Imaging with x-ray, MRI and ultrasound

Chapter 5 Imaging with x-ray, MRI and ultrasound





Introduction


X-ray, magnetic resonance imaging (MRI) and ultrasonic images play a key role in the diagnosis, staging, planning and delivery of treatment and follow up of patients with cancer.


In everyday language, an image is a picture and, more generally, it is a representation of the distribution of some property of an object. It is formed by transferring information from the object to an image domain. In practice, this requires the ordered transfer of energy from some source via the object of interest to a detector system. The detected signal may be processed in some way before being displayed and stored by suitable devices.


Medical imaging modalities covered in this chapter are classified according to the type of energy used to carry information: x-rays, radiofrequency waves and high frequency sound waves.


X-ray imaging enables tumours to be localized with respect to normal anatomical structures and to external markers. Because x-rays travel in straight lines until they are absorbed or scattered, they can produce images which faithfully represent spatial relationships within the body. It is principally for this reason that x-ray images of various kinds are essential to the planning and delivery of radiotherapy. A further reason is that interactions of ionizing radiation with matter are an essential feature of both imaging and therapy, so that information on properties of tissues relevant to treatment planning, such as electron density, may be obtained from suitable images.


Magnetic resonance imaging is an excellent technique for imaging soft tissue, and is often used to diagnose and stage cancer in the head, neck and body. It can also be used to monitor the response to treatment. The extent of the cancer can be seen on anatomical images. Other specialized MRI techniques, such as diffusion weighted imaging and dynamic imaging with a contrast agent can also be used to refine the diagnosis and cancer staging. Magnetic resonance spectroscopy provides information regarding the metabolism of the tumours and can also be used to monitor treatment response.


Diagnostic ultrasound imaging has several advantages over other imaging modalities [1]. It is relatively cheap, safe, gives real time images and has good soft tissue contrast. As well as anatomical detail, ultrasound can exploit the Doppler effect to give information about blood flow and the vascularity in tissues. The distortion of tissue under pressure in ultrasound images can give images related to the elasticity of tissues.


Radionuclide imaging, including PET-CT, which is primarily concerned with the function of organs and tissues is dealt with in Chapter 6.



X-ray imaging



Overview of x-ray imaging process


The energy source in medical x-ray imaging is usually an x-ray tube and electrical generator though, in the case of radiotherapy portal imaging, it is the linear accelerator. As the x-ray beam passes through the patient, some radiation is absorbed or scattered. The intensity of the emerging primary beam varies with position and carries information about the interactions that have occurred in the body. The emerging beam can be detected by a variety of devices, e.g. film/screen cassette, image intensifier, solid state electronic detector. These are typically large area devices and the image is a two-dimensional shadowgraph of the intervening anatomy. Radiographic film is unique in combining all three roles of image detection, recording and display. Image intensifiers are usually coupled to a television camera and display monitors: static images or dynamic (i.e. moving) series may be stored on analogue video media or digitized for storage on DVD or other computer-based media. Digital fluoroscopy and radiography systems use digital computers and their storage and display devices as integral components of the imaging system, as does computed tomography (CT). In CT, the x-ray beam is collimated in the longitudinal direction to a narrow slit and this is aligned with an arc of solid state detectors. The tube and detectors are mounted on a gantry which rotates about the patient. Essentially one-dimensional projection images are acquired from many angles and the data are processed in a digital computer to form images of transverse slices through the patient.



Production of x-rays for imaging


The general topic of x-ray production is covered in Chapter 2. This section highlights some aspects of specific relevance to imaging.


X-rays are generated by causing electrons, which have been accelerated to high energies in a vacuum tube, to collide with a metal target. The electrical supply is normally from a generator, which takes power from the mains three phase alternating current (AC) supply and converts it, using a transformer and associated circuits, to an approximately constant kilovoltage (kV) direct current (DC) output. Older models employed rectification and smoothing circuits which resulted in appreciable ripple on the kV waveform, i.e. the output voltage varied by several per cent over a mains cycle. For this reason, the kilovoltage is specified as the peak value, denoted by the abbreviation kVp. Modern generators employ converters, operating at a frequency of several kHz, which produce voltage waveforms with very little ripple. Diagnostic imaging work mostly uses accelerating potentials in the range 50 to 150   kVp, though lower values are used in mammography.


At megavoltage energies, as in linear accelerators used for radiotherapy, the x-rays are produced mainly in the forward direction of the electron beam and hence a transmission target is used. At kilovoltage energies, as used in diagnostic x-ray equipment, radiotherapy simulators and CT scanners, x-rays are produced more isotropically and a reflection target is used. This allows the tube to be constructed with a rotating anode (Figure 5.1), which permits the heat generated to be dissipated over a much larger area than with a stationary anode. This is important because more than 99% of the electron beam energy is converted to heat in the anode and less than 1% appears as x-rays. Moreover, to produce images with good spatial resolution, the focal spot must be as small as possible and short exposure times are used to reduce blurring due to patient movement. With a stationary anode, a large quantity of heat would be deposited in a short time over a very small area, resulting in serious damage to the target. In fact, most x-ray tubes offer two sizes of focal spot, the larger being used for higher exposure factors which impose higher heat loading demands on the tube.



The x-rays produced have a spread of energies, i.e. a spectrum as shown in Figure 5.2, and there are two main components. One is the bremsstrahlung produced when electrons experience large accelerations as they pass close to atomic nuclei. This produces the major part of the spectrum, the smooth curve. Superimposed on this is the second component, the line spectrum due to characteristic radiation emitted when orbital electrons move to lower energy levels to fill vacancies which have been caused by ionization. The area under the spectrum represents the total quantity of radiation produced.



The shape of the spectrum determines the quality of the radiation, i.e. its penetrating properties. Increasing the tube current (mA) or the exposure time (s) both increase the quantity of radiation produced but do not affect its quality. Increasing the applied voltage (kVp) increases both the quality and quantity of radiation produced and the output is approximately proportional to kVp2. Other factors, such as anode material and filtration of the beam, further affect the quality and quantity of radiation produced. For imaging, the lower energy components are usually selectively reduced by suitable filtration.



Information from absorption/scattering


When x-rays, generated from a suitable source, are incident upon an object, such as the human body, some pass straight through while others interact with the material in the object by processes of absorption and scattering. In biological tissues at kilovoltage energies, the interactions of importance are photoelectric absorption and Compton scattering. The photo-electric effect depends strongly on atomic number Z and the energy E of the x-rays. Calcium, found in bone, has a relatively high atomic number and hence bone strongly absorbs kV x-rays. At megavoltage energies, it is the Compton effect that predominates and this depends primarily on electron density ρe.


The beam emerging from the object contains primary radiation together with scattered radiation. It is the varying intensity of the transmitted primary beam which carries useful information to produce an image.






Anti-scatter grid


The anti-scatter grid consists of an array of long, thin lead strips, separated by some relatively radiolucent spacer material (Figure 5.5). Only radiation travelling perpendicular to the grid can pass through to the detector. Most of the scattered radiation is travelling at other angles and is intercepted and absorbed by the lead strips. Some primary radiation is absorbed too, but the net effect is greatly to increase the ratio of primary to scattered radiation reaching the detector, thus improving image contrast. If the angle between the primary beam and the perpendicular to the grid becomes too great, e.g. towards the edge of large fields, then a significant fraction of primary radiation will be absorbed. This can be overcome by using a focused grid, as shown in Figure 5.6. To avoid shadows from the lead strips producing distracting lines on the image, it is possible to move the grid to and fro laterally during the exposure and thus to blur out those lines.





Planar imaging



Film/screen detection


For many years, radiographic film has been used as a combined detector, storage and display device for x-ray images. It is usually used in conjunction with intensifying screens, which have a higher absorption efficiency than film for x-rays and which emit many visible light photons for each x-ray photon absorbed (Figure 5.7).



Radiographic film consists of a transparent polyester base, approximately 0.2   mm thick, usually coated on both sides with an emulsion containing crystals of silver bromide and this, in turn, is coated with a protective layer. When the emulsion is exposed to light or x-rays, some electrons are transferred from bromide ions to silver ions, which are reduced to silver atoms. These form a latent image which is not visible until it is chemically developed, a process in which the remaining silver ions in the affected crystals are also reduced to silver atoms, which cause blackening of the film. The more silver atoms present per unit area in the developed image, the darker the film appears.


Exposed films are normally processed automatically, in several stages:



Films may be manually loaded into the processor in a darkroom or automatically from suitable cassettes using a so-called daylight processor.


The intensifying screen (Figure 5.8) uses a fluorescent material which emits visible light when irradiated with x-rays and it is this visible light which is then detected by the film. (The same principle is used in image intensifier systems and in some digital imaging devices: see below.) A cassette is used which contains a separate screen for each side of the film and is constructed so as to ensure close contact between screen and film over their whole area. Many visible photons are produced for each x-ray photon absorbed and so the exposure required to produce a given degree of blackening on the film is greatly reduced compared with direct exposure of the film to x-rays. With modern rare earth screens, this reduction may be by a factor of about 1/100.




Characteristic curve


The degree of blackness of the film is measured in terms of optical density (D). If a beam of light of intensity Io is incident on a piece of film and intensity It is transmitted, then:



image     5.4



Hence, a region of film which transmits one-tenth of the incident light intensity has optical density 1.0, whereas a region which transmits one hundredth of the incident light intensity has optical density 2.0. A perfectly transparent region would have D = 0.


A graphical plot of D against log(exposure) is called the characteristic curve. A typical example is shown in Figure 5.9. If an unexposed film is developed, its optical density is a little greater than zero because the film base is not perfectly transparent and also because some of the silver bromide crystals are reduced to metallic silver (film fog). Over a range of exposures, the characteristic curve is approximately linear, and the gradient (slope) in this region is known as gamma for that film/screen combination. At very high exposures, all the silver bromide crystals are reduced on development and no increase in D occurs for higher exposures: the film/screen response is said to be saturated.



Contrast is the difference in D between different parts of an image. Under favourable conditions, the human eye can detect density differences as small as 0.02. If the slope of the characteristic curve is steep (i.e. has a high value of gamma), this means that the density increases rapidly over a relatively narrow range of exposure values, so the image has high contrast. On the other hand, only a narrow range of exposures can be represented before the image saturates, i.e. the latitude is low, and careful radiographic technique is needed to ensure that all features of interest are properly imaged. A lower gamma film/screen combination produces lower contrast but can encompass a wider range of exposure levels, i.e. it has greater latitude.


If only a relatively small exposure is required to produce a given density, as in curve A on Figure 5.10, the film/screen combination is said to be fast. Conversely, a slow combination requires a greater exposure to produce the same density (curve B). It might be thought that fast systems would always be desirable, to minimize the patient dose required to produce the image, but this is not necessarily so for two reasons:






Fluoroscopic imaging with image intensifier/TV chain


It is possible to view a time-varying (dynamic) image by using a fluoroscopic system, in which the x-rays are absorbed by a fluorescent material which emits visible light, as in the intensifying screens used with film. Because the brightness of this image is low, an image intensifier is used to increase the brightness and this secondary image is viewed by a TV camera system (Figure 5.11). The TV signal may be recorded in either analogue or digital format.



The image intensifier tube is an evacuated glass envelope with an input phosphor which is typically in the form of a layer of caesium iodide (CsI) crystals. In contact with this is a photocathode, which absorbs the visible light from the phosphor and emits photo-electrons. These are accelerated through a large potential difference (≈ 25   kV) and focused onto a much smaller output phosphor, which again produces visible light when it absorbs these electrons. As a consequence of the energy gained by the electrons and the fact that they are concentrated onto a smaller area, the brightness of the image at the output phosphor is much higher than at the input. This image is then viewed by a TV camera, usually via a mirror so that the camera is not in the primary x-ray beam.


At each stage in this process there is some loss of fidelity in the image and this can be serious if the electron optics are poorly adjusted or if there is significant interference from external magnetic fields (even the Earth’s magnetic field can affect the output image).



Mar 7, 2016 | Posted by in GENERAL RADIOLOGY | Comments Off on Imaging with x-ray, MRI and ultrasound

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