Parathyroid Disorders Flashcards

1
Q

Parathyroid chief cells secrete ___

A

PTH

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2
Q

Parathyroid oxyphil cells are ___ and contain ___

A

acidophilic; mitochondria

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3
Q

How does parathyroid detect changes in ECF calcium?

A

Decrease ECF calcium ↓ CaSR activity

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4
Q

PTH actions on kidney & bone

A

↑ Ca2+ resorption in kidney/bones (osteoclastic)

↓ PO43- resorption in kidney

vitamin D synthesis in kidney

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5
Q

Vitamin D promotes ___

A

Ca2+ absorption in small intestine (when vit D is converted to active dihydroxy form)

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6
Q

Phosphate action on calcium

A

Binds to calcium (↓ in serum)

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7
Q

Role of FGF 23

A

↓ sodium phosphate cotransporters in kidney PCT (↓ serum phosphate)

↓ 1,24 dihydroxy Vit D

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8
Q

RANKL action

A

Osteoblast protein that interacts with osteoclasts

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9
Q

RANK action

A

receptor on osteoclasts for interaction with osteoblasts

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10
Q

Osteoprotegerin action

A

binds RANKL to ↓ RANKL-RANK activity, ↓ osteoclast activity

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11
Q

M-CSF action

A

proliferation of osteoclast precursor cells

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12
Q

Three inducers of RANKL expression

A

progesterone, PTH, calcitriol (vit D3)

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13
Q

___ induces OPG, which ___ osteoclast activity.

A

Estrogen; decreases

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14
Q

1° hyperparathyroidism vs malignant hypercalcemia

A

1° hyperparathyroidism: ↑ PTH causes ↑ Ca2+

Malignancy: ↑ PTH-like polypeptide ↑ Ca2+

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15
Q

Three genetic causes of 1° hyperparathyroidism

A
  1. Cyclin D1 overexpression d/t Chr11p inversion
  2. MEN1 or MEN2A mutations
  3. Familial hypocalciuric hypercalcemia
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16
Q

Pathogenesis of familial hypocalciuric hypercalcemia

A

AD mutation in CASR ↓ activity

17
Q

Parathyroid adenoma vs parathyroid hyperplasia vs parathyroid carcinoma

A

Adenoma: solitary nodule in single gland

Hyperplasia: all 4 glands involved - asymmetry

Carcinoma: invasion of surrounding tissues & metastasis

18
Q

Kidney findings in hyperparathyroidism

A

nephrolithiasis & nephrocalcinosis (calcification)

19
Q

Describe osteitis fibrosa cystica

A

Bony pain due to cystic bone spaces w/ brown fibrous tissue. Most common in parathyroid carcinoma.

20
Q

Presentation of hyperparathyroidism

A

“Stones, thrones (polyuria), bones, groans, psychiatric moans”

21
Q

Labs in 1° hyperparathyroidism

A

↑ Ca2+, ↑ PTH, ↓ serum phosphate, hypercalciuria, hyperphosphaturia

22
Q

2° hyperparathyroidism usually caused by ___.

A

Renal insufficiency ↓ phosphate excretion (binds Ca2+) & ↓ active Vit D (↓ Ca2+ absorption)

23
Q

Labs in 2° hyperparathyroidism

A

↓ Ca2+, ↑ serum phosphate, ↑ PTH, ↓ vit D, ↑ ALP

24
Q

Most common causes of hypoparathyroidism

A

-Direct injury or vascular injury (surgery)
-autoimmune
-DiGeorge (22q11 deletion) - absence of parathyroids

25
Q

Clinical findings in hypoparathyroidism

A

Chvostek sign: facial twitch when cheek is tapped

Trousseau sign: carpopedal spasm with BP cuff

26
Q

Chronic manifestations of hypoparathyroidism include ___.

A

calcification of basal ganglia

27
Q

Labs in hypoparathyroidism

A

↓ PTH, ↓ Ca2+, ↑ serum phosphate

28
Q

Pathogenesis of pseudohypoparathyroidism

A

AD maternal imprinting mutation of GNAS → inactivated cell signaling w/ adenylate cyclase → PTH resistance in renal tubule

29
Q

Clinical features of pseudohypoparathyroidism

A

Albright hereditary osteodystrophy (short 4th/5th digits, obese, short stature, developmental delay)

30
Q

Labs in pseudohypoparathyroidism

A

↑ PTH, ↓ Ca2, ↑ serum phosphate