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244 Cards in this Set
- Front
- Back
this type of proliferative fibrocystic disease is associated with an increased risk of invasive breast cancer
|
sclerosing adenosis
|
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transformation of ductal epithelial cells to eosinophilic cells resembline apocrine sweat gland epithelium; not associated with increased CA risk
|
apocrine metaplasia
|
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testicular enlargement with obliterative endarteritis with perivascular cuffing of lymphocytes and plasma cells
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syphilis
|
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child infected in utero with DS DNA virus - petechiae, hepatosplenomegaly, jaundice; brain calcifications
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CMV
|
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what marker do leiomyomas express?
|
smooth muscle actin
|
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organism that lacks muramic acid?
|
chlamydia
|
|
most common bacterial STD in U.S.?
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chlamydia
|
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what complications account for the most maternal deaths in preeclampsia?
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cerebral hemorrhage and ARDS
|
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solitary, thickened, whitish plaque on penis - dysplastic epithelial cells with many mitoses, no stromal invasion
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Bowen's disease
|
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what is the posterior fornix in contact with - space that is the lowest part of the peritoneal cavity in the female pelvis
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rectouterine
|
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dermal lymphatic invasion by cancer cells?
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inflammatory breast cancer
|
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what maintains the corpus luteum during pregnancy?
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hCG
|
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tumor marker for serous papillary cystadenocarcinomas?
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CA-125
|
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initial event in pathogenesis of preeclampsia?
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placental ischemia
|
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bacteria causing amnionitis?
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listeria monocytogenes
|
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drainage of left ovary/testis?
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left gonadal vein - left renal ven - IVC
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drainage of right ovary/testis?
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right gonadal ven - IVC
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what does the suspensory ligament of the ovaries contain?
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ovarian vessels
|
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what does the transverse cervical/cardinal ligament contain?
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uterine vessels
|
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what does the round ligament of the uterus contain?
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no important structures
|
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what does the broad ligament of the uterus contain?
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round ligaments of uterus and ovaries and uterine tubules and vessels
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what is the acrosome derived from?
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golgi
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what is the flagellum (tail) of sperm derived from?
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one of the centrioles
|
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what is the sperm food supply?
|
fructose
|
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what does spermatogenesis begin with?
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spermatogonia (type A and B)
|
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where does spermatogenesis occur?
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seminiferous tubules
|
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what does type A spermatogonia form?
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both type A and type B
|
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what forms the blood-testis barrier?
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junctional complex (tight junction) between Sertoli cells
|
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what stimulates testosterone release from Leydig cells?
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LH
|
|
FSH stimulates sertoli cells to produce what?
|
androgen binding protein & inhibin (inhibits FSH)
|
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what converts testosterone and androstenedione to estrogen in adipose tissue?
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aromatase
|
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list the forms of estrogen in order of potency
|
estradiol > estrone > estriol
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what enzyme converts cholesterol to androstenedione in the theca cell? what stimulates it?
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desmolase; LH
|
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what converts androstenedione to estrogen in the granulosa cell? what stimulates it?
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aromatase; FSH
|
|
what is elevation of progesterone indicative of?
|
ovulation
|
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what does unopposed estrogen therapy increase the risk of? what can be added to decrease this risk?
|
endometrial cancer; progesterone decreases the risk
|
|
this hormone is responsible for stimulation of endometrial glandular secretions and spiral artery development
|
progesterone
|
|
what does progesterone do to myometrial excitability?
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decreases it
|
|
what influence does progesterone have on uterine smooth muscle?
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relaxes it
|
|
when is follicular growth the fastest?
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during 2nd week of proliferative phase
|
|
what stimulates endometrial proliferation?
|
estrogen
|
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what maintains the endometrium to support implantation?
|
progesterone
|
|
when does the estrogen surge occur?
|
day before ovulation - stimulates LH, inhibits FSH
|
|
what effect does progesterone have on temperature?
|
increases it
|
|
what is the role of OCPs?
|
prevent estrogen surge, LH surge so ovulation does not occur
|
|
what maintains the corpus luteum for the 1st trimester?
|
hCG
|
|
when does hCG appear in urine after fertilization?
|
8 days
|
|
what is the average age of onset of menopause?
|
51 - earlier in smokers
|
|
what happens to estrogen levels after menopause?
|
decrease
|
|
what happens to levels of FSH, LH, GnRH at menopause?
|
increase (FSH increases the most; no LH surge)
|
|
what does a bicornuate uterus result from?
|
incomplete fusion of the paramesonephric ducts; associated with UT abnormalities and infertility
|
|
what does hypospadias result from?
|
failure of urethral folds to close - opening on inferior/ ventral side
|
|
what does epispadias result from?
|
faulty positioning of genital tubercle - on superior/dorsal side
|
|
what is hypospadias associated with?
|
UTIs - more common than epispadias
|
|
what is epispadias associated with?
|
exstrophy of the bladder
|
|
what stage is an oocyte in prior to ovulation?
|
prOphase of meiosis I
|
|
what stage is a follicle in until fertilization?
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METaphase of meiosis II
|
|
what is Mittelschmerz
|
blood from ruptured follicle causes peritoneal irritation - can mimic appendcitis
|
|
ovaries present, but external genitalia are virilized or ambiguous - due to exposure to androgenic steroids during early gestation
|
female pseudohermaphrodite (XX)
|
|
testes present, but external genitalia are female or ambiguous
|
male pseudohermaphrodite
|
|
what is the phenotype in androgen insensitivity syndrome (46, XY)?
|
female - female external genitalia with rudimentary vagina, uterus and uterine tubes generally absent; develops testes
|
|
in androgen insensitivity, what levels of testosterone, estrogen, LH are seen?
|
all high
|
|
cryptorchidism is associated with an increased risk for what?
|
germ cell tumors, especially seminoma and embryonal carcinoma
|
|
what happens in 5-alpha reductase deficiency?
|
unable to convert T-DHT; ambiguous genitalia until puberty, when increased testosterone causes masculinization of genitalia
|
|
what levels of testosterone, estrogen, and LH are associated with 5-alpha reductase deficiency?
|
normal; LH normal or increased
|
|
in what location is nodular enlargement seen in BPH?
|
periuretheral (lateral and middle) lobes
|
|
from where does prostatic adenocarcinoma most often arise?
|
posterior lobe (peripheral zone)
|
|
what is the genotype of a complete hyatidiform mole? what is the origin?
|
46, XX- completely paternal in origin
|
|
what is HELLP syndrome?
|
Hemolysis, Elevated LFTs, Low Platelets
|
|
what is the treatment for eclampsia?
|
IV magnesium sulfate and diazepam
|
|
increased risk of abruptio placentae with what?
|
smoking, hypertension, cocaine use
|
|
painful uterine bleeding usually during 3rd trimester
|
abruptio placentae - premature separatino of placenta (may be associated with DIC)
|
|
defective decidual layer allows placenta to attach directly to myometrium
|
plaenta accreta
|
|
what stimulates theca cells to secrete androstenedione and testosterone?
|
LH
|
|
what stimulates aromatase activity in granulosa cells?
|
FSH
|
|
where is the deep inguinal ring?
|
about 1/2 inch above the midpoint of the inguinal ligament
|
|
how do indirect inguinal hernias enter the inguinal canal?
|
through the deep inguinal ring
|
|
in many cases of Paget disease of the breast, what else is present?
|
underlying adenocarcinoma
|
|
lump in breast with prominent multinucleated giant cell reaction?
|
fat necrosis
|
|
three types of ovarian tumors that can produce large amounts of steroid hormones?
|
sertoli-leydig cell tumors, fibroma-thecomas, granulosa cell tumors
|
|
what is the most likely condition predisposing to breast abscess/mastitis?
|
breast feeding
|
|
what predisposes to placenta accreta?
|
prior C-section or inflammation; may have massive hemorrhage after delivery
|
|
placenta previa?
|
attachment of placenta to lower uterine segement; may occlude cervical os
|
|
painless bleeding in any trimester
|
placenta previa
|
|
what is polyhydraminos (>1.5-2L) associated with?
|
esophageal/duodenal atresia; anencephaly
|
|
what is oligohydraminos (<0.5L) associated with?
|
bilateral renal agenesis or posteror urethral valves (in males)
|
|
koilocytes?
|
cervical dysplasia - HPV
|
|
what types of HPV are associated with CIN?
|
16, 18
|
|
how does HPV cause CIN?
|
HPV viral proteins E6 & E7 bind and inactivate gene products of p53 & Rb
|
|
endometrial hyperplasia puts one at an increased risk for what?
|
endometrial CA
|
|
abnormal endometrial gland proliferation usually caused by excess estrogen stimulation
|
endometrial hyperplasia
|
|
what is the most common gynecological malignancy?
|
endometrial carcinoma
|
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what is the peak age for endometrial carcinoma? how does it typically present?
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55-65; vaginal bleeding
|
|
risk factors for endometrial cancer?
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prolonged estrogen use, obesity, diabetes, and hypertension
|
|
leiomyomas are sensitive to what?
|
estrogen - increased sized with pregnancy and decreased with menopause
|
|
amenorrhea, infertility, obesity, hirsutism
|
polycystic ovarian syndrome
|
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increased LH production leads to anovulation, hyperandrogensim due to deranged steroid synthesis
|
PCOS
|
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treatment for polycystic ovarian syndrome?
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weight loss, OCPs, gonadotropin analogs, or surgery
|
|
what are antibodies directed against in type I DM?
|
glutamic acid decarboxylase (GAD)
|
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treatment for pituitary apoplexy?
|
glucocorticoids and thyroid hormone
|
|
most accurate test for hypothyroidism?
|
serum TSH
|
|
metabolic disturbance seen in primary adrenal insufficiency?
|
hypokalemia
|
|
what effect do alpha2 agonists have on insulin secretion?
|
directly inhibit it
|
|
what is Laron dwarfism?
|
congenital absence of growth hormone receptors
|
|
classical physical finding in Addison's disease?
|
hyperpigmentation
|
|
how does pregnancy/estrogen affect thyroid-binding globulin?
|
increases its synthesis
|
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Hashimoto's can be associated with disorders of what other organ?
|
thymus
|
|
how do you distinguish nephrogenic DI from neurogenic DI?
|
water deprivation will fail to increase urine osmolarity in both, but subsequent injeciton of vasopressin will concentrate the urine in the case of neurogenic DI but not nephrogenic DI
|
|
what are the secretory products of the zona glomerulosa?
|
aldosterone
|
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what are the secretory products of the zona fasciculata?
|
cortisol, sex hormones
|
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what are the secretory products of the zona reticularis?
|
sex hormones, e.g. androgens
|
|
what are the secretory products of the adrenal medulla?
|
catecholamines
|
|
what doe sthe posterior pituitary produce?
|
vasopressin and oxytocin
|
|
what embryonic layer is the posterior pituitary derived from?
|
neuroectoderm
|
|
what hormones is the alpha subunit common to?
|
TSH, LH, FSH, hCG
|
|
what subunit determines hormone specificity?
|
beta
|
|
in what part of the pancreas are the islets of Langerhans most numerous?
|
tail
|
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from what do the pancreatic islets arise?
|
pancreatic buds
|
|
what type of pancreatic cells secrete glucagon?
|
alpha
|
|
what type of pancreatic cells secrete insulin?
|
beta
|
|
what type of pancreatic cells secrete somatostatin?
|
delta
|
|
how does prolactin influence dopamine synthesis and secretion?
|
increases it
|
|
what effect does dopamine have on prolactin?
|
inhibits it's secretion
|
|
what effect do dopamine agonists (e.g. bromocriptine) have on prolactin secretion?
|
inhibit (antagonists - e.g. antipsychotics - stimulate
|
|
decreased sex hormones, decreased cortisol, increased mineralocorticoids - hypertension, hypokalemia; phenotypically female but no maturation
|
17alpha hydroxylase deficiency
|
|
what is the most common form of congenital adrenal hyperplasia?
|
21 beta hydroxylase deficiency
|
|
decreased cortisol (increased ACTH), decreased mineralocorticoids, increased sex homrones - masculinization, female pseudohermaphroditism, etc.
|
21 beta hydroxylase deficiency
|
|
what is the difference in BP between 17 alpha hydroxylase deficiency and 21 beta hydroxylase deficiency?
|
17=hyPERtension and 21=hyPOtension
|
|
increased plasma renin activity, volume depletion, hyponatremia, hyperkalemia are associated with what congenital adrenal hyperplasia?
|
21 beta hydroxylase deficiency
|
|
decreased cortisol, decreased aldosterone and corticosterone, increased sex hormones, masculinization, hypertension?
|
11 beta hydroxylase deficiency
|
|
what effect does PTH have on phosphate?
|
decreases serum phosphate, increases urine phosphate
|
|
what effect does PTH have on calcium?
|
increases serum calcium
|
|
where does PTH influence calcium resorption?
|
increases it in distal convuluted tubule
|
|
what type of vitamin D comes from sun exposure in skin?
|
D3
|
|
what increases absorption of dietary calcium and phosphate and increases bone resorption of them as well?
|
vitamin D
|
|
levels of calcium, phosphate, alk phos in osteoporosis?
|
all normal
|
|
levels of calcium, phosphate, alk phos in hyperparathyroidism?
|
increased calcium, decreased phosphate, increased alkphos
|
|
levels of calcium, phosphate, alk phos in Paget's disease
|
normal to increased calcium, normal phosphate, very high alk phos
|
|
levels of calcium, phosphate, alk phos in vitamin D intoxication?
|
all increased (alk phos normal or increased)
|
|
levels of calcium, phosphate, alk phos in renal insufficiency?
|
decreased calcium, increased phosphate, normal alk phos
|
|
what is the source of calcitonin?
|
parafollicular (C cells) of thyroid
|
|
waht is the function of calcitonin?
|
decreases bone resorption of calcium
|
|
what causes calcitonin secretion?
|
increased serum calcium
|
|
when is thyroid binding globulin decreased?
|
hepatic failure
|
|
how does thyroid hormone increase BMR?
|
increases Na/K ATPase activity - increased O2 consumption, RR, body temp
|
|
Cushing's disease?
|
primary pituitary adenoma - increased ACTH and cortisol
|
|
ACTH level in primary adrenal hyperplasia/neoplasia?
|
decreased (cortisol increased)
|
|
dexamethasone suppression in healthy person?
|
decreased cortisol after low does
|
|
dexamethasone suppression test in person with ACTH-producing tumor?
|
increased cortisol after low dose, decreased cortisol after high dose
|
|
dexamethasone suppression in person with cortisone-producing tumor?
|
increased cortisol after low and high dose
|
|
primary hyperaldosteronism/Conn's syndrome?
|
caused by an aldosterone-secreting tumor
|
|
findings in Conn's syndrome?
|
hypertension, hypokalemia, metabolic alkalosis
|
|
renin level in primary aldosteronism? in secondary?
|
low renin in primary, high renin in secondary
|
|
this type of hyperaldosteronism is due to renal artery stenosis, chronic renal failure, CHF, cirrhosis, or nephrotic syndrome
|
secondary - kidney perception of low intravascular volume results in overactive RAA system - high plasma renin
|
|
primary deficiency of aldosterone and cortisol due to adrenal atrophy
|
Addison's disease
|
|
hyponatremic volume contraction and skin hyperpigmentation
|
Addison's disease
|
|
how do you distinguish Addison's disease from secondary deficiency of aldosterone?
|
no skin hyperpigmentation in secondary (due to decreased pituitary ACTH production)
|
|
what is the cause of skin hyperpigmentation in Addison's?
|
MSH, a byproduct of increased ACTH production from POMC
|
|
what cells is a pheochromocytoma derived from?
|
chromaffin cells (arise from neural crest)
|
|
what MEN types is pheochromocytoma associated with? what other disorder is it associated with?
|
MEN II and III; neurofibromatosis
|
|
most common tumor of adrenal medulla in adults? kids?
|
pheochromocytoma; neuroblastoma (can occur anywhere along the sympathetic chain)
|
|
how is pheochromocytoma treated?
|
alpha antagonists, especially phenoxybenzamine
|
|
MEN I?
|
pancreas (e.g. Zollinger-Ellison syndrome, insulinomas, VIPomas), parathyroid, and pituitary tumors (3 P's)
|
|
how does MEN I present?
|
kindey stones and stomach ulcers
|
|
another name for MEN I?
|
Wermer's syndrome
|
|
MEN II?
|
medullary carcinoma of the thyroid, pheochromocytoma, parathyroid tumor
|
|
another name for MEN II?
|
Sipple's syndrome
|
|
MEN III?
|
medullary carcinoma of the thyroid, pheochromocytoma, and oral and intestinal ganglioneuromas (mucosal neuromas)
|
|
how are MEN syndromes inherited?
|
AD
|
|
what gene are MEN II and III associated with?
|
ret
|
|
what type of hypersensitivity reaction is Grave's?
|
type II
|
|
what is Riedel's thyroiditis?
|
thyroid replaced by fibrous tissue (hypothyroid)
|
|
histologic finding in hashimoto's?
|
lymphocytic infiltrate with germinal centers
|
|
self-limited hypothyroidism often following a flulike illness; elevated ESR, jaw pain, early inflammation, and very tender thyroid?
|
subacute thyroiditis (de Quervain's)
|
|
what is the most common type of thyroid cancer?
|
papillary carcinoma - excellent prognosis
|
|
ground-glass/Orphan Annie nuclei, psammoma bodies
|
papillary carcinoma of the thyroid
|
|
from what does medullary carcinoma of the thyroid arise?
|
parafollicular C cells
|
|
thyroid cancer that produces calcitonin, sheets of cells in amyloid stroma?
|
medullary carcinoma
|
|
type of thyroid cancer seen in older patients, very poor prognosis?
|
undifferentiated/anaplastic
|
|
defect in T4 formation or developmental failure in thyroid formation is seen in what?
|
sporadic cretinism
|
|
treatment for acromegaly?
|
octreotide
|
|
primary hyperparathyroidism is usually caused by what?
|
adenoma
|
|
findings in primary hyperparathyroidism?
|
hypercalcemia, hypercalciuria, hypophosphatemia, increased PTH, increased cAMP in urine
|
|
symptoms of primary hyperparathyroidism?
|
often asymptomatic; may present with weakness and constipation
|
|
what causes secondary hyperparathyroidism?
|
secondary hyperplasia due to decreased serum calcium, most often in chronic renal disease
|
|
findings in secondary hyperparathyroidism?
|
hypocalcemia, hyperphosphatemia, increased PTH
|
|
what causes hypoparathyroidism?
|
accidental surgical excision or DiGeorge's
|
|
findings in hypoparathyroidism?
|
hypocalcemia, tetany
|
|
what is Chvostek's sign?
|
hypocalcemia - tap facial nerve and see contraction of facial muscles
|
|
what is Trousseau's sign?
|
hypocalcemia - occlusion of brachial artery with BP cuff leads to carpal spasm
|
|
what is pseudohypoparathyroidism?
|
AR kidney unresponsiveness to PTH; hypocalcemia, shortened 4th/5th digits, short stature
|
|
excess of what vitamins can cause hypercalcemia?
|
vitamins A and D
|
|
what is usually the cause of DKA?
|
increase in insulin requirements from an increase in stress (e.g. infection) - excess fat breakdown and increased ketogenesis from the increase in free fatty acids, which are then made into ketone bodies
|
|
what is the metabolic disturbance associated with DKA?
|
increased H+, decreased HCO3-
|
|
|
anion gap metabolic acidosis; hyperkalemia but depleted intracellular K+
|
|
intensive thirst and polyuria with inability to concentrate urine?
|
diabetes insipidus
|
|
causes of central DI?
|
pituitary tumor, surgery, trauma, histiocytosis X
|
|
causes of nephrogenic DI?
|
hereditary or secondary to hpercalcemia, lithium, demeclocycline
|
|
what happens in a water deprivation test in DI?
|
urine osmolality doesn't increase
|
|
urine specific gravity is less than what in DI? osmolality greater that what?
|
<1.006, >290
|
|
what is the treatment for central DI?
|
intranasal desmopressin (ADH analog)
|
|
what is the treatment for nephrogenic DI (lack of renal resonse to ADH)?
|
hydrochlorothiazide, indomethacin, or amiloride
|
|
excessive water retention, hyponatremia, and urine osmolarity > serum osmolarity
|
SIADH
|
|
what is a dangerous potential effect of SIADH?
|
very low serum sodium levels can lead to seizures (correct slowly)
|
|
causes of SIADH?
|
ectopic ADH, CNS disorders/head trauma, pulmonary disease, cyclophosphamide
|
|
treatment for SIADH?
|
demeclocycine or water restriction
|
|
diarrhea, cutaneous flushing, asthmatic wheezing, right-sided valvular disease?
|
carcinoid syndrome
|
|
carcinoid syndrome?
|
rare syndrome caused by carcinoid tumors (neuroendocrine cells), especially metastatic small bowel tumors, which secrete high levels of serotonin - not seen if tumor is limited to GI tract (serotonin undergoes first-pass metabolism in GI tract)
|
|
what is the most common tumor of the appendix?
|
carcinoid
|
|
urine finiding in carcinoid syndrome?
|
increased 5-HIAA
|
|
what are carcinoid tumors derived from?
|
neuroendocrine cells of GI tract
|
|
treatment for carcinoid syndrome?
|
octreotide
|
|
rule of 1/3s for carciniod syndrome?
|
1/3 metastasize, 1/3 with 2nd pregnancy, 1/3 mutiple
|
|
what fascia encloses the thyroid gland?
|
pretracheal fascia
|
|
surgical resection of ileum causes what levels of calcium, 25-OH vitamin D, phosphate?
|
all decreased
|
|
mechanism of propylthiouracil?
|
inhibits deiodonation of T4
|
|
somatostatin inhibits the release of what 2 hormones?
|
GH and TSH
|
|
thyroid condition preceding lymphoma?
|
Hashimoto thyroiditis
|
|
pentagastrin-stimulated calcitonin secretion is a marker for what?
|
medullary carcinoma of the thyroid
|
|
treatment for DKA?
|
fluids, insulin, and potassium; glucose if necessary to prevent hypoglycemia
|
|
activation of pyruvate dehydrogenase and increased levels of acetyl CoA are associated with what?
|
type 2 DM
|
|
why does glucose taken orally cause a greater increase in insulin than when given IV?
|
increases duodenal secretion of gastric inhibitory peptide, increasing beta cell release of insulin
|
|
thyroid nodule with small 'solid balls' of neoplastic follicular cells containing microscopic blood vessels and fibrous stroma in their centers
|
papillary carcinoma
|
|
actions of insulin/insulin-like drugs?
|
TK activity: liver (increase glucose stored as glycogen), muscle (increased glycogen and protein synthesis, K+uptake), fat (aids TG storage)
|
|
what type of drug: tolbutamide & chlorpropamide?
|
first generation sulfonylureas
|
|
what type of drug: glyburide, glimepiride, glipizide?
|
second generation sulfonylureas
|
|
mechanism of action of sulfonylureas?
|
close K+ channel in beta cell membrane so cell depolarizes, triggering of insulin release via Ca2+ influx
|
|
what are sulfonylureas used for?
|
stimulate release of endogenous insulin in type 2 DM; require some islet function so useless in type 1
|
|
side effects of first generation sulfonylureas?
|
disulfiram-like reactions
|
|
side effect of second generation sulfonylureas?
|
hypoglycemia
|
|
what is the most grave side effect of metformin?
|
lacti acidosis
|
|
can metformin be used in patients without islet function?
|
yes
|
|
action of pioglitazone and rosiglitazone?
|
increase target cell response to insulin
|
|
action of acarbose and miglitol?
|
alpha glucosidase inhibitors - inhibit intestinal brush border alpha glucosidases; delayed sugar hydrolysis and glucose and glucose absorption lead to decreased postprandial hyperglycemia
|
|
mechanism of propylthiouracil, methimazaole?
|
inhibit organification and coupling of thyroid hormone synthesis - used for hyperthyroidism
|
|
toxicity of propylthiouracil, methimazole?
|
skin rash, agranulocytosis (rare), aplastic anemia
|
|
what are orlistat and dsibutramine used for?
|
obesity management (orlistat is long-term)
|
|
use of glucocorticoids?
|
Addison's disease, inflammation, immune suppression, asthma
|
|
mechanism of finasteride?
|
5 alpha reductase inhibitor
|
|
mechanism of flutamide?
|
nonsteroidal competitive inhibitor of androgens at the testosterone receptor
|
|
mechanism of leuprolide?
|
GnRH analog with agonist properties when used in pulsatile fashion and antagonist properties when used in continuous fashion
|
|
mechanism of clomephine?
|
partial agonist at estrogen receptors in hte pituitary - prevents normal feedback inhibition and increases release of LH and FSH from the pituitary, which stimulates ovulation
|
|
drug of choice for women with estrogen receptor + breast cancer?
|
tamoxifen - competitively inhibits estradiol at estrogen receptors
|
|
treatment for polycystic ovarian syndrome?
|
ketoconazole, spironolactone
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