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Related Subjects: |Chronic liver disease |Cirrhosis |Alkaline phosphatase (ALP) |Liver Function Tests |Ascites Assessment and Management |Budd-Chiari syndrome |Autoimmune Hepatitis |Primary Biliary Cirrhosis |Primary Sclerosing Cholangitis |Wilson disease |Hereditary Haemochromatosis |Alpha-1 Antitrypsin (AAT) deficiency |Non alcoholic steatohepatitis (NASH) |Spontaneous Bacterial Peritonitis |Alcoholism and Alcoholic Liver Disease |Hepatitis C
🩺 Liver Abscess = a pus-filled cavity in the liver parenchyma. ⚡ Pathophysiology: hepatocyte injury → local inflammation → neutrophilic infiltration → liquefaction → abscess formation. Remember: Klebsiella pneumoniae abscesses may disseminate to the eye causing endophthalmitis 👁️.
| Cause | Clinical Features | Diagnosis | Initial Treatment (UK, NICE-aligned) |
|---|---|---|---|
| Pyogenic | Fever, rigors, RUQ pain ± shoulder tip pain, jaundice, hepatomegaly, malaise, weight loss | USS/CT, blood cultures, aspiration & microbiology | IV broad-spectrum antibiotics (adjust per culture), image-guided drainage; surgery if refractory |
| Amoebic | Gradual fever, RUQ pain, ± diarrhoea, weight loss | USS (often single right lobe), serology (anti-amoebic IgG), aspiration if diagnosis unclear | Metronidazole → luminal agent (e.g., diloxanide furoate); drain only if large/persistent |
| Fungal | Fever, RUQ pain, weight loss; immunocompromised | CT (multiple abscesses), blood culture, biopsy | Systemic antifungals (amphotericin B, fluconazole); drainage if large |
| Echinococcus | Often asymptomatic; cyst rupture → anaphylaxis, urticaria, shock | USS/CT, serology (ELISA, WB), PCR if difficult | Surgical resection if feasible; otherwise PAIR (puncture, aspiration, injection ethanol, re-aspiration) + albendazole |
💡 Teaching tip: Always consider source of infection (biliary, portal, systemic), assess for immunosuppression, and monitor for sepsis. Early imaging and culture-guided therapy improve outcomes. Referral to hepatology or infectious disease recommended for complex cases.