Differentiated Thyroid Cancer Flashcards

1
Q

Some epidemiological facts regarding papillary thyroid cancer
(risk factors, prognosis)

A
  • 70-80% of thyroid carcinomas
  • peak incidence 30s-40s
  • most important risk factor = childhood radiation exposure
  • other risk factors: family history, Werner/Cowden syndrome, Carney complex, familial polyposis
  • 95% ten year survival rate
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2
Q

Papillary thyroid cancer- histological appearance (pathognomonic signs)

A

calcifications
psammoma bodies (concentric lamellated calcific structures)
squamous metaplasia & fibrosis

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3
Q

Histological variants of PTC?

A
classical PTC
follicular PTC
tall cell
columnar 
hobnail (tends to occur in older patients, prognosis less favourable)
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4
Q

What % of people with PTC have lymphatic mets? What are the two most common sites of lymphatic mets?

A

30-40% of people
3-5% metastatic at time of diagnosis
lungs and bones are two most common sites

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5
Q

Is lymphadenectomy routinely performed for PTC?

A

Nope

Intra-operatively checking for suspicious LN- then can take out if suspicious

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6
Q

What is the most common genetic mutation seen in PTC?

A

BRAF V600E

V= valine
E= glutamic acid

20% of patients with PTC have RET proto-oncogene

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7
Q

What other conditions is RET proto-oncogene associated with?

A

pheochromocytoma, FMTC, Hirschsprung’s disease

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8
Q

According to 2015 ATA guidelines, what are the recommendations for surgery based on size of tumour?

A

> 4 cm: total thyroidectomy
1-4 cm: total thyroid vs lobectomy
<1 cm: observe unless there are high risk features (extrathyroidal extension, lymphatic mets, etc)

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9
Q

What is a thyroid microcarcinoma?

A

papillary thyroid cancers <1 cm in size

-may be multifocal and are usually clinically silent until thyroidectomy for another indication

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10
Q

Epidemiology facts about follicular carcinoma.

A

10-20% of thyroid cancers

  • females>males
  • usually older population than PTC (40-60s)
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11
Q

Is radiation a risk factor?

What is the best prognostic factor?

A

Radiation is NOT risk factor

Age is best prognostic factor

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12
Q

Genetic mutations associated with Follicular carcinoma

A

PAX 8/PPARgamma genetic mutations

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13
Q

Most common route of spread for follicular thyroid cancer?

A

hematogenous
F - far away

LN spread in 10% of cases only
>80% of follicular carcinomas will take up iodine

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14
Q

What is a minimally invasive follicular carcinoma?

A

follicular neoplasms that capsular invasion but no vascular invasion

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15
Q

Hurthle cell carcinoma

A

5% of all thyroid carcinomas

  • likely follicular origin, considered DTC
  • less than 10% of HCCs take up iodine
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16
Q

Management of Hurthle cell carcinoma (HCC)

A

diagnostic thyroid lobectomy at minimum

usually advocate for total thyroid

17
Q

Indications for total thyroidectomy in Hurthle cell carcinoma

A
  • DTCs >4 cm in size
  • extrathyroidal extension
  • regional or distant mets
  • contralateral nodules/prior irradiation/familial DTC
  • patient preference
18
Q

What is the most common tumour to metastasie to thyroid gland?

A

Renal cell carcinoma

Other less common primaries: breast, lung, GI tract, melanoma, sarcoma

19
Q

What are some prognostic scoring systems for thyroid malignancy?

A

AGES, AMES, MACIS

AGES
A- age (low risk if women <50 years, men <40 years)
*most important prognistcator
G- grade
E- extrathyroidal disease
S- size of tumour (>4 cm bad)
AMES
A- age
M- mets
E- extrathyroidal invasion
S- size of tumour
MACIS
M- mets
A- age
C- completeness of resection
I- invasion of extrathyroidal structures
S- size of tumour
20
Q

How is age incorporated into TNM system?

A

if patient is less than 45 years old and does not have mets = Stage I (still favourable prognosis if younger)

21
Q

What is the follow-up protocol after thyroidectomy for recurrent thyroid cancer?

A

Low risk:
Annual:
-physical exam
-Neck ultrasound at 6-12 months then frequency depends on patient factors
-TSH levels
-serum Tg and anti-Tg levels (if total thyroidectomy) q12-24 months

High risk:
same stuff as above, except do the Tg and anti-Tg levels q6-12 months instead