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Cross-sectional imaging of the liver, biliary tree, and pancreas can be performed with ultrasound, computed tomography (CT), or magnetic resonance imaging (MRI). Positron emission tomography (PET) is most often performed in combination with CT (PET-CT) and has more recently been performed in conjunction with MRI (PET-MRI). This chapter will emphasize basic principles of ultrasound, CT, and MRI that highlight the strengths and limitations of each technique for the ordering clinicians.
Ultrasound as an imaging modality has tremendous versatility, is low-cost, and has real-time capability and portability. Ultrasound is considered safe at clinical, diagnostic levels, with no confirmed harmful biologic effects on the operator or patient. Use of Doppler ultrasound also allows for the assessment of blood flow dynamics (see Chapter 5 ). Despite these advantages, certain limitations influence the applicability of ultrasound. Ultrasound waves are unable to penetrate bone or air, which can obscure lesions and limit the field of view. The quality of ultrasound imaging and its interpretation are also operator dependent, which means they are influenced by skill and experience.
Different ultrasound transducers are optimized for specific frequencies. Lower-frequency transducers have poorer resolution with greater depth of penetration and thus are used to image deeper structures such as abdominopelvic tissues. Higher-frequency transducers have better spatial resolution, but higher-frequency sound attenuates rapidly and has poorer tissue penetration. Higher frequency ultrasound is best used for superficial soft tissues, such as the thyroid, and it can also be used to assess liver surface nodularity.
Echogenicity of tissue refers to the reflection or transmission of ultrasound waves relative to surrounding tissues. Based on gray scale imaging, a structure on the image display can be characterized as anechoic (uniformly black), hypoechoic (dark gray), or hyperechoic (light gray) ( Fig. 13.1 ). Acoustic artifacts often occur, many of which are clinically useful. For example, acoustic enhancement is described when there is increased through-transmission of sound waves in fluid-containing structures, making tissue behind the fluid appear artificially bright, a characteristic of cystic structures (see Fig. 13.1 ). Certain artifacts are useful to hepatobiliary imaging in particular. Acoustic shadowing occurs when a structure attenuates sound more rapidly than surrounding tissues and casts a dark acoustic shadow beyond the object. This occurs with strong reflectors, such as calcifications, or strong attenuators, such as dense tumors. Acoustic shadowing is a feature of gallstones and, in conjunction with mobility, aids in distinction between gallstones and gallbladder polyps (see Chapter 33 ). Comet tail artifact is a type of reverberation that occurs when two reflective interfaces are closely spaced, such as within a punctate crystal, producing posterior echoes that are parallel, evenly spaced echogenic bands with a triangular tapered shape. Comet tail artifact allows for the identification of surgical clips and is also a feature of gallbladder adenomyomatosis. Twinkle artifact is a color Doppler artifact that helps to detect and verify crystals and calcifications, particularly if a calculus does not demonstrate acoustic shadowing. Twinkle artifact occurs posterior to strong reflectors and appears as turbulent color Doppler flow with a mix of red and blue pixels; however, spectral Doppler tracing demonstrates noise. Additional artifacts have been described and are outside the scope of this chapter; the reader is referred to specialized texts.
A normal liver is smooth in contour and uniform in echogenicity. Hepatic parenchyma is hypoechoic to the spleen and either isoechoic or minimally hyperechoic to renal parenchyma (see Fig. 13.1 C). Liver size is most commonly determined sonographically by a longitudinal image of the right lobe. Treece et al. found that when the liver measures 15.5 cm or greater in the midhepatic line, hepatomegaly is present in 75% of patients. In the right midclavicular line, the normal mean length is 10 cm, with a standard deviation of 1.5 cm. In most patients the measurement of liver length suffices, but hepatic shape can be variable, and thus three-dimensional ultrasound volumetric analysis can aid evaluation. , Ultrasound images are obtained through available acoustic windows, avoiding bone and air, which will vary the appearance of the liver compared with the standard transverse planes of CT and MRI.
Doppler ultrasound is used to identify and evaluate blood flow in vessels based on the backscatter of blood cells (see Fig. 13.1 D). Doppler imaging allows for the assessment of vessel patency, direction of blood flow, flow velocity, and spectral waveforms. Three different Doppler displays are available: color, power, and spectral Doppler. Color Doppler provides information about the direction of motion and differences in flow velocity. Limitations of color Doppler imaging include dependence on angle of insonation, inability to display the entire Doppler spectrum in the image, and artifacts caused by aliasing and noise. Power (or amplitude) Doppler is a complementary technique that displays total amplitude of the echo signal but not flow direction. Power Doppler signal is more sensitive for flow detection than color Doppler and is less dependent on the angle of insonation. It is not subject to aliasing and is less sensitive to noise. Power Doppler is most useful in showing areas of low flow, depicting slow flow in an area of subtotal occlusion and demonstrating intralesional vascular patterns. In spectral Doppler, a sample volume cursor is placed within the target vessel and displays a waveform of the entire range of velocities during time, rather than the mean velocity as in a color Doppler image. Arterial waveforms are characterized as high resistance by limited flow during diastole or low resistance by continuous flow during diastole. At sites of stenosis, flow is not laminar; instead, flow becomes turbulent, and the spectral Doppler waveform reflects the red blood cells moving at varying velocities.
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