Endo Flashcards

(115 cards)

1
Q

cortisol causes

A
BP regulation
glucose metabolism
immune fxn 
inflammatory response 
insulin release
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2
Q

aldosterone causes

A

normally low K

inc Na, blood volume and pressure

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3
Q

androgens causes

A

produced DHEA

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4
Q

ACTH causes

A

release of cortisol from cortex (outer part) of adrenal gland

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5
Q

Addisons dz Patho

A

primary adrenal insufficiency
deficiency of aldosterone, cortisol, and androgen
zona fasciculata
problem w/ adrenal glands

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5
Q

Addisons dz Patho

A

primary adrenal insufficiency
deficiency of aldosterone, cortisol, and androgen
zona fasciculata
problem w/ adrenal glands

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6
Q

acute cause of primary adrenal insufficiency

A

massive adrenal hemorrhage

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7
Q

secondary adrenal insufficiency due to problem w/

A

pituitary

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8
Q

tertiary adrenal insufficiency due to problem w/

A

CRH secretion –> adrenal glands won’t product cortisol

head trauma or intracranial tumors

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9
Q

primary adrenal insufficiency labs

A
adrenal 
CRH: high
ACTH: HIGH
cortisol: LOW
CRH stim response: inc ACTH
aldosterone: low 
renin: high
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10
Q

secondary adrenal insufficiency labs

A
pituitary 
CRH: high
ACTH: LOW
cortisol: LOW
CRH stim response: no/dec ACTH
aldosterone: low 
renin: normal/low
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11
Q

tertiary adrenal insufficiency labs

A
hypothalamus  
CRH: low
ACTH: low
cortisol: low
CRH stim response: exaggerated/prolonged 
aldosterone: low 
renin: normal/low
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12
Q

adrenal crisis sx and labs

A

hypotension or shock, vomiting, abd pain
F, AMS
from withdrawal of steroids
dec Na, inc K, dec glu

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13
Q

primary adrenal insufficiency sx

A
hyperpigmentation (inc ACTH)
salt craving (dec aldosterone) 
hypoNa, orthostatic hypoTN (dec aldosterone) 
kyperK, metabolic acidosis (dec aldosterone)
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14
Q

secondary and tertiary adrenal insufficiency has normal

A

aldosterone levels

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15
Q

adrenal insufficiency BIT

A

AM serum cortisol level

low cortisol = adrenal insufficiency

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16
Q

adrenal insufficiency confirmation test

A

cosyntropin stimulation test (ACTH stim)

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17
Q

adrenal insufficiency tx

A

glucocorticoid and mineralocorticoid replacement: hydrocortisone/dexamethasone and fludrocortisone (primary only)
ER w/ hypoTN: IV fluids and IV hydrocortisone
secondary: glucocorticoid

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18
Q

cushings syndrome MOA

A

high cortisol levels in blood

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19
Q

cortisol function

A

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

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20
Q

MCC Cushing disease

A

pituitary adenoma

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21
Q

MCC Cushing syndrome

A

exogenous steroid use

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22
Q

Cushing BIT

A

overnight low dose dexamethasone test
24h free urine cortisol
suppression= Cushing
no suppression= adrenal/ectopic ACTH secreting tumor

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23
Q

GLP1 AE

A

“-tide”

pancreatitis

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24
SGLT2 AE
"-flozin" UTI yeast infx
25
metformin AE
lactic acidosis no IV contrast macrocytic anemia, renal impairment GI issues, metallic taste
26
type I DM pathophys
autoimmune pancreatic islet beta cell destruction and GAD abs
27
DMT1 labs
``` A1c > 6.5 fasting glucose >126 on 2 occasions random glucose >200 OGTT 2h >200 ABSENT C PEPTIDE islet leukocytic infiltrate ```
28
rapid insulin
lispro | aspart
29
short acting insulin
regular
30
intermediate acting insulin
NPH
31
long acting "basal" insulin
glargine Lantus Levemir
32
dawn phenomenon
hyperglycemia between 3AM and 8AM | increase night insulin
33
somogyi effect
nocturnal hypoglycemia at 3AM high glucose levels by 7AM decrease night insulin
34
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 ```
35
DM screening
adult w/ BMI >25 and triglycerides >250 or HDL <35 starting at 45yo repeat every 3yrs if normal
36
metformin CI if
GFR <45
37
hyperosmolar hyperglycemic state MC in pts w/
DMT2 | infection
38
hyperosmolar hyperglycemic state sx
polyuria, dehydration, lethargy, seizures, coma, death gradual onset, blurred vision, slurred speech, weakness, hypotension, AMS
39
hyperosmolar hyperglycemic state tests
``` glu 600-2400 high serum osmolality (>320) glycosuria, inc BUN/Cr negative ketones hyponatremia ```
40
hyperosmolar hyperglycemic state tx
agressive IV fluids w/ NS replete electrolytes (K) IV insulin after fluids
41
diabetic ketoacidosis causes
insulin non compliance new diabetic dx MCC infection
42
diabetic ketoacidosis sx
abd, N/V, dehydration, fruity breath | kussmaul respiration
43
diabetic ketoacidosis labs
``` ketonuria random glucose 250-600 metabolic acidosis total body K dec high anion gap leukocytosis ```
44
diabetic ketoacidosis tx
IV fluids K replacement before insulin IV insulin bicarb for severe acidosis
45
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
46
klinefelter sx
boy w/ gynecomastia | small testicles
47
Turner syndrome sx
girl w/ webbed neck | short stature
48
kallman syndrome sx
anosmia absent breast development uterus present syndactyly
49
MEN1
3Ps primary hyperparathyroidism: hypercalcemia, inc intact PTH, dec P, inc 24h urine calcium pancreatic tumor: ZES, gastronome, insulinoma pituitary adenoma: prolactinoma MC
50
MEN2A
1M and 2Ps medullary thyroid cancer pheochromocytoma primary hyperparathyroidism
51
MEN2B
``` 3Ms and 1P medullary thyroid cancer pheochromocytoma marfanoid body habits mucosal neuromas ```
52
pheochromocytoma rule of 10
``` bilateral familial pediatric malignant extra adrenal MEN2A/2B ```
53
pheochromocytoma sx
triad: episodic HA, HTN, diaphoresis 5Ps: pressure (HTN), pain (HA), perspiration, palpitation, pallor
54
pheochromocytoma BIT
24h urinary metanephrine and catecholamines: inc metanephrines and inc vanillylmandelic acid
55
pheochromocytoma MAT
CT/MRI adrenals
56
pheochromocytoma tx
surgical resection | preop: 1st alpha blockage (phenoxybenzamine) control BP then propranolol
57
primary hyperaldosteronism vs secondary hyperaldosteronism
primary: renin independent. adrenal hyperplasia, conns (adrenal aldosteronoma) secondary: increased renin. renal artery stenosis
58
Conns syndrome pathology
aldosterone secretion independent from RAAS
59
MCC conn syndrome
adrenal adenoma
60
Conns syndrome sx
refractory HTN muscle weakness (hypoK), palpitations, arrhythmias polyuria/polydipsia, N/V/abd dist dec DTR, dec Mg
61
Conns syndrome tests
screening: plamsa aldosterone to plasma renin if HTN (+ if inc ratio) definitive: saline infusion test hypernatremia, hypoK, metabolic alkalosis
62
conns syndrome tx
``` tx underlying (adrenalectomy) 1st line spironolactone or eplerenone ```
63
SIADH med causes
``` narcotics SSRI, NSAIDS carbamazepine TCA, HCTZ ecstasy ```
64
increased ADH secretion results in
``` concentrated urine (increased urine osmo) water retention (dec serum osmo) increased edema and increased ICP --> hyponatremia ```
65
ectopic ACTH secretion commonly from
small cell lung cancer
66
SIADH sx
hyponatremia, muscle weakness,, confusion, N/V/HA | severe: seizures, AMS from cerebral edema
67
SIADH tests
hyponatremia (isovolemic hypotonic) inc urine osmo, dec serum osmo inc plasma ADH dec uric acid, dec BUN
68
S|ADH tx
asx: fluid restriction and inc salt intake sx: hypertonic saline, ICU, furosemide demeclocycline, IV conivaptan/PO tolvaptan
69
medullary thyroid carcinoma produces
calcitonin
70
hyperparathyroidism sx
``` dec DTR moans: not feeling well groans: abd pain, GERD stones: kidney bones: bone pain psych overtonesL depression ```
71
primary hyperparathyroidism labs
inc Ca Inc PTH dec P shortened QT
72
hyperparathyroidism tx
IV fluids loop diuretics parathyroidectomy: if asx, can be candidate if T score <-2.5 or younger than 50yo
73
hypocalcemia EKG
prolonged QT interval
74
hypoparathyroidism sx
trousseau (BP cuff) chvostik sign (facial twitch) inc DTR, tetany
75
hypoparathyroidism lab triad
dec Ca dec intact PTH inc P
76
hypoparathyroidism tx
sx or Ca <7.6: IV Ca glutinate | Ca >7.6: PO Ca carbonate + VitD supplement
77
acromegaly/gigantism tx
transsphenoidal resection | octreotide
78
acromegaly/gigantism MAT
OGTT w/ serum GH in 2h
79
acromegaly/gigantism study of choice
MRI
80
acromegaly/gigantism BIT
inc IGF1 levels
81
acromegaly vs gigantism
acromegaly: adult gigantism: children
82
MC type of DI
central
83
rx that causes nephrogenic DI
lithium
84
DI labs
inc vol urine, dec ADH/vasopressin dec urine osmo (dilute) inc serum osmo (concentrated)
85
DI BIT
water deprivation test: if inc urine osmo --> psychogenic polydipsia
86
DI tx
central: tx underlying, IN DDAVP nephrogenic: thiazide, amiloride, indomethacin
87
nephrogenic DI CI
ahminoglycosides: nephrotoxic
88
dwarfism/achondroplasia patho
autosomal dominant: FGFR3
89
tx dwarfism
conservative | do not give GH
90
prolactinoma labs
dec LH/FSH dec estrogen inc serum prolactin
91
prolactinoma MAT
snowman appearance on MRI
92
prolactinoma tx
BItx: cabergoline/bromocriptine
93
MCC hyperthyroidism
graves dz
94
jod basedow phenomenon
iodine induced thyrotoxicosis | hyperthyroidism after IV iodine contrast
95
hyperthyroidism tx
``` methimazole PTU (pregnancy) BB prednisolone severe: thyroidectomy ```
96
graves triad
exophthalmos orbitopathy (lid lag) peritibial myxedema
97
thyroid storm sx
hyperthyroidism + fever, tachycardia, arrhythmia, and AMS
98
thyroid storm tx
``` ABC 1st step: BB 2nd: PTU/methimazole 3rd: iodine and steroids (dexamethasone) avoid aspirin ```
99
hashimotos thyroiditis labs
``` + thyroid ab thyroid peroxidase antimicrosomial dec RAIU HLADR3 ```
100
de quervains thyroiditis sx
follows flu-like illness | self limiting
101
de quervains thyroiditis phases
3 phases hyperthyroidism hypothyroidism return to normal fxn
102
riedel thyroiditis sx
chronic condition firm hard woody nodule fixed hard painless goiter tx w/ surgery
103
postpartum thyroiditis
up to 1yr after delivery transient hyperthyroidism then hypothyroidism self limiting, dont give thyroid meds + thyroid ab
104
wolff-chaikoff effect
auto regulatory w/ too iodine
105
medications that can cause thyroid issues
amiodarone lithium sulfonamides
106
silent (lymphocytic) thyroiditis
+ thyroid ab dec RAIU return to euthyroid in. 12-18mo wo tx tx w/ aspirin, no thyroid meds
107
hashimotos thyroiditis histology
hurtle cells
108
de quervain thyroiditis sx
1st: enlarged painful thyroid, jaw pain 2nd: weight gain, pretrial myxedema
109
de quervain thyroiditis tests
high ESR neg thyroid ab gold standard: RAIU dec
110
de quervain thyroiditis tx
self limiting 1st: NSAIDS and BB 2nd: steroids
111
myxedema coma sx
``` dec mentation hypothermia hypotension hyponatremia old lady w/ long standing hypothyroidism in cold weather ```
112
myxedema coma tx
ABC in ICU supportive IV levothyroxine and hydrocortisone
113
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) ```
114
diabetic meds that cause hypoglycemia
sulfonylureas: glyburide, glipizide meglitinides: repaglinide, nateglinide insulin: regular, lispro, aspart, NPH, glargine