Section: Hepatobiliary Sub-section: Liver Curriculum: Curriculum, page 86

Definition

Benign epithelial tumour comprised of hyperplastic hepatocytes

Epidemiology

  • 2nd most common benign solid liver tumour.
  • Prevalance 0.2%.
  • Mostly female
  • 20-40yrs.

Risk factors

  • Treatment for childhood cancer w haematopoietic stem cell transplantation
  • ?female hormones
  • No clear relationship with OCP

Aetiology/Pathology

  • Injury to the portal tract
  • Results in enlargement of arterial venous shunts
  • Causes hyperperfusion in local arteries resulting in oxidative stress that triggers a response from hepatic stellate cells to produce the typical central scar

Pathology

  • Lobulated lesion composed of nodules surrounded by fibrous septa originating from central scar.
  •  On histological analysis, a classic FNH shows nodular hyperplastic parenchyma
  • Development of FNH thought to be caused by injury to portal tract resulting in formation and enlargement of arterial to venous shunts.
  • This causes hyperperfusion in local arteries resulting in oxidative stress triggering hepatic stellate cells to produce typical central scar.

Clinical

  • Asymptomatic, incidental.
  • Some have abdominal pain or palpable mass.
  • Complications such as rupture causing intraperitoneal haemorrhage are rare.

Investigations

  • USS
    • Iso-echoic with central scar. Poorly able to differentiate
  • CT
    • Pre con: hypo or Iso
    • Arterial: Homogenous and rapid diffuse centrifugal filling, central scar nonenhanced
    • PV: slightly hyperattenuating or isoattenuating to liver and poorly visualised in many studies, the central scar remains hypodense.
    • Delayed: hyperattentuation of central scar and septae.
  • MRI
    • T1 iso or hypo, hypointense central scar
    • T2 hyperintense central scar
    • Arterial - homogeneous enhancement

Management and follow up

  • Usually dx on MRI or CT. Not routine biopsy unless uncertain dx.
  • FNH not premalignant.

Unclear diagnosis

  • Follow up imaging +/- biopsy

Asymptomatic

  • No treatment
  • No follow up

Symptomatic

  • Further evaluation

If women on OCP

  • f/u w annual USS 2-3 years in women on OCP.