Diseases of Adrenal Gland Flashcards
Clinical manifestations Adrenal insufficiency
- N/V
- Fatigue/weakness
- FTT
- Morning headache
- fasting hypoglycemia
- INC insulin sensitivity
- DEC gastric acidity
- DEC free water clearance
Primary AI specific
- S/S
- A/S
- Dark skin/mucosa, Hyperkalemia, Hyponatremia
- A/S Primary Hypothyroidism, DM1, Vitiligo,
2nd AI specific
- S/S
- A/S
- S/S: Pale skin, normal K + Na
- A/S: Central hypogonadism, GH def, DI, headache
Type 1 autoimmune polyglandular disease S/S + A/S
- Adrenal Failure
- Vitiligo
- Hypothyroidism
- Gonadal failure
- DM1
- Alopecia
- Penicious Anemia
- Chronic Candidia infx
Cortisol Levels
10-20 ug/dL = Normal
3.1 - 10 ug/dL = adrenal dynamic testing rq’d
<3 ug/dL = Adrenal insufficiency
When should patients with suspected AI be tested? Why?
In ICU + retested as outpatients
Prevent unnecessary long-term steroid use; hypoproteinemia can cause low levels
Dynamic tests available to assess adrenal function and ACTH reserve
- ACTH Test
- Insulin-induced Hypoglytcemia
- Metyrapone test
Adrenal Imaging findings
- Small heart
- Adrenal calcification (TB or fungal)
- small/enlarged adrenal glands
Acute adrenal crisis
- S/S
- Tx
- 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
Treatment of chronic adrenal insufficiency
- # 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
When should glucocorticoids replacement be increased?
Times of Stress like:
- Fevers
- Dental procedures
- invasive diagnostics
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?
Vascular instability
Corticosteroid dose major stress (SEPSIS, shock, etc)
50 mg IV Hydrocortisone q8
Cushing Syndrome Etiologies
- Iatragenic
- Cushing’s Disease
- Adrenal Neoplasms/Hyperplasia
- Ectopic ACTH (Lung, pancreas, kidney, thyroid, thymus)
- Psychiatric (Depression, EtOH, Anorexia, Panic Disorder)
- Familial (Carney’s)
Common presentation of ectopic ACTH
No active ACTH; No S/S besides Hyperpigmentation + weakness
Pseudo-Cushing’s Syndromes
Pregnancy Depression and other psychiatric conditions Alcohol dependence Glucocorticoid resistance Morbid obesity Poorly controlled diabetes mellitus
Bilateral micronodular or macronodular adrenal hyperplasia Tx
bilateral total adrenalectomy
Intractable Cushing’s or failed surgery Tx
Oral mefiprestone
SC pasireotide
Ketoconazole
Etomidate
Exogenous mineralocorticoids
Liquorice, carbenoxalone, fludrocortisone
Aldosterone-secreting adenoma Tx
- Treat BP + Hypokalemia w/ Spironolactone or Amiloride
- Unilateral adrenalectomy after
Bilateral Adrenal hyperplasia: Tx
- Control Hypokalemia w. Spironolactone or Amiloride
- Control HTN w/ antihypertensive agent
- evaluate for glucocorticoid-responsive hyperaldosteronism (trial of dexamethasone)
What can induce PCC S/S’s?
Emotions, excercise, abdominal pressure, + tyrosine-containing foods
Diagnostic testing PCC
- Plasma free metanephrine or normetanephrine OE urine catecholamines
- Check during spell
- If normal, Perform clonidine suppression test -> No Suppression = PCC
- CT/MRI can confirm
PCC Tx
- Sx for localizes tumor
- Phenoxybenzamine (a-block) 2 weeks prior, then B-blockers before surgery