Adrenal Glands - Sheet1 Flashcards

1
Q

↑ cortisol caused by a pituitary adenoma resulting in ↑ ACTH secretion which causes the adrenal gland to secrete excess cortisol

A

Cushing’s Disease: secondary

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2
Q

↑ cortisol secretion from an adrenal tumor

A

Cushing’s Syndrome: primary

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3
Q

Adrenal gland destruction causing lack of cortisol and aldosterone secretion usually autoimmune

A

Primary adrenocortical insufficiency (Addison’s disease)

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4
Q

In a patient with secondary corticoadrenal insufficiency, what would happen to cortisol levels after a cosyntropin stimulation?

A

Cortisol levels would increase

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5
Q

What is cosyntropin?

A

ACTH

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6
Q

What does no change in cortisol levels after initiation of a cosyntropin stimulation indicate?

A

Primary corticoadrenal insufficiency

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7
Q

How does hyperpigmentation differentiate hypocortisol states?

A

Hyperpigmentation occurs with primary corticoadrenal insufficiency (Addison’s disease)

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8
Q

What is the treatment of choice for Cushing’s Disease?

A

Trans sphenoidal resection of the pituitary adenoma or surgical resection of ectopic cortisol producing tumor and cortisol (hydrocortisone or fludrocortisone) replacement if needed

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9
Q

What are the cardinal signs and symptoms of Cushing syndrome or disease?

A

Buffalo hump - Moon face - Blue abdominal striae - Truncal obesity - Hyperglycemia - Hypertension

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10
Q

Salt craving hyperpigmentation of skin and fatigue represent which disorder?

A

Addison’s

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11
Q

Pheochromocytoma

A

24 hour catecholamines including metabolites (metanephrine and vanillylmandelic acid)

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12
Q

List three medications which may be used for Cushing patients who can not have surgical correction?

A

Mitotane - Metyrapone - Ketoconazole

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13
Q

What screening should long term Cushing syndrome or disease patients have?

A

DEXA (Osteoporosis common in long term hyper-cortisol states)

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14
Q

Decreased ACTH and high cortisol levels in a high dose dexamethasone suppression test is diagnostic for which disorder?

A

Cushing syndrome (primary) will result in decreased ACTH from the dexamethasone

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15
Q

Increased ACTH result from a high dose dexamethasone suppression test is diagnostic for which disorder?

A

Cushing disease (secondary) will continue with increased ACTH despite the dexamethasone

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16
Q

What result is expected with a low dose dexamethasone suppression test?

A

Decreased cortisol = Normal - Cushing disease or syndrome will result in persistent increased cortisol

17
Q

Cushing Syndrome

A

Buffalo hump, moon face, blue abdominal striae, truncal obesity, increased glucose, increased BP

18
Q

List three causes of Cushing syndrome?

A

Adrenal adenoma - Adrenal hyperplasia - Adrenal cancer

19
Q

Is Cushing’s disease or syndrome more common?

A

70% of patients have secondary (Cushing’s disease) from ACTH secreting tumors

20
Q

What test other than the dexamethasone suppression test can be used for Cushing disease?

A

Serum ACTH will be increased in Cushing’s disease (secondary)

21
Q

What test other than the dexamethasone suppression test can be used for Cushing syndrome or disease?

A

24 hour urine for cortisol will be increased in both

22
Q

What is the difference between Cushing syndrome and Cushing’s disease?

A

Syndrome is primary - Disease is secondary

23
Q

What happens to glucose blood pressure inflammation and metabolism in Cushing’s syndrome or disease?

A

Increased glucose - Increased blood pressure - Decreased inflammation - Increased metabolism

24
Q

PITUITARY FAILURE which results in ↓ ACTH (from pituitary failure), ↓ Cortisol, and normal aldosterone

A

Secondary adrenocortical insufficiency (Addison’s disease)

25
Q

What is the treatment for corticoadrenal insufficiency?

A

Hydrocortisone or fludrocortisone

26
Q

List four less common causes of primary corticoadrenal insufficiency?

A

Tuberculosis - Adrenal infection - Metastasis to adrenal gland - Adrenal trauma

27
Q

What is the most common cause of primary corticoadrenal insufficiency?

A

Addison’s disease

28
Q

What symptoms may result from abrupt withdrawal of long term high dose steroids?

A

Severe N/V/D - Significant hyponatremia - Hyperkalemia - Hypoglycemia

29
Q

A test in which one or more small doses of dexamethasone are given. The level of cortisol is checked from a sample of blood or from urine that is collected for three days. This test is done to check if the adrenal gland is making too much cortisol. In general, a clear failure to suppress cortisol levels in response to low-dose dexamethasone establishes the diagnosis.

A

Low-dose dexamethasone suppression test - used to diagnose cushing’s syndrome

30
Q

A test in which one or more high doses of dexamethasone are given. The level of cortisol is checked from a sample of blood or from urine that is collected for three days.

A

High-dose dexamethasone suppression test (done in response to a positive low dose test)

31
Q

A patient has decreased ACTH and increased cortisol. Is this primary or secondary disease?

A

Primary

32
Q

What basic metabolic panel finding might one find in a patient with Addison’s disease?

A

Hyponatremia

33
Q

What CBC finding might one find in a patient with Addison’s disease?

A

Eosinophilia

34
Q

What are you concerned about in a patient who has no change in ACTH levels and has increased cortisol levels on a high dose dexamethasone suppression test?

A

Ectopic source of ACTH - e.g. lung tumor

35
Q

What is the best way to test cortisol levels in a patient with a suspect hypercortisol state?

A

24 hour urine cortisol

36
Q

Are increased cortisol levels with a cosyntropin test consistent with primary or secondary corticoadrenal insufficiency?

A

Secondary

37
Q

Is hyperpigmentation a sign of primary or secondary corticoadrenal insufficiency?

A

Primary

38
Q

What is Sipple syndrome?

A

MEN 2a (Hyperparathyroid - Medullary thyroid cancer - Pheochromocytoma)