Endocrine Quiz #4 Flashcards

(56 cards)

1
Q

Where does hypothalamus secrete hormones and what systems do these hormones control?

A
  • to ant pituitary

- control thyroid, adrenals, gonads, growth

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2
Q

What is the difference between primary and secondary endocrine disorders?

A

primary: originating in peripheral endocrine gland.
secondary: from over or under stimulation by pituitary/HTH

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3
Q

What questions do you want to be sure to ask in HPI?

A

HA, heat or cold intolerance, response to exercise, changes in menses, erectile function, skin, vision, weight.

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4
Q

Empty Sella

A

anterior pit lobe disorder

enlarged sella turcica is not entirely filled

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5
Q

primary vs secondary empty sella

A

primary: congenital defect in diaphragm allows CSF pressure to enlarge sella
sec: mass enlarges sells

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6
Q

imaging for empty sella

A

xray

MRI of brain

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7
Q

cause of hypofunction of ant pituitary

A

pituitary tumors, sarcoidosis, thrombosis, traumatic brain injury, ischemic stroke, etc.

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8
Q

sx of hypo ant pit

A
  • GH def in children: growth retardation, lack of maturation
  • Los of GN (LH and FSH) decreases sexual function
  • depends on hormones that are deminished or absent.
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9
Q

lab workup and imaging for hypofunction of ant pit

A
cortisol
TSH
Gonadotropins
GH
CT or MRI
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10
Q

What does low cortisol and high ACTH indicate?

A

adrenal insufficiency

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11
Q

Pituitary apoplexy

A

sudden hem of pituitary adenoma causing edema and hypofunction

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12
Q

sx of pituitary apoplexy

A

sudden onset severe HA
stiff neck
visual field defects

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13
Q

complications of pit apoplexy

A

coma or death

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14
Q

DX of pit apoplexy

A

MRI

lumbar puncture to see if blood in CSF

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15
Q

Pituitary infarction (Sheehan syndrome)

A

pituitary necrosis as a result of postpartum hemorrhage and hypovolemic shock

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16
Q

sx of sheehan syndrome

A

severe: lethargy, anorexia, weight loss, inability to lactate
less severe: failure to lactate, menses do not resume, loss of sexual hair

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17
Q

pituitary dwarfism

A

decreased GH from pit or HTH disease

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18
Q

causes of pit dwarfism

A

idiopathic, emotional deprivation, hereditary

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19
Q

PE and lab for pit dwarfism

A

PE: growth charts
Lab: IGF-1 and GH levels may be low

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20
Q

what hormones are over-produced in hyperfunction of ant pit

A

adenomas over secrete hormones: PRL, GH, ACTH

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21
Q

sx of hyperprolactinemia in women

A

premenopausal: lactation after pregnancy, amenorrhea, menstrual abnormalities
post men: HA, vision impairment,

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22
Q

sx of hyperprolactinemia in men

A

decreased libido, erectile dysfunction, infertility, gynecomastia

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23
Q

Acromegaly vs gigantism

A

acromegaly: start out looking normal and then have changes in adulthood
gigantism: starts as kids

24
Q

sx of acromegaly

A

enlargement of jaw, hands, feet, coarse facial features, CVD, sleep apnea, DM2, vision loss, carpal tunnel

25
Workup for acromegaly
PE: organomegaly, enlarged tongue Lab: serum IGF-1 elevated glucose test
26
Central Diabetes Insipidus (neurogenic)
deficiency of ADH leads to large amounts of very dilute urein and excessive thirst
27
causes of central diabetes insipidus
hypothalamus or post pit disease, autoimmune, familial
28
sx of central diabetes insipidus
abrupt onset polyuria, poludipsia, nocturia | dry skin, dry mucus membranes, tachycardia
29
****What tests can you run for central diabetes insipidus? How do you run it?
water restriction test: measure urine volume and osmolality every hr and plasma sodium every 2 hrs. In DI: urine is more dilute than plasma
30
SIADH
increased secretion of ADH without stimulus | hyper function of posterior pituitary caused by stroke, head trauma, drugs, pneumonia, HIV
31
sx SIADH
lethargy, HA, difficulty concentrating, gait disturbances, vomiting, coma, seizures
32
insidious progressive weakness, fatigue, anorexia, N/V, diarrhea or constipation, abdominal pain, cold intolerance, dizziness, fainting, low resistance to infection, salt craving, joint pain, gait disturbance?
Addisons Disease (primary adrenal insufficiency)
33
etiology of Addisons disease
70% idiopathic (autoimmune) atrophy of adrenal gland
34
What is the gold standard test for Addisons disease?
ACTH stimulation test: IV cortisol administered and measured at baseline, 30 min, 60 min - if elevated, primary adrenal insufficiency - not elevated, secondary to pituitary insufficiency
35
profound weakness, peripheral vascular collapse, renal failure/azotemia, pain in legs, back, abdomen
Adrenal Crisis (emergency)
36
What is the difference between primary and secondary adrenal insufficiency with low cortisol?
secondary has no hyperpigmentation
37
what is the mechanism of the problem with secondary adrenal deficiency with low cortisol?
secondary to low ACTH stimulation which is a result of destructive pituitary or pituitary lesion *issue with pituitary (not adrenal).
38
permanently high ACTH levels due to defects in cortisol hydroxylation with accumulation of precursors of cortisol.
Congenital adrenal hyperplasia (CAH)
39
sx of congenital adrenal hyperplasia
F: masculinization of fetus in utero, ambiguous genitalia males: infant hercules syndrome * adrenal crisis in early two weeks of age from salt loss
40
workup for congenital adrenal hyperplasia
very high serum 17 hydroxyprogesterone | increased testosterone
41
excess ACth production leads to hyper pigmentation (80% due to tumors of pituitary gland)
Cushing's Disease
42
due to longterm use of corticosteroids or cortisol secreting tumors
Cushings syndrome
43
sx of cushing disease/syndrome
``` moon face buffalo hump truncal obesity skinny limbs easy bruising purple striae poor wound healing ```
44
adrenal adenoma/hyperplasia leads to increased aldosterone
primary hyperaldosteronism (conn syndrome)
45
sx of primary hyperaldosteronism
hypervolemia, muscle weakness, parasthesias, transient paralysis, personality disturbances
46
tumor of sympathetic ganglia or adrenal medulla with excess catecholemines.
pheochromocytoma
47
sx of pheochromocytoma
``` sudden increases in BP with severe HA diaphoresis flushing cold clammy skin angina palpitations tremor N/V epigastric pain visual disorders dyspnea parasthesias panic attack ```
48
what are actions of parathyroid hormone?
increased bone, tubular, and intestinal resorptions of Ca. | Decreased tubular resorption (increased excretion) of PO4 and activation of Vit D.
49
What is normal serum Ca level?
8.5-10.5 (40% bound to serum protein)
50
hypo secretion of PTH leading to hypocalcemia.
hypoparathyroidism
51
sx of hypoparathyroidism
``` asymptomatic tetany numbness tingling carpo-pedal spasm laryngeal stridor seizure psychiatric findings (depression, confusion, psychosis) ```
52
lab findings for hypoparathyroid
low ca (les than 8.5mg) low PTH high PO4 hypomagnesemia
53
what causes pseudohypoparathyroidism?
end organ insensitivity to PTH | lab: hypercalcemia
54
excess PTH secretion high Ca low PO4 bone resorption
hyperparathyroid
55
causes of hyperparathyroid
adenoma PTH producing carcinoma hypercalcemia
56
sx of hyperparathyroid
``` kidney stones constipation anorexia N/V with abdominal pain muscular weakness renal impairment ```