Parathyroid Flashcards

1
Q

Parathyroid:

Normal PTH secretion and calcium homeostasis?

A

low Ca stimulates PTH secretion from the parathyroid gland

Results in:

  • increased vitamin D synthesis
  • calcium resorption from bone, absorption from gut, reabsorption from kidney
  • phosphate resorption from bone kidney
  • increased magnesium reabsorption
  • reduction in bicarbonate reabsorption

Calcium measurement
Total Ca = free and bound combined

bound = to albumin and phosphate

Acidosis = increased free Ca = reduced PTH
Alkalosis = reduced free Ca = elevated PTH
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2
Q

Parathyroid:

Types of parathyroid derrangement?

A

Primary (parathyroid tumour) = increased/normal PTH, increased Ca

Secondary (Chronic Renal Failure or vitamin D deficiency) = increased PTH often due to hypertrophy), low/normal Ca

Tertiary (treated but residual hyperplasia) = very elevated PTH, very elevated Ca

Malignancy = low PTH (appropriately suppressed), increased Ca

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3
Q

Parathyroid:

Renal osteodystrophy mechanism?

A

1) As renal function declines vitamin D synthesis declines and calcium reabsorption is limited
2) Cycle of Ca levels drops/phosphate elevation which the PTH levels rise in response to
3) Eventually Ca levels drop too much to be compensated for despite continued elevations of PTH

https://www.fortunejournals.com/fulltext-images/chronic-kidney-diseasemineral-and-bone-disorders-ckdmbd-03.png

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4
Q

Parathyroid:

Primary Hyperparathyroidism?

A

post menopausal women

risk factors:

  • lithium therapy
  • head or neck irradiation

Symptoms:
Hypercalcaemia (Stones, bones, groans and psychic moans)

85% cause by solitary parathyroid adenoma

95% cure rate with surgical removal

**Must exclude Familial Hypercalciuric Hypercalcaemiua (FHH)

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5
Q

Parathyroid:

Familial Hypercalciuric Hypercalcaemia (FHH)?

A

benign condition
autosomal dominant
hypercalcaemia from birth
result of inactivated calcium sensing receptors

how to rule it out?
Fraction of urinary calcium = (Urine Ca x Serum Ca)/(Serum Ca x Urine Creatinine)
If > 0.02 = primary hyperparathyroidism
if < 0.01 = FHH

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6
Q

Parathyroid:

Hypercalcaemia?

A

Causes:

  • malignancy (inappropriate release of PTH-related peptide from tumour cells, associated with lung, breast, prostate, colon and T-cell malignancies and MM)
  • post-hypocalaemic hypercalcaemia (recovery from pancreatitis, ARF, rhabdomyolysis)
  • primary hyperparathyroidism
  • adrenal insufficiency
  • prolonged immobilisation
  • granulomatous disease – sarcoidosis, TB, beryliosis, leprosy, histoplasmosis (increase in 1,25(OH)2D production from macrophages in granuloma)
  • vit A and D intoxification
  • thyrotoxicosis
  • acromegaly
  • phaeochromocytoma
  • chronic lithium therapy
  • secondary hyperparathyroidism
  • tertiary hyperparathyroidism

Symptoms:
Stones, bones, groans and psychic moans

  • RENAL – polyuria, stones, dehydration
  • bone aches
  • GIT = constipation, anorexia, nausea, vomiting, pancreatitis
  • NEURO – lethargy, hypotonia, confused, coma
  • CVS – arrhythmias (shortened QTc and Osborne waves)
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7
Q

Parathyroid:

Hypocalcaemia?

A

Causes:

  • reduced intake
  • increased losses - diuretics
  • redistribution (hyperphosphataemia, alkalosis, pancreatitis, rhabdomyelitis, tumour lysis, hypoparathyroidism)

Symptoms:

  • perioral numbness
  • paraesthesia
  • cramps
  • seizures

Signs:

  • tetany
  • Trousseau (BP cuff inflation traps excitable median nerve resulting in carpal spasm
  • Chvostek (tap facial nerve results in facial muscle spasm)
  • hypotension
  • long QT
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