Pituitary Disorders Flashcards

(45 cards)

1
Q

size of microadenoma

A

<1cm-1cm

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2
Q

size of macroadenoma

A

> 1cm

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3
Q

physiological causes of raised prolactin

A

breast feeding
pregnancy
stress
sleep

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4
Q

pharmacological causes of raised prolactin

A
dopamine antagonists e..g metoclopramide
phenothiazines
TCA
SSRIs
oestrogens
cocaine
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5
Q

pathological causes of raised prolactin

A

hypothyroid
stalk lesions
prolactinoma

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6
Q

how does hypothyroidism cause raised prolactin?

A

dopamine requires tyrosine- thyroxine is made from tyrosine and iodine

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7
Q

what is a prolactinoma?

A

adenoma of the pituitary gland that overproduces prolactin

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8
Q

presentation in females with prolactinoma

A
earlier presentation usually
galactorrhoea
menstrual irregularity
infertility
visual field abnormality
headache
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9
Q

presentation in males with prolactinoma

A

impotence
visual field abnormality
headache

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10
Q

diagnosis of prolactinoma

A

high serum prolactin
MRI
visual fields e.g. bitemporal hemianopia

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11
Q

prolactin levels in macroadenoma?

A

20,000+

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12
Q

prolactin levels in microadenoma?

A

3,000+

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13
Q

management of prolactinoma

A

dopamine agonist e.g. cabergoline causes tumour shrinkage

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14
Q

adverse of cabergoline

A

nausea
vomiting
low mood
fibrosis of heart valves and retroperitoneum

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15
Q

what is acromegaly?

A

excess of GH

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16
Q

presentation of acromegaly

A
children gigantism (if before epiphyseal fusion)
thickened soft tissues
hypertension, early CV death
headaches
DM
sleep apnoea, snoring
carpal tunnel 
colonic polyps and colon cancer
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17
Q

thickened soft tissues examples in acromegaly

A

increased shoe size
spade hands
wedding ring too tight

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18
Q

diagnosis of acromegaly

A

measure IGF1
OGTT
visual fields
visualise the pituitary e.g. MRI

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19
Q

why do you measure IGF1 in acromegaly?

A

GH secretion is pulsatile

GH stimulates release of IGF1 from the liver

20
Q

describe the OGTT in acromegaly

A

75g PO glucose and check GH every 30 minutes

normal= <0.4ug/l after glucose whereas in acromegaly it is unchanged/risen

21
Q

management of acromegaly

A
transsphenoidal pituitary surgery
radiotherapy
somatostatin analogues
dopamine agonists
GH antagonists
cancer surveillance, cardiovascular RF and sleep apnoea management
22
Q

what can radiotherapy on the pituitary lead to?

A

hypopituitarism

23
Q

somatostatin analogue use in acromegaly

A

sandostatin, octreotide and lareotide

relieve headaches and reduce tumour size

adverse if GI upset

24
Q

dopamine agonist use in acromegaly

A

cabergoline and bromocriptine

better if co-secreting prolactin)

25
what is Cushing's disease?
an excess of cortisol caused by pituitary adenoma secreting excess ACTH
26
what is Cushing's syndrome?
signs/symptoms of excess cortisol caused by adrenal adenomas, ectopic or pseudo causes
27
ectopic production of ACTH
thymus lung pancreas
28
pseudo production of ACTH
alcohol | steroids
29
presentation of Cushing's
myopathy, proximal wasting (proteolysis) thin skin, striae, bruising OP hypertension, obesity, DM (stress hormone) oedema (mineralocorticoids) virilism, hirutism, oligo/amenorrhoea (androgen excess)
30
diagnosis of Cushing's
screening= urine free cortisol and diurnal variation low dose dexamethasone test measure ACTH
31
management of Cushing's disease
hypophysectomy (radiotherapy and bilateral adrenalectomy if recurs)
32
management of Cushing's if unfit for surgery?
metyrapone
33
what is panhypopituitarism?
absence of pituitary hormones
34
causes of panhypopituitarism
pituitary tumours surgery granulomatous disease
35
presentation of panhypopituitarism
``` hypothyroid face abdominal obesity infertility, menstrual irregularity gynaecomastia loss of facial hair ```
36
diagnosis of panhypopituitarism
PFTs | can do suppression/stimulation tests
37
management of panhypopituitarism
hormone replacement
38
which hormone is abused in sport?
GH
39
why is cortisol replaced before levothyroxine in panhypopituitarism?
activates sympathetics and can cause adrenal crisis
40
adverse of testosterone therapy?
risks making cancers grow more polycythaemia (stroke/MI) hepatitis (LFTs)
41
cranial DI
problem with ADH in posterior pituitary
42
causes of cranial DI
familial (DIDMOAD) | acquired (tumour, trauma, idiopathic, inflammation)
43
diagnosis of cranial DI
water deprivation test/ desmopressin
44
water deprivation test result in cranial DI
osmol ratio >2 is negative | if low and improves after desmopressin, then cranial not nephrogenic
45
management of cranial DI
desmospray or desmopressin tablets/injections