26: Parathyroid Flashcards
(23 cards)
Three major cell types of parathyroid
Chief cells, oxyphil cells, adipocytes
Chief cells on histology
Central round nuclei, light pink/white cytoplasm, secretory granules
Oxyphil cells on histo
Smaller darker nuclei, eosinophilic granules
Two effects of PTH on kidney
Ca resorption, converts 25(OH)D to 1,25(OH)2D
CaSR
Ca-sensing receptor on parathyroid: regulates amount of PTH secreted
What leads to Rugger jersey sign on spinal XR
Renal osteodystrophy -> dissecting osteitis
Biggest way to tell difference between primary and tertiary hyperparathyroidism
Tertiary always comes after a prolonged period of secondary hyperparathyroid
Major EKG change due to hypercalcemia
Shortened QT interval
DEXA: where to scan central vs screening exam
central: lower spine and hip
screening: writs, heel, leg, fingers (can also be used if pt isn’t mobile enough to get onto hard xray table)
Risks for developing osteoporosis
estrogen depletion, age 70+, anorexia, malapsorption, obesity, steroids, hypogonadism, immobility
three things that cause high PTH, high Ca
- parathyroid adenoma
- primary hyperparathyroidism
- parathyroid carcinoma
two thing that cause low PTH, high Ca
- humoral hypercalcemia of malignancy
2. local osteolytic hypercalcemia
two things that cause low PTH, low Ca
- Di George
2. CaSR activation mutation
two things that cause high PTH, low Ca
- kidney disease causes secondary parathyroid hyperplasia
2. calciphylaxis
____ is usually asx, but when it does present, it presents with stones, bones, moans, and groans
primary hyperparathyroidism
what causes osteitis fibrosis cystica
primary hyperparathyroidism
sx of high Ca, low PTH
AMS, N/V, shortened QT interval
how does humoral hypercalcemia of malignancy work?
tumor produces PTHvP
local osteolytic hypercalcemia
breast CA or myeloma -> metz to bone -> osteoclast bone resoprtion -> releases Ca
sx of low Ca
numbness and tingling, stupor, muscle cramps/spasms, tetany, Trousseau and Chovstek signs
how does kidney disease cause low Ca
less PO is excreted -> binds Ca in the blood
labs in pseudohypoparathyroidism
nl/high PTH, low Ca, high PO
mutation in Albright’s hereditary Osteodystrophy
GNAS