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51 Cards in this Set
- Front
- Back
Q200. Etiology of Hypopituitraism; (3)
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A200. Tumors;; Medical/surgical destruction;; Sheehan's syndrome
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Q201. Dx: 36-yo woman complains of amenorrhea for 1 year, increasingly bad HA, clumsiness and sporadic nipple discharge; beta-hCG levels are normal
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A201. Prolactinoma
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Q202. Drugs that inhibit DA and as a result, cause hyperprolactinemia; (6)*
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A202. The Prolactin Has Magnified My C-cups: TCAs;; Prochlorperazine;; Haloperidol;; Methyldopa;; Metoclopramide: Cimetidine
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Q203. Difference b/t Central DI and Nephrogenic DI with respect to ADH
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A203. Central DI: inadequate pituitary secretion of ADH; Nephrogenic DI: lack of renal response to ADH
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Q204. Etiology of Central DI; (4, 3 are systemic)
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A204. PENS:; 1. Posterior pituitary damage (tumor, trauma, etc); 2. Encephalitis;; 3. Neurosyphillis;; 4. Sarcoidosis
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Q205. Dx: Psychiatric disorder of compulsive water drinking common in young to middle aged women; polyuria and dilute urine. How is it distinguished from DI?
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A205. Psychogenic Polydipsia; difference with DI: PP has a low plasma osmolality
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Q206. Etiology of Nephrogenic DI aside from Drugs, renal Dz and electrolyte disorders
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A206. Sickle cell
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Q207. (3) Drugs that can cause nephrogenic DI
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A207. "Liquid DM": Lithium;; Demeclocycline;; Methoxyflurane
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Q208. Dx: polyuria (3-15 L/day); thirst; dilute urine (sp gravity < 1.005)
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A208. DI
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Q209. Dx test for DI; (3)
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A209. 1. plasma Osmolality: High; 2. Exogenous ADH: leads to Water deprivation; 3. Infusion of hypertonic saline: no response
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Q210. Compare the urine osmolality before and after the infusion of exogenous ADH in: 1. Normal patient; 2. Central DI patient; 3. Nephrogenic DI patient
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A210. Normal: High urine Osm -> high urine Osm; Central DI: Low urine Osm -> high urine Osm; Nephrogenic DI: Low urine Osm -> low urine Osm
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Q211. Tx for Central DI
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A211. Desmopressin (DDAVP)
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Q212. Tx for Nephrogenic DI
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A212. Thiazide Diuretics
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Q213. Definition: Excess production of ADH
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A213. SIADH
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Q214. basic Etiology of SIADH; (3)
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A214. PIE:; Pharmacologic stimulation of hypo-pit axis;; Idiopathic overproduction of axis;; Ectopic production from tumors
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Q215. what (2) tumors cause SIADH?
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A215. Small cell lung CA; Pancreatic CA
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Q216. what are the Idiopathic causes of the overproduction of ADH in SIADH?; (5 in 2 categories)
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A216. CNS: encephalitis, trauma, stroke; Pulmonary Dz: TB, pneumonia; *any problem to Lungs or Brain (+ Pancreatic CA) can cause SIADH!
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Q217. (4) Pharmacologic causes of SIADH
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A217. Carbamazepine;; Chlorpropamide;; Clofibrate;; Vincristine
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Q218. (4)* other causes, aside from small cell and pancreatic cell cancer, of ADH secretion
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A218. Adrenal failure;; Renal failure;; Edema;; Fluid loss
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Q219. Dx: hyponatremia; low serum osmolality; high urinary sodium; urine osmolality > serum
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A219. SIADH
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Q220. Tx for SIADH; (2 with fluids, 1 drug)
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A220. Fluid restriction;; Hypertonic saline in severe HypoN;; Demeclocycline (lowers CD response to ADH)
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Q221. Definition: Disease of impaired bone mineralization
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A221. Osteomalacia; (Mineralization = Malacia)
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Q222. Osteomalacia in children
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A222. Rickets
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Q223. Basic etiology of Osteomalacia; (4)
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A223. Decreased Calcium absorption;; Dietary Calcium deficiency;; Vitamin D deficiency;; Hypophosphatemia
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Q224. Causes of dietary Calcium deficiency; (3)*
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A224. Malabsorption syndromes;; Gastrectomy;; Dumping syndrome
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Q225. Main Causes of Vitamin D deficiency; (2)
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A225. Hepatobiliary and Pancreatic diseases (loss of bile acids or pancreatic lipase reduce absorption of fat-soluble vitamins);; Renal Osteodystrophy
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Q226. Causes of Hypophosphatemia; (2)
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A226. Renal Tubular Acidosis;; Falconi's syndrome
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Q227. Dx: Bone pain, weakness, difficulty walking: broad-based waddling gait with short strides; thoracic kyphosis
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A227. Osteomalacia; (Rickets in children)
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Q228. What do blood tests show to Dx Osteomalacia?; (3)
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A228. Labs:; 1. Low - nml Calcium;; 2. Low - nml Phosphate;; 3. High Alk-phos (possible high PTH)
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Q229. Tx for Osteomalacia; (2)
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A229. Tx underlying disorder;; Calcium and Vitamin D supplements
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Q230. Definition: Systemic disorder resulting in a reduction of bone mass that leads to increased risk of fracture
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A230. Osteoporosis
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Q231. Risk factors for Osteoporosis; (6)
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A231. Elderly Female;; Post-menopause;; Family Hx;; Smoking;; Thin body;; Sedentary lifestyle
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Q232. Pathophysiology of Osteoporosis
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A232. Reduction of bone mass occurs due to an imbalance b/t bone acquisition and bone reabsorption;; without change in the ratio of mineral to organic bone
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Q233. Histology of Osteoporosis
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A233. Decreased cortical thickness and number (and size) of cancellous bone trabeculae; (especially horizontal)
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Q234. When does osteoporosis usually become symptomatic?; (2) types
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A234. when Fracture occurs:; Vertebral body fracture;; Hip fracture
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Q235. Dx lab blood test results for Osteoporosis
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A235. Everything is normal: Serum Ca++ and PO4- are usu normal;; Alk-phos is normal unless there is a fracture, then it's increased
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Q236. How is bone mineral density measured?; (2) Dx results
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A236. Dual X-ray Absorptiometry (DEXA) scan; T-score < -2.5 = Osteoporosis; T-score -2.5 to -1 = Osteopenia
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Q237. Differential in Osteoporosis; (4)*
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A237. Malignancy;; Hyperparathyriodism;; Osteomalacia;; Padget's disease of the bone
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Q238. Prevention and Tx for Osteoporosis; (4)
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A238. Dietary Calcium and Weight-bearing exercises;; Estrogen replacement therapy;; Calcitonin;; Bisphosphonates (Alendronate) with Vitamin D and Calcium supplements
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Q239. Definition: Chronic Dz of adult bone in which localized areas of bone becomes hyperactive, and the normal bone matrix is replaced by softened and enlarged bone
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A239. Padget's Disease of the bone
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Q240. If Alkaline Phos is elevated, what is the next step?; (2)
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A240. Send GGT to determine if it is Hepatic (elevated GGT) or bone (not elevated); or Check to see if it is heat-labile (Bone), where hepatic is not
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Q241. Histology: Hyperactive bone turnover with enlarged multinucleated osteoclasts
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A241. Padgets Disease of the bone
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Q242. Dx: 45-yo male is found to have an elevated alkaline phosphatase during a routine blood test. No other abnormalities were found. Further workup reveals the enzyme to be heat labile
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A242. Padget's Disease of the bone
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Q243. Radiologic finding: area of hyperlucency of the bone surrounded by a hyperdense border
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A243. Padget's Disease of the bone
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Q244. Tx for Padget's Disease of the Bone for: 1. Pain relief; 2. Anatomic deformity or impingement; 3. to Decrease bone reabsorption; 4. to assist with cardiac failure or neurologic deficits
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A244. 1. Pain = Indomethacin; 2. Deformity = Osteotomy of the bone; 3. Decrease Reabsorption = Bisphosphonates; 4. Assist in CardiacNeuro = Calcitonin
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Q245. What is the Normal serum Calcium range?
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A245. 8.5 - 10.2 mg/dL
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Q246. Etiology of Hypocalcemia; (8)*
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A246. IV STRAP:; Insufficient PTH;; Vitamin D deficiency;; Sepsis / Severe Mg deficiency;; Toxins;; Rhabdomyolysis;; Albright's Osteodystrophy (Pseudohypoparathyroidism);; Pancreatitis
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Q247. Osteoporosis Risk factors; (8)*
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A247. FACELESS:; Family history;; Alcohol;; Corticosteroids;; Elderly Female;; Low Calcium;; Estrogen low (Menopause);; Smoking;; Sedentary lifestyle
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Q248. First sign/Sx of Hypocalcemia; Name and describe (2) other common signs seen in PE
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A248. first sign:; Circumoral Paresthesia; Chvostek's sign: Facial muscle spasm with tapping of the facial nerve; Trousseau's sign: Carpal spasm after occluding blood flow in forearm with BP cuff
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Q249. What is seen with EKG for Hypocalcemia?
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A249. Prolonged QT and ST intervals; (also peaked T-waves can be seen as in HyperK)
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Q250. How can Calcium correct for Hypoalbuminemia?
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A250. Adjust Calcium upward by 0.8mg/dL for each 1.0g/dL of albumin below normal
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