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42 Cards in this Set

  • Front
  • Back
List the arterial supply to the adrenal glands
Superior adrenal - inferior phrenic artery
Middle adrenal - aorta
Inferior adrenal - renal artery
List the venous drainage of the adrenal glands
Left adrenal vein goes to left renal vein
Right adrenal vein goes to inferior vena cava
When is sx indicated for ASYMPTOMATIC ADRENAL MASS
Surgery is indicated if mass has ominous characteristics (nonhomogenous) or is
>4-6 cm, functioning, or enlarging
What are the Common metastases to the adrenals?
Lung CA (# 1), breast CA, melanoma, renal CA
Cancer history with asymptomatic adrenal mass - need biopsy
ADRENAL CORTEX
What hormone is produced by
Glomerulosa
Aldosterone
ADRENAL CORTEX
What hormone is produced by
Fasciculata
Glucocorticoids
ADRENAL CORTEX
What hormone is produced by
Reticularis
Androgens/ estrogens
is released from the anterior pituitary gland and causes the release of cortisol
ACTH
ADRENAL CORTEX
All zones have ________ hydroxylase
21 - and 11 -beta hydroxylase
stimulates renal sodium resorption and secretion of potassium, hydrogen ion , and ammonia
Aldosterone
What stimulates Aldosterone secretion?
Angiotensin II
Hyperkalemia
and to some extent ACTH
Excess estrogens and androgens by adrenals is _______ until proven otherwise
Cancer
Congenital adrenal hyperplasia (enzyme defect in cortisol synthesis)
most common; precocious puberty in males, virilization in females
increase in17-0H progesterone leads to increase production of testosterone
salt wasting (decrease in sodium and increase in potassium) and causes hypotension
21 -Hydroxylase deficiency (90%)
• Tx: cortisol, genitoplasty
Congenital adrenal hyperplasia (enzyme defect in cortisol synthesis)
precocious puberty in males, virilization in females
Increase 11 - Deoxycortisone
Is salt saving (deoxycortisone acts as a mineralocorticoid) and causes hypertension
11 - Hydroxylase deficiency
• Tx: cortisol, genitoplasty
Congenital adrenal hyperplasia (enzyme defect in cortisol synthesis)
ambiguous genitalia in males at birth; salt saving
17-Hydroxylase deficiency
Symptoms: HTN 2/2 sodium retention with out edema; hypokalemia; also have weakness, polydipsia, and polyuria
Hyperaldosteronism (Conn's syndrome)
Low renin - # 1 cause
adenoma (80%-90%)
hyperplasia (10%- 20% ), ovarian tumors (rare), cancer (rare)
Primary disease Hyperaldosteronism (Conn's syndrome)
(high renin) - more common
CHF, renal artery stenosis, liver failure, pregnancy, diuretics, Bartter's syndrome (renin secreting tumor)
Secondary disease Hyperaldosteronism (Conn's syndrome)
Dx for primary hyperaldosteronism
Urine aldosterone after salt load best (will stay high)
decreased serum K, increased urine K,
increased serum Na,
metabolic alkalosis
• Plasma renin activity will be low
• Aldosterone: renin ratio > 20
Tx for Hyperaldosteronism (Conn's syndrome) 2/2 hyperplasia
Medical therapy first with hyperplasia using spironolactone, calcium channel blockers, and potassium
Tx: adenoma cuasing Hyperaldosteronism (Conn's syndrome)
resection has good results with adrenalectomy
Localizing studies for Hyperaldosteronism (Conn's syndrome
MRI, NP- 59 scintigraphy (shows hyperfunctioning adrenal tissue; differentiates adenoma from hyperplasia; 90% accurate)
#1 cause - withdrawal of exogenous steroids
#1 primary disease - autoimmune disease
Hypocortisolism (adrenal insufficiency, Addison's disease)
Decreased cortisol and aldosterone
Dx of Hypocortisolism (adrenal insufficiency, Addison's disease)
Decreased cortisol and aldosterone
Dx: decreased serum Na , increased serum K,
ACTH stimulation test
sx hypotension, fever, lethargy, abdominal pain,
decreased glucose, decreased mental status, nausea and vomiting, increased K
Acute adrenal insufficiency
most common cause Hypercortisolism (Cushing's syndrome)
iatrogenic
#1 noniatrogenic cause of Cushing's syndrome
Pituitary adenoma (Cushing's disease)
Most sensative test for dx Hypercortisolism (Cushing's syndrome)
24hr Urine cortisol (most sensitive test)
Bimodal distribution (before age 5 and in the 5th decade); more common in females
• 5O% are functioning tumors - cortisol, aldosterone, sex steroids
precocious puberty in boys, virilization in females
Sx abdominal pain, weight loss, weakness
• 80% have advanced disease at the time of diagnosis
• Tx: radical adrenalectomy; mitotane for residual or recurrent disease
• 20% 5-year survival rate
Adrenocortical carcinoma
What structure?
From ectoderm neural crest cells
• Catecholamine production tyrosine> dopa> dopamine> norepinephrine> epinephrine
ADRENAL MEDULLA
What is the rate- limiting step in catecholamine production?
tyrosine > dopa
Tyrosine hydroxylase
enzyme that converts norepinephrine> epinephrine
(requires methylation)
• Enzyme is found only in adrenal medulla (exclusive producers of epinephrine)
PNMT
converts:
norepinephrine >
normetanephrine,
epinephrine > metanephrine,
VMA produced from these
MAO monoamine oxidase
Usually slow growing; arise from sympathetic ganglia or ectopic neural crest cells
R side predominance
• "Extra"adrenal tumors more likely malignant
• Sx: HTN (frequently episodic), HA, diaphoresis, palpitations
• Dx: urine metanephrines and VMA - breakdown products of epi and norepinephrine
Pheochromocytoma
chromaffin cells
Most sensitive test for Pheochromocytoma
VMA in urine most sensitive
#2 noniatrogenic cause of Cushing's syndrome
small cell lung CA
Cortisol is not suppressed with either low- or high-dose dexamethasone
suppression test
Tx: resection of primary if possible; medical suppression or bilateral adrenalectomy for inoperable lesions
Tx for Adrenal hyperplasia
(macro or micro)
bilateral adrenalectomy
Medical therapy for ectopic ACTH production or adrenocortical cancer with
residual or metastatic disease after resection
1. Ketoconazole and metyrapone - inhibit steroid formation
2. Aminoglutethimide - inhibits cholesterol conversion
• Op-DDD ( mitotane) - adrenal - lytic, used for metastatic disease
,- --
def.
inhibits tyrosine hydroxylase causing decrease synthesis of catecholamines
Metyrosine
Most common site of extramedullary tissue
organ of Zuckerkandl (inferior
aorta near bifurcation)
What can cause falsely elevated VMA
coffee, tea, fruits, vanilla , iodine contrast, labetalol alpha and beta- blockers
Def. rare benign, asymptomatic tumor of neural crest origin in the
adrenal medulla or sympathetic chain
Gianglioneuroma