Literature DB >> 25088350

Quantitative analysis of the dual-energy CT virtual spectral curve for focal liver lesions characterization.

Qi Wang1, Gaofeng Shi2, Xiaohui Qi3, Xueli Fan4, Lijia Wang5.   

Abstract

OBJECTIVE: To assess the usefulness of the spectral curve slope of dual-energy CT (DECT) for differentiating between hepatocellular carcinoma (HCC), hepatic metastasis, hemangioma (HH) and cysts.
METHODS: In total, 121 patients were imaged in the portal venous phase using dual-energy mode. Of these patients, 23 patients had HH, 28 patients had HCC, 40 patients had metastases and 30 patients had simple cysts. The spectral curves of the hepatic lesions were derived from the 40-190 keV levels of virtual monochromatic spectral imaging. The spectral curve slopes were calculated from 40 to 110 keV. The slopes were compared using the Kruskal-Wallis test. Receiver operating characteristic curves (ROC) were used to determine the optimal cut-off value of the slope of the spectral curve to differentiate between the lesions.
RESULTS: The spectral curves of the four lesion types had different baseline levels. The HH baseline level was the highest followed by HCC, metastases and cysts. The slopes of the spectral curves of HH, HCC, metastases and cysts were 3.81 ± 1.19, 1.49 ± 0.57, 1.06 ± 0.76 and 0.13 ± 0.17, respectively. These values were significantly different (P<0.008). Based on ROC analysis, the respective diagnostic sensitivity and specificity were 87% and 100% for hemangioma (cut-off value ≥ 2.988), 82.1% and 65.9% for HCC (cut-off value 1.167-2.998), 65.9% and 59% for metastasis (cut-off value 0.133-1.167) and 44.4% and 100% for cysts (cut-off value ≤ 0.133).
CONCLUSION: Quantitative analysis of the DECT spectral curve in the portal venous phase can be used to determine whether tumors are benign or malignant.
Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Dual-energy computed tomography; Focal liver lesions; Quantitative analysis; Spectral curve

Mesh:

Substances:

Year:  2014        PMID: 25088350     DOI: 10.1016/j.ejrad.2014.07.009

Source DB:  PubMed          Journal:  Eur J Radiol        ISSN: 0720-048X            Impact factor:   3.528


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