02b: Adrenal HT Flashcards
(29 cards)
Adrenal mechanisms for HT can be caused by excess:
- Glucocorticoids (ZF)
- Mineralocorticoids (ZG)
- Catecholamines (medulla)
90% of all congenital adrenal hyperplasia is due to (X) deficiency. Is HT a symptom?
X = 21-a hydroxylase
No (but other enzyme deficiencies causing CAH do have HT)
List the causes of primary aldosteronism. Star the most common. Double-star the severe causes.
- Bilateral hyperplasia*
- Adrenal adenoma/carcinoma**
- Glucocorticoid-remediable
Pt with treatment-resistant BP makes you suspicious for (X), especially if (Y) serum levels are (low/high).
X = hyperaldosteronism
Y = K
Low
Screening for hyperaldosteronism via which test/lab?
Plasma aldo:renin ratio (aka aldo:PRA ratio)
Aldo:PRA ratio cutoff greater than (X) as well as plasma (Y) greater than 10 suggests diagnosis of…
X = 30
Y = aldosterone
Hyperaldosteronism
List the guidelines for screening with aldo:PRA ratio
- BP over 150/100 despite 3 BP meds
- Low K
- Adrenal incidentaloma
Pt has high serum aldosterone and a high aldo:PRA ratio. What’s the next step?
Confirm diagnosis of hyperaldosteronism by V-loading maneuver (oral salt loading, saline infusion); normal response is to lower aldosterone
Hyperaldosteronism: (X) is the most reliable test to distinguish unilateral adenoma from bilateral hyperplasia
Venous aldosterone and cortisol samples from adrenal veins
Hyperaldosteronism from adenoma: what’s the Rx?
Surg (often curative) and maybe medical therapy (K-sparing diuretics)
Hyperaldosteronism from bilateral hyperplasia: what’s the Rx?
- K sparing diuretics
- Ca channel blockers
- ACEi
T/F: Pheochromocytomas make up only 1% of hypertensive cases
True
Patient has spike in BP during surgery. What should he/she be screened for?
Pheo
T/F: FHx of Pheo is reason to screen patient
True
Which familial syndromes put patient at risk for Pheo?
- Familial Pheo
- MEN-2
- Neurofibromatosis
- VHL syndrome
Diagnostic tests for Pheo. Star the one with the highest sensitivity and double-star the one with highest specificity.
- Plasma metanephrines*
- Urine metanephrine/normetanephrines
- Urine VMA**
T/F: Pheo screening is limited by certain requirements due to too many false positives.
True
T/F: Pheochromocytoma is limited to adrenal medulla.
False - 90% are located there, but can appear at other sites
The “Rule of 10’s” applies to which disease?
Pheo
10% are extra-adrenal
10% are familial
10% are bilateral
10% are malignant
Pheo Rx:
- Surg
2. Med (pre-op/palliative)
Medical Rx for Pheo includes:
- Alpha-blocker
- Ca channel blocker
- Beta-blocker (ONLY after alpha-blocker)
Patient has been diagnosed with unilateral adrenal pheochromocytoma. First step for Rx is:
Pre-op prep with alpha blockers (10-14 days before surg) to prevent severe BP changes during/after surg
Incidentalomas are seen in (X)% of CTs and MRIs. (Y)% make some hormone and (Z)% are malignant.
X = 2-4 Y = Z = 10
You discover an adrenal incidentaloma on patient’s abdominal CT. If this is a functioning mass, what is it most likely to be secreting?
Cortisol
less likely: pheo, aldosteronoma