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51 Cards in this Set

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Q150. Tx for adrenal insufficiency; what additional Tx for Addison's only?
A150. Tx: Glucocorticoid replacement (especially at times of stress); additional for Addisons: Mineralcorticoid replacement
Q151. What disease presents with the exact opposite of Addison's?
A151. Cushing's Dz
Q152. Definition: Symptoms of excess Cortisol production
A152. Cushing's syndrome
Q153. Definition: Cushing's syndrome caused by excess ACTH secretion of pituitary
A153. Cushing's disease
Q154. What lung cancer is associated with ectopic ACTH production?
A154. Small (Oat) cell lung CA
Q155. Etiology of Cushing's syndrome (Adrenal excess); (3)
A155. Exogenous corticosteroid therapy;; Adrenal neoplasm;; Ectopic ACTH production
Q156. Dx: HTN, hair loss, central obesity, hump on the back of neck, abdominal purplish striae, hirsuitism, proximal muscle weakness, osteoporosis
A156. Cushing's syndrome
Q157. How is the ectopic ACTH Sx different from the ACTH Sx released directly from the adrenals?; Why?
A157. Ectopic ACTH Sx: Weight gain and proximal muscle weakness only; B/c: the ACTH in ectopic from is usually the inactive form.
Q158. How can Cushing's Dz be distinguished from Cushing's Syndrome?
A158. Cushing's Dz: presence of Hyperpigmentation
Q159. Dx: 42-yo woman on long-term steroids for asthma has excess adipose tissue in her neck and upper trunk, a wide "moon face", and very fine hair
A159. Cushing's Syndrome
Q160. (2) main lab tests to Dx Cushing's Syndrome; which is more specific as to finding the etiology?
A160. Overnight Dexamethasone Suppression test; High-Dose Dexamethasone Suppression test (more specific)
Q161. Describe the Overnight Dexamethasone test
A161. 1 mg of dexamethasone is given at night, then plasma cortisol is measured in the morning. if < 5ug/100mL, it EXCLUDES Cushing's as the Dx
Q162. What are the 3 Dx from Dexamethasone Suppression test & ACTH that follows?; (3 results from test)
A162. Give 8 mg dexamethasone, then measure ACTH: 1. If ACTH is decreased or undetectable with no supression = Adrenal etiology; 2. ACTH is Normal or Increased with no supression = Ectopic ACTH etiology; 3. ACTH is High with partial supression = Pituitary etiology
Q163. What are the electrolyte (Cl, K and Na) findings with Cushing's syndrome?; (3); What is found in urine?
A163. Hypochloremia;; HypoK;; HyperN; In Urine: 24-hour Urinary free cortisol > 100 ug/24hr
Q164. Tx of Cushing's from Pituitary adenomas
A164. Transsphenoidal surgery; (radiation for children and refractory to surgery)
Q165. Tx of Cushing's from Adrenal Adenoma
A165. Unilateral resection, followed by 3 to 12 months of glucocorticoid replacement (until normal adrenal comes out of suppression)
Q166. Tx of Cushing's from Bilateral Adrenal Hyperplasia
A166. Bilateral resection and lifelong replacements of glucocorticoids and mineralcorticoids
Q167. Tx of Cushing's from Ectopic ACTH production
A167. Remove source of neoplasm
Q168. Definition: Isolated excess production of Aldosterone; Another name for it?
A168. Hyperaldosteronism; "Conn's syndrome"
Q169. Etiology of Conn's syndrome; (2); Which is MCC?
A169. 1. Unilateral aldosterone-producing Adenoma (MCC); 2. Bilateral hyperplasia of ZoNa Glomerulosa (idiopathic)
Q170. Dx: HTN, signs of HyperK (muscle cramps, palpitations), signs of glucose intolerance (polyuria, polydipsia); may also be asymptomatic
A170. Conn's syndrome
Q171. Dx test for Conn's syndrome
A171. Measure plasma aldosterone to plasma renin activity ratio; a ratio > 20 = Conn's syndrome (hyperaldosteronism)
Q172. Dx: 44-yo woman has HTN, muscle cramps and excessive thirst
A172. Hyperaldosteronism; (Conn's syndrome)
Q173. What is the Tx for Conn's syndrome if it is due to hyperplasia?; (2)
A173. 1. Spirolactone or ACEi to control BP; 2. Low-sodium diet
Q174. Definition: tumor of the adrenal medulla resulting in the intermittent release of catecholamine excess
A174. Pheochromocytoma
Q175. (4) Disease Etiologies of Pheochromocytomas
A175. MEN II: (Pheochromocytoma, PTH tumor, medullary thyroid CA);; MEN III: (Pheochromocytoma, PTH tumor, mucosal Neuromas);; Neurofibromatosis;; Von Hippel-Lindau Dz
Q176. Dx: Pheochromocytoma, retinal angioma, CNS hemangioblastomas, renal cell CA, pancreatic pseudocysts, ependymal cystenoma
A176. Von Hippel-Lindau Dz
Q177. Dx: 38-yo woman on labetalol presents with poorly controlled hypertension, frequent headaches and palpitations
A177. Pheochromocytoma
Q178. what are the 5 "H" Sx of pheochromocytoma?
A178. HA;; HTN;; Hot (diaphoretic);; Heart palpitations;; Hyperhidrosis (hand sweating)
Q179. Dx test for Pheochromocytoma
A179. Elevated urine Vanillylmandelic Acid; (urine catecholamines)
Q180. Tx for pheochromocytoma; (2)
A180. Surgical resection of mass;; Alpha-adrenergic blocker (may also add B-blocker)
Q181. What is a possible misdiagnosis of Pheochromocytoma?
A181. Anxiety disorder
Q182. What Dx is known for the "Rule of 10s": 10% are extra- adrenal; 10% are bilateral; 10% are malignant; 10% are familial; 10% are pediatric; 10% calcify; 10% recur after resection
A182. Pheochromocytoma
Q183. Where is the anterior pituitary derived from?
A183. Rathke's pouch
Q184. Where is the posterior pituitary derived from?
A184. Hypothalamic neuronal axon terminals of the brain
Q185. what multiendocrine problem includes pituitary tumors?
A185. MEN-1; (pituitary, pancreas, parathyroid)
Q186. where is the site of the primary tumors of the pituitary?
A186. Anterior pituitary only; (none in posterior)
Q187. MC pituitary tumor, it presents with glactorrhea and amenorrhea; Tx?
A187. Prolactinoma; Tx: Bromocriptine (DA agonist)
Q188. Dx: pituitary tumor that presents with visual changes or slightly high prolactin levels; Tx?
A188. Nonfunctioning Tumor; Tx: surgery
Q189. Definition: MC tumor of the suprasellar region in children that arises from the remnants of Rathke's pouch and is solid or cystic; usually calcified
A189. Craniopharyngioma
Q190. Dx: HA, compression of optic chiasm "tunnel vision", signs of increased intracranial pressure
A190. Craniopharyngioma
Q191. Dx Test for Craniopharayngioma; (3)
A191. X-ray - shows enlarged sella; CT / MRI; Hormone studies: excess deficiencies
Q192. Tx for craniopharyngioma; (3 together)
A192. 1. Surgery; 2. Hormone replacement; 3. Dopamine agonist if prolactin-related Sx are noticed
Q193. specific Etiology of Acromegaly
A193. pituitary Somatotrophic Adenoma secreting GH
Q194. Dx: progressive enlargement of the peripheral body parts, particularly head, hands, and feet; decreased glucose tolerance; hyperphosphatemia
A194. Acromegaly
Q195. Acromegaly in children
A195. Gigantism
Q196. What hormone in excess is related to acromegaly?
A196. GH
Q197. Dx tests that confirm Acromegaly; (3)
A197. 1. Serum GH levels - measured in bed in am; 2. Lack of GH suppression by glucose; 3. Elevated serum IGF-I levels
Q198. Aside from surgery and radiation, what is the medicine used to Tx Acromegaly?
A198. GH receptor blocker: Pegvisomant (Somavert)
Q199. Dx: 29-yo woman with inability to lactate after childbirth. Delivery was complicated by blood loss and hypotension
A199. Sheehan's syndrome
Q200. Etiology of Hypopituitraism; (3)
A200. Tumors;; Medical/surgical destruction;; Sheehan's syndrome