Adrenal Flashcards

1
Q

What is synthesised and released from the zona glomerulosa?

A

Aldosterone in response to angiotensin II & K+

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2
Q

What is synthesised and released from the zona fasiculata?

A

Glucorticoids (i.e. cortisol) in response to ACTH

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3
Q

What is synthesised and released from the zona reticularis?

A

Sex hormones in response to ACTH & CASH

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4
Q

What are the effects of cortisol?

A

Anti-inflammatory.
Stimulates gluconeogenesis > increased blood glucose.
Stimulates catabolism of proteins > increased blood AAs.
Stimulates FA release > increased blood FAs.

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5
Q

What is Cushing’s syndrome?

A

Elevated plasma [cortisol]

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6
Q

Name some causes of Cushing’s

A

Cushing’s disease - adenoma of the AP.
Adenoma of the adrenal cortex.
Abnormal hypothalamus function > elevated CRH release.
LT treatment with glucocorticoids.

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7
Q

What affect will primary cushings syndrome have on ACTH levels?

A

ACTH levels will be reduced.

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8
Q

What affect will secondary cushings have on ACTH levels?

A

ACTH levels will be elevated.

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9
Q

How can you differentiate between primary and secondary cushings?

A

Give dexamethasone - if ACTH levels fall = secondary cushings.

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10
Q

What are the symptoms of cushings?

A
Weight gain & central obesity.
Moon faced.
Plethoric.
Easily bruised.
Hypertension.
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11
Q

What is the treatment for cushings?

A

Removal of adenoma.
11-beta hydroxylase inhibitor (metyrapone) - blocks 11-B hydroxylase which is required for cortisol synthesis.
Mitotane.

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12
Q

What is 21-hydroxylase deficiency?

A

Most common cause of CAH.

Autosomal recessive disorder which leads to 21 hydroxylase deficiency - required for cortisol & aldosterone synthesis.

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13
Q

What are the symptoms of 21-hydroxylase deficiency?

A

Hypotension.
Hypovolaemia.
Salt wasting.
Sexual ambiguity and hirsuitism.

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14
Q

What will investigations for 21-hydroxylase deficiency show?

A

Elevated 17 hydroxyprogesterone levels.
Low cortisol levels.
Elevated androgen levels.

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15
Q

What is the treatment for 21-hydroxylase deficiency?

A

Hydrocortisone

Fludrocortisone

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16
Q

What is addisons disease?

A

Dysfunctioning adrenal gland > decreased cortisol & aldosterone synthesis.

17
Q

What is the most common cause of addisons disease?

A

UK - autoimmune disease.

Worldwide - Tb.

18
Q

What will primary addisons show?

A

Low aldosterone.

Elevated ACTH.

19
Q

What will secondary addisons show?

A

Low aldosterone.

Low ACTH.

20
Q

What are the symptoms of addisons?

A

skin pigmentation.
Weight loss, fatigue, fever & abdo symptoms.
Addisons crisis - hypotension > coma.

21
Q

What is the treatment for addisons?

A

Hydrocortisone.

Fludrocortisone.

22
Q

What is conns syndrome?

A

Hyperaldosteronism > hypertension.

23
Q

What is pheochromocytoma?

A

Tumour of the adrenal medulla (chromaffin cells) or an extra-adrenal tumour > excess catacholamine release > hypertension.

24
Q

What are the symptoms of pheochromocytoma?

A

Hypertension.

Episodes of sweating, palpitations and panic attacks