Pituitary and Hypothalmic Disorders Flashcards Preview

Endocrine > Pituitary and Hypothalmic Disorders > Flashcards

Flashcards in Pituitary and Hypothalmic Disorders Deck (31):
1

What hormones are manufactured in the hypothalamus?

ADH, oxytocin

2

What is hyperprolactinemia?

elevated prolactin levels. caused by prolactinoma, trauma, meds (SSRIs, antipsychotics, cocaine, alpha methyldopa), hypothyroidism

3

What is a prolactinoma?

a tumor of the anterior pituitary that secretes prolaction. may cause compression of the optic chiasm and bitemporal hemianopsia. most common type of pituitary adenoma.

4

What happens to prolactin levels if the stalk of the hypothalamus is damaged?

prolactin inhibiting hormone (dopamine) will not be transmitted to the pituitary. Prolactin levels then increase unchecked

5

What medications increase serotonin and may lead to increased prolactin levels?

Antidepressants, Antipsychotics, Alpha methyldopa (antihypertensive). Serotonin is a prolactin releasing factor

6

What does prolactin block?

gonadotropins FSH and LH

7

What are the symptoms of prolactinoma in women?

microadenoma more common in women. Amenorrhea, galactorrhea, infertility

8

What are the symptoms of prolactinoma in men?

macroadenoma more common in men. Decreased libido, gynecomastia, erectile dysfunction, infertility, bitemporal hemianopsia, headache. decreased testoterone levels

9

How is prolactinoma diagnosed?

best initial test is the prolactin level. additional tests to rule out secondary hyperprolactinemia: TSH, beta-HCG (pregnancy test), CMP, LH, FSH, serum estradiol (wm) or serum/total testosterone (mn). MRI to confirm the diagnosis

10

How is prolactinoma treated?

dopamine agonists: cabergoline (best tolerated) or bromocriptine. transsphenoidal pituitary surgery, radiation, or chemo w/temozolomide. depends on symptoms and size of tumor.

11

What is acromegaly?

excess growth hormone. almost always caused by a pituitary tumor. occurs btw 20-40. may be associated w/tumors of the pancreas or parathyroids.

12

What are signs and symptoms of acromegaly?

skeletal changes, coarsening of facial features (jaw protrusion, prominent brow), enlargement of the hands and feet, deepening of the voice, carpal tunnel, CHF (organ enlargement)

13

How is acromegaly diagnosed?

best initial test is IGF-1 level. Serum GH not suppressed following oral glucose. MRI

14

How is acromegaly treated?

transsphenoidal resection is best choice. Gamma knife radiosurgery is transsphenoidal fails. meds: cabergoline. or ocreotide, lanreotide, pegvisomant (sub Q injections)

15

What is gigantism?

excessive growth hormone in youth prior to closure of epiphyses. work up and treatment is the same as acromegaly

16

What are the different possible etiologies of hypopituitarism?

pituitary apoplexy, Sheehan's syndrome, infiltration, non-functioning adenoma, trauma, stroke, mass effect

17

What is the order of hormone deficiency of hypopituitarism?

GH-->LH/FSH-->TSH-->ACTH

18

What is pituitary apoplexy and its symptoms?

Hemorrhage into the pituitary. Usually secondary to existing adenoma. headache, nausea, vomiting, altered mental status, low blood pressure, low blood glucose

19

What is Sheehan's syndrome and its symptoms?

Post partum ischemic necrosis of the pituitary. Secondary to hypotension, emboli, HELLP syndrome. Difficulty breastfeeding, extended amenorrhea

20

How is hypopituitarism diagnosed?

check anterior pituitary hormones: LH/FSH, IGF-1 or GH insulin response test, TSH, ACTH (measured thru cortisol levels). MRI

21

What is a GH insulin response test?

administer insulin to lower blood glucose level. GH should increase due to insulin release

22

What is SIADH (Sudden Inappropriate Diuretic Hormone)?

characterized by euvolemic hyponatremia due to elevated ADH levels. Reabsorption of excess fluid, low sodium, low serum osmolality.

23

What are symptoms of SIADH?

if chronic it's asymptomatic. HA, N/V, altered mental status, seizures

24

What are possible etiologies of SIADH?

trauma, malignancy, meningitis, meds

25

How is SIADH diagnosed?

CMP, urine sodium is inappropriately high >20mEg/L with low serum sodium <130. CT. Rule out SIADH producing cancers: CXR small cell cancer of lung, CT abdomen pancreatic cancer

26

How is SIADH treated?

increase sodium levels by fluid restriction (1200-1800ml/day). For patients w/neuro sx-hypertonic saline IV over 3-4hrs (may cause central pontine myelinolysis if administered too quickly)

27

What is diabetes insipidus?

lack of appropriate levels of ADH leads to elevated plasma sodium w/inability to concentrate urine . Central- deficiency of ADH or resistance to ADH. Nephrogenic- defect in kidney tubules that interferes w/water reabsorption.

28

What are symptoms of diabetes insipidus?

intense thirst, polydipsia, craving for ice water, polyuria, nocturia, enuresis, hypernaturemia

29

What is the etiology of diabetes insipidus?

Central- deficiency of ADH or resistance to ADH due to trauma or tumor. Nephrogenic- defect in kidney tubules that interferes w/water reabsorption due to lithium, demeclyocyline, infiltrative disease, Sjogren's syndrome

30

How is diabetes insipidus diagnosed?

CMP, plasma osmolality, plasma ADH, urine sodium. Water deprivation test- serum sodium will increase but urine sodium will be low. DDAVP test- urine sodium increases if central DI

31

What is the treatment of diabetes insipidus?

Central- DDAVP. Nephrogenic- hydrochlorothiazide or amiloride: block reabsorption of sodium in the kidneys to keep the plasma sodium levels down