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23 Cards in this Set

  • Front
  • Back
Pituitary close to ...
Internal carotids
CN III, IV, V1, V2, VI
optic chiasm
anterior pituitary
positive control from hypothalamus (except prolactin under negative tonic dopaminergic control)
ACTH, TSH, GH, LH, FSH, Prolactin
ACTH
regulated by corticotropin releasing hormone (CRH)
stimulates cortisol release from adrenal glands
cortisol has neg feedback
excess cortisol leads to Cushing's syndrome, deficiency leads to adrenal insufficiency
TSH
regulated by Thyrotropin Releasing Hormone (TRH)
stimulates thyroid hormone release from thyroid
Thyroid hormone has negative feedback
excess leads to central hyperthyroidism, deficiency leads to central hypothyroidism
FSH & LH
Regulated by GnRH
stimulates testes and ovaries to ...
males: testosterone secrete & spermatogenesis
females: estradiol secrete & gametogenesis
excess leads to precocious puberty, deficiency leds to hypogonadism
Prolactin
under tonic inhibition by dopamine
targets the breast to lactate
excess leads to galactorrhea and amenorrhea, deficiency leads to inability to lactate
Posterior Pituitary
ADH, Oxytocin
synthesized in neurosecretory cells (supraoptic & paraventricular)
ADH
regulated by plasma osmolality and blood volume
affects H2O permeability in collecting tubule
excess leads to Syndrome of Inappropriate Secretion of ADH, deficiency leads to Diabetes Insipidus
Oxytocin
Regulated by neurotransmitters (cholinergic & alpha adrenergic
causes milk let down from breasts and uterine contractions during labor
Cushing's Syndrome
Result of chronic glucocorticoid excess
ACTH-dependent - Cushings disease, Ectopic ACTH, Ectopic CRH
ACTH-independent: Adrenal adenoma, Adrenal carcinoma, micro/macronodular hyperplasia
Pseudo: Depression, EtOH
DX: centripetal obesity, buffalo hump, hyperpigmentation
Confirm: Urine Free Cortisol >3x normal limit x2 catches, Dexamethasone suppression test, loss of diurnial variation
TX: surgical resection w/ radiation, tumor removal, unilateral adrenalectomy
Dexamethasone Variation Test
synthetic glucocorticoid given leading to ACTH suppression via neg feedback in healthy individuals, no suppression in Cushing's syndrome
10-20% false positive b/c obesity, depression, EtOH
Differentiating ACTH-independent from ACTH-dependent Cushings
Plasma ACTH levels
<5 pg/ml --> adrenal cushings (independent) --> CT adrenals
>10 pg/ml --> pituitary (ectopic) cushings (dependent)
5-10 pg/ml not definitive
worry about ACTH secreting tumor w/ increased ACTH release
Differentiating pituitary v. ectopic ACTH dependent Cushings
High Dose Dexamethasone suppression test: high dose dexamethasone should suppress serum ACTH in pituitary Cushings but serum ACTH should remain high with ectopic ACTH

Petrosal sinus sample (last resort invasive surgical procedure)

MRI pituitary once positive results for pituitary Cushings. can't use to DX b/c 10-20% false positive
Acromegaly
excess GH from pituitary tumor (99%) after epiphyseal plate closure (before --> gigantism)
presents: acral enlarge, facial changes, arthralgias, sweating, skin tags, greasy skin, HTN, DM, sleep apnea
Increased incidence: arthropathy, neuropathy, CV dz, HTN, resp dz, colon ca, carb intolerance
TX: transsphenoidal surg (50% effective), somatostatin analoges (preferred), radiation, DA agonists, GH antagonists
Diagnosis of Acromegaly
Failure of GH to suppress Oral Glucose Tolerance Test (gold standard)
IGF-1 increased, 10-15% false neg due to lever dz, hyperglycemia, malnutrition
Prolactinomas
most common secretory pit tumor
female: amenorrhea, infertility, galactorrhea
men: decreased libido, impotence, galactorrhea, mass effects (headache & vision changes)
DX: increased prolactin, abnormal pit MRI
Exclude: hypothyroid, renal fail, cirrhosis, preg, stress, haloperidol, compression of pit stalk
TX: DA agonists (Bromocriptine, Cabergoline), surgery and rad if medical fails
Thyrotrope Adenoma
TSH secreting, rare
Hyperthyroidism
Mass effects (headache, abnormal visual field)
TX: surgery
Gonadotrope Adenoma
FSH (most common), LH, or alpha subunit secreting
no obvious clinical syndrome
Mass Effects
Hypopituitarism from deficiency of other hormones
TX: surgery
Diabetes Insipidus
Insufficient ADH
polyuria, polydypsia, thirsty
central - abrupt onset
nephrogenic - slow onset
Central: Congenital, iatrogenic, trauma, neoplasm, ischemia (sheehan), granuloma (sarcoid), infection, autoimmune
Nephrogenic: Congenital (X-link), renal dz, electrolyte disorder, drugs (lithium, demeclocyclin)
DX: polyuria, low urine specific gravity + osmolality
central responds to ddAVP (vasopression analog)
TX: ddAVP (central), NSAIDs & thiazids (nephrogenic)
hypopituitarism
deficiency of one or multiple pit hormones
GH, FSH, LH most often
TSH, ACTH, ADH last to diminish
Sheehan's Syndrome
Ischemic pituitary necrosis following childbirth. associated w/ postpartum hemorrhage and HOTN
Failure to lactate
Pituitary Apoplexy
Hemorrhagic infarct of pituitary adenoma.
presents w/ headache, mental status changes, opthalmoplegia, visual loss
DX: MRI, endocrine test
TX: surgical, hormone replace
Pituitary Incidentalomas
10-20% MRIs pick up incidental adenomas.
exclude hormonal hypersecretion, hypopituitirism & visual change w/ macro
follow up MRIs at 6 mo, 1,2,5 yrs