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
DDx: Benign liver masses
- 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
- 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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