Diseases of Adrenal Gland Flashcards

1
Q

Clinical manifestations Adrenal insufficiency

A
  • N/V
  • Fatigue/weakness
  • FTT
  • Morning headache
  • fasting hypoglycemia
  • INC insulin sensitivity
  • DEC gastric acidity
  • DEC free water clearance
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2
Q

Primary AI specific

  • S/S
  • A/S
A
  • Dark skin/mucosa, Hyperkalemia, Hyponatremia

- A/S Primary Hypothyroidism, DM1, Vitiligo,

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3
Q

2nd AI specific

  • S/S
  • A/S
A
  • S/S: Pale skin, normal K + Na

- A/S: Central hypogonadism, GH def, DI, headache

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4
Q

Type 1 autoimmune polyglandular disease S/S + A/S

A
  • Adrenal Failure
  • Vitiligo
  • Hypothyroidism
  • Gonadal failure
  • DM1
  • Alopecia
  • Penicious Anemia
  • Chronic Candidia infx
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5
Q

Cortisol Levels

A

10-20 ug/dL = Normal
3.1 - 10 ug/dL = adrenal dynamic testing rq’d
<3 ug/dL = Adrenal insufficiency

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6
Q

When should patients with suspected AI be tested? Why?

A

In ICU + retested as outpatients

Prevent unnecessary long-term steroid use; hypoproteinemia can cause low levels

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7
Q

Dynamic tests available to assess adrenal function and ACTH reserve

A
  • ACTH Test
  • Insulin-induced Hypoglytcemia
  • Metyrapone test
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8
Q

Adrenal Imaging findings

A
  • Small heart
  • Adrenal calcification (TB or fungal)
  • small/enlarged adrenal glands
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9
Q

Acute adrenal crisis

  • S/S
  • Tx
A
  • S/S: Circulatory collapse, dehydration, N/V, Hypoglycemia, Hyperkalemia
  • Tx: Plasma ACTH. Cortisol, renin, + Aldosterone; 2-3 L Na Saline or D5 NSal; dexamethasone IV bolus and q12 hours thereafter OR IV hydrocortisone, 100 mg immediately and q 6h thereafter
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10
Q

Treatment of chronic adrenal insufficiency

A
  • # 1 Hydrocortisone 10-12 mg/m^2 per day; ~15 mg am, 5 mg pm
  • Oral Fludrocortisone (0.05-0.2); adjust dose to S/S
  • Sexual Dysfx -> DHEA 50 mg daily
  • Advise liberal Na intake
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11
Q

When should glucocorticoids replacement be increased?

A

Times of Stress like:

  • Fevers
  • Dental procedures
  • invasive diagnostics
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12
Q

A patient was given an increased does of GCs for a dental procedure. He developed N/V, and was switched to parental. What is the major risk?

A

Vascular instability

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13
Q

Corticosteroid dose major stress (SEPSIS, shock, etc)

A

50 mg IV Hydrocortisone q8

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14
Q

Cushing Syndrome Etiologies

A
  • Iatragenic
  • Cushing’s Disease
  • Adrenal Neoplasms/Hyperplasia
  • Ectopic ACTH (Lung, pancreas, kidney, thyroid, thymus)
  • Psychiatric (Depression, EtOH, Anorexia, Panic Disorder)
  • Familial (Carney’s)
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15
Q

Common presentation of ectopic ACTH

A

No active ACTH; No S/S besides Hyperpigmentation + weakness

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16
Q

Pseudo-Cushing’s Syndromes

A
Pregnancy
Depression and other psychiatric conditions
Alcohol dependence
Glucocorticoid resistance
Morbid obesity
Poorly controlled diabetes mellitus
17
Q

Bilateral micronodular or macronodular adrenal hyperplasia Tx

A

bilateral total adrenalectomy

18
Q

Intractable Cushing’s or failed surgery Tx

A

Oral mefiprestone
SC pasireotide
Ketoconazole
Etomidate

19
Q

Exogenous mineralocorticoids

A

Liquorice, carbenoxalone, fludrocortisone

20
Q

Aldosterone-secreting adenoma Tx

A
  • Treat BP + Hypokalemia w/ Spironolactone or Amiloride

- Unilateral adrenalectomy after

21
Q

Bilateral Adrenal hyperplasia: Tx

A
  • Control Hypokalemia w. Spironolactone or Amiloride
  • Control HTN w/ antihypertensive agent
  • evaluate for glucocorticoid-responsive hyperaldosteronism (trial of dexamethasone)
22
Q

What can induce PCC S/S’s?

A

Emotions, excercise, abdominal pressure, + tyrosine-containing foods

23
Q

Diagnostic testing PCC

A
  1. Plasma free metanephrine or normetanephrine OE urine catecholamines
  2. Check during spell
  3. If normal, Perform clonidine suppression test -> No Suppression = PCC
  4. CT/MRI can confirm
24
Q

PCC Tx

A
  • Sx for localizes tumor

- Phenoxybenzamine (a-block) 2 weeks prior, then B-blockers before surgery