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kwartalnik polskiego towarzystwa ultrasonograficznego

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Characterization of focal liver lesions<br />

in non-cirrhotic liver<br />

Dietrich C.F. 1 , Jędrzejczyk M. 2<br />

1. innere Medizin 2, caritas-krankenhaus, Bad Mergenthein<br />

2. Department of Diagnostic imaging, 2 nd Medical faculty of Warsaw Medical University<br />

Correspondence:<br />

Prof. Dr. med. christoph f. Dietrich<br />

innere Medizin 2<br />

Uhlandstr. 7, D-97980 Bad Mergentheim<br />

telefon: 07931 / 58 2201, fax: 07931 / 58 2290<br />

E-mail: christoph.dietrich@ckbm.de<br />

Summary<br />

focal liver lesions are characterised sonographically not only by analysis of differences in echogenicity<br />

from the surrounding liver tissue, but also by the enhancement pattern of contrast media. as a result of<br />

the double blood supply of the liver via both the portal vein and the hepatic artery, focal lesions in the<br />

liver often exhibit no sustained hyper- or hypo perfusion, but depending on the perfusion phase and the<br />

histology, present with a complex spatio-temporal picture of increased and reduced contrast enhancement.<br />

conventional B-scan ultrasound makes it possible to characterize the frequently occurring typical<br />

liver cysts and calcifications by differences in echogenicity in comparison with the surrounding liver<br />

tissue. the characterisation of focal liver lesions by conventional B-mode ultrasound and colour Doppler<br />

imaging in an otherwise healthy person is sufficient in typical cases (about 70 %). contrast enhanced<br />

ultrasound (cEUs) has markedly improved the characterisation of liver lesions. certain lesions display<br />

a characteristic contrast enhancement pattern (e.g., wheel-spoke phenomenon of focal nodular hyperplasia<br />

[fnH]) or a distinctive perfusion pattern (e.g., iris diaphragm phenomenon [Haemangioma]),<br />

allowing the lesions to be characterised.<br />

Key words<br />

focal liver lesions, contrast enhanced ultrasound<br />

Introduction<br />

the EfsUMB-guidelines and recommendations 2008<br />

provide general advices for the use of Ucas to improve<br />

the management of patients. the initial EfsUMBguidelines<br />

have been published in 2004 and have been<br />

further discussed in other papers. individual patients<br />

must be managed in an individual fashion, therefore the<br />

present article and illustrations of focal liver lesions in<br />

the non-cirrhotic liver are intended to help in the decision<br />

making process. focal liver diseases have evolved<br />

into the single most important application of cEUs.<br />

this technique now equals contrast enhanced computed<br />

tomography (cEct) and in some instances exceeds<br />

it in accuracy. Due to the dual blood supply of liver tissue<br />

by the hepatic artery (25-30 %) and the portal vein<br />

(70-75 %), three overlapping vascular phases can be<br />

defined and visualized using contrast enhanced ultrasound<br />

which is helpful for liver tumour characterisation.<br />

18 ULTRASONOGRAFIA nr 34, 2008<br />

Differentiation of benign and malignant liver lesions<br />

Characterisation of a liver lesion starts once an<br />

abnormality is found. an imaging procedure that is used<br />

to detect liver masses should also enable the examiner<br />

to differentiate between benign and malignant lesions,<br />

since benign and malignant lesions have been reported<br />

to vary in their uptake during the portal venous phase<br />

[(1;2)]. the non-enhancing nature of malignant liver<br />

lesions is explained by the lack of liver specific tissue,<br />

e.g. portal veins, sinusoids and reticulo-endothelial cells<br />

[figure 1]. contrast enhanced ultrasound may discriminate<br />

between benign liver specific tissue and non-liver<br />

specific tissue-mainly malignant focal liver lesions in<br />

the portal venous and liver specific late phase in almost<br />

all patients [table 1-3] [(1)] if cysts and calcifications<br />

are excluded by conventional B-mode ultrasound. only

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