Endo Flashcards
Which CN affected in pituitary apoplexy?
acute pituitary hemorrhage. will cause severe HA, bitemporal visual defects, likely adrenal insuff and CN3 paresis.
initial tests for suspecting Cushing
Pick any:
- overnight dexamethasone suppression test
- 24 hour urinary free cortisol assay
- late-night salivary cortisol measurement
tx for hyperecalcemia from granulomatous dz
- decrease calcium/oxalate intake
- avoid sun exposure
- volume expansion
- low dose steroids
T/F: Bisphophonates are safe in CKD
FAlse! Don’t use if CrCl <30
Can use denosumab in renal insuff (monitor for hypocalcemia)
acromegaly testing
Step 1: Measure IGF-1 levels (note: GH fluctuates diurnal so not used)
Step 2: confirmatory testing with oral glucose suppression test (75g glucose). + = GH >2
Step 3: brain MRI (pituitary mass found in 70%)
T/F: statins can worsen hypothyroid myopathy
true and vice versa
Mgmt of pituitary incidentaloma
<10mm: prolactin levels or targeted hormone testing if any sxs
>10mm: check pituitary hormonal functions, consider surgery (can also follow,and prolactinomas respond well to medical therapy)
T/F: Hyperprolactinemia is common in CKD
true. does not respond to HD, can normalize with dopamine agonists however sexual dysfunction often persists due to multifactorial
Difference in presentation of hyperparathyroidism and hypercalcemia of malignancy
HyperPTH: Insidious onset, often asx/mild, Ca elevated mild (<11)
Malignancy: acute onset, significant sxs and severe hyperCa (>13)
Osteoporosis in men should prompt screening for:
Screen for hypogonadism with an early-morning serum testosterone assay
initial eval in hyperthyroid patient without features of Graves
Radioactive iodine uptake (RAIU)
High RAIU scan
Diffuse uptake pattern: Graves
Nodular uptake: Toxic adenoma, Multinodular goiter
Low RAIU
Measure Tg
- decreased: exogenous hormone
- elevated: thyroiditis, iodide exposure, extraglandular production
why is cosyntropin test needed prior to levothyroxine in central hypothyroidism?
This is an ACTH stimulation test. Levothyroxine can precipitate adrenal crisis in patients with concurrent adrenal insufficiency.
Anti-tpo (thyroperoxidase)
chronic lymphocytic thyroiditis aka Hashimoto (PRIMARY HYPOTHYROIDISM WITH ELEVATED TSH)
T/F: Risk of malignancy of thyroid nodule is independent of TSH
False.
Elevated TSH = higher risk malignancy.
Suppressed TSH suggests hyperfunctioning nodule, which is typically benign.
Other descriptors which increase risk of malignancy = >1cm, hypoechoic, vascular, microcalcifications
Hormonal testing after adrenal incidentaloma
All incidental tumors need at least hormone testing.
Must eval for:
- excess cortisol (i.e. overnight dexamethasone suppression test)
- pheo: urinary fractionated catecholamines and metanephrines
If hypertension: plasma aldosterone and aldosterone:renin activity ratio
T/F: Patients with type 2 diabetes and obesity commonly have hypogonadotropic hypogonadism
True. If it is borderline low (200-300), do not routinely need pituitary imaging.
If markedly low (<200) or signs of other pituitary hormone abnormalities, pituitary MRI to eval for mass
Testing in all patients with medullary thyroid cancer
RET mutation genetic testing.
- also eval for co-existing tumors (i.e. metanephrines for pheo) and for mets
- calcium for hyperparathyroidism
- MTC is seen in MEN 2A and 2B
T/F: Hereditary hemochromatosis causes secondary hypogonadism
True. Look for a patient with sick sinus syndrome. Iron deposits in the pituitary gonadotrophs.
Next step when RAIU shows toxic adenoma (mildly elevated, high-normal RAIU) or multinodular goiter with over hyperthyroidism (low TSH, high T4)
Radioactive iodine ablation (definitive tx)….or surgical thyroidectomy
side effects of SGLT2 inhibitors
UTI, hypotension, vaginal candidiasis
**use cautiously if hx of PVD/diabetic ulcer/neuropathy b/c increased risk of LE amputation
**inc in DKA (euglycemic)
**they decrease glucose reab in kidney - osmotic diuresis = hypotension. reduce doses of diuretics
(note, they don’t cause wt loss)
Which DM med causes wt loss
GLP-1 (liraglutide, exenatide, dulaglutide), low risk of hypoglycemia, good add on to metformin . AE = pancreatitis, GI side effects (n/v/d), wt loss
T/F: Hypogonadism is common in men with obesity and diabetes
True, HPA axis dysfunction. If other features are present (loss of body hair, gynecomastia, hot flashes, osteoporosis), should prompt workup for androgen def
initial step in eval of male hypogonadism
morning serum total testosterone level. Next step after testosterone is FSH and LH
(measuring free testosterone is not recommended initially, is expensive and inaccurate)
When would you do MRI of pituitary in workup of hypogonadism?
First check serum total testosterone. If low, check FSH and LH. If low (secondary hypogonadism), it should be considered if severe hypogonadism (testosterone <150), other pituitary deficiencies (TSH, GH), high prolactin or mass effect sxs
Which patients definitely need stress dose steroids perioperatively?
- daily pred for >3 weeks
- any patient who has developed Cushingoid features (including wt gain)
T/F: Subclinical hypothyroidism does not require treatment
False.
Indications for tx: TSH >10
if TSH 7-9.9 and <70, tx
if sxs, enlarging goiter or anti-TPO titer detected, tx
T/F: All patients with central hypothyroidism should undergo neuroimaging and chemical testing
True
especially adrenal, i.e. ACTH stimulation test known as cosyntropin stim test…since giving levo to central patients can precipitate adrenal crisis
workup in a patient with Cushing appearance
- Confirm the dx: abnormal results on 2 screening tests (low dose dex suppression test, 24 hour urine free cortisol, late night salivary cortisol)
- Establish etiology: ACTH independent (low) vs ACTH-dependent (normal/high). Measure ACTH level
- F/u imaging:
ACTH independent usually have a cortisol-secreting adrenal mass or adrenal hyperplasia (CT adrenal glands); ACTH-dependent usually have ACTH-secreting pituitary adenoma (Cushing dz), or ectopic
How do you evaluate a patient with ACTH-dependent Cushings?
-can include high dose dexamethasone suppression tests, corticotropin-releasing hormone stim testing, MRI pituitary, desmopressin stim test, inferior petrosal sinus sampling
Suppression of cortisol following high-dose dex = corticotroph pituitary adenoma
ectopic ACTH secreting tumors will have no suppression of cortisol fellowing high dose dex (resistant to feedback inhibition)
High dose dexamethasone suppresses pituitary ACTH and adrenal cortisol means
source is pituitary. If MRI negative, do intrapetrosal sinus sampling for ACTH to confirm source is pituitary
ACTH is high but high dose dexamethasone does not suppress cortisol production
ectopic tumor is release ACTH. Most common tumors = SCLC, pheochromocytoma, medullary thyroid carcinoma and bronchial carcinoid.
Get chest/abdomen CT
Tx for Cushing syndrome
Surgical resection of the adrenal gland (ACTH independent), pituitary gland (ACTH dependent) or ectopic tumor (ACTH dependent)
Bisphosphonate if low bone density
T/F: Patient found to have an incidental adrenal mass >1 cm but no sxs can be reassured and observed
False. This defines an incidentaloma, all patients require biochemical workup for:
- Cushings: 1-mg overnight dexamethasone suppression test
- Pheo: 24-hour urine metanephrines and catecholamines
**If htn or hypokalemia, measure plasma aldosterone-renin ratio
if no surgical resection, repeat imaging in 6-12 months
Next steps if secondary hypogonadism is confirmed (i.e. low/inappropriately normal LH and FSH)
- check prolactin
- check iron studies to rule out hemochromatosis
- MRI to eval for hypothalamic/pituitary lesions
fever or sore throat in a patient take methimazole or PTU
agranulocytosis until proven otherwise