MEH 18 - Adrenal Disorders Flashcards

1
Q

What are the clinical presentations of cortisol/mineralocorticoid/androgen/ACTH excess and deficiency?

A

Excess

Cortisol = weight gain + cushingoid features
Mineralo =  High BP, High Na+ + Low K+
Androgen = Increased male characteristics in women
ACTH = Skin pigmentation (melanocyte stimulation)

Deficiency

Cortisol = weakness, tiredness, weight loss
Mineralo = Dizziness, low Na, high K
Androgen = low libido + loss of body hair in women
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2
Q

How can adrenal disorders be assessed?

A

1) Clinically - via symptoms
2) Biochemical - e.g.: via electrolytes, urine concentration of hormones + suppression tests
3) Imaging - CT scans, MRI scans, PET scans etc

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3
Q

What is primary adrenal failure (Addison’s disease)

What are the symptoms + signs?

A
  • Underactive adrenal gland, caused by autoimmune disorder, infection, malignancy, iatrogenic etc.
  • Symptoms = fatigue, weakness, anorexia, weight loss, nausea, dizziness
  • Signs = underweight, general malaise, postural hypotension, pigmentation etc.
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4
Q

How is Addison’s disease treated?

A
  • Lifelong replacement of glucocorticoids (hydrocortisone) and mineralocorticoids (fludrocortisone) + education to prevent crisis.
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5
Q

What is Cushing’s syndrome + how is it caused?

A
  • Cushing’s syndrome is an overexposure to excess glucocorticoids.
  • Pituitary tumours, adrenal tumours, ectopic ACTH
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6
Q

What are the signs + symptoms of Cushing’s syndrome?

A
  • Round pink face with round abdomen
  • Skinny + weak arms/legs
  • Thin skin + easily bruised
  • Red stretch marks (striae) on abdomen
  • High BP + diabetes
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7
Q

What is primary hyperaldosteronism + how is it caused?

How does it present clinically?

A
  • Excess production of aldosterone from adrenal glands, either by aldosterone-secreting adrenal adenoma (Conn’s syndrome) or bilateral adrenal hyperplasia.
  • Hypertension, hypokalaemia + hypernatraemia (think about aldosterone action)
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8
Q

What is congenital adrenal hyperplasia?

How does it present?

A
  • Rare inherited disorder caused by enzyme deficiency in adrenal cortex pathway. Can lead to low cortisol, aldosterone or high sex steroids.
  • Hypotension, hyponatreamia, hyperkalaemia, hypoglycaemia + ambiguous genitalia.
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9
Q

What are the symptoms of a phaechromocytoma?

A
  • Acute episodes, sweating, panic attacks, palpitations, high or low BP, collapsing.
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