๐ Hepatocellular carcinoma (HCC) is the most common primary liver cancer, frequently arising in patients with cirrhosis. Biannual ultrasound ยฑ alpha-fetoprotein (AFP) screening is recommended in high-risk groups to allow diagnosis at an early stage when potentially curative therapies are feasible.
๐ About
- HCC is a leading cause of cancer deaths worldwide.
- Highest incidence: Southeast Asia & sub-Saharan Africa ๐.
- Not all cases arise in cirrhosis โ HBV can predispose directly via viral DNA integration.
โ ๏ธ Risk Factors
- Chronic hepatitis B or C infection ๐ฆ
- Alcoholic liver disease ๐บ
- Non-alcoholic steatohepatitis (NASH, metabolic syndrome link) ๐
- Haemochromatosis ๐ฉธ
- Aflatoxin B exposure (contaminated grains/nuts in endemic regions) ๐ฝ
- Primary biliary cholangitis (rare cause)
๐ฉบ Clinical Features
- Systemic: Weight loss, anorexia, fever, fatigue.
- Hepatic: Right upper quadrant pain, hepatomegaly, jaundice in late disease.
- Background of cirrhosis (ascites, varices, encephalopathy).
๐ Screening
- Surveillance: Ultrasound ยฑ AFP every 6 months for cirrhotics or HBV carriers at risk.
- Helps detect subclinical disease when resection/transplant is feasible.
๐งช Investigations
- Bloods: FBC, U&E, LFTs, coagulation, CRP.
- Tumour marker: Alpha-fetoprotein (AFP), though not diagnostic alone.
- Ultrasound: Initial modality to detect lesions.
- Triple-phase CT / MRI: Gold standard to confirm arterial enhancement & venous washout.
- Biopsy: Usually avoided due to seeding risk unless diagnosis uncertain.
๐ ๏ธ Management
- Resection: Best for solitary tumours with preserved liver function (Child-Pugh A, no portal hypertension).
- Liver Transplantation: For unresectable cases meeting Milan criteria (single tumour โค5 cm or โค3 tumours โค3 cm, no vascular invasion/metastases).
- Ablation (RFA/Microwave): Effective for small lesions; less so for large or deep tumours.
- Transarterial chemoembolisation (TACE): Used for multifocal disease without vascular invasion/extrahepatic spread.
- Systemic therapy: Sorafenib (tyrosine kinase inhibitor), Lenvatinib (non-inferior alternative), Regorafenib for progression. Newer immunotherapies (atezolizumab + bevacizumab) showing survival benefit ๐.
๐ References