Interactive Transcript
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Now let's focus on selecting the
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appropriate target for biopsy.
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So which lesion or which part
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of a lesion should be biopsied?
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Here's some general guidelines you wanna biopsy the most
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suspicious area.
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So it is a very heterogeneous lesion, uh,
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particularly if it's a mixed, solid or cystic lesion.
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You wanna get the solid portion if it is a lesion
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that appears necrotic.
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Make sure you get the wall.
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You don't want to get just necrotic debris.
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If you're biopsying a cyst, you wanna get the wall of it.
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Again, generally if there are multiple suspicious masses,
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you biopsy all of them, but usually not more than three.
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Um, be very, very careful to differentiate
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between these different lesions
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and use different clips for each lesion.
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If you've got three
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or more lesions, you may want
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to just biopsy the most suspicious or the most distance.
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So if you have a lesion in the upper inner quadrant
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of the breast and multiple other lesions in the upper inner
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quadrant, but also one in the lower outer quadrant,
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you're gonna want to make sure that you have
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that lower outer quadrant lesion biopsy
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as this is really going to affect surgical decision making.
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If you have a satellite lesion, you do not need
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to biopsy that separately.
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Just to confirm the standard nomenclature
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multifocal lesions.
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So when there's more than one lesion within one quadrant
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of the breast multicentric when there's more than one lesion
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within different quadrants of the breast.
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And that differentiation used to be more important
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as multicentric disease used
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to mean the patient was always recommended for a mastectomy
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that's no longer true.
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Uh, patients with multiple lesions, multiple multicentric
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or multifocal lesions may frequently end up now
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having multiple lumpectomies.
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Now, a satellite lesion is different.
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That is when there are additional lesions which are two
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centimeters or less.
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And these don't need to be separately biopsied, as I said,
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they'll be excised at the time, a lumpectomy
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and they won't change the staging or other treatment.
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Now, it is super important for patients
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who have multiple lesions for the clinical management
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that you have strict and consistent name ring.
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Um, I'm gonna give you how we name ours.
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Uh, you can do something similar,
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but as long as you're consistent
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and is very clear, which lesion is which,
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and this same naming convention should be continued
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through further imaging such as MRI, surgical management,
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pathology and so on.
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Do not change lesion one to be lesion two
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at some point during the workup.
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That gets very confusing.
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Um, and I found that our surgeons really
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like this consistency.
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So the way that we name it is,
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we name it separate for each breast.
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So we have right lesion
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One, lesion two, lesion three, and so on.
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And then we would have left lesion one, lesion two,
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and lesion three and so on.
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And for each lesion we have its size.
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What type of lesion is I? Is it a mass?
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Is it a non mass lesion, et cetera,
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radian or clock face?
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And how many centimeters from the nipple?
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So for example, right lesion one, 1.2 centimeter mass,
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12 o'clock four centimeters from the nipple, right lesion,
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two three centimeter calcifications,
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two o'clock five centimeters in the nipple left lesion,
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one 2.3 centimeter nomas lesion, five o'clock,
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two centimeters, the nipple and so on.
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When you're choosing your lesions to biopsy
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and certainly right
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before you do a biopsy, always check for flow.
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Using color doppler, obviously you want
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to avoid large vessels.
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This may affect what lesion you biopsy.
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It may affect or angle you come at them.
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Um, especially those big ones in the ax are good to avoid.
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And sometimes if it's a very vascular lesion, you might want
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to add epinephrine, especially if the patient is on any form
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of antithrombotic therapy.
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And on occasions you might want to reduce the needle size,
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for example, from a 14 gauge to an 18 gauge.
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So just a reminder that the blood flow
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to lesions in the breast can be very affected
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by your transducer pressure.
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Um, this is particularly important with superficial lesions.
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Papillo is the classic example because there's soft tumors
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and you can see here how this papillo,
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there is color flow on both these images,
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but you don't see any flow whatsoever
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where the pressure is being applied
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by the transducer in the left hand image.
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But when you release that pressure suddenly pop,
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that color flow comes back in.
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So just always remember to put minimal pressure on, um,
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before you exclude flow.