Imaging features facilitate diagnosis of porto-sinusoidal vascular disorder

被引:15
|
作者
Lampichler, Katharina [1 ]
Semmler, Georg [2 ,3 ,4 ]
Woeran, Katharina [5 ]
Simbrunner, Benedikt [2 ,3 ,4 ,6 ,7 ,8 ]
Jachs, Mathias [2 ,3 ,4 ]
Hartl, Lukas [2 ,3 ,4 ]
Bauer, David Josef Maria [2 ,3 ,4 ]
Balcar, Lorenz [2 ,3 ,4 ]
Burghart, Lukas [2 ,3 ,4 ]
Trauner, Michael [2 ,4 ]
Tamandl, Dietmar [1 ]
Ba-Ssalamah, Ahmed [1 ]
Mandorfer, Mattias [2 ,3 ,4 ]
Reiberger, Thomas [2 ,3 ,4 ,6 ,7 ,8 ]
Scheiner, Bernhard [2 ,3 ,4 ]
Scharitzer, Martina [1 ]
机构
[1] Med Univ Vienna, Dept Biomed Imaging & Image Guided Therapy, Vienna, Austria
[2] Med Univ Vienna, Dept Internal Med 3, Div Gastroenterol & Hepatol, Waehringer Guertel 18-20, A-1090 Vienna, Austria
[3] Med Univ Vienna, Dept Internal Med 3, Div Gastroenterol & Hepatol, Vienna Hepat Hemodynam Lab, Vienna, Austria
[4] Med Univ Vienna, Rare Liver Dis RALID Ctr, European Reference Network ERN RARE LIVER, Vienna, Austria
[5] Med Univ Vienna, Clin Inst Pathol, Vienna, Austria
[6] Med Univ Vienna, Christian Doppler Lab Portal Hypertens & Liver Fi, Vienna, Austria
[7] Ludwig Boltzmann Inst Rare & Undiagnosed Dis, Vienna, Austria
[8] Austrian Acad Sci, CeMM Res Ctr Mol Med Austrian, Vienna, Austria
关键词
Liver cirrhosis; Portal vein; Multiparametric magnetic resonance imaging; Contrast agent; TRANSIENT ELASTOGRAPHY; DISEASE; CT;
D O I
10.1007/s00330-022-09132-4
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Objectives Porto-sinusoidal vascular disorder (PSVD) is a recently defined vascular liver disease. Since diagnosis remains challenging, we aimed to evaluate radiological features that are distinct between PSVD and cirrhosis. Methods Clinical, laboratory, and radiological parameters (CT/MRI) of patients with histologically-confirmed PSVD vs. cirrhosis vs. non-cirrhotic parenchymal liver disease were retrospectively evaluated. Results Sixty-three PSVD, 155 cirrhosis, and 41 non-cirrhotic patients were included. As compared to cirrhosis, PSVD patients were younger and had lower HVPG, liver stiffness, and MELD. Routine clinical and imaging findings indicative of portal hypertension were similarly common. Intrahepatic portal tract abnormalities (49% vs. 15%; p < 0.001), FNH-like lesions (30% vs. 1%; p < 0.001), and abnormal liver morphology defined as peripheral parenchymal atrophy and compensatory hypertrophy of central segments (32% vs. 7%; p < 0.001) were significantly more common in PSVD patients. Hypertrophy of segment I (70% vs. 84%; p = 0.019), atrophy of segment IV (24% vs. 47%; p = 0.001), and nodular liver surface (22% vs. 89%; p < 0.001) were more common in patients with cirrhosis. In patients with gadoxetic acid-enhanced MRI, we identified the distinct imaging feature of "periportal hyperintensity" in the hepatobiliary phase (HBP) in 42% of patients with PSVD (14/33) vs. 1% in cirrhosis (1/95) vs. 0% in non-cirrhotic controls (0/41); p < 0.001). Conclusions Diagnosis of PSVD must be considered in younger patients presenting with clinical features of portal hypertension, portal tract abnormalities, and FNH-like lesions on CT/MRI. 'Periportal hyperintensity' in the HBP of gadoxetic acid-enhanced MRI was identified as a specific radiological feature of PSVD.
引用
收藏
页码:1422 / 1432
页数:11
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