EXAM #1: PARATHYROID DISEASES Flashcards

1
Q

What is the embryologic origin of the parathyroid glands?

A
Superior= 4th pouch
Inferior= 3rd pouch
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2
Q

What is a common location of ectopic parathyroid gland?

A

Superior mediastinum

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3
Q

What are the two major types of cells in the parathyroid gland?

A

1) Chief cells

2) Oxyphil cells

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4
Q

What chromosome is the gene that is responsible for PTH located on?

A

Chromosome 11

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5
Q

How should you order PTH levels?

A

iPTH–intact PTH

*Note that the breakdown products also have biologic activity

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6
Q

What controls PTH secretion?

A

Ca++

  • Mg++
  • Vitamin D
  • Catecholamines

*Low Ca++ leads to PTH secretion

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7
Q

What are the three target organs for PTH?

A

1) Bone
2) Intestinal mucosa
3) Kidney

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8
Q

What is the effect of PTH on bone?

A

Increased osteoclast activity causing resorption (release into circulation) of Ca++ and phosphate

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9
Q

What is the effect of PTH on the kidney?

A
  • Retain Ca++

- Excretion of phosphate

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10
Q

What is the effect of PTH on the gut?

A

Increased gut absorption of Ca++

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11
Q

What is the NET effect of elevated PTH?

A

1) Increased serum Ca++

2) Decreased serum phosphate

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12
Q

Where does Ca++ absorption occur in the kidney?

A

Proximal tubule

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13
Q

Where does PTH fine-tune Ca++ in the kidney?

A

DISTAL nephron

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14
Q

What is the effect of PTH on bicarbonate?

A

Impaired reabsorption of HCO3-

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15
Q

What is the acid/base effect of elevated PTH?

A

Hyperchloremic metabolic acidosis

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16
Q

What is the first line test in a hypercalcemic patient?

A

PTH level

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17
Q

What is the most common cause of hypercalcemia in ambulatory patients? What about hospitalized patients?

A

Ambulatory= Hyperparathyroidism

Hospitalized= malignancy

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18
Q

What is the most common cause of primary hyperparathyroidism?

A

Single parathyroid adenoma

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19
Q

What is the mnemonic to remember the major clinical features of primary hyperPTH?

A
  • Bones= long bone pain
  • Stones= kidney stones
  • Groans= gastric ulcers
  • Moans= psychiatric sx. -depression
20
Q

What are the expected labs for hyperPTH?

A
  • Increased Ca++ (chronic)
  • Decreased phosphate
  • Increased or normal iPTH*
  • Increased urine Ca++
21
Q

Generally, how does hyperPTH effect bone?

A

Decreased bone density, especially in cortical bone

22
Q

What bone must be checked for a DEXA scan with likely hyperPTH?

A

Wrist

Hip/spine is different type of bone that is not usually as implicated in the osteoporosis caused by hyperPTH

23
Q

What is the definitive treatment for primary hyperPTH?

A

Surgery

24
Q

What are the indications for surgery in primary hyperPTH?

A

1) Symptoms
2) Serum Ca++ greater than 1 over upper normal limit
3) Creatinine clearance less than 70%
4) Less than 50 y/o

25
Q

What are the complications of surgery in primary hyperPTH?

A

1) Recurrent laryngeal nerve damage
2) Hypocalcemia
3) Hungry bone syndrome

26
Q

What is hungry bone syndrome?

A
  • Severe disease drastically drives Ca++ OUT of bones
  • That drive is removed
  • Bones react by “mopping up” Ca++ as PTH drive stops

*Results in severe acute cases of hypocalcemia

27
Q

What are the medical therapies for primary hyperPTH?

A

1) Avoid dehydration
- No diuretics
- H20
2) Bisphosphonates (decrease bone turnover)
3) Calcimimetics
4) Monitoring with Ca++, creatinine, DEXA

28
Q

What are the most common causes of secondary hyperPTH?

A

1) Vitamin D deficiency

2) Renal failure

29
Q

What causes tertiary hyperparathyroidism?

A

Renal failure

*This is when there are renal failure leads to autonomously functioning parathyroid glands

30
Q

What is FHH?

A

Familial Hypocalciuric Hypercalcemia

31
Q

What is Familial Hypocalciuric Hypercalcemia?

A
  • Inactivating mutation of Ca++ receptor
  • Mild hypercalcemia/ iPTH
  • Low urinary Ca++
32
Q

Is treatment indicated for FHH?

A

NO

33
Q

What are the basic causes of hypoPTH?

A

1) Low PTH production

2) Resistance to PTH (receptor level problem)

34
Q

What is the most common cause of hypoPTH?

A

Surgical excision

35
Q

What are the symptoms of hypoPTH dependent on?

A

The DEGREE and RAPIDITY of hypocalcemia

36
Q

What are the major sx. associated with hypoPTH?

A

asdf

Pathoma

37
Q

What are the net physiologic effects of hypoPTH?

A
  • Decreased Ca++

- Increased phosphate

38
Q

What cancer is associated with hypocalcemia?

A

Prostate cancer i.e. an “osteoblastic metastasis”

39
Q

What do you need to correct a serum Ca++ for?

A

Serum albumin

  • Albumin greater than 4= lower Ca++
  • Albumin less than 4= higher Ca++
40
Q

How should you approach hypocalcemia?

A

1) Measure iPTH
2) Measure Vitamin D
3) Measure Mg++

41
Q

How is hypocalcemia treated?

A

1) IV or PO calcium
2) Vitamin D

AND
3) Synthetic PTH analog (NATPARA)

*Note expensive and subQ; good for non-compliant patients

42
Q

What are the two types of pseudo pseudohypoPTH?

A

Types 1A and 1B

*Both are problems with end-organ resistance to PTH

43
Q

What are the labs associated with Type 1A and 1B pseudohypoPTH?

A

1) Low Ca++
2) High Phosphate
3) High iPTH

44
Q

What is the major difference between pseudohypoPTH 1A and 1B?

A

No physical manifestations

45
Q

What is pseudo pseudohypoparathyroidism?

A

Physical manifestations without lab abnormalities