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19 Cards in this Set

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What are the 4 basic mechanisms of hyperprolactinemia?
(1) lack of hypothalamic DA
(2) hypothalamic DA can't be delivered adequately to the ant. pituitary
(3) ant. pituitary is insensitive to hypothalamic DA
(4) lactotroph cells are being stimulated by something else (estrogen, TRH)
What classes of drugs contain things that can cause hyperprolactinemia?
antiHTN, GI meds, Antipsychotics, AntiD, cocaine, opiates, protease inhibitors.
What are clinical sx of hyperprolactinemia in women? men?
- women: 30-80% galactorrhoea, menstrual irreg, infertility
- men: <30% galactorrhoea, impotence, viz field abnormalities, HA, extraocular muscle weakness, ant. pituitary malfunction
Sx of gonadotrophin deficiency in women? men?
- women: amenorrhoea/oligomenorrhoea, infertility, dyspareunia, breast atrophy, loss of 2ndary sexual hair
- men: poor libido/impotence, infertile, small/soft testicles, loss of 2ndary hair.
What is the primary tx for almost all pts with pathological hyperprolactinemia?
- current drug options for this in the US?
+ common SE?
DA agonist therapy.
- bromocriptine, cabergoline
+ N&V, orthostatic hypotension
Which subunit (a or b) of pituitary glycoprotein hormones is the active one?
- which do most nonfunctioning pituitary tumors secrete?
Beta.
- alpha
When dealing with a tumor causing mass effects on the way to panhypopituitarism, what is hte order of hormone loss?
GH, LH, FSH, TSH, ACTH, PRL
TSH deficiency causes what clinical sx in children? adults?

ACTH deficiency in all ages causes what?
- growth retardation
- \energy, constipation, sensitivity to cold, dry skin, weight gain

weakness, tiredness, dizziness on standing (orthostatic hypotension), pallor, hypoglycemia
Generally speaking, what sorts of medical problems should make us think of a pitutary tumor?
unexplained HA, impotence, loss of pubic/axillary hair, galactorrhea, amenorrhea, infertility, anorexia/WL
acral enlargement/coarse features, sweating, menstrual upset, HA, arthriris, carpal tunnel syndrome, diabetes, impaired libido, HTN....and many others are sx (in decreasing prevalence order) on presentation of what endocrine disorder?
acromegaly.
What effect does G loading have in agromegaly?
their plasma glucose stays high on oral glucose challenge. Normally, it should drop.
What is the surgical tx for acromegaly?

Other tx?
transsphenoidal hypophysectomy.

Xrt, Somatostatin analogs, Dopamine Agonists, growth hormone receptor antag (directly inhib IGF-1 secretion)
Can dopamine agonists like bromocriptine and cabergoline cause tumor shrinkage?
- what percentage of pts achieve adequate control re: IGF-1 lvls on these meds
very little clearly documented data on this.
- 10-20%.
What is octreotide?

Pegvisomant?
- efficacy at normalizing IGF-1 lvls?
- SE?
somatostatin mimic, more potent than biological version.

Growth Hormone receptor antagonist.
- can be 97%+ on higher doses.
- rare LFT elevations.
Fatigue, cold intolerance, bradycardia, constipation, dry skin, hair loss, etc. Top of the DDx?
- of these disorders, which is more severe, primary or secondary?
hypothyroidism.
- primary
Midline facial defects, such as cleft palate, central incisor, etc. are common in which hormone deficiency?
GH deficiency
Aplasia and hypoplasia of the pituitary are often due to deletions in which genes?

Howabout isolated GH deficiency?
Prop-1 and Pit-1 (both pituitary transcription factors)

GH-N gene
What can insulin induced hypoglycemia directly test for?
GH secretion
What is the metyrapone test?
Tests the pituitary's capacity to secret ACTH by blocks 11 hydroxylation of 11- deoxycortisol, and resulting in a fall in serum cortisol and a rise in 11-deoxycortisol.

In normals the fall in cortisol results in a rise in ACTH secretion secondary to negative feedback of cortisol on ACTH (which has now been decreased b/c cortisol has dropped)