Adrenocortical, Aldosterone, Pituitary Flashcards

1
Q

How do you distinguish primary hypogonadism from secondary hypogonadism?

A
History
Exam
Check LH/FSH
- If elevated: primary gonadal failure
- If low: secondary gonadal failure
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2
Q

Clinical presentation includes anorexia, nausea/vomiting, weight loss, weakness/fatigue, abdominal pain, lightheadedness

A

Adrenal Insufficiency

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3
Q

Cushing’s disease is a condition of

A

Excess cortisol

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4
Q

Frequent cause of hyperaldosteronism

A

bilateral adrenal hyperplasia

may also be caused by a single adrenal adenoma

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5
Q

Caused by destruction of both adrenal cortices

A

Primary adrenal insufficiency

Low cortisol, low aldosterone, high ACTH

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6
Q

In primary adrenal insufficiency, there is ___________ hyperkalemia

A

Pronounced hyperkalemia (++)

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7
Q

______ is produced by the adrenal cortex after ______ stimulation via the hormone ________

A

CORTISOL is produced by the adrenal cortex after PITUITARY stimulation via the hormone ACTH

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8
Q

What is the most common pituitary adenoma?

A

Prolactinoma

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9
Q

Due to hypothalamic or pituitary disease that decreases secretion of CRH/ACTH

A

Secondary adrenal insufficiency
Low cortisol, normal aldosterone, low ACTH

–> associated with other pituitary hormone deficiencies, rarely isolated

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10
Q

Secondary gonadal failure or pituitary disease causes hypogonadism via

A

decreased GnRH, LH, FSH –> impaired gonadal function

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11
Q

Clinical presentation includes central weight gain, round facies, striations, thin skin/bruising, mood disturbance, insomnia, HTN, diabetes, sexual dysfunction, bone loss

A

Cushing’s disease

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12
Q

How are pituitary tumors treated?

A

ALL - except prolactinoma - are treated surgically

Can give radiation after surgery

Medical:

  • Acromegaly: octreotide, pegvisomant
  • Cushing’s: metyrapone, ketoconazole, mifepristone

Replace missing hormones

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13
Q

What accounts for most of the differences in symptoms between primary and secondary adrenal insufficiency?

A

Aldosterone secretion (or lack of)

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14
Q

Nuances of ectopic Cushing’s

A
  • May not present with weight gain (underlying malignancy)
  • More severe HTN/hyperglycemia
  • Low potassium due to very high cortisol levels
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15
Q

How do you treat hypogonadism?

A

Estrogen +/- progesterone if premenopausal woman

Testosterone if man (SE: polycythemia, oily skin/acne, prostate enlargement, progression of prostate cancer)

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16
Q

In secondary adrenal insufficiency, there is ______ hyperkalemia

A

NO hyperkalemia (-)

17
Q

How do you diagnose Cushing’s disease?

A

1) Establish high cortisol (urinary, midnight control, suppression test)

2) Establish if ACTH dependent or not
- dependent = pituitary tumor, ectopic
- independent = adrenal tumor

3) If dependent, establish if pituitary or ectopic with suppression test
4) Localize tumor (CT, MRI)

18
Q

Treatment for secondary adrenal insufficiency includes

A

ONLY glucocorticoids

19
Q

Consequences of high aldosterone

A
  • -> sodium retention + water retention
  • -> potassium wasting
  • -> feedback suppression of renin
20
Q

How do you evaluate a pituitary adenoma?

A

1) Tumor function (prolactin, ACTH, GH, TSH, none)
2) Surrounding tissue (compression, hormonal impairment)
3) Surrounding structures (optic chiasm, CN, temporal lobe)

21
Q

What is the best treatment for Cushing’s disease?

A

Remove the cause (tumor/cancer)

Then:

  • enzyme inhibitors (metyrapone, ketoconazole)
  • cortisol receptor blocker (mifepristone)
22
Q

Presents with hypogonadism and galactorrhea (W)

A

Prolactinoma (pituitary adenoma)

–> diagnose with elevated prolactin level

23
Q

High aldosterone + high aldosterone/renin ratio

A

Hyperaldosteronism (diagnostic)

–> follow with adrenal CT

24
Q

Hypotension may indicate _________ Adrenal Insufficiency.

A

Primary - yes

Secondary - yes or no

25
Q

Hyperaldosteronism patients tend to have

A
  • HTN at a young age
  • Resistant hypertension
  • Spontaneous hyperkalemia
26
Q

Hyperpigmentation is characteristic of ________ Adrenal Insufficiency

A

Primary (elevated ACTH)

27
Q

How do you treat hyperaldosteronism?

A
  • After diagnosis (high aldosterone + high aldosterone/renin ratio) perform adrenal CT to find tumor
  • Adrenal venous sampling to see if bilateral
  • Excise tumor if unilateral
  • Aldosterone receptor blocker if bilateral (spironolactone or eplerenone)
28
Q

Tissue swelling and enlargement is characteristic of

A

Acromegaly

–> diagnose with elevated IGF-1 level

29
Q

Treatment for primary adrenal insufficiency includes

A

glucocorticoids and mineralocorticoids

30
Q

How do you diagnose Acromegaly?

A

Elevated IGF-1, failure to suppress GH with glucose load

31
Q

How do you treat prolactinomas?

A

With dopamine agonists cabergoline or bromocriptine
–> lower prolactin, shink tumor

With BCP if patient premenopausal (testosterone in men)

Observe if postmenopausal/older male

32
Q

How do you treat acromegaly?

A

surgical + ocreotide (somatostatin analog to decrease GH secretion) or pegcisomant (GH receptor blocker, inhibits production of IGF-1)

33
Q

What are the possible causes of increased prolactin?

A
If high HCG --> pregnancy
If high TSH --> hypothyroidism
If high Creatinine --> renal failure 
Medications
Pituitary prolactinoma