Adrenal Disorders Flashcards

1
Q

What is Cushings?

A

Hypercortisolism

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2
Q

What is Conn’s?

A

Hyperaldosteronism

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3
Q

What is Addison’s?

A

Hypoadrenalism

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4
Q

What happens in Conn’s?

A

Excessive aldosterone causes Na retention, increased plasma and ECF volume, hypokalaemia and HTN
All supresses Renin
Alkalosis

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5
Q

What causes Conn’s?

A
Adrenal adenoma (70%)
Bilateral adrenal hyperplasia
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6
Q

What causes secondary hyperaldosteronism?

A

Renal artery stenosis/obstruction
Heart Failure
Causes high renin which stimulates aldosterone production

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7
Q

What are symptoms and signs of Excessive aldosterone?

A

HTN- LVH/MI renal failure
Hypernatraemia signs
Hypokalaemia- DI, thirst, polyuria, polydipsia, neuromuscular weakness, tetany and paraesthesia

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8
Q

How do you investigate Hyperaldosteronism?

A

Exclude other causes of hypokalaemia (diuretics/laxatives)
Measure aldosterone:renin ratio
Imaging

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9
Q

What is the mechanism of Cushings?

A

Chronic excessive cortisol and loss of circadian rhythms

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10
Q

Who gets cushings?

A

Male

Prepubescent

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11
Q

What is the difference between Cushings disease and syndrome?

A

Syndrome- Adrenal adenoma/ steroids/ paraneoplastic- 30%

Disease- Pituitary tumour (ACTH dependent)- 70%

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12
Q

What are clinical features of cushings?

A
HTn
Central obesity
Hirsutism
DM
Osteoporosis
Straie
Red Moon face
Bufalo hump
Depression and psychosis
Impotence
Hypokalaemia
Acne
Recurrent achilles tendonitis
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13
Q

How is Cushing investigated?

A

Repeated tests and clinical judgement needed
DEXAMETHASONE supression test- then measure ACTH and cortisol in the morning to see if morning spike reduced. First low dose then high
If pit cause= ACTH low, cort low
If adrenal cause+ ACTH low cort high

24 hour free cortisol (>2 measurements) and measure ACTH

Imaging

Refer to endocrinology

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14
Q

When do you get high cortisol physiologically?

A
Pregnancy
Depression
Morbid obesity
DM
Alcohol dependence
Stress
Malnutrition
Chronic excercise
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15
Q

How is Cushings managed?

A

Surgery/radio

Cabergoline to act on pit or Ketoconadazole or mifepristone to act on adrenals

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16
Q

What is the mechanism in Addisons?

A

Adrenal insufficiency means reduced aldosterone and cortisol

17
Q

What causes primary adrenal insufficiency?

A

Addisons- autoimmune destruction of cortex
TB
Lymphoma

18
Q

How is primary adrenal insufficiency diagnosed?

A

9am cortisol low
Increased ACTH
Low Aldosterone
Syntrophin test

19
Q

What causes secondary adrenal insufficiency?

A

Steroid excess supresses adrenal axis
Pituitary tumours
Head trauma

20
Q

What is most common cause of adrenal insufficiency

21
Q

What are symptoms of adrenal insufficiency>

A
Anorexia
Weakness and fatigue
Weight loss
Hyperpigmented palms (lean and tanned)
Nausa and pain
Hypotension
Salt cravings
Loss of libido
Tachycardia
Postural dizziness
Tearful
22
Q

What are biochemical signs of adrenal insufficiency?

A
Hyponatramia
Hypoglycaemia
Hypercal
Hyperkal
Anaemia
Eosinophilia
Lymphocytosis
Increased liver transaminases
High TSH
23
Q

What is management of adrenal insufficiecy?

A

Daily Hydrocortisone
Daily Fludrocortisone
Double doses when sick

24
Q

What is the syacthen test?

A

syACTHen test- given synthetic ACTH and cortisol measured baseline, 30 and 60 mins after and cortisol response measured

25
What happens in an acute addisonian crisis?
Imbalance caused by vomit/diarrhoea, infection, surgery, MI, hypoglycaemia meaning acute lack of steroids
26
How does an addisonian crisi present/
``` Nausea Abdo pain Muscle cramps Confusion Hypotension Hyponat HyperK ```
27
How is an addisonian crisis managed?
IV HYDROCORTISONE bolus then infusion Fluid resus Correct glucose and monitor UandE
28
What is a phaemochromocytoma?
Adrenaline producing tumour of chromaffin cells in adrenals
29
How is adrenaline produced in phaeochromocytoma?
in bursts
30
WHat is phaeochromocytoma associated with?
Multiple Neuroendocrine Neopolasia (MEN 2) | Neurofibromatosis
31
What are clinical features of phaeochromocytoma?
``` HTN Palpitations Pallor Anxiety Tremor Sweating Weakness Fatigue Weight loss Hyperglycaemia ```
32
How is phaeochromocytoma investigated?
24 hour urine catecholamine collection and plasma metanephrine CT/MRI
33
How is phaeochromocytoma managed?
BP control- alpha blocker (PHENOXYBENZAMINE) or CCBs then BBs once established on alpha blockers Adrenalectomy with alpha blocker to prevent hypertensive crisis in theathre
34
What does Aldosterone do?
Causes increased sodium and water retention increasing BP
35
What does ADH do?
Increases absorbtion of sodium and water in the collecting ducts through the AQP-2 channels and therefore concentrating the urine