B6.050 Post CBCL Formative Info Flashcards

1
Q

what are reasons you might expect a rare parathyroid carcinoma?

A

palpable neck mass
hypercalcemia > 14 mg/dL
parathyroid adenoma and hyperplasia do not present as palpable masses

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

histology of a parathyroid malignancy

A

marked mitotic activity, dense fibrous stroma, evidence of local invasion into capsule or surrounding vessels
metastasis most common to lymph nodes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

histology of parathyroid hyperplasia

A

diffuse proliferation of clear cells with little remaining normal tissue

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

histology of parathyroid adenoma

A

single focus of chief cells, surrounded by a compressed rim of normal tissues

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

first sign of MEN 1

A

parathyroid adenomas and 4 gland hyperplasia
presents with increased PTH and Ca
typically in 3rd or 4th decade w no gender predilection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

symptoms of hypercalcemia in MEN 1 patients

A

involve urinary tract rather than the skeleton

many are asymptomatic

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

treatment of MEN 1 parathyroid disease

A
  1. 5 gland (subtotal) resection

goal: achieve normocalcemia for as long as possible while avoiding hypoparathyroidism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

other tumors associated with MEN 1

A

pancreatic endocrine tumors
pituitary tumors
thymic carcinoids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

pancreatic tumors in MEN 1

A

gastrinoma (Zollinger Ellison, PUD and diarrhea)
insulinomas
VIPomas
glucagonomas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

pituitary tumors in MEN 1

A

prolactin

GH

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

mutation in MEN 1

A

MENIN tumor suppressor on chromosome 11

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

significance of lithium induced HPTH

A

more likely to need a 4 gland exploration since all 4 glands are exposed to the effects of lithium
higher tendency to cause 4 gland hyperplasia than in the normal population

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

3 Ps of MEN 1

A

parathyroid
pancreas
pitutitary

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

describe pseudohypoparathyroidism

A

target tissue resistance to PTH
low serum calcium
elevated serum PO4
defect in skeletal growth and development

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

disorder associated with pseudohypoparathyroidism

A

mutations in GNAS1

PTH function is normal, but kidney cannot respond to PTH stimulation due to loss of functional signaling pathway

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

additional surgery in MEN 1 parathyroid disease

A

bilateral thymectomy

patients have a greater incidence of thymic carcinoids as well as ectopic parathyroid glands

17
Q

when you resect a parathyroid gland that you thought was the cause of HPTH, and the PTH doesn’t go down, what do you do?

A

check ipsilateral gland next
if adenomatous, resect this one too
if PTH still doesn’t drop, move to contralateral side and do a total parathyroidectomy
auto implantation follows

18
Q

EKG finding with hypocalcemia

A

prolonged QT interval

T wave inversion

19
Q

treatment for severe hypocalcemia

A

IV 10% calcium gluconate to achieve serum conc of 7-9 mg/dL

also correct associated deficits in Mg, K, and pH

20
Q

how does severe hypomagnesemia perpetuate hypocalcemia

A

low Mg can suppress PTH release

low Mg can stimulate osteoblastic activity

21
Q

how does modest hypomagnesemia perpetuate hypocalcemia

A

impair end organ response to PTH

22
Q

earliest clinical feature of hypocalcemia

A

numbness

tingling in circumoral region or tips of fingers

23
Q

profound clinical features of hypocalcemia

A

tetany
seizure
Trousseau sign
Chvostek’s sign

24
Q

where is calcitonin produced

A

perifollicular C cells of thyroid

25
Q

when would calcitonin be elevated

A

medullary thyroid carcinoma

26
Q

functions of calcitonin

A

decreases BOTH serum concentrations of Ca and PO4
inhibits osteoclasts
stimulates osteoblasts

27
Q

when is calcitonin used

A

treatment of hypercalcemic crisis