Diagnosis of Adrenal Disorders Flashcards

1
Q

How many rings are in a steroid?

A

4

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2
Q

What is hydrocortisone?

A

cortisol

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3
Q

What is cortisone?

A

a biologically inactive metabolite of cortisol - needs to be metabolised in the liver to be active

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4
Q

What are the synthetic glucocorticoids?

A

prednisolone and dexamethasone

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5
Q

What causes the hyperglycaemia in Cushing’s syndrome?

A

stimulation of gluconeogenesis in the liver, breakdown of protein in the muscle, lipolysis

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6
Q

What is Cushing’s disease?

A

pituitary adenoma which produces ACTH

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7
Q

What are the two different types of hypercortisolism?

A

ACTH dependent and ACTH independent

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8
Q

What is an ACTH dependent cause of hypercortisolism that is not Cushing’s disease?

A

an ectopic tumour producing ACTH e.g. in the lung

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9
Q

What are the ACTH independent causes of hypercortisolism?

A

adrenal adenoma or carcinoma, ACTH independent nodular hyperplasia, administration of glucocorticoids

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10
Q

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

A

moon face, obesity, hypertension, menstrual disorders, hirsuitism, weakness, striae, bruisability, osteoporosis, ankle oedema, buffalo hump

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11
Q

Why is it important to do diagnose with biochemical tests before doing any radiological tests?

A

because radiology may show something that is unrelated and lead to a misdiagnosis

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12
Q

What are the tests for Cushing’s?

A

24 hour urine cortisol, diurnal cortisol variation, dexamethasone suppression test, pituitary MRI, adrenal CT

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13
Q

What is Addison’s disease and what are the symptoms?

A

chronic primary adrenocortical insufficiency due to destruction of adrenals (autoimmune)- symptoms are anorexia, nausea, vomiting, diarrhoea, weight loss, low blood pressure, tachycardia, darkening of the skin, muscle weakness, increased susceptibility to infection

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14
Q

What are the causes of adrenocortical insufficiency?

A

enzyme defect in cortisol synthesis, adrenoleukodystrophy, autoimmune adrenal destruction, infectious disease

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15
Q

What is the treatment for Addison’s disease?

A

cortisol and fludrocortisone (aldosterone analogue)

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16
Q

Where on the body does Addisonian pigmentation occur?

A

knuckles of hands, knees, gums, oral mucosa and general pigmentation

17
Q

What is CAH and what are the symptoms?

A

defiency in the enzyme 21-hydroxylase so can’t synthesise cortisol and aldosterone which leads to over production of androgens - symptoms are premature pubic hair, hirsuitism, acne, enlargement of penis/clitoris, behavioural changes, linear growth spurt, rapid epiphyseal fusion, muscular habitus, deepening of voice

18
Q

What is prednisolone?

A

synthetic glucocorticoid

19
Q

What is dexamethasone?

A

synthetic glucocorticoid

20
Q

What is fludrocortisone?

A

synthetic mineralocorticoid

21
Q

What stimulates aldosterone secretion?

A

potassium in extracellular fluid, angiotensin II, ACTH

22
Q

What is the action of aldosterone?

A

salt and water absorption, potassium excretion

23
Q

What is Conn’s syndrome and what are the symptoms?

A

an adrenocortical tumour secreting aldosterone - symptoms are hypertension (due to fluid retention) and weakness (due to potassium deficiency)

24
Q

What are the symptoms of aldosterone deficiency?

A

dehydration, postural hypotension and cardiac arrhythmias

25
Q

What is pheochromocytoma and what are the symptoms?

A

a tumour of the adrenal medulla leading to overproduction of catecholamines - causes episodes of pallor, palpitations, hypertension, sense of doom