Pathology Part II Flashcards

1
Q

These cells regulate free ionized calcium via PTH

A

Chief cells (of the parathyroid)

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2
Q

How to do chief cells regulate ionized calcium?

A
  1. increase bone osteoclast activity - releasing Ca and Phosphate
  2. Increase small bowel absorption of calcium and phosphate (indirect vit D activation)
  3. Increase renal calcium reabsorption (distal tubule) and decrease phosphate reabsorption (proximal tubule)
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3
Q

Increased serum calcium provides this type of feedback to the parathyroid

A

Negative.

Increased serum Ca leads to a decrease in PTH secretion.

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4
Q

Define primary hyperparathyroidism

A

Excess PTH due to a disorder of the parathyroid gland itself

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5
Q

Most common cause of hyperparathyroidism?

A

Parathyroid adenoma (80%)
Sporadic parathyroid hyperplasia
parathyroid carcinoma

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6
Q

How do parathyroid adenomas most often present?

A

benign hypercalcemia

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7
Q

Laboratory findings of hyperparathyroidism?

A
increased PTH
increased Ca
decreased Phos.
Increased urinary cAMP
increase serum alk phos
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8
Q

Most common cause of secondary hyperparathyroidism?

A

Chronic renal failure

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9
Q

Pathophysiology of CRF and secondary hyperparathyroidism?

A

Renal insufficiency - decreased phosphate excretion
Increased serum phosphate - binds free Ca
Decreased free Ca stimulates parathyroid glands
Increased parathyroid gland activity stimulates bone resorption

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10
Q

Lab findings of secondary hyperparathyroidism?

A

Increased PTH
decreased Ca
increased serum phos
increased alk phos

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11
Q

What differences in lab findings will you see between primary and secondary hyperparathyroidism?

A

Primary: Increased Ca, decreased phosphate

secondary: decreased Ca, increased phosphate

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12
Q

List some causes of hypoparathyroidism

A

Autoimmune damage
surgical excision
Di George syndrome

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13
Q

How do symptoms of low serum calcium often present?

A

Numbness and tingling

Muscle spasm

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14
Q

Lab results of hypoparathyroidism

A

Low PTH

Low serum calcium

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15
Q

End organ resistance to PTH (high PTH levels)

A

Pseudohypoparathyroidism

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16
Q

The endocrine pancreas is composed of these types of cells

A

Islet cell cluster
B cells - insulin
A cells - glucagon

17
Q

Insulin MOA

A

upregulates insulin dependent glucose transporter protein (GLUT4) on skeletal muscle and adipose tissue

18
Q

Type I diabetes HLA

A

DR3 and DR4

19
Q

Etiology of CV disease among diabetics

A

Nonenzymatic glycosylation (NEG) of vascular membranes

20
Q

What number measures the NEG of Hgb (glycated Hgb)

A

HbA1C

21
Q

Pancreatic endocrine neoplasms often are a component of this endocrine syndrome

A

MEN 1

along with Parathyroid hyperplasia and pituitary adenoma

22
Q

Lab values in pt with insulinoma

A

Decreased serum glucose
Increased insulin
increased C peptide

23
Q

Three layers of adrenal cortex and the hormones they produce

A

Glomerulosa - mineralocorticoids
Fasciculata - glucocorticoids
Reticularis - androgens

24
Q

What are all steroid hormones derived from

A

Cholesterol

25
Q

Primary hyperaldosteronism is most commonly due to this condition

A

Bilateral adrenal hyperplasia

26
Q

Tx for primary hyperaldosteronism

A

mineralocorticoid receptor antagonist such as spironolactone or eplerenone
if adenoma – surgically resect

27
Q

Classical presentation for hyperaldosteronism?

A

HTN
Hypokalemia
metabolic alkalosis

28
Q

How will Liddle syndrome vary from hyperaldosteronism when running tests

A

Will have LOW aldosterone