ADC similarity predicts microvascular invasion of bifocal hepatocellular carcinoma
Purpose This study aimed to investigate whether ADC similarity can predict microvascular invasion (MVI) in patients with bifocal hepatocellular carcinoma (HCC). Materials and Methods Between January 2015 and September 2015, 51 patients with two HCC lesions were included. All patients underwent conve...
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Published in | Abdominal imaging Vol. 43; no. 9; pp. 2295 - 2302 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.09.2018
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Purpose
This study aimed to investigate whether ADC similarity can predict microvascular invasion (MVI) in patients with bifocal hepatocellular carcinoma (HCC).
Materials and Methods
Between January 2015 and September 2015, 51 patients with two HCC lesions were included. All patients underwent conventional magnetic resonance imaging including diffusion-weighted imaging (DWI) before the HCC lesions were surgically resected; the tumor specimens were examined histopathologically. Similarity between two HCC lesions regarding DWI signal intensity (SI) and ADC value was calculated as the difference between the two lesions: Value Similarity = [1-(|value
large lesion
-value
small lesion
|)/(value
large lesion
+ value
small lesion
)] × 100%. Univariate and multivariate logistic regression analyses were performed to assess the presence of MVI.
Results
Risk factors significantly related to MVI of bifocal HCC in univariate analysis were cirrhosis (
P
= 0.010), histological grade (
P
= 0.040), DWI SI similarity (
P
= 0.027) and ADC similarity (
P
= 0.003). In multivariate analysis, cirrhosis (odds ratio 0.068,
P
= 0.022) and ADC similarity (odds ratio 1.204,
P
= 0.008) were independent risk factors for MVI of bifocal HCC.
Conclusion
In patients with two HCC lesions, highly similar ADC values for the two HCC lesions may be a preoperative predictor of MVI. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2366-004X 2366-0058 |
DOI: | 10.1007/s00261-018-1469-4 |