Hepatocellular carcinoma

Case contributed by Naim Qaqish , 15 Mar 2021
Diagnosis certain
Changed by Mostafa Elfeky, 17 Mar 2021

Updates to Case Attributes

Presentation was changed:
Elevated AFP more than 400 ng/mL, suspected HCC.
Body was changed:

Hepatomas, present a hypervascular tumor. Charestrictsic early vivid enhancement (mainly during late arterial phase) and early washout (portal and later phases) to become indistinct or hypodense relative to adjacent hepatic parenchyma. Multiphase CT with a late arterial phase is essential as many lesions are only visible during the arterial phase.

Some lesions may show a ‘mosaic’ pattern of enhancement on CT with an enhancing grid-like pattern as well as later rim enhancement. 

Any enhancing lesion in a cirrhotic background of the liver is considered hepatoma until proven otherwise.

Large lesions may demonstrate vascular invasive features, undergo hemorrhage, and contain areas of fat, thrombosis, and necrosis.

Any new solid lesion on US hyperechoic/hypoechoic in relation to adjacent parenchyma in a high-risk patient is considered a potential HCC. Large lesions may show internal heterogeneity, due to hemorrhage, necrosis, or fat and often cause portal vein thrombosis or tumor thrombus, which can expand the vein. High-velocity Doppler signals from within the lesion occur in the majority of cases as a result of arterioportal shunting. 

The patient underwent resection of the left  lobelobe and gallbladder. Tissue specimen of the lesion confirmed moderately differentiated HCC with lymphovascular invasion. No pathological changes of gallbladder.

  • -<p><a href="/articles/hepatocellular-carcinoma">Hepatomas</a>, present a hypervascular tumor. Charestrictsic early vivid enhancement (mainly during late arterial phase) and early washout (portal and later phases) to become indistinct or hypodense relative to adjacent hepatic parenchyma. Multiphase CT with a late arterial phase is essential as many lesions are only visible during the arterial phase.</p><p>Some lesions may show a ‘mosaic’ pattern of enhancement on CT with an enhancing grid-like pattern as well as later rim enhancement. </p><p>Any enhancing lesion in a <a href="/articles/cirrhosis">cirrhotic</a> background of the liver is considered <a href="/articles/hepatocellular-carcinoma">hepatoma</a> until proven otherwise.</p><p>Large lesions may demonstrate vascular invasive features, undergo hemorrhage, and contain areas of fat, thrombosis, and necrosis.</p><p>Any new solid lesion on US hyperechoic/hypoechoic in relation to adjacent parenchyma in a high-risk patient is considered a potential <a href="/articles/hepatocellular-carcinoma">HCC</a>. Large lesions may show internal heterogeneity, due to hemorrhage, necrosis, or fat and often cause portal vein thrombosis or tumor thrombus, which can expand the vein. High-velocity Doppler signals from within the lesion occur in the majority of cases as a result of arterioportal shunting. </p><p>The patient underwent resection of the left  lobe and gallbladder. Tissue specimen of the lesion confirmed moderately differentiated <a href="/articles/hepatocellular-carcinoma">HCC</a> with lymphovascular invasion. No pathological changes of gallbladder.</p>
  • +<p><a href="/articles/hepatocellular-carcinoma">Hepatomas</a>, present a hypervascular tumor. Charestrictsic early vivid enhancement (mainly during late arterial phase) and early washout (portal and later phases) to become indistinct or hypodense relative to adjacent hepatic parenchyma. Multiphase CT with a late arterial phase is essential as many lesions are only visible during the arterial phase.</p><p>Some lesions may show a ‘mosaic’ pattern of enhancement on CT with an enhancing grid-like pattern as well as later rim enhancement. </p><p>Any enhancing lesion in a <a href="/articles/cirrhosis">cirrhotic</a> background of the liver is considered <a href="/articles/hepatocellular-carcinoma">hepatoma</a> until proven otherwise.</p><p>Large lesions may demonstrate vascular invasive features, undergo hemorrhage, and contain areas of fat, thrombosis, and necrosis.</p><p>Any new solid lesion on US hyperechoic/hypoechoic in relation to adjacent parenchyma in a high-risk patient is considered a potential <a href="/articles/hepatocellular-carcinoma">HCC</a>. Large lesions may show internal heterogeneity, due to hemorrhage, necrosis, or fat and often cause portal vein thrombosis or tumor thrombus, which can expand the vein. High-velocity Doppler signals from within the lesion occur in the majority of cases as a result of arterioportal shunting. </p><p>The patient underwent resection of the left lobe and gallbladder. Tissue specimen of the lesion confirmed moderately differentiated <a href="/articles/hepatocellular-carcinoma">HCC</a> with lymphovascular invasion. No pathological changes of gallbladder.</p>

References changed:

  • Adam A, et al. Grainger & Allison's Diagnostic Radiology E-Book. (2014): 745-747 <a href="https://books.google.co.uk/books?vid=ISBN9780702061288">ISBN: 9780702061288</a><span class="ref_v4"></span>
  • Adam A, et al. Grainger & Allison's Diagnostic Radiology: A Textbook of Medical Imaging, 6th edn. Churchill Livingstone, 2015: 745-747

Systems changed:

  • Hepatobiliary

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