Hepatocellular Carcinoma

 

  • Background

    Pathophysiology

    • HCC accounts for 90% of primary hepatobiliary cancers. Most of the others are cholangiocarcinoma.
    • Characterised by aggressive angiogenesis.
    • Most liver tumours are in fact secondary.

    Causes and risk factors

    • NAFLD is overtaking ALD as the commonest cause.
    • Viral hepatitis is a major worldwide cause. HBV vaccination reduces this.
    • Diabetes is an independent risk factor.
  • Presentation

    Symptoms of chronic liver disease or acute decompensation, the latter being a bad prognostic sign.

  • DDx: Benign liver masses

    Tumours:

    • Haemangioma: commonest. Hyperechoic on US.
    • Focal nodular hyperplasia: 2nd commonest. Affects young to middle age, women > men.
    • Hepatic adenoma: linked to contraceptive pill. Hypodense on CT.
    • Mesenchymal hamartoma: congenital.

    Cysts and abscesses:

    • Simply cyst: congenital.
    • Abscess: can be pyogenic (linked to abdominal infection) or amoebic.
    • Hydatid cyst: Echinococcus infection. Large, thick walled cyst with septa.
  • Investigations

    If liver US shows nodules:

    • Nodules <1 cm → repeat US in 6 months.
    • Nodules >1 cm → CT or MRI → biopsy if radiological findings not definitive (but beware seeding).

    Alpha fetoprotein (AFP):

    • Only 50% sensitive, and usually just in later disease.
    • Used in combination with US for HCC monitoring in cirrhosis.
  • Management

    • Surgical resection is 1st line for solitary tumours <5 cm in patients with good liver function.
    • Transplantation if unresectable (usually due to poor liver function) and Milan criteria are met: 1 lesion ≤5 cm or 2-3 lesions ≤3 cm, and no extrahepatic or vascular disease.
    • Radiofrequency ablation is an alternative to surgery for localized but unresectable disease. May be curative, especially for small tumours.
    • Trans-arterial chemo-embolization (TACE) is a non-curative treatment for larger tumours >5 cm. Also used as bridge to transplant.
    • Chemotherapy with sorafenib for advanced disease.
  • Prognosis

    • 50% detected too late for any treatment.
    • 5 year survival: 10%.

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