Parathyroid Flashcards

1
Q

Which cells secrete PTH and calcitonin

A

PTH: chief cells of parathyroid
calcitonin: C-cells of thyroid

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2
Q

Hyperparathyroidism etiologies

A

adenoma > hyperplasia > carcinoma

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3
Q

Osteitis fibrosa cystica

A

complication of hyperparathyroidism

resorptin of bone leading to fibrosis and cystic changes

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4
Q

Lab findings in primary hyperparathyroidism
urine cAMP
serum alkaline phosphatase

A

elevated urine cAMP (Gs cascade)
elevated serum alkaline phosphatase
*because PTH activates blasts, which then activate clasts

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5
Q

Complications of hypercalcemia

A

metastatic calcifications, esp renal tubules
acute pancreatitis (Ca2+ activates enzymes)
nephrolithiasis
osteitis fibrosa cystica

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6
Q

2˚ hyperparathyroidism

most common etiology

A

renal failure
decreased phosphate excretion
hyperphosphtemia –> phosphate binds Ca2+, which lowers free serum Ca2+
low free serum Ca2+ => release of PTH

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7
Q
Labs in 2˚ hyperparathyroidism
PTH
serum Ca2+
serum phosphate
alkaline phosphatase
A
high PTH
low serum Ca2+
high serum phosphate
high serum alkaline phosphatase
*b/c PTH activates blasts first, blasts activate clasts
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8
Q

Hypoparathryoidism
boring etiology
interesting etiology

A

autoimmune or due to surgical excision
DiGeorge syndrome
-upper pair from 4th pharyngeal pouch
-lower pair from 3rd pharyngeal pouch

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9
Q

Trousseau sign

Chvostek sign

A

tetany when filling BP cuff

tetany when tapping on facial nerve

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10
Q

First sign of hypocalcemia

A

perioral numbness

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11
Q

Pseudohypoparathyroism labs

A

high PTH

low serum calcium

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12
Q

Hypoparathyroidism labs

A

low PHT

low serum calcium

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13
Q

Pseudohyperparathyroidism

etiology

A

end organ resistance to PTH
commonly in Gs receptor mutation
short stature and 4th and 5th digits

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14
Q

Inheritance pattern of common form of pseudohyperparathyroidism

A

dominant

Gs receptor mutation

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