Endocrine Flashcards
(135 cards)
a 25-year-old man concerned about some “bizarre symptoms” that he has been. He tells you that approximately 6 months ago, he began to experience the following symptoms: headaches, visual defects, weight gain, an appearance of his forehead growing, enlarging hands and feet (he could no longer get his gloves and shoes on), and increased sweating. On examination, mental status is normal, and the apical impulse is felt in the fifth intercostal space, midclavicular line. His blood pressure is 170/ 105 mm Hg. He does have a protruding brow, and three discrete visual field defects are noted (two in the left eye and one in the right eye). His tongue appears enlarged, and he is sweating profusely. What is the likely diagnosis
Acromegaly
What is the different between acromegaly and gigantism
igantism occurs if growth hormone (GH) hypersecretion begins in childhood, before the closure of the epiphyses
Acromegaly involves growth hormone GH hypersecretion beginning in adulthood; a variety of bony and soft tissue abnormalities develop
What is the main cause of both gigantism and acromegaly q
a pituitary adenoma that secretes excessive amounts of Growth Hormone; rarely, they are caused by non-pituitary tumors that secrete GHRH
What are the diagnostic tests for gigantism and acromegaly
GH test 2 hour after glucose load
Increased IGF-1
MRI/CT shows a pituitary tumor
What is the treatment of gigantism and acromegaly
Removal of pituitary tumor
a 25-year-old male presents complaining of fatigue, weight loss, and recurrent nausea and vomiting. On physical exam, he appears weak and has skin that appears abnormally tan. Her blood pressure is 90/70. A basic metabolic panel reveals hyponatremia and hyperkalemia. What is the likely diagnosis
Addisons disease
What causes Addisons disease
Typically autoimmune. May be due to Tuberculosis in endemic areas
What is Addison’s disease
Destruction of the adrenal cortex resulting in loss of cortisol production (↓ cortisol)
What are the typical lab findings with Addisons disease
↓ sodium, ↓ 8 AM cortisol, ↑ ACTH (primary), ↑ potassium (primary), low DHEA
What is the role of DHEA and where is it produced
It is produced in the adrenal gland and helps with the production of testosterone and estrogen
How do you diagnose Addison’s disease
High dose cosyntropin (synthetic ACTH) stimulation test
-Blood or urine cortisol is measured after an IM injection of cosyntropin (synthetic ACTH)
*The normal response is a rise in blood and urine cortisol levels after synthetic ACTH is given
Primary adrenal insufficiency results in little or no increase in cortisol levels (< 20 mcg/dL) after ACTH is given
How do you treat Addison’s disease
Hydrocortisone/prednisone PO daily
If someone is experiencing an Addisonian crisis, what will their presenting symptoms be and how would you treat it.
Hypotension, altered mental status
treatment: emergent IV saline, glucose, steroids
a 32-year-old woman who comes to the clinic because of new skin markings on her abdomen. Physical exam shows a round face, large purple striae over the abdomen, and several ecchymoses over her trunk, arms, and legs. She describes easy bruising, as well as a significant weakness when she tries to stand up from sitting on the ground. Her 24-hour urine free cortisol is 3 x the upper limit, her late-night serum cortisol is elevated and her plasma ACTH level is < 5 pg/mL. What is the likely diagnosis
Cushings disease
What is cushings disease
Cushing’s syndrome is a collection of signs and symptoms due to prolonged exposure to excess cortisol
-ACTH secreting pituitary microadenoma usually very small on anterior pituitary
Which gender is more susceptible to cushings disease
Females (3x)
What are common symptoms seen with cushings disease
buffalo hump, moon facies, supraclavicular pads, HTN, thirst, polyuria, hypokalemia, Proximal muscle weakness, pigmented striae; backache, headache, oligomenorrhea/amenorrhea emotional lability/psychosis
How do you diagnose cushings disease
Confirming high cortisol with a 24 hr urine free cortisol, late-night serum cortisol, and/or low-dose dexamethasone suppression test
What is the most reliable index of cortisol secretion
24-hour urinary free cortisol
How do you confirm the source of the high cortisol
ACTH level
*If it is an ACTH dependent cause, an MRI of the brain should be done to look for a pituitary adenoma (Cushing disease). If it is an ACTH independent cause, a CT of adrenals should be done to look for an adrenal mass such as an adenoma
How does the dexamethasone suppression test work to diagnose cushings syndrome
Give a steroid (dexamethasone) ⇒ failure of steroid to decrease cortisol levels is diagnostic ⇒ proceed next to high dose dexamethasone suppression test ⇒ no suppression = Cushing’s syndrome
How do you treat cushings syndrome
Transsphenoidal selective resection of pituitary tumor cures 75-90%
a 25-year-old male complaining of an unabated thirst that began three weeks ago. He is constantly drinking and goes to the bathroom around five times a night. He has lost five pounds over the last few weeks. The patient is on lithium for bipolar disorder. His BP is 115/70. The patient’s labs are significant for serum Na of 145 mEq/L (normal: 135-145). Urine osmolality is 185 mOsm/kg, and urine specific gravity is 1.004 (normal: 1.012 to 1.030). What is the likely diagnosis
Diabetes insipidus
What is diabetes insipidus
Diabetes insipidus (DI) is caused by a deficiency of or resistance to vasopressin (ADH), which decreases the kidneys’ ability to reabsorb water, resulting in massive polyuria