Hypercalcaemia/parathyroid disease and hypocalcaemia Flashcards

1
Q

How many parathyroid glands are there and where are they?

When is parathyroid hormone secreted?

What does it do?

A
  • There are 4 parathyroid glands, lying posteriorly to the thyroid
  • The chief cells are responsible for secreting parathyroid hormone (PTH)
    • PTH is secreted when plasma calcium levels are low
    • PTH can also be secreted in response to low vitamin D, or high phosphate levels
  • PTH works to increase plasma calcium reabsorption from bone by:
    • Directly stimulating calcium resabsorption from bone
    • Directly increasing renal tubular calcium reabsorption
    • Indirectly stimulating increased GI calcium absorption
      • By increasing vitamin D activation in the kidney
    • PTH has a secondary effect of increasing renal phosphate excretion
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2
Q

What is the role of vitamin D?

How is ‘active’ vitamin D formed?

A

Vitamin D acts to sustain plasma calcium and phosphate levels by increasing their inflow from the GI tract

  • It i also required for normal bone formation
  • Endogenously it is synthesized in the skin, forming D3, cholecalciferol
  • Exogenously it is ingested as D2, ergocalciferol (common in fish, liver and dairy products)
  • ‘Active’ vitamin D is then formed by a second hydroxylation in the kidney, to produce to 1,25-(OH)2-D2/3
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3
Q

What are causes of vitamin D deficiency?

A

Most commonly occur in people with inadequate sunlight exposure, malabsorptive conditions and liver/kidney disease

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4
Q

Where is calitonin secreted from?

What is its function?

A
  • Calcitonin is secreted by parafollicular/’C’ cells of the thyroid gland in response to increased plasma calcium levels
  • It acts to decrease plasma calcium levels, by antagonism of the effect of PTH on the bone
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5
Q

Why is the importance of calcitonin in humans is controversial?

A
  • Removal of thyroid, and complete calcitonin deficiency does not lead to overt hypercalcemia
  • Extreme hypersecretion of calcitonin by tumours rarely produces hypocalcaemia
  • It is likely that PTH/Vitamin D levels are adjusted in response to calcitonin changes
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6
Q

Give an overview of the normal control of serum calcium

A
  • Intestinal uptake of calcium depends on the amount of ionized calcium in the lumen, and the presence of activated vitamin D
  • 90% of renal excretion of calcium is related to sodium reabsorption in the proximal tubule, with 10% regulated by PTH in the distal tubule
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8
Q

What are the common causes of raised serum calcium?

A

In a patient with hypercalcaemia, 97% of cases are due to primary hyperparathyroidism or malignacy (PTH high in hyperparathyroidism, low in malignancy)

Causes:

  • Excessive PTH secretion
    • Primary hyperparathyroidism
    • Tertiary hyperparathyroidism
    • Ectopic PTH secretion (very rare)
  • Malignancy
    • Myeloma
    • Metastatic deposits in bone
    • Paraneoplastic
      • PTHrp secretion: e.g. SCC (of lung or other tissues)
      • Production of osteoclastic factors
  • Excess Vitamin D
    • Exogenous excess
    • Granulomatous disease: TB/sarcoid
    • Lymphoma
  • Excess calcium intake
    • ‘Milk-alkali’ syndrome (antacids + large amounts of calcium lead to excessive absorption
  • Other endocrine disease
    • Thyrotoxicosis
    • Addison’s
  • Renal disease
    • Severe AKI
  • Drugs
    • Thiazide diuretics
    • Lithium
  • Hereditary
    • Familial hypocalciuric hypercalcaemia
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9
Q

What are the symptoms of hypocalcaemia?

A
  • Peripheral irritability:
    • Tetany/cramps
    • Carpo-pedal spasm
      • Wrist flexion and fingers drawn together
      • Happens especially after occulusion of brachial artery, e.g. with a blood pressure cuff: Trosseau’s sign
      • Tapping over the facial nerve causes twitches: Chvostek’s sign
  • Central irritability
    • Seizures
  • Depression/anxiety
  • Perioral paraesthesia
  • Cataracts
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10
Q

What the common causes of hypocalaemia?

A

With low PTH (hypoparathyroidism)

  • Idiopathic/primary hypoparathyroidism (autoimmune)
  • Post thyroid/parathyroid surgery
  • Post neck irradiation
  • Infiltration: sarcoid/malignancy
  • Congential absence of the gland: Digeorge syndrome
  • Severe hypomagnesia: impairs PTH secretion

With high PTH

  • Vitamin D deficiency
  • Acute pancreatitis
  • Alkalosis
  • Acute hyperphosphataemia
    • renal failure
    • rhabdomyolysis
    • tumour lysis
  • Drugs: bisphosphonates, calcitonin
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