Parathyroid Disorders Flashcards

1
Q

What are the functions of parathyroid hormone

A

PTH is released in response to low blood calcium / high phosphate

PTH acts on:

  1. Catalysing VITAMINE D3 Activation ->Calcitriol
    Calcitriol acts on intestines to increase Abdo Ca2+ absorption + kidney to reduce Ca2+ excretion
    2.Increase bone resorption: Indirectly increase osteoclast activity + Directly inhibit osteoblast activity
  2. Decrease phosphatase resorption
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2
Q

Which hormone opposes the action of PTH?

A

Calcitonin released by Thyroid gland oppose PTH and reduce blood calcium levels by

Inhibiting Bone resorption

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3
Q

What are the different types of hyperparathyroidism and associated causes>

A

Primary Hyperparathyroidism - Parathyroid adenoma (MC), Hyperplasia
Secondary Hyperparathyroidism - Low VITD (CKD/DEFICIENCY)
Tertiary Hyperparathyroidism - Autonomic secretion following long term 2o causes

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4
Q

Which serum levels is to be taken when assessing parathyroid function and how would it look for each type of hyperparathyroidism?

A

Also ALP will be up in all of them

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5
Q

What signs and symptoms will present in hyperparathyroidism?

A

Sx is associated with hypercalcemia - BSGM

Bones - Bone pain / Osteoperosis
Stone - Renal Stones, Haematuria; due to renal stones
Abdo groan - Abdo pain
Psychic moans - Anxiety/depression

+polyuria/polydispsia

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6
Q

hyper Parathyroid DX

A

PTH profile - indicates which source
ECG - Hypercalcaemia ~ Short QT (primary)

other
Dexa Scan - Assess bones
CT KUB - Kidney Urethra Bladder- Assess kidney function and stones

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7
Q

Hyperparathyroid TX

A

Parathyroidectomy
+
Bisphosphonates - bone protection
Calcimimetics - Calcitrol - Reduce PTH=Ca2+

2o:
Tx underlying cause - CKD - renal transplant / vit d def - vit supplements
+
Ca2+ Suuplements

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8
Q

What are the causes of hpoparathyroidism

A

Iatrogenic - MC Neck surgery
Metabolic - Hypo magnesium (MG need for secretion)
Autoimmune - Isolated autoimmune hypoparathyroidism
Congenital: DiGeorge syndrome: 22q11

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9
Q

What the associated signs with DiGeorge syndrome: 22q11

A

22q11 deletion leads to failure to develop the 3rd and 4th pharyngeal arches.

Features can be summarised by the mnemonic, CATCH22

CATCH22: cardiac abnormalities, abnormal facies, thymic aplasia, cleft palate, hypoparathyroidism, 22q11 deletion

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10
Q

How would hypo parathyroid present?

A

Hypocalcemia - CATS go numb

CONVULSION
ARRYTHMIAS
TETANY - SPASM
and
numbness/ Paresthesia

+ Signs
Chvostek’s sign
Trousseau’s Signs

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11
Q

FACIAL NERVE TAP CAUSES FACIAL TWITCHING

A

CHVOSTEK’S SIGN

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12
Q

BP CUSS CAUSES WRIST/HAND SPASM

A

TROUSSEAU’S SIGNS

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13
Q

Hypoparathyroidism Dx

A

PTH profile
U/E - Ca2+/Mg and Vit D
ECG - PROLONGED QT

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14
Q

Hypoparathyroidism TX

A

IV calcium gluconate
Calcitrol (vitd3)
thiazides

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