Adrenal Pathology Flashcards

1
Q

What are the 3 layers of the adrenal cortex? What does each layer secrete?

A

From outside-in:

zona glomerulosa - aldosterone in response to angiotensin II
zona fasiculata - cortisol in response to ACTH
zona reticularis - androgens

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2
Q

What is the effect of Addison’s on the blood?

A
Hypotension
Hyperkalaemia
Hyponatreamia
Hypoglycaemia
Metabolic acidosis
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3
Q

What are 2 primary and 2 secondary causes of adrenal insufficiency?

A

Addison’s
Congenital adrenal hyperplasia

Pituitary disease
Exogenous steroid use

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4
Q

What is the test for adrenal insufficiency? What is the anticipated result?

A

Short synacthen test

normally cortisol should have baseline >250 nmol/l and rise to >550 nmol/l after IM Synacthen

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5
Q

What does aldosterone normally do?

A

Increases blood pressure

Causes excretion of K+ and H+

Causes resorption of Na+

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6
Q

What is the treatment for adrenal insufficiency?

A

Hydrocortisone and fludrocortisone

Hydrocortisone - Split over the day, most given in the morning.

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7
Q

What are the sick-day rules for treatment of adrenal insufficiency?

A

Double hydrocortisone, maintain fludrocortisone dose

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8
Q

What is the management of Addisonian crisis?

A

Hydrocortisone 100 mg
Normal saline with dextrose if hypoglycaemic
Continue hydrocortisone 6 hourly until the patient is stable - no need for fludrocortisone

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9
Q

What test is used in Cushing’s syndrome?

A

Overnight dexamethasone suppression test

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10
Q

Cushing’s syndrome may be ACTH-dependant (pituitary adenoma, small cell cancer) or -independant (adrenal adenoma or carcinoma).

How may the the underlying be determined to be ACTH-dependant or -independant?

A

9am and midnight plasma ACTH + cortisol levels

low- and high-dose dexamethasone suppression test

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11
Q

What are the 3 features of primary hyperaldosteronism?

A

Significant, resistant hypertension.
Hypokalaemia
Metabolic alkalosis

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12
Q

What are the 2 potential underlying causes of primary hyperaldosteronism?

A

Conn’s syndrome (adrenal adenoma)

bilateral adrenocortical hyperplasia

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13
Q

What tests may diagnose primary hyperaldosteronism?

A

Aldosteron-Renin ratio

CT and adrenal vein sampling can determine if Conn’s or bilateral hyperplasia is cause.

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14
Q

How would you treat Conn’s syndrome?

A

Surgical adrenelectomy

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15
Q

How would you treat bilateral adrenocortical hyperplasia?

A

Spironolactone

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16
Q

What is congenital adrenal hyperplasia?

A

A congenital disease in which there may be inappropriate secretion of hormones:

In 21alpha hyroxylase deficiency subtype:
Aldosterone and cortisol may be low
Testosterone may be high

Although different subtypes exist

17
Q

What is the treatment of congenital adrenal hyperplasia?

A

Hydrocortisone and fludrocortisone

Surgical correction of ambiguous genitals

18
Q

What are the symptoms of congenital adrenal hyperplasia

A

Adrenal insufficiency (similar to Addison’s = lack of aldosterone)

  • Hyponatraemia
  • Hyperkalaemia
  • Hypoglycaemia

Salt-loss crisis

Poor weight gain

Genital ambiguity in females

19
Q

What is the classical triad of phaeochromocytoma?

A

Hypertension, headache, sweating

20
Q

What blood abnormalities may be seen in pheochromocytoma?

A

Hyperglycaemia
Hypokalaemia
Hypercalcaemia

High haematocrit
Lactic acidosis without shock

21
Q

What test confirms pheochromocytoma?

A

24hr urinary metinephrines

22
Q

What is the treatment for phaeochromocyotoma?

A

alpha-blocker THEN beta-blocker

Surgery - aim to excise, debulk if not possible

Chemo if malignant