Parathyroid Flashcards

1
Q

What are the two cells of the parathyroid gland?

A

Chief cells- produce PTH

Oxyphil cells- packed with mitochondria (granular/pink on H and E)

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2
Q

What triggers the release of PTH from chief cells of the parathyroid?

A

Low serum (ionized) calcium levels

not under Hypothalamic-pituitary axis..

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3
Q

What is the effect of PTH?

A

Increase serum calcium

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4
Q

How does PTH increase serum calcium levels?

A

Increase renal tubular reabsorption
Increase vitamin D to its active form
Decrease serum phosphate by increasing urinary excretion
Increase GI calcium absorption

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5
Q

What are two causes of hypercalcemia with elevated PTH levels?

A

Primary Hyperparathyroidism

Familial hypocalciuric hypercalcemia

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6
Q

What are a few causes of hypercalcemia with low PTH levels?

A
Hypercalcemia of malignancy
Vitamin D toxicity
Immobilization
Thiazide diuretics
Granulomatous disease (like sarcoidosis)
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7
Q

How can malignancy cause hypercalcemia?

A

Tumors to the bones –> increased resorption

-or-

Paraneoplastic syndrome: release of parathyroid hormone-related peptide (PTH-RP)

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8
Q

What is far and away the most common lesion of the parathyroid gland?

A

Parathyroid adenoma

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9
Q

What is the gene involved in MEN1 syndrome?

A

MEN1- (parathyroid, pancreas and pituitary)

MEN1 is a tumor suppressor gene

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10
Q

What is the gene mutated in MEN2A syndrome?

A

Activating mutation of RET (tyrosine kinase)

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11
Q

What is the genetic mutation associated with familial hypocalciuric hypercalcemia

A

CASR- AD disorder

Ca2+ sensing receptor gene in the renal tubules

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12
Q

What is the half life of PTH? Why is this useful?

A

3 minutes-

You can remove an parathyroid gland suspected of causing primary hypercalcemia and check the PTH levels. If you got the right one, the levels will drop in half within a few minutes

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13
Q

What type of cells are missing from parathyroid adenomas?

A

Fat

Can occupy up to 30% of adult parathyroid glands

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14
Q

Define parathyroid hyperplasia

A

When the disease affects more than one gland.

Parathyroid adenomas are localized to a single gland

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15
Q

What are the clinical manifestations of hypercalcemia?

A

Painful bones, renal stones, abdominal groans and psychic moans

Osteofibrosis cystica, osteoporosis, nephrolithiasis, nephrocalcinosis, gallstones, PUD, acute pancreatitis, CNS depression, seizures…

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16
Q

What is the most common cause of secondary hyperparathyroidism?

A

Renal failure (often with diabetes)

17
Q

What is secondary hyperparathyroidism?

A

Process of chronic depression or decrease in calcium that causes compensatory over activity of the parathyroid glands

18
Q

What does renal insufficiency cause secondary hyperparathyroidism?

A

Renal insufficiency causes decreased phosphate excretion –> hyperphosphatemia –> decreased ionized serum calcium

19
Q

What is tertiary hyperparathyroidism?

A

Autonomous hyperparathyroidism without symptomatic hypercalcemia- follows chronic hypercalcemia due to secondary hyperparathyroidism (again, often due to renal insufficiency)

20
Q

Which is more common: hyper or hypoparathyroidism?

A

Hyperparathyroidism is way more common than hypoparathyroidism

21
Q

What is the most important cause of hypoparathyroidism?

A

Surgically induced

22
Q

With what syndrome can you have congenital absence of parathyroid?

A

DiGeorge’s Syndrome

23
Q

What are the CNS manifestations of hypoparathyroidism?

A

Tetany: especially perioral numbness
Chvostek sign: tap along course of facial nerve
Trousseau sign: carpal spasms following occlusion of circulation of the forearm

Mental status change

24
Q

How is the QT interval affected by hypoparathyroidism?

A

Prolonged QT (with low calcium)