Adrenal Disorders Flashcards

1
Q

This deck covers the main adrenal disorders:

A
  • Cushing’s Syndrome
  • Addison’s Disease
  • Conn’s Syndrome
  • Pheochromocytoma
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2
Q

What is Addison’s Disease also known as?

A

Primary Adrenal Insufficiency

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3
Q

What is Addison’s Disease?

A

Insufficiency in adrenal cortex causing insufficient glucocorticoids and mineralocorticoids

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4
Q

What causes Addison’s?

A

Mainly Autoimmune

  • Infection
  • Infarction
  • Iatrogenic
  • Infiltration
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5
Q

How does Addison’s Present?

A

In decreasing order of likelihood:

  • Weakness, fatigue, weight loss & anorexia
  • Skin pigmentation or vitiligo (loss of pigment)
  • Hypotension
  • Unexplained hypoglycaemia
  • Salt Craving
  • Postural Symptoms
  • N&V + Diarrhoea
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6
Q

What tests do you do if you suspect Addison’s?

A
  • Routine bloods
  • Random Cortisol
  • Synacthen Test
  • Plasma ACTH
  • Adrenal Auto-antibodies
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7
Q

What does a random cortisol test tell you about addison’s?

A

ITs the first test you do

If they’re cortisol is >700nmol/l then it’s not Addison’s

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8
Q

What does a synacthen test tell you about Addison’s?

A

Give ACTH to see how muhc their cortisol goes up

In addison’s they should produce very little cortisol

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9
Q

Why test plasma ACTH in Addison’s?

A

If its elevated it confirms Primary Adrenal Insufficiency.

If its suppressed however the source is secondary

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10
Q

How do you treat Addison’s disease?

A

Glucocorticoid replacement e.g. Hydrocortisone

Mineralocorticoid replacement e.g. Fludrocortisone

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11
Q

What do you have to think about when people are Exogenous steroid dependant?

A

During stressfull stimuli they need an increased dose, as their own production if suppressed.

Double dose on minor illness
IV hydrocortisone on major illness, tapered off at 50% a day

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12
Q

What would indicate autoimmune addison’s?

A

Other autoimmune conditions like:

  • Type 1 DM
  • Thyroid disease
  • Premature ovarian failure
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13
Q

How does Cushing’s Disease present?

A
  • Moon face & pendulous breasts/abdomen
  • Muscle wasting, particularly in small hands/feet muscles and proximal muscles
  • Thin skin +ulcers
  • Bruising (purpura) & Oedema
  • DM
  • Cardiac failure due to muscle atrophy
  • Hirsutism
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14
Q

Types of Cushing’s?

A

ACTH dependant

  • Pituitary Tumour - 75% (cushings disease)
  • Extopic ACTH - 5% (lung cancer)

ACTH independant:

  • Adrenal adenoma or carcinoma -20%
  • CCS therapy
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15
Q

How do you investigate suspected Cushing’s disease?

A

Screen with overnight dex test or 24 hour urine cortisol

Confirm with 24 hour urine cortisol repear

Paired morning/midnight cortisol/ACTH test to check ACTH dependancy

If ACTH dependant do a High dose Dex test to check pituitary vs ectopic

Localise with MRI/CT/CT chest as appropriate

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16
Q

What is Conn’s Syndrome?

A

An aldosterone secreting tumour in the adrenal cortex

I.e. Primary Hyperaldosteronism

17
Q

Whats the presentation of Conn’s Syndrome?

A

Hypertension with Hypokalemia

18
Q

TEsts for Conn’s Syndrome?

A

If you see hypertension & hypokalemia:

  • Plasma aldosterone/renin ratio.
  • > 20 & a raised aldosterone indicates Conn’s syndrome

Follow up with a 24hr urine aldosterone to confirm

Then CT the adrenal glands

19
Q

What is a pheochromocytoma?

A

A tumour of the adrenal medulla that secretes excess catecholamines

20
Q

How does pheochromocytoma present?

A

Hypertension along with paroxysmal attacks of:

  • Headaches
  • Sweat
  • Palpitations
  • Tremor
  • Pallor
  • Anxiety/fear
21
Q

How do you investigate a pheochromocytoma?

A

patient with High BP & paroxysmal adrenaline attacks

24 hour urine total catecholamines

Followed by adrenal MRI/CT

22
Q

How do you manage pheochromocytoma?

A

Surgically