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32 Cards in this Set

  • Front
  • Back
Role of PTH
Inc release of Ca and Phosphate from bones
Inc absoprtion of Ca and phosphate by kidneys
Promote Ca absorption in GI tract
Age and sex of Hyperparathyroidism
Women 2x more than men
Most like >60 yo
Etiology of hyperparathyroidism
PRIMARY: Regulatory relationship btw serum calcium and PTH is interrupted - the balance gets inteupted due to: adenoma, hyperplasia in the gland
SECONDARY: glands become hyperplastic due to malfxt of another sytem seen in kidney dx and padget's dx
TERTIARY: PTH is inc or overactive in ppl with low serum Ca levels
Primary and secondary causes of hyperparathyroidism
Primary: adenoma and hyperplasia of gland
Secondary: Kidney dx and padget's dx
General clinical manifestations of hyperparathyroidism
Bone damage
Due to hypercalcemia: abdominal pain, peptic ulcers, pancreatitis, kidney damage, muscle symptoms, nuerological symptoms
What happens to bone in parahyperthyroidism
Excess extraction of Ca from bone leads to bone damage
Demineralization of bone, lytic bone lesions, fractures, and pain
Kidney issue with parahyperthyroidism
Deposite of cacium phosphate in renal tubule
Nephrocalcinosis
Kidney stones b/c calcium salts are insoluble in urine
Muscle symptoms due to hyperparathyroidism
Paresthesia, mm cramps, loss of pain and vibratory sensation along a stocking glove distribution
Diagnosis of hyperparathyroidism
Elevated serum Ca
Serum phosphate dec'd (counterintuitive but true)
High levels of Ca and phosphorus in urine
Diffuse demineralization on X-ray
PT implications for hyperparathyroidism
Chronic LBP
Marked mm weakness/atrophy
CPPD (gout in 35% of cases)
Osteogenic synovitis in achilles and triceps
Inc'd risk of fx
Hypoparathyroidism:
Ca and phosphate levels
Etiology
Sex and age
Low Ca, high phosphate
Latrogenic (accidental removal) or idioathic
Children 9x more than adults, Women 2x more than men
Clinical manifestations of Hypoparathyroidism
Bone resrption dec's
Severe NM irritability
Calcification o various organs = eye and BG
Severe symptoms down the line of hypoparathyroidism
Tingling in finger tips and around mouth
Progresses to tetani during exacerbations
Dx of hypoparathyroidism
Hx and clinical presentation
Lab values: dec Ca and high phosphate
Signs of acute tetany with hypoparathyroidism
Minor mm twitching
Laryngospasm (voice)
What does therapy revolve around for hypoparathyroidism?
Gait training
Technique to prevent falls
What is secreted by the adrenal cortex and main function?
Mineralcorticoids - Steroid hormone imp in regulating fluid and mineral balance
Glucocorticoids - Steroid hormone responsible for controlling glucose metabolism
Androgens - sex hormone

Adrenal glands are small glands on the upper part of the kidney
Difference between Cushing's syndrome and dx
Syndrome - excessive glucocoricoids due to externally administered cortisol--commonly occurs in autoimmune dz or post-transplant
Dx - Hypercortisolism due to excess excretion of ACTH (primary cause = pituitary hypersecretion due to pituitary or adrenocorticol tumors)
What do inc levels of cortisol cause?
Inc'd liberation of AA from mm
Weakening of protein stucture
Protuberant abdomen with striated stretch marks
Generalized mm weakness
Marked osteoporosis (secondary to loss of Ca thru urine)
Primary tx of Cushing's Disease?
Radiation (if tumor of pituitary or adrenal cortex)
Drug therapy
Surgery

Goal is reduction of cortisol levels
What is Conn's syndrome? Cause
Excess release of Aldosterone from adrenal cortex
Primary cause: Adrenal lesion which leads to hypersecretion
Secondary: Renal HTN, sclerosis of the liver, and cardiac failure
Consequences of too much Aldosterone (Conn's syndrome)
Inc resorption of Na and H2O by kidney
Hypernatremia
Hypervolemia
Hypokalemia
Metabolic alkalosis
Clinical presentation of Conn's dx
HTN
CVA
Heart failure
Visual disorders
MM weakness
Excess thirst
DM
Tx of Conn's dx
diuretics
Beta blockers
Remove or radiation of hypersecreting tumors
Causes of Primary adrenal insufficiency
Addison's dx (main cause)
Bilateral adrenectomy
Adrenal hemorrhage or inflammation
Radiation
Malignant adrenal neoplasm
Infections (cytomegalovirus)
Chemical agents
Etiology of Addison's dx
Idiopathic or autoimmune
Risk factors for developing or exacerbating adrenal insufficiency
Surgery
Prego (postpartum hemorrhage)
Injury or trauma
Salt loss d/t diffuse diaphoresis
Failure to take steroid therapy in person with Addison's dx
Outcome of Adrenal insufficiency
Dec'd cortisol
Glucoeneogenesis dec'd
Glycogen deficiency
Hypoglycemic: weak, exhausted, hypotensive, anorexia, wt loss, n/v, emotional disturbance (depresseon and dec'd resistance to stress)
What happens to ACTH with primary adrenal insufficiency?
Increases due to neg feedback loop
Causes inc in MSH too which results in hyperpigmentation (bronzed, tanned look)
What does dec'd aldosterone result in in adrenal insufficiency?
Hyponatremia and hyperkalemia = hypotensive
Could cause circulatory colaps
Dec tolerance to minorstress, ppor coordination, craving for salty foods, retard axillary and pubic hair growth in females, dec'd libido, amenorrhea
Dx and tx of adrenal insufficiecy
Dx: blood, urine, and hormonal assays
Tx: life long administration of synthetic corticosteroids
Function of Aldosterone
Increase the reabsorption of Na+ and H20 and increases the release or secretion of potassium

Causes increased blood volume