PA Boards App Flashcards
Syndrome caused by overproduction of growth hormone (GH); Usually affecting pts in their 40s; MC etiology is from a pituitary tumor*
Acromegaly
Pts may present w/ symptoms of tumor compression (HA, double vision, or visual field defects); Presentation is from soft tissue overgrowth; enlarged jaw, hands, and feet with coarsening of the facial features; HTN, cardiomegaly, insulin resistance & colonic polyps/cancer;
Acromegaly
MC reason for increased mortality is from cardiovascular disease
Acromegaly
First initial test is an insulin-like growth factor (IGF-1)-increased! MRI of pituitary
Acromegaly
Adrenal insufficiency; MC cause is from autoimmune destruction
Addisons Disease
Pts present with fatigue, weakness, anorexia, nausea, weight loss; Hyperpigmentation occurs from long-standing elevated ACTH levels; pt will also have hypotension, hyponatremia, hypoglycemia, hyperkalemia, and metabolic acidosis
Addison’s DIsease
Dx is confirmed with ACTH stimulation test (cosyntropin)-if cortisol levels DO NOT rise, adrenal insufficiency is confirmed
Addisons Disease
Tx of choice is Fludrocortisone (mineralocorticoid)
Addison’s Disease
Increased cortisol levels from any source=
Cushing’s Syndrome
Increased cortisol levels from a pituitary adenoma=
Cushing’s Disease
Pts present with central obesity, facial plethora, proximal weakness, striae, moon face, buffalo hump, HTN, diabetes, supraclavicular fat pads, and atrophy of the skin;
Cushing’s
Screen with 24H urine free cortisol, low dose dexamethasone test, or late night salivary test
Cushing’s
Autoimmune destruction of the pancreatic beta cells; will result in insulin dependence; can lead to DKA
T1DM
Characterized by insulin resistance related to obesity
T2DM
May present with obesity or acanthosis nigricans; consider dx in pts with prolonged or recurrent fungal infections
T2DM