Hepatic Neoplasms
Definition | Aetiology | Pathophysiology | Risk Factors | Signs and Symptoms | Investigations | Management | Referral
Definition
Hepatic neoplasms refer to tumours originating in or metastasising to the liver. These may be benign (e.g., haemangiomas, adenomas) or malignant (e.g., hepatocellular carcinoma, metastatic liver cancer).
Aetiology
- Primary hepatic neoplasms:
- Hepatocellular carcinoma (HCC): most common primary liver cancer.
- Cholangiocarcinoma: cancer of the bile ducts.
- Hepatic adenoma: benign tumour often linked to oestrogen use.
- Haemangioma: the most common benign liver tumour.
- Secondary (metastatic) liver tumours:
- Commonly from colorectal, breast, lung, or pancreatic cancers.
Pathophysiology
The mechanisms vary depending on the tumour type:
- Hepatocellular carcinoma (HCC): chronic inflammation and fibrosis (e.g., from hepatitis B/C or cirrhosis) lead to dysplasia and eventual malignant transformation.
- Metastatic liver tumours: spread occurs via haematogenous dissemination, typically through the portal vein.
Risk factors
- Chronic hepatitis B or C infection.
- Liver cirrhosis (e.g., from alcohol misuse or non-alcoholic fatty liver disease).
- Exposure to aflatoxins (common in developing countries).
- Metabolic conditions (e.g., haemochromatosis, alpha-1 antitrypsin deficiency).
- Use of oral contraceptives (associated with hepatic adenomas).
- Family history of liver cancer or related genetic conditions.
Signs and symptoms
Symptoms:
- Right upper quadrant pain or discomfort.
- Fatigue and malaise.
- Unexplained weight loss and anorexia.
- Jaundice (in advanced cases).
- Abdominal distension (due to ascites).
Signs:
- Palpable liver mass or hepatomegaly.
- Jaundice and scleral icterus.
- Signs of chronic liver disease (e.g., spider naevi, palmar erythema).
- Ascites (fluid accumulation in the peritoneal cavity).
Investigations
- Blood tests:
- Alpha-fetoprotein (AFP): elevated in HCC.
- Liver function tests (LFTs): may show raised bilirubin, ALP, and GGT.
- Clotting profile: prolonged in advanced liver disease.
- Imaging:
- Ultrasound: first-line for detecting liver masses.
- CT or MRI: for detailed characterisation and staging of lesions.
- Biopsy: only if imaging and clinical findings are inconclusive.
Management
1. Curative Options (if applicable):
- Surgical resection: indicated for resectable primary or solitary secondary tumours in patients with good liver function.
- Liver transplantation: for selected patients with small, unresectable HCC (e.g., meeting Milan criteria).
2. Localised Treatments (as per specialist):
- Ablative therapies: radiofrequency ablation (RFA) or microwave ablation (MWA) for small tumours.
- Transarterial therapies: transarterial chemoembolisation (TACE) or radioembolisation (TARE) for intermediate-stage HCC.
3. Systemic Therapy (as per specialist input):
- Targeted therapy: Sorafenib or lenvatinib for advanced HCC.
- Immunotherapy: Checkpoint inhibitors (e.g., atezolizumab) for selected cases.
- Chemotherapy: For metastatic liver tumours (e.g., colorectal metastases).
4. Palliative Care:
- Symptom control (e.g., pain management, relief of ascites).
- Management of complications (e.g., jaundice, encephalopathy).
Referral
- Urgent referral: if liver masses are detected on imaging or AFP is elevated.
- Specialist hepatology team: for further evaluation and management planning.
- Oncology referral: for systemic or palliative therapies.