01a: Ant Pit Flashcards

1
Q

Disruption of hypothalamus connection/blood supply to anterior pituitary will cause hypersecretion of (X) ant pit hormone. Why?

A

X = prolactin

Normally under inhibitory regulation by DA from hypothalamus

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2
Q

List some intrinsic hypothalamic peptides that, if increased, will also cause hyperprolactinemia.

A

TRH (ex: hypothyroidism) and VIP (ex: breast stimulation)

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3
Q

Prolactin levels greater than (X) value is always from (Y) cause.

A
X = 250 ng/mL
Y = prolactinoma
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4
Q

Most common pituitary adenoma

A

Prolactinoma

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5
Q

Clinical symptoms of hyperprolactinemia in women

A
  1. Galactorrhea (30-80%)
  2. Amenorrhea
  3. Infertility
  4. Hirsutism
  5. Osteoporosis
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6
Q

Clinical symptoms of hyperprolactinemia in men

A
  1. Galactorrhea (under 10%)
  2. Impotence
  3. Hypogonadism
  4. Mass effects (visual, eye muscles, HA)
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7
Q

Prolactin adenomas can be medically treated with:

A

DA agonists

Bromocriptine or Cabergoline

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8
Q

T/F: DA agonists treat prolactinomas by inhibiting prolactin synthesis/secretion, but don’t treat mass effects of tumor.

A

False - also cause reduction in tumor size

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9
Q

T/F: Surgical success and tumor recurrence rates are both low for prolactin microadenomas.

A

False - both high (over 70% success, 50% recurrence over 5y)

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10
Q

T/F: Both pituitary micro- and macro-adenomas have high surgical success rates.

A

False - macroadenomas difficult to cure with surgery (success about 30%)

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11
Q

Which two opposing peptides regulate GH secretion?

A

Stim: GHRH
Inhib: Somatostatin

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12
Q

GH is secreted in (constant/pulsatile) fashion. List some states/molecules that stimulate its secretion.

A

Pulsatile (and more secreted at night);

Hypoglycemia, exercise, stress, AA

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13
Q

Actions of GH are primarily due to its (direct/indirect) effect on tissues.

A

Indirect (via secretion of IGF-1/somatomedin C)

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14
Q

T/F: Unlike GH and its pulsatile secretion, IGF-1 level is constant.

A

True

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15
Q

T/F: Nighttime GH levels in normal person can spike as high as the levels seen in acromegaly patient.

A

True - but acromegaly patients lose normal pulsatile rhythm of GH

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16
Q

(Hyper/hypo)-secretion of (X) causes gigantism in kids and acromegaly in adults.

A

Hypersecretion

X = GH

17
Q

Acromegaly, if left untreated, can lead to which devastating complications?

A
  1. CV disease (HT, cardiomyopathy)
  2. Cancers (colon)
  3. Resp impairment (sleep apnea)
  4. Skeletal overgrowth/deformity; arthralgias
18
Q

Diagnosis of acromegaly confirmed by:

A

Administering glucose load and demonstrating that GH secretion is not suppressed (below 2 ng/mL)

19
Q

Majority of acromegaly patients have (micro/macro)-adenomas. How are these patients treated?

A

Macroadenomas (due to insidious nature of disease);

Meds (surg/radiation have low success rate for macroadenomas)

20
Q

Unlike true Cushing’s, pseudo-Cushing’s has preserved:

A

Circadian rhythm control of cortisol

21
Q

Treatment of Cushing’s disease - which, by definition, is due to (X) - is primarily via (Y).

A
X = pit adenoma (ACTH-secreting)
Y = surg (most are microadenomas)
22
Q

If the first-line Rx option for Cushing’s disease doesn’t provide cure, what are other options?

A
  1. Radiation/gamma knife therapy
  2. Med therapy

(first-line = surg)

23
Q

Inferior pituitary growth into (X) structure results in which key symptom?

A

X = sphenoid sinus

Nasal discharge of CSF

24
Q

Superior pituitary growth into (X) structure results in which key symptom?

A

X = hypothalamus

Hormonal imbalances

25
Q

Lateral pituitary growth into (X) structure results in which key symptom?

A

X = cavernous sinus

Eye movement issues/diplopia

26
Q

(X) adrenal mass lights up bright white on T2 weighted images due to (high/low) (Y).

A

X = pheo
High
Y = catecholamines

27
Q

The DIRECT cause of osteomalacia in adults and rickets in children is (low/high) levels of (X).

A

Low

X = serum phosphate (so low Ca-P and poor bone mineralization)

28
Q

Any chronic granulomatous disease, like Sarcoidosis, can result in high serum and urine (X).

A

X = Ca

Macrophages have active 1a hydroxylase

29
Q

(X) are the most numerous anterior pituitary cell types

A

X = somatotrophs

30
Q

Pheochromocytomas can occur at (X) landmark of the aorta, where (Y) chromaffin body is located

A
X = bifurcation (into common iliacs)
Y = Organ of Zuckerkandl
31
Q

Traid of precocious puberty, cystic bone lesions, and unilateral café-au-lait spotting

A

McCune-Albright Syndrome