ENDOCRINE Flashcards

(48 cards)

1
Q

rapid onset hirsutism suggests…

hirsutism in general should make you think…

A

high androgen levels due to androgen secreting neoplasm

pcos

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2
Q

tumor in kids that causes precocious puberty with estrogen secretion

A

granulosa cell tumors

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3
Q

botulism vs GBS

A

botulism is descending paralysis with early cranial involvement and pupillary changes

GBS is ascending symmetrical paralysis over days

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4
Q

what level do you treat hypercalcemia?

A

> 14 mg/dL

treat with NS hydration plus calcitonin

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5
Q

niacin deficiency
sx?
tx?

A

B3 deficiency
PELLAGRA ( dementia, dermatitis, diarrhea)

niacin replacement

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6
Q

thiamine (B1) deficiency

A

beri beri or wenicke-korsakoff

ass with alcoholics or weight loss surgery

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7
Q

riboflavin deficiency

A

B2 deficiency

cheilosis, glossitis, seborrheic dermatitis

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8
Q

pyridoxine deficiency

A

B6

irritability, depression, dermatitis, stomatitis

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9
Q

B12 deficiency

A

cyanocobalamin deficiency

macrocytic anemia and peripheral neuropathy

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10
Q

what can be elevated in a patient with B12 deficiency?

A

methylmalonic acid

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11
Q

kallman syndrome

A

decreased GnRH and decreased FSH/LH

anosmia +/- renal agenesis

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12
Q

ADH deficiency is known as…

A

central diabetes insipidus

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13
Q

2 hormones of the posterior pituitary

A

ADH and oxytocin

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14
Q

central DI vs nephrogenic DI

presentation of DI?

A

central is decreased ADH production
nephrogenic is decreased response to ADH in kidneys

high volume urine output and excessive thirst resulting in volume depletion and hypernatremia -> can lead to confusion, lethargy

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15
Q

classically what medication can cause nephrogenic DI?

A

lithium

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16
Q

best diagnostic test to determine central vs nephrogenic DI

A

vasopressin (desmopression) stimulation test

central = urine V will decrease and urine osmolality will increase

nephro = no effect

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17
Q

treatment for central and nephro DI?

A

central = vasopressin

nephro = tx underlying cause + HCTZ, amiloride, and NSAIDs

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18
Q

acromegaly

usually caused by?
presentation?
dx?
tx?

A

overproduction of GH

usually d/t pituitary adenoma
enlarging soft tissue = increased hat, ring sizes, carpal tunnel, OSA, body odor, coarsening of facial features, deep voice, big tongue

best initial test is IGF-1
most accurate test is glucose suppression test (glucose should suppress GH)

tx: transphenoid resection of the pituitary
or meds
-ocreotide (somatostatin will suppress GH)
-pegvisomant (GH receptor antagonist)

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19
Q

should a head MRI ever be an initial diagnostic test?

A

NO!! never first test for endocrine disorders

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20
Q

if prolactin is elevated, next tests?

A

pregnancy test
thyroid function tests
BUN/Cr (kidney disease can elevate prolactin)

21
Q

best first initial test for thyroid issues

22
Q
findings and tx for hyperthyroid dz:
1 graves dz
2 subacute thyroiditis
3 painless silent thyroiditis
4 exogenous thyroid hormone use
5 pituitary adenoma
A

1 proptosis, TSH receptor abs, low TSH, high RAIU –> tx with radioactive iodine (ablation)

2 tender thyroid, low TSH, decreased RAIU –> tx with aspirin

3 normal exam, low TSH, decreased RAIU –> no tx

4 involuted/nonpalpable gland, low TSH, decreased RAIU –> stop exogenous use!

5 HIGH TSH, MRI of head –> surgery

23
Q

thyroid nodules must be biopsied when?

A

must FNA nodule if it is >1 cm if they have normal thyroid function

24
Q

cardiac sx of hypercalcemia?

A

short QT and htn

25
tx for acute hypercalcemia
saline hydration at high volume and bisphosphonates (aledronate, pamidronate, zeledronic acid) if that doesnt bring ca down, you can use calcitonin
26
labs seen in primary hyperparathyroidism
``` high PTH high serum Ca low phosphate ekg with short QT alk phos may be elevated due to bone effects ```
27
tx for primary hyperparathyroidism
surgical removal of parathyroid glands or cinacalcet if nonoperable
28
labs seen in hypocalcemia due to low albumin
low albumin causes a decrease in total calcium but free calcium is normal = no sx
29
signs of hypocalcemia
``` chvosek sign (facial nerve hyperexcitable) carpopedal spasm perioral numbness mental irritability seizures tetany (treausseau sign) prolonged QT ```
30
tx for hypocalcemia
replace ca and vit D orally if mild sx IV if severe
31
HPA axis
hypothalamus --> CRH --> pituitary gland ---> ACTH ---> adrenal glands ---> cortisol
32
cushings syndrome | 4 main causes
hypercortisolism! pituitary overproduction of ACTH (cushing disease) adrenals unknown source extopic ACTH (cancer, carcinoid)
33
dx tests for hypercortisol/cushings
best initial test = 24 hr urine cortisol (second best option is overnight dexamethasone suppression) if 24 hr urine is elevated = confirms hypercortisolism if suppression on dexa test occurs, can rule out hypercortisolism ACTH testing is best test to identify the SOURCE of hypercortisolism - -low ACTH means adrenal source - -high ACTH means either pituitary of ectopic --> scan brain with MRI if high ACTH and nonsuppressible
34
``` addisons disease aka? presentation? dx? tx? ```
chronic hypoadrenalism weakness, ams, n/v, hypoNa, HyperK, hyperpigmentation hypoglycemia, hyperK, met. acidosis, hypoNa, high BUN, EOSINOPHILIA if pituitary failure = ACTH is low if primary adrenal failure = ACTH high cosyntropin test (synthetic ACTH) --> if normal should cause a rise in cortisol tx steroids
35
acute adrenal crisis presentation? first step?
profound hypotension, fever, confusion, coma high eosinophils, hyperK, hypoNa, hypoglycemia draw cortisol level and give HYDROCORTISONE **hydrocortisone is more important than diagnosis in acute adrenal crisis
36
``` primary hyperaldosteronism main causes? presentation? dx? tx? ```
solitary adenoma or bilateral hyperplasia high BP despite low renin and hypokalemia best initial test is ratio of aldosterone to renin only do a CT if testing shows: 1) low K, 2) high aldosterone, and 3) low renin adenoma = surg laparotomy bil, hyperplasia = tx w eplerenone or spironolactone
37
pheochromocytoma presentation? dx? tx?
nonmalignant autonomous lesion of adrenal medulla that produces catecholamines despite high BP episodic htn, headache, sweating, and palpitations best initial test is free plasma metanephrines and 24 hr urine metanephrines then do CT tx phenoxybenzamine (alpha blocker) --> surg removal
38
DM diagnosis
2 fasting BG >125 single glucose >200 with symptoms or increased glucose on oral glucose tolerance testing or hgA1c>6.5% (best test to follow therapy effect)
39
how does exercise help in DM
exercising muscle does not need insulin so it decreases insulin requirement/decreases insulin resistance by decreasing adipose tissue
40
best initial med for DM? mech? but it is contraindicated in?
metformin - it bocks gluconeogenesis (does not increase weight gain and does not cause hypoglycemia) contraindicated in renal dysfunction (can accumulate and cause met acidosis)
41
sulfonylureas
not first line for DM since they increase insulin release from pancreas and increase weight gain
42
if oral agents are not controlling DM, start patient on...
insulin insulin glargine = 1x/day long acting NPH would be 2x/day long acting + lispro or aspart (short acting) goal is hgba1c<7%
43
DKA tx
large volume saline and insulin
44
best indicator of severity of DKA?
serum bicarbonate **if very low (big anion gap), there is risk of death
45
all DM patients should receive
``` pneumococcal vaccine yearly eye exam yearly foot exam statin if LDL>100 acei/arb if BP >140/90 or if urine + microalbuminuria aspirin if >30yo ```
46
tx for DM associated gastroparesis (decreased bowel mobility due to decreased stretch feedback)
metoclopromide and erythromycin (increase gastric mobility)
47
retinopathy seen w DM? | tx?
nonproliferative retinopathy --> tighter gluc control proliferative retinopathy (vitreous hemorhage and neovascularizatuion) --> laser photocoagulation
48
to dx amyloidosis
abdominal fat pad biopsy