IntroductionConventional ultrasound (US) is the preferred imaging technique used to screen for focal liver lesions (FLLs) because of its noninvasiveness and accuracy. However, it has a low specificity rate for characterization of these lesions, and therefore other imaging techniques like dynamic computed tomography (CT) or magnetic resonance imaging (MRI) are usually required. The limitations of CT and MRI are well known: both increase the cost and time of diagnosis, CT is associated with radiations problems, the intravenous contrast medium used for CT scans can be dangerous for patients with renal failure or iodinate contrast allergy, and the presence of certain biomedical implants and devices may pose hazards for patients undergoing MRI procedures. Thus, it would be advantageous if a correct diagnosis could be reached immediately during the US study. Recent advances in US technology including the availability of US contrast agents and the development of nonlinear specific contrast imaging methods have led to US imaging playing a bigger role in the characterization of FLLs, with an accuracy similar to that of dynamic CT and MRI.
Contrast-specific imaging with ultrasoundContrast agents are based on gas microbubbles stabilized with different substances. When injected intravenously, microbubbles pass through the pulmonary bed and not only increase the Doppler signal but also produce enhancement of the gray-scale echostructure using specific imaging sequences [1]. Microbubbles interact with the ultrasound beam depending on the insonation energy. At very low acoustic powers [i.e., low mechanical index (MI)], they reflect ultrasound thereby increasing the echoes. As the acoustic power increases, the bubbles undergo nonlinear oscillation which produces harmonic signals. At higher acoustic powers, bubble disruption occurs, producing a strong but transient effect that may be seen as an intense signal [2]. Therefore, specific software systems capable of canceling fundamental linear components and highlighting the nonlinear harmonic components of the insonated structures have been introduced. Techniques such as pulse and phase inversion allow the microbubble enhancement to be evaluated in gray-scale. The initial imaging methods of displaying the microbubble signals used a high MI in order to destroy the microbubbles. However, these methods had several limitations including (a) a transient effect due to the microbubble disruption, (b) limited resolution, and (c) lack of penetration. Recently, further improvements have been made in order to achieve higher resolution, higher sensitivity, and good penetration, thus overcoming the problem of transient effect [3,4]. With the development of more stable and pressure-resistant second-generation contrast agents (e.g., SonoVue, Definity and Optison), combined with new low-MI contrast methods, very small blood vessels and tissue perfusion can be evaluated in real time [5].
Characterization of focal liver lesionsCharacterization of FLLs with conventional US is not possible in many case...