tailored to visualize
different tissue properties and pathologies. Here are some of the
main MR imaging techniques:
101
MR Imaging Techniques
59.
1. T1-Weighted Imaging
Appearance:
Tissues with short T1 relaxation
time (like fat) appear bright
Tissues with longer T1 times
(like fluid, water) appear dark
Muscles appear intermediate
102
MR Imaging Techniques
Brain T1 MRI
(Axial ‘Horizontal’ View)
Brain T1 MRI
(Coronal View)
4. Short TauInversion Recovery (STIR)
A special technique that suppresses the
signal from fat
Appearance:
Fluids and water → bright
Fat (suppressed) → dark
Bone → dark
114
MR Imaging Techniques
Ankle STIR MRI
(Sagittal View)
Clinical use:
Effectivein distinguishing
between fat and other tissue
types
In musculoskeletal imaging →
edema, inflammation, tumors
and others
116
MR Imaging Techniques
Shoulder Metastasis
Inflamed SI Joint
74.
Summary of themain imaging techniques:
117
MR Imaging Techniques
Tissue Type T1 Weighted T2 Weighted T2 FLAR STIR
CSF Dark Bright Dark (suppressed) Bright
Pathological Fluid Dark Bright Bright Bright
Fat Bright Darker than T1 Darker than T1 Dark (suppressed)
Muscle Intermediate Darker than T1 Darker than T1 Intermediate to dark
75.
◉ Gadolinium isa rare earth metal with
paramagnetic properties (it enhances
the signal in MRI) → makes tissues
appear brighter on T1 images.
◉ Used in MRI to improve the visibility of
internal structures and the contrast
between normal and abnormal tissues.
◉ Administered to the human body
through intravenous (IV) injection.
118
Gadolinium-Based Contrast Agent
◉ Items suchas jewelry, watches, credit
cards, cell phones and any metal objects
must be removed before entering the
MRI room.
◉ Patients usually are provided with
earplugs, as MR machines produce loud
knocking sounds.
120
MRI Safety
78.
◉ Materials usedin and around MR
scanners must be non-ferromagnetic
and non-metallic to prevent interactions
with the magnetic field.
◉ The scanning room is prepared with a
compatible materials (MRI table,
contrast injector, lighting lamps …)
121
MRI Safety
79.
◉ Neurology
○ Brainand spinal imaging.
◉ Musculoskeletal System
○ Examining muscles, ligaments, tendons, and bones.
◉ Cardiology
○ Cardiomyopathies, congenital heart disease and vascular imaging.
◉ Oncology
○ Tumor detection and monitoring treatment response.
◉ Abdominal imaging, vascular imaging and others …
122
Clinical Applications of MRI
80.
◉ Time consuming
○Scan duration ranges between 15 minutes to over an hour.
○ May lead to patient movement during scan → motion artifacts.
◉ Patient contraindications
○ Metal implants and devices as pacemakers and other electronic devices.
○ Claustrophobia.
◉ Limited information on bones
○ MRI is not the best imaging modality for examining bones. CT scan is typically
preferred for imaging bones.
◉ Small risk of allergic reactions to contrast media
◉ High cost
123
Limitations of MRI
81.
Heart Electrophysiology andElectrocardiography
Biophysics II Course
Washington University of Health and Science
Summer 2025
Lecturer: Huda Nasser
Heart Electrophysiology
Theheart is a muscular organ
comprised of four chambers with
two atria (right and left) opening
into right and left ventricles via
tricuspid and mitral valves,
respectively.
A wall of muscle called the septum
separates all four chambers.
4
made up
-
85.
Heart Electrophysiology
5
Theheart is a mechanical pump whose
activity is governed by the electrical
conduction system.
This mechanical work of pumping blood
to the whole body occurs in a
synchronized manner and is under the
control of the cardiac conduction system.
86.
Heart Electrophysiology
Itis comprised of two types of cells,
pacemaker and non-pacemaker cells.
Pacemaker cells are located primarily
in the SA and AV node, and it is the SA
node that drives the rate and rhythm
of the heart.
The AV node gets suppressed by the
more rapid pace of the SA node.
6
87.
Heart Electrophysiology
Thespecialized function associated
with the pacemaker cells is their
spontaneous depolarization with no
true resting potential.
When spontaneous depolarization
reaches the threshold voltage, it
triggers a rapid depolarization
followed by repolarization.
7
88.
Heart Electrophysiology
Thenon-pacemaker cells mainly comprise the atrial and
ventricular cardiac muscle cells and Purkinje fibers of the
conduction system.
8
89.
Heart Electrophysiology
Theyconsist of true resting
membrane potential, and upon
initiation of an action potential, rapid
depolarization is triggered, followed
by a plateau phase and subsequent
repolarization.
Action potentials are generated by
ion conductance via the opening
and closing of the ion channels.
9
Electricity issimply the flow of electric charge across a gradient.
In living organisms, charge gradients across membranes
produce electricity in the form of flowing ions.
The flow of charged ions causes heart to beat and muscles to
contract.
11
Heart Electrophysiology
Electrocardiography
The electrocardiogram(abbreviated as
ECG or EKG) is a test that records the
electrical activity of the heart,
including the rate and rhythm to
diagnose heart disorders.
It is recorded non-invasively from the
surface of the body.
14
95.
Electrocardiography
It wasinvented in 1902 by the Dutch physician William
Einthovan.
This invention laid the foundation of the most fundamental
technique for investigating heart disorders.
ECG was soon recognized as a robust screening and clinical
diagnostic tool, and today it is used globally in almost every
healthcare setting.
15
96.
Electrocardiography
The goalof the electrocardiogram interpretation is to
determine whether the ECG waves and intervals are normal or
pathological. Electrical signal interpretation gives a good
approximation of heart pathology.
16
97.
Electrocardiography
The equipment forperforming a
conventional 12-lead ECG includes:
Electrodes (sensors)
Gauze and skin preparation (alcohol
rub) solution
Razors, clippers, or a roll of tape (for
hair removal)
Skin adhesive and/or antiperspirant
ECG paper
Cardiac monitor or ECG machine
17
found inside the electrodes
Cadiff
reading from diff places
-
-
① -> 10 of them (physical
②
③
be it causes artifacts
⑨
-
antisweat
⑤ -
> beforePrinting on/after printing is called ECC
Trace
⑯
Electrocardiography
The conventional12-lead ECG consisting of six limbs and six
precordial leads is organized into ten wires (electrodes).
The limb leads include I, II, III, aVL, aVR, and aVF and are
named RA, LA, RL, and LL.
The limb leads are color-coded to avoid misplacement (red -
right arm, yellow - left arm, green - left leg, and black - right
leg).
19
-
>
4 electrodes (contain 6 limb leads)
100.
Electrocardiography
The precordial(chest) leads V1 to V6 are attached to the
surface of the chest.
Electrodes: is the physical sticky patches (wires attached)
placed on the body.
Leads: the electrical views or recordings the ECG machine
makes.
10 electrodes → 12 leads
20
u
Samenamefor elected
as
Electrocardiography
Principle
The fundamentalprinciple behind recording an ECG is an
electromagnetic force, current, or vector with both magnitude
and direction. When a depolarization current travels towards
the electrode, it gets recorded as a positive deflection, and
when it moves away from the electrode, it appears as a
negative deflection.
23
104.
Electrocardiography
Principle
A currentof repolarization traveling away from the positive
electrode is seen as a positive deflection and towards a
positive electrode as a negative deflection.
When the current is perpendicular to the electrode, it touches
the baseline and produces a biphasic wave.
24
105.
Electrocardiography
Principle
Electrocardiogram machinesare designed to record changes
in electrical activity by drawing a trace on a moving
electrocardiograph paper.
The electrocardiograph moves at a speed of 25 mm/sec. Time
is plotted on the x-axis and voltage on the y-axis. On the x-
axis, 1 second is divided into five large squares, each
representing 0.2 sec.
Each large square is further divided into five small squares of
0.04 sec each.
25
Electrocardiography
ECG Waveform
P-wave:represents atrial depolarization
on the ECG.
As atrial depolarization initiates by the SA
node located in the right atrium, the right
atrium gets depolarized first, followed by
left atrial depolarization. So the first half of
the P wave represents right atrial
depolarization and the second half shows
left atrial depolarization.
27
108.
Electrocardiography
ECG Waveform
PRInterval: represents the time from
the beginning of atrial depolarization to
the start of ventricular depolarization
and includes the delay at the AV node.
QRS complex: represents ventricular
depolarization as current passes down
the AV node.
28
109.
Electrocardiography
ECG Waveform
Q-wave:represents the depolarization of
the interventricular septum.
R-wave: represents the electrical stimulus
as it passes down the ventricles during
depolarization.
S-wave: represents the final depolarization
of the Purkinje fibers.
29
110.
Electrocardiography
ECG Waveform
ST-segment:depicts the end of
ventricular depolarization and the
beginning of ventricular repolarization.
T-wave: represents ventricular
repolarization.
QT interval: represents the start of
depolarization to the end of the
repolarization of ventricles.
30
Electrocardiography
1. Rate:
For thecalculation of rate:
The number of either small or large squares between an R-R
interval should be calculated.
The rate can be calculated by either dividing 300 by the
number of big squares or 1500 by the number of small
squares between two R waves.
32
113.
Electrocardiography
1. Rate:
The heartrate can be calculated as:
Heart Rate (bpm) = 300 / R-R interval (no. of large squares)
or Heart Rate (bpm) = 1500 / R-R interval (no. of small squares)
Normal HR is 60 to 99 beats per minute.
If it is less than 60, it is called bradycardia, and if greater than
100, it is referred to as tachycardia.
33
Electrocardiography
2. Heart rhythm:
Foran accurate interpretation of rhythm. It involves looking for
several points:
1. The presence or absence of regular P waves
2. The duration of QRS complexes (narrow or wide)
3. The correlation between P waves and QRS complexes, whether
the rhythm is regular or irregular
4. The morphology of P waves
35
116.
Electrocardiography
2. Heart rhythm:
Thosefeatures also help identify if the arrhythmia originates in the
atria or ventricles. Many disorders are related to rhythm
abnormalities.
36
117.
Electrocardiography
Several types ofECG monitoring
equipment are available, including:
Continuous ECG monitoring
Telemetry ECG system
Ambulatory ECG
Wireless mobile cardiac monitoring
systems, etc.
37
Continuous
Ambulatory
Telemetry
Wireless (Portable)
118.
Electrocardiography
With theevolution of technology, there are electronic
wristwatches that can also monitor the heart rate and rhythm.
However, the accuracy of these devices may be somewhat
inferior compared to a 12-lead ECG. When prompted for
abnormal findings, these require confirmation by standardized
clinical testing available in the cardiology office.
38
119.
Electrocardiography
Preparation
Before theprocedure, a brief history regarding drugs and allergies
to adhesive gel is necessary.
For good contact between the body surface and electrodes, it is
advised to shave the chest hair.
Any metallic object requires removal.
Limb and precordial leads should be accurately placed to avoid
vector misinterpretation.
Finally, the patient must lie down and relax before recording the
standard 10-second strip.
39
120.
Indications of theECG
Symptoms are the foremost indication of the ECG, including
palpitation, dizziness, chest pain, seizure, and poisoning.
Symptoms or signs associated with heart disease include
tachycardia, bradycardia, and clinical conditions including
hypothermia, shock, hypotension, and hypertension.
To detect myocardial injury, ischemia, and the presence of
prior infarction.
Rheumatic heart disease.
40
00 ⑤
121.
Indications of theECG
Detecting pacemaker or defibrillator device malfunction,
evaluating their programming and function.
Helpful for the assessment of blunt cardiac trauma.
Perioperative anesthesia monitoring, as well as preoperative
assessment and postoperative monitoring.
41
122.
Limitations of theECG
Limited structural (anatomical) and blood flow information.
May miss early heart disorders.
Incorrect electrode placement can lead to false readings.
Less reliable in some patients, e.g. obese, muscular, or those
with lung disease.
42
◉ Radiation therapy(also called
radiotherapy) is a cancer
treatment that uses high doses of
radiation to kill cancer cells and
shrink tumors.
3
Radiation Therapy
126.
◉ Ionizing radiationsgenerate free radicles, which subsequently
damage vital cellular components and lead to double-stranded DNA
breaks (DSBs), resulting in chromosomal aberrations and
rearrangements.
◉ Some cells undergo apoptosis due to the resulting damage, and
some cells die during mitosis due to improperly repaired
chromosomal damage.
◉ Normal cells can repair DNA breaks better than tumor cells.
4
Radiation Therapy
127.
◉ At highdoses, radiation kills cancer cells or slows their growth by
damaging their DNA. Cancer cells whose DNA is damaged beyond
repair stop dividing or die. When the damaged cells die, they are
broken down and removed by the body.
◉ Radiation therapy does not kill cancer cells right away. It takes days
or weeks of treatment before DNA is damaged enough for cancer
cells to die. Then, cancer cells keep dying for weeks or months after
radiation therapy ends.
5
Radiation Therapy
• The mostcommonly used radiotherapy treatment employs a beam
of high-energy X-Rays (photon beam) generated external to the
patient and directed toward the tumor.
• Electron beams
• Protons and neutrons (these particles offer more precise targeting
compared to X-rays but are less commonly available).
• Implanted radioactive sources (gamma, beta and alpha emitters).
7
Types of Radiation Used in Cancer Treatment
①
⑫
③
④
130.
◉ There aredifferent types of radiation therapy.
◉ The two major types are:
○ External-beam radiation therapy
○ Internal radiation therapy
8
Types of Radiation Therapy
131.
External-beam radiation therapy
◉Is the most common type and delivers radiation from a machine
outside the body.
◉ The types of external-beam radiation therapy are:
○ Three-Dimensional Conformal Radiation Therapy (3D-CRT)
○ Intensity Modulated Radiation Therapy (IMRT)
○ Proton Beam Therapy
○ Stereotactic Radiation Therapy (SRT)
9
Types of Radiation Therapy
132.
Three-Dimensional Conformal RadiationTherapy (3D-CRT)
Three-dimensional images of the cancer are created, from CT or
MRI scans.
Directs radiation beams toward the tumor that “conform” or fit the
tumor’s exact size and shape.
This allows aiming the radiation therapy more precisely.
It means that higher doses of radiation therapy can be used while
reducing damage to healthy tissue.
10
Types of Radiation Therapy
133.
Intensity Modulated RadiationTherapy (IMRT)
This is a more complex form of radiation (an advanced form of 3D-
CRT).
With IMRT, each beam also contains several small beams with
variable intensities, or strengths, unlike conventional 3D-CRT, which
uses the same intensity throughout each beam.
IMRT targets the tumor and avoids healthy tissue better than
conventional 3D-CRT.
11
Types of Radiation Therapy
134.
Stereotactic Radiation Therapy(SRT)
This treatment delivers extremely precise, and very intense radiation
therapy dose to a small tumor area.
Stereotactic surgery (SRS) and stereotactic body radiation therapy
(SBRT).
SRS: delivers a high dose of radiation in a single session.
SBRT: delivers high doses over several sessions (fractions).
12
Types of Radiation Therapy
135.
Stereotactic Radiation Therapy(SRT)
Single fraction treatment (SRS) or multi-fractional (SBRT)
administration of high dose radiation to particular target areas from
multiple directions to maximize dose delivery at highly specific
points helps reduce exposure to surrounding normal tissues.
Commonly utilized in intracranial, spinal, or extracranial sites in
sensitive tissues (e.g., lungs, pancreas, head and neck cancers).
13
Types of Radiation Therapy
Proton Beam Therapy
This treatment uses protons rather than x-rays.
At high energy, protons can destroy cancer cells.
The protons deposit the specific dose of radiation therapy to the
targeted tissue.
There is very little radiation dose beyond the tumor as compared to
x-rays.
This limits damage to nearby healthy tissue.
15
Types of Radiation Therapy
·
138.
Internal-beam radiation therapy
◉Also called brachytherapy.
◉ A radiation source (radioactive material) is placed inside the tumor or
next to the target area and slowly emits radiation, which is active only
for a short distance.
◉ Commonly utilized for prostate cancer and gynecological malignancies.
◉ Types of internal radiation therapy include:
○ Permanent Implants
○ Temporary Internal Radiation Therapy
16
Types of Radiation Therapy
·
139.
Permanent Implants
◉ Theseare tiny steel seeds about the size of a grain of rice that
contains radioactive material.
◉ They deliver most of the radiation therapy around the implant area.
17
Types of Radiation Therapy
140.
Temporary Internal radiationtherapy
◉ Radiation therapy is given via needles, catheters, and special
applicators.
◉ The radiation stays in the body from a few minutes to a few days.
◉ Most people receive radiation therapy for just a few minutes, some
may receive for more time.
18
Types of Radiation Therapy
141.
◉ A linearaccelerator, abbreviated as ‘linac,’
refers to a device that accelerates ions
(electrons) along a linear path to produce
electrons or high-energy X-rays (by colliding
the electrons with a target).
◉ The most commonly used radiation therapy
machine.
◉ Used in 3D-CRT, IMRT, SRS and SBRT.
19
Linear Accelerator
142.
◉ Gamma Knife(GK) radiosurgery is the
most frequently used SRS technique
worldwide.
◉ The GK system consists of an array of 192
or 201 sources of cobalt-60 that align
with an inner collimator to direct the
resulting photon beams delivered by the
decay of Cobalt 60 (gamma rays).
20
Gamma Knife
143.
◉ GK allowsto precisely deliver high
doses of radiation to small targets
minimizing the volume of normal brain
structures irradiated to high doses.
◉ Frequently employed in patients with
brain tumors.
◉ GK is usually given in single fraction or,
less frequently, in a reduced number of
fractions (from 2 to a maximum of 5).
21
Gamma Knife
144.
• The radiotherapyplanning process begins by defining the tumor
target and susceptible normal tissues.
• The process then involves arranging the radiation beams such that
they cover target tissues while minimizing exposure to the adjacent
normal organs.
• The optimal beam angles, dose distribution, and fractionation
(dividing the total dose into smaller doses over several treatments)
are determined by the radiation oncologist.
22
Treatment Planning
D ② ③
145.
• Simulation isa critical step in the radiation
treatment planning process.
• It is performed at the simulation room
equipped with a dedicated big-bore CT
scanner.
• During the simulation, the treatment setup
will be simulated by positioning the
patient on the flat couch immobilized by
specially designed devices.
23
Simulation
146.
• The patientwill then be aligned to the reference low-energy lasers in
the room and be marked on the skin with ink marks.
24
Simulation
147.
• Then, aCT scan will be performed to
acquire the anatomy involved in the
treatment.
• CT scan will be used to identify the
tumor and surrounding normal critical
organs for developing a treatment plan
that will guide the treatment machine to
target the tumor accurately and spare
critical organs as much as possible.
25
Simulation
148.
Acute side effects:
•Fatigue: feeling tired or exhausted.
• Skin reactions: redness, dryness, itching, or peeling in the treated area.
• Hair loss: in the area being treated.
• Nausea and vomiting: although less common than with chemotherapy.
• Diarrhea or constipation: if the treatment area includes the abdomen or
pelvis.
• Mouth sores: if the head and neck area is treated.
26
Side Effects of Radiotherapy
D
⑪
⑤
④
⑤
G
149.
Long-term side effects:
•Chronic fatigue.
• Fibrosis: scar tissue formation.
• Secondary cancers: a small risk of developing a new cancer in the treated
area.
• And others
27
Side Effects of Radiotherapy
150.
Electroencephalography (EEG) andMagnetoencephalography (MEG)
Biophysics II Course
Washington University of Health and Science
Summer 2025
Lecturer: Huda Nasser
Brain Electricity
Electricityis simply the flow of electric
charge across a gradient.
In living organisms, charge gradients
across membranes produce electricity
in the form of flowing ions.
The brain contains roughly a hundred
billion electrically conductive biological
wires (neurons).
3
153.
Brain Electricity
Neurons= nerve cells.
The basic unit of structure and
function in the nervous system.
Collect and send information to
and from sensory organs,
muscles, glands, and other
neurons.
4
Axon
Cell Body
154.
Brain Electricity
Whenthe neurons fire, electrical
impulses cause us to dream, laugh,
think, see, and move.
Plasma membrane of all living cells
have a membrane potential (polarized
electrically), due to differences in
concentration.
5
155.
Brain Electricity
Membrane Potential
A resting membrane potential is the
difference between the electric
potential in the intracellular fluid
(ICF) and extracellular fluid (ECF) of
the cell when it is not excited (at
rest).
Results from the uneven distribution
of electrical charge (ions) between
ECF and ICF.
6
156.
Brain Electricity
Membrane Potential
Neurons (excitable cells) can change
membrane potential and generate an
action potential, when neurons are
excited (stimulated).
Changes in potential are directly
proportional to the intensity of the
stimulation.
7
157.
Brain Electricity
Membrane Potential
An action potential can be thought
of as the firing of the neuron.
Action potentials will propagate
down the length of a neuron’s axon.
Action potentials are the electrical
signals that move down a neuron.
8
Conduction of action potentials
158.
Brain Electricity
Whenan action potential occurs in one
region of a neuron membrane, it causes
a bioelectric current to flow to adjacent
portions of the membrane.
This propagation of action potentials
along a nerve axon constitutes a nerve
impulse.
9
159.
Brain Electricity
Everytime one of neurons fires, it
produces a charge gradient of about
105 millivolt (mV) → the net change
between resting potential and peak.
This tiny change in voltage causes a
tinier amount of current to flow (about 1
nano-ampere).
10
Electroencephalography
An electroencephalogram(EEG) is
an essential tool that studies the
electrical activity of the neuronal cells
in the brain.
Records the voltage differences
caused by summed action potentials
in the cerebral cortex.
There are at least 10 billion neurons in
the outermost layer of the brain, the
cerebral cortex.
12
162.
Electroencephalography
The basicequipment includes
electrodes, an amplifier, and an EEG
system (monitor and processor).
Metal electrodes are used to pick up
the electrical potentials in the scalp.
13
163.
Electroencephalography
Typically, atleast 21 electrodes are
placed on the scalp.
EEG electrodes are sensitive to the
potential changes over the head surface.
The difference in electrical potential
between two electrodes ranges in
micro-volt (μV).
An amplifier is used to amplify it in a
range where digitization can be
performed precisely.
14
164.
Electroencephalography
The strongestEEG signal comes when the
neurons are perpendicular to the scalp.
The fact that the cortex is folded, forming gyri
and sulci implies that:
Some populations of neurons have apical
dendrites that are perpendicular to the scalp,
i.e. those are at the top of a gyrus.
Others are parallel to the scalp, i.e. those that
are on the wall of a sulcus
15
165.
Electroencephalography
Excitatory postsynapticpotential (EPSP) and inhibitory
postsynaptic potential (IPSP) are the two main kinds of
postsynaptic potentials.
The summation of EPSP and IPSP over a selected cortical region
creates an electrical field with positive and negative ends (dipole).
The dipole is typically parallel to the pyramidal cell orientation.
The EEG measures this summation.
16
166.
Electroencephalography
The recordedEEG signals can be
classified into four basic groups at
various frequency bands (waves).
Each is associated with various
functional state.
Alpha (8 to 12 Hz), beta (13 to 30
Hz), theta (4 to 7 Hz), and delta
(less than 4 Hz).
17
167.
Indications of theEEG
Primarily used to assess seizure disorders, such as epilepsy.
To classify the type of seizure and localize the onset of
seizures.
To determine the hemisphere dominance for language and
memory.
Patients with altered mental status from various etiologies like
toxic metabolic encephalopathies.
18
168.
Indications of theEEG
Symptoms of loss of consciousness with a negative cardiac
workup.
Identify delayed ischemic changes after brain hemorrhage.
Brain death determination.
19
169.
Limitations of theEEG
EEG cannot precisely locate the source of brain activity.
Mainly records surface activity (cortex), missing deeper brain
structures.
EEG shows function (electrical activity), not anatomy, unlike
CT or MRI.
EEG signals can be distorted by motion, such as eye
movements, muscle activity, blinking, …
20
Magnetoencephalography
The currentis always associated
with a magnetic field
perpendicular to its direction.
Magnetoencephalography (MEG) is
based on the ability to detect very
weak magnetic fields that originate
from electrical activity within the
brain.
22
172.
Magnetoencephalography
These signalsare detected with an array of
devices that are placed close to the scalp,
known as SQUIDS (superconducting
quantum interference devices).
SQUID is an ultra-sensitive detector of
magnetic flux.
23
173.
Magnetoencephalography
SQUIDs candetect tiny magnetic signals,
much less than one-billionth the strength
of the Earth's magnetic field.
SQUIDS convert these magnetic signals
into recordable electric voltages.
The SQUID array is mounted in a close-
fitting helmet, can measure field changes
of the order of 10-15 femto-Tesla.
24
174.
Magnetoencephalography
That requiressensitive magnetic detectors, and has the ability to
deal with environmental noise (shielding and smart sensor
design).
These tiny signals are picked up by SQUID sensors, but they are
too weak to be analyzed directly.
Therefore, the system uses amplifiers to boost the signals before
digitization and analysis.
25
175.
Magnetoencephalography
MEG seesonly the magnetic fields that
have a component perpendicular to the
skull.
At least 10,000 neighboring neurons
firing simultaneously for MEG to detect.
26
Magnetoencephalography
Magnetic Shielded Room
A special room made with materials
that block external magnetic noise to
ensure accurate and clean recordings.
Most shielded rooms comprise either
2 or 3 shells.
28
178.
Magnetoencephalography
Different patternsof brain waves
can be recognized by their
frequencies and amplitudes.
Brain waves are categorized
based on their level of activity
and frequency.
Slow activity: lower frequency
and high amplitude.
Fast activity: refers to higher
frequency and often smaller
amplitude.
29
Magnetoencephalography
Types of brainwaves:
Alpha: indicates physical and mental relaxation.
Awake but relaxed and not processing much information, when
getting up in the morning and just before sleep.
32
182.
Magnetoencephalography
Types of brainwaves:
Beta: indicates normal alert consciousness, active thinking.
Active conversations, making decisions, solving a problem,
focusing on a task, learning a new concept, ...
33
Magnetoencephalography
Types of brainwaves:
It is very hard to capture gamma wave in an EEG, they originate
in the thalamus (center of the brain) and move from the back
part of the brain to the front with incredible speed.
35
185.
Indications of theMEG
Tumor and lesion evaluation
Stroke and brain injury assessment
Assess brain function post-injury
Cognitive neuroscience and research
Language processing
Memory
Neurodevelopmental and psychiatric disorders
Autism spectrum disorder (ASD)
Schizophrenia
ADHD
36
186.
Limitations of theMEG
MEG systems are very expensive to purchase and maintain.
Limited in availability (not widely accessible compared to EEG
or MRI).
Less effective at detecting activity from deep brain structures.
Movement sensitivity (even small head movements can distort
results).
Does not provide structural (anatomical) information.
37
◉ Ultrasound imaging,also known as sonography or
ultrasonography, is a diagnostic technique that uses high-
frequency sound waves to create cross-sectional images of the
human body.
◉ Real-time imaging technique (the ability to see moving structures
and changes within the body instantly).
◉ It relies on the principles of sound wave propagation and their
interactions with biological tissues.
126
Ultrasound Imaging
190.
◉ Sound wavesare mechanical waves
that require a medium to propagate.
◉ They are able to travel through air,
water and biological tissues.
127
Physical Principle
-onefoldspeed
di
require
adium
↳2 feilds Perpendiciar le speed
t
T
o TQ light
↳ electrmagnetic
↳ doesn't require medium
191.
◉ Sound wavetransmits their energy
mechanically, through pressure
variations on the particles.
◉ Regions of high pressure and density
are called “compressions” while
regions of low pressure and density
are called “rarefactions”.
128
Physical Principle
192.
Properties of SoundWaves:
Frequency: number of oscillations
(cycles) per second, measured in Hz.
Wavelength: distance between
successive compressions or
rarefactions.
Amplitude: height of the wave, also
called intensity/strength of the wave.
Speed: speed at which the wave
travels through the medium.
129
Physical Principle
(nm or mm)
↓
decreases
themore
it travels
193.
◉ Ultrasounds referto sound waves with
frequencies above the audible range
for humans (20 Hz – 20 kHz).
◉ In medical ultrasound the frequency
of sound waves is in the range of
millions of cycles per second (2 MHz
to 20 MHz).
130
Physical Principle
T lowerthan higher than normal
normal human human
Mega Dange range
194.
Longitudinal wave vs.transverse wave
• Longitudinal wave → the movements of particles in a medium are
parallel to the direction of propagation of the sound wave.
• Longitudinal sound waves are used in ultrasound imaging.
• Transverse wave → the movements of particles in a medium are
perpendicular to the direction of propagation of the sound wave.
131
Physical Principle
-
-
195.
Generation of Ultrasound
An ultrasound transducer (probe):
ultrasound waves are produced by
piezoelectric crystals in the
transducer.
• The electric signal is converted into
vibrations of the piezoelectric crystal,
which then generates ultrasound
waves.
132
Physical Principle
Pressure
[
me
In the pico electic crystal
converted into ultrasound
the electic Signals -
> wares
196.
The transducersends an ultrasound pulse into tissue → ultrasound
images are produced relying on properties of acoustic physics
(reflection, refraction, absorption, and scattering) → these properties
cause attenuation of ultrasound that is used to localize and
characterize different tissue types.
Acoustic impedance is a physical property of a tissue in which how much
resistance it offers to stop the transmission of an ultrasound beam.
Differences between the acoustic impedance of two mediums govern the
proportions of reflected and transmitted sound waves.
133
Physical Principle
forsoundware
.
a
goes
back
(
tothe C
probe
generates
theimage
.
C
fortheeself
197.
If thesound waves encounter an impedance (resistance) on their way,
e.g. at the boundary between fatty tissue and water → then they are
reflected (echoed) → and received by the transducer → enough data
are recorded to form a rapidly moving real-time image.
134
Physical Principle
198.
What happens toultrasound waves in the body?
1. Absorption: a large part of the ultrasound waves is completely
absorbed into a medium.
• Absorption increases with increasing image depth and the applied
frequency.
2. Reflection: occurs when sound waves encounter a boundary
between two different tissues with varying acoustic impedance.
135
Physical Principle
b< when frequency inc qualit inc , but
Absorptionina so won't
b. we
limitation
helpinimage need reflection.
a
-
199.
What happens toultrasound waves in the body?
3. Refraction: bending of the ultrasound wave as it passes through a
boundary between two media with different propagation speeds.
4. Scattering: redirection of ultrasound waves in multiple directions
due to small inhomogeneities within the tissue.
136
Physical Principle
V
araying
↳ lung or stone in Kidney /some pathologies / you use scattering ba
some might reflect back to from image
The speed ofpropagation of the sound waves depends on the medium
which they pass through, and its elasticity and density.
The propagation speed of sound is higher in tissues with increased
stiffness (decreased elasticity) and reduced density.
• Density relates to the amount of matter in a given space.
• Elasticity relates to a material's ability to deform and recover its
original shape.
138
Physical Principle
202.
Types of Transducers(Probes)
Transducers are subdivided according
to the propagation of the sound waves:
a. Linear transducers: the sound waves
propagate in parallel, which has the
advantage of geometrically accurate
imaging.
139
Basic Principles
203.
Types of Transducers(Probes)
b. Convex transducers (curved array):
the sound waves spread out like a fan. A
large area can be imaged.
c. Sector transducers: the sound wave
propagation is fan-shaped and radial.
Typical application is cardiac ultrasound
with a transcostal access (between the
ribs).
140
Basic Principles
Convex
Sector
-
> for pregnant
women
204.
Image Formation
• Ultrasoundimages are formed by sending short pulses of sound
waves into the body and receiving echoes from tissue interfaces
(reflected sound waves).
• The time taken for echoes to return helps calculate the distance
and create the image.
141
Basic Principles
-
gives location
205.
Image Formation
• Thetime it takes for the ultrasound waves to reflect back to the
transducer varies depending on the density and composition of the
tissues.
• By analyzing the timing and intensity of these echoes, ultrasound
machines create detailed images that represent the internal
structures of organs, blood flow, and abnormalities.
142
Basic Principles
·
·
·
aplitude
T
-
206.
Ultrasound Gel
• Becausesound waves have a difficult
time traveling through the air, ultrasound
gel is used to reduce the air between the
transducer and the skin (to reduce the
acoustic impedance and reflection).
143
Basic Principles
207.
1. A-Mode
• TheA-mode is the oldest method.
• “A” stands for amplitude modulation.
• Today, this mode is still used for distance determination in ENT,
ophthalmology and neurology.
144
Imaging Techniques (Modes)
208.
2. B-Mode
• TheB-mode (for “brightness”)
• Is the most frequently used method.
• In the 2D image, the different pixels
are detected with different
brightness grey dots, depending on
the strength of the reflected signal.
145
Imaging Techniques (Modes)
209.
3. M-Mode
• TheM-mode (motion).
• Can be used to map the temporal
behavior of a tissue.
• It is used particularly in cardiology. A
typical example is the imaging of the
movement of a heart valve or the
myocardium.
146
Imaging Techniques (Modes)
210.
4. Doppler Sonography
•Is used to assess blood flow through
blood vessels.
• Detect a frequency shift in echoes,
and determine whether the tissue
(blood) is moving toward or away
from the transducer.
147
Imaging Techniques (Modes)
proble pobt
V ~
Fed ↑ d ()
blue
↳ also depends
on way you
hold the
-
can
see
stenosisstels
movina again
Probe
211.
4. Doppler Sonography
Ageneral guide to the color scheme:
• Red: indicates blood flow towards the ultrasound probe. This color
typically appears when the blood is moving in the same direction as
the sound waves emitted by the probe.
• Blue: represents blood flow away from the ultrasound probe. This
color is used when the blood is moving in the opposite direction from
the sound waves.
148
Imaging Techniques (Modes)
◉ Depth ofPenetration
○ Ultrasound waves have limited penetration depth compared to other imaging
modalities like CT or MRI.
○ Higher frequency ultrasound waves provide better resolution but penetrate less
deeply, limiting visualization of structures deep within the body.
◉ Obesity and Air
○ Ultrasound waves are attenuated by air and bone, which can hinder imaging
quality in obese patients or in regions where there is significant gas (e.g., bowel
loops). This can make it challenging to obtain clear images in these situations.
◉ Operator Dependency
150
Limitations
for
abdomen
they
a
214.
◉ Limited Fieldof View
◉ Limited Tissue Characterization
○ Ultrasound provides limited information on tissue composition or specific tissue
characteristics (e.g., distinguishing between different types of liver masses)
◉ Patient Factors and Positioning
○ Patient factors such as body habitus, patient cooperation, and the need for specific
patient positioning can affect the ability to obtain optimal ultrasound images
151
Limitations
18
History of X-Ray
Wilhelm Roentgen discovered X-Ray in
1895 by accident while experimenting
with cathode rays. He observed a
fluorescent glow from a nearby screen,
he named the new rays "X-rays“, where
"X" stood for an unknown.
Roentgen’s discovery quickly led to the
development of medical imaging.
221.
19
Wall Bucky
X-Ray Tube
X-RayTable
X-Ray detector
is located here
X-Ray Machine Components
ag
theinteractia
X-ray
Production-
1 % X-ray
/Characteristic
breaking
dete
222.
Basic Principles
◉ X-Raybeam is generated in the X-Ray tube.
20
tungsten (high atomic #)
- Produces
is
chase
on
j Charged
e-
so
C all e-
be
has
e-
& They'retalea & releasa
pulledit
e-gotow
and
amodeeurgett
223.
Basic Principles
◉ WhenX-Rays are emitted towards the body,
one of three situations will happen:
○ X-Rays pass through the body (body parts with
low density ‘low atomic number’ e.g. air and fat).
○ X-Rays are blocked and absorbed by the body
(body parts with high density ‘high atomic
number’ e.g. bone and implanted metals).
○ X-Rays may be deflected or scattered.
◉ X-Rays pass through the body, with varying
degrees of absorption (attenuation).
21
&The film itself is
white ,
oncexray passes
a
itmakes
e
air
for
e WHITE
film
spot
of
↳ never waso
attentuation
224.
Basic Principles
◉ Adevice located behind the patient, called
X-Ray detector, captures the transmitted X-
Rays, converting them into an image.
○ X-Rays that pass through the body render the
film dark (black) → Radiolucent.
○ X-Rays that are totally blocked and absorbed
render the film light (white) → Radiopaque.
○ The varying degrees of the X-Ray attenuation
make the various radiographic densities in the
image (gray-scale).
22
if X-ray passes
clothing ,
that part
of film
tenuations
remains
white diffrent
a
give
us
aspectiae
225.
◉ Plain X-Ray,also called conventional radiography, is the simplest
and most common type of X-Ray imaging that offers a quick and
cost-effective way to visualize certain internal structures.
◉ Uses a beam of X-rays to create a two-dimensional image
(superimposed view) of the internal structures within the body.
○ Multiple views (projections) from different angles may be necessary for a
comprehensive understanding.
◉ A valuable tool for initial evaluations and diagnosing various
conditions.
23
X-Ray Imaging
226.
X-Rays may betaken in various patient positions, based on patient
condition and the body part being examined.
Common patient positions include:
24
Standing Supine Decubitus
Prone
X-Ray Imaging
227.
X-Ray projections describethe direction the X-ray beam travels in
relation to the body part being imaged. Common projections include:
25
AnteroPosterior (AP)
X-Ray Imaging
Path -> where X-ray
enter & exits
29
X-Ray Imaging
Why dowe need more than one view?
We need more than one view for an X-ray because a 2D image
can hide details. Structures can overlap, and we may miss
fractures, fluid, or masses seen only from another angle
232.
kVp (Kilovolt Peak)
•Kilovolt peak (kVp) refers to the maximum voltage applied across
the X-ray tube during an exposure.
• It determines the energy and penetrating ability of the X-ray
photons produced.
• Higher kVp results in more energetic X-rays that can pass through
denser tissues.
30
X-Ray Imaging
233.
mAs (Milliampere-Seconds)
• Milliampere-seconds(mAs) is the product of the tube current
(measured in milliamperes) and the exposure time (measured in
seconds).
• It controls the total quantity of X-ray photons generated during an
exposure.
• It has a direct relationship with patient dose, where higher mAs
increases radiation dose.
• mAs = mA x exposure time (seconds)
31
X-Ray Imaging
Clinical Indications:
• Evaluatingfractures and bone injuries.
• Examining joints for signs of arthritis or other problems.
• Checking for pneumonia or other lung diseases.
• Identifying foreign objects swallowed or lodged in the body.
• Monitoring the progress of certain medical conditions.
30
X-Ray Imaging
>
romatizim
236.
Limitations:
• Does notprovide detailed information about soft tissues or organs
other than bones and lungs.
• Can be difficult to distinguish between certain structures that have
similar densities.
• Involves exposure to ionizing radiation, although the amount is
relatively low for plain X-Rays.
31
X-Ray Imaging
◉ Fluoroscopy usesa continuous X-Ray
beam to create live images on a
monitor, similar to an X-Ray but with
the added benefit of motion.
○ Allowing physicians to observe the
movement of organs and tissues.
◉ It allows real-time visualization of the
internal structures of the body.
33
Fluoroscopy
239.
Applications of fluoroscopy
◉Diagnostic imaging:
a. Gastrointestinal tract (barium
swallow and barium enema)
34
Fluoroscopy
·
↳ Liquid/gadin
tum
oraly
240.
Applications of Fluoroscopy
◉Diagnostic imaging:
b. Assessing blood flow
(angiography = arteriography)
35
Fluoroscopy
Coronary Angiography Cerebral Angiography
- the more
you cen
construct
here
not due
colo's
& ability to
distinguish
-
> differentiatiate (less
its the
diff in
colors) so more contrast
& btw
obj thathave
ity - many densities= low contrast
similar
IV
Apex of
Brain
heart
Angio
steries
Used in eatherization
241.
Applications of Fluoroscopy
◉Diagnostic imaging:
c. Assessing joint movement
36
Fluoroscopy
↳bone is black because
its postprocessing
,
so
its negative
editting
after
recording it to see
morearly
242.
Applications of Fluoroscopy
◉Interventional procedures:
a. Angioplasty and stents implantation
37
Fluoroscopy
We put needle
through femeral
artem first ba
its widest
Circumflex
Y
narrowing
↓
Stenosis
243.
Applications of Fluoroscopy
◉Interventional procedures:
b. Biopsy needle guidance
38
Fluoroscopy MRF ,
neck, Sagittal
rig
lung
②
244.
Applications of Fluoroscopy
◉Interventional procedures:
c. Joint injections
39
Fluoroscopy
·
↳ ex) oily needle injection
forsmoother flow
◉ Mammography isa specialized
medical imaging technique used to
examine the breasts, primarily for the
early detection of breast cancer.
◉ It involves using low-energy X-Rays
to create detailed images of the
breast tissue.
44
Mammography
↳ 2D
250.
Types of Mammography:
◉Screening mammography: this is used for routine, asymptomatic
patients to detect early signs of breast cancer, often before
symptoms appear.
◉ Diagnostic mammography: used for patients who have signs or
symptoms (such as a lump or abnormal physical exam) or those
with an abnormal screening mammogram.
45
Mammography
251.
Clinical Applications:
• Screeningfor breast cancer.
• Breast cancer staging.
• Monitoring post-treatment changes.
• Biopsy guidance.
46
Mammography
252.
Limitations:
• Inability todetect small tumors in dense breasts.
• Limited sensitivity in young women (under 40 years).
• Involves exposure to ionizing radiation.
47
Mammography
runger
women
Y
usually havedensyou
e
sound
X use ul
-
> Ultrasoundhe40
◉ Panoramic X-Rayis a type of
dental radiograph that captures
a broad, panoramic image of
the entire mouth area, including
the teeth, jaws, and surrounding
structures, in a single shot.
◉ It provides a comprehensive
view of the upper and lower
jaws, teeth, and the surrounding
bones and tissues.
49
Panoramic X-Ray
LBLT
-
istypeatdetailed
Than
Panoramic
be its 3D ,
but its
higher close
of
X-ray
used for these alot
-
Sinuses & TMjoints
mastonr cells
Shows
O
255.
◉ In apanoramic X-Ray, a machine rotates
around the patient's head to capture a full, 180-
degree view of the mouth, teeth, and jaw.
◉ The machine creates a single image by
capturing X-Rays from all angles, which are
then combined into one large panoramic image.
50
Panoramic X-Ray
#
1888
tube 2 detecter
↳ putyour tongue on the roof of e
rotate
mouth to
prevent air
from Coming in -
256.
Clinical Applications:
• Evaluationof teeth and jaw structures.
• Orthodontic treatment planning.
• Implant planning.
• Oral and Maxillofacial pathology (cysts, tumors or infections within
the jawbone or surrounding structures).
• Sinus evaluation.
• Temporomandibular joint (TMJ) assessment.
51
Panoramic X-Ray
257.
Limitations:
• Not idealfor small-scale issues (between teeth or along the root
surfaces).
• Image distortion.
• Involves exposure to ionizing radiation.
52
Panoramic X-Ray
-
> betube itself is moving