Lecture 2 – Adrenal Flashcards

1
Q

What do the cortex and the medulla of the adrenal glands produce?

A

The cortex produces adrenaline and the medulla produces catecholamines.

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

What are the different layers of the adrenal medulla and what do they produce?

A

The zona glomerulosa produces mineralacorticoids such as aldosterone
The zona fasciculata produces glucocorticoids such as cortisol
The zona reticularis produces androgens such as DHEA

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

What is congenital adrenal hyperplasia and how does it occur?

A

It is a number of autosomal recessive conditions that result in problems with enzymes in the synthesis of steriods. Typically there is blockage of the cortisol pathway resulting in overproduction of DHEA. This can cause female babies to be born with virilised genitalia.

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

What deficieny most commonly causes CAH and how would this be tested diagnostically?

A

21-hydroxylase enzyme is most commonly deficient and this causes a lack of conversion to 17OHP. This means that 17OHP levels can be measured before and after ACTH is given to detect 17-hydroxylase deficiency.

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

Why does DHEA production increase when there is a deficiency in 21-hydroxylase?

A

As there are no mineralcorticoids or glucocorticoids being produced there is greatly reduced negative feedback to the pituitary. This means excessive ACTH is produced resulting in overproduction of androgens.

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

Why is CAH a medical emergency?

A

The child is not producing enough glucocorticoids so will go into adrenal crisis if not given cortisol.

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

What is the growth pattern of an undiagnosed child with CAH?

A

They will grow quickly however their growth plates will fuse early due to excessive androgens. This will result in short stature later in life.

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

What is an adrenal incidentaloma?

A

An adrenal mass that is dicovered icidentally when investigating other things.

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

What is adrenocortical carcinoma and how common is it?

A

It is a highly malignant tumour but is rare at only 2-11% of adrenal masses.

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

It is hard to differentiate between benign and malignant adrenal masses, why is this?

A

Imaging of the adrenals is difficult so hard to tell if they are benign.

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

Once an adrenal mass has been identified what can be looked at other than imaging?

A

Can look at hormone levels to see if the tumour is hypersecreting. All layers of the adrenals can hypersecrete with a tumour.

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

What three conditions must you exclude when looking at bloods for an adrenal mass?

A

Cushings
Phaeochromocytoma - adrenaline
Primary Hyperaldosteronism - renin levels high

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

What is phaeochromocytoma and what would you test to exclude this?

A

This is a hypersecretory tumour in the cortex of the adrenal gland. This could be excluded by looking at plasma metanephrines because these are the breakdown products of adrenaline so would be increased with phaeochromocytoma.

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

How would you exclude cushings when looking at an adrenal mass?

A

An overnight dexamethasone supression test would be used. This provides negative feedback to the pituitary which should decrease ACTH and cortisol if it is was not cushings. Also do 24 hr urinary free cortisol.

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

How would you exclude hyperaldosteronism with an adrenal mass?

A

measure renin and aldosterone levels, always test pairs of hormones (diagnostic pairs) e.g. ACTH and cortisol.

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

What is a hazard of removing a hypersecreting tumour?

A

If it is hypersecreting cortisol then negative feedback would have been dampened. This means that if the tumour is removed and cortisol falls then negative feedback will not increase it so the patient can go into adrenal crisis.

17
Q

What are the criteria for surgery of a likely adrenal corticocarcinoma on imaging?

A

The tumour must be greater than 4cm, it must have a density of greater than 20 hounsfield units on CT. It must also appear irregular shape on MRI.

18
Q

What are the causes of phaeochromocytoma?

A

25% are from a mutation in RET which is a proto oncogene.
multiple endocrine neoplasia type 2
Von hippel lindau syndrome

19
Q

What are the signs and symptoms of phaeochromocytoma?

A

90% of cases have hypertension
Headaches, sweating, nausea and general signs of adrenaline release.
Postual hypertension

20
Q

How is phaeochromocytoma treated medically?

A

With alpha and beta blockers.

Or Mitotane or Cytotoxic Chemotherapy

21
Q

How is phaeochromocytoma treated surgically and what precautions must be taken?

A

It is treated with alpha blockers whilst surgery is taking place. This is because even touching the tumour can cause adrenaline release which can cause heart attacks and brain aneyrysms from sudden changes in vasodilation.