Endocrinology Flashcards

1
Q

Outline the mechanism of primary hypothyroidism.

A

Low T4

High TSH and TRH

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2
Q

What are the causes of primary hypothyroidism?

A

Autoimmune: Hashimoto’s thyroiditis

Atrophic thyroiditis

Thyroidectomy

Radioactive iodine

Drugs

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3
Q

What is the management of primary hypothyroidism?

A

Replace thyroxine

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4
Q

Outline the mechanism of secondary hypothyroidism.

A

Pituitary gland failure

Low T4

TSH and TRH are low

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5
Q

Outline the mechanism of thyrotoxicosis.

A

Negative feedback loop

High T4

TSH and TRH are low

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6
Q

What are some of the causes of thyrotoxicosis?

A

Autoimmune: Graves’ disease

Multinodular goitre

Single toxic nodule

Thyroiditis: viral, post-partum, drugs

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7
Q

What is the management of thyrotoxicosis?

A

Beta-blocker for symptoms

Antithyroid medication: carbimazole

Radioactive iodine

Surgery

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8
Q

Outline the mechanism of a TSH-secreting pituitary tumour.

A

High T4

High TSH

Low TRH

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9
Q

What is the general theory behind dynamic testing?

A

If you think there is not enough hormone –> try to stimulate
e.g. short synacthen test, insulin tolerance test

If you think there is too much hormone –> try to suppress
e.g. glucose tolerance test, dexamethasone suppression test

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10
Q

What are the signs and symptoms of acromegaly?

A

Excess growth hormone production

  • large, “spade-shaped” hands and feet
  • coarse features: prominent supraorbital ridge, large nose, separated teeth, protruding jaw
  • headache
  • visual field defects: bitemporal hemianopia
  • excessive sweating
  • carpal tunnel syndrome
  • cardiomegaly and hypertension
  • glucosuria and polyuria
  • abnormal glucose tolerance test
  • arthrosis
  • sexual dysfunction
  • peripheral neuropathy
  • galactorrhoea
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11
Q

Outline the hormones produced by the pituitary gland.

A

HYPOTHALAMUS PITUITARY GLAND END-ORGAN
GnRH LH & FSH Ovaries/testes (androgens –> sperm, oestrogens –> ovulation)
GHRH GH Liver (growth factor)
Dopamine (-)Prolactin Breasts/gonads (lactation)
TRH TSH Thyroid (thyroxine)
CRH ACTH Adrenals (steroid hormones)
ADH Renal tubules
Oxytocin Breasts/uterus

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12
Q

What are the investigations in acromegaly?

A
  • TSH & T4
  • prolactin
  • FSH & LH
  • GH
  • insulin growth factor-1
  • glucose tolerance test
  • MRI pituitary fossa
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13
Q

What is the management of acromegaly?

A

Surgery: transphenoidal

Radiotherapy: conventional or gamma-knife

Medical: somatostatin analogue (octreotide), GRH blockers (pegvisomant)

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14
Q

What is growth hormone?

A

Peptide hormone causing musculoskeletal and vertebral growth and gluconeogenesis

Inhibited by somatostatin

Pulsatile

Glucose tolerance test: increases somatostatin –> should suppress GH

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15
Q

What does an excess or deficiency of growth hormone cause?

A

EXCESS

  • children = gigantism (epiphyses fail to fuse)
  • adults = acromegaly

DEFICIENCY

  • children = proportional dwarfism
  • adults = weight gain, muscle loss (insulin tolerance test - contraindicated in IHD and epilepsy)
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16
Q

What are the signs and symptoms of Cushing’s syndrome?

A
  • plethoric, moon facies, dorsal hump
  • bruising, thin skin, purpura, poor wound healing, abdominal striae
  • central obesity
  • cardiac hypertrophy and hypertension
  • adrenal tumour/hyperplasia
  • myopathy
  • amenorrhoea
  • diabetes
17
Q

What is Nelson’s syndrome?

A

Development of ACTH-secreting tumour following bilateral adrenalectomy for Cushing’s disease

18
Q

What are the investigations in Cushing’s disease?

A
  • 24hr urinary cortisol x 3
  • ACTH
  • midnight cortisol
  • low dose dexamethasone suppression test = 0.5mg qds 48hrs (excludes pseudo-Cushing’s)
19
Q

What are the differentials for Cushing’s disease?

A
  • ACTH secreting pituitary
  • ectopic ACTH-secreting tumour
  • adrenal tumour

Differentiate using high dose dexamethasone suppression test, CRH test, petrosal sinus sampling, MRI pituitary fossa

20
Q

Contrast pituitary and adrenal Cushing’s.

A

Pituitary:

  • high cortisol
  • high ACTH

Adrenal:

  • high cortisol
  • low ACTH
21
Q

Outline the mechanism of Addison’s disease.

A

Low steroid hormones

High ACTH

22
Q

What are the signs and symptoms of Addison’s disease?

A
  • hyponatraemia
  • hyperkalaemia
  • postural hypotension
  • bronze pigmentation
  • GI disturbance
  • weight loss
  • weakness
  • hypoglycaemia
  • change in distribution of body hair
23
Q

What are the causes of primary adrenal insufficiency?

A

Autoimmune

TB

Iatrogenic

Sepsis

Infiltrative disease

Friedrich-Waterhouse syndrome (haemorrhagic adrenalitis, fulminant meningoccocaemia)

Adrenal leucodystrophy

24
Q

What is the management of a hypoadrenal crisis?

A
  • fluids
  • glucose
  • steroids: hydrocortisone 100mg IV 6hrly
  • treat sepsis
  • find cause
25
What are the investigations in Addison's disease?
- 9:00AM cortisol - ACTH level - renin - short synacthen test: giving ACTH fails to increase cortisol levels
26
What is the long-term management of Addison's disease?
- hydrocortisone (10/5/5mg) - fludrocortisone (50-100mg) - education - emergency hydrocortisone injection kit - endrocrinology follow-up
27
Outline the mechanism of hyperprolactinaemia.
Prolactin is under tonic inhibitory control by dopamine Prolactin elevated by dopamine antagonists e.g. haloperidol, olanzapine, domperidone, metoclopramide Prolactin decreased by dopamine agonists e.g, bromocriptine, pregabalin
28
What are the signs and symptoms of hyperprolactinaemia?
- galactorrhoea - secondary amenorrhoea/oligomenorrhoea - dysmenorrhoea - infertility
29
What are the causes of hyperprolactinaemia?
Macroadenoma of pituitary gland --> low blood supply to desc. dopaminergic inhibition --> reduced inhibition of prolactin Non-functioning prolactinoma 5Ps = pregnancy, physiological, pharmacology, PCOS, primary hypothyroidism