Lecture 19 Flashcards

1
Q

What does hyperactivity of the adrenal cortex cause?

A

Increased secretion of cortisol: Cushing’s Syndrome

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2
Q

Why may you get Cushing’s syndrome?

A
  • primary cortisol producing adrenal adenoma
  • disorders in secretion of ACTH by a pituitary adenoma: Cushing’s Disease
  • ectopic secretion of ACTH from a tumour at a site remote from the pituitary
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3
Q

What are the signs and symptoms of excess cortisol?

A
  • increased muscle proteolysis: wasting of proximal muscles= thin arms and leg and weakness
  • increased hepatic gluconeogenesis: hyperglycaemia with polyuria and polydipsia
  • increased lipogenesis in adipose tissue leading to depositions of fat in abdomen, neck and face: moon shaped face
  • purple striae: catabolic effects on protein structures in skin leading to easy bruising due to thinning of skin
  • mineralcorticoid effects of excess cortisol may produce hypertension due to sodium and fluid retention
  • disturbances to calcium metabolism: osteoporosis
  • immunisuppressive, anti-inflammatory, anti-allergic reactions of cortisol leading to bacterial infections and acne
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4
Q

What patients experience the symptoms of Cushing’s syndrome?

A

Patients receiving long term treatment with glucocorticoids for chronic inflammatory conditions
e.g. hydrocortisone, prednisone

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5
Q

Difference between Cushing’s disease and syndrome?

A

Syndrome refers to collection of symptoms due to excessive exposure to cortisol (more common)
Disease refers to a benign ACTH secreting pituitary adenoma

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6
Q

What is it called when you have too little cortisol and what causes it?

A

Addison’s Disease

  • diseases of adrenal cortex (autoimmune destruction)
  • disorders in pituitary/hypothalamus leading to decreased secretion of ACTH/CRF
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7
Q

What does autoimmune destruction of adrenal gland cause?

A

Loss of cortisol and mineralcorticoids

May present as a clinical emergency: Addisonian Crisis or Addison’s Disease

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8
Q

What are the symptoms of Addison’s disease?

A
  • hypoglycaemic episodes
  • postural hypotension
  • decreased BP due to sodium and fluid depletion
  • increased skin pigmentation in exposed areas of body, buccal mucosa, scars, palmar creases due to increase in ACTH as well as other products of POMC which stimulate melanocytes to produce more melanin
  • extreme muscular weakness/anorexia
  • dehydration
  • weight loss
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9
Q

How do you treat Addison’s Disease?

A

Intravenous cortisol

Fluid replacement

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10
Q

What clinical tests can be used to diagnose adrenocortical disease?

A
  • measurement of plasma cortisol and ACTH levels, and 24 urinary excretion of cortisol
  • dynamic function tests (dexamethasone suppression/ACTH stimulation)
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11
Q

How do dynamic function tests work to diagnose adrenocortical disease?

A

Dexamethasone: synthetic steroid given orally suppresses secretion of ACTH and therefore cortisol

  • suppression of cortisol is characteristic of Cushing’s disease because the diseased pituitary retains some sensitivity to synthetic steroids
  • suppression does not normally occur in adrenal tumours/ectopics
Syncathen intramuscularly (synthetic analogue of ACTH)
-normally increase plasma cortisol, normal response excludes Addison disease
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12
Q

What is congenital adrenal hyperplasia?

A

Genetic defect in an enzyme required for synthesis of corticosteroid hormones from cholesterol
-lack of cortisol= more ACTH via negative feedback causing hyperplasia of adrenal cortex
= deficiency in enzyme 21-hydroxylase: less glucocorticoid and mineralcorticoid production and more androgen synthesis resulting in genital ambiguity and salt-wasting crises (unable to retain enough salt) due to high rate of sodium in urine because of lack of aldosterone

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13
Q

What is Conn’s syndrome?

A

Primary hyperaldosteronism: hyperactivity of one/both adrenal glands
Unilateral form: adenoma
Bilateral form: rare genetic syndromes

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14
Q

What are the symptoms of Conn’s syndrome?

A
  • high BP
  • muscular weakness/spasms
  • excessive urination
  • tingling sensations
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15
Q

What effect does excess aldosterone have on the kidney?

A

Increases sodium reabsorption and potassium secretion via Na/K ATPase, resulting in increased BP and volume
-increase in blood volume and renal perfusion causes a decrease in renin release
In Conn’s disease, decreased renin levels does not lead to a decrease in aldosterone

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16
Q

What receptors does cortisol bind to?

A

Glucocorticoid receptors
Mineralcorticoid and androgen receptors with a low affinity: this becomes significant when high levels of cortisol are present

17
Q

What do androgens stimulate in men and women?

A

Men: male genital tract, male secondary characteristics (height, body shape, facial and body hair, lower pitch voice), anabolic actions on muscle protein
Women: female genital tract, breasts, female secondary characteristics (broad hips, accumulation of fat in breasts and buttocks, body hair distribution), anabolic, decrease circulating cholesterol levels

18
Q

What does oversecretion of adrenal androgens in females cause?

A
Excessive body hair growth (hirsutism)
Acne
Menstrual problems 
Virilisation (development of male physical characteristics)
Increased muscle
Deepened voice