Endocrinology Flashcards
1st line test for Cushing’s
Overnight / low dose dexamethasone suppression test
Cortisol raised after low-dose dexamethasone suppression test.
Cortisol normal after high-dose dexamethasone suppression test.
Diagnosis + investigation?
Pituitary adenoma
MRI pituitary gland
Bilateral adrenal disease - drug used to manage hypokalaemia?
Potassium-sparing diuretic e.g. sprinolactone
Describe Cushing’s DISEASE (different to Cushing’s syndrome)
Cushing’s disease =
- pituitary adenoma
- increased ACTH
- increased cortisol production
(which causes a Cushing’s syndrome)
Causes of Cushing’s syndrome?
CAPE
- Cushing’s disease (pituitary adenoma)
- Adrenal adenoma
- Paraneoplastic syndrome (small cell lung cancer)
- Exogenous steroids
Tests for adrenal insufficiency
9 am cortisol
U + E
Short synacthen test
Explain a short synacthen test
Synacthen = synthetic ACTH
(SYNthetic ACTH ENjection = SYNACTHEN)
Stimulates cortisol production.
Cortisol should double. If it doesn’t, there is adrenal insufficiency.
How to differentiate between primary and secondary adrenal insufficiency ?
ACTH raised = primary adrenal insufficiency (because pituitary gland is producing ACTH with no cortisol no act as a negative feedback)
ACTH low = secondary adrenal insufficiency (because pituitary gland is not producing ACTH)
All the causes of adrenal insufficiency to be aware of:
Primary adrenal insufficiency (Addison’s disease) can be caused by:
- Auto-immune destruction (most common)
- Surgical removal of the adrenal glands
- Trauma to the adrenal glands
- Infectious diseases, such as tuberculosis (more common in developing countries)
- Haemorrhage (e.g., Waterhouse-Friderichsen syndrome)
- Infarction
- Less commonly, neoplasms, sarcoidosis, or amyloidosis
Secondary adrenal insufficiency can occur due to:
- Congenital disorders
- Fracture of the base of the skull
- Pituitary or hypothalamic surgery or Neoplasms in the pituitary or hypothalamus
Infiltration or infection of the brain - Deficiency of corticotropin-releasing hormone (CRH)
Management of Addisonian Crisis =
- Aggressive fluid resuscitation
- Administration of intravenous/IM (if no access) steroids STAT
- Glucose administration if hypoglycaemia is present
Basic distinctions between Cushing’s syndrome, Conn’s syndrome, and Addison’s disease
Cushing’s syndrome = too much cortisol
Conn’s syndrome = too much aldosterone
Addison’s disease = not enough cortisol/aldosterone
Which steroids to give in Addisonian crisis?
IV hydrocortisone
Patient is on hydrocortisone and fludrocortisone - then gets a severe infection e.g. pneumonia
How to adjust steroid doses?
Double the hydrocortisone
(don’t need to double fludrocortisone as the high-dose hydrocortisone has some mineralocorticoid effects)
Aldosterone vs cortisol
Which is a glucocorticoid and which is a mineralocorticoid?
Aldosterone = mineralocorticoid
Cortisol = glucocorticoid
AMCOG
What is Waterhouse-Friedrichsen syndrome?
What is the most common cause?
Bilateral adrenal haemorrhage secondary to infection.
Most commonly, meningococcal septicaemia.
Visual field defect in pituitary tumour
(how do they first present and what do they become?)
Smaller pituitary tumours = bitemporal superior quadrantanopia
Bigger pituitary tumours = bitemporal hemianopia
Medication used to shrink pituitary adenoma?
Cabergoline (dopamine agonist)
What hormones are produced in the anterior pituitary?
The anterior pituitary gland releases:
Thyroid-stimulating hormone (TSH)
Adrenocorticotropic hormone (ACTH)
Follicle-stimulating hormone (FSH) and luteinising hormone (LH)
Growth hormone (GH)
Prolactin
What hormones are produced in the posterior pituitary?
The posterior pituitary releases:
Oxytocin
Antidiuretic hormone (ADH)
Explain pretibial myoedema
Specific to Graves’ disease
Deposits of mucin under shin skin
(discoloured, waxy)
Caused by reaction of tissues to TSH receptors antibodies
Thyrotoxic crisis (thyroid storm)
Acute, severe hyperthyroidism
- pyrexia
- tachycardia
- delirium
Admit + supportive care
- fluid resuscitation
- anti-arrhythmic drugs (if there’s an arrhythmia)
- beta blockers (symptomatic control)
Treatment for Graves disease
First line = Carbimazole
- normal function after 4 - 8 weeks
- titrate down for maintenance dose / “block and replace” (block all production of thyroid hormone then replace with levothyroxine)
- normally complete remission by 18 months
2nd line =
Propylthiouracil
- small risk of fatal hepatic reactions
or,
Radioactive iodine
- destroys thyroid cells which can cause hypothyroid
(contraindicated in pregnancy, avoid close contact with children and pregnant women for 3 weeks, avoid everyone for 3 days
following the treatment due to radiation)
or,
Surgery
- removes thyroid
- require levothyroxine for life
What happens to PTH levels in hypercalcaemia?
PTH should be low.
If PTH is normal and calcium is high, PTH is “inappropriately normal”.
This indicates primary hyperthyroidism.