Parathyroid Flashcards

1
Q

PTH function

A

directly releases Ca from bone
renal Ca resorption (phosphate secretion)
renal conversion of 25(OH)D to 1,25(OH)D2

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2
Q

causes of primary hyperparathyroidism

A

adenoma
primary hyperplasia
parathyroid carcinoma

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3
Q

sx of primary hyperparathyroidism

A

bones - osteoporosis/osteitis fibrosis cystica
stones - nephrolithiasis
groans - constipation, gallstones
moans - depression, lethargy, seizures

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4
Q

parathyroid adenoma

A

benign neoplasm of parathyroid chief or oxyphil cells
normal and abnormal tissue may be present
usually affects one gland
due to germline or somatic mutations in MEN1

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5
Q

parathyroid hyperplasia

A

presents in multiple glands
MEN syndrome may be responsible
abnormal tissue only

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6
Q

what is more common: primary or secondary parathyroid hyperplasia?

A

secondary

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7
Q

parathyroid carcinoma

A

metastasis is most telltale sign!

elevated PTH that doesn’t go down after surgery

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8
Q

non-parathyroid hypercalcemia causes

A

malignancy
vitamin D excess
calcium excess
medication (thiazide diuretics)

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9
Q

humoral hypercalcemia of malignancy

A

PTHrP mediated - SSC

vitamin D mediated - lymphomas

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10
Q

local osteolytic hypercalcemia

A

osteoclastic bone resorption due to:
breast carcinoma
multiple myeloma

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11
Q

cause of secondary parathyroid hyperplasia

A

*reduced kidney function
gastric bypass
vit D deficiency
pseudohypoPTH

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12
Q

presentation of secondary hyperparathyroidism

A

dissecting osteitis/”rugger jersey sign”

calciphylaxis - calcific occlusion of blood vessels causing ischemic necrosis

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13
Q

describe tertiary hyperparathyroidism

A

prolonged hypocalcemia causes continuous production of PTH even when Ca levels have normalized

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14
Q

clinical features of hypocalcemia

A

behavioral disturbance/stupor
numbness/parasthesias
muscle cramps/spasms
convulsions

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15
Q

PE findings of hypocalcemia

A

Trosseau sign
Chvostek sign
Prolonged QT interval on EKG

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16
Q

causes of acquired primary hypoparathyroidism

A

iatrogenic (surgical)

autoimmune

17
Q

causes of congenital primary hypoparathyroidism

A

DiGeorge syndrome
CaSR mutation
familial isolated hypoparathyroidism

18
Q

describe CaSR LoF mutation

A

hypercalcemia and hypocalcuria

  • parathyroid thinks there isn’t enough Ca when there is
  • turns on PTH and reduces renal excretion
19
Q

describe CaSR GoF mutation

A

hypocalcemia and hypercalciuria

  • parathyroid thinks there’s plenty of Ca when there isn’t
  • turns off PTH and increases renal excretion
20
Q

pseudohypoparathyroidism

A

PTH resistance in renal tubular cells and bone

hypocalcemia and hyperphosphatemia despite normal or elevated PTH

21
Q

what disease and mutation is associated with pseudohypoparathyroidism

A

Albright hereditary osteodystrophy

*GNAS mutation

22
Q

presentation of Albright’s hereditary osteodystrophy

A

*short stature
*obesity
*short phalanges of UE and LE
dental abnormalities
subcutaneous ossifications
cataracts
seizures and tetany