Addison's Disease Flashcards

1
Q

What is it?

A

Primary adrenocortical insufficiency resulting in a lack of production of steroid hormones

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2
Q

What steroids are implicated? (3)

A

Glucocorticoids e.g Cortisol, Mineralocorticoids e.g Aldosterone, Androgens e.g Testosterone

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3
Q

What is the most common cause?

A

80% are caused by autoimmune disease

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4
Q

What are the other causes? (7)

A

TB, Adrenal metastases, lymphoma, opportunistic infections, adrenal haemorrhage, congenital, LONG TERM IATROGENIC STEROID USE

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5
Q

What is the autoantibody seen in addisons disease?

A

21 Hydroxylase

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6
Q

Is it common?

A

No it is relatively rare-1 in 10,000 people

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7
Q

Who is affected?

A

It can affect all age groups but is most common in 30-50 year olds and affects more women

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8
Q

Symptoms (16)

A

Lean, tanned, tired, tearful, weakness, anorexia, dizziness, fainting, flu like aches, depression, low self esteem, nausea, vomiting, abdominal pain, diarrhoea, constipation

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9
Q

Signs (8)

A

Pigmented palmar creases, pigmented buccal mucosa, postural hypotension, vitilligo, shock, hypovolaemia, tachycardia, temperature, coma

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10
Q

What bloods would you do? (6)

A

FBC, U&E (high potassium, low sodium), LFT, Glucose (low), Calcium (high), Cortisol

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11
Q

Other investigations (4)

A

ACTH stimulation tests, 21 Hydroxylase Adrenal Autoantibodies, Plasma renin and aldosterone, Cortisol

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12
Q

What is the treatment? (3)

A

Steroid replacement therapy e.g 15-25mg Hydrocortisone, mineralocorticoids to correct postural hypotension and electrolyte balance e.g Fludrocortisone 200mg, patient education about addisonian crises

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13
Q

Complications (3)

A

Adrenal Crisis, Reduced quality of life due to fatigue, osteoporosis

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14
Q

Is there a good prognosis? (4)

A

Lose several years of life expectancy, treatment is lifelong, more susceptible to infection, risk of sudden death

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