18 - Disorders of Adrenocortical Function Flashcards

1
Q

What is Cushing’s syndrome caused by?

A

Excess cortisol secretion

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2
Q

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

A

Cushing’s disease is due to a specific case of benign ACTH secreting pituitary adenoma, but syndrome is due to general symptoms from chronic cortisol exposure

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3
Q

What are some of the signs and symptoms of Cushing’s disease and the reasons behind these?

A

- Hyperglycaemia with polyuria and polydipsia due to increased muscle proteolysis and hepatic gluconeogenesis

- Thin arms and legs and muscle weaknesss due to proteolysis

- Fat in abdomen and weight gain due to increase lipogenesis

- Stria on lower abs, arms and thighs due to proteolysis and easy bruising

- Bacterial infections and acne due to immunosupression, antiinflammatory and anti-allergic effects of cortisol

- Back pain and collapse of ribs due to osteoporosis due to loss of bone matrix protein

  • Hypertension from sodium retention
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4
Q

A patient is taking hydrocortisone and prednisone for rheumatoid arthiritis, they start to develop a buffalo hump and hyperglycaemia, what do they have and what should the treatment be?

A
  • Cushing’s syndrome as these are steroid drugs and have the same effects as cortisol and mineralcorticoids
  • Take them off of the drugs slowly
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5
Q

What can steroid drugs be used to treat and what are some examples?

A
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6
Q

What is a chronic cortisol insufficiency referred to as and what is this caused by?

A

Addison’s disease

  • Disease of the adrenal cortex e.g autoimmune
  • Disorders of the pituitary or hypothalamus decreasing ACTH or CRF
  • Rare causes: fungal infection, adrenal cancer, adrenal haemorrhage after trauma
  • Leads to insufficiency of cortisol and mineralcorticoids if autoimmune so can lead to crisis
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7
Q

What is the difference between Addison’s disease and an Addisonian crisis?

A
  • Addison’s is a chronic dehabilitating disorder
  • Addisonian is an acute life threatening emergency when you have addison’s disease
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8
Q

What are some symptoms of Addison’s disease?

A
  • Initial non-specifific symptoms: tiredness, muscle weakness, anorexia, vague ab pain, weight loss, diziness
  • Dehydration
  • Increased skin pigmentation
  • Postural hypotension due to fluid depletion
  • Hypotension
  • Hypoglycaemic episodes, especially on fasting
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9
Q

Why do you get hyperpigmentation in Addison’s disease?

A
  • Occurs mainly on exposed areas of body, points of frction, scars, palmar creases and buccal muscosa
  • Increase in ACTH as well as other products of POMC that stimulate melanocytes to make more melanin
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10
Q

What is an Addisonian crisis exacerbated by and what are the symptoms?

A
  • Severe stress
  • Salt deprivation
  • Infection
  • Trauma
  • Cold exposure
  • Steroid drug withdrawal
  • Overexertion
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11
Q

How can you treat an Addisonian crisis?

A

- IV cortisol (hydrocortisone)6

- Fluid replacement (dextrose in saline)

TO AVOID COMA AND DEATH

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12
Q

How do you test adrenocortical function clinically?

A
  • Measure plasma cortisol and ACTH
  • 24h urinary excretion of cortisol and break down products (17-hydroxysteroids)
  • ACTH stimulation test
  • Dexamethasone supression test
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13
Q

How do you distinguish between Cushing’s disease and between adrenal tumours/ectopic ACTH production?

A

- Dexamethasone: steroid that when given orally would supress ACTH and therefore coritsol

  • In Cushings, will suppress plasma cortisol by more than 50% as still sensitive to potent steroids.
  • Supression won’t occur in the other two cases
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14
Q

How can you dynamically test for Addison’s disease?

A

- Administer Synacthen IM (analogue of ACTH)

  • Will normally increase plasma cortisol by >200nmol/L
  • With Addison’s, this does not happen
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15
Q

What is congenital adrenal hyperplasia?

A
  • Genetic defect in one or more of the enzymes involved in synthesis of corticosteroid hormones from cholesterol
  • Lack of cortisol, PG releases lots of ACTH causing adrenal hyperplasia
  • Mainly 21-hydroxylase deficiency
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16
Q

What are the symptoms of congenital adrenal hyperplasia and why?

A
  • Precursor of gluco and mineralcorticoids, 17a-hydroxypredenolone is diverted to more androgen synthesis (androstenedione and testosterone)
    • Salt wasting crisis* due to loss of aldosterone
    • Genital ambiguity* in female infants
17
Q

What is Conn’s syndrome?

A

- Primary hyperaldosteronism due to hyperactive adrenal glands

- Unilateral form: adenoma

- Bilateral form: familial hyperaldosteronism type I and II

  • Low renin compared to secondary hyperaldosteronism
18
Q

What are some examples of nuclear receptors and what is their structure?

A
  • Steroid
  • Vitamin D
  • Thyroid
  • Hydrophobic hormon binding region, DNA binding region and variable region. Sequence homology in hormone binding regions of the receptors
19
Q

When high levels or cortisol are present, what receptors does it start binding to and why?

A
  • Sequence homology so binds to their hormone binding site with low affinity
  • Will bind to mineralocorticoid and androgen receptors when at high levels!!
20
Q

What do androgens stimulate?

A

Growth and development of male genital tract and sexual characteristics like height, body shape, facial and body hair, low voice pitch, anabolic muscle protein

21
Q

What happens when there is an oversecretion of androgens in females?

A
  • Acne
  • Hirsutism
  • Menstrual problems
  • Virilisation
  • Increased muscle bulk
  • Deepening voice
22
Q

What do oestrogens stimulate in females?

A
  • Growth and development of female genital tract
  • Breasts
  • Broad hips
  • Accumulation of fat in breast and buttocks
  • Body hair distribution
  • Weakly anabolic
  • Decrease circulating cholesterol levels
23
Q

How can you tell the cause of Cushing’s syndrome>

A
24
Q

Explain why purple striae as depicted in the patient below are often seen in Cushing’s syndrome?

A
25
Q

Which type of enzyme catalyses the conversion of noradrenaline to adrenaline?

A

Methyltransferase

26
Q

Which time of day would be best to take a blood sample for cortisol measurement if Cushing’s syndrome is suspected?

A