ScanFlo

Resources/Protocols

Liver / abdomen

A constantly moving target where the battle is against breathing and bowel motion, and the diagnosis lives in the timing. Multi-phase contrast catches lesions leaking dye — arterial wash-in, portal peak, delayed fill-in — so a consistent breath-hold and precise phase timing decide the exam.

Protocols/Abdomen

When this study is used

  • Characterising a focal liver lesion — cyst, haemangioma, HCC or metastasis.
  • Metastasis screening in known malignancy.
  • Biliary obstruction assessment (with MRCP).

Patient & coil positioning

  • Head-first supine, perfectly straight and centred; arms raised above the head to clear phase wrap over the liver edges.
  • Torso phased-array coil centred at the xiphoid process for full liver, diaphragm and upper-abdomen coverage.
  • Rehearse the breath-hold: 'breathe in, breathe out, hold' at gentle exhalation — exhalation gives a reproducible diaphragm position and standardises slice planning.

Localizer

Fast three-plane localizer in a single breath-hold. The coronal must show the whole liver from dome to the inferior tip of the right lobe, including both adrenals and the diaphragm.

Sequence planning

Each sequence below lists how the slice group is positioned — the reference line it follows, its coverage, and why it earns its place in the protocol. Plan against the localizer, not by eye.

Axial T2 fat-sat

Axial

Planning — Angle parallel to the dome of the liver, following the diaphragm's curve — not a flat axial block. Extend to include pancreas and kidneys.

Why — Fluid-content lesions (cysts, haemangiomas bright as 'light bulbs') versus solid lesions.

Axial DWI (b=50, 800) + ADC

Axial

Planning — Match the T2 coverage; free-breathing with several averages if breath-hold is unreliable.

Why — Restricted diffusion (bright DWI, dark ADC) as a hallmark of malignancy.

Axial T1 in/out-phase

Axial

Planning — Dual-echo in one breath-hold.

Why — Microscopic fat (adenoma, steatosis) or iron — the liver darkens out-of-phase.

Dynamic T1 fat-sat (multi-phase)

Axial

Planning — Same volume repeated across phases; time the arterial phase with a test bolus or fluoro-trigger.

Why — Arterial (~20–35 s) for hypervascular lesions, portal (~60–70 s) for hypovascular metastases, delayed (3–5 min) for haemangioma fill-in.

MRCP (thick + thin slab)

Coronal oblique

Planning — Heavily T2-weighted slab centred on the common bile duct, from intrahepatic ducts to the pancreatic head; MIP reconstruction.

Why — Non-contrast map of the biliary tree — stones, strictures.

Representative parameters

Ranges, not commandments — field strength, coil and vendor move the numbers. What must not move is understanding why each sits where it does.

SequenceBreathingNotes
T2 fat-satBreath-hold or triggeredDome-parallel; lesion signal
DWI (b=50, 800)Free-breathing, NEX 4–8Malignancy hallmark
T1 in/out-phaseSingle breath-holdFat/iron detection
Dynamic T1 FSBreath-hold per phaseArterial 20–35 s, portal 60–70 s, delayed 3–5 min
MRCPRespiratory-triggeredThick slab + 3D thin slab, MIP

Artifacts & how to fix them

ArtifactTypical causeMitigation
Breathing motionInconsistent breath-holdsRehearse; respiratory triggering; parallel imaging
Chemical shift (liver–kidney)Fat–water mismatch at interfacesRaise bandwidth; spectral fat-sat; swap phase
Poor fat-sat over the liverB0 inhomogeneity, bowel gasRe-shim on the right lobe; Dixon; STIR for non-contrast
Venous contamination (dynamic)Arterial phase mistimed lateTest bolus / fluoro-trigger for exact timing

What am I looking at?

You are not reporting the study, but recognising pathology helps you keep it in the field of view and know when to add a sequence or contrast. How the common findings read on the console:

FindingSequence to checkHow it reads
HCCDynamic T1 (arterial + delayed)Arterial enhancement then wash-out — darker than liver on delayed
HaemangiomaT2 FS + delayed T1Very bright 'light bulb' on T2; peripheral nodular delayed fill-in
MetastasisDWI + portal T1Restricts on DWI; hypovascular (dark) on portal phase
Fatty liverT1 in/out-phaseLiver darkens on the out-of-phase image

Review checklist

  • Whole liver covered dome to inferior tip on every phase.
  • Arterial phase caught at true wash-in, not late.
  • In/out-phase acquired at the same level for comparison.
  • MRCP MIP shows the biliary tree continuously (if acquired).

Mistakes that cost repeats

  • Inconsistent breath-holds smearing the dynamic series.
  • Arterial phase timed late, so hypervascular lesions are missed.
  • Flat axial block instead of dome-parallel, clipping the liver top.
  • Fat-sat shimmed on the whole abdomen rather than the right lobe.

Common questions

Why hold the breath at exhalation for liver MRI?
Exhalation puts the diaphragm in a consistent, reproducible position between breath-holds. That standardises slice planning and keeps the liver in the same place across the dynamic phases, which is essential for comparing enhancement.
Why is contrast timing so critical in the liver?
Lesions are characterised by how they enhance over time. HCC lights up in the arterial phase and washes out later; metastases are best seen in the portal phase; haemangiomas fill in on delayed images. Miss the timing and you miss the diagnosis.
What does the in/out-phase sequence show?
It detects microscopic fat or iron within tissue. On the out-of-phase image, tissue containing both fat and water loses signal — so a fatty liver or a fat-containing adenoma visibly darkens compared with the in-phase image.

Try it in ScanFlo: Run a dynamic series and step through the arterial, portal and delayed phases on the same slice. Watch a lesion enhance and then wash out — reading that time-course, not a single image, is how liver lesions are told apart.

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