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Porto-sinusoidal vascular disease with portal hypertension versus liver cirrhosis: differences in imaging features on CT and hepatobiliary contrast-enhanced MRI

Authors
Kang, Ji HunKim, Do HyungKim, So YeonKang, Hyo JeongLee, Jung BokKim, Kyoung WonLee, Seung SooChoi, JonggiLim, Young-Suk
Issue Date
May-2021
Publisher
Springer Science and Business Media LLC
Keywords
Gadoxetate disodium; Liver cirrhosis; Magnetic resonance imaging; Portal hypertension; Porto-sinusoidal vascular disease
Citation
Abdominal Radiology, v.46, no.5, pp.1891 - 1903
Indexed
SCIE
SCOPUS
Journal Title
Abdominal Radiology
Volume
46
Number
5
Start Page
1891
End Page
1903
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/189647
DOI
10.1007/s00261-020-02831-w
ISSN
2366-004X
Abstract
Purpose: To differentiate the computed tomography (CT) and magnetic resonance imaging (MRI) features of porto-sinusoidal vascular disease (PSVD) and liver cirrhosis (LC). Methods: In this retrospective case–control study of patients with PSVD matched in a 1:3 ratio with LC patients according to liver function, initial diagnosis and time to final diagnosis were analyzed. Imaging features on CT and the parenchymal enhancement on hepatobiliary phase of hepatobiliary agent-enhanced MRI (HBA-MRI) were compared using a generalized linear mixed model. Focal hepatic lesions in the PSVD group were analyzed. Results: In total, 43 PSVD patients and 129 LC patients were included. Among PSVD patients, 72.1% were initially misdiagnosed with LC. PSVD patients had a longer diagnostic delay than LC patients (32 months vs. 4 months; p < 0.001). Liver surface nodularity was less common in the PSVD group than in the LC group (16.3% vs. 89.2%, p < 0.001). Increased caudate-to-right lobe ratio, heterogeneous parenchymal enhancement, and portal vein abnormalities were more frequently noted in the PSVD group than in the LC group (all p < 0.001). The grade of portal hypertension was significantly higher in the PSVD group than in the LC group (p < 0.001), and they also had brighter parenchymal enhancement during the hepatobiliary phase of HBA-MRI (p < 0.001). In the PSVD group, 14% patients had at least one focal hepatic lesion, primarily a focal nodular hyperplasia (FNH)-like nodule. Conclusions: Some imaging features on CT and HBA-MRI can distinguish PSVD from LC. Benign focal lesions, most commonly FNH-like nodules, can develop in PSVD.
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