Adrenal gland physiology and disorders Flashcards

1
Q

What are the secretions of the adrenal glands?

A

Aldosterone
Cortisol
Androgens (DHEAA)
Catecholamines

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is the main cause of primary adrenal insufficiency?

A

Addisons disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What causes Addisons disease?

A

Autoimmune destruction of the adrenal cortex

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are the main features of Addisons?

A

Non-specific symptoms such as anorexia, fatigue, malaise, lethargy
Dizziness and low BP
Abdominal pain, nausea and vomiting
Skin pigmentation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What is the main diagnostic test in Addisons?

A

Short synacthen test

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

How is Addison’s treated?

A

Replacement of hydrocortisone and fludrocortisone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Why is it not necessary to treat with fludrocortisone in secondary adrenal insufficiency due to pituitary disease?

A

Because RAAS is still intact

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Name three situations where primary aldosteronism may be considered as a diagnosis.

A

Resistant hypertension in the young
Hypokalaemia
Alkalosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How does primary aldosteronism present?

A

Often asymptomatic
Signs of hypokalaemia
Polyuria, polydipsia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are the two main causes of primary aldosteronism?

A

Conn’s syndrome (adrenal adenoma)

Bilateral adrenal hyperplasia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Which suppression test is used to confirm primary aldosteronism?

A

Saline suppression test (saline should suppress aldosterone)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

How is a) Conn’s b) bilateral adrenal hyperplasia managed?

A

a) Adrenalectomy

b) Spironolactone (mineralocorticoid receptor antagonist)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What causes congenital adrenal hyperplasia?

A

Inherited autosomal recessive mutations in corticosteroid synthesis. Usually 21-hydroxylase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

How does C.A.H. typically present in a) infants b) young boys c) young girls d) late onset (atypical)?

A

a) salt-losing crisis b) precocious puberty c) ambiguous genitalia d) signs of androgen excess e.g. hirsutism, oligomenorrhoea, subfertility

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

How is C.A.H. diagnosed?

A

Basal 17-OH progesterone

Synacthen test- inappropriate rise in progesterone

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

How is C.A.H. managed a) in paediatrics b) in adults

A

a) steroid replacement, surgical correction of genitalia b) control androgen excess, restore fertility

17
Q

Where does phaeochromocytoma usually arise from?

A

Chromaffin cells of the adrenal medulqla

18
Q

What familial cancer conditions is phaeochromocytoma associated with?

A

MEN2a
Von-Hippel Lindau
Neurofibromatosis

19
Q

What is the classic triad of symptoms of phaeochromocytoma?

A

Episodic headache, sweating and tachycardia

20
Q

What is the main test if phaeochromocytoma is suspected?

A

Urine catecholamines