Hyperparathyroidism Flashcards

1
Q

What is hyperparathyroidism?

A

“Abnormally high PTH levels in blood due to overactivity of the parathyroid glands”
- PTH → increases serum calcium & decreases serum phosphate. Secretion is stimulated by decrease in serum calcium.

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2
Q

Describe the epidemiology of hyperparathyroidism?

A
  • F>M (3:1)
  • most cases occur >50 yrs old
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3
Q

What are the different types of hyperparathyroidsm?

A
  1. Primary Hyperparathyroidism - increased secretion of PTH unrelated to the plasma calcium concentration or (inappropriately NORMAL given the raised calcium)
  2. Secondary Hyperparathyroidism - increased secretion of PTH secondary to hypocalcaemia
  3. Tertiary Hyperparathyroidism - autonomous PTH secretion (despite high calcium) following chronic secondary hyperparathyroidism – glands undergo hyperplastic or adenomatous changes.
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4
Q

What are the causes of hyperparathyroidism?

A
  1. Primary
    o Parathyroid adenoma 80%
    o Parathyroid hyperplasia 20%
    o Parathyroid carcinoma <0.5%
    o MEN syndrome
  2. Secondary
    o Chronic renal failure
    o Vitamin D deficiency – causes reduced calcium absorption in gut hence hypocalcaemia
    - Pure vitamin D deficiency would lead to low calcium and phosphate
  3. Tertiary:
    o Occurs after prolonged secondary hyperparathyroidism due to conditions like chronic kidney disease.
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5
Q

Summarise the epidemiology of hyperparathyroidism

A

● Primary - incidence of 5/100,000
● Twice as common in FEMALES
● Peak incidence: 40-60 yrs

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6
Q

What are the presenting symptoms and signs of hyperparathyroidism?

A
  1. pHPT → polydipsia, polyuria, anorexia, nausea, constipation, bone pain (esp. back pain), renal stones, low mood.
    - Majority of patients are asymptomatic, abdominal groans & psychic moans (Symptoms of Hypercalcaemia)
  2. sHPT + tHPT → symptoms related to underlying cause (ie. renal failure).
    - Bone pain and increased risk of fractures.
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7
Q

What investigations are used to diagnose/ manage hyperparathyroidism?

A
  1. U&Es
  2. Serum calcium (high in primary and tertiary, low/normal in secondary)
  3. Serum phosphate (low in primary and tertiary, high in secondary)
  4. Albumin
  5. ALP
  6. Vitamin D
  7. PTH - high
    Primary Hyperparathyroidism:
    o Hyperchloraemic acidosis
    o Normal anion gap
    o Due to PTH inhibition of renal reabsorption of bicarbonate
    o Urine - high PTH in the presence of high calcium can also be caused by familial hypocalciuric hypercalcaemia (FHH)
    *Calcium: creatinine clearance ratio can help differentiate between primary hyperparathyroidism and FHH
  8. Renal ultrasound - can visualise renal calculi
  9. DEXA scan to check bone density 
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8
Q

How is hyperparathyroidism managed?

A
  1. pHPT → total parathyroidectomy (definitive management). Calcimimetics (Cinacalcet) are drugs that inhibit PTH release.
    - IV Fluids for treat hypercalcaemia
  2. sHPT → treat underlying cause (ie. CKD, Vitamin D deficiency)
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9
Q

What are some complications that may arise from hyperparathyroidsim?

A
  1. Primary
    o Increased bone resorption
    o Increased tubular calcium reabsorption
    o Increased 1-hydroxylation of vitamin D
    o All of these lead to hypercalcaemia
  2. Secondary
    o Increased stimulation of osteoclasts and increased bone turnover
    o This leads to osteitis fibrosa cystica – seen on X-ray as subperiosteal erosions, cysts, brown tumours, pepper pot skull
  3. Complications of surgery
    o Hypocalcaemia
    o HypoPTH
    o Recurrent laryngeal nerve palsy
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10
Q

Summarise the prognosis for patients with hyperparathyroidism

A

● Primary - surgery is curative for benign disease in most cases
● Secondary or Tertiary - same prognosis as chronic renal failure

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