common endocrine presentations Flashcards

1
Q

what is the deawhat investigation is used for the definitive diagnosis of acromegaly ?

A

first line iis IGF-1
if raised then perform oral glucose test to see the suppression of the growth hormone

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2
Q

what is the GI association with acromegaly ?

A

carries a high risk for colonic polyps and cancer colon

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3
Q

what is the cause of acromegaly ?

A

mostly due to pituitary adenoma
if not - then GH secreting tumors

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4
Q

what is the first line management of acromegaly ?

A

trans-sphenoidal surgery

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5
Q

if surgery is not possible for cases of acromegaly what is the best management ?

A

somatostatin analogue ( octreotide )
or radiotherapy

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6
Q

what are the different result interpretations associated with thee dexamethasone suppression test ?

A

used to test the level of ACTH and cortisol

1- not suppressed by low dose - cushing syndrome
2- not suppressed by low dose but suppressed by high dose - cushing disease
3- not suppressed by high or low dose - ectopic secretion of ACTH

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7
Q

what is the cut off value to exclude cushing syndrome in association with the low dose dexamethasone suppression test ?

A

less than 1.8 mcg or 50 nmol

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8
Q

what is the best treatment for cushing disease ?

A

transsphenoidal surgery
or adrenalectomy

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9
Q

what is the second line treatment for cushing’s disease ?

A

bilateral adrenalectomy or radation

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10
Q

what is the medical treatment for cushing’s disease ?

A

11 SAGA
1-11 beta hydroxylase : osilodrostat
2- somatostatin analogues : pasireotide
3- adrenal steroid inhibitors : ketoconazole
4- glucocorticoid receptor antagonist : Mifepristone
5- adrenolytic agents : Mitotane

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11
Q

what is the action of somatostatin analogues ?

A

inhibits the production of ACTH which leads to decreased cortisol production

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12
Q

what test is used to test for primary adrenal insufficiency ?

A

short synacthen test
a synthetic form of ACTH (synacthen ) is given in an attempt to stimulate the adrenal gland

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13
Q

what is the difference in lab findings between primary and secondary hypoadrenalism ?

A

in primary hypoadrenalism - High ACTH with low cortisol levels
in secondary ACTH - Low ACTH and Low cortisol

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14
Q

what hematological malignancies are associated with primary adrenal insufficiency ?

A

hodgkin and non hodgkin lymphoma

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15
Q

what is the main autoantigen in idiopathic autoimmune adrenocortical insufficiency ?

A

21 hydroxylase

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16
Q

what is the association of hashimoto’s and addison’s known as ?

A

schmidt syndrome
HHAI DOC

17
Q

what is polyglandular autoimmune syndrome type 1 ?

A

addisons disease
hypoparrathyroidism
candidiasis

18
Q

what is the other name for polyglandular autoimmune syndrome type 1 ?

A

APECED

19
Q

what mutation results in APECED ?

A

AIRE mutation

20
Q

what are the diseases in polyglandular autoimmune syndrome type 2 ?

A

addison’s
type 1 DM
hashimotos
Graves

21
Q

what is the treatment for addison’s disease ?

A

replacement with oral steroids
dose to be increased in infection and surgery

22
Q

what is the treatment of hyperprolactinemia secondary to pituitary adenoma ?

A

1st line - bromocriptine , cabergoline
transsphenoidal pituitary adenomectomy if medical therapy fails

23
Q

what are the causes of hyperprolactinemia ?

A

pituitary adenoma
drug induced hyperprolactinemia
pregnancy
primary hypothyroidism

24
Q

what must first be excluded in hyperprolactinemia ?

A

pregnancy

25
Q

if a patient presents with hypothyroidism and hyperprolactinemia , what is the best next step in management ?

A

treat thee hypothyroidism first

26
Q

what is the best test used to diagnose cushing ?

A

24h urinary cortisol
dexamethasone suppression test

27
Q

how should serum prolactin samples be taken ?

A

preferably in the morning and the patient should be fasting