ENDO-Adrenal Flashcards

1
Q

Which adrenal layer secretes catecholamines (epinephrine & norepinephrine)?

A

medulla (inner)

richly innervated, extension of sympathetic nervous system

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2
Q

Which layer Secretes steroid hormones

A

adrenal Cortex (outer)

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3
Q

List the 5 steroid hormone groups based on their receptor binding sites

A
1] Mineralocorticoids: Aldosterone, 
2] Glucocorticoids: Cortisol, 
3] Androgens: Testosterone, DHEA, 
4] Estrogens: Estradiol, estrone, 
5] Progestins: progesterone- corpus luteum
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4
Q

Descibe the HPA axis

A
Stress -> 
hypothalamus -> 
CRH -> 
Anterior Pituitary -> 
ACTH -> 
adrenal glands -> cortisol
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5
Q

HIGH ACTH

LOW serum CORTISOL

A

Primary adrenal insufficiency
pituitary is pumping out lots of ACTH
adrenal gland is not responding by NOT making cortisol, problem is the adrenal

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6
Q

LOW ACTH

LOW serum cortisol,

A

Secondary adrenal insufficiency

pituitary is not responding to feedback signal of low cortisol
problem is the pituitary

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7
Q

PT c/o Weakness, abdominal pain, fever, confusion, N/V/D.

PE/Vitals: Low BP, dehydration; skin pigmentation

A

Acute (adrenal crisis) Adrenal Insufficiency

Emergency caused by cortisol insufficiency.

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8
Q

PT c/o Weakness, easy fatiguability, anorexia, weight loss, N/V/D. abdominal pain; MSK pains; amenorrhea,

PE/Vitals Sparse axillary hair, increased skin pigmentation (esp at creases, pressure areas, nipples),
Low BP,
small heart -quiet sounds

A

Chronic (Addison’s disease) Adrenal Insufficiency

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9
Q

Describe the causes of Primary Adrenal Insufficiency

A
1] Autoimmune diseases, 
2] Adrenal infections and inflammation, 
3] Bilateral metastases, 
4] After adrenalectomy, 
5] Adrenal hemorrhage or necrosis,
 6] Idiopathic,
 7] Drug-induced, 
8] Congenital disorders
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10
Q

Describe the causes of Secondary Adrenal Insufficiency

A

1] Pituitary or hypothalamic tumor,
2] Pituitary irradiation, surgery or brain trauma,
3] Pituitary infections, inflammation, hemorrhage or necrosis,
4] Acute interruption of prolonged glucocorticoid therapy, 5] Acute adrenal crisis (shock syndromes)

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11
Q

PT c/o Weakness, abdominal pain, fever, confusion, N/V/D.

PE/Vitals: Low BP, dehydration; skin pigmentation

What is next step to check?

A

ADDison Adrenal Insufficiency -cortisol and aldosteronelow
1] CMP with high K+, low Na+, high Ca2+, high BUN,
2] CBC anemia, neutropenia with lymphocytosis, and eosinophilia (chronic),

3] Low plasma cortisol at 8:00am

4] High plasma ACTH in primary adrenal disease

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12
Q

PT c/o Weakness, abdominal pain, fever, confusion, N/V/D.

PE/Vitals: Low BP, dehydration; skin pigmentation
Describe the diagnositic test

A

secondary Adrenal Insufficiency
Cosyntropin stimulation test: Synthetic ACTH given parenterally;

draw blood 30-60 min later;

failure of serum cortisol to rise is POSTIVE FOR PRIMARY- adrenal not responding
IF give DEXA(cortisol) ACTH still stays high, then pituitary

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13
Q

What is treatment for Adrenal Insufficiency

A

1] Replace cortisol with hydrocortisone (or other form),

2] Treat infections aggressively; stress dosing appropriate

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14
Q

Pt C/o poor wound healing, psych changes,

Obj-“moon face,” acne, “buffalo hump,” supraclavicular fat pads, protuberant abdomen, thin extremities

PE/Vitals
Central obesity, muscle wasting, thin skin, hirsutism, purple striae, Osteoporosis, HTN,

A

Cushing’s Syndrome-Due to excess corticosteriods

Massive fat redistribution

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15
Q

What are some reproductive dysfunction of Cushing’s Syndrome

A

Oligomenorrhea/amenorrhea, impotence

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16
Q

Describe the other dysfunctions of Cushing’s Syndrome

A

1] Weakness, backache, HA, polyuria, polydipsia, 2] HTN, osteoporosis, bone AVN, nephrolithiasis, 3] Decreased concentration, mood lability or psychosis

17
Q

What would you order first and find for the next stepss of Cushing’s Syndrome

A
#1] Late evening salivary cortisol level, 
2] 24 hour urine for free cortisol, 
3] Low-dose dexamethasone suppression test 

4] CMP-Impaired glucose tolerance and insulin resistance, hyperglycemia; hypokalemia (normal sodium)
5]CBC Leukocytosis, lymphocytopenia

18
Q

What are the requirements for diagnosis of Cushing’s Syndrome?

A

1] Cortisol levels should be checked at least twice,

2] At least two of these tests should be abnormal

19
Q

What is the next step once hypercortisolism is confirmed

What would findings suggest?

A

plasma ACTH is ordered to find the cause

low ACTH; high serum cortisol,
high cortisol shuts off ACTH production from pituitary, so cause is adrenal tumor

20
Q

If after dexa test, cortisol is till high, ACTH is high then…What is condition?

A

Cushing’s disease ***
high serum cortisol, high ACTH; high cortisol does not shut off ACTH

pituitary, caused by benign pituitary adenoma

21
Q

What is the next step in management if the patient has Cushing’s disease?

A

Refer to endocrinology for CRH stimulation test to determine if cause is hypothalamus or pituitary,

22
Q

What are the classic signs and sx of Primary Hyperaldosteronism

A

PE/Labs:HTN (Resistant HTN primary reason to consider this dx),
hypokalemia
Elevated plasma and urine aldosterone
low plasma renin level- NOT kidneys affectin Aldo

Pt-Polyuria, polydipsia, muscular weakness

23
Q

What are the most common subtypes of Primary Hyperaldosteronism? What test to confirm?

A

1] aldosterone-producing adenoma and
2] bilateral idiopathic hyperaldosteronism
Adrenal CT scan

24
Q

Describe the treatment of Primary Hyperaldosteronism

A

adrenalectomy

25
Q

Pt c/o Attacks of HA, perspiration, palpitations, tachycardia, anxiety,

Vital- HTN

A

Pheochromocytoma

Tumor in adrenal medulla; rare cause of HTN

26
Q

Describe the HTN in Pheochromocytoma

A

may be sustained, resistant to therapy or paroxysmal, esp in relation to stress

27
Q

Pt c/o Attacks of HA, perspiration, palpitations, tachycardia, anxiety,

Vital- HTN
What is the work up?

A

Pheochromocytoma
URine- elevated catecholamines or metanephrines;

CBC-plasma fractionated free metanephrines most sensitive but many false positives

28
Q

What is next step in management if catecholamines or metanephrines positive?

A

Refer to Endocrinology

Followed by imaging of adrenals (CT or MRI)

29
Q

treatment of Pheochromocytoma

A

surgical resection of tumor

30
Q

When should you refer to an endocrinologist?

A

1] If positive, refer to Endocrinology,
2] If you’re not sure, refer to Endocrinology,
3] Treatment and follow up will be done by the Endocrinologist