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Diagnostic Ultrasound - Abdomen and Pelvis

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Hepatocellular Carcinoma<br />

TERMINOLOGY<br />

Abbreviations<br />

• Hepatocellular carcinoma (HCC)<br />

Definitions<br />

• Malignant neoplasm originating from hepatocytes<br />

IMAGING<br />

General Features<br />

• Best diagnostic clue<br />

○ Solid, intrahepatic mass > 1 cmin patient with risk factors<br />

such as chronic hepatitis or cirrhosis<br />

○ Portal vein or hepatic vein tumor invasion highly<br />

suggestive of HCC<br />

• Size<br />

○ Small or large: < 3 cm to> 5 cm<br />

○ Diffuse or infiltrative: Subcentimeter to > 5 cm<br />

• Key concepts<br />

○ Most frequent primary visceral malignancy globally<br />

– Accounts for 80-90% of all adult primary liver<br />

malignancies<br />

– Usually arises in cirrhotic liver, due to chronic viral<br />

hepatitis (HBV, HCV) or alcoholism<br />

○ 2nd most common malignant liver tumor after<br />

hepatoblastoma in children<br />

○ Growth patterns of HCC: 3 major types<br />

– Solitary, often large mass<br />

– Multinodular or multifocal<br />

– Diffuse or infiltrative<br />

○ Metastases to lung, bone, adrenal, lymph node<br />

Ultrasonographic Findings<br />

• Grayscale ultrasound<br />

○ Hypoechoic: Most common sonographic appearance<br />

– Solid tumor<br />

– May be surrounded by thin, hypoechoic halo (capsule)<br />

○ Hyperechoic<br />

– Indicates fatty metamorphosis/hypervascularity<br />

– Simulates hemangioma/focal steatosis<br />

□ If risk factors are present <strong>and</strong> hyperechoic lesion > 1<br />

cm detected, cannot assume hemangioma<br />

○ Mixed echogenicity: More common in larger HCC<br />

– Indicates tumor necrosis/fibrosis<br />

– Focal fat in some HCCs appear echogenic<br />

○ Background cirrhosis (except for fibrolamellar HCC <strong>and</strong><br />

hepatitis B)<br />

○ Calcification is rare unless treated<br />

○ Invasion of portal vein & less commonly hepatic vein<br />

highly suggestive of HCC<br />

○ Hemoperitoneum if subcapsular or exophytic HCC<br />

ruptures<br />

○ Associated signs of portal hypertension: Ascites,<br />

splenomegaly, portosystemic collaterals<br />

○ Fibrolamellar carcinoma<br />

– Rare, < 1% of all cases of primary liver cancer<br />

– Well-defined partially/completely encapsulated mass<br />

– Prominent central fibrous scar often with calcification<br />

– Intralesional necrosis/hemorrhage<br />

– Regional adenopathy <strong>and</strong> metastases to lung <strong>and</strong><br />

peritoneum<br />

– Typically without chronic liver disease<br />

– AFP usually negative or mildly elevated<br />

• Pulsed Doppler<br />

○ Arterial feeding vessels with low-resistance waveforms<br />

indicate tumor vessels<br />

○ Tumor thrombus with arterial neovascularity<br />

• Color Doppler<br />

○ Irregular hypervascularity within neoplasm<br />

○ Tumor thrombus, typically in portal vein, with<br />

neovascularity<br />

CT Findings<br />

• NECT<br />

○ Iso- or hypodense liver mass, occasionally fat content<br />

detected<br />

– Characterization of lesion not possible on NECT<br />

• CECT<br />

○ Characterization <strong>and</strong> diagnosis of HCC can be made with<br />

triphasic CT: Late arterial, portal venous,<br />

delayed/equilibrium phase<br />

– Late arterial phase: Hyperenhancing compared to<br />

background liver<br />

– Portal venous phase: Variable enhancement, may be<br />

iso-, hypo-, or hyperdense compared to background<br />

liver<br />

– Delayed or equilibrium phase (3-5 min after contrast<br />

injection): "Washout" is characteristic of HCC; lesion<br />

hypodense compared to liver<br />

□ May see delayed enhancing pseudocapsule<br />

MR Findings<br />

• T1WI<br />

○ Typically hypointense compared to background liver but<br />

may be iso- or hyperintense depending on fat content or<br />

necrosis<br />

• T2WI<br />

○ Typically slightly hyperintense, similar intensity to spleen<br />

• T1WI C+<br />

○ Late arterial phase: Hyperenhancing compared to<br />

background liver<br />

○ Portal venous phase: Variable but typically hypointense<br />

○ Delayed or equilibrium phase: "Washout" is characteristic<br />

of HCC with lesion hypointense to background liver<br />

– Hyperintense pseudocapsule typically best seen on<br />

delayed or portal venous phase images<br />

○ Hepatobiliary contrast (gadoxetate, Eovist, Primovist):<br />

Uptake in hepatocytes related to OATP8 receptor, downregulated<br />

in most HCC, up-regulated in focal nodular<br />

hyperplasia (FNH)<br />

– Pitfall: Up to 10% of HCC can be isointense or<br />

hyperintense on hepatobiliary phase<br />

Angiographic Findings<br />

• Hypervascular tumor<br />

○ Marked neovascularity <strong>and</strong> AV shunting<br />

○ Large hepatic artery <strong>and</strong> vascular invasion<br />

○ "Threads <strong>and</strong> streaks" sign in portal vein tumor thrombus<br />

Nuclear Medicine Findings<br />

• Hepatobiliary scan: Uptake in 50%<br />

http://radiologyebook.com/<br />

Diagnoses: Liver<br />

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