Liver - Original Article

Vol. 29 No. 4 (2018): 2018.29.4-Turkish Journal of Gastroenterology

The role of acoustic radiation force impulse elastography in the differentiation of benign and malignant focal liver masses

Main Article Content

Emin Akdoğan
Feyza Gelebek Yılmaz

Abstract

 
Background/Aims: The aim of this study was to evaluate elasticity of benign and malign focal liver lesions and surrounding parenchyma as measured by acoustic radiation force impulse (ARFI).
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Materials and Methods: 34 hemangiomas, 4 focal nodular hyperplasia (FNH), 10 hepatocellular carcinoma (HCC) and 22 metastatic lesions from a total of 62 patients were examined with ARFI elastography. ARFI measurements for each tumor type were expressed as mean ± standard deviation for liver mass and surrounding parenchyma. ARFI values were compared between tumor types and surrounding parencyhma.
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Results: The mean stiffness values were 2.15±0.73 m/s for hemangiomas (n=34), 3.22±0.18 m/s for FNH (n=4), 2.75±0.53 m/s for HCC (n=10) and 3.59±0.51 m/s for metastasis (n=22). Although there was not a significant difference between hemangiomas and HCC lesions in ARFI values (p>0.05), hemangiomas showed significantly different ARFI values from FNH and metastases (p<0.05). Also, there were significant differences in ARFI values between malignant and benign masses. The area under the receiver-operating characteristics curves for discriminating the malignant from benign liver masses was 0.826 (p<0.001). An ARFI value of 2.32 m/s was selected as cut-off value to differentiate malignant liver masses from benign ones (sensitivity: 0.93, specificity: 0.60).
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Conclusion: Although currently ARFI is not a definitive method for the primary diagnosis of focal solid liver lesions, it provides additional important information non-invasively for differential diagnosis.
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Cite this article as: Akdoğan E, Gelebek Yılmaz F. The role of acoustic radiation force impulse elastography in the differentiation of benign and malignant focal liver masses. Turk J Gastroenterol 2018; 29: 456-63.

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