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85 Cards in this Set
- Front
- Back
in DKA one will see what symptoms
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diaphoretics,
NV but no D - b/c there is NO ENTERITIS. seen usually w/ type1 and unusually w/ type2 |
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viral causes for autoimmune DM (type1)
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coxsackie
mumps rubella |
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habitus of a DM1 pt
habitus and usual outlook of a DMtype2 pt? |
skinny, autoimmunity,
fat, develops insulin Resistance over time, B-islet cells produce too much insulin and this over time causes the b-iselt cells to atrophy |
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Dx criteria for DM
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random plasma glucose >200 w/ sx
random plasma after 2 hr OGT >200 on 2 visits fasting plasma glucose >126 |
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examples of different types of insulin:
rapid acting regular long acting |
lispro, aspart
pump nph glargine and detemir - onset w.in 2 hrs and last till maxx - 24+ hrs. |
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management for type2DM
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start w/ metformin and then put on sulfonylurea or thiazolidonenoe if hba1c >7 after 2-3 mo
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if hba1c after 2nd drug added is still >8.5 then start on insulin additionally or?
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third agent, acrarbose, etc?
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#1 complication for dm2
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hhnk
then retinopthy, nepropathy, neuroapthy, atherosclerosis |
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dka patho and sx?
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extremely low insulin levels leads to too much glucose 300-800 and sx: dry membranes, kussmal = slow deep breaths, and mental status change, polyuria, polydip, and hypervent, and hypovolemic
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tx
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aggressive IVF and insulin, kcl and tx the cause
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causes of dka
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mi or high stress, infections, mucromycosis, burns, etoh high use
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hhnk >800 seen in
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type 2 dm pts w/ same reasons as above card and NO ACIDOSIS seen w/ this versus in DKA
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dm drug that causes gi issues most comonly and acidosis most rarely usually first line, what is its moa?
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decreases hepatic gluconeogenesis, increases insulin activity - metformin
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dm drug that causes a 24hr hypoglycemia and are contraindicated in pts w/ RF and hepatic issues most common problem is weight gain, moa?
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stimulate insulin release from the b-islet cells - sulfonyl - glyburide
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dm drug that causes a 24hr hypoglycemia and $$$, like a sulfonyls and even have same moa, moa?
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stimulate insulin release - meglitinide
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causes flatulence and decreases gi carb absportion
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acarbose
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moa for glitazones and issues w/ them?
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cause hpeatic gluconegenesis reduction and wt gain and increase serum ldl and rare liver tox also a/w chf!!
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2 types of diabetic retinonopathy?
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background retinopathy (no neo vascularazation) -cotton wooling and edema.
proliferative retinopathy ( w/ neovasc) - hemmoraghic type - use laser photocoag to correct |
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kimmelstein gn - findings?
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see nodules, mesangial expansion, basement membrane degeneration and, see labs w. hypoalbuminurura
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diabteic neuropathy sx
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begins in feet, and ascend w/ stocking glove pattern
decreased pain and vibratory sense can also get gastroparesis and impotence commonly and tx w/ gabapentin and carbamzapeine, PHEYNTOIN |
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complications w/ dm neuropathy
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charcot joints = repetitive foot trauma can cause foot deformity and joint destruction.
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htnsive pt/ dm never give?
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bb they mask hypoglycemia
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hypoglycemia common causes:
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reactive - decrease in serum gluc after eating so eat smaller meals more frequently
iatrogenic = too much insulin, excess administration due to sulfonylurea (glipizde) problem, cpep will be elevated, will see a high insulin lvl and low glucose. insulinoma - b-iselt tumor, cpep elevated and will see on ct or mri get surgery done or use octreotide fasting etoh induced - pit/adrenal insuff -lo cortisol, so tx is replace cortisol. do acth stim test, if still high then - d/t a non renal/adrenal cause (small cell) if low levels of acth - adrenal tumor |
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in pregnancy tbg is high and total t3,4 is high but?
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free t3,4 is normal
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______________ can occur from increase basal metabolic rate, from hyperthyroid
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osteoporosis
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a factituous hyperthyroidism will show a ___________ scan
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normal thy uptake scan
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a increased thy scan seen w._________________
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graves and adenomas (tox multinodular goiter)
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main indications for calcitonin
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paget's bone disease ( disease of too much osteoblasts and osteoclasts and you get tibial bowing, deafness, kyphosis and increased cranial diameter
and post menopausal osteoprosis |
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graves sx -
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exopthalmos, pretibial myxedema, painless goiter, and tsi ab's found on serum
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tx for graves
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subtotal thyroidectomy and radioablation
prorpthyouracil and methimazole atenolol |
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plummer's disease or toxic multinodular goiter sx or labs?
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single or multiple hyperactive nodules
increased scan at site of nodule, and hot nodule seen on labs |
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subacute thyroiditis - de quervain's thyroidits sx and labs?
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enlarged goiter and hyper then hypo condition due to viral stimulus
PAINFUL GOITER AND FEVER AND INCREASED ESR AND DECREASED UPTAKE ON THYROID SCAN. NSAIDs and b-b |
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decreased uptake on thyroid scan seen w. (2) disease?
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silent thyroiditis - post partum and bx shows inflammation ( not really hypo, hyper)
de quervain's- painful, fever, decreased uptake on thyroid scan. |
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ab's seen w/ hashimoto thryoidsitis
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increased tsh, antimicrosmal abs, antithyrolgobulin abs, decreased uptake on thyroid scan - cold scan!! - HYPO CONDItion
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THYROID CA - nodules should be worked up by?
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tsh levels, thyroid function tests and us, fna w/ biopsy
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most common form of thyroid cancer
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papilary- of columnar gland cells
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most aggressive cancer form for thyroid
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anaplastic - poorly diff, can cause hoarseness and dysphagia and can hit the recurrent laryngeal nerve and prognosis is poor
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produces calcitonin, thyroid cancer?
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produces calcitonin - medullary thyroid ca a/w men type 2a,2b cancer of the parafolicular c cells see spiral things.
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malignant nodule workup?
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scan - cold usually,
observe - small and cystic nodules solid and benign - do sx and radioablation levothyroxine malignant tumor - resect - <1cm lobectomy if larger do total thyroidectomy w/ ablation synthroid post surgery for replacement |
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labs:
primary hyperPTH |
HIGH PTH
HIGH CA LO PO4 |
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MAIN CAUSES OF HYPERPTH
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ADENOMA (PIT) OR/AND HYPERPLASIA OF THE GLAND
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sx of hyperpth
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bones, groans, stones, and psych overtones
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tx for hyperPTH
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single adenoma- remove nodule
hyperplasia - remove all 4 and implant a portion of one in the forearm muscle so there is some endogenous pth tx hypercalcemia w/ ivf and alendronate |
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hyperpth - secondary causes
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malnurtition, malabsp, and renal disease, or ca-wasting drugs
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secondary hyperpth (NON RENAL) labs
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HIGH PTH
LO PO4 LO CA AND VIT D |
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SECONDARY HYPERPTH ( RF) LABS
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HIGH PTH
HIGH PO4 LO CA, VITD |
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HYPOPTH MOST COMMON CAUSE
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D/T SURGICAL REMOVAL - OF PARATHYOID OR AUTOIMMUNE GLAND DESTRUCTION - LEADS TO HYPO CA
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HYPO PTH LABS
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lo ca, high phos, lo pth
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signs and symptoms seen w/ hypopth
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trosseou sign - carpal spasm w/ bp cuff inflation
chvostek sign - tap facial nerve |
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tx for hypopth
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ca and vitD suuplementaion
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psuedohypoparathyroidism
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hypocalcemia resulting from tissue non responsiveness to pth
high pth lo calcium high po4 --- looks like secondary hyperpth w/rf |
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tx of psueohypopth?
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ca supplementation. vitD
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TRH stimulates? (2)
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tsh and PTL
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drugs that cause hyperPTL
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phenothiazines
risperidone haldol m-dopa verapamil |
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sx for hyperPTL
tx? |
amenorrhea, galatorrhea, lo libido, ED, bilateral hemianopsia, gynecomastia
cabergoline, bromocriptine, pergolide, transphenoidal surgery |
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to test for excess GH like in acromegaly?
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give 1 hr 100g glucose test look for increased GH
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sx for acromegaly?
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organomegaly,LVH, diastolic dysfunction, dm, cord compression,vision loss, insulin resistance
childhood form - gigantism |
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tx for acromegaly?
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surgical resection for adenoma ( adenoma is mcc)
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ORDER OF HORMONE DEFICIENCIES SEEN IN PANHYPOPIT
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GOOD LUCK FINDING TX FOR PITUITARY ACCIDENTS
GH - GROWTH FAILURE LH - AMENORHEA, IMPOTENCE FSH TSH - HYPOTHY PTL - NO LACTTAION ACTH - DECREASED SKIN PIGMENT, FATIGUE, WT LOSS, LO APPETITE. |
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TEST FOR LO LH?
LO GH? LO TSH? LO PTL? LO ACTH? |
GIVE MEDROXYPORGESTERONE - STILL LOW
GIVE 2 HR INSULIN OGT - STILL LOW LO TSH, T4 T3 CORTISOL DOES NOT INCREASE FOLLOWING ADMINISTRATION OF INSULIN |
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CUSHINGS DISEASE
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EXCESS ACTH BY PIT ADENOMA
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CUSHINGS SYNDROME
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EXCESS CORTISOL INTAKE - MCC FOR CUSHINGS
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DETERMINE CAUSE OF CORTISOL EXCESS
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LO DEXAME TEST SUPP TEST - 1-2 MG GIVEN PM AND LO CORTISOL NORMALLY FOUND
HIGH SUPP TEST - 8MG/DAY FOR 2 DAYS AND USED TO DETERMINE CAUSE OF CORTISOL EXCESS. |
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WHAT WILL LOW DOSE DEXAMTHASONE SUPPRESSION TEST SHOW FOR A CUSHING'S SYNDROME PT?
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NO DECREASE
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cushing's syndrome sx
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mr. cushings
menstural iregularities rounded facies central obestiy cervical fat pad urinary cortisol increase glucose increased = insensitivity purple striae on abdomen suppression of immune system htn, hyper cortisolism, hirsutism iatrogenic neoplasm glucose intolerance growth retardation |
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cushings labs
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hyperglycemia, glycosuria, hypokalemia
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if after low dose dexameth test the next am the cortisol level is still found low that means
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cushing's not due to intrisnsic cause, due to exogenous steroid administration - remove the pills
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if after low dose dexameth test there is no change in cortisol following the morning then we will say:
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dx of cuhsing's do 24 hr urinary cortisol
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if after no change is seen on dexameth test and ater 24hr urinary cortisol is done, we see high urinary cortisol, what does that tell us?
normal urinary cortisol? |
high- do high dose dexamth test to determine exact cause, if suppressed this time - think pit adenoma
if not suppressed - get acth level - think adrenal tumor if level is low, if high, no adrenal acth secreting tumor like paraneoplastic small cell normal not cushings |
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most common complication for cushin's adrenal tumor sugrery
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avn of hip
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excess aldosterone secretion caused by a unliateral adenoma
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hyperaldosteronism
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labs seen w/ hyperaldosteroneism
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lo k
hi na met alkalosis lo renin - in conns always whether its primary or secondary hyperaldos will see - increased 24hr urinary aldosterone |
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adrenal insufficiency types:
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primary - addison's - autoimmune destruction due to hemorrhage (waterhous F syndrome - meningococcal sepsis and hemorrhage into adrenals bilaterally) - see increased msh, and skin pigment (only seen w/ primary!!)
secondary - due to decreased acth production to chronic steroid use (adrenal atrophy) or insufficient acth production by pit. - Tertiary - hypothalamic failure - CRH not produced. |
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labs in hyperaldosteroneism
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decreased na and increased k ( like on k sparer) secondary to low aldosterone, decreased cortisol (adrenal insuff) and eosiniophillia
addisons/primary adrenal insuff - see increased acth, increase msh. secondary insfuff/tertiary - see decreased acth the low cortison goes UPPP w/ acth analog administration (cosyntropin stim test- dx test for addisons) in primary insuff/addisons - NO CHANGE in secondary/tert insuff - see increase!! |
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tx for adrenal insuff
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mineralocorticoid and glucocorticoid replacment
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complications of adrenal insuff
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Addisonian crisis- weakness, fever, ams, vascular collapse, in times of stress, need for cortisol.
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causes of eosinophilia -
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drugs, neoplasm, allergies, addisons, ain, collagen vasc disease, parasitic pneumonitis, ascaris lumbracoides
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cah - types:
recall: 1 first number - then we see htn 1 2nd number - then we see virilization |
17a - amenorrhea, ambiguous genatalia, htn lo k, hi na, decreased androgens
21a- excess testoserone, ambiguous genitalia, virilization, precocious puberty, hotn, hi k lo na. 11b- virilization, precpuberty in males, ambig genitalia in women and htn, and increased secondary dexoycorticosterone, + androgens. WE SEE BOTH HTN AND VIRILIZATION!!!! **21 is the most common form of cah |
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what is the pheocromocytoma rule of 10s?
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10% malignant
10% multiple 10% bilateral 10% extradrenal 10%kids 10%familial 10%calcify |
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diaphorectic w/ intermittent tachycardia and htn, headache
tx? |
pheo
get 24hr urinary metanphrines, catecholamines and vma surgery a, before beta |
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men 1 a/w
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PITY - acromegaly (GH secreting adenoma), cushings (excess cortisol- syndrome), galactorrhea
PARA- hyperPTH, hypercalcemia Pancreas - zollinger ellison -gastrin producing tumor in duoenum or panc - increased fasting gastrin levels. |
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men2a a/w
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medullary thyroid carcinoma (recall- psammoma bodies a/w papillary) - increased calcitonin lvls
parathroid - increased PTH - hypercalcemia pheo- increased urine and serum catcholamines |
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men2b a/w
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medullary thyroid ca
pheo mucosal neuroma - NF? marfanoid habitus |
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baby born w/ poor feeding, lethargy, bulgining fontanelles, thick tongue, constipation, umbilical hernia, poor growth, hypotonic, skin dry, jaundice prolonged
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severely hypothryoid infant - cretinism.
which sx is seen fist?? - prolonged jaundice! |
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bx shows thyroid w/ germinal centers
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hypothyroidism
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