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Hepatic Venous Occlusion Type of Budd-Chiari Syndrome versus Pyrrolizidine Alkaloid-Induced Hepatic Sinusoidal
Yaru Tong1, Ming Zhang1, Zexue Qi2
1Department of Gastroenterology, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing 210008, China.
Insights
Budd-Chiari syndrome (BCS-HV) and pyrrolizidine alkaloid-induced hepatic sinusoidal obstructive syndrome (PA-HSOS) often present with similar symptoms. Key imaging differences include hepatic vein collateral circulation and caudate lobe enlargement in BCS-HV, which are absent in PA-HSOS.
Area of Science:
- Hepatology
- Radiology
- Internal Medicine
Background:
- Hepatic venous occlusion type of Budd-Chiari syndrome (BCS-HV) and pyrrolizidine alkaloid-induced hepatic sinusoidal obstructive syndrome (PA-HSOS) exhibit overlapping clinical and imaging features, increasing the risk of misdiagnosis.
- Accurate differentiation between BCS-HV and PA-HSOS is crucial for appropriate patient management and treatment strategies.
Purpose of the Study:
- To identify distinct clinical, laboratory, and imaging indicators for differentiating BCS-HV from PA-HSOS.
- To evaluate the diagnostic value of various imaging modalities, including Doppler ultrasonography (DUS), CT, and MRI, in distinguishing these two conditions.
Main Methods:
- Retrospective analysis of 139 patients with BCS-HV and 257 patients with PA-HSOS across six university-affiliated hospitals.
- Comparison of clinical manifestations, laboratory test results, and imaging features between the two patient groups.
- Detailed assessment of specific imaging findings such as hepatic vein occlusion, collateral circulation, caudate lobe enlargement, and early liver enhancement nodules.
Main Results:
- BCS-HV patients were younger on average than PA-HSOS patients (p < 0.05).
- Hepatic vein collateral circulation (73.90%), enlarged caudate lobe (47.70%), and early liver enhancement nodules (8.46%) were significantly more prevalent in BCS-HV compared to PA-HSOS (p < 0.05).
- Doppler ultrasonography (DUS) demonstrated higher sensitivity (86.29%) for detecting hepatic vein occlusion and collateral circulation in BCS-HV than CT or MRI (4.55%) (p < 0.001).
Conclusions:
- Hepatic vein stenosis and collateral circulation are key differentiating imaging features for BCS-HV, especially when PA-containing plant exposure is confirmed.
- Enhanced CT and MRI may overlook crucial imaging findings, potentially leading to misdiagnosis of BCS-HV as PA-HSOS.
- DUS is a valuable tool for identifying hepatic vein abnormalities in BCS-HV, aiding in accurate differential diagnosis.
Abstract:
(1) Background: Hepatic venous occlusion type of Budd-Chiari syndrome (BCS-HV) and pyrrolizidine alkaloid-induced hepatic sinusoidal obstructive syndrome (PA-HSOS), share similar clinical features, and imaging findings, leading to misdiagnoses; (2) Methods: We retrospectively analyzed 139 patients with BCS-HV and 257 with PA-HSOS admitted to six university-affiliated hospitals. We contrasted the two groups by clinical manifestations, laboratory tests, and imaging features for the most valuable distinguishing indicators.; (3) Results: The mean patient age in BCS-HV is younger than that in PA-HSOS (p < 0.05). In BCS-HV, the prevalence of hepatic vein collateral circulation of hepatic veins, enlarged caudate lobe of the liver, and early liver enhancement nodules were 73.90%, 47.70%, and 8.46%, respectively; none of the PA-HSOS patients exhibited these features (p < 0.05). DUS showed that 86.29% (107/124) of patients with BCS-HV showed occlusion of the hepatic vein, while CT or MRI showed that only 4.55%(5/110) patients had this manifestation (p < 0.001). Collateral circulation of hepatic veins was visible in 70.97% (88/124) of BCS-HV patients on DUS, while only 4.55% (5/110) were visible on CT or MRI (p < 0.001); (4) Conclusions: In addition to an established history of PA-containing plant exposure, local hepatic vein stenosis and the presence of collateral circulation of hepatic veins are the most important differential imaging features of these two diseases. However, these important imaging features may be missed by enhanced CT or MRI, leading to an incorrect diagnosis.
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