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Typical and Atypical Imaging Findings of Intrahepatic Cholangiocarcinoma Using Gadolinium Ethoxybenzyl Diethylenetriamine Pentaacetic Acid-Enhanced Magnetic Resonance Imaging

Authors
Kim, So HeeLee, Chang HeeKim, Baek HuiKim, Wan BaeYeom, Suk KeuKim, Kyeong AhPark, Cheol Min
Issue Date
11월-2012
Publisher
LIPPINCOTT WILLIAMS & WILKINS
Keywords
gadoxetic acid; Gd-EOB-DTPA; cholangiocarcinoma; liver; MRI
Citation
JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY, v.36, no.6, pp.704 - 709
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY
Volume
36
Number
6
Start Page
704
End Page
709
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/107069
DOI
10.1097/RCT.0b013e3182706562
ISSN
0363-8715
Abstract
Purpose: The objective of this study was to examine the imaging features of classic mass-forming intrahepatic cholangiocarcinoma (MICC) and nonclassic hypervascular MICC on gadolinium ethoxybenzyl diethylenetriamine pentaacetic acid-enhanced magnetic resonance imaging. Methods: Twenty pathologically confirmed MICCs were included. Two radiologists retrospectively reviewed the imaging characteristics on T2-weighted imaging, diffusion-weighted imaging, dynamic contrast-enhanced images, and hepatobiliary phase (HBP) of each MICC. For the morphologic feature of defect, HBP signal intensity (SI) ratio was calculated by dividing the SI of the MICC by nearby normal liver parenchyma SI. Results: Classic MICCs (n = 14) showed classic rim or peripheral enhancement at arterial dominant phase with centripetal enhance in the delayed phases. Hypervascular MICCs (n = 6) showed complete (n = 4) or near-complete (n = 2) arterial enhancement and washout (n = 6) on delayed phases. On HBP, 13 classic MICCs (93%) and 2 hypervascular MICCs (33%) showed cloud-like SI in the center ("EOB cloud") with peripheral defect. Mean SI ratio was 0.77 in classic MICCs and 0.59 in hypervascular MICC (P = 0.057). Conclusions: Classic MICCs (70%) frequently showed progressive centripetal enhancement on dynamic phase, and central EOB-cloud appearance with distinct peripheral defect on HBP. Nonclassic hypervascular MICCs comprised 30% of the MICCs in this study. Compared with classic MICCs, hypervascular MICCs showed wash-in on arterial dominant phase and washout on delayed phase.
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