Ch 4 TIRADS + Biopsies Flashcards

1
Q

What does TIRADS stand for?

A

Thyroid imaging reporting + data system

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2
Q

What is TIRADS?

A

-A 5 point classification system that uses u/s characteristics to determine the risk + suspicion for malignancy in thyroid nodules

-Developed TIRADS to help reduce the amount of biopsies being done

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3
Q

List the 5 TIRAD classifications?

A

TR 1: benign (no FNA, 0 points)
TR 2: not suspicious (no FNA, 2 points)
TR 3: mildly suspicious
(FNA if >2.5cm, follow up if >1.5cm, 3 points)
TR 4: moderately suspicious
(FNA if >1.5cm, follow up if >1cm, 4-6 points)
TR 5: highly suspicious - some exceptions here
(FNA if >1cm, follow up if >0.5cm, >7 points)

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4
Q

When would we not use TIRADS?

A

When a lesion is under 5mm or 0.5cm

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5
Q

What size must a lesion be to have a biopsy done?

A

> 1cm

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6
Q

What are the 4 composition options?

A

-Cystic or almost completely cystic (0 points)
-Spongiform (0)
-Mixed cystic + solid (1)
-Solid or almost completely solid (2)

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7
Q

If composition can’t be determined, which option do we choose?

A

Solid

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8
Q

What is spongiform composition?

A

When at least 50% of the nodule is comprised of tiny cysts

(if there are other features present like peripheral or macro calcs, do NOT classify as spongiform)

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9
Q

What are the 4 echogenicity options?

A

-Anechoic (0 points)
-Hyperechoic/isoechoic (1)
-Hypoechoic (2)
-Very hypoechoic (3)

(all echogenicity is compared to thyroid, except very hypoechoic is compared to surrounding neck muscles)

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10
Q

If the echogenicity can’t be determined, which option do we choose?

A

Isoechoic

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11
Q

What are the 2 shape options?

A

-Wider than tall (0 points)
-Taller than wide (3 points)

(measured in TRV)

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12
Q

What are the 4 margin options?

A

-smooth (0 points)
-ill defined (0)
-lobulated or irregular (2)
-extra thyroidal extension (3)

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13
Q

If the margin can’t be determined, which option do we choose?

A

ill-defined

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14
Q

What are the 4 echogenic foci options?

A

-None or large comet tail artifact (0 points)
-Macrocalcifications, large enough to produce shadowing (1)
-Peripheral rim calcifications (2)
-Punctate echogenic foci (3)

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15
Q

What defines a large comet tail?

A

When the tail is >1mm + is V shaped

(this is a non-suspicious finding)

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16
Q

Peripheral rim calcifications can be dense enough to obscure the internal components of the nodule, how would we describe the composition + echogenicity of it now?

A

Composition: solid
Echogenicity: isoechoic

17
Q

Do punctate echogenic foci have comet tails?

A

Foci <1mm sometimes can have a small comet tail

18
Q

Mixed cystic + solid lesions should be characterized by what?

A

The soft tissue component

19
Q

No further characterization is required for what type of nodule?

A

A spongiform nodule that is identified as TR 1

20
Q

What is a fine needle aspiration (FNA)?

A

-Cytological evaluation used to test for malignancy, confirm benignity or determine the nature of other lesions

-Considered minimally invasive
-Is an outpatient procedure
-Uses a smaller needle than a core biopsy

21
Q

What are complications with FNA?

A

-Risk of bleeding or infection (m/c)
-Voice hoarseness
-Seeding/spreading of cancer (rare)

22
Q

Does FNA or a core biopsy use a smaller needle?

A

FNA

23
Q

What is a core needle biopsy?

A

-Biopsy gun with a hollow core needle
-Obtains a larger amount of tissue
-Uses a larger needle than FNA
-Associated with more complications than FNA

(less repeat biopsies are needed b/c they are taking a greater sample, but this increases risk of complications)

24
Q

Explain how an u/s guided FNA procedure works?

A

-Sterile technique, local anesthetic + 25g needle used
-Same pt set up as for a thyroid u/s
-U/s guides the needle into the lesion of interest
-Multiple samples obtained from the lesion, placed into cytology fluid + sent to lab for testing

25
Q

What are limitations of an FNA?

A

-Inconclusive results or repeat biopsies needed (2/10)

-Lacks specificity for certain cancers (follicular carcinoma, hurthle cell carcinoma + lymphomas)

26
Q

How can we reduce the repeat rate of FNA’s?

A

-Can use u/s guidance
-By having an onsite tech to check the cells right away once they are drawn to ensure they will work for testing