Chemical pathology - Thyroid Flashcards

1
Q

What % of T4 is typically bound to TBG?

A

75%

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2
Q

To which proteins can T4 bind?

A

TBG
TBPA
Albumin

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3
Q

Recall 6 possible aetiologies of primary hypothyroidism

A

Hashimoto’s
Atrophic (1st in UK)- no goitre, small thyroid due to lymphocytic infiltration
Lihtium, Amiodarone
Iodine deficiency (1st worldwide)
Riedel’s thyroiditis = dense fibrosis, stony hard
Post thyroidectomy/radioiododine

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4
Q

What is the expected TSH and T4 levels in primary hypothyroidism?

A

TSH high
T4 low

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5
Q

What test should always be done before thyroid-replacement medication is initiated?

A

ECG - because T4 increases cardiac contractility

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6
Q

How does thyroid function change in pregnancy?

A

In 1st trimester, there is a huse rise in hCG
hCG has the same configuration as TSH - this then stimulates the thyroid gland to produce supra-physiological amounts of thyroxine
However, this is normal in pregnancy, so the woman doesn’t become clinically hyperthyroid

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7
Q

What type of non-thyroid malignancy can cause thyrotoxicosis?

A

Malignancy that produces hCG

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8
Q

What test is used to detect neonatal hypothyroidism?

A

Guthrie test on day 2/3 of life

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9
Q

What does the term ‘sick euthyroid’ refer to?

A

Any severe illness –> reduced T4, increased TSH and decreased T3
This is normal physiology in sepsis

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10
Q

Recall 5 differentials for the cause of hyperthyroidism, and how each would appear on a technetium scan

A
  1. Grave’s (40-60% of cases) - high uptake
  2. Toxic multinodular goitre (30-50%) - high uptake
  3. Single toxic adenoma - high uptake
  4. Subacute de quervain’s thyroiditis - low uptake
  5. Postpartum thyroiditis - low uptake
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11
Q

What drugs can be used to treat an overactive thyroid? What is their mechanism of action?

A

Carbimazole and propylthiouracil
Inhibit thyroid peroxidase

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12
Q

What is the main risk of carbimazole and propylthiouracil treatment?

A

Agranulocytosis
- if sore throat or fever, stop testament and seek advice

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13
Q

Over how long should carbimazole and propylthiouracil treatment be titrated ?

A

18 months

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14
Q

How should papillary thyroid Ca be treated?

A

Removal of thyroid gland
Then radioiodine treatment
Then give supraphysiological thyroxine (so Ca cells not reactivated)

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15
Q

Recall 2 tumour markers for medullary thyroid cancer

A

CEA and calcitonin

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16
Q

Which type of thyroid cancer is associated with Men II?

17
Q

is T3 or T4 active? which is more abundant

A
T3 = active 
T4 = abundant
18
Q

is the TSH high or low in subclinical hypothyroidism

A

TSH = high but T4 is NORMAL

19
Q

TSH and T4 levels in hyperthyroidism

A

low TSH
high T3 and T4

20
Q

what cell is associated w Hashimoto’s

A

hurthle cell

21
Q

solitary hot nodule on isotope scan =

A

toxic adenoma

22
Q

initially hyperthyroid, then hypothyroid =

A

de quervain’s thyroiditis - self limiting, post viral painful goitre

23
Q

what’s Plummer’s disease

A

toxic multi nodular goitre = painless goitre

24
Q

what psychiatric drug commonly causes hypothyroidism

25
types of thyroid neoplasia (cancer) and prevalence
PFMA(L) papillary (75%) - female, aged 20-40, v good prognosis follicular (15%) - aged 40 - 60 (increases w age down) medullary (5%) anapaestic lymphoma (maltoma - rf = chronic hashimoto's)
26
tumour marker of papillary thyroid cancer?
thyroglobulin
27
presentation of papillary thyroid cancer?
painless cervical lymphadenopathy - spreads to lymph nodes and lung
28
2 histological fin finds of papillary thyroid cancer
``` psammoma bodies (foci of calcification) orphan annie eyes (empty appearing nuclei w central clearing) ```
29
thyroglobulin is a marker of what thyroid cancers
papillary and follicular
30
medullary thyroid cancer is associated with what condition?
MEN2
31
medullary thyroid cancer is dervived from what cell? what do they secrete
neuroendocrine neoplasm derived from parafolllicular C cells secreting calcitonin
32
2 tumour markers of medullary thyroid cancer?
calcitonin CEA
33
what's the inheritance of the multiple endocrine neoplasia conditions? outline the types
autosomal dominant MEN 1 = 3Ps = pituitary adenoma, pancreatic tumour and parathyroid hyperplasia MEN2a = 3Cs = Calcitonin (medullary thyroid cancer), Calcium (parathyroid hyperplasia), Catelcholamines (phaeo) MEN2b = B for Big (marfanoid) & Belly problems (mucosal neuromas)