endo Flashcards
inheritance pattern congential adrenal hyperplasia
pathology
which deficiency?
recessive
in response to low cortisol levels, the anterior pituitary secretes high levels of ACTH
- 21-hydroxylase deficiency (90%)
- 11-beta hydroxylase deficiency (5%)
- 17-hydroxylase deficiency (very rare)
X-ray changes in hyperparathyroidism
- osteopenia (low bone density)
- erosion of the terminal phalyngeal tufts
pepperpot skull
primary / secondary / teritary hyperPTH
primary (oversecretion of parathyroid):
high PTH, high calcium, low phos
secondary (vit D def, CKD):
high PTH, low calcium, high phos
teritary (CKD, hyperplasia):
v high PTH, high calcium, high phos
where does PTH act to increase Ca levels
bowel
kidneys
bone
chief cels secrete PTH
electroylte imbalance seen in cushing
hypokalaemic metabolic acidosis
with impaired glucose tolerance
Ectopic AC
features of cushings
hyperglycaemia (central obesity) osteoporosis muscle wasting / weakness skin thinning / brusing / striae ulcers immunosuppression / infection (neutropenia)
moon face
buffalo hump
diagnostic tests for cushings
- 24 urinary cortisol sample
- dexamethasone suppression test
low (1mg) / (8mg)
serum cortisol
serum ACTH
c-peptide significance?
low in T1DM
- pancreas is not making enough insulin precursor –> which breaks down to form C-peptide + insulin)
high/normal levels in T2DM
how do you diagnose insulinoma?
whipple’s triad
- hypoglycaemia in mornings (before eating)
- reversal of symptoms with glucose/food
- recorded low BMs at time of symptoms
high c peptide
conn’s blood results
hypernatraemia
hypokalaemia
metabolic alkalosis
aldosterone Na/K
H ions pumped out
1st line conn’s investigation
aldosterone:renin ratio
conn’s:
high aldosterone
low renin
CT abdo/adrenal after
Maturity-onset diabetes of the young inheritance pattern
autosomal dominant
define fasting glucose
fasting glucose 6.1 to 7mmol/l
define impaired glucose tolerance
fasting glucose < 7
OGTT 2 hr 7.8 - 11mmol/L
mx for acute addisonian crisis
iv hydrocortisone