» Articles » PMID: 20843994

Selective Atrophy of the Middle Hepatic Venous Drainage Area in Hepatitis C-related Cirrhotic Liver: Morphometric Study by Using Multidetector CT

Overview
Journal Radiology
Specialty Radiology
Date 2010 Sep 17
PMID 20843994
Citations 19
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: To retrospectively analyze the morphologic changes of hepatitis C-related cirrhosis, which commonly show macronodular cirrhosis, in relation to the portal venous supply and hepatic venous drainage, by using multidetector computed tomographic volumetry.

Materials And Methods: Institutional ethics committee approval and informed consent were obtained. The volume of the entire liver, each portal segment, and hepatic venous drainage area with the respective proportion relative to the entire liver and the volume of hepatic area with the respective proportion relative to the anterior segment of the right lobe were measured in 74 patients without cirrhosis and with normal liver function and in 64 patients with cirrhosis classified as Child-Pugh class A and in 68 with that classified as Child-Pugh class B. The diameter and length of each hepatic vein were measured in normal liver. All measurements were statistically analyzed by using the Kruskal-Wallis test, and multiple comparisons were made by using a Bonferroni correction (P < .05).

Results: The entire liver volume was significantly smaller in patients with Child-Pugh class B cirrhosis (P = .002), whereas there was no significant difference in volume between the normal liver and the liver with Child-Pugh class A cirrhosis (P > .99). Middle hepatic venous (MHV) drainage area revealed significant atrophy in cirrhosis (P < .0001), more markedly in Child-Pugh class B. The right hepatic venous (RHV) and left hepatic venous drainage areas showed significant hypertrophy in cirrhosis (P < .0001). The anterior and medial segments showed significant atrophy (P < .0001), and the lateral and posterior segments and caudate lobe showed significant hypertrophy in cirrhosis (P < .05). In the anterior segment, the MHV drainage area showed significant atrophy (P < .0001), and the RHV drainage area demonstrated relative hypertrophy in cirrhosis, more definitely in Child-Pugh class B. The diameter of MHV was significantly the smallest (P < .0001), and the length of MHV was relatively longer in normal livers.

Conclusion: The morphologic changes in hepatitis C-related cirrhosis (mainly macronodular cirrhosis) were attributed to a selective volume reduction of the MHV drainage area and relative enlargement of the other areas.

Citing Articles

Modeling Liver Fibrosis Progression in Patients With Viral Hepatitis Using the Machine Learning Tool Subtype and Stage Inference (SuStaIn).

Suzuki A, Sano K, Saito Y, Wijeratne P, Yamamoto K, Fujita S Cureus. 2025; 17(2):e78744.

PMID: 40065901 PMC: 11893182. DOI: 10.7759/cureus.78744.


Benefits of Liver Volume and Serum Zinc Level Assessment for the Screening of Covert Hepatic Encephalopathy in Patients with Child-Pugh Class A Cirrhosis.

Fukushima M, Miyaaki H, Sasaki R, Nakao Y, Haraguchi M, Takahashi K Diagnostics (Basel). 2025; 15(1.

PMID: 39795551 PMC: 11719456. DOI: 10.3390/diagnostics15010023.


An improved model based on quantitative features of right liver lobe, maximum varices, and portal vein system measured on magnetic resonance imaging to predict oesophagogastric variceal haemorrhage secondary to hepatitis B-related cirrhosis.

Tan B, Tang Z, Ou J, Zhou H, Li R, Chen T Quant Imaging Med Surg. 2023; 13(12):7741-7752.

PMID: 38106265 PMC: 10722043. DOI: 10.21037/qims-23-353.


L-distance ratio: a new distance ratio-based evaluation method for the diagnosis of cirrhosis using enhanced computed tomography.

Ye H, Wang Q, Huang H, Zhao K, Li P, Liu Z Quant Imaging Med Surg. 2023; 13(3):1499-1509.

PMID: 36915361 PMC: 10006107. DOI: 10.21037/qims-22-861.


Validation of 4D flow cardiovascular magnetic resonance in TIPS stent grafts using a 3D-printed flow phantom.

Riedel C, Ristow I, Lenz A, Schoennagel B, Hoffmann M, Piecha F J Cardiovasc Magn Reson. 2023; 25(1):9.

PMID: 36775827 PMC: 9923912. DOI: 10.1186/s12968-023-00920-5.