MedEd thyroid and misc endo Flashcards

(59 cards)

1
Q

What cells produce T3 and T4?

A

Follicular thyroid cells

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2
Q

What does negative feedback to the pituitary?

A

T3 and T4

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3
Q

What are hyperthyroid symptoms?

A
Tremor 
Anxiety
Palpitations
Diarrhoea
Oligomenorrhea
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4
Q

What are hypothyroid symptoms?

A
lethary
weight gain
cold intolerance
constipation
menorrhagia 
reduced deep tendon reflexes
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5
Q

What are causes of hyperthyroid?

A

Graves
toxic multinod goitre
viral thyroiditis
drugs

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6
Q

What drug causes hyperthyroidism?

A

Amiodarone

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7
Q

What are causes of hypothyroid?

A

hashimotos
de quervains thyroiditis (subacute)
drugs
iodine deficiency

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8
Q

what drugs cause hypothyroidism?

A

amiodarone

lithium

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9
Q

How is hyperthyroid amanged?

A

Propanolol
Carbimazole
Radioiodine

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10
Q

How does carbimazole work in hyperthyroidism?

A

It is a TPO inhibitor and TPO is needed to make thyroxine

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11
Q

What is a side effect of carbimazole?

A

angranulocytosis ie no neutrophils

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12
Q

how is hypothyroidism managed?

A

Levothyroxine

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13
Q

what causes exopthalamos?

A

anti TSH receptor antibodies binding to TSH receptors behind the eyes

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14
Q

what are the defining features of graves?

A

bilateral exopthalamos
lid lag
pre tibial myexodema
thyroid acropachy

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15
Q

what are features of thyroid cancer?

A
non functional
painless
rapidly growing 
solitary 
irregular in shape 
palpable nodule thats hard and fixed
hoarse voice 
dysphagia
haemoptysis 
airway obstrcution
cervical lymohadenopathy
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16
Q

what is the most common thyroid cancer?

A

papillary carcinoma

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17
Q

what are defining features of thyroid cancer?

A

hoarse voice

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18
Q

what is seen on hisotology in papillary thyroid cancer?

A

psammoma body

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19
Q

what thyroid cancer is associated with low dietary iodine intake

A

follicular carcinoma

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20
Q

what thyroid cancer is associated with MEN 2A and MEN 2B

A

medullary

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21
Q

what is the GS ix for thyroid cancer?

A

fine needle aspiration with biopsy

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22
Q

what is MEN 1 syndrome? what organs and cells are involved

A

parathyroid adenomas which are functional
pancreatic islet cells
pituitary problems eg prolactinoma
other cells can also be involved

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23
Q

what 3 cells/organs are involved with MEN 1 syndrome?

A

parathyroid gland
pancreas
pituitary

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24
Q

what are hypercalcaemia symtpoms?

A

stones
abdo groans
bones
psychic moans

25
what is GS ix for MEN 1 syndrome?
CT/MRI body
26
what causes non MEN 1 gastrinomas?
zollinger ellinson syndrome
27
what characterises MEN 2A and 2B?
meduallry thyroid cancer
28
what organs/cells are involved with MEN 2A?
parathyroid | phaeochromocytoma
29
what tumors/features are involved with MEN 2B?
phaeochromocytoma neuromas marfanoid habitus
30
what MEN syndrome is someone with marfans like habitus likely to have? what are some examples of this?
``` MEN 2B tall stature pectus excavatum long limbs eye problems ```
31
what is GS ix for MEN 2A and 2B? what else might you do
``` genetic testing for RET oncogene might also do: calcitonin urine catecholamines CT/MRI ```
32
what gene is tested for in MEN 2A and B?
RET oncogene
33
what are the types of MEN syndrome, what are they associated with and hwo do you remember this?
MEN 1- parathyroid, pancreas, pituitary (3Ps) MEN 2A- phaeo, parathyroid (2Ps) MEN 2B- phaeo, neuromas, marfanoid habitus (1P) 3Ps, 2Ps, 1P
34
what is the most common feature of carcinoid syndrome?
flushing
35
what is carcinoid syndrome? ie how does it arose
uncontrolled division of neuroendocrine tumors which mets to the liver
36
what is there buildup of in carcinoid syndrome?
serotonin bardykinin histamine
37
what are features of carcinoid syndrome?
``` flushing dairrhoea SOB pulmonary stenosis abdo pain itching ```
38
how fastly do tumors grow in carcinoid syndrome
slow growing
39
what gene mutation is carcinoid syndrome associated with?
MEN 1 mutation
40
what are ix for carcinoid syndrome?
urinary 5-HIAA CT scan ocreotide scan- specific
41
what is a specific ix for carcinoid syndrome?
ocreotide scan
42
describe what LH acts on in males v females and what it produces
males: acts on leydig cells, makes testosterone females: acts on theca cells, makes progesterone
43
describe what FSH acts on in males v females and what it produces
males: acts on sertoli cells and makes sperm (spermatogenesis) females: acts on granulosa cells and makes oestrogen
44
what are features of PCOS?
hirtuism oligomenorrhea polycycstic ovaries infertility/trouble concieving
45
what causes physiological hypogonadism?
pregnancy
46
what causes negative feedback onto the gonadotrophs on the anterior pituitary
LH and FSH
47
what is a defining symptom of kallmanns syndrome hypogonadism
anosmia
48
where are gonadotrophs found
anterior pituiatry
49
what are some causes of primary hypogonadism in females
degenesis of the gonadotrophs eg turners gonadal damage primary ovarian failure pcos
50
what are some causes of secondary hypogonadism
``` kallmann syndrome pituitary or hypothalamic tumor hyperprolactinaemia functional (low bmi, excess exercise, stress) ocp use ```
51
what are some causes of primary hypogonadism in males
gonadal degenesis eg klinefelters, cryptorchidism gonadal damage post orchitis eg mumps
52
what are features of hypogonadism?
``` delayed puberty infertility reduced libido amenorrhea night sweats/hot flushes erectile dysfunction symptoms of cause eg visual changes if tumor ```
53
what ix are done for hypogonadism?
``` preg test LH/FSH prolactin testosterone/oestradiol TFTs karyotyping MRI ```
54
what does gnrh stimulate the production of and where does it act?
growth hormone- acts on all organs | igf-1- made in organs and also acts everywhere
55
what is acromegaly usually caused by?
pituitary adenoma
56
what are features of acroomegaly
``` coarse facial features large tongue large jaw spade like hands and feet excess sweating organomeagly headaches, visual disturbance (bitemp hemianopia), hyperprolactinaemia etc- due to tumor ```
57
what are common complications of acromegaly?
carpal tunnel syndrome colorectal cancer diabetes hypertension
58
what investigation is done to diagnose acromegaly? what is seen?
OGTT | there will be a paradoxical rise in GH if the patient has acromegaly
59
how is acromegaly managed? give GS and other treatments
GS: trans sphenoidal surgery to resect tumor | can also do radiotherapy, somatostatin analogues, dopamine receptor agonists and GH receptor antagonists