Endo Flashcards
cortisol causes
BP regulation glucose metabolism immune fxn inflammatory response insulin release
aldosterone causes
normally low K
inc Na, blood volume and pressure
androgens causes
produced DHEA
ACTH causes
release of cortisol from cortex (outer part) of adrenal gland
Addisons dz Patho
primary adrenal insufficiency
deficiency of aldosterone, cortisol, and androgen
zona fasciculata
problem w/ adrenal glands
Addisons dz Patho
primary adrenal insufficiency
deficiency of aldosterone, cortisol, and androgen
zona fasciculata
problem w/ adrenal glands
acute cause of primary adrenal insufficiency
massive adrenal hemorrhage
secondary adrenal insufficiency due to problem w/
pituitary
tertiary adrenal insufficiency due to problem w/
CRH secretion –> adrenal glands won’t product cortisol
head trauma or intracranial tumors
primary adrenal insufficiency labs
adrenal CRH: high ACTH: HIGH cortisol: LOW CRH stim response: inc ACTH aldosterone: low renin: high
secondary adrenal insufficiency labs
pituitary CRH: high ACTH: LOW cortisol: LOW CRH stim response: no/dec ACTH aldosterone: low renin: normal/low
tertiary adrenal insufficiency labs
hypothalamus CRH: low ACTH: low cortisol: low CRH stim response: exaggerated/prolonged aldosterone: low renin: normal/low
adrenal crisis sx and labs
hypotension or shock, vomiting, abd pain
F, AMS
from withdrawal of steroids
dec Na, inc K, dec glu
primary adrenal insufficiency sx
hyperpigmentation (inc ACTH) salt craving (dec aldosterone) hypoNa, orthostatic hypoTN (dec aldosterone) kyperK, metabolic acidosis (dec aldosterone)
secondary and tertiary adrenal insufficiency has normal
aldosterone levels
adrenal insufficiency BIT
AM serum cortisol level
low cortisol = adrenal insufficiency
adrenal insufficiency confirmation test
cosyntropin stimulation test (ACTH stim)
adrenal insufficiency tx
glucocorticoid and mineralocorticoid replacement: hydrocortisone/dexamethasone and fludrocortisone (primary only)
ER w/ hypoTN: IV fluids and IV hydrocortisone
secondary: glucocorticoid
cushings syndrome MOA
high cortisol levels in blood
cortisol function
circadian rhythm
rise in AM to help us wake up, and decreases in PM to help go to sleep
maintain BP
dec inflammatory and immune response
MCC Cushing disease
pituitary adenoma
MCC Cushing syndrome
exogenous steroid use
Cushing BIT
overnight low dose dexamethasone test
24h free urine cortisol
suppression= Cushing
no suppression= adrenal/ectopic ACTH secreting tumor
GLP1 AE
“-tide”
pancreatitis
SGLT2 AE
“-flozin”
UTI
yeast infx
metformin AE
lactic acidosis
no IV contrast
macrocytic anemia, renal impairment
GI issues, metallic taste
type I DM pathophys
autoimmune pancreatic islet beta cell destruction and GAD abs
DMT1 labs
A1c > 6.5 fasting glucose >126 on 2 occasions random glucose >200 OGTT 2h >200 ABSENT C PEPTIDE islet leukocytic infiltrate
rapid insulin
lispro
aspart
short acting insulin
regular
intermediate acting insulin
NPH
long acting “basal” insulin
glargine
Lantus
Levemir
dawn phenomenon
hyperglycemia between 3AM and 8AM
increase night insulin
somogyi effect
nocturnal hypoglycemia at 3AM
high glucose levels by 7AM
decrease night insulin
DMT2 criteria labs
A1c >6.5 fasting glucose >126 on 2 occasions random glucose >200 OGTT 2h >200 ELEVATED C PEPTIDE amyloid polypeptide deposits in pancreas
DM screening
adult w/ BMI >25 and triglycerides >250 or HDL <35
starting at 45yo
repeat every 3yrs if normal
metformin CI if
GFR <45
hyperosmolar hyperglycemic state MC in pts w/
DMT2
infection
hyperosmolar hyperglycemic state sx
polyuria, dehydration, lethargy, seizures, coma, death
gradual onset, blurred vision, slurred speech, weakness,
hypotension, AMS
hyperosmolar hyperglycemic state tests
glu 600-2400 high serum osmolality (>320) glycosuria, inc BUN/Cr negative ketones hyponatremia
hyperosmolar hyperglycemic state tx
agressive IV fluids w/ NS
replete electrolytes (K)
IV insulin after fluids
diabetic ketoacidosis causes
insulin non compliance
new diabetic dx
MCC infection
diabetic ketoacidosis sx
abd, N/V, dehydration, fruity breath
kussmaul respiration
diabetic ketoacidosis labs
ketonuria random glucose 250-600 metabolic acidosis total body K dec high anion gap leukocytosis
diabetic ketoacidosis tx
IV fluids
K replacement before insulin
IV insulin
bicarb for severe acidosis
metabolic syndrome criteria
waist circumference: >40in (M), >35in (F)
glucose >100 or tx of hyperglycemia
HDL: <40 M, <50 F or tx HDL
BP: >135 systolic or >85 diastolic or tx HTN
triglyceride: >150 or tx triglyceride
klinefelter sx
boy w/ gynecomastia
small testicles
Turner syndrome sx
girl w/ webbed neck
short stature
kallman syndrome sx
anosmia
absent breast development
uterus present
syndactyly
MEN1
3Ps
primary hyperparathyroidism: hypercalcemia, inc intact PTH, dec P, inc 24h urine calcium
pancreatic tumor: ZES, gastronome, insulinoma
pituitary adenoma: prolactinoma MC
MEN2A
1M and 2Ps
medullary thyroid cancer
pheochromocytoma
primary hyperparathyroidism
MEN2B
3Ms and 1P medullary thyroid cancer pheochromocytoma marfanoid body habits mucosal neuromas
pheochromocytoma rule of 10
bilateral familial pediatric malignant extra adrenal MEN2A/2B
pheochromocytoma sx
triad: episodic HA, HTN, diaphoresis
5Ps: pressure (HTN), pain (HA), perspiration, palpitation, pallor
pheochromocytoma BIT
24h urinary metanephrine and catecholamines: inc metanephrines and inc vanillylmandelic acid
pheochromocytoma MAT
CT/MRI adrenals
pheochromocytoma tx
surgical resection
preop: 1st alpha blockage (phenoxybenzamine) control BP then propranolol
primary hyperaldosteronism vs secondary hyperaldosteronism
primary: renin independent. adrenal hyperplasia, conns (adrenal aldosteronoma)
secondary: increased renin. renal artery stenosis
Conns syndrome pathology
aldosterone secretion independent from RAAS
MCC conn syndrome
adrenal adenoma
Conns syndrome sx
refractory HTN
muscle weakness (hypoK), palpitations, arrhythmias
polyuria/polydipsia, N/V/abd dist
dec DTR, dec Mg
Conns syndrome tests
screening: plamsa aldosterone to plasma renin if HTN (+ if inc ratio)
definitive: saline infusion test
hypernatremia, hypoK, metabolic alkalosis
conns syndrome tx
tx underlying (adrenalectomy) 1st line spironolactone or eplerenone
SIADH med causes
narcotics SSRI, NSAIDS carbamazepine TCA, HCTZ ecstasy
increased ADH secretion results in
concentrated urine (increased urine osmo) water retention (dec serum osmo) increased edema and increased ICP --> hyponatremia
ectopic ACTH secretion commonly from
small cell lung cancer
SIADH sx
hyponatremia, muscle weakness,, confusion, N/V/HA
severe: seizures, AMS from cerebral edema
SIADH tests
hyponatremia (isovolemic hypotonic)
inc urine osmo, dec serum osmo
inc plasma ADH
dec uric acid, dec BUN
S|ADH tx
asx: fluid restriction and inc salt intake
sx: hypertonic saline, ICU, furosemide
demeclocycline, IV conivaptan/PO tolvaptan
medullary thyroid carcinoma produces
calcitonin
hyperparathyroidism sx
dec DTR moans: not feeling well groans: abd pain, GERD stones: kidney bones: bone pain psych overtonesL depression
primary hyperparathyroidism labs
inc Ca
Inc PTH
dec P
shortened QT
hyperparathyroidism tx
IV fluids
loop diuretics
parathyroidectomy: if asx, can be candidate if T score <-2.5 or younger than 50yo
hypocalcemia EKG
prolonged QT interval
hypoparathyroidism sx
trousseau (BP cuff)
chvostik sign (facial twitch)
inc DTR, tetany
hypoparathyroidism lab triad
dec Ca
dec intact PTH
inc P
hypoparathyroidism tx
sx or Ca <7.6: IV Ca glutinate
Ca >7.6: PO Ca carbonate + VitD supplement
acromegaly/gigantism tx
transsphenoidal resection
octreotide
acromegaly/gigantism MAT
OGTT w/ serum GH in 2h
acromegaly/gigantism study of choice
MRI
acromegaly/gigantism BIT
inc IGF1 levels
acromegaly vs gigantism
acromegaly: adult
gigantism: children
MC type of DI
central
rx that causes nephrogenic DI
lithium
DI labs
inc vol urine, dec ADH/vasopressin
dec urine osmo (dilute)
inc serum osmo (concentrated)
DI BIT
water deprivation test: if inc urine osmo –> psychogenic polydipsia
DI tx
central: tx underlying, IN DDAVP
nephrogenic: thiazide, amiloride, indomethacin
nephrogenic DI CI
ahminoglycosides: nephrotoxic
dwarfism/achondroplasia patho
autosomal dominant: FGFR3
tx dwarfism
conservative
do not give GH
prolactinoma labs
dec LH/FSH
dec estrogen
inc serum prolactin
prolactinoma MAT
snowman appearance on MRI
prolactinoma tx
BItx: cabergoline/bromocriptine
MCC hyperthyroidism
graves dz
jod basedow phenomenon
iodine induced thyrotoxicosis
hyperthyroidism after IV iodine contrast
hyperthyroidism tx
methimazole PTU (pregnancy) BB prednisolone severe: thyroidectomy
graves triad
exophthalmos
orbitopathy (lid lag)
peritibial myxedema
thyroid storm sx
hyperthyroidism + fever, tachycardia, arrhythmia, and AMS
thyroid storm tx
ABC 1st step: BB 2nd: PTU/methimazole 3rd: iodine and steroids (dexamethasone) avoid aspirin
hashimotos thyroiditis labs
\+ thyroid ab thyroid peroxidase antimicrosomial dec RAIU HLADR3
de quervains thyroiditis sx
follows flu-like illness
self limiting
de quervains thyroiditis phases
3 phases
hyperthyroidism
hypothyroidism
return to normal fxn
riedel thyroiditis sx
chronic condition
firm hard woody nodule
fixed hard painless goiter
tx w/ surgery
postpartum thyroiditis
up to 1yr after delivery
transient hyperthyroidism then hypothyroidism
self limiting, dont give thyroid meds
+ thyroid ab
wolff-chaikoff effect
auto regulatory w/ too iodine
medications that can cause thyroid issues
amiodarone
lithium
sulfonamides
silent (lymphocytic) thyroiditis
+ thyroid ab
dec RAIU
return to euthyroid in. 12-18mo wo tx
tx w/ aspirin, no thyroid meds
hashimotos thyroiditis histology
hurtle cells
de quervain thyroiditis sx
1st: enlarged painful thyroid, jaw pain
2nd: weight gain, pretrial myxedema
de quervain thyroiditis tests
high ESR
neg thyroid ab
gold standard: RAIU dec
de quervain thyroiditis tx
self limiting
1st: NSAIDS and BB
2nd: steroids
myxedema coma sx
dec mentation hypothermia hypotension hyponatremia old lady w/ long standing hypothyroidism in cold weather
myxedema coma tx
ABC in ICU
supportive
IV levothyroxine and hydrocortisone
Sheehan syndrome
postpartum pituitary infarction lactation failure (dec prolactin) amenorrhea, hot flashes, vaginal atrophy (dec FSH/LH) fatigue, bradycardia (dec TSH) anorexia, WL, hypoTN (dec ACTH) dec lean body mass (dec GH)
diabetic meds that cause hypoglycemia
sulfonylureas: glyburide, glipizide
meglitinides: repaglinide, nateglinide
insulin: regular, lispro, aspart, NPH, glargine