Portal vein embolisation — the future liver remnant

CT

First and second year — the floor first, then every step

Measure the future liver remnant (FLR) volume as a percentage of the total functional liver on CT volumetry before and 3–6 weeks after portal vein embolisation; hypertrophy and the kinetic growth rate decide whether major hepatectomy can proceed.

Orient first

  • Thresholds: FLR ≥ 20–25% in a normal liver, ≥ 30% after chemotherapy, ≥ 40% in cirrhosis (verify the surgeons' thresholds).
  • Kinetic growth rate over about 2% per week predicts safety.
  • Portal anatomy variants (trifurcation, right posterior from the main portal vein) change the approach.

Acquire the study

  • Portal venous phase CT with thin sections for volumetry; repeat at 3–6 weeks after embolisation.

The manoeuvre

  • Portal venous anatomy on coronal reformats: bifurcation, trifurcation, segment IV supply.
  • Volumetry: FLR segments and total liver volume in mL, excluding tumour; FLR as % of total or of standardised liver volume.
  • After PVE: FLR volume in mL and %, degree of hypertrophy, kinetic growth rate per week.
  • Non-target embolisation into the FLR portal branches; tumour progression during the wait.
  • Complications: portal thrombosis, subcapsular haematoma.

What confirms it

  • FLR percentage and growth reported against the surgical threshold.

What licenses you to exclude it

  • Not applicable — a volumetric read.

The classic misread

  • Including tumour in the functional liver volume.
  • Missing embolic material in the FLR branches.

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