Endo Diagnosis Flashcards
Elevated plasma LDL
Elevated plasma triglyceride
Premature atherosclerosis, thus elevated cardiovascular morbidity
Mild obesity (inc fat mass)
GH deficiency
Excessive & sustained GH release even in daytime
acromegaly
When GH is in excess in children of growing ages what occurs?
gigantism
Frontal bossing
increased base of nose
thickening of naso-labial sulcus and lips
parotid hypertrophy
loss of oval features
thickened tongue and skin, increased skin folds, enlarged visceral organs (can lead to HTN due to cardiomegaly)
acromegaly
If acromegaly is due to enlarged anterior pituitary what sx would you expect to see?
HA, peripheral vision loss and double vision
How do you diagnosis acromegaly?
measure IGF-I levels and if elevated test glucose intolerance test and GH measure and if inadequately suppressed then do pituitary MRI to find mass if none then do chest and abd CT to find extrapituitary cayse
What tests would you use to assess adrenal fn?
Measure urinary hormone or degradation products- 24 hour collection
Dexamethasone suppression test (corsitol levels should decrease if HPA is normal and ectopic ACTH tumors do not respond)
Metyrapone Stimulation Test (inhibits cortisol via inhibition of 11-beta hydroxylase)
CRH Stimulation Test (excessive rise in ACTH in corticotroph tumors but not in ectopic ACTH producing tumors)
K+ depletion
Na+ retention
Hypertension
Hyperaldosteronism
What is conn symdrome
primary aldosteronism
excess secretion of aldosterone due to adrenal disease
What is Secondary hyperaldosteronism- renin dependent?
High plasma renin activity often due to cirrhosis, heart failure or nephrosis
What happens to cortisol, CRH and ACTH when a patient has Primary (adrenal) excess?
Cortisol: ↑
CRH: ↓
ACTH: ↓
What happens to cortisol, CRH and ACTH when a patient has Secondary (pituitary) excess?
Cortisol: ↑
CRH: ↓
ACTH: ↑
What happens to cortisol, CRH and ACTH when a patient has Primary (adrenal) deficiency?
Cortisol: ↓
CRH: ↑
ACTH: ↑
What happens to cortisol, CRH and ACTH when a patient has Secondary deficiency?
Cortisol: ↓
CRH: ↑
ACTH: ↓
Hypersecretion of epinephrine and norepinephrine
Pheochromocytoma
Effect of Pheochromocytoma
sustained HTN
glycosuria
increased urinary excretion of catecholamine metabolites
What type of thyroid cancer has the best outcome?
Papillary thyroid cancers
95% 10 yr survival
What is the best test for Cushing’s?
24 hr urine or midnight salivary cortisol
How do you test for adrenal crisis?
ACTH stim test is the Gold standard
If patient presents with cushings symptoms and ACTH is high what is the most likely cause?
Pituitary (primary) cushings or ectopic cushing’s
Sodium levels with SIADH
low
Sodium levels with central diabetes insipidus
high
high BP and low K+
hyperaldosteronism
episodic HA, tachycardia, sweating, feeling of impending doom
Pheochromocytoma
Best initial screening test for pheochromocytoma?
plasma metanephrines
What test should you order if you suspect hyperaldosteronism?
renin aldosterone levels
Parathyroid adenoma
Pituitary adenoma
Pancreatic islet cell tumor
MEN type 1
Pheochromocytoma
Medullary carcinoma of thyroid
Parathyroid hyperplasia
MEN type 2A
Pheychromocytoma
Medullary carcinoma of thyroid
Marfanoid habitus with mucosal and visceral ganglioneuromas
MEN type 2B
What test do you order if you suspect Hashimodos?
TPO
What antibodies are associated with graves?
TSI and TRAB
Low TSH and high free T4
Graves disease