15.10 Adrenal Cortex Flashcards

1
Q

What is generated in the glomerulosa?

A

Mineralocorticoids - aldosterone

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2
Q

What is generated in the fasciculata?

A

Glucocorticoids - cortisol

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3
Q

What is generated in the reticular?

A

Sex Steroids

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4
Q

Cushing Syndrome

A

Excess cortisol

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5
Q

What are the features of Cushing syndrome?

A
  • Moon facies
  • Buffalo hump
  • Truncal obesity
  • Muscle weakness
  • HTN
  • Osteoporosis
  • Immune suppression
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6
Q

How does cortisol cause HTN?

A

Upregulation of alpha-1 receptors

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7
Q

How does cortisol cause immunosuppression?

A
  • Inhibition of IL-2
  • Inhibition of phospholipase A2
  • Inhibits histamine
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8
Q

What are the causes of Cushing syndrome?

A
  • Exogenous corticosteroids
  • Adrenal adenoma, hyperplasia or carcinoma
  • ACTH-secreting pituitary adenoma
  • Paraneoplastic ACTH secretion
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9
Q

What tumor can cause paraneoplastic ACTH secretion?

A

SCC of the lung

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10
Q

What cause of Cushing syndrome will cause bilateral adrenal atrophy?

A

Exogenous corticosteroids

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11
Q

What will respond with decreased ACTH in response to dextromethasone?

A

Pituitary adenoma - SCC of the lung will NOT

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12
Q

Hyperaldosteronism

A

Excess aldosterone

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13
Q

What are the features of hyperaldosteronism?

A
  • Hypernatremia
  • Hypokalemia
  • Metabolic Alkalosis
  • HTN
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14
Q

What is the most common cause of primary hyperaldosteronism?

A

Adrenal Adenoma

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15
Q

What are the lab findings for renin and aldosterone in primary hyperaldosteronism?

A
  • High aldosterone

- Low renin

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16
Q

What are the causes of secondary hyperaldosteronism?

A

Activation of the RAA system leading to high aldosterone with high renin - often due to renovascular HTN

17
Q

Congenital Adrenal Hyperplasia

A

Excess sex steroids with hyperplasia of both adrenal glands

18
Q

What is the most common cause of congenital adrenal hyperplasia?

A

21-hydroxylase deficiency

19
Q

Why is there hyperplasia in the adrenals in congenital adrenal hyperplasia?

A

There is a deficiency of cortisol as all steroid genesis is shunted towards sex steroids - leads to increased ACTH and adrenal hyperplasia

20
Q

What is 21-hydroxylase required for?

A

Mineralcorticoid and cortisol production

21
Q

What are the clinical features of congenital adrenal hyperplasia?

A
  • Hyponatremia
  • Hyperkalemia
  • Hypovolemia
  • Hypotension that is life threatening
22
Q

What happens with 11-hydroxylase deficiency?

A
  • No cortisol
  • Only weak mineralocorticoid production so no salt wasting
  • Most is shunted to sex steroid production
23
Q

What is required for pregnenolone to enter into the synthesis pathway and become cortisol or sex steroids?

A

17-hydroxylase - if deficient there will be excess mineralocorticoids

24
Q

Adrenal Insufficiency

A

Lack of adrenal hormones

25
Q

Waterhouse-Friderichsen Syndrome

A

Often in a young child with N. meningitides who develops DIC with bilateral adrenal atrophy - “sack of blood”

26
Q

Chronic Adrenal Insufficiency

A

Slow destruction of the adrenal glands

27
Q

What are some of the causes of chronic adrenal insufficiency?

A
  • Autoimmune (common in West)
  • TB (common in 3rd world)
  • Metastatic Carcinoma
28
Q

What cancer often metastasizes to the adrenal glands?

A

Lung cancer