Imaging the breast Flashcards

1
Q

When is imaging of the breast indicated?

A

Symptomatic patients:
¥ Lumps
¥ Unilateral or blood-stained nipple discharge
¥ Skin tethering or dimpling
¥ Signs of inflammation
¥ Axillary lumps
¥ NOT for pain; tenderness; symetrical nodularity!

Screening

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2
Q

What is mammography?

A

¥ A low dose xray designed specifically to maximise contrast between the breast tissues, whilst minimising radiation dose

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3
Q

What are the BIRADS parenchymal patterns seen on mammography

A

¥ a: nearly all fat
¥ b: scattered fibroglandular densities (25-50%)
¥ c: heterogeneously dense (51-75% glandular)
¥ d: extremely dense (> 75% glandular)

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4
Q

What are features of malignant calcification?

A

¥ Distribution - cluster or segmental vs. scattered or diffuse
¥ Cluster shape/size - rhomboid forms
¥ Individual particle shape -linear/branching/Y shaped forms
¥ Pleomorphic nature - size/density

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5
Q

How is a calcification assessed?

A
¥	Mammography  
¥	microfocus magnification - ML, mag cc and lat      
¥	tangential views (skin calcifications)
¥	digital manipulation - contrast, zoom 
¥	Ultrasound 
¥	MRI?? – not if you can biopsy it!
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6
Q

When is USS indicated?

A

¥ Characterisation of mammographic findings - differentiation of cystic and solid lesions
¥ Palpable lesions, women < 40y
¥ Nipple Discharge
¥ Breast Implants or augmentation
¥ Other - inflammatory conditions (abscesses)
¥ Evaluation of response to chemotherapy

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7
Q

What do cystic lesions look like on USS?

A

¥ Cysts: fluid collections
¥ Shape, contents, internal echoes
¥ Clustered cysts
¥ Complex cysts

can use US guided aspiration

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8
Q

What do benign solid nodules look like on USS?

A
¥	Circumscribed
¥	Hypoechoic/hyperechoic
¥	“Wider than Tall”
¥	Homogeneous
¥	Peripheral/no vascularity
¥	Often Multiple
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9
Q

What do malignant solid nodules look like on USS?

A
¥	Poorly Circumscribed
¥	Hypoechoic
¥	Heterogeneous
¥	“taller than wide”
¥	Spiculate
¥	Oedema/peritumoral fat (blurriness surrounding it)
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10
Q

What is elastography?

A
this is a new US technique based on tissue compression indicating how ‘stiff’ a tissue is.
¥	MRI based elastography
¥	US based elastography:
¥	sonoelasticity (vibration)
¥	single/multi-step compression
¥	compression devices
¥	freehand method 
¥	shear wave elastography
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11
Q

What is a vacuum assisted biopsy?

A

use device to create vacuum and suck up biopsy with help of USS

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12
Q

Why is MRI breast needed?

A

• Mammography has limitations:
o sensitivity in dense breasts ( 55%)
o Limited contrast inherent in technique- up to 15% ca’s mammographically occult
o Observer limitations
o High % indeterminate lesions needing biopsy
o Compression, irradiation

•	US has limitations:
o	Operator-dependent
o	Time-consuming
o	Reproducibility
o	Misses calcifications
o	Unproven in screening - false positives and negatives
•	MRI:
o	Excellent intrinsic tissue contrast
o	Multiplanar tomographic capacity
o	No compression
o	No ionising radiation
o	Accuracy independent of breast density
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13
Q

When is MRI used in breast ?

A

Malignant disease: postcontrast scans
¥ i.v gadolinium based contrast
¥ Rapid dynamic imaging of entire breast

Accuracy:
morphological pattern – can see shape temporal pattern - can see how the contrast moves in time

Look for enhancement and neovascularity:

  • More enhancement in malignancy
  • More neovascularity = correlation with tumour grade and risk of met.s
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14
Q

Contraindications to MRI breast

A

¥ Absolute – as for any other MR exam
(cardiac pacemakers, ferromagnetic aneurysm clips, cochlear implants, renal impairment etc.)
¥ Relative – pregnancy, lactation
(effect of gadolinium based contrast, increased background breast enhancement)

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15
Q

Indications for breast MRI

A

Benign disease:
¥ implants (integrity) – gold standard for implants
¥ problem solving (lesion characterisation)

Malignant disease: 
¥	diagnosis (occult 1° breast cancer)
¥	staging and treatment planning
¥	residual disease post WLE
¥	response assessment - chemotherapy
¥	recurrent disease – breast, reconstructed breast, axilla

screening – high risk groups (genetic) annually
¥ 30-49 yrs with >30% probability of BRCA
¥ 30-49 yrs with known BRCA
¥ 20-49 yrs with >30% probability of TP53
¥ 20-49 yrs with known TP53 mutation

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