Clinical aspects of the adrenal gland Flashcards

What could go wrong?

1
Q

What could cause hyposecretion of the adrenal gland?

A
  • Addison’s disease

- Adrenal enzyme defects

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2
Q

what are the causes of addison’s disease?

A
  • Immune destruction (auto)
  • > 85% UK cases of adrenal failure
  • +ve adrenal autoantibodies (to 21-OHase) in 70% cases
  • lymphocytic infiltrate of adrenal cortex
  • associated autoimmune diseases are common
  • thyroid disease (20%)
  • Type 1 diabetes mellitus (15%)
  • premature ovarian failure (15%)
  • Invasion
  • Infiltration
  • Infection
  • Infarction
  • Iatrogenic
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3
Q

What are the symptoms of hyposecretion?

A
  • Weakness, fatigue, anorexia, weight loss 100%
  • Skin pigmentation or vitiligo 92%
  • Hypotension 88%
  • Unexplained vomiting or diarrhoea 56%
  • Salt Craving 19%
  • Postural symptoms 12%
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4
Q

What are the possible clues to the diagnosis of adrenal failure?

A
  • Disproportion between severity of illness & circulatory collapse / hypotension / dehydration
  • Unexplained hypoglycemia
  • Other endocrine features (hypothyroidism, body hair loss, amenorrhoea)
  • Previous depression or weight loss
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5
Q

How do you diagnose adrenal insufficiency?

A
  • Non-specific symptoms: so must think of the diagnosis in the first place!
  • Routine bloods: U&E, glucose, FBC
  • Random cortisol
    □ >700 nmol/l (not Addison’s)
    □ <700 nmol/l (adrenal status uncertain)
  • Synacthen test (and basal ACTH)
  • If suspicion high & patient unwell, treat with steroids and do Synacthen test later
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6
Q

How does one replace glucocorticoids?

A
  • Usual total daily doses & relative potencies
    □ Hydrocortisone 20-30mg =
    □ Prednisolone 7.5mg =
    □ Dexamethasone 0.75mg
  • Given in divided doses to ‘mimic normal diurnal variation’
    □ e.g. HC 20mg at 08.00h & 10mg at 18.00h
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7
Q

How does one replace mineralocorticoids?

A
  • Synthetic steroid, fludrocortisone
  • Binds to mineralocorticoid (aldosterone) receptors
  • 50-300 micrograms daily
  • Adjust dose according to:
    □ clinical status (postural BP, oedema)
    □ U&E
    □ plasma renin level
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8
Q

What should one do (in regards to the treatment of adrenal hyposecretion) when one has a minor short lived illness or stress?

A

double glucocorticoid dose

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9
Q

What should be done (in regards to the treatment of adrenal hyposecretion) when one has a major illness or operation (especially if nil by mouth or GI upset)?

A
  • 100mg hydrocortisone iv stat
  • 50-100mg HC iv 8-hourly
  • as stress abates, reduce HC by 50% per day until back on usual replacement dose
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10
Q

What are the endocrine causes of hypertension?

A
○ Primary hyperaldosteronism
- unilateral adenoma 
- bilateral hyperplasia
○ Rarer causes
- Pheochromocytoma
- Conn's syndrome (aldosterone)
- Cushing’s syndrome (corticosteroids)
- Acromegaly
- Hyperparathyroidism
- Hypothyroidism
- Congenital Adrenal hyperplasia
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11
Q

What are the investigations for Cushing’s disease

A
  • screening for hypercortisolism: overnight Dex test and 24 hour urine free cortisol
  • Confirmation of hypercortisolism: 24 hour urine free cortisol and low dose dex test
  • ACTH dependent or not: Paired morn-midnight ACTH cortisol
  • ACTH (pit/ no pit): high dose dex test
  • Localisation: MRI sella, CT adrenal, BIPSS, CT chest
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12
Q

What are the clinical features of phaeochromocytoma?

A
  • Hypertension (persistent in 70%)
  • Paroxysmal attacks
    □ headache
    □ sweating
    □ palpitations
    □ tremor
    □ pallor
    □ anxiety/fear
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13
Q

Explain adrenal hyperplasia

A
• >90% cases due to 21-hydroxylase deficiency
• Severe cases
○ neonatal salt-losing crisis
○ ambiguous genitalia (girls)
• Incomplete defects
○ pseudo-precocious puberty (boys)
○ hirsutism (women)
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