Adrenal Gland Flashcards

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1
Q

anatomy of the adrenal gland

A

has the medulla and the cortex. Cortex consists of 3 zones.

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2
Q

Adrenal cortex hormones

A
  1. Glucocorticoids, produced in Zona Fasciculata (Cortisol) 2. Mineralcorticoids, produced in Zona Glomerulosa (aldosterone) 3. Sex steroids, produced in Zona Reticularis (Androgens)
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3
Q

Adrenal medulla hormones

A

produces catecholamines: epinephrine, NE and dopamine.

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4
Q

Cortisol test

A

24 HOUR URINE TEST IS BEST A random cortisol sample collection tells you nothing because cortisol levels naturally fluctuate throughout the day.

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5
Q

Dexamethasone Suppression Test

A

Dexamethasone is a synthetic glucocorticoid that is more potent than Cortisol Give a dose of dexamethasone and it should suppress pituitary activity. This test will tell you if the Cushings syndrome is adrenal or pituitary in nature.

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6
Q

ACTH

A

In patients that have an abnormal Dexamethasone suppression test, you will do an ACTH test to determine if the Cushings is ACTH dependent or not.

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7
Q

ACTH Stimulation Test

A

The most useful test for Adrenal Insufficiency It tests the adrenal response when pt given an ACTH-like substance. Normal response is a cortisol level greater than 20mg/dl, one hour later. Lack of a rise indicates adrenal insufficiency

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8
Q

CRH Stimulation Test

A

CRH can be given to evaluate to Pituitary response to stimulation from the Hypothalamus. Give CRH and measure Cortisol and ACTH This test is used to differentiate primary vs. secondary adrenal insufficiency.

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9
Q

Primary (Pituitary) Adrenal Insufficiency determined by CRH stim test

A

test will show elevated ACTH but no Cortisol production

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10
Q

Secondary Adrenal Insufficiency determined by CRH stimulation test

A

test will show Low ACTH and Low Cortisol

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11
Q

Aldostrone Concentration

A

Most important test to diagnose Hyper and Hypoaldosteronism. Can be measured in serum or in urine.

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12
Q

Testing for Primary Aldostronism

A

order an aldostrone concentration and a Plasma renin activity (PRA)

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13
Q

Plasma Renin Activity

A

when kidneys are stressed, PRA goes up. Elevated PRA seen in Hyperaldosteronism. This test measures the ability to convert Angiotensinogen to Angiotensin I

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14
Q

Cushings Syndrome

A

Excess ACTH Not typically an endogenous disease process, usually caused by medications.

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15
Q

Cushings Disease

A

Cushings syndrome but as a result of a pituitary adenoma. Get excess ACTH production from the pituitary.

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16
Q

Cushings diagnosis

A
  1. 24 hour urine cortisol (could also be 24 hour salivary cortisol) is the GOLD STANDARD. 2. Determine if the cortisol deficiency is ACTH suppressible or CRH sensitive by getting an ACTH suppression test and a CRH sensitivity test. This determines the level of the problem. 3. Get imaging for potential surgical fix.
17
Q

Primary Cortisol and ACTH defeciency

A

There is low production at the Adrenal Level

Addisons disease or Adrenal insuffeciency

18
Q

Secondary ACTH and Cortisol Defeciency

A

Because of some failure in the hypothalmic/Pituitary Axis

19
Q

Primary Addisons Disease

A

Destruction of the Renal Cortex

  • autoimmune disorder
  • TB
  • Chronic infection

Cortisol and Aldosterone levels are low

When you to an ACTH stimulation test, there is no increase in cortisol, this is how you know it is primary.

20
Q

Secondary Addisons disease

A

Due to lack of ACTH

  • Drugs
  • Tumors
  • infection of pituitary

Cortisol only is low

you do an ACTH stimulation test and you get an increase in cortisol

21
Q

Addisons manifestations

A

Hypoglycemia

Weight loss

Fatigue

Hypotension

Dizziness

N/V/D

Tanning of skin

22
Q

Diagnosing Addisons

A
  1. Look for Low cortisol Level–> 24 hour urine cortisol, plasma aldosterone
  2. Demonstrate if ACTH is sensitive–> ACTH sensitivity Test

If not ACTH sensitive –> Primary/Adrenal cause

If ACTH sensitive–> Secondary cause –> order CRH stimulation test: Hypothalmic or pituitary level.

  1. look for treatable cause–> imaging.
23
Q

Primary Addisons treatment

A

Replacement therapy

Replace Cortisol levels with hydrocortisone.

Replace Aldosterone with Fludrocortisone.

24
Q

Secondary Addisons Treatment

A

Find/treat tumors

stop the offending drugs

treat the infection

25
Q

Conns Syndrome

A

Primary Hyperaldosteronism

Pts have hypertension, decreased blood potassium, and are tired, have muscle weakness and polyuria. Pts do not respond to hypertension drugs.

This is caused by an adrenal adenoma- treatment is surgical

Labs: aldosterone is high, potassium low, normal sodium, PRA is low

26
Q

Secondary Hyperaldosteronism

A

More common

oIncreased Aldosterone is due to decreased renal perfusion which causes elevated PRA
Commonly caused by: CHF, nephrotic syndrome, cirrhosis

27
Q

Primary hypoaldosteronism

A

o- Usually due to destruction of adrenal glands. Hypo is rare.
oCauses; misuse of steroids, TB, auto immune.

PRA is elevated.

28
Q

Secondary hypoaldosteronism

A

the problem is outside of the adrenal gland- usually a pituitary tumor.

29
Q

CAH

A

Congenital Adrenal Hyperplasia

Characterized by genital abnormalities due to adrenal gland defeciencies.

The adrenal gland is unable to make cortisol and aldosterone, so it makes the only other thing it knows how to make, and that is androgen. The body produces too much androgen. This causes male sex characteristics to appear innaproriately or early.

30
Q

21-Hydroxylase Deficiency

A

90–95% of CAH cases are caused by 21- OHD

Females affected with severe, classic 21- OHD are exposed to excess androgens prenatally and are born with virilised external genitalia–> ambiguous genitalia.

Males born with 21-OHD present early with a salt-wasting crisis –> dehydration.

31
Q

Best test for adrenal medulla

A

Plasma Metanephrine, or 24 hour urine metanephrine

32
Q

Phenochromocytoma

A

Benign or malignant chromaffin tumor of the Adrenal Medulla
Can be fatal if untreated, but is usually treatable with surgery.

Display the 5 P’s

  1. Pressure (HTN)
  2. Pain (headache)
  3. Perspiration
  4. Palpitation
  5. Pallor