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