Endocrinology Flashcards
Connection of thyroid to tongue
thyroglossal duct (foramen cecum= normal remnant)
Where thyroid diverticulum arise
primitive pharynx
Layers and products of adrenal medulla
Zona glomerulosa: Aldosterone
Zona fasciculata: cortisol
zona reticularis: sex hormones
Common tumors of adrenal medulla in adults vs kids
adults: pheo
kids: neurobalstoma (HTN uncommon)
Venous drainage of L vs R adrenal gland
L: L adrenal vein, L renal vein, IVC
R: R adrenal vein, IVC
Rathke pouch- what does it become
Anterior pituitary
Secreted by posterior pituitary
vasopressin, oxytocin
secreted by anterior pituitary
FSH, LH, ACTH, TSH (Basophils)
prolactin, GH (Acidophils)
a cells of pancrease: secreted and location
glucagon, peripheral
b cells of pancreas: secreted and location
insulin, central
delta cells of pancreas: secreted and location
somatostatin, interspersed
Insulin R is a ___
tyrosine kinase
pathways induced by insuline receptor
PI3 kinase, RAS/MAP kinase
Gluc transporter in adipose tissue, skeletal muscle
GLUT-4 (insulin dependent)
Gluc transpoter in RBC, brain, cornea
GLUT-1 (insulin independent)
Gluc transporter in spermatocytes, GI tract
GLUT-5 (Fructose, insulin independent)
Gluc transporter in b islet, liver, kidney, SI
GLUT-2 (bidirectional, insulin independent)
What inhibits glucagon?
insulin, hyperglycemia, somatostatin
what is the action of glucagon?
glyocgenolysis, gluconeogenesis, lipolysis, ketone production
Effect of CRH
incr ACTH, MSH, b-endorphin
Effect of dopamine on pituitary
decr prolactin
Effect of Prolactin on pituitary
decr GnRH
Affect of somatostatin on pituitary
decr GH, TSH
Effect of TRH on pituitary
Incr TSH, prolactin
Effect of GnRH on pituitary
Tonic: supresses HPA
Pulsatile: puberty, fertility
via FSH, LH
Bromocriptine
Dopamine agonist, used to inhibit prolactin secretion
what stimulates prolactin secretion
dopamine antagonists (antipsychotics), estrogens
What 2 factors inhibit GH
glucose, somatostatin
What mediates GH effects
IGF-1/somatomedin
Which nucleus synthesizes ADH
supraoptic nuclei of hypothalamus
What is treatment of central DI
desmopressin (ADH analog)
What receptors sense ADH, what to they regulate?
V2- serum osmolarity (primary function)
V1- blood pressure
mineralocorticoid, cortisol, sex hormone levels in 17a-hydroxylase deficiency
incr mineralocorticoid, decr cortisol, decr sex hormone levels
mineralocorticoid, cortisol, sex hormone levels in 21-hydroxylase deficiency
decr mineralocorticoid, decr cortisol, incr sex hormone levels
mineralocorticoid, cortisol, sex hormone levels in 11b-hydroxylase deficiency
decr mineralocorticoid, decr cortisol, incr sex hormone levels; incr BP due to incr 11-deoxycorticosterone
Presents as hypertension, hypokalemia, lack secondary sexual development in females
17a hydroxylase deficiency
Presents as hypotension, hyperkalemia, incr renin; salt wasting in infants, precocious puberty in children
21 hydroxylase deficiency
presents as hypertension with low renin, virilization in females
11b hydroxylase deficiency
Functions of cortisol (BIG FIB)
INCR: Blood pressure Insuline resistance Gluconeogensis, lipolysis, proteolysis DECR: Fibroblast activity Inflammatory response Bone formation
What are patients on exogenous cortisol susceptible to? what is mechanism
TB, candidiasis; blocked IL-2 production
Regulation of cortisol secretion
CRH produced by hypothalamus, ACTH produced by pituitary
Cells that produce PTH
chief cells of parathyroid
Effect of PTH on bone
incr resorption of Ca2+, PO43-
Effect of PTH on kidney (3)
incr reabsoprtion Ca2+ DCT
decr reabsorption PO43- in PCT
incr production calctriol
Effect of Mg on PTH levels
moderate decreae Mg: incr PTH
severe decrease Mg: decr PTH
Causes if hypomagnesemia: diarrhea, aminoglycosides, diuretics, alcohol abuse
Effect of incr pH on Ca levels
incr affinity to albumin, symptoms of hypocalcemia
Source of calcitonin
Parafollicular C cells of thyroid
T3 functions (4 Bs)
Brain maturation
Bone growth (synergize with GH)
B-adrenergic effects (incr B1 on heart)
Basal metabolic rate
Cushing disease vs cushing syndrome
Cushing Disease= ACTH secreting pituitary adenoma
Cushing syndrome= incr cortisol (multiple causes)
Cushing syndrome with low ACTH, diagnostic test
primary adrenal adenoma, hyperplasia, or carcinoma; MRI to confirm tumor; expect atrophy of uninvolved gland
Cushing syndrome with high ACTH, suppression via high dose dexa
Cushing disease, usually pituitary adenoma
Cushing syndrome with high ACTH, no suppression via high dose dexa
ectopic ACTH secretion
Hypertension, hypokalemia, metabolic acidosis, low renin
primary hyperaldonsteronism
Conn syndrome- define
aldosterone-secreting adrenal adenoma
Causes of secondary hyper aldost
renal artery stenosis, CHF, cirrhosis, nephrotic syndrome (renal perception of low intravascular volume)
treatment of secondary hyperaldost
spironolactone
distinguis primary vs secondary hyperaldosterone
primary: low renin
secondary: high renin
Addison disease- define
chronic primary adrenal insuffeciency, deficiency of aldosterone and cortisol
Hypotension, hyperkalemia, acidosis, hyperpigmentation
Addison disease
Primary vs secondary adrenal insufficiency
Secondary: no hyperpigmentation, hyperkalemia (decr pituitary ACTH)
Waterhouse-friedrichsen syndrome- describe
acute primary adrenal insufficiency due to hemorrhage
causative organism of waterhouse-friedrichsen syndrome
N. meningitidis
Oncogene assoc with neuroblastoma
N-myc
Neuroblastoma vs Wilms tumor- presentation
Neuroblastoma: firm irregular mass, can cross the midline
Wilms: smooth, unilateral
Urine and histology marker for neuroblastoma
Homovanillic acid in urine
Bombesin + with rosettes
Syndromes associated with pheo (3)
von Hippel-Lindau, MEN 2A, 2B
Treatment for pheo
a antagonist (phenoxybenzamine) before b blocker; resection
what cell type makes pheo
chromaffin cell
Cholesterol levels in hypothyroidism and mechanism
hypercholesteremia; decr LDL receptor expression
Assoc with Hurthle cells
Hashimoto’s thyroiditis
HLA type assoc with Hashimoto’s thyroiditis
HLA-DR5
Pot-bellied, pale, protruding umbilicus, protuberant tongue, poor brain function
congenital hypothyroidism (cretinism)
Riedel thyroiditis
thyroid is replaced by fibrous tissue; can extend to local structures
Tender vs nontender thyroiditis
Tender= de Quervain (usually self-limiting) Nontender= hashimoto
Histologic finding of de Quervain thyroiditis
granulomatous inflammation
Cause of toxic multinodular goiter
Mutation in TSH receptor- fxn independent of TSH
Jod-Basedow phenomenon
thyrotoxicosis when pt with iodine-deficiency goiter is given iodine
Wolf-Chaikoff effect
excess iodine temporarily inhibits thyroid peroxidase
Treatment of thyroid storm
propanolol, propylthiouracil, corticosteroids
Describe thyroid storm
stress-induced catecholamines– agitation, delirium, fever, diarrhea, coma, tachyarrythmia
Mutations associated with papillary thyroid carcinoma
RET, BRAF
Assoc with “orphan annie” eye nuclei
papillary thyroid carcinoma
Follicular adenoma vs follicular carcinoma
follicular carcinoma invades thyroid capsule
Amyloid stroma assoc with
medullary thyroid carcinoma
Syndromes associated with medullary carcinoma
MEN 2A, MEN 2B
Osteitis fibrosa cystica
cystic bone spaces filled with brown fibrous tissue, assoc with hyperparathyroidism
Hypercalcemia, hypercalciuria, hypophosphatemia, Incr ALP, incr cAMP in urine
hyperparathyroidism
Renal osteodystrophy
bone lesion due to secondary or tertiary hyperparathyroidism
Cause of secondary, tertiary hyperparathyroidism
chronic renal disease
Albright hereditary osteodystrophy
psuedohypoparathyroidism; AD, kidney unresponsive to PTH; hypocalcemia, shorthened 4th, 5th digit, short stature
Chvostek sign
tapping of facial nerve induces contraction of facial muscle; indicates hyocalcemia
Trousseau sign
carpal spasm when brachial arterl occulded; indicates hypocalcemia
Treatment of prolactinoma
bromocriptine, cabergoline (dopamine agonist)
Pegvisomant
growth hormone receptor antagonist
GH response to oral glucose challenge
should suppress, will not suppress in acromegaly
Intense thirst and polyuria, inability to concentrate urine
diabetes insipidus
Demeclocycline
ADH antagonist
Destinguish central vs nephrogenic DI
ADH levels (decr in central) Water restriction test (no response in nephrogenic) Vasopressiin administration (no response in nephrogenic)
treatment of central DI
intranasal DDAVP
treatment of nephrogenic DI
HCTZ, indomethacin, amiloride
Causes of SIADH (3)
Small cell lung cancer, CNS, pulmonary disease
what drug can cause SIADH
cyclophosphamide
Treatment of SIADH
fluid restriction, IV hypertonic saline, conivaptan, tolvaptan, demeclocycline
Define SIADH
excess water retention, dilutional hyponatremia, urine osmolarity> serum osmolarity
Sheehan syndrome
ischemic infarct of pituitary (esp ant pituitary) after postpoartum bleeding
Kimmelstiel-Wilson nodules
assoc with diabetic nephropathy
Most common cause of death in diabetic
MI
Small vessel disease in diabetics
retinopathy, glaucoma, nephropathy
Large vessel disease in diabetics
atherosclerosis, CAD, peripheral vascular occlusive disease, gangrene
Osmotic damage in diabetics
neuropathy, cataracts
HLA types associated with Type 1 diabetes
HLA-DR3, DR4
Histologic finding T1 DM
Islet leukocytic infiltrate
Histologic finding T2 DM
islet amyloid polypeptide deposits
Kussmaul respirations, n/v, abdominal pain, delirium, dehydration
DKA
Lethargy, syncope, diplopia
whipple triad; insulinoma
Infection associated with DKA
mucormycosis (Rhizopus)
MEN syndrome associated with marfanoid habitus
MEN 2B
MEN syndrome associated with pancreatic endocrine tumors
MEN 1
Also called Wermer syndrome
MEN 1
MEN associated with pituitary tumors
MEN 1
Also called Sipple syndrome
MEN 2A
MEN syndrome associated with mucosal neuromas
MEN 2B
MEN syndromes associated with medullary thyroid carcinoma
MEN 2A, 2B
MEN syndromes associated with parathyroid tumor/hyperplasia
MEN 1, 2A
MEN syndromes associated with Pheo
MEN 2A, 2B
Treatment of carcinoid syndrome
resection, somatostatin analog
Diarrhea, cutaneous flushing, asthmatic wheezing, right-sided valvular disease
carcinoid syndrome
Assoc with incr 17-OH progesterone
21a-hydroxylase deficiency