Looks like no one added any tags here yet for you.
etiology primary hyperparathyroidism
parathyroid adenoma
primary hyperplasia of parathyroid
parathyroid carcinoma
primary hyperparathyroidism is characterized by abnormal regulation of _________
pth secretion by calcium
are caused by mutations in the dna of parathyroid cells
parathyroid adenomas
clinical features primary hyperparathyroidism
asymptomatic hypercalcemia + elevated intact pth conc
clinical pic hypercalcemia
patients w/ osteoporosis, fx, low bone density or nephrolithiasis
sumptomatic severe hypercalcemia (parathyroid crisis) or osteitis fibrosa cystic
signs and symptoms primary hyperparathyroidism
stones, bones, abd groans and pyschic moans
cns effects - memory loss, lethargy, confusion
neurom - prox myopathy, arthritis
cardiovasc - htn, brady
renal - stones
gi - nausea, constipation, epulis
band keratopathy, metastatic calcification
clinical characteristics of bone disease in PHPT
bone pain, generalized demineralization bone (@ cortical sites), manifestations osteitis fibrosa cystican→ subperiosteal bone resorption @ hands, bone cysts, brown tumours, patho fx
labs PHPT
hypercalcemia, low-normal phosphorus, hyperchloremic metabolic acidosis, markers bone turnover
what is measurement urinary calcium excretion required for
distinguishing phpt from familial hypocalciuric hypercalemia (increased in phpt)
what can obscure lab results phpt
vit d deficiency
parathyroid crisis
severe hypercalemia, high ca conc, cns dysfxn (agitation, lethargy, confusion, coma), abd pain, peptic ulcer, pancreatitis
treatment phpt
excision abnormal parathyroid tissue - parathyroidectomy
when does acute postop hypocalcemia occur after parathyroidectomy for phpt
severe bone mineral deficits present (hungry bones syndrome) or injury to all normal parathyroid glands
what should patients avoid after parathyroidectomy for phpt
avoid inativity, mod. calcium intake, avoid thiazides and lithium, lots vit d
meds for phpt if surgery not possible
estrogen-progestin in postmenopausal, biphosphonates, raloxifene, calcimimetics
treatment parathyroid crisis
rehydration, furosemide, biphosphonate, zolendronate, calcitonin, iv glucocorticoids, dialysis, urgent parathyroidectomy
osteoporosis
reduction strength of bone leading to fx from loss bone tissue and deterioration skeletal microarchitecture
primary osteoporosis - causes
reduced bone mass and fx in postmenopausal women or old men from age due to
estrogen deficiency
progressive deficits renal and intestinal fx
failure to reach peak bone mass in young
secondary osteoporosis - causes
bone loss from
endocrinopathies - thyrotoxicosis, hyperprolactinemia, phpt, DM
gi - vit d deficiency, chronic liver disease, malabsorption
hema - hemochromatosis, leukemia, mm
glucocorticoids, OCs, immunosuppressants, antiseizure meds
genetics - hypophosphatasia, osteogenesis imperfecta
clinical manifestations osteoporosis
no symptoms until fx (vertebral is most common)
colles fx
common osteoporosis fx in women right after menopause
risk factors for osteoporosis fx
history fx, female sex, old, white, low calcium intake, estrogen deficiency, alcoholism
investigations osteoporosis
xray, bmd, dxa
cbc, calcium, renal + hepatic fxn, vit d
bone formation markers - akp, osteocalcin
bone resorption markers - n-telopeptide, c-telopeptide, deoxypyridinoline
pharma therapy for postmenopausal women w/ osteoporosis
antiresorptives - biphosphonates, SERM, tibolone
anabolic therapy - parathyroid, strontium, steroids
se biphosphonates
upper gi, jaw osteonecrosis, bone pain, flu symptoms
COs biphosphonates
hypersensitivity, hypocalcemia, esophagus abnormalities
COs HRT for osteoporosis
abnormal vaginal bleeding, thrombophlebitis or v thromboembolic disorders, breast carcinoma