Adrenocortical, Aldosterone, Pituitary Flashcards
How do you distinguish primary hypogonadism from secondary hypogonadism?
History Exam Check LH/FSH - If elevated: primary gonadal failure - If low: secondary gonadal failure
Clinical presentation includes anorexia, nausea/vomiting, weight loss, weakness/fatigue, abdominal pain, lightheadedness
Adrenal Insufficiency
Cushing’s disease is a condition of
Excess cortisol
Frequent cause of hyperaldosteronism
bilateral adrenal hyperplasia
may also be caused by a single adrenal adenoma
Caused by destruction of both adrenal cortices
Primary adrenal insufficiency
Low cortisol, low aldosterone, high ACTH
In primary adrenal insufficiency, there is ___________ hyperkalemia
Pronounced hyperkalemia (++)
______ is produced by the adrenal cortex after ______ stimulation via the hormone ________
CORTISOL is produced by the adrenal cortex after PITUITARY stimulation via the hormone ACTH
What is the most common pituitary adenoma?
Prolactinoma
Due to hypothalamic or pituitary disease that decreases secretion of CRH/ACTH
Secondary adrenal insufficiency
Low cortisol, normal aldosterone, low ACTH
–> associated with other pituitary hormone deficiencies, rarely isolated
Secondary gonadal failure or pituitary disease causes hypogonadism via
decreased GnRH, LH, FSH –> impaired gonadal function
Clinical presentation includes central weight gain, round facies, striations, thin skin/bruising, mood disturbance, insomnia, HTN, diabetes, sexual dysfunction, bone loss
Cushing’s disease
How are pituitary tumors treated?
ALL - except prolactinoma - are treated surgically
Can give radiation after surgery
Medical:
- Acromegaly: octreotide, pegvisomant
- Cushing’s: metyrapone, ketoconazole, mifepristone
Replace missing hormones
What accounts for most of the differences in symptoms between primary and secondary adrenal insufficiency?
Aldosterone secretion (or lack of)
Nuances of ectopic Cushing’s
- May not present with weight gain (underlying malignancy)
- More severe HTN/hyperglycemia
- Low potassium due to very high cortisol levels
How do you treat hypogonadism?
Estrogen +/- progesterone if premenopausal woman
Testosterone if man (SE: polycythemia, oily skin/acne, prostate enlargement, progression of prostate cancer)
In secondary adrenal insufficiency, there is ______ hyperkalemia
NO hyperkalemia (-)
How do you diagnose Cushing’s disease?
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)
Treatment for secondary adrenal insufficiency includes
ONLY glucocorticoids
Consequences of high aldosterone
- -> sodium retention + water retention
- -> potassium wasting
- -> feedback suppression of renin
How do you evaluate a pituitary adenoma?
1) Tumor function (prolactin, ACTH, GH, TSH, none)
2) Surrounding tissue (compression, hormonal impairment)
3) Surrounding structures (optic chiasm, CN, temporal lobe)
What is the best treatment for Cushing’s disease?
Remove the cause (tumor/cancer)
Then:
- enzyme inhibitors (metyrapone, ketoconazole)
- cortisol receptor blocker (mifepristone)
Presents with hypogonadism and galactorrhea (W)
Prolactinoma (pituitary adenoma)
–> diagnose with elevated prolactin level
High aldosterone + high aldosterone/renin ratio
Hyperaldosteronism (diagnostic)
–> follow with adrenal CT
Hypotension may indicate _________ Adrenal Insufficiency.
Primary - yes
Secondary - yes or no
Hyperaldosteronism patients tend to have
- HTN at a young age
- Resistant hypertension
- Spontaneous hyperkalemia
Hyperpigmentation is characteristic of ________ Adrenal Insufficiency
Primary (elevated ACTH)
How do you treat hyperaldosteronism?
- 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)
Tissue swelling and enlargement is characteristic of
Acromegaly
–> diagnose with elevated IGF-1 level
Treatment for primary adrenal insufficiency includes
glucocorticoids and mineralocorticoids
How do you diagnose Acromegaly?
Elevated IGF-1, failure to suppress GH with glucose load
How do you treat prolactinomas?
With dopamine agonists cabergoline or bromocriptine
–> lower prolactin, shink tumor
With BCP if patient premenopausal (testosterone in men)
Observe if postmenopausal/older male
How do you treat acromegaly?
surgical + ocreotide (somatostatin analog to decrease GH secretion) or pegcisomant (GH receptor blocker, inhibits production of IGF-1)
What are the possible causes of increased prolactin?
If high HCG --> pregnancy If high TSH --> hypothyroidism If high Creatinine --> renal failure Medications Pituitary prolactinoma