Endocrine: adrenal medulla and cortex Flashcards

1
Q

What is the primary hormone deficiency in Addison’s disease, and how does it manifest clinically?

A

CORTISOL AND ALDOSTERONE

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2
Q

Why does secondary adrenal insufficiency not typically result in hyperkalemia?

A

Aldosterone levels are preserved

since it is regulated by RAAS and not by ACTH which is deficient in secondary adrenal insufficiency

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3
Q

How does the ACTH stimulation test differentiate primary from secondary adrenal insufficiency?

A

Suboptimal cortisol response in primary; normal in secondary.

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4
Q

What biochemical feature distinguishes pheochromocytoma from other causes of hypertension?

A

elevated plasma or urinary metanephrines

metabolites of catecholamines that are overproduced in pheochromocytoma

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5
Q

How does Conn’s syndrome (primary hyperaldosteronism) lead to metabolic alkalosis?

A

Excess aldosterone increases sodium reabsorption and potassium/hydrogen ion excretion.

the resulting hypokalemia and loss of hydrogen ion shifts pH towards alkalosis

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6
Q

Why does congenital adrenal hyperplasia (CAH) cause virilization in females?

A

excess androgen production

deficiency in cortisol synthesis leads to increased ACTH stimulation = converts precursors to androgen

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7
Q

What imaging modality is preferred for localizing an adrenal incidentaloma?

A

CT/MRI

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8
Q

What is the most common cause of Cushing’s syndrome?

A

EXOGENOUS glucocorticoid use (iatrogenic cushing’s syndrome)

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9
Q

How can adrenal insufficiency lead to hyponatremia?

A

Lack of aldosterone causes sodium loss; cortisol deficiency leads to inappropriate ADH secretion.

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10
Q

Hallmark feature of adrenal crisis

A

HYPOTENSION unresponsive to fluids

Lack of cortisol impairs vascular tone and stress response, necessitating immediate steroid replacement.

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11
Q

How does a 21-hydroxylase deficiency impact adrenal hormone synthesis?

A

overproduction of 17-hydroxyprogesterone and androgen imparing cortisol and aldosterone production

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12
Q

Why is hyperpigmentation observed in primary adrenal insufficiency but not secondary?

A

Elevated ACTH levels in primary stimulate melanocyte activity

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13
Q

How can you differentiate adrenal Cushing’s syndrome from pituitary Cushing’s disease?

A

LOW ACTH levels in ADRENAL cushing’s syndrome

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14
Q

What electrolyte abnormalities are expected in pheochromocytoma?

A

hyperglycemia
hypercalcemia

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15
Q

What is the significance of a “dex suppression test” in hypercortisolism evaluation?

A

Failure to suppress cortisol suggests Cushing’s syndrome.

Normal feedback mechanisms are disrupted in endogenous cortisol overproduction.

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16
Q

What role does aldosterone-renin ratio (ARR) play in diagnosing primary hyperaldosteronism?

A

HIGH ARR is diagnostic

17
Q

What is the treatment of choice for a pheochromocytoma?

A

Surgical resection after pre-op alpha-blockade preventing hypertensive crises during surgery