End Part 2 Flashcards

1
Q

Difference between Cushing Syndrome and Disease?

A

Syndrome = Excess Cortisol
Disease = ACTH producing tumor

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2
Q

Cushing Syndrome is often caused by exogenous steroids. List some physical exam findings

A

Central obesity with striae
Moon facies
Buffalo hump
Bruising/purpura
Muscle weakness
Thin skin

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3
Q

If you suspect high cortisol levels, what should be done first?

A

24 hour urine cortisol levels

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4
Q

If 24 hour cortisol is elevated, then what?

A

Low-dose Dexamethasone suppression test

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5
Q

What will be the result of a Low-dose Dexamethasone suppression test with Cushing Syndrome?

A

FAILS to suppress cortisol

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6
Q

Once the cortisol fails to suppress with a low-dose dexamethasone test, what should be done next?

A

Measure ACTH – Is the high cortisol ACTH independent or dependent?

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7
Q

If ACTH is low with high Cortisol, where is the likely source?

A

Adrenals – get a CT/MRI

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8
Q

If ACTH is high with high Cortisol, what should be done?

A

High-dose dexamethasone suppression test

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9
Q

If the High-dose dexamethasone suppression test suppresses cortisol, what is the diagnosis?

A

Pituitary adenoma

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10
Q

If the High-dose dexamethasone suppression test does NOT suppress cortisol, what is the diagnosis?

A

Ectopic ACTH producing tumor

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11
Q

List as many Cushing syndrome signs as possible

A

Abdominal obesity with striae
Moon facies
Buffalo hump
Bruising/purpura
Muscle weakness
Thin skin

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12
Q

If you suspect a GH secreting tumor, what should be measured?

A

IGF-1

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13
Q

If IGF-1 is HIGH, what should be done next?

A

Glucose suppression test

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14
Q

GH secreting tumors present as Gigantism in children and Acromegaly in adults. What is the treatment options?

A

Surgery
Somatostatin analogs to (-) GH secretion

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15
Q

Medical treatment for GH tumors?

A

Somatostatin analogs to (-) GH secretion
ex. Octreotide

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16
Q

What are 2 complications of Acromegaly?

A

Diabetes
Cardiomyopathy

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17
Q

What are the levels of the Adrenal Cortex and what do they secrete?

A

GFR
- Glomerulosa –> Aldosterone
- Fasciculata –> Cortisol
- Reticularis –> Androgens

18
Q

What regulates the levels of the Adrenal Cortex?

A

Glomerulosa – Angiotensin 2
Fasciculata and Reticularis – ACTH

19
Q

What is in the Adrenal Medulla?

A

Chromaffin cells that produce catecholamines Epinephrine and Norepinephrine

20
Q

What is Adrenal Insufficiency?

A

Inadequate production of Glucocorticoids +/- Mineralocorticoids

21
Q

Common causes of Primary Adrenal Insufficiency?

A

Autoimmune (Addison’s)
TB
Hemorrhage (Waterhouse-Friderichsen)

22
Q

Describe the lab values with Primary Adrenal Insufficiency

A
  • Low Aldosterone –> High K+
  • Low cortisol
  • High ACTH
23
Q

What are the signs of Primary Adrenal Insufficiency?

A

Fatigue, anorexia, weight loss and skin hyperpigmentation

24
Q

What causes the skin hyperpigmentation with Primary Adrenal Insufficiency?

25
If you suspect Primary Adrenal Insufficiency, what test should be done?
Cosyntropin ACTH stimulation test
26
What will be the result of Cosyntropin ACTH stimulation test with Primary Adrenal Insufficiency?
NO RISE in Cortisol
27
What is the treatment for Primary Adrenal Insufficiency?
Replace glucocortiocoids +/- mineralocorticoids (fludracortisone)
28
Secondary/Tertiary Adrenal Insufficiency is due to?
LOW ACTH
29
What will the lab values be with Secondary/Tertiary Adrenal Insufficiency?
LOW ACTH - Low cortisol - Aldosterone, Na and K UNAFFECTED because they are regulated by Angiotensin 2
30
An Acute Adrenal Crisis is due to abruptly stopping long-term steroids. How may that present?
Confusion Hypotension Coma
31
What is the treatment for an Acute Adrenal Crisis? (2)
Volume resuscitation + STEROIDS
32
Congenital Adrenal Hyperplasia is due to enzyme deficiencies. What is the most common?
21-hydroxylase
33
In general, what is present with 21-hydroxylase deficiency?
LOW mineralocorticoids and glucocorticoids HIGH Androgens
34
How will 21-hydroxylase deficiency present?
Ambiguous genitalia and hypotension
35
What marker is specific for adrenals?
DHEA-S
36
Besides androgens, what will be elevated with 21-hydroxylase deficiency?
17-OHP and Renin!
37
If 11beta-hydroxylase deficiency is to blame for CAH, how does that differ from 21-hydroxylase?
NO LOW BP -- 11-deoxycorticosterone is produced and is able to raise the BP
38
MEN 1
Pituitary Parathyroid Pancreas
39
MEN 2A
Parathyroid Pheochromocytoma Medullary thyroid carcinoma
40
MEN 2B
Pheochromocytoma Medullary thyroid carcinoma Marfanoid habitus