mix of endo Flashcards

1
Q

Diabetes insipidus is due to lack of ___

A

ADH

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2
Q

classification of Dibaetes insipidus

A

cranial or nephrogenic

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3
Q

2 symptoms of diabetes insipidus

A

polyuria & polydipsia

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4
Q

type of diabetes where the collecting ducts of the kidney do not respond to ADH

A

Nephrogenic diabetes insipidus

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5
Q

type of diabetes where the hypothalamus does not produce ADH

A

cranial diabetes insipidus

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6
Q

drug causing nephrogenic DI

A

lithium

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7
Q

electrolyte imbalance in diabetes insipidus

A

hypernatraemia

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8
Q

osmolality findings in diabetes insipidus

A

low urine osmolality
&
high serum osmolality

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9
Q

test for diagnosing diabetes insipidus?

A

Water deprivation test
/
desmopressin stimulation test

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10
Q

where is ADH released from

A

posterior pituitary gland

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11
Q

ectopic ADH secretion?

A

small cell lung ca

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12
Q

mechanism of ADH

A

acts on distal convoluted tubule & collecting duct to increase water reabsorption independant of sodium

ADH stimulates the insertion of aquaporin-2 channels onto the luminal membrane, allowing free entry of water

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13
Q

sodium level in SiADH

A

euvolemic hyponatraemia

due to dilution

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14
Q

urine osmolality is ___

A

low

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15
Q

what can severe hyponatraemia cause?

A

seizures & reduced consciousness

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16
Q

medications that can cause SiADH

A
  • thiazide diuretics
  • carbmazepine
  • cyclophosphamide
  • antipsychotivs
  • SSRI
  • NSAIDs
17
Q

why is it important to correct sodium level slowly?

A

prevent; ‘Central pontine myelinolysis’

18
Q

e.g. of ADH receptor blockers

A

Tolvaptan

19
Q

1st phase of central pontine myelinolysis & why?

A

water moves from blood to cells in the brain across BBB. causing brain to swell

  • encephalopathic
  • confused
20
Q

2nd phases of central pontine myelinolysis

A

demyelination of the neurones, particularly in the pons. May present as cog&behavioural changes, spastic quadriparesis, pseudobulbar palsy

21
Q

what is ADH produced by?

A

magnocellular neurons in the paraventricular & supraoptic nuclei of the hypothalamus

22
Q

what triggers release of ADH

A

rising plasma osmolality

23
Q

urinary test results in SiADH

A

high urine osmolality
&
high urinary sodium

24
Q

what produces calcitonin?

A

parafollicular C cells

25
Q

effect of Calcitonin on: a) intestines b) bones c) kidneys

A

Intestines - reduces calcium absorption

Bones - stimulates osteoblasts & inhibits osteoclasts

Kidneys - inhibits phosphate reabsorption

26
Q

what electrolyte imbalance calcitonin be used to treat?

A

hypercalcaemia

27
Q

what marker can be used for recurrence of medullary thyroid cancer?

A

calcitonin

28
Q

inheritance pattern of MEN 1&2

A

autosomal dominant

29
Q

3 P’s of MEN 1

A
  • Parathyroid hyperplasia
  • Pituitary adenoma
  • Pancreatic tumours
30
Q

syndrome characterised by gastrinoma & recurrent peptic ulcers & diarrhoea

A

Zollinger-Ellison syndrome

31
Q

what mutation causes MEN 2

A

mutation of RET proto-oncogene

32
Q

3 conditions predominantly in MEN 2

A
  • Parathyroid hyperplasia
  • Medullary thyroid ca
  • Phaechromocytoma
33
Q

difference between MEN 2a & 2b

A

2a - normal appearance & parathyroid hyperplasia is common

2b - marfanoid habitus & parathyroid hyperplasia is rare