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Endocrine Function III Part 2

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

Card preview (24)

#1
Front (Question)

Addison’s disease -clinical symptoms due to mineralcorticoid deficiency

Back (Answer)

Dehydration, hypotension, hyperkalemia, metabolic acidosis, hyponatremia

#2
Front (Question)

Addison’s disease -clinical symptoms due to glucocorticoid deficiency

Back (Answer)

Fatigue, weakness, weight loss, GI disturbances, post parandial hypoglycemiaz

#3
Front (Question)

Addison’s disease -reason for hyperpigmentation and infertility

Back (Answer)

No negative feedback on anterior pituitary (ex hyperpigmentation not present because ACTH excess is not present to stimulate MSH production)

#4
Front (Question)

Addison’s disease -typical Na, K, blood sugar, cortisol, and ACTH lab results

Back (Answer)

Increased ACTH, decreased cortisol, decreased blood sugar, decreased sodium, and increased potassium

#5
Front (Question)

Cause of addisonian crisis?

Back (Answer)

During infection or acute stress, Addison’s patient cannot respond with increased aldosterone and cortisol and can go into shock with hypotension, fever, hypovolemia, and hyperkalemia (life threatening)

#6
Front (Question)

What is the cause of Waterhouse-Friderichsen?

Back (Answer)

Caused by meningococcal meningitis and septicemia; this causes acute adrenal insufficiency

#7
Front (Question)

What is the most common cause of tertiary adrenal insufficiency ?

Back (Answer)

Chronic pharmacological administration of glucocorticoids

#8
Front (Question)

What are four conditions associated with a hyperfunctioning adrenal cortex?

Back (Answer)

1 primary aldosteronism (Conn’s Syndrome) 2 secondary aldosteronism 3 cushing’s syndrome 4 Congenital adrenal hyperplasia

#9
Front (Question)

Primary Aldosteronism (Conn's Syndrome) -cause

Back (Answer)

Adenoma in outermost layer (tumors)

#10
Front (Question)

Primary Aldosteronism (Conn's Syndrome) -outstanding clinical symptom

Back (Answer)

Hypertension

#11
Front (Question)

Primary Aldosteronism (Conn's Syndrome) -typical serum and urine K,Na,aldosterone, and renin levels

Back (Answer)

Decreased Potassium, increased sodium, increased aldosterone, decreased renin, increased urine potassium, metabolic alkalosis caused by increased H secretion in urine (caused by increased Na reabsorption)

#12
Front (Question)

What are two general causes in secondary aldosteronism?

Back (Answer)

1 decreased blood flow to kidney causing decreased GFR 2 hyperactivity of RAAS causing increase in renin production

#13
Front (Question)

Cushing’s Syndrome -five clinical symptoms

Back (Answer)

Moon face, buffalo hump, truncal obesity, purple striae, hypertension

#14
Front (Question)

Cushing’s Syndrome -three general causes

Back (Answer)

Exogenous glucocorticoid therapy (prednisone), ACTH-dependent syndrome, ACTH-independent

#15
Front (Question)

Cushing’s syndrome -two specific causes of ACTH-dependent cushing’s

Back (Answer)

Cushing’s, Ectopic ACTH secreting tumors

#16
Front (Question)

Cushing’s Syndrome -Two specific causes of ACTH-independent cushing’s

Back (Answer)

Adrenal adenoma, nodular adrenal hyperplasia

#17
Front (Question)

Cushing’s syndrome -two recommended screening tests and typical results if patient has syndrome

Back (Answer)

• 24 hr free cortisol (>120=cushing’s) • overnight dexamethasone suppression test • AM/PM cortisol levels

#18
Front (Question)

Cushing’s syndrome -expected morning and afternoon cortisol levels

Back (Answer)

Increased in AM, decreases over the day normally (cushing’s is increased all the time)

#19
Front (Question)

Cushing’s syndrome -typical sodium, potassium, blood sugar, cortisol

Back (Answer)

Increased Na, decreased K, increased blood sugar, and increased cortisol

#20
Front (Question)

Cushing’s syndrome -typical ACTH results in Cushing’s syndrome, cushing’s disease, and ectopic ACTH secreting tumors

Back (Answer)

Increased ACTH due to the adrenal cortex being stimulated

#21
Front (Question)

Congenital adrenal hyperplasia (CAH) (adrenogenital syndrome) -pathogenesis

Back (Answer)

Caused by enzyme deficiencies in the pathways to produce the glucocorticoids and mineralocorticoids; no negative feedback since cortisol not produced and aldosterone is decreased

#22
Front (Question)

Congenital adrenal hyperplasia (CAH) (adrenogenital syndrome) -two common enzyme deficiencies

Back (Answer)

21-hydroxylase and 11-beta-hydroxylase

#23
Front (Question)

Congenital adrenal hyperplasia (CAH) (adrenogenital syndrome) -expected cortisol, ACTH, progesterone, DHEA, sodium, and potassium levels

Back (Answer)

Decreased cortisol, increased ACTH, increased progesterone, increased DHEA, decreased sodium, and increased potassium

#24
Front (Question)

Congenital adrenal hyperplasia (CAH) (adrenogenital syndrome) -typical symptoms in boys and girls

Back (Answer)

Females: abnormalities of external genitalia at birth (cannot tell if male or female); hirsutism, infertility, breast atrophy Males: appear normal at birth, but have sexual precocity (too much testosterone) Both: acne, coarsening of voice, scalp recession early in life Both: