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1000 Cards in this Set
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- 3rd side (hint)
What are the 5 main platelet abnormalities? |
1) ITP: peripheral platelet destruction, antiplatelet antiboides, increased megakayrocytes
2) TTP: increased platelet aggregation leads to thrombosis and schistocytes, increased LDH (There are neurologic & renal symptoms, & fever) 3) DIC: schistocytes & increased fibrin split products 4) Aplastic anemia 5) Drugs (e.g. immunosuppressive agents) |
A schistocyte or schizocyte (from Greek schistos for "divided" or schistein for "to split", and kytos for "hollow" or "cell") is a fragmented part of a red blood cell.
- irregularly shaped, jagged and asymmetrical. - a true schistocyte does not have central pallor. |
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What are the signs of platelet abnormalities?
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1) MICROhemorrhage: mucous membrane bleeding, epistaxis, petechiae, purpura
2) increased bleeding time |
- Epistaxis = nosebleed
- Petechiae = a small (1-2mm) red or purple spot on the body - Purpura - small (0.3-1 cm) red or purple discolorations on the skin that do not blanch on applying pressure. Caused by bleeding underneath the skin. |
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What are the 3 main coagulation factor defects?
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1) Hemophilia A (factor VIII deficiency)
2) Hemophilia B (factor IX deficiency) 3) vW disease: mild, most-common (deficiency of vonWillebrand factor leads to a defect in platelet adhesion and a decrease in factor VIII survival) |
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What are the signs of a coagulation factor defect?
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1) MACROhemorrhage: hemarthroses (bleed into joints), easy bruising
2) Increased PT &/or PTT time |
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What is the initial response to high-altitude induced hypoxia?
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1) Hemoglobin-O2 curve shifts right as a result of increased 2,3-DPG) in order to release more O2 to tissue
2) The P50 (partial pressure of O2 @ 50% saturation of hemoglobin) will increase |
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What is one chronic response to high-altitude induced hypoxia?
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Increased hemocrit due to increased erythropoietin
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What is the action of 2,3-DPG?
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1) It binds to the beta chains of deoxyhemoclogin and DECREASES the affinity of hemoglobin for O2
2) This right-shifts the Hemoglobin-O2 curve 3) Is a response to high-altitude hypoxia |
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What is the pulmonary vascular response to increased altitude?
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B/C barometric pressure decreases, there is a decrease in alveolar partial O2 pressure.
- This causes hypoxic vasoconstriction in the pulmonary vessels - This increases pulmonary arterial pressure (i.e. pulmonary vascular resistance) - If prolonged = Right heart hypertrophy |
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What causes acromegaly?
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Unsuppressed secretion of growth hormone (GH), usually due to a pituitary adenoma
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What causes the visual disturbances often seen with acromegaly?
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If the cause is a pituitary adenoma, this tumor can press on the optic chiasm
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What are the main functions of growth hormone (GH)?
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1) Human growth and development
2) Stress response to starvation |
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How does growth hormone (GH) respond to starvation?
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GH is released in response to hypoglycemia & acts directly to REDUCE glucose uptake by cells & to increase lipolysis inorder to INCREASE blood sugar levels
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How is growth hormone (GH) used in the Dx of acromegaly?
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- In a healthy person, a glucose tolerance test should depress GH levels.
- However, in acromegaly, the GH levels would not be affected |
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What is the growth hormone (GH) response to obesity? |
it's secretion is reduced
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What is the growth hormone (GH) response to pregnancy?
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GH secretion decreases
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What are somatomedins and when are they released?
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1) Somatomedins = insulin-like growth factors
2) Mediate metabolic changes necessary for growth & development 3) Act on hypothalamus & anterior pituitary via negative feedback to reduce growth hormone (GH) secretion |
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What is somatomedin's effect on GH secretion
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1) It is part of the negative feedback system that regulates GH secretion
2) Synthetic forms can be used to treat acromegaly |
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What are the primary findings in acromegaly?
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1) Cause: excess GH in adults
2) Features: - Large tongue with deep furrows - Deep voice - Lg. hands & feet - Coarse facial features - Impaired glucose tolerance (insulin resistance) |
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What does excess GH cause in adults? In children?
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In adults: acromegaly
In kids: gigantism |
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What is the Tx for acromegaly?
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Pituitary adenoma resection followed by octreotide administration
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Octreotide: mimics natural somatostatin pharmacologically; a more potent inhibitor of growth hormone, glucagon, & insulin than the natural hormone.
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How is acromegaly diagnosed?
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1) Increased serum IGF-1
2) Failure to suppress serum GH following oral glucose tolerance test |
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When is growth hormone (GH) normally increased?
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Stress, exercise, & hypoglycemia
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How does acetazolamide work?
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Inhibits carbonic anhydrase in the PCT (luminal/basolateral membrane & cytoplasm)
- t/f decreases kidney reabsorption of bicarbonate in the proximal tubule & increases K+, Na+, & Cl- loss - ALKALINIZES Urine |
ACIDazolamide causes ACIDosis
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What is acetazolamide used for?
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ACE family:
- Altitude sickness - metabolic Alkalosis - Alkalinizing urine - glauComa - Epilpsy - Familial periodic paralysis |
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What is the potential toxicity of acetazolamide?
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PACE:
- Potassion depletion (hypokalemia) - Acidosis (Hyperchloremic metabolic) due to excretion of HCO3 - Allergy (SULFA-based) - Ca nephrolithiasis - Encephalopathy in patients with hepatic cirrhosis due to decreased NH4+ excretion |
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What drugs increase urine NaCl?
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ALL diuretics:
- Carbonic anhydrase inhibitors - Loops - Thiazides - K+-sparing |
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Which drugs increase urine K+
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All diuretics, except K+ sparing
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Which diuretics cause acidemia?
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1) Carbonic anhydrase inhibitors
- reduced HCO3- reabsorbtion 2) K+ sparing - hyperkalemia leads to K+ entering all cells (via H+/K+ exhcanger) & H+ exiting cells |
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Which diuretics cause alkalemia?
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Loops & Thaizides:
1) "Contraction Alkalosis": Volume contraction -> increased ATII -> Na+/H+ exchange in proximal tubule-> increased HCO3- 2) K+ loss leads to: K+ exiting all cells (via H+/K+ exchanger) & H+ enters cells 3) "Paradoxical aciduria": In a low K+ state, H+ (rather than K+) is exchanged for Na+ in principle cells, leading to alkalosis |
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Which diuretics cause an increase in urine Ca2+?
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1) Loops
2) Mechanism: - Abolish lumen-positive potential in thick ascending limb of loop of Henle -> decrease in paracellular Ca+ reabsorption -> hypocalcemia |
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Which diuretics cause a decrease in urine Ca2+?
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1) Thiazides
2) Mechanism: - Block luminal Na+/Cl- cotransport in DCT -> increased Na+ gradient -> increased interstitial Na+/Ca2+ exchange -> hypercalcemia |
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In acute renal failure, what is the indication for dialysis?
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1) Severe hyperkalemia (elevated blood level of potassium)
2) A rapidly-rising potassium value 3) Severe acidosis 4) BUN >80 mg/dl or S/S uremia 5) Na Concentration <120mEq/L or >155mEq/L 6) Toxins: lithium or salicylates |
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What is a broad definition of acute renal failure?
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Abrupt decline in renal function + increased creatinine and BUN over a short period of several days
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What are the 3 stages of acute renal failure?
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1) prerenal azotemia
2) intrinsic renal 3) postrenal |
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What are the characteristics of prerenal azotemia?
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1) Decreased RBF (e.g. hypotension)
2) Reduced GFR 3) Na+/H2O & urea retained by the kidney |
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What are the characteristic lab values of prerenal azotemia?
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1) Urine osmolality: >500
2) Urine Na: <10 3) Fe of Na: <1% ***4) BUN/Cr ratio: >20 |
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What are the characteristic lab values of the intrinsic renal stage of acute renal failure?
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1) Urine osmolality: <350
2) Urine Na: >20 3) Fe of Na: >2% 4) BUN/Cr ratio: <15 |
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What are the characteristic lab values of the postrenal stage of acute renal failure?
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1) Urine osmolality: <350
2) Urine Na: >40 3) Fe of Na: >4% 4) BUN/Cr ratio: >15 |
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What are the characteristics of the intrinsic renal stage of acute renal failure?
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1) Causes: acute tubular necrosis or ischemia/toxins.
2) Patchy necrosis leads to debris obstructing tubule & fluid backflow across necrotic tubule leads to a decrease in GFR 3) Urine has epithelial/granular casts |
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What are the characteristics of the postrenal stage of acute renal failure?
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1) Cause: outflow obstruction (stones, BPH, neoplasia)
2) NB: ONLY develops with bilatral obstruction |
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What are the 2 forms of renal failure?
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1) Acute: usually due to acute tubular necrosis
2) Chronic: usually caused by hypertension & diabetes |
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What are the 8 possible consequences of renal failure?
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1) Anemia: failure of erthropoietin production
2) Renal osteodystophy: no vit. D production 3) Hyperkalemia: possible cardia arrhythmias 4) Metabolic acidosis: decreased acid secretion & reduced HCO3- production 5) Uremic encephalopathy 6) Na & H20 excess: CHF & pulmonary edema 7) Chronic pyelonephritis 8) Hypertension |
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What is uremia?
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A clinical syndrome marked by increased BUN & creatinine & associated symptoms
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What type of exchange limitation is caused by emphysema?
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1) Diffusion-limited exchange
2) Destruction of alveoli leads to a decreased surface area for gas exchange 3) T/F increased perfusion will not improve the exchange |
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In a diffusion-limited situation, will O2 fully equilibrate along the length of the pulmonary capillary?
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1) No.
2) As blood is oxygenated, the gradient driving O2 into the blood decreases. 3) T/F further equilibration would take more time &, in a diffusion-limited situation, there is not enough time & O2 will not equilibrate by the time it reaches the end of the capillary. |
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What gasses are perfusion-limited?
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1) O2 (in normal health)
2) CO2 3) N2O |
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What does it mean for a gas to be perfusion-limited?
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1) Gas equilibrates early along the length of a pulmonary capillary
2) Diffusion can be increased ONLY with an indrease in blood flow |
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What does it mean for a gas to be diffusion-limited?
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Gas does not equilibrate by the time the blood reaches the end of the pulmonary capillary
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What gasses are diffusion-limited?
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1) O2 (emphysema & fibrosis)
2) CO |
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What is the most severe consequence of pulmonary hypertension?
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Cor pulmonale & RV failure (JV distention, edema, hepatomegaly)
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How is the diffusion equation affected by emphysema?
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Decrease in Area
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How is the diffusion equation affected by pulmonary fibrosis?
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Increase in Thickness
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Give the diffusion equation.
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Vgas = A/T x Dk(P1-P2)
A = area T = thickness Dk(P1-P2) = difference in partial pressures |
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What are the pulmonary function findings in a case of COPD?
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Obstructive Pattern:
Increase in RV Decrease in FVC Decrease in FEV1 Decrease FVC Decrease FVC1/FVC ration (**) V/Q mismatch |
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What is the pathology of Chronic Bronchitis (Blue Bloater)?
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1) Hypertrophy of mucus-secreting glands in the bronchioles (small airways)
2) Reid index >50 3) Productive cough for > 3 consecutive months in 2(+) years 4) Findings: wheezing, crackles, cyanosis (early-onset hypoxemia due to shunting), late-onset dyspnea |
Reid index = gland depth / total thickness of bronchial wall
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What are the types of emphysema?
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1) Centriacinar: smoking
2) Panacinar: alpha-1-antitrypsin deficiency (or liver cirrhosis) 3) Paraseptal: bullae that rupture causing pneumothorax (often = otherwise healthy, young males) |
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What is the pathology of Emphysema (Pink Puffer with barrel-shaped chest)?
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1) Enlargement of air spaces and decrease in recoil resulting from destruction of alveolar walls
2) Increased elastase activity 3) Increased compliance due to loss of elastic fibers 4) Px exhale through pursed lips to increase airway pressure and prevent airway collapse during exhalation |
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What are the clinical findings in Emphysema?
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- Dyspnea
- Decreased breath sounds - Tachycardia - Late-onset hypoxemia due to eventual loss of capillary beds (loss of alveolar walls) - Early-onset dyspnea |
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What is the pathology of asthma?
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1) Bronchial hyperresponsiveness causes reversible bronchoconstriction
2) Smooth muscle hypertrophy & Curschmann's spirals (shed epithelium from mucous plugs) |
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What triggers asthma?
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- Viral URIs
- Allergens - Stress |
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What are the clinical findings of asthma?
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- Cough, wheezing, dyspnea
- Tachypnea - Hypoxemia - Reduced I/E ratio - Pulsus paradoxus - Mucus plugging |
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What is the pathology of Bronchiectasis?
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Chronic necrotizing infection of bronchi leads to permanently dilated airways, purulent sputum, recurrent infections, and hemoptysis
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What is Bronchiectasis associated with?
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- Bronchial obstruction
- CF - Poor ciliary motility - Kartagener's Syndrome - Development of Aspergillosis |
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What does an isolated prolonged PTT indicate?
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One of the following:
1) Factor XI, IX, & VIII deficiency 2) Presence of factor VIII inhibitor 3) Use of Heparin 4) Presence of lupus anticoagulant |
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If the PT test is prolonged, what other test will automatically be abnormal?
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the INR will be prolonged as well (that is, what is monitored in Warfarin Therapy
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What does a prolonged PT (& INR) indicate?
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One of the following:
1) Warfarin therapy 2) Liver Disease 3) Factor VII deficiency 4) Vitamin K deficiency |
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What does a combination of prolonged PT, INR, and bleeding time indicate?
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One of the following:
1) Warfarin therapy 2) Liver Disease 3) Factor VII deficiency 4) Vitamin K deficiency 5) vWF deficiency NB: the same as PT & INR, + vWF for platelet |
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What does prolongation of all coagulation parameters indicate?
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vWF deficiency or DIC
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What are the lab test results that indicate thrombocytopenia?
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1) Reduced Platlet Count
2) Increased Bleeding time 3) NORMAL PT & PTT |
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What are the lab test results that indicate Hemophilia A or B?
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All normal, except increased PTT
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What are the lab test results that indicate von Willebrand disease?
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1) Increased Bleeding Time
2) Increased PTT |
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What are the lab test results that indicate DIC?
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1) Decreased: platlet count
2) Increased: PT, PTT, & Bleeding Time |
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What are the lab test results that indicate Vitamin K deficiency?
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Increased PT & PTT
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What are the lab test results that indicate Bernard-Soulier disease?
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1) Decreased platelet count
2) Increased bleeding time |
Bernard-Soulier Disease: defect of platelet adhesion (reduced GP Ib)
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What are the lab test results that indicate Glanzmann's thrombasthenia?
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1) Increased bleeding time
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Glanzmann's Thrombasthenia = defect of platelet aGgredation (reduced GP IIb-IIIa)
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What factors are tested by PT?
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Extrinsic factors: II, V, VII, & X
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What factors are tested by PTT?
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Intrinsic: ALL, except VII
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What are Lewy bodies?
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1) Pink inclusions (aggregation of alpha-synclein proteins) in neurons of the substantia nigra
2) Patients with Parkinson's or Lewy body dementia |
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What are the clinical characteristics of Parkinson's?
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TRAP
1) Tremor (At rest) 2) cogwheel Rigidity 3) Postural instability 4) Bradykinesia |
bradykinesia: "slow movement", a slowness in the execution of movement.
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What disease classically presents with myoclonic fasciculations?
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Creutzfeld-Jacob
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1) Myoclonus: sudden, involuntary jerking of a muscle or group of muscles.
2) Fasciculation (or "muscle twitch"): a small, local, involuntary muscle contraction (twitching) visible under the skin arising from the spontaneous discharge of a bundle of skeletal muscle fibers. |
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What type of muscle weakness is seen in Guillain-Barre syndrome and amyotrophic lateral sclerosis?
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symmetrical
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What types of diseases present with tongue fasciculations?
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degenerative neurological diseases (e.g. spinal muscular atrophy & amyotrophic lateral sclerosis)
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What is the pathology of Parkinson's disease?
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1) A degenerative disorder of the CNS
2) Histo: Lewy bodies (alpha-synuclein) 3) Gross: depigmentation of the substantia nigra pars compacta (loss of dopaminergic neurons) 4) Rare cases linked with exposure to MPTP (a contaminnant in illicit street drugs) |
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Define "aphasia"
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Higher-order inability to speak
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Define "dysarthria"
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motor inability to speak
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Define Broca's aphasia.
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Broca's Broken Boca:
1) Nonfluent aphasia with intact comprehension 2) Broca's area: infereior frontal gyrus |
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Define Wernicke's aphasia.
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Wernicke's is Wordy buy makes no sense: Wernicke's = "What?"
1) Fluent aphasia with impaired comprehension 2) Wernicke's area: superior temporal gyrus |
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Define Global aphasia.
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1) Nonfluent aphasia with impaired comprehension
2) Both Broca's and Wernicke's areas are affected |
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Define Conduction aphasia.
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1) Poor repetition, but fluent speech
2) Intact comprehension 3) Arcuate fasciculus: connects Broca's & Wernicke's areas |
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Where is a lumbar puncture taken?
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Between L4 & L5 (Level of iliac crests)
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What structures are pierced in a lumbar puncture?
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1) Skin/Superficial fascia
2) Ligaments (Supraspinous, interspinous, ligamentum flavum) 3) Epidural space 4) Dura mater 5) Subdural space 6) Arachnoid NOT PIA: Pia is not Pierced |
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What is the likely tumor at the epiphyseal end of the femur in a 30-year-old woman?
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Giant cell:
1) Benign, primary bone tumor, aggressive 2) Radiography: double bubble or soap bubble sign 3) Histo: oval or spindle-shaped cells along with scattered multinucleated giant cells 4) Epidemiology: 20-40 year old, usually women |
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What patients are most susceptible to chondrosarcoma?
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1) Older men (30-60)
2) Malignant cartilaginous tumor of the pelvis, spine, scapula, humerus, tibia, or femur. 3) May be primary bone or from an osteochrondroma 4) Gross: expansile glistening mass within the medullary cavity |
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What is the most common benign bone tumor?
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osteochondroma: it occurs in men less than 25 years old, in the metaphysis of long tubular bones
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What is Ewing's sarcoma?
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Going out for Ewings & onion rings!
1) Aggressive malignant bone tumor; early met but responsive to chemo 2) Epidemiology: boys less than 15 years old 3) Histo: lamellated, "onion skin" periosteal reaction: uniform sheets of anaplastic, small blue cells 4) Gross: DIAPHYSIS of bones, pelvis, scapula, ribs 5) 11:22 translocation |
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What is osteosarcoma?
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2) Epidemiology: Males, 10-20 years old
3) Gross: METAPHYSIS of long bones 4) Radiography: 2 growth patterns: - Codman's Triangle: elevated periosteum - Sunburst growth pattern: reactive bone formation |
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List the 6 benign bone tumors.
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1) Osteoma
2) Osteoid Osteoma 3) Osteoblastoma 4) Giant Cell (Osteoclastoma) 5) Osteochondroma (exostosis) 6) Enchondroma |
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List the 3 malignant bone tumors.
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1) Osteosarcoma (osteogenic sarcoma)
2) Ewing's Sarcoma 3) Chondrosarcoma |
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What is an osteoma?
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1) Benign bone tumor
2) New pieces of bone grows on another piece of bone, often in the SKULL 3) Associated with Gardner's syndrome (FAP) |
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What is an osteoid osteoma?
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1) Benign bone tumor
2) Interlacing trabeculae of woven bone are surrounded by osteoblasts 3) <2cm; proximal tibia or femur 4) Men <25 years old |
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What is an osteoblastoma?
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1) Benign bone tumor
2) Interlacing trabeculae of woven bone are surrounded by osteoblasts 3) can be large; vertebral column 4) 20-40 year old Px |
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What is a Giant Cell tumor?
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1) Locally aggressive benign tumor often around the distal femur, proximal tibial region (KNEE)
2) Radiology: "double bubble" or "soap bubble" 3) Spindle-shaped cells with mutinucleated giant cells 4) 20-40 year old Px |
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What is a Osteochondroma?
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1) MOST COMMON BENIGN bone tumor
2) Mature bone with cartilaginous cap 3) Males <25 years of age 4) Origin: long metaphysis |
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What is an enchondroma?
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1) Benign cartilaginous neoplasm found in intramedullary bone
2) Usually DISTAL extremities |
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What is an osteosarcoma?
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1) 2nd most common primary malignant tumor of bone (after multiple myeloma)
2) Peat incidence: males 10-20 years old 3) METAPHYSIS of long bones: distal femur, proximal tibial region (knee) 4) Predisposing factors: Paget's disease of bone, bone infarcts, radiation, familial retinoblastoma 5) Radiography: Codman's triangle or sunburst pattern 6) Poor prognosis |
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What is the mechanism of albuterol?
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Increases conversion of cAMP by adenylate cyclase:
- activates B2-adrenergic receptors on smooth muscle cells to activate adenylate cyclase. - Adenylate cyclase then converts ATP to cAMP - SMOOTH MUSCLES RELAX |
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What lymphoma presents with aggressive onset of thrombocytopenia, anemia, and a lg. mediastinal mass?
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ALL (Acute Lymphoblastic Lymphoma):
- lymphoblasts in blood and bone marrow - Epidemiology: children < 15 years old |
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What makes a pneumonia "atypical"?
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1) insidious onset
2) Nonproductive cough 3) streaky interstitial infiltrate on chest radiograph 4) Most common cause: Mycoplasma (confirm with cold agglutinin test): contains cholesterol in membrane 5) Rx: Erythromycin or tetracyclin (b/c NO CELL WALL) |
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What is the pathogenesis of acute intermittent porphyria (AIP)?
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1) Deficiency is porphobilinogen deaminase
- leads to a deficiency in heme synthesis & buildup of intermediates like aminolevulinic acid & porphobilinogen 2) Acute attacks of GI, neurological/psychiatric, & heart symptoms 3) Onset after puberty, more common in women 4) Symptoms can be brought on by drugs that INDUCE cytochrome P450 |
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What drug prevents growth, survival, and division of Estrogen-positive cancer cells and is thereby prescribed to certain breast cancer patients?
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Raloxifene: it also increases bone mass
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What is the expected respiratory carbon dioxide change expected for every 1-mEq/L bicarbonate increase?
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- The PCO2 should increase by 0.7mm Hg per 1mEq/L increase in bicarbonate.
- A normal bicarbonate is 24 mEq/L & a normal PCO2 is 40 mmHG. |
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What are the causes of secondary cardiac tamponade?
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1) Trauma
2) hypothyroidism 3) Myocardial rupture 3) Complication of pericarditis (esp. due to malignancy or uremia) |
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What is Beck's Triad?
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Signs of cardiac tamponade:
1) Distant heart sounds 2) Increased JVP 3) Hypotension Also, pulsus paradoxus: systolic Bp drops by >10mmHg on inspiration |
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What is the best treatment for cardiac tamponade?
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1) First: Immediate volume resuscitation (IV fluids) to maintain cardiac output & increase preload
2) 2nd: Positive iontropes (dobutamine & pericardiocentesis) |
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What drug has the side effect of a brown darkening of the iris?
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Latanoprost: prostaglandin prodrug used to increase the outflow of aqueous humor in glaucoma or increased intraocular pressure
- side effect occurs in 10% of patients |
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What is Wallenberg's syndrome?
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AKA: lateral medullary syndrome:
1) Stroke: dissection & thrombosis of vertebral artery & posterior inferior cerebellar artery |
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What symptoms indicate an infarction of the lateral medulla?
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1) Spinal trigeminal nucleus: loss of pinprick sensation on the right face
2) Spinothalamic track: loss of pinprick sensation on the left below the neck 3) Inferior cerebellar peduncle: ataxia 4) Vestibular nucleus: nystagmus 5) Dorsal motor nucleus of vagus: hoarsness 6) Descending sympathetic fibers: Horner's syndrome (ptosis, miosis, anhidrosis) |
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Where in the medulla do vibratory & proprioceptive info course?
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Medial: medial lemniscus
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What paraneoplastic syndrome is produced by small cell carcinoma?
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Cushing's syndrome (ectopic ACTH)
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What paraneoplastic syndrome is caused by squamous cell carcinoma of the lungs?
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Hypercalcemia: cells produce parathyroid homone-related peptide.
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What type of drugs for CHF cause a urinalysis with the following findings:
- pH 5.5 - increased NaCl, K, Ca concentrations |
Loops (like furosemide): Loops Lose calcium, stimulate acidification by increasing distal Na delivery & transport (this causes a favorable electric gradient for K & H+ secretion)
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Can there be "carriers" of AD diseases?
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No.
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In diseases that cause a decrease in intestinal cells, what step of lipid digestiong & absorbtion is impaired?
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Chylomicron formation, this step occurs within the intestinal cells (reestrification)
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What cause croup?
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Parainfluenza virus is a common cause
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What is arcus lipoides
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Opaque rings found on the endge of the iris that indicate type IIa familial dyslipidemia (familial hypercholesterolemia)
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What is the difference in prognosis for those heterozygous and homozygous patients with familial hypercholesterolemia?
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This disease is AD:
1) Homozygous: MI in 1st decade of life 2) Heterozygous: elevated LDL that may manifest in middle age |
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What brain tumor is a feature of vonHippel-Lindau disease?
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Hemangioblastoma (benign) of the cerebellum or retina:
- Patients present with headache - Findings include papilledema, nystagmus, & ataxia (& 2ndary polycytemia due to epo secretion by the tumor) - Tx: surgical resection |
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What is the cause of von Hippel-Lindau disease?
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- AD disease that results in a deletion of a tumor suppressor gene on Chromosome 3
- Features: cysts of kidney, pancrease, polycytemia, hemangioblastoma of cerebellum or retina |
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What are the signs of chronic vitamin A (retinol toxicity)?
|
- Ataxia
- Alopeica - Headache - Fatigue - Bone & joint pain - Muscle pain - Visual disturbances - Hyperlipidemia - Hepatotoxicity - Dry mucous membranes - Lip Fissures |
|
|
What are the signs of acute vitamin A (retinol toxicity)?
|
1) Nausea
2) Vomiting 3) Vertigo 4) Blurry vision Severe: drowsiness & altered mental status |
|
|
What is the pathogenesis of the allergic reaction to aspirin
|
increase leukotriene syntheses leads to bronchoconstriction: b/c the cyclooxygenase-catalyzed prostaglandin pathway is blocked
|
|
|
What drug can stop the bronchoconstriction due to aspirin allergy?
|
Zileuton: Inhibits the 5-lipoxygenase pathway to block the conversion of arachidonic acid to leukotrienes
|
|
|
What are the most common arteries targed by peripheral atherosclerosis?
|
1) abdominal aorta
2) Iliac 3) Femoral 4) Popliteal (can present with intermittent claudication) 5) tibial 6) popliteal |
|
|
What is the mechanism of action of zanamivir?
|
Inhibits neuraminidase enzyme that is critical to the influenza life cycle (A & B) & blocks the release of progeny virons as there is no cleavage of neuraminic acid to release the viron with host cell membrane cover.
|
|
|
What cell types and cytokines drive asthma?
|
1) hyperresponsive T lymphocytes in the lung (esp. Th2)
2) Il-4, Il-5, Il-3 |
|
|
What are the main causes of eosinophilia?
|
- Asthma
- Neoplasms - Parasites - Collagen vascular diseases - Allergic processes |
|
|
What is the microscopic pathology of hypertrophic obstructive cardiomyopathy (or asymmetric septal hypertrophy and idiopathic hypertrophic subaortic stenosis)
|
AD in 50% of cases:
myofiber hypertrophy & disarray |
|
|
What triad indicates classic carcinoid syndrome?
|
1) Chronic diarrhea
2) Intermittent facial flushing 3) Tricuspid stenosis murmur |
|
|
Under what conditions are carcinoid syndrome present?
|
When there is a liver metastases of a GI carcinoid (b/c then the liver cannot metabolize the serotonin produced within the liver)
|
|
|
What is the pathogenesis of the right heart valvular disease of cardinoid syndrome?
|
Serotonin-mediated fibroelastosis
|
|
|
What urine test finding is diagnostic of carcinoid syndrome?
|
Elevated 5-HIAA
|
|
|
Which viruses establish latency in the dorsal root gangila?
|
1) Herpes simplex 1 & 2
2) Varicella-zoster |
|
|
What is one of the 1st signs seen in a post-MI biopsy within 12 hours of the infarction?
|
Contraction bands @ the margin of the necrotic area due to elevated intracellular calcium & the resultant hypercontraction.
|
|
|
What is the principle function of the anterior cruciate ligament?
|
To prevent anterior subluxation (misalignment) of the knee relative to the femur anterior in the fully extended position.
|
|
|
How does hydroxyurea help sickle cell patients?
|
It increases fetal hemoglobin production in place of hemoglobin S & thereby reduces RBC sickling and complications there of.
|
|
|
What infects does the spleen clear? What if the spleen is gone?
|
1) Encapsulated bacteria
2) Prophylaxis with fluorquinolones and macrolides |
|
|
What are the 2 major clinical features of nephrotic syndrome?
|
1) Edema: low plasma oncotic pressue due to protein wasting & sodium retention from the collecting tubules
2) Massive proteinuria, hypoalbuminemia, hypercholesterolemia |
|
|
What is Ortner's syndrome?
|
An enlarged left atrium compresses the left recurrent laryngeal nerve:
- Causes hoarseness - Is a branch of the vagus & innervates on "glossus", the palatoglossus |
|
|
What muscles does the hypoglossal nerve innervate?
|
All intrinsic & extrinsic tongue muscles (except the palatoglossus, which is innervated by the vagus & helps to raise the back of the tongue)
|
|
|
Explain the process of serum sickness? What type of immune reaction is it?
|
- Type III: immune complex deposition (in skin: rash, in kidney: glomerulonephritis)
- Humoral immune response against foreign protein: 7-10 days later as antibodies must be produced (requires T-helper cells) |
|
|
What is the toxicity of oligomycin?
|
This antibiotic blocks ATP synthesis by binding to the stalk of the ATP synthases. T/F it blocks protein re-entry to the matrix.
|
|
|
What is the toxicity of 2.4 Dinitrophenol?
|
It is an uncoupling protein that results in decreased ATP
|
|
|
What is the toxicity of Antimycin A?
|
Binds to cytochrome c reductase & prevents further continuation of the electron transport chain in ATP synthesis.
|
|
|
What is the toxicity of Cyanide?
|
Binds the Fe3+ of cytochrome oxidase a3 & prevents the last enzyme of oxidative phosphorylation & ATP production?
|
|
|
What is Rotenone's toxicity?
|
Inhibits transfer of electrons to ubiquinone & thus stops ATP production
|
|
|
How does E. coli acquire the Shiga-like toxin that can cause bloody diarrhea & hemolytic-uremic syndrome?
|
specialized tranduction transfer: a lysogenic bacteriophage incorporates foreign DNA into its host.
|
|
|
What is conjugation?
|
1 bac extends its mating pili to another without the F plasmid & transfers this plasmid to the 2nd bac (& maybe also some adjacent DNA)
|
|
|
What is bacterial transformation?
|
DNA is taken up directly from the environment by a bac
|
|
|
What is bacterial transposition?
|
DNA segments can jumpt to various locations within a genome as well as in a plasmid & can then by passed on.
|
|
|
What does the trochlear nerve innervate?
|
IV: superior oblique muscle. Injury leads to CN IV palsy: diplopia that worsens when they look down and away from the affected side
|
|
|
What is the first line drug choice for BPH & what is that drug's mechanism of action?
|
Tamsulosin:
- Smooth muscle tension is mediated by alpha-1-adrenergic receptors and these are selectively blocked. |
|
|
How do integrases treat HIV?
|
Prevents the formation of a proviral infection
|
|
|
What is the mechanism of the gram-negative rod Bordetella pertussis's toxin?
|
- The A subunit inhibits membrane-bound Gi proteins that results in the accumulation of cAMP.
- This results in histamine sensitization, increased insulin synthesis, lymphocytosis, and the inhibition of phagocytosis. - Result: whooping cough |
|
|
What is the mechanism of the alpha toxin of S. aureus and Streptolysin O of S. pyrogens?
|
Binds to the membrane and allows ions and small molecules to enter the cell. This leads to swelling & eventual cell lysis.
|
|
|
What is the mechanism of action of C. diptheriae's exotoxin & P. aeruginosa's exotoxin A?
|
Inactivates elongation factor 2, causing pharyngitis & the pseudomembrane of the throat.
Rx: antitoxin (to prevent membrane spread & airway obstruction), penicillin or erthyromycin & DTP vaccine |
|
|
What is the mechanism of action of C. botulinum's toxin?
|
Inhibition of the release of acetylcholine into the synaptic cleft. This leads to muscle weakness and paralysis?
|
|
|
What is an endotoxin?
|
Lipopolysaccharide-lipid A, a part of the bacterial membrane of all gram-negative bac (except L. monocytogenes)
|
|
|
What is a common extraintestinal manifestation of Chron's disease?
|
migratory polyartheritis
|
|
|
Which has a higher cancer risk: UC or Crohn's?
|
Ulcerative colitis
|
|
|
Which disease almost always affects the rectum: UC or Crohn's
|
UC: 50% of UC cases are even limited exclusively to the rectum
|
|
|
Which condition is associated with sclerosing cholangitis: UC or Crohn's
|
UC. This results in dilation of the biliary ducts, fibrosis of the liver & eventual hepatic failure.
|
|
|
What is another name for Guillain-Barre syndrome?
|
acute inflammatory demyelinating polyradiculopathy.
NB: radiculopathy: disease of spinal nerve roots and spinal nerves |
|
|
What is the histological findings in Guillain-Barre syndrome?
|
- Segmental demyelination of areas of peripheral nerves (possibly including inflammation of the axons themselves)
- This results in slower conduction velocity of action potentials through peripheral nerves & spinal nerve roots |
|
|
How do you calculate Mean Corpuscular volume (MCV)?
|
[Hematocrit/RBC count] x 10
|
|
|
How can you histologically distinguish iron deficiency anemai from a thalassemia?
|
- Thalassemia will have target cells
- Both will be microcytic & hypochromatic |
|
|
What is the Mentzer index?
|
- RBC MCV/RBC
- < 13 in Px with iron deficiency anemia & <13 in patients with thalassemia |
|
|
What Mentzer index values distinguish iron deficiency anemia from thalassemia?
|
> 13 is iron deficiency
< 13 is thalasemia |
|
|
What is Lambert-Eaton syndrome?
|
Oat (small) cell carcinoma produces antibodies against presynaptic Ca channels @ the neuromuscular junction:
- proximal muscle weakness - decreased deep tendon reflexes - diplopia |
|
|
What is another name for nonbacterial thrombotic endocarditis?
|
Libman-Sacks endocarditis (a symptom of SLE):
- single or multiple 1- to 3-mm verrucous deposits on the edge of either surface of the valve leaflets on any heart valve - Usually, mitral, aortic, & tricuspid - Histo: immune complexes, mononuclear cells, hematoxylin bodies, fibrin, & platelet thrombi - Healing = fibrosis, scarring, & calcification = valve damage, regurg, & predisposition to bac. endocarditis - fibrin & platelet thrombi may embolize systemically |
|
|
What is the Whipple triad & what does it indicate?
|
1) episodic hypoglycemia, CNA symptoms (confusion, stupor, convulsions, & coma), & reversal of CNS symptoms with glucose
2) insulinoma (islet; that is, B cell tumor), either benign or malignant = elevated C peptide & insulin levels |
|
|
What are the characteristic symptoms of Hodgkin's lymphoma?
|
- Night sweats, fever, & weight loss
- Also, mediastinal lymphadenopathy - Histo: Reed-Sternberg cells: cells with large, "owl eye" binucleate cells; and reactive lymphocytes |
|
|
What is the short-term compensation for high-altitude hypoxia?
|
An increase in 2,3-diphosphoglycerate (2,3-DPG) to release more O2 to tissues)
- This causes an increase in the P50 (partial pressure of O2 at 50% saturation of hemoglobin) and a right shift in the hemoglobin-O2 curve |
|
|
What are the principle functions of thyroid hormone in development?
|
Bone Growth
CNA maturation |
|
|
What are the primary functions of somatostatin?
|
1) Inhibits all GI & pancreatic exocrine & endocrine functions & inhibits the release of insulin
2) Inhibits GH & prolactin release by the pituitary |
|
|
What are the side effects of octreotide (exogenous somatostatin) administration?
|
Nausea
Vomiting Diarrhea Gallstone-related illness |
|
|
What are the characteristics of Renal Tubular Acidosis (RTA)?
|
Non-anion gap, hyperchloremic, metabolic acidosis
|
|
|
What problem is associated with ngiotensin-converting enzyme inhibitors, timethoprim, and heparin?
|
RTA IV: inability to secrete sufficient acid into the urine due to hypoaldosteronism
- hypoaldosteronism leads to decreased Na reuptake in the distal convoluted tubule & collecting duct - This decreases excretion of K into the urine = kyperkalemia - Hyperkalemia results into H+ ion shift to the extracellular fluid to maintain a K balance = metabolic acidosis - The alkalotic environment of the renal tubule cells = low ammonia & H+ production & secretion. T/F the kidney cannot secrete the excess bodily acid - Low ammonia = unbuffered urine & a low pH (below 5.5) |
|
|
What are the stimuli for insulin secretion?
|
1) Hyperglycemia (primary stimulus)
2) Increase in fatty acids in the blood 3) Increase in amino acids in the blood 4) Cortisol 5) GH 6) Gastrointestinal inhibitory peptide |
|
|
What causes a physiological right-shift of the Oxygen-Hemoglobin curve in exercising persons?
|
Right shift = decrease affinity of hemoglobin for O2 & more tissue-unloading of O2:
1) Decrease: tissue pH (up H+ concentration) 2) Increase: Temperature & partial pressure of CO2 |
|
|
Why are excercising patients not loosing too much CO2 due to increased respiration?
|
Tissue CO2 production due to aerobic respiration
|
|
|
What is the formula for physiologic dead space (Vd)?
|
tidal vlume x ([arterial CO2 pressure - expired air CO2 pressure] divided by the arterial CO2 pressure
or Vt x ([PaCO2 - PeCO2] / PaCO2) |
|
|
What is the equation for renal blood flow? What can be done to increase flow?
|
1) Flow = (change in pressure) / resistance
2) Decreasing resistance will increase flow: - low levels of dpamine dilate renal arterioles - bradykinin induces vasodilation of arterioles |
|
|
What is the equation for renal blood flow? What can be done to decrease flow?
|
1) Flow = (change in pressure) / resistance
2) Increasing resistance will decrease flow: - Stimulating afferant alpha1-adrenergic receptors will vasoconstrict the arteriole - Stimulating afferant angiotension II receptors will vasoconstrict the arteriole |
|
|
What is the iodine status of a pregnant woman?
|
Relative deficiency: due to increased renal clearance
|
|
|
What lab values indicate an isolated respiratory alkalosis?
|
low CO2 and low HCO3- levels
|
|
|
What can cause an isolated respiratory alkalosis?
|
hyperventilation due to anxiety/panic/pain (sympathetic stimulation) or high altitude or low O2
|
|
|
What type of limited gas is O2, diffusion or perfusion?
|
Perfusion: gas exchange can only increase or decrease with an increase or decrease in blood flow.
|
|
|
What hormone maintains lactation?
|
Prolactin from the anterior pituitary
|
|
|
How does lactation prevent ovulation?
|
- Inhibits secretion of GnRH (Gonadotropin-releasing hormone) from the hypothalamus.
- This inhibits secretion of LH and FSH from the anterior pituitary |
|
|
What are 2 common causes of hyperprolactinemia?
|
1) Tumors
2) Antipsychotic drugs (dopamine antagonists = increase prolactin as dopamine usually inhibits prolactin release) |
|
|
Is pepsin a high or low pH active enzyme?
|
Low; if antacids or used protein digestion can be impaired and patients will often have constipation
|
|
|
What are the steps to DNA binding from circulation that a steroid hormone undergoes?
|
1) Enters cell membrane (lipophilic)
2) Binds to an intracellular receptor in the cytoplasm or within the nucleus 3) The hormone-receptor complex transforms to reveal the hormone's DNA binding domain 4) The hormone binds to the DNA enhancer element & generates gene transcription. |
|
|
What respiratory cause of hypoxemia cannot be overcome by supplimental O2?
|
A shunt, e.g. alveolar collapse, where blood flows through some capillaries without any gas exchange
|
|
|
Which respiration problems result in a large A-a gradient?
|
1) Shunt
2) ventilation-perfusion mismatch 3) Diffusion impairment |
|
|
How does imipramine change a patient's sleep pattern?
|
- Decrease in stage 4 or slow wave (delta: large & slow wave) sleep.
- Stage 3 &4 is when disorders including night terrors, sleepwalking, and enuresis take place. |
|
|
How do central chemoreceptors respond to blood pH and partial gas pressures?
|
1) Increase PCO2 or decreased pH = increase in total peripheral resistance
2) Mechanism: systemic vasoconstriction via sympathetic outflow |
|
|
How does the Na+/H+ exchanger in the proximal tubule facilitate Na & water resorption?
|
1) H+ is pumped into the tubual lumen
2) Luminal H+ then returns to the tubular cell in the process of HCO3- resorption: - H+ & HCO3- join to form H2O via carbonic anhydrase at the brush boarder - H20 & CO2 diffuse into the tubular cell 3) HCO2 is regenerated in the tubular cell (& sent to the bloodstream) & H+ is left behind to participate in the exchanger again. |
|
|
What is the physiology of high fat food pain in patients with gallstones?
|
CCK (cholecystokinin) is released in the duodenum after a fatty meal (& amino acids) to induce gallbladder contraction & thus the stone obstruction causes pain.
|
|
|
Which Coombs test detects antibodies attached to RBCs & which detects antibodies circulating in serum?
|
Direct: antibodies on RBCs
Indirect: antibodies in serum |
|
|
What is the correct order of MI blood test markers?
|
1) Troponin I (elevated w/in 4 hours; remains for 7-10 days)
2) CK-MB (peaks w/in 24 hours & falls off) - best for monitoring post-MI for a new infarct w/in 1 wk 3) AST (increases over 1st 2 days; slowly declines): NOT SPECIFIC, like myoglobin 4) LDH (elevated 2-day post MI; remains elevated for 7 days) |
|
|
What is contraction alkalosis?
|
- Loss of volume without losing bicarbonate
- E.G. Excessive diuresis with a loop diuretic; CF patient outside too long on a hot day |
|
|
What is the mechanism of action of Losartan?
|
Inhibits angiotension II receptor: angiotension II is formed from angiotension I by the ACEnzyme in the lung capillaries
|
|
|
During which interval does isovolumetric relaxation occur in the heart?
|
During early ventricular diastole: ventricles relax with aortic & matral valves closed
|
|
|
What side effect is shared by Demeclocycline & lithium?
|
- Nephrogenic diabetes insipidus: these drugs inhibit the kidneys' response to ADH.
- DDx: Exogenous ADH administration or a hold on fluids will not improve symptoms. |
|
|
Which form of diabetes insipidus will be corrected by exogenous ADH administration?
|
Central DI
|
|
|
How is prolactin secretion regulated?
|
- Prolactin increases dopamine synthesis & secretion from the hypothalamus
- Dopamine itself inhibits prolacin secretion from the anterior pituitary |
|
|
In what environment is one more likely to isolate deoxyhemoglobin? What about oxygemoglobin
|
1) Deoxyhemoglobin (T form): low-O2 affinity state = peripheral capillaries
2) Oxyhemoglobin (R form): high O2 affinity state = pulmonary capillary bed |
|
|
What does the P wave represent?
|
Depolarization of the atria (NOT contraction)
|
|
|
What does the PR segment represent?
|
- isoelectric (flat) portion of AV node conduction
|
|
|
What does the PR interval represent?
|
Time of initial depolarization of the atria to the initial depolarization of the ventricles (a pathological delay can occur here)
|
|
|
What does the QRS complex represent?
|
Vetricular depolarization
|
|
|
What does the T wave represent?
|
ventricular repolarization
|
|
|
What does the ST segment represent?
|
- Legnth from the end of QRS to initial deflection of T wave
- That is, the end of ventricular depolarization to the beginning of ventricular repolarization |
|
|
What does the QT interval represent?
|
Time between the start of ventricular depolarization and the end of ventricular repolarization
- from the onset of the QRS complex to the end of the T wave |
|
|
What is the change in menapause that brings on the usual lab results of increased LH and FSH?
|
Follicular depletion with a resultant decrease in estrogen secretion; this leads to no negative feedback on:
- gonadotropin-releasing hormone - follicle-stimulating hormone (FSH) - luteinizing hormone (LH) |
|
|
What is the action of infliximab?
|
- It is a chimeric monoclonal antibody. It bings to soluble TNF-alpha (secreted by macrophages & found in high [] in Crohn's patients)
- Rx: Crohn's; a single infusion = clinical response in 65% of Px - Side Effects: Headache, GI distress, increased upper respiratory infections |
|
|
What drugs, in combo with St. John's wort cause serotonin syndrome?
|
SSRs (liek sertraline)
Seratonin Syndrome: mental status changes, autonomic changes (fever, diaphoresis, tachycardia, tremor, rigidity) |
|
|
What CSF findings indicate bacterial meningitis?
|
- Increased protein
- Decreased glucose |
|
|
What is the most common cause of meningitis in infants (0-3 months old)?
|
- Lysteria monocytogenes (gram positive rod)
- E. coli (gram - rod) - Group B strep (gram + cocci) |
|
|
What is the anti-cancer action of etoposide?
|
G2 phase action: inhibits topoisomerase II (results in irreversibel ds breaks in DNA) & prevents synthesis of components needed for mitosis
|
|
|
Which cells are "output" cells of the cerebellum? What neurotransmitter do they employ?
|
1) Purkinje cells
2) GABA: all these outputs are inhibitory |
|
|
What artery supplies both the head of the pancreas & the duodenum?
|
gastroduodenal artery (branch of the celiac trunk) & superior mesenteric
|
|
|
What are the 3 ps of Multiple Endocrine neoplasia type 1?
|
3 tumors:
Pancrease Pituitary Parathyroid |
|
|
What physical diagnosis finding is characteristic of parathyroid-hormone-secreting adenoma?
|
History of renal stones & neck nodule
|
|
|
What is the genetics of myotonic dystrophy?
|
Autosomal dominate with a CTG trinucleotide repeat with anticipation
E.G. a mom with a 50-100 repeat can have a symptomatic child with a 1000-1500 repeat |
|
|
Where is the narrowing in a Px with infantile coarctation of the aorta?
|
Preductal: between subclavian artery & ductus arteriosus
|
|
|
What is the MOPP regiment & what is it used to treat?
|
1) Mechlorethamine, vincristine (Oncovin), Procarbazine, & Prednisone
2) lymphoma, Wilm's tumor, Choriocarcinoma |
|
|
What is the action of Vincristine?
|
Vinca alkaloid: binds to tubulin & prevents polymerization into microtubules. T/F there is no mitotic spindle formation & no mitosis.
Rx: testicular carcinoma & Hodgkin's & non-Hodgkin's lymphomas |
|
|
What is the action of methotrexate?
|
- It is a DNA and protein synthesis inhibitor
- Folic acid antagonist: inhibits dihydrofolate reducatase during the S phase |
|
|
What is a good drug to compliment methotrexate therapy?
|
- Leucovorin: it is folinic acid & helps to replinish the body's supply of folic acid.
- T/F it inhibits the myelosuppressive effects of methotrexate |
|
|
What is the equation for PPV?
|
- True Positives divided by those who tested positive
- Higher prevalence = higher PPV (increased numerator & denominator) & lower NPV (increased denominator only) - Lower prevalence = lower PPV (increase in denominator only) & greater NPV (increase in numerator & denominator) PPV = TP/(TP+FP) NPV = TN(TN+FN) |
|
|
What is a complication of neonatal meningitis?
|
1) Menigeal scarring: can lead to a decrease in CSF absorption by arachnoid villi (= nonobstructive/communicating hydrocephalus)
2) Tx: shunt |
|
|
What is a side effect of nonselective B-blockers?
|
Vasoconstriction of peripheral vessels by blocking B2-mediated vasodilation
|
|
|
How is T. gondii transmitted?
|
Cysts in raw meat
Cat feces |
|
|
What is the treatment for toxoplasmosis?
|
Sulfadiazine & pyrmethamine
|
|
|
What class of antiarrhythmics is Lidocaine?
|
Class Ib:
- it blocks sodium channels & decrease action potential duration - selective for ischemic or depolarized purkinje & ventricular tissue Other Ib: mexiletine & tocainide |
|
|
Which part of the myocardium is the first to undergo necrosis due to prolonged ischemia?
|
ventricular wall (last to be perfused)
|
|
|
Where is a Pancoast tumor located?
|
Superior pulmonary sulcus; grows towards thoracic inlet & can damage structures that exit that region:
- bracial plexus, stellate ganglion, & sympathetic chain |
|
|
What are the 3 major mechanisms that limit the extent of coagulation?
|
1) activity of tissue factor pathway inhibitor
2) activity of antithrombin III 3) activity of activated proten C with cofactor protein S |
|
|
When a Px is vitamin K deficient, why do they exhibit a coagulation overactivation?
|
Protein C is not gamma-carboxylated & thus does not become active to cleave factors Va & VIIIa
|
|
|
Where are bile acids recirculated to the liver?
|
Terminal ilium via a Na-bile cotransporter
|
|
|
Where is iron absorbed?
|
Duodenum
|
|
|
What drugs cause a lupus-like syndrome?
|
1) quinidine
2) minocycline 3) isoniazid 4) valproate 5) hydralazine 6) penicillamide 7) sulfasalazine 8) procainamide |
|
|
What are the % risks for needle-stick contraction of Hep B, C, & HIV
|
Hep B: 30%
Hep C: 10% HIV: 0.3 - 0.45% |
|
|
What is Waldenstrom's macroglobinemia?
|
B-cell neoplasm secreting lg. amounts of IgM:
- headaches & vision problems (impaired crania blood flow) - weakness - weight loss - increased bleeding (due to inhibited clotting factors) - monoclonal M spike on serum protein electrophoresis (lg. spike in the gamma region) |
|
|
Why are some B-blockers nephrotoxic?
|
- B/C they can induse rhabdomyolysis & T/F excretion of myoglobin by the kidneys.
- Myoglobin is nephrotoxic = ATN |
|
|
What is an early sign of salicylate toxicity?
|
Tinnitus
|
|
|
What part(s) of the body are associated with the 2nd stage of Lyme disease?
|
Skin, CNS, heart, & joins
|
|
|
What is damaged when a Px presents with expressive aphasia?
|
Broca's area (inferior frontal gyrus)
NB: this is near the primary motor cortex, so lower arm & face paralysis can also occur. |
|
|
What is the symptoms of a C. trachomatisis congenital infection?
|
1) Eye inflammmation with purulent discharge & eyelid swelling at 5-14 days after birth
2) Can spread to the lungs & cause pneumonia between 4-11 weeks of life: rapid breathing, cough, & respiratory distress 3) Histo: BIG intracytoplasmic inclusions push the nucleus to the cell periphery. |
|
|
What bacteria presents with abdominal cramps, fever, & bloody diarrhea? (There are C-shaped organisms on stool analysis)
|
Campylobacter jejuni (Rx: erythromycin)
- Untreated: Guillain-Barre syndrome - acute symmetric ascending muscle weakness with parethesias that begins in the lower extremities that results from an inflammation & demyelination of peripheral nerves |
|
|
How does the kidney respond to hypovolemic shock?
|
Increases glomerular capillary hydrostatic pressure through intravascular fluid retention & efferent arteriole constriction to retain GFR
|
|
|
What is the clinical presentation of Lesch-Nyhan syndrome?
|
1) Hyperuricemia
2) Excessive production of uric acid = GOUT 3) Neuro: self-mutilation choreoathetosis, spasticity, mental retardation, aggressive behavior |
|
|
What kind of disorder is Lesch-Nyhan and what is the pathogenesis?
|
1) Genetic: X-linked recessived
2) Deficiency in the production of hypoxanthine guanine phosphoribosyltransferase (HGPRTase) --> overproduction of purine & the accumulation of uric acid |
|
|
Patients with what genetic disorder are at risk for anemia when treated with isoniazid?
|
1) G6PD deficiency
2) The anemia will show histologically as Heinze bodies (dark inclusions of precipitated globin chains) & bite cells 3) anemia can also be produced after exposure to sulfonamides, antimalarial drugs and oxidative stress. |
|
|
What intermediate of the TCA cycle inhibits the rate-limiting enzyme of glycolysis & activates the rate-limiting enzyme of fatty acid synthesis?
|
Citrate
- inhibits phosphofructokinase - activates acetyl CoA arboxylase |
|
|
What is the mechanism of diptheria toxin?
|
Inhibits elongation factor EF2-alpha:
- Normally: EF2-alpha complexes with guanosine triphosphate & binds to the ribosome to initiate the translocation step of protein synthesis. |
|
|
Which antibiotics inhibit the 30S subunit of prokaryotic ribosomes?
|
Tetracycline
Aminoglycosides |
|
|
What is the mechanism of action of the botulinum toxin?
|
inhibition of acetylcholine release, which results in flaccid paralysis
|
|
|
What results from damaging the accessory nerve root?
|
winging of the scapula (trapezius) and impaired neck rotation (sternocleidomastoid)
|
|
|
Damaging which nerve will result in a monotone voice?
|
external laryngeal nerve (terminal branch of the superior laryngeal, a branch of the vagus)
|
|
|
What does the phrenic nerve supply?
|
- diaphragm, mediastinal pleura, pericardium
- it arises from C3-C5 |
|
|
What nerve damage results in "waiter's tip" palsy?
|
suprascapular nerve: loss of lateral roation of the humerus at the shoulder (supraspinatus & infraspinatus)
|
|
|
What are the symptoms of 17-alpha-hydroxylase deficiency?
|
- primary amenorrhea
- lack of 2ndary sexual characteristics - elevated aldosterone = hypokalemia (low potassium) & hypertension |
|
|
What is the inheritance pattern for hereditary spherocytosis?
|
Autosomal dominant defect in spectrin protein of erythrocyte membranes
- increased mean corpuscular hemoglobin concentration - large RBCs w/o a central pallor - Dx: osmotic fragility test - late complications: bilirubin gallstones & cholecystitis |
|
|
How is autoimmune hemolytic anemia differentiated from hereditary spherocytosis?
|
Autoimmune hemolytic anemia will have a positive direct Coomb's test
|
|
|
What is the mechanism of HIV encephalitis?
|
Infection of brain macrophages & microglia:
- Histo: microglial nodule = multinucleated giant cells (fusion of HIV-infected microglial cells |
|
|
What cells are infected by the JC virus?
|
oligodendrocytes: results in progressive multifocal leukoencephalopathy
|
|
|
What is the immunofluorescent picture in Berger's disease?
|
AKA: IgA nephropathy (post-infectious nephritic)
- Nonlinear IgA deposits in the mesangium - Rx: ACE inhibitors & corticosteroids |
|
|
How does Horner's syndrome affect pupil constriction?
|
The pupil cannot dilate b/c there is an absence of norepinephrine (there is a lesion in the postganglionic neuron, which prevents neuroepinephrine from being released) & t/f no stimulation of the ciliary muscle
|
|
|
How does cocaine dilate pupils?
|
It inhibits norepinephrine reuptake and thus keeps the ciliary muscle stimulated
|
|
|
What is the action of hydroxyamphetamine?
|
It causes the release of norepinephrine
|
|
|
If hydroxyamphetamine is given as an eye drop to diagnose a nerve lesion, what would a pupilary dilation indicate? What if there is no response?
|
Dilation: a problem from the preganglionic neuron:
- since this drug initiates norepinephrine release in the postganglionic neuron, if the pupil dilates, then this neuron is not damaged and the problem is earlier in the pathway. No change: the problem is with the postganglionic neuron as it SHOULD dilate with this drug |
|
|
What are the main "things" innervated by the 3-neuron oculosympathetic pathway?
|
Sweat glands of the forehead
Smooth muscles of the eyelid Pupilary ciliary muscle - Interruption of any of the 3 neurons results in Horner's syndrome |
|
|
What characterizes the optical pathology of Horner's syndrome?
|
Abscence of norepinephrine & no stimulation of the ciliary muscle: NO DILATION
|
|
|
What is the usual presentation of preeclampsia?
|
1) Hypertension
2) Proteinuria 3) Nondependent edema (face & hands) |
|
|
What are the symptoms of sever preeclampsia?
|
1) Headache
2) Blurry vision 3) Right upper quadrant abdominal pain 4) Hyperreflexia Rx: magnesium sulfate as a seizure prophylaxis |
|
|
What type of anti-depressants cause serotonin syndrome when combined?
|
SSRIs (e.g. paroxetine, fluoxetine, sertraline, citalopram) + MAO inhibitors (e.g. Tanylcypromine, phenelzine)
|
|
|
What are the symptoms of serotonin syndrome?
|
1) Hyperpyrexia
2) Muscle rigidity 3) Cardiovascular collapse 4) Mental status changes |
|
|
What is the common presentation of glioblastoma?
|
headache, focal neurologic findings, nausea, vomiting, seizure
|
|
|
What is the histological difference between an anaplasitc astrocytoma and a glioblastoma?
|
Astrocytoma lacks necrosis and vascular or endothelial cell proliferation
|
|
|
Where in the brain are anaplasic oligodendrogliomas located?
|
usually: frontal lobes
|
|
|
Where are cystic astrocytomas found?
|
posterior fossa of children (these are low-grade astrocytomas)
|
|
|
What is tumor lysis syndrome?
|
complicationof lymphomas & other bulky cancers due to cytotoxic therapy & dying tumor cell contents overwhelm the body:
- Excess potassium = heart arrhythmias & weakness - Excess uric acid (DNA breakdown) = gout & renal failure Rx: allopurinol (to reduce uric acid production) & glucose/insulin to combat hyperkalemia |
|
|
What are the Ann Arbor staging notation for lymphoma?
|
I = single lymph node or single extralymph organ
II = >/=2 sites on the same side of the diaphragm III = >/=2 sites on both sides of the diaphragm - A without constitutional symptoms - B without constitutional symptoms IV = disseminated disease (extralymphatic organs) |
|
|
What is the Rx for chronic hepatitis B?
|
Interferon-alfa to block viral RNA & DNA synthesis
|
|
|
What is Foscarnet used for?
|
Ganciclovir-resistant cytomegalovirus: binds to pyrophosphate binding site of viral DNA polymerase
|
|
|
What is Ganciclovir used for?
|
Cytomegalovirus
|
|
|
What is Ivermectin used for?
|
Onchocerciasis (River Blindness)
|
|
|
What usually causes systemic miliary TB?
|
Mycobacterium tuberculosis: hematogenous spread via seeding of the pulmonary venous return to the heart to affect the liver, bone marrow, spleen, adrenal glands, meninges...
|
|
|
How does cirrhosis show up in a liver biopsy?
|
bridging fibrous septae (that look like brad scars linking portal tracts)
|
|
|
What processes lead to centrolobular necrosis of the liver?
|
hypoperfusion + retrograde congestion = left or right-sided heart failure or shock
|
|
|
What is the liver histological picture of a chronic alcoholic?
|
Clear, macrovesicular globules of hepatic steatosis
- Grossly: large, yellow, & greasy - Reversible |
|
|
What is the usual triad for adult normal pressure hydrocephaus (NPH)?
|
"Wet, wobbly, & wacky": excessive cerebrospinal fluid production, decreased absorption, or both
1) Incontinence 2) Gait difficulty (Magnetic: feet appear to stick to the floor) 3) Mental decline Rx: ventriuloperitoneal shunt Dx: MRI to rule out a mass lesion |
|
|
What is the most common etiology of acute-onset of pleuritic chest pain in otherwise young, healthy men?
|
Pneumothorax
|
|
|
What is bronchiectasis?
|
dilation of the bronchial tree secondary to mucus plugging (usually seen in Px with a history of repeated lung infections; e.g. CF Px)
|
|
|
What are the cluster C personality disorders?
|
Anxiour or worried with abnormal fears about relationships, separation, & control:
1) Avoidant 2) Obsessive-compulsive 3) Dependent |
|
|
What are the 2 most common porphyrias?
|
Acute intermittent (AIP)
Porphyria Cutanea tarda (PCT) |
|
|
What is the mechanism of AIP (Acute intermittent porphyria)?
|
Defect in the enzyme PBG (3rd step in heme synthesis): porphobilinogen deaminase (aka: uroporphyrinogen I synthase)
- Result: aberrant accumulation of ALA (aminoleuvlinate) & PBG - Symptoms: neurovisceral: abdominal pain, muscle weakness, & anxiety/paranoia/depression & high PBG in urine (severe: port wine urine) |
|
|
What is the mechanism of Porphyria cutanea tarda (PCT)?
|
Defect in the enzyme URO decarboxylase (5th step in heme pathway):
- aberrant accumulation of URO - deficiency is inherited or acquired (iron, alcohol, estrogens, Hep C or HIV) - Symptoms: photosensitivity, chronic, blistering lesions on sun-exposed skin, no neuropsychiatric signs |
|
|
What is the pathology of X-linked sideroblastic anemia?
|
ALA synthase deficiency (the 1st & rate-limiting step in heme synthesis)
|
|
|
What is erythropoeitic porphyria?
|
Deficiency of ferrochelatase (no iron incorporation into protoheme)
- disorder begins in childhood with marked photosensitivity |
|
|
What catalyzes the oxidation of heme to biliverdin?
|
Heme oxygenase
|
|
|
What genetic defect results in Marfan's?
|
Mutation of the fibrillin-1 gene on chromosome 15 = defective microfibrils
- elastin in aorta - suspensory ligaments of the lens of the eye |
|
|
What precipitates DeQuervain's throiditis?
|
Viral illness causes a transient hypothyroidism:
- tender thyroid gland - elevated ESR - fatigue, cold intolerance, cool skin, decreased delirium tremens Rx: nothing |
|
|
What are the key dermatome locations for the following disc locations:
C2 C3 C4 T4 T7 T10 L1 |
C2 = head (covers the poserior 1/2 of a skull cap)
C3 = upper neck C4 = between neck & shoulders T4 = nipples "T4 at the teat pore" T7 = xiphoid process T10 = umbilicus L1 = inguinal ligament (Oblique in shape) |
|
|
What is the action of metformin?
|
Stimulates glycolysis in peripheral tissues, decreases intestinal glucose absorption, & decreases hepatic gluconeogensis
- Side effects (of all biguanides): lactic acidosis; t/f always give hospitalized patients (who have to stop their metformin) IV insulin |
|
|
What is the mechanism of insul & insulin analogs?
|
Bind to insulin receptor on cell membranes that activate tyrosine kinase that leads to glucose absorption.
- Result: increased glycogen storage in the liver & glycogen & protein synthesis in muscle |
|
|
What is the mechanism of sulfonylureas (glyburide & glipizide)?
|
Stimulate the release of endogenous insulin stores: close potassium channels in B-cells that leads to an influx of Ca, cell, depolarization, & insulin release
|
|
|
What is the mechanism of glitaxones (rosiglitazone, pioglitazone)?
|
Thiazolidinediones: increase sensitivity to insulin
- Stimulate peroxisome proliferator-activated receptor-gamma; this leads to increased glucose uptake in muscle & adipose |
|
|
What is undulant fever?
|
Infection by Brucella:
- E.G.: B. melitensis (gram -, coccobacilli, intracellular bac that stains with a modified acid-fast) - From contaminated milk products or contact with sick livestock - Symptoms: undulating fever, weakness, loss of appetite |
|
|
What bac is the cause of cat scratch?
|
Bartonella henselae
|
|
|
How does Pasteurella infection present?
|
- Cellulitis, high fever, hepatosplenomegaly (septic arthritis in PEDs)
- Route of infection: Dog or cat bite |
|
|
What causes a rapid-onset food poisoning with nonbloody diarrhea after eating reheated rice?
|
- Bacillus cereus exotoxin
- S/S: nausea, vomiting, diarrhea - "food poisioning from Reheaded Rice (diarrhea)? Be Cerious!" |
|
|
What causes a late-onset food poisoning with bloody diarrhea after eating reheated rice?
|
Campylobacter jejuni: enterocolitis
Rx: erythromycin or ciprofloxacin |
|
|
What is the treatment for Cholerae?
|
- Prompt H2O & electrolytes replacement
- Tetracyclines to reduce the disease course |
|
|
What is used to treate a severe Shigella infection (bloody diarrhrea)?
|
Fluroquinolones
|
|
|
What are the 4 major causes of food poisioning, nonbloody diarrhea?
|
1) Staphylococcus aureus
2) Clostridium perfringens 3) Enterotoxigenic E. coli (traveler's diarrhea) 4) Bacillus cereus |
|
|
What is the mechanism of Gemfibrozil?
|
1) increases the activity of lipoprotein lipase & enhances clearance of triglycerides
2) Fibric acid derivative that acts on peroxisome proliferator-activated receptor-alpha protein |
|
|
What is the action of statins?
|
Reduce cholesterol biosynthesis in the liver by preventing the formation of the precursor mevalonate
|
|
|
What is the mechanism of action of ezetimibe?
|
- Blocks cholesterol absorption in the small intestine brush boarder
- Usually dosed along with statins |
|
|
What is the action of resins (cholestyramine & colestipol)?
|
Bind bile acids and steroids in the small intestine & prevent their absorption
|
|
|
What is the most common cause of pneumonia in CF patients?
|
Pseudomonas
Rx: Gentamicin |
|
|
What is the mechanism of action of aminoglycosides like gentamicin?
|
Bactericidal: inhibit formation of the initiation complex & cause misreading of mRNA
- require O2 for uptake (ineffective against anaerobes) - Use: severe gram - rod infections - Tox: nephrotox, Oto, teratogenic |
|
|
What type of drug is Ampicillin & what is it used for?
|
- Aminopenicillin
- penicillnase-sensitive - combined with clavulanic acid to enhance spectrum - Rx: Gram + & Gram - : H. influenzae, E. coli, Listeria, Proteus, Salmonella, enterococci, Shigella - Tox: hypersensitivity & pseudomenbraneous colitis |
|
|
What can cause SIADH?
|
- Cancer: lymphoma, sarcoma, carcinoma of duodenum or pancreas
- CNS: meningitis, brain abscess, trauma - Pulmonary: oat cell carcinoma, TB, pneumonia, abscess |
|
|
What is the key call mediator in the pathogenesis of atherosclerotic plaque?
|
Platlet-Derived Growth Factor: recruits platlets and smooth muscle to intimal lining to produce an extracellular matrix that becomes a fibrous plaque
|
|
|
What is the pathogenesis of a vascular fatty streak?
|
1) Endothelial Injury
2) Subendothelial space accumulates lipoproteins 3) lipoproteins are glycoslyated or oxidized and this recruits monocytes to the vessel walls 4) Monocytes enter the subendothelial space and convert to macrophages 5) Unregulated macrocytosis of the LDL cholestrol occurs that yields foam cells |
|
|
What does a hydrops fetalis newborn look like?
|
- Gross hepatosplenomegaly & Ascities
- Peripheral edema & purpura - Placenta is pale, thickened, & enlarged |
|
|
What are the finding in a patien with toxic aspirin ingestion?
|
- Metabolic Acidosis with Respiratory alkalosis or Acidosis with anion gap
- Symptoms: coma, respiratory depression, cardiovascular collapse Asprin Tox: increase sensitivity of respiratory centers in the brain, uncouple oxidative phosphorylation, increase metabolism, inhibit Krebs cycle & platelet aggregation |
|
|
When does Acetaminophen become toxic?
|
When its metabolism is saturated & N-acetyl-p-benzoquinone imine (NAPQI) is produced. This damages hepatocytes
- NAPQI cannot be detoxified by endogenous glutathione - Lab: Huge elevations in aspartate aminotransferase & alanine aminotransferase (due to centrilobar necrosis) Rx: activated charcoal within 4 hours & N-acetylcysteine |
|
|
What confirms a Benzo overdose?
|
Reversal of symptoms (coma & respiratory depression: both are rare) by flumazenil
|
|
|
What is the toxicity of Ephedra?
|
CNS & cardiovascular stimulation, arrhythmia, stroke, seizures
|
|
|
What is the toxicity of drain cleaners?
|
NaOH or KOH = GI erosion & metabolic alkalosis
|
|
|
What is the equation for clearance? (L/min)
|
Rate of drug elimination / plasma drug concentration
|
|
|
How does spironolactone cause gynocomastia, testicular atrophy, and decreased libido?
|
- It binds to steroid receptors outside the kidney
- Its therapeutic effect is as an antagonist at the renal aldosterone receptor in the DC tubule - It is potassium-sparing |
|
|
What are the main side effects of B-blockers?
|
impotence
bronchoconstriction hypoglycemia cold extremities |
|
|
What is the main action (& side effects) of hydrochlorothiazide?
|
- Action: Inhibit luminal Na & Cl entry to the DC tubule cells, Potassium-wasting
- SE: hypokalemia, give potassium supplements |
|
|
How does long term steroid use induce diabetes?
|
Decreased glucose tolerance & counterregulatory action of the hormone:
- increase glucose production by the liver by stimulating glconeogenesis & proteolysis in the skeletal muscle to release glucogenic amino acides into the vasculature |
|
|
What are teh 2 main causes of Diabetes insipidus?
|
- Pituitary dysfunction
- Failure of kidneys to respond to ADH |
|
|
Why do Cushing's disease patients develop hyperpigmentation of the skin?
|
- Primary pituitary adenoma secretes ACTH
- ACTH stimulates melanocytes |
|
|
Does steroid use result in hyper or hypotension?
|
Hypertension due to the mineralocorticoid properties of steroids (increased Na retention)
|
|
|
How does Cushing's syndrome manifest in muscle tissue?
|
Wasting due to catabolic effects of cortisol
|
|
|
What ADHD medication is not a controlled substance?
|
- Atomoxetine - a selective norepinephrine reuptake inhibitor
- it has no abuse potential |
|
|
What is the drug treatment for carcinoid syndrome?
|
Octreotide: somatostain analog that inhibits secretion from neuroendocrine tumors (also used with VIPomas that secrete vasoactive intestinal polypeptide)
|
|
|
What does aflatoxin cause?
|
1) Hepatocellular carcinoma
2) This toxin is produced by Aspergillus flavus growing on peanuts & grains and intercaltes into host DNA 3) Contamination is a problem in Asia & Africa |
|
|
How does AZT stop reverse transcriptase on a molecular level?
|
It is converted in cells into a nucleoside triphosphate & becomes incorporated into DNA. However, without a hydroxyl at the 3' carbon, it cannot form a phosphate bond & elongate.
|
|
|
What is the function of zonula occludens?
|
Tight Junctions:
- Prevent leakage across the intracellular space - Found toward luminal side of epithelial cells |
|
|
What is the function of zonula adherens?
|
- Components: actin filaments & E-cadherins
- Connects cytoskeletal elements of neighboring cells - Below zonula occludens - Allows cells to create a functional unit |
|
|
What is the function of a desmosome?
|
Aka: Spot-adhering junction
- Contents: keratin & desmoplakin (desmoglein), actin, & E-cadherin - Function: joins small, discrete sections of neighboring cells |
|
|
What is the function of Gap junctions?
|
- Function: Cell communication
- Structure: connexins with central channel |
|
|
What are the causes of eosinophilia?
|
NAACP: (release Major Basic Protein)
1) Neoplasia 2) Asthma 3) Allergies 4) Collagen vascular diseases 5) Parasitic infection |
|
|
What are the main infections that can result in Gillain-Barre?
|
1) Herpesvirus, CMV, EBV, HIV
2) Campylobacter jejuni gastroenteritis + stress |
|
|
How does E. histolytica infection present?
|
It is an amoebal dysentery associated with liver abscess formation
|
|
|
What foods can be contaminated with L. monocytogenes?
|
- Delicatessen meats & soft cheese
- Gram + rod with tumbling motility |
|
|
What is prophylthiouracil used to treat?
|
- hyperthyroidism: inhibits the synthesis of T4 & the peripheral conversion of T4 to triiodothyronine.
- (rare) Tox: agranulocytosis, rash, edema |
|
|
What is the clinical use of Leuprolide?
|
- Infertility, prostate cancer, uterine fibroids
- MOA: Gonadotropin-releasing hormone analog = dosage suppresses release of LH & downregulates the hypothalamic-pituitary-gonad axis - SE: gynecomastia, decreased libido, nausea, vomiting |
|
|
Which anticoagulant does not require any laboratory monitoring?
|
LMWH = low-molecular-weight heparin
- activates antithrombin III - administer subcutaneously |
|
|
What is the MOA of spironolactone?
|
Potassium-Sparing diuretic:
- Competitive aldosterone receptor antagonest: Na reabsorption & K secretion are inhibited @ the cortical collecting duct - it is a steroid |
|
|
What is the molecular picture of nephrogenic diabetes insipidus?
|
Loss of arginine vasopressin receptor 2 function
|
|
|
Which stage of the cardiac cycle is prolonged in a patient with atrial stenosis?
|
- Isovolumetric contraction: it must overcome the resistance of the valve & open it
- Sound: ejection click & cresendo-decrescendo murmur @ right sternal boarder that radiated to the neck |
|
|
What is the pathogenesis of the tetralogy of Fallot?
|
Anterosuperior displacement of the infundibular septum during development in utero:
- overriding aorta - pulmonary stenosis - right ventricular hypertrophy |
|
|
What is the classic behavior of a child with tetralogy of Fallot?
|
They squat during cyanotic spells to compress the femoral arteries to decrease their right-to-left shunt
|
|
|
What causes venous abnormalities that can lead to impotence?
|
- Insufficient relaxation of smooth muscle due to excessive adrenergic tone or damaged parasympathetic innervation
- this can result in a leak into the dorsal & saphenous veins & results in venous outflow abnormality |
|
|
What is the normal physiology of an erection?
|
Accelerated blood flow increases pressure within the intracavernosal spaces & this blocks penile venous outflow.
- abnormalities in venous outflow (e.g.e leak from dorsal vein to saphenous vein) can result in failure to attain &/or maintain an erection |
|
|
What is accumulated in Lesch-Nyhan syndrome?
|
Uric Acid:
- There is a deficiency of HGPRT in the purine salvage pathway. - T/F guanine & hypoxanthine cannot be recycled to IMP & GMP respectively - Guanine & hypoxanthine are instead converted to uric acid - ALSO: de novo purine synthesis is increased & this results in MORE uric acid |
|
|
What gene fusion is characteristic in Acut promyelocytic leukemia (APL)?
|
t(15:17) = PML + retinoic acid receptor
Rx: retinoic acid to mature the leukemic cells |
|
|
What gene fusion is characteristic in Chronic myelogenous leukemia (CML)?
|
- Philadelphia chromosome
- t(9:22): BCR-ABL fusion protein |
|
|
What genetic translocation results in Burkitt's lymphoma?
|
t(8:14): C-myc (Ch. 8) & immunoglobulin heavy chain (Ch. 14) locus
|
|
|
What is Ras?
|
- a plasma membrane protein that has GTP binding and GTPase abilities.
- its activity is increased in some cancers BUT, it is not associated with translocations |
|
|
Which anti-inflammatory drug is best to avoid gastric side effects?
|
Celecoxib: selective COX-2 inhibitor
- decreases conversion of arachiodonic acid to prostaglandin G2 - Prescribe with caution due to heart side effects |
|
|
How does COX-1 inhibition lead to ulcers?
|
Removes the prostaglandin syntheses that is protective to gastric mucosa
|
|
|
What is the mechanism of primary hemochromatosis?
|
AR inheritance: mutation in HFE gene
- body over absorbs iron in the GI |
|
|
What are some causes of sideroblastic anemia?
|
incomplete synthesis of heme:
- Drug interactions (ethanol, isoniazid, chloramphenicol) - Lead poisoning - Nutritional deficiencies of pyridoxine/copper - genetic disorders |
|
|
What is the toxicity of tricyclic antidepressants?
|
MOA: inhibit neuronal reuptake of norepinephrine, seratonin, & other amines
- Mental status changes - Hypotension - Anticholinergic tox: flushing, hyperthermia, dilated pupils, intestinal ileus, urinary retention - Ventricular arrhythmias |
|
|
What day post MI is a patient at risk for ventricular wall rupture?
|
4-7: severe hypotension & results in cardiogenic shock
|
|
|
What is the preferred antibiotic for community-acquired lobal pneumonia (high fever, productive cough, acute onset)?
|
ceftriaxone: broad spectrum, 3rd-generation cephalosporin against:
- S. aureus - H. influenzae - S. pneumoniae |
|
|
What is clindamycin used for?
|
Anaerobics: (often combined with an aminoglycoside)
- penetrating wound infections of abdomen - UTIs in women |
|
|
What is doxycycline particularly useful for?
|
Px with renal failure needing an antibiotic:
- it binds to the 30S subunit & prevents attachment of aminoacylt-tRNA - Rx: atypical pneumonia (Chlamydia & Mycoplasma) - SE: GI distress, photosensitivity, rash |
|
|
What is the 1st line therapy for P. jiroveci pneumonia?
|
Trimethoprim-sulfamethoxazole
|
|
|
Which anemia is caused by lead poisoning?
|
sideroblastic:
- Lead binds to sulfhydryl groups of heme-synthesis enzymes: alpha-aminolevulinic acid dehydratase & ferroketolase) |
|
|
What are the 4 toxicities of lead?
|
1) inhibits heme synthesis (binds to alpha-aminolevulinic acid dehydratase & ferroketolase)
2) competes with Ca ions for binding to other molecules 3) inhibits membrane enzymes (e.g. 5'-nucleotidase & Na-K pumps) causing hemolysis, renal cell damage & hypertension 4) inhibits active vit. D production |
|
|
What drugs cause aplastic anemia?
|
Chloramphenicol
Sulfonamides Alkylating agents |
|
|
What lab test can distinguish between iron deficiency anemia and lead poisoning anemia? They both present with hypochromatic, microcytic anemia
|
Transferrin saturation:
- In iron-deficiency, it is increased (b/c there is no iron to saturate) - in lead poisoning, it is elevated or normal (b/c there is no iron loss) |
|
|
What is elevated in Vit. B12 deficiency?
|
1) Homocysteine = No B12 co-enzyme for its conversion to methionine
2) Methylmalonic acid = No B12 for methylmalonyl-CoA mutase to convert this to succinyl-CoA & metabolize odd-chain fatty acid |
|
|
What are the clinical symptoms of B12 deficiency?
|
1) Fatigue
2) Peripheral neuropathy 3) Macrocytic anemia Lab: elevated homocysteine & Methylmalonic Acid |
|
|
What is the most common serum antibody seen in Multiple Myeloma?
|
IgG (55%)
Iga (25%) |
|
|
In what cancer will a pathologist be able to see Auer rods?
|
- Acute myelogenous leukemia
- These are in myeloblast cytoplasm |
|
|
What are the characteristics of Waldenstrom's macroglobulinemia?
|
- Monoclonal IgM
- Epistaxis - Bleeding Gums |
|
|
What are the common symptoms of Multiple Myeloma?
|
CRAB:
hyperCalcemia Renal insufficiency/failure Anemia Bone/Back pain (lytic lesions) |
|
|
What are the common physical findings in Rickets?
|
Areas of bone growth:
- wrists (widened) - ankles (widened) - costrochondral junctions (rachitic rosary) These are all unmineralized, soft oseoid |
|
|
What are the common lab findings in Rickets?
|
Decreased: Ca, PO3, vit D, alkaline phosphatase
Increased: PTH |
|
|
What is vitamin D's main function?
|
Promotes Ca & PO3 absorption from the GI
|
|
|
What genetic mutation renders a patient immune to infection with certain strains of HIV?
|
Mutated CCR5 (homozygous):
- CCR5 receptor is a chemokine receptor on macrophages that facilitates viral entry into cells. |
|
|
What is injured in the "straddle injury"?
|
- When the urethra below the urogenital diaphragam (at the junction of the membranous & penile) ruptures due to trauma
- Result: urine flows into the scrotum & perineal region. |
|
|
What are the 3 parts of the male urethra?
|
1) prostatic
2) membranous - through the urogenital diaphragm 3) penile |
|
|
What will cause the anterior bladder wall to rupture?
|
- Fractured Pelvis
- Urine wile flow into the retropubic space |
|
|
What would cause a penile urethra rupture?
|
- Crush Injury
- Urine will flow into the deep fascia of Buck within the penis |
|
|
What will cause the superior bladder wall to rupture (dome rupture)?
|
- Forceful compression of a full bladder
- Urine will flow into the peritoneal cavity |
|
|
What will cause a urethral rupture above the urogenital diaphragm (@ the junction of the prostatic & membranous urethra)?
|
- Fractured pelvis or improper catheter insertion
- Urine will flow into the retropubic space |
|
|
What is the toxicity of polymyxins?
|
Nephro & Neuro: dizziness, drowsiness, confusion, nystagmus, blurred vision
|
|
|
What is the MOA of polymxins?
|
Bind to Gram - bacterial cell membrane phospholipids & act like a detergent
|
|
|
What drugs commonly cause granulocytopenia (neutrophils, eosinophis, & basophils)?
|
- Clozapine
- Ticlopidine - Sulfasalazine - Antithyroid drugs - Trimethoprim - Dapsone |
|
|
What drugs, especially in combination, cause ototoxicity?
|
Aminoglycosides
Vancomycin |
|
|
What drugs ill precipitate a severe anemia with jaundice, pallor, dark urine, & back pain in patients with G6PD?
|
Primaquine
Sulfonamides |
|
|
What is the treatment for ulcerative colitis?
|
Sulfasalazine: compo of sulfapyridine (antibacerial) & mesalamine (anti-inflammatory)
- SE: malaise, nausea, sulfonamide tox, reversible oligospermia Also, 6-mercatopurine & methotrexate can be used |
|
|
What is Sucralfate used for?
|
Ulcers & traveler's diarrhea: it binds to an ulcer base & provides protection
|
|
|
What is Infliximab used for?
|
- Monoclonal antibody to tumor necrosis factor alpha
- Crohn's & a 2nd line for UC |
|
|
What is Nizatidine used for?
|
- Peptic ulcer, gastritis, mild GERD
- Reversible histamine-2 blocker |
|
|
What is Omeprazole used for?
|
- HYPERsecretory states:Peptic ulcer, gastritis, esophageal reflux, ZE syndrome
- Proton pump (H+/K+ATPase) of stomach parietal cells inhibitor - SE: headache, GI distrubances |
|
|
What is Ondansetron used for?
|
- Antiemetic
- 6-hydroxytryptamine-3 agonist that is centrally-acting |
|
|
What are the symptoms of atropine poisoning?
|
- Blind as a bat: mydriasis
- Red as a beet: flushed skin - Mad as a hatter: delirium & disorientation - Hot as a hare: fever from inhibited sweat glands - Dry as a bone: lacrimal gland inhibition - no tears or saliva - Plugged Up: constipation & urinary retension |
|
|
What is the antidote for atropine poisoning?
|
Physostigmine: reversibly inhibits acetylcholinesterases to increase the amount of acetylcholine at the cholinergic receptor
- ONLY use in SEVER overdose Light poisoning: supportive care, activated charcoal, benzos |
|
|
What is Clonidine used for?
|
Hypertension: it is an alpha2-receptor agonist
|
|
|
What type of drug is Lisinopril?
|
ACE inhibitor used for hypertensive Px.
|
|
|
What type of drug is Metoprolol?
|
Hypertension: a cardioselective B-blocker
|
|
|
What are natural sources of atropine & scopolamine?
|
Poisonous plants: deadly nighshade & jimson weed
|
|
|
Which part of the nervous system controls accomodation or cycloplegia?
|
parasympathtic control of the ciliary muscle via cholinergic receptors
|
|
|
What action does Acetylcholine have at muscarinic receptors in the eye?
|
- Miosis (pupil constriction)
- Ciliary muscle contraction (accommodation) NB: atropine (a muscarinic agonist) has the oppose effect: mydriasis & cyloplegia. Physostigmine restores the parasympathtic response in atropine poisoning |
|
|
What is the MOA of Pilocarpine?
|
It is an acetylcholine mimetic - causes miosis & contraction of the ciliary muscle
- Rx: open (wide-angle) & closed (narrow-angle) glaucoma |
|
|
How can you calculate the PPV if given the sensitivity, specificity and pre-test probability?
|
PPV =
1) Convert the pre-test probability to an odds ratio 2) Calculate the the test's positive likelihood ratio (LR+) = sensitivity / (1-specificity) 3) Multiply #1 x #2 |
|
|
How does etoposide induct apoptosis?
|
It stabilizes topoisomerase II-DNA complex during the G2 phase & prevents G2 completion & DNA strands break. This triggers apoptosis.
|
|
|
What is the MOA of paclitaxel?
|
- Hyperstabilizes microtubules and directly prevent anaphase (M1 arrest)
- Rx: ovarian & adjuvant to breast cancer |
|
|
What is the MOA of Beomycin?
|
Causes the formation of free radicals after binding DNA, which causes single- & double-strand breaks within the DNA
|
|
|
Which TB drug induces p450?
|
Rifampin
|
|
|
What are the main drug types that induce the cytochrome p450 system?
|
Rifampin
Fluconazole Protease inhibitors Digoxin Warfarin Oral Controceptives |
|
|
What is the MOA of ethanbutol?
|
It inhibits arabinsyl transferase enzymes needed for mycobacterial cell wall formation
Tox: hyperuricemia, GI distress, optic neuritis, visual loss |
|
|
What is the toxicity of isoniazid?
|
Hepatitis
hemolysis in G6PD Px lupus-like syndrome Neurotoxicity |
|
|
What is the MOA of streptomycin?
|
Aminoglycoside that binds the 30S subunit & inhibits protein synthesis.
Tox: neuromuscular blockade & ototoxicity |
|
|
Which cancer causes parathyroid hormone-related peptide problems?
|
- Squamous Cell
- Results in hypercalcemia & suppressed levels of PTH |
|
|
What causes central diabetes insipidus?
|
- decreased ADH production
- hypernatremia & increased plasma osmolaity |
|
|
What newborn umbilical cord abnormality can indicated another congenital abnormality (usually cardiovascular)?
|
A single umbilical artery (there should be 2: to take deoxygenated blood from the fetus to the placenta)
|
|
|
What is the MOA of Methotrexate?
|
- It is an analog of folic acid & inhibits dihydrofolate reducatase & thus prevents tetrahydrofolate regeneration (metabolically active folic acid
- Therefore DNA, RNA, & protein synthesis is decreased |
|
|
What is pyridoxine used for?
|
Pyridoxine = vit. B6
- cofactor in amino acid catabolism, heme synthesis, & glycogen breakdown Deficiency: angular stomatitis, glossitis, dermatitis, & seizures |
|
|
What does cobalamin deficiency result in?
|
Vit B12 deficiency: decreased methionine synthesis from homocysteine
- megaloblastic anemia (no folate derivatives for DNA synthesis are recycled b/c methyltetrahydrofolate is not converted to tetrahydrofolate) - paresthesias & ataxia due to subacute combined degeneration (of the dorsal & lateral spinal columns) - Reduced epinephrine, creatine, & melatonin b/c methionine is a precursor |
|
|
What is the treatment for a benzodiazepam overdose?
|
Flumazenil: a competitive antagonist of the GABAergic receptor
|
|
|
What is the treatment for opiate overdose?
|
Naloxone
|
|
|
What can be given to counter a B-blocker overdose?
|
Glucagon
|
|
|
What happens after vasopressin binds to the V2 receptor?
|
- Activation of a Gs to activate adenylyl cyclase
- Increased AMP then leads to the insertion of aquaporin proteins into the apical membrane of the collecting duct epithelium - mutations in the V2 receptor can cause diabetes insipidus |
|
|
How do fibrates increase HDL?
|
Induce the synthesis of the major HDL cholesterol apolipoproteins (apoA-1 & apoA-2)
|
|
|
How do fibrates reduce lipids?
|
- Increase lipoprotein lipase-mediated lipolysis & this removes triglycerides from the peripheral circulation
- E.G. Gemfibrozil & fenofribrate |
|
|
What is the mechanism of statins?
|
Inhibit HMG-CoA reductase (3-Hydroxyl-3-methylglutaryl-CoA) the rate-limiting step of cholesterol biosynthesis
|
|
|
What is the enzyme that converts arachidonic acid to leukotrienes?
|
5-lipoxygenase
|
|
|
What is the 1st committed step of fatty acid synthesis?
|
The synthesis of malyonyl-Coa via Acetyl-CoA carboxylase
|
|
|
What is the MOA of thrombolytics?
|
- Indirect or direct assistance of the conversion of plasminogen to plasmin
- plasmin cleaves thrombin & fibrin clots |
|
|
What extra problem is associated with ovarian teratomas?
|
Can contain thyroid tissue (struma ovarii) & cause a hyperthyroid state
|
|
|
What lab value indicates that a fetus will have Down's?
|
AFP reduction: "AFP goes down in Down's Syndrome"
|
|
|
What lab value indicates a neural tube defect in a fetus?
|
Dramatic increase in AFP (reduce risk with prenatal folate)
|
|
|
What is the MOA of abciximab
|
- Monoclonal antibody against the glycoprotein IIb/IIIa receptor on the surface of platelets
- It impairs platelet aggregation Rx: acute coronary syndrome |
|
|
What is the MOA of heparin?
|
Complexes with Antithrombin II and increases its activity by 2000-fold
|
|
|
What is the treatment for Enterobacter species?
|
Carbapenems (i.e. imipenem & meropenem) when resistant to penicillin/penicillinase via B-lactamase
|
|
|
What is the mechanism of C. difficile infection?
|
- Pseudomembranous colitis: Exotoxin that results in enterocyte death & watery diarrhea
- Often follows ampicillin or clindamycin treatment |
|
|
What is the toxicity of C. perfringens?
|
Lecithinase exotoxin that results in myonecrosis, gas gangrene, & hemolysis
|
|
|
What are the signs of nephrotic syndrome?
|
1) Azotemia
2) Hematuria 3) Oliguria 4) Hypertension |
|
|
What is the initial treatment for esophageal dysmotility?
|
Metoclopramide: promotility agent
|
|
|
What is Ondansetron used for?
|
- 5-HT3 receptor antagonist
- Used to treat refractory or severe nausea & vomiting |
|
|
What are the two types of diabetes insipidus (DI)
|
- Central (reduced ability to produce ADH)
- Nephrogenic (lack renal response to ADH) & can be a rare toxicity of Lithium |
|
|
What is the toxicity of valproic acid
|
- Liver & pancreatic toxicity along with neural tube defects if the patient is pregnant.
- This drug is an antiepileptic |
|
|
What is the risk factor for developing Ebstein's anomaly?
|
Lithium exposure during gestation:
- apical displacement of the septal & posterior tricuspid valve leaflets = atrialization of the right ventricle & displacement of the anterior leaflet |
|
|
What is fetal hydantoin syndrome?
|
Phenytoin-associated fetal defects:
- growth deficiencies - skull & facial feature abnormalities - mental retardation - underdevelopment of nails in the fingers & toes |
|
|
What are the risk factors for the Tetralogy of Fallot?
|
Phenytoin
Alcohol Also: 22q11 syndrome association |
|
|
What physical symptoms characterize ALS?
|
- Upper & lower motor neuron signs: fasciculations, hyperreflexia in lower extremities and areflexia in the upper limbs
- Biopsy of muscle: muscular atrophy due to lack of neuronal input |
|
|
What type of viruses are capable of genetic/antigenic shift?
|
Those with segmented genomes that can exchange segments (e.g. influenza: negative-stranded RNA virus) & can result in periodic changes int he surface antigen of the virus:
- H antigens: hemaglutinin - N antigens: neuraminidase |
|
|
What family of viruses is Influenza a member?
|
Orthomyxovirus
|
|
|
What viruses are a member of the paramyxovirus family?
|
Parainfluenza
RSV Mumps Measles |
|
|
What is the MOA of amphetamines for ADD treatment?
|
Promote the release of catecholamines (dopamine & norepinephrine):
- increases the concentration in the synaptic cleft - Dopaminergic activity in the CNS stimulates & leads to increased attention |
|
|
When is atropine indicated for heart therapy?
|
Advanced cardiac life support to block parasympathetic input to the heart:
- Increases heart rate |
|
|
What is the common MOA of cocains and tricyclic antidepressants?
|
Block reuptake of catecholamines into the presynaptic terminals
|
|
|
What is the MOA of Reserpine?
|
Blocks catecholamine storage within the presyaptic neuron by preventing storage withing the presynaptic vesicles
|
|
|
What tract is responsible for the dopaminergic control of prolactin?
|
tuberoinfundibular: antagonists to D2-receptors in this region will cause hyperprolactinemia.
E.G. Chlorpromazine (antipsychotic) is such a drug that antagonizes this receptor. |
|
|
What tract is antagonized by typical anti-psychotics and thought to exacerbate negative symptoms of schizophrenia?
|
Mesocortical (cognition pathway) D2-receptors
|
|
|
What results in D2-receptor antagonism by chlorpromazine in the mesolimbic tract?
|
Decrease in positive symptoms of schizophrenia (hallucination, delusions, & frank psychosis)
|
|
|
What is the function of the nigrostriatal tract?
|
Basal ganglia involved in movement production:
- antagonism of D2-Receptors results in Parkinson-like movement & tardive dyskinesia (typical antipsychotics act here) |
|
|
What is the DDx for organisms causing long branching filaments?
|
Fungi
Nocardia asteroides Actinomyces israelii |
|
|
What is the treatment for a Nocardia pneumonia?
|
Sulfa-based antibiotic, IV, high dose: sulfamethoxazole
|
|
|
What are the catalase, hemolytic, and coagulase properties of S. aureus?
|
Catalase-positive
Coagulase-positive B-hemolytic |
|
|
What are the catalase and coagulase properties of S. epidermis?
|
Catalase-positive
Coagulase-negative |
|
|
What bacterial cause of pneumonia is a gram-positive cocci that grows in chains and possesses a glycoprotein capsule?
|
S. pneumoniae; it is also bile soluble
|
|
|
Which type of ulcer results in weight loss & pain with food?
|
gastric
Rx: 14-day triple therapy - Bismuth - Omeprazole - Amoxicillin or tetracycline |
|
|
What are the symptoms of acut gastritis?
|
Nausea
Vomiting Hematemesis Histo: diffuse erythematous patches on the lumen of the stomach |
|
|
What is the MOA of Sildenafil?
|
Inhibits cGMP phosphdiesterase (PDE5) which increases cGMP leading to smooth muscle relaxation in the corpus cavernosum to increase blood flow to the corpus vascularity
|
|
|
What is Clomiphene used for?
|
Female infertility:
- it is a selective estrogen receptor modulator and partial agonist of the estrogen binding site on the hypothalamus & pituitary - it increases secretion of gonadotropin-releasing hormone |
|
|
What is the MOA of Alprostadil?
|
Intraurethral prostaglandin pellet that increases arterial inflow & decreases venous outflow via binding G proteins & stimulating adenylyl cylase
Tox: priapism if given as an intracavernosal injection |
|
|
What structures run through the tarsal tunnel (posterior to the medial malleolus)?
|
Superior to Inferior: "Tom, Dick, And Very Nervous Harry":
- Tibialis posterior tendon: plantar flexion & inversion - flexor Digitorum longus tendon: plantar flexion of foot & flexion of the 2nd-5th toes - posterior tibial Artery - posterior tibial Vein - tibial Nerve - flexor Hallucis longus tendon |
|
|
What are fibromuscular dysplasias of the kidney?
|
Inherent structural defects of the renal artery wall that impair perfusion:
- leads to stimulation of the renin-angiotension-aldosterone axis that leads to vasoconstriction & volume expansion - Rx: surgery |
|
|
What is a catecholamine-screting tumor of the adrenal medulla?
|
Pheochromocytoma:
- increased plasma epinephrine & norepinephrine - Symptoms: hypertension, diaphoresis, headaches, heart palpitations |
|
|
What are the symptoms of Conn's syndrome (primary hyperaldosteronism)? What is the treatment?
|
- New-onset hypertension
- Alkalosis & hypokalemia (can manifest as muscle weakness or paralysis) - Low plasma renin Rx: Aldosterone antagonist (e.g. spironolactone) |
|
|
What antidepressants have the best cardiac profile?
|
1st Choice: SSRIs
2nd Choice: Monoamine oxidase inhibitors (MAOs) - also good for BPH patients b/c there are no anticholinergic activity |
|
|
What causes "red man" syndrome (RMS)?
|
Too rapid infusion of vancomycin
Rx: slow or pretreat with antihistamine |
|
|
What is a common sequela of Rotavirus infection?
|
Transient lactose intolerance due to brush border of the small intestine being shed.
|
|
|
Where can patients contract Chagas disease?
|
Central & South America via the reduvidd bug
- chagomas (dermal granuloma) - myocarditis - CHF if not treated Chronic: arrhythmias, dilated cardiomyopathy, megacolon, megaesophagus |
|
|
Where do G. lamblia trophozoites colonize?
|
Duodenum & jejunum: cause malabsorption & diarrhea
Rx: Metronidazole |
|
|
What is Oral Rehydration Therapy? as used for Cholera?
|
Glucose-containing sodium solution in a ration not exceeding 2 glucose molecules per 1 sodoum molecules
- prevents dehydration by shifting fluid from the intestinal lumen into the circulation as a 2ndary effect of glucose-coupled Na transport into the mucosal cells |
|
|
What is Gerstmann's syndrome
|
Damage to the visual association cortex (angular gyrus):
1) Inability to distinguish right from left 2) Inability to identify fingers 3) Agraphia 4) Acalculia or dyscalcuia |
|
|
What results from injury to the left posterior inferior frontal lobe?
|
Broca's (expressive aphasia) & (sometimes) brachiofacial weakness
|
|
|
What results from injury to the left posterior superior temporal gyrus?
|
Wernicke's (fluent/receptive) aphasia & may involve visual dificits
|
|
|
What results from injury to the left sylvian region?
|
global aphasia, hemianopia, hemiplegia
|
|
|
What results from injury to the left temporopareto-occipital junction?
|
Transcoritical sensory aphasia:
1) poor comprehension 2) good repetition 3) nonfluent speech |
|
|
What cause of sudden death does malignant hypertension predispose to?
|
Thoracic aortic dissection: pain radiates to the back & ECG will appear normal!
|
|
|
What does the Achilles tendon reflex test?
|
S1-2 nerve roots
- a diminished deep tendon reflex = LMN injury NB: "Count up" Achilles reflex (S1, S2) Knee jerk (L3, L4) Biceps (C5, C6) Triceps (C7, C8) |
|
|
What infections does the complement pathway clear?
|
gram negative
|
|
|
What are the most common causes of otitis & sinusitis?
|
H. influenzae (gram -)
Moraxella catarrhalis (gram -) |
|
|
How do IgG & IgM bind to gram - back in the classical complement pathway?
|
with the Fc region
|
|
|
What is C7 radiculopathies?
|
Damage (usually via herniation) to the C7 nerve root:
- Tricep weakness: elbow extension limited - Weakness in extension of wrist & fingers - Sensory: pain & paresthesia of the middle finger |
|
|
Do cervical roots emerge on top or below corresponding vertebrae?
|
ABOVE
|
|
|
What would a C4-C5 disc herniation result in?
|
Impingement upon the C5 root: limited shoulder abduction
- Weak deltoid - Weak infraspinatus - Sensory: shoulder & upper, lateral arm |
|
|
What would a C5-C6 herniation result in?
|
C6 nerve root problems:
-weak wrist extensors & biceps - Absence of right bicep & brachioradialis relex - Sensory: 1st & 2nd fingers |
|
|
Why is alkalosis coupled with potassium wasting?
|
Kidneys avidly take up H+ to restore the pH and these are exchanged with potassium
|
|
|
What is the DDx for target cells on a peripheral blood spear?
|
HALT:
Hemoglobin C disease Asplenia Liver disease Thalassemia |
|
|
What is within the omental foramen?
|
hepatoduodenal ligament that contains the common bile duct, hepatic artery proper & hepatic portal vein
|
|
|
What is the MOA of isoniazid?
|
Inhibits mycobacterial cell wall formation by inhibiting enzymes required for mycolic acid synthesis.
|
|
|
What is the MOA of Ethambutol?
|
It inhibits arabinosyl transferase to decrease arabinogalactan (a component of mycobacterial cell walls)
|
|
|
What is the MOA of pyrazinamide?
|
Unknown; however, its activity requires conversion by pyrazinamidase
|
|
|
What is the presentation of a patient with pheochromocytoma?
|
Neoplasm of the chromaffin cells (neural crest derivatives that synthesize & release catecholamines):
- Hypertension (bursts or chronic) - Palpitations - Headache - Tremor - Sweating - Sense of apprehension |
|
|
What syndrome develops rapidly (days to weeks) with adrenocortical insufficiency and an overwhelming bacterial infection (N. meningitidis), rapidly progressive hypotension, shock, DIC, & widespread purpura?
|
Waterhouse-Friderichsen syndroma
|
|
|
What is bronchiectasis?
|
abnormal dilation of the proximal & medium-sized bronchi (>2mm in diameter) caused by destruction of the muscular and elastic components of the bonchial walls
|
|
|
What Reid index value indicates chronic bronchitis and hyperplasia of submucosal glands?
|
>0.4
|
|
|
How can you definitively diagnose a B12 deficiency?
|
Check methylmalonic acid levels:
- B12 is a cofactor for the conversion of of Methylmalonyl CoA to succinyl CoA - Without B13, Methylmalonyl CoA is converted to methylmalonic acid |
|
|
What causes the "penis-at-12" phenomenon?
|
5alpha-reducatase deficiency:
- genetic males with testes & ambiguous or female external genitalia - @ puberty, increased testosterone causes masculinization of the external genitalia 5alpha reductase converts testosterone to dihydrotestosterone that is required in utero to develop external genitalia |
|
|
What does 21-hydroxylase do?
|
It converts progesterone to deoxycorticosterone on the way to aldosterone
- without this, there is a virilization of the female genitalia at birth - without this, there is no feedback inhibition on renin & Px have elevated Bp |
|
|
What does 17alpha-hydroxylase do?
|
Converts pregnenolone & progesterone to 17alpha-hydroxypregnenolne & 17alpha-hydroxyprogesterone respectively
- Deficiency leads to increased sex hormone levels, decreased corisol levels & increased mineralocorticoid levels |
|
|
What deficiency causes chronic granulomatous disease?
|
NADPH oxidase: no superoxides from molecular O2
|
|
|
What is pregnenolone?
|
an intermediate in the conversion of cholesterol into adrenal steroids
|
|
|
What ovarian tumor presents with symptoms of hyperthyroidism in 5-15% of patients?
|
Struma ovarii:
- monodermal teratoma that contains thyroid tissue - Increased risk of malignant thyroid carcinoma arising from this tumor |
|
|
What can cross the vilous epithelial cell membrane of the small intestine via simple diffusion?
|
free fatty acids & monoglycerides: breakdown product of triglycerides by pancreatic lipase & bile salts
|
|
|
How are carbohydrates absorbed across the apical membranes?
|
SGLT-1: glucose & galactose
GLUT5: fructose Portal circulation access is through GLUT2 cotransporter |
|
|
What is the histological sign of extramedulllary hematopoiesis?
|
dacryocytes or "teardrop cells"
|
|
|
What is idopathic myelofibrosis?
|
myeloproliferative syndrome in which bone marrow is gradually replaced by collagen fibrosis
- Lab: anemia, mild thromocytosis, mild neutrophilia - Gradual bone marrow failure results in extramedullary hematopoiesis in spleen |
|
|
What is the DDx for target cells
|
1) asplenia
2) alpha & beta thalassemia |
|
|
What is another term for hemoglobin clumping?
|
Heinz Bodies (e.g. G6PD deficiency)
|
|
|
What is the histological appearance of intravascular hemolysis?
|
helmet cells & schistocytes
|
|
|
What is the lab finding in a child with ITP (idiopathic thrombocytopenia purpura)?
|
- Antiplatelet antibodies
- Thrombocytopenia - Blood smear: large platelets due to increased production |
|
|
What is the genetics of Hunters & Hurlers?
|
X-linked recessive
|
|
|
What is the pathology of Hunter's & its clinical presentation?
|
1) Pathology: deficiency in lysosomal iduronate sulfatase; accumulation of dermatan & heparan sulfate
2) Clinical: Mild mental retardation, hearing loss, coarse facies, hepatosplenomegaly, agressive behavior, airway obstuction, but NO corneal clouding |
|
|
What is the clinical presentation of Job's syndrome?
|
1) Recurrent staph abscesses
2) Pruritic eczema (papulovesicular dermatitis) 3) Multiple "cold" (i.e. noninflamed) skin lesions LAB: High levels of IgE: - T-helper cells cannot produce IFN-gamma & thus do not activate phagocytic cells - T/F -> a failure of neutrophil chemotatic response |
|
|
What are the lab values & symptoms of a patient with Wiskott-Aldrich
|
MALE (x-linked)
Symptoms: (TRIAD) - Recurrent pyrogenic infections - Eczema (itchy erythematous rash) - Thrombocytopenia LAB: - Elevated IgA, IgE - Normal IgG - Low IgM = pathology b/c there is no IgM response |
|
|
When is Amiodarone indicated & what are its toxicities?
|
Indication: Vfib
TOX: hypotension, PULMONARY FIbrosis, thyroid dysfunction, hepatotox, ocular changes, bradyarrhythmia & torsades |
|
|
When are Class IC agents (flecainide & encainide) indicated?
|
Vtach or intractable supraventricular tachycardia
MOA: phase 3 of the action potential Tox: increased post-MI mortality |
|
|
When is Procainamide indicated?
|
1) Re-entrant & ectopic suptraventricular & ventricular tachycardia
2) MOA: (Class 1a Na-channel blocker) increase action potential duration & increased QT interval = decrease in myocardial excitability & conduction velocity |
|
|
What are the digoxin toxicities?
|
- Color vision disturbances (esp. yellow-green)
- Nausea - Vomiting - Diarrhea - Arrhythmias |
|
|
What is the MOA of Digoxin?
|
Directly inhibits Na+/K+ATPase, this indirectly inhibits the Na+/Ca2+ exchanger & increases intercellular calcium.
- POSITIVE INOTROPY - Rx: CHF & atrial fib |
|
|
What is a toxicity of Quinine?
|
torsades de pointes
- This drug is an isomer of quinidine, an antiarrhythmic - Antiprotozoal action: prevents separation of dsDNA & thus inhibits DNA replication & transcription |
|
|
What is the treatment for Chagas?
|
nifurtimox
|
|
|
What are the 6 most common causes of DIC?
|
1) Gram - sepsis
2) Malignancy 3) Acute pancreatitis 4) Trauma 5) Transfusion reactions 6) Obstetric complications |
|
|
What infections are sickle cells, asplenic patients more at risk for?
|
Encapsulated Organisms:
- Pneumococci - Meningiococci - Haemophilus & Salmonella osteomyelitis |
|
|
@ what level of saturation does glucose stop being reabsorbed in the proximal tubule via the Na-gluclose cotransport?
|
200 mg/dl
|
|
|
What is the pathogenesis of Bruton's?
|
X-linked agammaglobulinemia:
- NO signaling molecule (Bruton's tyrosine kinase) to tell B cells to develop = NO immunoglobulins (low IgG & IgM, NO IgA) b/c of a mutation on the X chromosome (Xq21.22) - Susceptible to extracellular pyogenic bacterial infections: H. influenzea, S. pyogenes, S. aureus, S. pneumoniae |
|
|
If a patient has no T lymphocytes, what infections are they susceptible to?
|
Viral & intracellular bacteria
|
|
|
What cell type should be stimulated when a patient is at risk for neutropenia & throbocytopenia (e.g. because of cancer chemo)?
|
Meloid stem cell: progenitor of neutrophils, basophils, eosinophils, macs, & platelets
|
|
|
What enterococcus infection treatment can lead to pseudomembrane formation?
|
ampiclin
|
|
|
What anaerobic bacteria infection can result in pseudomembranous colitis when treated with Clindamycin?
|
Bacteroides Fragilis
|
|
|
What metabolic disease can mimic Parkinson's?
|
Wilson's: copper builds up in the putamen
- Dx: low leves of serum ceruloplasmin, increased heaptic copper content, & increased urinary copper excretion - Rx: D-penicillamine (copper chelator) |
|
|
Why do patients on repeated broad spectrum antibiotics develop spontaneous bleeds?
|
- Gut flora are wiped out & thus Vit. K is not produced & there is a deficiency in the Vit. K clotting factors: II, VII, IX, X, C & S.
- VII is deficient 1st b/c it has the shortest 1/2 life & thus prothrombin time is prolonged 1st. |
|
|
What vein is the source of the bleed when an alcoholic bleeds from the mouth?
|
Left gastric (b/c of the anastomoses between the left gastric and the azygos)
|
|
|
What is the MOA of Gemcitabine?
|
- Inhibits DNA polymerase & ribonucleotide reductase when phosphorylated intracellularly
- It inhibits nucleotide synthesis by inhibiting the formation of deoxyribonucleotides |
|
|
What is the MOA of Cyclophosphamide?
|
- Alkylating agent: alkylates DNA (esp. at the N7 position of guanine) that results in interstrand linkages
- This leads to DNA strand breaks & abnormal base pairing. - T/F Interferes with DNA replication |
|
|
What is the MOA of Dactinomycin?
|
Binds to & intercalates with dsDNA to prevent RNA synthesis (particularly rRNA)
|
|
|
What is the MOA of Etoposide?
|
- Inhibits topoisomerase II & t/f causes dsDNA breaks & interferes with cell division at the late-S to G2-phase
|
|
|
What drugs should not be combined with cephalosporins (e.g. cefoxitin)?
|
- Aminoglycosides (Tobamycin, gentamicin, streptomycin).
- The combination results in ATN which reduces GFR & increases serum creatinine. Can be reversed with discontinuation of the drugs |
|
|
What is the scope of Azithromycin and what are it's SEs?
|
- Gram + organisms
- Allergic hepatitis & Thrombophlebitis |
|
|
What is the main SE of piperacilin?
|
- Hypersensitivity in 10% of patiensts
- Effective against Klebsiella |
|
|
What is the difference in cough between croup & epiglottitis?
|
- Croup: barking (leads to inspiratory stridor)
- Epiglottitis: stridor & hoarseness (leads to respiratory distress & can require surgery to establish an airway) |
|
|
What two diseases can causes a dilation of the aorta & dilation of the aortic ring that results in aortic regurgitation?
|
1) T. pallidum (syphilis)
2) Coarctation of the aorta |
|
|
What heart murmur is associated with congenital bicuspid aortic valves?
|
Crescendo-decrescendo sytolic ejection following an ejction click: aortic stenosis (resulting from valvular calcification)
|
|
|
What heart pathology is associated with Ehlers-Danlos syndrome?
|
Mitral valve prolapse
|
|
|
What is the most common heart pathology after chronic rheumatic heart disease?
|
mitral stenosis
|
|
|
What does an ST-elevation indicate? What about an ST-depression? Q wave?
|
ST-Elevation = transmural
ST-Depression = subendocardial Q wave = transmural |
|
|
What is the MOA of the cholera toxin
|
- ADP ribosylation of the GTP-binding protein
- Keeps adenylate cyclate in the active state & thereby increases chloride secretion |
|
|
What is the most common non-Hodgkin's lymphoma?
|
Follicular t(14:18), bcl-2 protein (antiapoptotic) overproduced
|
|
|
What translocation is associated with APL version of AML?
|
t(15:17)
- Rx: all-trans retinoic acid to restore differentiation & conventional chemo |
|
|
What receptors do Heroin & other opiates target?
|
u stimulation in brain and GI:
- Brain = pleasure - GI = decreased motility & constipation |
|
|
How does Clofibrate increase the risk of gallstones?
|
- It up regulates lipoprotein lipase (to increase triglyceride clearance from the bloodstream) but down regulates the rate of bile acid secretion.
- Bile is supersaturated with cholesterol & this increases the risk for stones |
|
|
What is the fucntion of Transforming growth factor-Beta?
|
Dampens the immune response
|
|
|
What is the function of Clara cells?
|
1) Location: terminal bronchiole
2) Produce the protein component of surfactant 3) Transport Cl ions 4) Site of cytochrome p450-dependent mixed-function oxidase in the lung |
|
|
What are Bronchial cells of Kulchitsky?
|
Endocrine cells of the trachea:
- vesicles contain ADH, serotonin, calcitonin, somatostatin |
|
|
Where do gram + organisms inhibit penicillin?
|
Those with B-lactamase--including some S. aureus strains--secrete it into the surrounding space (there is no space between the cytoplasmic membrane & the peptidoglycan layer of the cell wall)
|
|
|
What acne drug is absolutely contraindicated for pregnant women?
|
isotretinoin
|
|
|
What are the microbio risk factors for B12 deficiency?
|
H. pylori
D. latum infection (both can affect directly/indirectly absorption in the terminal ilium) |
|
|
What areas of the CNS are affected by a B12 deficiency?
|
1) Dorsal Columns: loss of propioception, pressure, vibration, & light touch
2) Lateral corticospinal tract: descending fibers to control limb movement 3) Spinocerebellar tract: modulation of movement & gait |
|
|
What is the triad of a molar pregnancy?
|
1) Hyperemesis
2) Vaginal bleeding 3) Hyperthyroidism |
|
|
Why does a molar pregnancy present with hyperthyroidism?
|
B-hCG has a alpha subunit shared with TSH & can sometimes cross-react with the TSH receptor
|
|
|
What Bunyavirus can cause ARDS?
|
Hantavirus - transmitted via rodent droppings & saliva
|
|
|
What are the symptoms of PMR associated with giant cell arteritis?
|
Aching of proximal muscles & girdle stiffness
|
|
|
What is the MOA of Vancomycin?
|
Gram +s: prevents the cross-linking of D-ala-D-ala subunits of the bacterial cell wall
|
|
|
What is the MOA of Doxycycline?
|
Binds the 30S ribosomal subunit and prevents aminoacyl-tRNA attachment
|
|
|
What is the definitive test for chronic granulomatous disease?
|
- Nitroblue tetrazolium dyn reduction: negative result
|
|
|
What is the pathogenesis & presentation of Ataxia-telangiectasia?
|
- Defect in DNA repair enzyme (Ch. 11q22-23 mutation) & IgA deficiency
- Presentation: cerebellar problems (ataxia) & spider angiomas (telagiectasia) @ a young age - Also: impaired organ maturation, x-ray hypersensitivity, predisposition to malignancy |
|
|
What is the most common selective immunoglobulin deficiency?
|
IgA: sinus & lung infections
|
|
|
What is the classic presentation of Bruton's agammaglobulinemia?
|
- X-linked affected Male
- Normal T-cell count - Recurrent bac infections after 6m = . influenzae, S. pneumo, S. aureus |
|
|
What is neuroleptic malignant syndrome?
|
Life-threatening extrapyramidal side effect of antipsychotic agents:
- hyperpyrexia - autonomic instability - severe rigidity Rx: Dantrolene (muscle relaxant), discontinuation of all neuroeptics, & supportive care |
|
|
What is treatment for a benzo overdose?
|
Flumazenil (competative antagonist at the y-aminobuteric acid receptor
|
|
|
What is the period of maximum susceptibility to teratogens?
|
Organogenesis: between weeks 3 & 8 of development
|
|
|
What is the fetal period of resistance?
|
Week 1 & 2: either the fetus will be survive the teratogen or it will fail to survive at all. "all-or-none" response
|
|
|
What are possible squalae of celiac sprue?
|
1) T-cell lymphoma
2) Dermatitis herpetiformis (pruritic papular lesions located on the trunk & extensor surfaces) |
|
|
What is the electron & light microscopic picture for membranoproliferative glomerulonephritis (MPGN)?
|
- Electron: subendothelial "hump-like" immune deposits & mesangial interposition into the capillary wall
- Light: tram-tracking of capillaries - Young Px (8-30 years old) |
|
|
What is the difference between primary and 2ndary Membranoproliferative glomerulonephritis?
|
1) Primary = idiopathic
2) 2ndary = hep C & B, cryoglobulinemia, lupus, rheumatoid arthritis, maligancy cause - In either case, 20 years to end-stage renal disease |
|
|
What is Berger's disease?
|
IgA nephropathy:
- IgA in the mesangium - most common cause of nephritic syndrome worldwide - Concurrent with an upper respiratory infection |
|
|
How is Warfarin monitored?
|
Prothrombin time (PT): prevents synthesis & gamma-carboxylation of vitamen K-depenent factors (II, VII, IX, & X, proteins C & S) via vit. K antagonism
Mneumonic: WEPT: Warfairin, Extrinsic, PT |
|
|
What muscle lowers the jaw?
|
Lateral pterygoids: innervated by mandibular branch of the trigeminal
"Lateral Lowers, M's Munch" M = Masseter, teMporalis, Medial pterygoid |
|
|
What are the classic lab findings for obstructive jaundice?
|
- Elevation in alk phosphatase & Direct bilirubin
- Decreased Urine urobilnogen Light stools |
|
|
What is the treatment for Gilbert's disease?
|
Indirect hyperbilirubinemia: mild decrease in glucoronyltransferase activity
Rx: phenobarbital |
|
|
What is the difference between direct and indirect bilirubin?
|
Direct: conjugated
Indirect: unconjugated |
|
|
What are the 2 main risk factors for hepatocellular carcinoma?
|
1) Chronic hepatitis
2) Exposure to toxins (aflatoxin) |
|
|
What is the histological pattern of Creutzfeld-Jakob disease (CJD)?
|
spongiform degeneration:
- vaculated appearance of the cortex due to deposition of abnormal PrPsc prtoein along with reactive astrocytosis - decreased number of neurons in the cortex in the absence of inflammatory changes |
|
|
What is the clinical presentation of Creutzfield-Jakob disease (CJD)?
|
- Rapidly progressive demintia & ataxia (cerebellar involvement) & involuntary muscle jerks "startle myoclonus)
- Die within 6 m., onset in the 7th decade |
|
|
What disease causes hemosiderosis & gliosis of the mamillary bodies?
|
Wernicke-Korsakoff syndrome = secondary to vitamin B1 (thiamine) deficiency in chronic alcoholics
- Hemosiderin is due to repeated hemorrhages |
|
|
What are the 3 phases of posterior pituitary acute trauma?
|
1) Ceasation of secretion of ADH
2) Death of pituitary: release of all stored ADH 3) Persistent diabetes insipidus dues to injury to posterior pituitary |
|
|
What does a mild B6 deficiency cause?
|
- Reduced decarboxylation reactions
- Inhibited neurotransmitter production: symptoms of depression, irritability, confusion, convulsions - Cheliosis & glossitis - Microcytic anemia - Always supplement with isoniazid treatment b/c isoniazid inactivates pyridoxine by binding with B6 |
|
|
What distinguishes a case of phyelonephritis from a UTI?
|
Presence of WBC casts in the urine. Indicates renal parenchyma involvement
|
|
|
What causes bilateral acoustic neuromas?
|
Aka: vestibular schwannomas
Cause: Neurofibromatosis Type 2 - Mutation of the summor suppressor on Chromosome 22q Symptoms: hearing loss, headache, tinnitus, vertigo |
|
|
What is the mutation involved with Wilms' tumor?
|
Loss of WT1 tumor suppressor gene on chromosome 11q
|
|
|
What genetic mutation ca result in reintoblastoma and osteosarcoma?
|
Rb tumor suppressor gene on chromosome 13q
|
|
|
What chromosomal abnormality results in Li-Fraumeni syndrome?
|
- AD: Loss of p53 tumor suppressor on Chromosome 17p
- Leaves patients at a significant rick for malignancy as children or young adults: osteosarcoma, soft-tissue sarcomas, early-onset breast cancers, adrenocortical tumors, leukemias |
|
|
What genetic mutation can cause colorectal cancer?
|
Loss of the APC tumor suppressor gene on chromosome 5q
|
|
|
What is the role of the pylorus?
|
limit the rate of gastric emptying: it contracts in response to each peristalic wave
|
|
|
How does swallowing work?
|
1) Initiation: touch receptors near the pharyngeal opening are stimulated
2) Signals are sent to the swallowing center in the medulla & lower pons 3) Swallowing center sends impulses to the muscles of the pharynx & esophagus via cranial nerves |
|
|
What nerve ends mediate pressure, coarse touch, vibration, & tension
|
Pacinan (large, ovid, 1-2 mm by 0.1-0.7 mm)
|
|
|
What nerve structures are involved in proprioception?
|
Golgi tendon organs & muscle spindles (encapsulated mechanoreceptors)
|
|
|
What nerve structures are responsible for light discriminatory touch?
|
Meissner's (small, encapsulated, on dermal papillae of glabrous/hairless skin)
|
|
|
What nerve receptors are sensitive to pain caused by mechanical stress, extreme temperatures, & cytokines such as bradykinin & histamine?
|
nociceptors
|
|
|
What nerve structures respond to temperature changes?
|
Thermoreceptors (naked, small, nonmyelinated nerve fibers)
|
|
|
What nerve structures respond to static touch?
|
Merkel's disks (cup-shaped, encapsulated)
|
|
|
What can help DDx a chest pain to be a pulmonary embolism?
|
Low O2 saturation
|
|
|
What type of familial hypercholesterolemia is associated with a defect of LDL cholesterol receptors?
|
Type IIa
|
|
|
What syndrome is associated with a defect in collagen type III?
|
Ehlers-Danlos
Triad: Loose joins, decreased skin elasticity, genu recurvatum of the knee (knee is fixed in hyperextension) |
|
|
What causes scurvy?
|
Vit. C deficiency resulting in a defect in hydroxylation of proline & lysine residues of collagen
|
|
|
What does a P. aeruginosa ear infection present with?
|
(Swimmer's Ear) External or malignant otitis externa: ear pain & itchiness
MOA: produces exotoxin A that ADP ribosylates elongation factor 2 & impairs host cell protein synthesis P. aerugoinoa: gram -, non-lactose-fermenting rod that forms blue-green colonies & has a fruity odor |
|
|
What is the MOA of lipopolysaccharidea (LPS)?
|
Binds & activates toll-like receptor 4
|
|
|
What is the MOA of Shiga toxin?
|
cleaves rRNA of the host cell
|
|
|
What is the MOA of the superantigen that causes TSST-1 (toxic shock syndrome) by S. aureus?
|
Nonspecificallly binds & activates lympocytes: fever, rash, shock
|
|
|
What is the primary defect in diabetes type 2?
|
Peripheral insulin resistance due to decreased glucose uptake in muscle & adipose
- Possible cause: defective downstream signaling pathways causing either a decreased number of insulin receptors on the cell surface or signaling errors after insulin has bound to the receptor Hyperglycemia presents with polyuria, polydipsia |
|
|
Why do obese patients often have hyperestrogenism?
|
Adipose contains aromatase that converts androgens into estrogens
|
|
|
Why is there an increase in hepatic glucose production in type 2 DM?
|
insulin resistance results in a decreased ability to suppress gluconeogensis in the liver
|
|
|
What is the pathogenesis of paroxysmal nocturnal hemoglobinuria?
|
There is an insufficient synthesis of glycosyl-phosphatidylinositol anchors, which stabilize proteins that protect RBCs from complement-mediated cell lysis
|
|
|
What is the pathogenesis of throbotic thrombocytopenic purpura?
|
Absences of von Willebrand factor protease & there is hemolysis due to shear trauma in the vessels
|
|
|
What causes RBC lysis in autoimmune hemolytic anemai?
|
IgG targets RBC antigens
|
|
|
How is a PDA maintained in an infant & how is it medically closed?
|
Prostaglandin I2
Rx: indomethacin inhibits PGI2 formation |
|
|
What are the 3 congenital heart lesions that cause late cyanosis (L to R shunt)?
|
VSD
ASD PDA |
|
|
What does Thromboxane A2 cause?
|
- Platelet aggregation & vasoconstriction
- Inhibited by aspirin |
|
|
What results from prostaglandin E2 activation?
|
increase in body temperature
|
|
|
What results from prostaglandin F2alpha activation?
|
Uterine contractions & bronchoconstriction
|
|
|
What are the symptoms of Kawasaki's? What is the treatment?
|
1) Px < 5 years old
2) Fever (40C/104F) 3) Red eyes = injected conjunctivae 4) Erythematous rash on palms & soles + edema 5) Tachycardia & mucosal inflammation 6) Lymphademopathy 7) Lab: Normocytic anemia & neutrophilic leukocytosis & elevated ESR Rx: Aspirin & IV Ig (prevent coronary artery aneurysm due to necrotizing vasculitis of sm/m muscular arteries) |
|
|
What is Busulfan used for?
|
Alkylator used to treat CML
|
|
|
What is cylophosphamide used for?
|
Nitrogen mustard alkylating agent
Rx: cancer, Wegener's granulomatosis & polyarteritis nodosa |
|
|
What are the main uses of penicillin G?
|
- Syphilis
- Gram- & gram +s that are not penicillin resistant |
|
|
For what autoimmune disease is prednisone contraindicated?
|
Kawasaki's b/c it might increase the risk for coronary aneurysm
|
|
|
What amino acid can donate methyl groups?
|
Methionine (S-adenosyl-L-methionine)
E.G. used in the synthesis of phosphatidylcholine |
|
|
What are the lab results that indicates Edwards' syndrome?
|
Low: maternal AFP, estradiol, B-human chorionic gonadotropin
|
|
|
What genetic mutation results in DiGeorge's? What are the characteristic features of this disease?
|
22q11 microdeletion
CATCH-22: Cleft palate Abnormal facies Thymic aplasia Cardiac defects Hypocalcemia 22 deletion |
|
|
What lab value distinguishes Edwards' from Downs?
|
1) b-hCG: elevated in Down's and decreased in Edwards
2) SAME: low AFP & low estradiol |
|
|
What is the picture of Pneumocystis infection?
|
S/S: dry cough, dyspnea, hazy bilateral hilar infiltrate on chest X-ray
Rx: Trimethoprim/Sulfamethoxzaole |
|
|
What type of fracture is most likely due to child abuse from bone twisting?
|
Spiral fracture
|
|
|
What type of fracture is caused by compression and results in a bulging or buckling of the periosteum?
|
Buckle: usually caused by accidents
|
|
|
What catalyzes the production of testosterone by Leydig cells?
|
17alpha-hydroxylase (& 17beta-hydroxysteroid dehydrogenase)
|
|
|
What does 11beta-hydroxylase assist in the formation of?
|
- Cortisol & corticosterone in the adrenal cortex
- without this, biological males will be born with female external genitalia that will be virilized @ puberty |
|
|
What is type 1 5alpha-reductactase for?
|
Conversion of testosterone to dihydrotestosterone in the skin
|
|
|
What is type 2 5apha-reductase for?
|
Conversion of testosterone to dihydrotestosterone in the prostate & genital target tissues
|
|
|
What is the maximum point value for APGAR & what is each area evaluated?
|
10:
- 7(+) = good survival - 4(<) = mortality risk 0-2 for each: Appearance Pulse Respiration Grimace Activity |
|
|
What is the treatment for mycoplasma pneumoniae infection?
|
Macrolides (e.g. azithromycin)
|
|
|
What is a common cause of nosocomial UTI & subacute endocarditis?
|
Enterococcus
Rx: ampicillin or vancomycin (if resistant) |
|
|
What is the MOA & use of piperacillin?
|
Inhibits bacterial cell wall synthesis
Rx: gram +, P. aeruginose, Enterobacteriaceae Use in combo with B-lactamase inhibitor such as tazobactam |
|
|
What is female pseudohermaphroditism?
|
Ovaries are present & external genitalia are virilized/ambiguous
|
|
|
What is required for development of the penis & scrotum during embryogenesis?
|
Dihydrotestosterone via functional 5alpha-reductase to convert testosterone to dihydro...
Deficiency causes phenotypical female with bilateral testes & male internal urogenital tract. @ puberty, external genitalia will be masculinized |
|
|
What are the symptoms of rhabdomyolysis?
|
muscle pain, weakness, "coca-cola colored" urine
|
|
|
What is the muscle-related complication of statin use?
|
myalgia or rhabdomylosis
Especially when combined with any inhibitor of cytochrome P450 enzyme CYP3A4 (that metabolizes statins) - E.G. erythromycin |
|
|
What is the pathogenesis of pyomyositis?
|
S. aureus infection of skeletal muscle
- due to bacteremia from IV drug use or dental work) - often large leg muscles - S/S: muscle pain, swelling, fever |
|
|
What genetic disorder predisposes patients to thromboses in unusual locations (e.g. mesenteric veins) at an early age (<50)?
|
Factor V Leiden thrombophilia
- heterozygous have a higher risk for thrombotic events |
|
|
What does Fanconi's anemia predispose patients to?
|
These patients have pancytopenia and have an increased risk of infection, anemia, fatigue, & bleeding
|
|
|
How is von Hippel-Lindau disease characterized?
|
abnormal blood vessel growth leading to angiomas and hemangioblastomas in the:
- Retina - Brain - Spinal Cord - & elsewhere |
|
|
How does von Willebrand's present?
|
Prolonged bleeding time after trauma, surgery, nosebleeds, & hematomas
|
|
|
How does Giant Cell arteritis present histologically?
|
- Nodular thickening that reduces the size of the lumen
- Granulomatous inflammation with mononuclear & giant cells - Fragmentation of the internal elastic membrane |
|
|
What infection causes tabes (i.e. shriveled) dorsalis?
|
T. pallidum = neurosyphilis progressively demyelinates & scleroses the posterior nerve roots
- reduced reflexed, decreased pain, decreased proprioception (will show a positive Romberg test) Rx: doxycycline |
|
|
What is Pott's disease?
|
- When TB invades the spinal column & causes bone destruction & compresses region of the spinal cord
- 1st symptom is pain Rx: isonizaid + rifampin |
|
|
Where does poliovirus affect the spinal cord?
|
Motor neurons in the anterior horn
Rx: prevent via vaccine |
|
|
How does alpha1-antitrypsin deficiency harm the liver?
|
intrahepatic accumulation of abnormal alpha1-antitrypsin protein
|
|
|
What are the ester-type local anesthetics?
|
Tetracaine
Chloroprocaine Procaine Novacaine Propoxycaine If a Patient is allergic to one, avoid all |
|
|
What are the amide-type local anesthetics?
|
Bupivacaine
Etidocaine Lidocaine Prilocaine |
|
|
What vessel prohibits a horseshoe kidney from ascending?
|
inferior mesenteric artery
|
|
|
What is Waterhouse-Friderichsen syndrome?
|
Bilateral necrosis & hemorrhage of the adrenals cause by infection with N. meningiditis
Dx: high potassium level, low Na, & no increase in serum cortisol level in response to ACTH administration Rx: cephalosporin, penicillin, chloramphenicol & glucocoritcoid replacemtn therapy with hydrocortisone |
|
|
What is the MOA of statin-inducted ATN?
|
secondary to obstruction or via toxic effect on renal tubules
|
|
|
What color is a patient's urine when they have myoglobinuria?
|
Tea-colored
|
|
|
What are causes of interstitial nephritis?
|
- Allergic reaction to drugs (NSAIDS, diuretics, antibiotics)
- Infections - Infiltrative process |
|
|
What is the typical presentation of a Becker's (BMD) patient?
|
- Muscle weakness &/or cardiac disease a mid adolescence
- Cause: an in-frame deletion in the dystrophin gene: partially functional protein is produced (vs. DMD = out of frame that results in truncated or absent dystrophin) |
|
|
What is the most common cause of mitral stenosis?
|
Rheumatic heart disease
- delayed, rumbling, late diastolic murmor |
|
|
What is the most common valvular lesion?
|
mitral prolapse
- late systolic murmor with a midsystolic click - predisposes to infective endocarditis |
|
|
What are the main causes of aortic stenosis?
|
Calcified valve
Congenital bicuspid aortic valve Rheumatic heart disease |
|
|
What are the physical exam finding that indicate aortic regurg?
|
high-pitched blowing diastolic murmur with widened pulse pressure
|
|
|
What are the physical exam finding that indicate aortic stenosis?
|
- Crescendo-decrescendo systolic ejection murmur that radiates to the carotid
- Weak peripheral pulse (pulsus parvus et tardus) |
|
|
What are the physical exam finding that indicate mitral regurg?
|
holosytoci high-pitched blowing murmor @ the base of the heart with a radiation to the left axilla
|
|
|
What are the physical exam finding that indicate mitral stenosis?
|
Opening snap with a delayed, rumbling late-diastolic murmur
|
|
|
How does the kidney respond to a high sodium diet?
|
- Volume expansion will increase stretch in baroreceptors located in the afferent arteriole
- This leads to a reduced sympathetic activity - This leads to vasodilation of the glomerular afferent arterioles - Increases GFR & decreases Na reabsorption |
|
|
When is atrial natriuretic peptide secreted?
|
By the atria in response to increased extracellular fluid volume & causes dilation of the glomerular afferent arterioles
|
|
|
What are the toxicities of cisplatin?
|
- Nephrotoxicity & acoustic nerve damage
- It is a cell cycle nonspecific drug that alkylates DNA (cross-links and inhibits DNA synthesis) |
|
|
What are the side effects of Busulfan?
|
DNA alkylator
- PULMONARY FIBROSIS - hyperpigmentation - bone marrow suppression - GI & CNS: insomnia, anxiety, headache |
|
|
What is the toxicity of Doxorubicin?
|
DNA intercalator that leads to strand breaks (Rx: breast cancer)
- Cardiotox (dilated cardiomyopathy) - Myelosuppression & alopecia |
|
|
What are the side effects of etoposide
|
plant alkaloid that acts in the late S and early G2 & inhibits topoisomerase II
- Tachycardia - Nausea, vomiting - Shortness of breath - hematuria - melena - myelosuppression - alopecia |
|
|
What is methotrexate used for?
|
Antimetabolite that inhibits dihydrfolate reductase in the S phase b/c it is structurally similar to folic acid: decreases purine nucleotide synthesis
carcinoma leukemia trophoblastic disease rheumatoid arthritis ectopic pregnancy psoriasis abortifactant |
|
|
What are the side effects of methotrexate?
|
myelosuppression
mucositis elevated liver enzymes renal toxicty |
|
|
What is the use of ondansetron?
|
antiemetic: selective serotonin receptor antagonist
SE: headache, malaise, constipation |
|
|
What is the MOA of Vinblastine?
|
binds tubulin and blocks microtubule polymerization & mitotic spindle assembly
SE: bone marrow suppression, alopecia, SIADH |
|
|
What is the MOA of acyclovir, ganciclovir, and famciclovir?
|
Inhibits viral DNA polymerase
|
|
|
What 5 types of antibiotics inhibit protein synthesis?
|
1) chloramphenicol & clindamycin
2) linezoid 3) erythromycin 4) tetracycline & doxycycline 5) aminoglycosides |
|
|
What is the treatment for Rocky Mountain spotted fever (R. rickettsii) & Lyme disease (B. burgdorferi) infection?
|
Doxycycline (inhibits protein synthesis)
|
|
|
What is the treatment for ectopic pregnancy?
|
laparoscopic rescection
|
|
|
What is the frequency of the slow waves of the stomach and small intestine?
|
Stomach: 3Hz
Small intestine: 12 Hz |
|
|
What is Whipple's triad for an insulinoma?
|
1) Hypoglycemia
2) Hypoglycemic symptoms (headache/irritability) 3) Relief of symptoms with calorie intake LAB: high C-peptide (indicates taht serum insulin is endogenous) |
|
|
How is Pneumocystis jiroveci pneumonia diagnosed?
|
Methenamine silver stain of lung biopsy tissue
Rx: - Sulfamethoxazole-trimethoprim - pentamidine - dapsone |
|
|
What is the MOA of sulfamthoxayole-trimethoprim & trimethoprim?
|
Inhibit folate synthesis: pteridine & PABA are incorporated into folic acid
= inhibition of nucleic aci & amino acid formation |
|
|
What is the MOA of antifungals like fluconazole & terbinafine?
|
Inhibition of ergosterol synthesis
|
|
|
What antibiotics inhibit the 50S subunit?
|
Chloramphenicol
Erythromycin Clindamycin Linezolid |
|
|
How is N. gonorrhoeae cultured?
|
Thayer-Martin agar (chocolate agar plate suffused with vancomycin, colistin, & nystatin (VCN) to suppress endogenous growth)
|
|
|
What is Bordet-Gengou (aka potato) agar or Regan-Lowe medium used to culture
|
- Bordetella pertussis (gram + rod: whooping cough)
- Also collect with calcium alginate swabs |
|
|
What agar is used to cuture Legionella pneumophilia?
|
Charcoal yeast extract with increased iron & cysteine
|
|
|
What agar is used to culture TB
|
Lowenstein-Jensen (no growth of gram-positive respiratory flora)
|
|
|
What is MacConkey's agar used to culture?
|
Lactose-fermenting enterics:
E.coli Klebsiella |
|
|
What drugs can cause SIADH?
|
1) High-dose IV cyclophosphamide
2) Carbamazepine 3) Vincristine 4) Vinblastine 5) Amitriptyline 6) Amiodarone 7) MAO inhibitors |
|
|
What are the clinical features of SIADH?
|
nausea
lethargy seizures coma Lab: - hyponatremia - serum hypo-osmolality - urine hyperosmolarity - decreased hemocrit (2ndary to dilution |
|
|
What are 2 drugs that can be used to treat nephrogenic DI?
|
Indomethacin
HCTZ (hydrochlorothiazide) |
|
|
What is a direct Coomb's test?
|
1) Coombs reagent is added to the patient's blood
2) Binds to autimmune Ig bound to several RBCs & causes agglutination |
|
|
What can IgM cold agglutinin immune hemolytic anemia occur concuurently with?
|
- Mononucleosis
- Mycoplasma pneumoniae - Lymphoid neoplasm (chronic anemia only) |
|
|
What is an indirect Coombs' used to assess
|
Blood compatibility (before a transfusion): detects unbound antibodies that can bind to RBCs from a normal, healthy doner.
|
|
|
What is a neural complication of overaggressive treatment of hyponatremia (correction of the Na level at a rate faster than 1mEq/L/Hr)?
|
Central pontine myelinolysis (Osmotic demyelination): rate of osmolarity outstrips the brain's ability to adapt to the rising osmolarity -> neuronal shrinkage & death
Clinical: dysarthria, dysphagia, flaccid quadriparesis (can lead to spastic or locked-in syndrome) |
|
|
What is locked-in syndrome?
|
When a patient is fully aware, but can move only the extraocular muscles
|
|
|
What is the treatment for bulimia?
|
SSRIs (e.g. fluoxetine)
|
|
|
What are the clinical signs of bulimia?
|
- Calluses/Scars on the dorsum of the hand (abrasion by teeth during induced gaggin)
- Parotid enlargement - Erosion of tooth surfaces from enamel dissolution |
|
|
What is Lorazepam used to treat?
|
Anxiety disorders
|
|
|
What are amphetamines used to treat (main 2)?
|
ADD/ADHD
Narcolepsy Modulate dopamine, serotonin, & NE |
|
|
What is Thioridazine used to treat?
|
Schizophrenia (as a last resort b/c of SE)
SE: neuroleptic malignant syndrome, cardiotoxicity, retinopathy |
|
|
At what point in meiosis does trisomy 21 occur (i.e. the nondisjunction)?
|
Anaphase I or II (mitotic spindle unequally separates 21, usually in the mother's gamete)
|
|
|
Where is a Robertsonian translocation?
|
A translocation between chromosome 21 & long arm of a second acrocentric chromosome (usually 14 or 22)
|
|
|
When does crossover or recombination occur in meiosis?
|
Phrophase I
|
|
|
What is characteristic of MS (anatomical changes & symptoms)?
|
CNS demyelination with neurologic lesions within the white matter
- S/S that are separated in time & anatomic location - Can have difficulty urinating or incomplete voiding - IMPORTANT: episodic symptoms last >24 hours; MRI: periventricular plaques in >90% of Pxs |
|
|
What do intention tremors & ataxia indicated?
|
Cerebellar disease (e.g. with MS)
|
|
|
What is the triad for Huntington's?
|
- Chorea (forceful, spastic involuntary movements of the limbs &/or facial muscles with gradual onset but become permanent)
- Muscle rigidity - Dementia Cause: nucleotide repeat expansion on the short arm of Ch. 4 |
|
|
What happens in late-stage amyotrophic lateral sclerosis?
|
Paralysis of the respiratory muscles
|
|
|
What are the 4 main manifestations of NF2 (neurofibromatosis type 2)?
|
- Bilateral schwannoma (neoplasm at cerebellopontine angle (CN VII & VIII can be affected)
- Eye lesions (juvenile cataracts) - Ependymomas - Meningiomas - NF2 - tmor-suppressor on Ch.22 that encodes a membrane cytoskeletal protein |
|
|
What are the manifestations NF1 (Neurofibromatosis type 1)?
|
- Cafe-au-lat spots
- neurofibromas -iris hamartomas - optic pathway gliomas - pheochromocytoma - scoliosis (or other skeletal disorders) - UNILATERAL schwannomas) |
|
|
What is the origin of neurofibromas
|
Schwann cells + perineural & endoneural components
|
|
|
What is the classical presentation of Charcot-Marie-Tooth?
|
- Distal muscle (esp. calve) atrophy
- Clumsiness Genetic disorder that affects peripheral nerves via mutations in various myelin genes |
|
|
What are the characteristic facial features of fragile X?
|
Large Ears & Jaws, & Macro-Orchidism in males
EVERYTHING (chromosome, face...) is BIG |
|
|
What is the treatment for Bruton's agammaglobulinemia?
|
IV Ig
No tyrosine kinase gene = no B lymphocyte differentiation |
|
|
What lab results show elevated mineralocorticoids (along with a lack of other cortical steroids)?
|
- Hypertension
- Hypokalemia - Female w/o sexual maturation 17alpha-Hydroxylase deficiency |
|
|
What 2 enzymes are needed to produce cortisol? sex hormones?
|
Cortisol:
21beta-hydroxylase 17alpha hydroxylase Sex: 17alpha hydroxylase |
|
|
What are the ocular manifestations of a Berry aneurysm?
|
Cranial nerve (CN III) compression due to the rupture of a thin-walled outpouching at a cerebral arterial branch point (anterior cerebral & communicating)
- parasympathic fibers are compressed and this results in dilated, unreactive pupils (palsy) |
|
|
How does blockage of a penetrating artery in the internal capsule present?
|
pure motor or sensory deficits
|
|
|
How does the blockage of an anterior cerebral artery present?
|
Stroke: contralateral motor & sensory deficits in the leg & foot
|
|
|
How do subdural hematomas present on CT?
|
"crescent-shaped" density - bridging veins (between dura & arachnoid) rupture do to shearing forces
|
|
|
What is the usual cause & presentation of a middle meningeal artery rupture?
|
Epidural hematoma due to a lateral blow to the head
CT: "lens-shaped" density |
|
|
How does Ketoconazole or metyrapone inhibit ACTH effects?
|
- Both inhibit cytochrome P450 in the adrenal glands (& ketoconazole inhibits ACTH)
- Can be used to treat SIADH from small cell lung cancer |
|
|
What is the MOA of Desmopressing acetate (DDAVP)?
|
It is a synthetic analog of ADH & binds to V2 receptors in the collecting ducts to increase water resorption
- Used to treat diabets insipidus - Stimulates release of vonWillebrand factor & factor VIII by stimulating the V1a receptor (used to treat coagulation disorders: vW disease, mild Hemophilia A, thrombocytopenia) |
|
|
What is the MOA & use for Finasteride?
|
- MOA: Decreases conversion of testosterone to dihydrotestosterone
- Rx: BPH hypertrophy |
|
|
What is Pamidrone used to treat?
|
(Bisphosphonate)
Rx: Hypercalcemia |
|
|
What is spironolactone used to treat (besides hypertension)?
|
Can be used to treat Conn's (primary hyperaldosteronism)
- It is a potassium-sparing diuretic & also competitively inhibits the mineralcorticoid receptor - It is a steroid |
|
|
What is commonly used to treat neuroleptic malignant syndrome?
|
Bromocriptine (a dopamine agonist to restore the depletion of dopamine signaling caused by drugs like haloperidol that blocks dopamine receptors)
|
|
|
What is Benztropine used for?
|
It is an antimuscarinic that improves the tremor & rigidy in patients with Parkinson's
|
|
|
What 2 antipsychotics have the highest rist of neuroleptic malignant syndrome?
|
Chlorpromazine
Haloperidol |
|
|
What is the MOA of Clozapine?
|
Atypical antipsychotic that blocks serotonin & dopamine receptors (D1 & D2)
SE: agranulocytosis & seizures in nonepileptic Px |
|
|
What is the MOA of Fluoxetine?
|
Serotonin-specific reuptake inhibitor
|
|
|
What is the pathogenesis of midgut volvulus?
|
Complication of intestinal malrotation in the 1st month of life when the midgut rotates less that 270 degrees (between week 10 & 12)
|
|
|
How does midgut volvulus present on X-ray? Clinically? What are possible complications?
|
X-ray: Twisted & overdistened colon with a coffee-bean shape & lack of septa & haustra
Clinical: vomiting & constipation Complications: compromised blood supply -> ischemic necrosis & perforation |
|
|
Describe the Measles rash.
|
Blanching red that starts on the face & then moves down the trunk & limbs
+ fever |
|
|
What is a rare complication of measles?
|
SSPE: subacute sclerosing panencephalitis
- 7-9 years after infection - personality changes - lethargy, difficulty in school, odd behavior - Late changes: dementia, severe myoclonic jerking, eventyal flaccidity & decorticate rigitiy -> rip |
|
|
What is the presentation of pediatric roseola?
|
High fever (3-5 days)
conjunctivits otitis media malaise - Blanching macular rash on the neck and trunk that spreads to face & extremities |
|
|
What is the Rubella of rash like?
|
Descending: starts on the face
- fever before (& resolves) rash, lymphadenopathy |
|
|
What is the presentation of Scarlet fever?
|
Strep pyrogenes: fever, soar throat, strawberry tongue
Rash: trunk, neck, limbs, NO palms/soles. Post rash: desquamation of palms & soles |
|
|
What is the MOA of fluoroquinolones (such as ciprofloxacin)?
|
Inhibit DNA gyrase & topoisomerase of gram-negative bac.
|
|
|
What nerve roots contribute to the axillary nerve?
|
C5-6 (posterior cord branch)
|
|
|
What is the clinical presentation of a cocaine user?
|
Tachycardia
Dilated pupils Angina Nosebleed MOA: sympathomimetic that inhibits neurotransmitter reuptake (e.g. NE) |
|
|
What causes prerenal azotemia?
|
Reduction of GFR due to a decreased vascular supply to the kidney
- Heart failure - Sepsis - Renal artery stenosis |
|
|
What are the classic lab values of prerenal azotemia?
|
Accumulation of BUN & Cr in blood:
- BUN rises out of proportion to Cr (Cr is filtered, no reabsorbed) = elevated BUN: Cr ratio |
|
|
How does AIN (acute interstitial nephritis) present?
|
eosinophilic casts in the urine
elevated fractional excretion of Na |
|
|
What distinguishes postrenal from prerenal azotemia?
|
Post: normal BUN: Cr ratio, lack of highly concentrated urine
Pre: increased BUN:Cr ration, highly concentrated urine |
|
|
What level are the nerves that control erection?
|
S2-4 (sympathetic fibers)
|
|
|
What level are the nerves that control erection?
|
S2-4 (sympathetic fibers)
|
|
|
When does fibrinous pericarditis occur post MI?
|
3-5 days
S/S: sharp, pleuritic chest pain, fever, pericardial friction rub |
|
|
When is a thrombotic emboli a risk post MI?
|
weeks to months later
|
|
|
When is a heart rupture a risk post MI?
|
4-10 days
|
|
|
What are the main functions of smooth ER?
|
steroid biosynthesis
membrane synthesis repair detoxification (liver has a lot) |
|
|
What are the S/S of Rocky Mountain spotted fever?
|
fever
sever headache red conjunctivae rash on palms and soles Rx: tetracycline (e.g. doxycycline) or chloramphenicol FAST (or death) |
|
|
What lab test can confirm a rickettsial infection (rash on palms & soles)?
|
Weil-Felix reaction for this gram - bac
- Serologic fluorescent antibody screen - Positive: cross-reacting antigens from Proteus vulgaris |
|
|
What type of infection is cold antibody agglutination used to detect?
|
Mycoplasma
|
|
|
What are the vectors for Rickettsia rickettsii?
|
Dermacentor andersoni & D. variabilis (ticks)
|
|
|
What is the tumor marker for breast cancer?
|
CA-15-3
|
|
|
In what cancers is alpha-fetoprotein elevated?
|
hepatocellular carcinoma and nonseminomatous germ cell tumors (yolk sac tumor)
|
|
|
What is Bombesin a tumor marker for?
|
neuroblastoma, lung, & gastric cancer
|
|
|
What tumors can CA-125 mark?
|
Ovarian & malignant epithelial tumors
|
|
|
What is S-100 a tumor marker for?
|
melanoma
neural tumors astrocytoma |
|
|
What tumors is Tartrate-resistant acid phosphatase a marker for?
|
Hariy cell leukemia (a B-cell tumor)
|
|
|
What is volvulus?
|
A twisting of a portion of the bowel around its mesentery
- PEDs & elderly |
|
|
How doe spyloric stenosis present?
|
- S/S: nausea & vomiting at 3- to 6-weeks post birth; olive-shaped mass on physical exam
- Patho: pyloric muscle hypertrophies & causes gastric outlet obstruction - Rx: surgical pyloroplasty |
|
|
What is the pathogenesis of Meckel's diverticulum?
|
Incomplete obliteration of the vitelline duct (yolk stalk)
2% of population & 2 ft. from ileocecal junction; usually asymptomatic Complication: bleeding |
|
|
What is intussusception & how does it present?
|
Invagination of intesting upon itself (usually at ileocecal junction) @ 6-36 m. old
S/S: intermittent & crampy abdominal pain with current-jelly stool due to rectal bleeding |
|
|
What is cystinuria?
|
Increased levels of lysine & arginine in the urine due to a defect in amino acid reabsorption in the proximal tubule leading to a wasting of:
- lysine, arginine, cystine Elevated cystine leads to recurrent stone formation (S/S severe pelvic pain & elevated creatinine due to postrenal failure caused by the stone) Rx: hydration & alkalization of urine |
|
|
What level are the nerves that control erection?
|
S2-4 (sympathetic fibers)
|
|
|
What is the classic presentation for prolactinoma (most common pituitary adenoma) in a woman?
|
Headaches
Galactorrhea Bitemporal hemianopsia |
|
|
How does prolactin suppress menstration?
|
inhibits FSH and GRH & promotes breast milk production
|
|
|
What is thyroid dermopathy?
|
- Pretibial myxedema (nonpitting & thickening of skin)
- Characteristic of hyperthyroidism due to Graves |
|
|
When there is truncal obesity due to a pituitary adeonma, what is the cause of the obesity?
|
ACTH hypersecretion
|
|
|
What are the neurofibrillary tangles of Alzheimer's composed of?
|
intracellular inclusions of microtubule binding protein tau
|
|
|
What is the most common cardiovascular abnormality seen in congenital rubella syndrome?
|
PDA
|
|
|
What is the presentation of congenital CMV infection?
|
petechial rashes
jaundice hepatosplenomegaly sensorineural hearing loss |
|
|
How does congenital herpes infection present?
|
skin (vesicles), eyes (keratoconjunctivitis), and mouth (vesicles) or localized CNS infection, all within 4 weeks of birth
- CNA: temp. instability, RDS, poor feeding, letharcy |
|
|
What is the triad for congenital toxoplasmosis?
|
chorioretinitis
hydrocephalus intracrainal calcifications Early: maculopapular rash, jaundice, hepatomegaly |
|
|
How does congenital syphilis present?
|
asymptomatic at birth
- Cranial VIII defect (hearing problems) - Cutaneous lesions (palms & soles) - Anemia, jaundice, hepatomegaly |
|
|
What spinal nerve controls the inguinal region dermatome?
|
L1: also includes the femoral triangle and superolateral quadrant of the buttock
|
|
|
What spinal nerve controls the anterior & lateral thigh dermatome?
|
L2
|
|
|
What spinal nerve controls the dermatome at the level of the umbilicus?
|
T10
|
|
|
What spinal nerve controls the dermatome directly inferior to the umbilicus?
|
T11
|
|
|
What spinal nerve controls the dermatome region interior to the anterior iliac crest?
|
T12
|
|
|
What lab values indicate an inability to dilute urine?
|
- Urine osmolaity > plasma osmolality
- Normal specific gravity - Urine Na >40mEq/L |
|
|
What ECG is indicative of WPW (Wolff-Parkinson-White) syndrome?
|
Wide QRS with relatively short PR invervals & slurring of the initial parts of the QRS complex
- Cause: congenital accessory pathway leads to pre-excitation of the ventricle; the slurred upstroke is the delta wave - Result: suptraventricular tachycardia: palpitations followed by syncopy |
|
|
What causes an S4 heart sound?
|
stiffness of hypertrophied ventricle
|
|
|
What heart sounds indicate hypertrophic cardiomyopathy?
|
S4 (due to stiff walls)
Ejection murmur (mild outflow tract obstruction due to septal hypertrophy) Rx: b-blocker or non-dyhydropyrine Ca channel blocker (verapamil) |
|
|
Which rotator cuff muscle medially rotates the arm?
|
subscapularis
|
|
|
What is the action of the infraspinatus?
|
adducts the arm and laterally rotates the glenohumoral joint
|
|
|
Which rotator cuff muscle is most often injured?
|
supraspinatus: initiator of abduction (first 15 degrees of the arc; deltoid does the rest)
|
|
|
What is the action of teres minor?
|
adduct & laterally rotates the arm
|
|
|
What is the key component of fungal endospores that allow them to resist dehydration, heat, & chemicals?
|
dipicolinic acid (e.g. present in Coccidioides immitis: causes coccidioidomycosis in the southwest US)
|
|
|
Which virus is known for its hemagglutinin antigen
|
influenza
|
|
|
What bacteria has a capsule made of D-glutamate
|
Bacillus anthracis
|
|
|
What is the action of Teichoic acid on gram + bacteria?
|
induces tumor necrosis factor alpha and interleukin-1 production
|
|
|
What is the ECG finding in tamponade?
|
- Sinus tachycardia & low QRS voltages
- Elecrical alternans (alternations of QRS height with each beat) is pathognomonic |
|
|
What does an ECG result of PR elongation indicate?
|
1st degree atrioventricular block
|
|
|
What does a peaked or hyperacute T wave indicate?
|
hyperkalemia (or, early MI or myocaridal ischemia)
|
|
|
What are the causes of QT prolongation?
|
1) Drugs:
- Class IA or III antiarrhytmics - Phenothizines - TCAs 2) Hypocalcemia 3) Hypothermia 4) Cerebrovascular diseases 5) Ischemic heart disease 6) Idiopathic |
|
|
What is the site of lymph drainage of the liver?
|
Space of Diss (between sinusoidal endothelial cells & hepatocytes)
|
|
|
What heaptic vein carries deoxygenated blood from the liver back to the heart?
|
hepatic vein
|
|
|
What proteins are affected by tuberous sclerosis?
|
AD (Ch. ( & 16): tuberin & hamarin, they regulated cellular growth & differentiation
Tumors: cortical tubers, renal angiomyolipomas, cardiac rhadbdomyomas, astrocytomas, pulmonary lymphangioleiomyomatosis Physical: ash-leaf spot, Shagreen patch, facial angiofibromas Presentation: mental retardation & epilepsy |
|
|
What is the pathogenesis of Leber's hereditary optic neuropathy?
|
- Mitochondrial mutation that causes degeneration of the optic nerve with rapid loss of central vision, leading to a permanent central scotoma
- Males are more affectwith & symptoms usually start in the 3rd decade |
|
|
What is the bac most often responsible for osteomyelitis in diabetic patients?
|
pseudomonas aeruginosa
|
|
|
What is the cellular lining of the epididymis (where sperm acquire motility)?
|
pseudostratified columnar epithelium with stereocilia
|
|
|
What is the cellular lining of the vas deferens (where the sperm travel after maturing in the epididymis)?
|
pseudostratified columnar epithelium
|
|
|
What is the cellular lining of the rete testes (@ the testicular hilum & where the sperm is transfered from the sminiferous tubules to the ductuli efferentes to the epididymis)?
|
simple cuboidal cells
|
|
|
What cell type lines the bladder, calyces, ureters, & upper urethra?
|
transitional cell epithelium
|
|
|
What is the treatment for Clozapine-induced agranulocytosis?
|
1) Discontinuation of clozapine &
2) Administration of Granulocyte colony-stimulating factor (GC-SF) |
|
|
What lab results indicate primary hyperparathyroidism?
|
Hypercalcemia -> metastatic calcification & duodenal peptic ulcers
hypophosphatemia increased alk phos increased PTH levels -> osteitis fibrosa cystic (excessive bone resoption & fibrous replacement of the marrow leaving cystic spaces (brown tumors) |
|
|
What is Osteitis fibrosa cystica and what causes it?
|
- Excessive bone resoption & fibrous replacement of the marrow leaving cystic spaces (brown tumors)
- Increased PTH levels - Presentation: bone pain & fractures |
|
|
On what chromosome is the FAP (familial adenomatous polyposis) genetic mutation found?
|
5: APC locus, loss of tumor suppression & increased risk of:
- duodenal - gastric - liver - thyroid - CNS |
|
|
What is the DOC for H. ypylori infection?
|
Clarithromycin, amoxicillin, & PPI
- 14 day regiment OR Metronidazole, tetracycline, bismuth subsalicylate, & PPI |
|
|
What is the most common cause of 2ndary hyperparathyroidism?
|
- Renal failure
- Symptoms: diffuse bone pain & proximal muscle weakness (+ pruritis if there is a deposition of excess Ca) |
|
|
What is renal osteodystrophy?
|
1) Nephron damage (Lab: increased creatine) reduces Ca reabsorption, impaired phosphate excretion & impaired vit. D activation.
2) Result: decreased serum Ca & increased phosphate = hypocalcemia 3) PTH increases & bone is reabsorbed: increased alk phos. |
|
|
What are the symptoms of hypocalcemia?
|
tetanny & incrased neuromuscular excitability + decreased serum PTH
|
|
|
How does maligancy cause hypercalcemia?
|
1) Lytic metastases to bone
- up serum alk phos & hyperphosphatemia 2) PTH-related peptide production (with hypophosphatemia) |
|
|
What are the lab results that indicated Vitamin D intoxication?
|
hypercalcemia
hyperphosphatemia decreased serum intact PTH levels |
|
|
When do extrapryamidal adverse effects of typical antipsychotic set in?
|
1) acute dystonia (1st hours after dose)
2) akinesia (1st few days after dose) 3) tardive dyskinesia (several months) |
|
|
What renal disease often presents in otherwise healthy young males with hemoptysis?
|
Goodpasture's: Dx with anti-GBM antibodies in blood & kidney biopsy
Rx: plasmapheresis & airway protection + steroids & cyclophosphamide |
|
|
Which strands of strep tend to cause poststreptococcal glomerulonephritis?
|
- M type
- Autoimmune attack begins 2-6 wks. after skin infection & 1-3 weeks after pharyngitis |
|
|
What drug can be used to "rescue" bone marrow after methotrexate administration?
|
It delivers folinic acid that can be reduced to methylene tetrahydrofolate & will thereby bypass the dihydrofolate reducate enzyme that is inhibited by methotrexate
|
|
|
What is Mesna used for?
|
Prevent hemorrhagic cystitis in patients taking cyclophosphamide:
- supplies a free thiol group to bind to & inactivate the toxic metabolite acrolein in the kidney |
|
|
What is compartment syndrome?
|
when a lacerated artery bleeds into a closed space:
- greater than expected pain - decreased blood flow @ the site of injury |
|
|
What are the HLA b27 diseases?
|
PAIR:
Psoriasis Ankylosing spondylitis IBD Reiter's syndrome |
|
|
Disorders of peroxisomes result in what 2 diseases?
|
1) Refsum's
2) Adrenoleukodystrophy - peroxisomes can no longer metabolize very-long-chain fatty acids & this results in problems with making myelin & hydrogen peroxide formation = progressive neurological damage |
|
|
What test approaches 100% sensitivity for detecting syphilis?
|
Veneral Disease Research Laboratory (VDRL) test: FTA-ABS absorption test
|
|
|
Describe the 3 stages of syphilis?
|
1) painless chancre (localized)
2) SYSTEMIC (6 wks later): maculopapular rash (palms & soles), condylomata lata 3) Gummas (chronic graulomas), aoritis (vasa vasorum destruction), neurosphyilis (tabes dorsalis), Argyll Robertson pupil. SIGNS: broad-based ataxia, positive Romberg, Charcot joints, stroke w/o hypertension |
|
|
What are the signs of congenital syphilis?
|
Broad-based ataxia
Positive Romberg Charcot joints Stroke w/o hypertension |
|
|
What is the Tzanck preparation with Giemsa stain used for?
|
1) HSV: reveals multinucleated giant cells
2) Vesicular stomatitis virus infection |
|
|
When can an individual possess the capacity for awareness of a full rectum/bladder & are able to control bowel & urinary tract sphincters?
|
19-36 months
|
|
|
When is the oedipal/phallic phase?
|
36-6 years: strong attachment to parent of the opposite sex
|
|
|
When is the oral stage of life?
|
1st year: passive dependence on eating & sucking
|
|
|
When is the latency phase of life?
|
6 years - puberty: children do not fixate
|
|
|
What infection & CD markers are associated with Hodgkin's disease?
|
EBV
CD45-,CD30+, CD15+/- |
|
|
What are the risk factors for Hodgkin's lymphoma?
|
- Male Gender
- Age 15-40 or 50+ - EBV infection (history, not current) - Immunodeficiency/AIDS - Prolonged use of growth hormone |
|
|
How are the lymph nodes changed in Bartonella heniselae infection?
|
stellate abscesses & tender
Also, there can be sterile, suppurative papules at the site of inoculation |
|
|
What does mucosis fungoides initially present as?
|
- Eczematous, psoriatic-like rash
- It is a cutaneous T-lymphocyte lymphoma |
|
|
What H2-antagonist is an inhibitor of the cytochrome p450 system?
|
cimetidine (Rx: ulcers; SE: headache, confusion, gyncomastia, thrombocytopenia)
|
|
|
What FEV1/FVC ratio is indicative of a restrictive disease?
|
>80
|
|
|
What can be a severe compication of bleomycin therapy?
|
pulmonary fibrosis (~1 month after initiation of treatment) & ARDS
|
|
|
What prostaglandin E1 analog is contraindicated in pregnancy (& why)?
|
Misoprostol: increases producing & secretion of gastric mucous barrier
- it is an abortifactant & can cause diarrhea |
|
|
What are the most common causes of IUGR (intrauterine growth restriction)?
|
- Poor maternal nutrition
- Hypertension - Infections - Congenital anomalies - Smoking |
|
|
What are the risks of placenta previa?
|
(Placenta covers the cervical os):
- Prior cesarean section - Multiparity - Advanced maternal age - Multiple gestations - Prior placenta previa |
|
|
Where does Triatoma cruzi infect?
|
- Heart: myocarditis (ventricular dilation & congestive heart failure 2ndary to myocyte necrosis & fibrosis)
- Nerve cells of the myenteric plexus: dysmotility of hollow organs (esophagus, colon, ureter) = acquired achalasia (distal 1/3) & mega-colon/ureter |
|
|
How does psoriatic arthritis present?
|
psoriasis (nonpuritic scaly or silvery erthematous plaques with well-defined borders) + joint symptoms with acute onset in 1/3 of patients
- Joint swelling asymmetrically in distal interphalangeal joints - some patients have sausage-like finger from inflammation of the digital tendon sheaths |
|
|
What skin disorder goes along with celiac disease?
|
dermatitis herpetiformis: pruritic papules & vesicles
|
|
|
What is deposited in joints in pseudogout?
|
Ca pyrophosphate dihydrate crystals in CONNECTIVE tissues: weakly bifringent & rhomboidal in shape
|
|
|
What is the most common selective Ig deficiency syndrome & how does it present?
|
IgA: mucosal deficiency leads to sinus & lung infections
|
|
|
What is the most common type of primary malignant tumor found in the liver?
|
HCC: hepatocellular carcinoma
|
|
|
What causes a bicornuate uterus?
|
Failure of complete fusion of the paramesonephric ducts at there superior end.
|
|
|
What causes uterus didelphys?
|
- Complete failure of fusion of the paramesonephric (Mullerian) ducts
- Results in 2 seperate uterine cavities that each have a cervix & vagina |
|
|
What cause a arcuate uterus?
|
(aka septate uterus)
Failure of resorption of the midline uterine septum |
|
|
Where is Schistosoma hematobium endemic? What does it cause?
|
- North Africa & Middle East (parasitic flatworm)
- Infection via snails; enters bladder can cause squamous cell carcinoma of the bladder - Rx: Praziquantel |
|
|
What does Dracunculus medinensis cause?
|
(aka Guinea worm)
- Cutaneous nodules & ulceration: resides in subcutaneous tissue & the tail of adult female can protrude to from a small ulcer (usually found on the Patient's lower limb) |
|
|
Where is Necator americanus found (in the world)?
|
(aka hookworm)
- Americas - sub-Saharan Africa - Southeast Asia |
|
|
What does Schistosoma masoni cause?
|
intestinal schistosomiasis
- Intestinal cancer - Liver infection - Katayama fever (sub-Saharan Africa, South America) |
|
|
What is used to treat endometriosis?
|
Danazol (androgen): to decrease GRH to reduce luteinizing hormone & FSH secretion (decrease growth of endometrium)
SE: menstrual irregularities, thrombotic events, benign hepatic adenomas, benign intracranial hypertension (psuedotumor cerebri), weight gain, & acne |
|
|
What antiantrogen is used to treat BPH & male pattern balness?
|
finasteride (5alpha-reductase inhibitor)
|
|
|
What antiantrogen is used to treat prostate cancer?
|
flutamide (competitive androgen inhibitor @ the testosterone receptor)
|
|
|
What antiantrogen is used to treat hirsutism & polycystic ovarian syndrome?
|
ketoconazole (inhibits adrenal desmolase needed for steroid synthesis)
|
|
|
What antiantrogen is used to treat class III/IV congestive heart failure, primary hyperaldosteronism, diuretic-induced hypokalemia)?
|
sironolactone (steroid binding inhibitor)
|
|
|
What differentiates clomiphene & tamoxifen?
|
- Tamoxifen: has agonist activity & promotes endometrial hyperplasia
- Cloomiphenes: has antagonist activity: inhibits endometrial hyperplasia |
|
|
In which tissues does clomiphene & tamoxifen act as an antagonist?
|
1) CNS = vasomotor symptoms & sleep irregularities
2) Breast = breast cancer protection 3) bone PTH hormone = bone pain, hypercalcemia, arthralgias 4) Lipid profile = incrases HDL & triglycerids and decreased total & LDL cholesterol 4) Liver = increased protein synthesis, including clotting factors |
|
|
What drug often given to treat breast cancer in postmenopausal woman can cause Steven-Johnson syndrome?
|
Anastrozole (aromatase inhibitor)
|
|
|
What is a patient at risk for post-thyroidectomies if not given levothyroxine?
|
Reduced:
- Glycogenolysis - Gluconeogenesis - Lipolysis B/C thyroid receptors are located on bones in both the CNA & autonomic nervous systems |
|
|
What is the only human glycerophospholipid that is antigenic?
|
Cardiolipin (Diphosphatidylglycerol): it is recognized by antibodies against Treponema pallidum
|
|
|
What is the most common presentation of Burkitt's in North America?
|
Loss of appetite
Sever Constipation Abdominal pain or distention Cause of symptoms: enlarged lymph nodes in the abdomen |
|
|
What catalyses the prodrug prednisone into prednisolone?
|
11-beta-hydroxysteroid dehydrogenase
|
|
|
What is the MOA of imatinib mesylate (Gleevec)?
|
- Tyrosine receptor kinase inhibior that acts on Philadelphia chromosom fusion protein product Bcr-ABl in CML.
- Stops autophosphorylation & the unchecked proliferation of granulocytes in CML. |
|
|
What do glomeruli of diabetic patients with ESRD (End-Stage Renal Disease) look like histologically?
|
Nodular glomerulosclerosis
|
|
|
What is the most common congenital heart disease in adults? How can it present?
|
Patent foramen ovale (PFO)
- Migraine with aura - Right-to-left cardiac shunts - Stroke in a young patient (venus thrombi bypass pulmonary circulation and cause paradoxical emboli) |
|
|
What is the treatment for a suspected rapies infection?
|
1) Administer human rabies immune globulin to provide passive immunity
2) Followed with a series of 5 injections of killed rabies virus vaccination to develop active immunity |
|
|
What 2 steps make bilirubin soluable?
|
1) Noncovalent binding to albumin (in liver)
2) Conjugation with glucuronate (in hepatocytes via UDP-glucuronyl transferase) to form bilirubin diglucuronide |
|
|
Where is urobilinogen producted?
|
Gut: bilirubin diglucuronide is reduced by gut bacteria
|
|
|
What is the typical presentation for MEN1?
|
Hyperparathyroidism (hypercalcemia & hypophosphatemia)
|
|
|
Besides hyperparathyroidism, what 2 signs can be indicative of MEN1?
|
1) Pituitary prolacinoma (galactorrhea)
2) Duodenal ulcers (gastrinoma in the pancreas causing Sollinger-Ellison syndrome) |
|
|
What nerve roots is the pudendal nerve derived from?
|
S2-4
|
|
|
What is the karyotype of a complete mole?
|
46 XX (haploid sperm replicates within an empty egg)
|
|
|
What is the karyotype of a partial mole?
|
69 XXX (2 haploid sperm fertilize a haploid egg)
|
|
|
What "essential" amino acids can be synthesized by a healthy adult?
|
histidine & arginine
|
|
|
What is the embryological source of cranial nerve VII & muscles of facial expression
|
2nd branchial arch
|
|
|
Which test for syphilis is the most specific?
|
FTA-ABS: dlurescent treponemal antibody absorption
|
|
|
What are the early cellular changes due to ischemia? late ones?
|
Early: cellular swelling, organelle swelling, ribosomal disaggregation
Late: organelle membrane damage & morphologic changes (cell blebs), cell surface deformities caused by cyoskeletal dysfunction, & nuclear changes (pyknosis, karyolysis, & karyorrhexis) |
|
|
How do renin levels distinguish 1 from 2ndary hyperaldosteronism?
|
Primary: high renin
Secondary: low renin |
|
|
What is the hemodynamic picture for septic shock?
|
- Increased CO
- Decreased SVR (Systemic Vascular Resistance) & PCWP (Pulmonary Capillary Wedge Pressure) |
|
|
What is the hemodynamic picture of neurogenic shock?
|
- Loss of vasomotor tone
- Decreased CO - Decreased PCWP (Pulmonary Capillary Wedge Pressure) |
|
|
What hemodynamic picture indicates hypovolemic shock?
|
- Increased SVR
- Decreased CO - Decreased PCWP (Pulmonary Capillary Wedge Pressure) |
|
|
What hemodynamic picture is seen with cardiac shock?
|
- Increased SVR
- Decreased Co - Increased PCWP (Pulmonary Capillary Wedge Pressure) |
|
|
What bacteria cause skin abscesses & are most likely transmitted via dog/cat bite?
|
Pasteurella multocida (gram - rod)
|
|
|
What does infection by Brucella canis cause?
|
fever, malaise, hepatosplenomegaly
|
|
|
What are the HACEK organisms?
|
Haemophilus
Actinobacillus Actinomycetemcomitans Cardiobacterium hominis Eikenella corrodens Kingella kingae Can all cause culture negative endocarditis |
|
|
What bacterium can be transmitted to humans via handling of rabbit tissue (or a tick or deerfly bite)?
|
Francisella tularensis
- Well-demarcated skin lesion with a black base!! - Later: systemic symptoms (fever, headache, malaise) |
|
|
What is the leading theory about how vaccine use has increased the number of allergies/autoimmune diseases?
|
- Low stimulation of Th1 lymphocytes (b/c they are stimulated by bac/viruses)
- This leads to an overproduction of Th2 lymphocytes and allergen-specific IgE |
|
|
What drug is used to treat narcolepsy daytime sleepiness>
|
- Modafinil: increases monoamines in the brain somehow (MOA unknown)
- Safer than amphetamines & methylphenidate |
|
|
What nerve innervates the adductor muscles of the thigh? What patients are at risk for damage?
|
Obturator (athletes: can be entrapped between muscles)
|
|
|
What nerve innervates the anterior compartment of the thigh?
|
femoral (flexes the thigh & extends the knee)
|
|
|
What nerve innervates the gluteus maximus?
|
Inferior gluteal: extends & laterally rotates the thigh
|
|
|
What nerve innervates the obturator internus & superior gemellus?
|
Obturator internus: laterally rotates & flexes the thigh
|
|
|
What muscles does the sciatic nerve (tibial & common peroneal divisions) innervate?
|
Hamstrings (posterior thigh muscles): extend the thigh & flex the leg
|
|
|
How is the kidney changed in hepatorenal syndrome?
|
- It is not. It remains of normal shape & size.
- There change is only physiological: vasoconstriction in the vascular beds due to the activation of the renin-angiotensin system. |
|
|
In what disease do the kidneys appear grossly flea-bitten?
|
Malignant hypertension
|
|
|
What is the MOA of hydralazine?
|
increases cGMP & causes smooth muscle relaxation (greater effect on arterioles than veins) to reduce afterload
- Rx: essentail hypertension and CHF SE: compensatory tachycardia (angina), Up fluid retention, & lupus-like syndrome with long-term use |
|
|
What is a rare complication of long-term heparin therapy? What's the treatment?
|
HIT: heaprin-induced thrombocytopenia
- Heparin-specific antibodies form complexes with heparin & platelets - Results in platelet activation, clot formation, & steadily dropping platelet levels Rx: Direct thrombin inhibitors (Argatroban & Lepirudin) |
|
|
What are the direct thrombin inhibitors & why aren't they 1st line therapy?
|
- Argatroban & Lepirudin
- Effects are not readily reversible |
|
|
What are the physical findings that indicate I-cell disease?
|
Coarse facial features
Developmental delay Restricted joint movement Histo: intracytoplasmic inclusions in mesenchymal-origin cells. |
|
|
What is the pathogenesis of I-cell disease?
|
Improper intracellular trafficing:
- Failure to add a mannose-6-phosphate residue to proteins that should be directed to lysosomes - Result: membrane-bound intracytoplasmic vacuoles that are filled with fibrillogranular material (lipids, mucopolysaccharides, oligosaccharides) |
|
|
How is congenital rubella infection characterized?
|
Cataracts
Glaucoma Pigmented retinopathy Cardiac malformations Deafness |
|
|
What is the MOA of bacterial/viral superantigens?
|
Proteins that nonspecifically cross-link MHC class II molecules with certain T-cell receptor (TCR) subsets
- Inappropriate activation of these T-cells (2-20% of all T-cells) - Supraphysiologic production of cytokins: IL-1, TNFalpha, IL-6, IL-12, interferon-gamma. |
|
|
What is oculocutaneous albinism?
|
A mutation in tyrosinase (converts tyrosine into dopa) that is the key, rate-limiting step in melanin production from phenylalanine
|
|
|
What enzyme is deficient in Maple syrup urine disease?
|
alpha-ketodehydrogenase:
- inability to degrade branched amino acids (isoleucine, leucine, valine) I LoV Maple Syrup |
|
|
What enzyme deficiency results in galactosemia & galactosuria?
|
galactokinase: converts galactose into glucose
|
|
|
What disorder is characterized by black urine (especially after long periods of standing) & arthralgias?
|
Alkaptonuria (deficiency of homogentisic acid oxygenase)
|
|
|
What 3 different enzyme deficiencies can result in homocystinuria?
|
1) Methionine synthase
2) Cystathionin synthases (converts homocysteine into cysteine): REQUIRES B6!! 3) Decreased affinity of cystathionine synthase for pyridoxal phosphate Result: mental retardation, osteoporosis, tall statue, kyphosis, lens subluxation |
|
|
What is the presentation of giardiasis?
|
- Bloating
- Flatulence - Foul-smelling, nonbloody, diarrhea - Light-colored fatty stools |
|
|
What infection presents with macrophages containing amastigotes and clinical symptoms of hepatosplenomegaly, malasie, anemia, & weight loss?
|
Leishmainia donovani (sandfly transmission)
Rx: Sodium stibogluconate |
|
|
What 2 important cystic infections are acid-fast staining?
|
- Cryptosporidium (water: fecal-oral): severe/mild, nonbloody diarrhea (severe = HIV Px)
- Toxoplasma (raw meat or cat feces): brain abscesses in HIV Px & birth defects if congenital |
|
|
What is the treatment for T. gondii?
|
Sulfadizine & pyrimethamine
|
|
|
What are RBCs containing schizonts characteristic of?
|
Plasmodium infection (late stage of the asexual form of the parasite) transmitted by the female Anopheles mosquito: flu-like symptoms
|
|
|
What endogenous hormone inhibits HCl secretion?
|
somatostatin
|
|
|
How do NSAIDS cause peptic ulcer disease?
|
Disrupt the mucus barrier by inhibiting prostaglandin synthesis
|
|
|
What cells secrete cholecystokinin?
|
I cells: promotes gallbladder contraction after ingestion of fatty acids or amino acids
|
|
|
What is the action of VIP (vasoactive intestinal polypeptide)?
|
Increases intestinal water & electrolyte secretion
|
|
|
What is the 1st line therapy of ulcerative colitis?
|
Sulfasalazine:
- Metabolized to 5-aminosalicylic acid in GI tract & decreases local inflammation - SE: Renal insufficiency & increased risk of a bleed |
|
|
When is ciprofloxacin used to treat UC?
|
When it is complicated by strictures & infections of the GI (NOT 1st line Rx)
|
|
|
What do the acidophils of the pituitary secrete?
|
Growth hormone
Prolactin |
|
|
What do the basophils of the pituitary secrete?
|
FSH
LH ACTH TSH |
|
|
What are oxyphils?
|
Cells of the parathyroid gland
|
|
|
@ what receptors does ADH act?
|
V2 (basolateral side of principal cells)
- activates Gs-mediated cyclic AMP - This mobilizes aquaporin transmembrane channels to the luminal surface - Net water moves from the collecting duct lumen to the hyperosmolar interstitium |
|
|
What is the course of the ureters in the female pelvis?
|
- Cross iliac artery anteriorly @ its bifurcation
- Continues into the pelvis, where it passes posterior to the uterine artery "water under the bridge" |
|
|
What presents in 10% of patients with pancreatic adenocarcinoma?
|
Trousseau's Syndrome: migratory thrombophlebitis
+ normal signs of acute weight loss, steatorrhea, & atypical DM (increase thirst & urination) |
|
|
What is the blood supply of the liver?
|
75%: portal vein
25%: hepatic artery BUT, they give equal O2 |
|
|
How does Brown-Sequard present?
|
(spinal cord hemisection)
- ipsilateral loss of motor function & vibration/proprioception - contralateral loss of pain & temperature sensation |
|
|
How does Syringomyelia present?
|
bilateral sensory defects in the upper extremities dues to enlargement of the central canal of the spinal cord
|
|
|
What is the most commonly obstructed artery in the gut & what does it supply?
|
SMA (superior mesenteric artery): embryonic midgut (duodenum to the proximal 2/3 of the transverse colon)
|
|
|
What artery supplies the gallbladder, stomach to proximal duodenum, pancrease & the liver?
|
celiac: embryonic foregut
|
|
|
What infection causes undulating fever (peaks in the evening & falls at nighttime)?
|
Brucella (contaminated milk or direct livestock contact)
|
|
|
Where are Yersinia pestis buboes located?
|
Buboes (painful, enlarged lymph nodes) in the groin & armpits.
- then can enter bloodstream and cause sepsis, DIC, pneumonia or meningitis |
|
|
How is renal osteodystrophy treated?
|
- Ca
- Phosphate binders - calcitriol (synthetic vitamin D3) supplimentation |
|
|
What lung parameter is changed equally in obstructive & restrictive lung disease?
|
decrease in vital capacity (insufficient amount of air exhaled or inhaled)
|
|
|
What are the 2 ways that glucose can enter a cell?
|
1) Na-independent facilitated diffusion with glucose transporters
2) Na-monosaccharide cotransporter system (intestinal cells, renal tubules, choroids plexus) SGLT-1 |
|
|
Where is the GLUT-2 receptor?
|
Basal surface of intestinal cells & transmits glucose into the blood
|
|
|
Where is the GLUT-4 receptor?
|
Muscle & adipose tissues
|
|
|
Where is the GLUT-5 receptor?
|
Lumen of the gut: Na-dependent absorbtion of fructose
|
|
|
What is the MOA of beta-blockers that allows them to help with coronary artery disease?
|
Slows phase 4 depolarization & prolong's diastole: increase coronary artery filling
- Decreased sympathetic tone decreases the inward Na+ current |
|
|
What characterizes the 2nd phase of Lyme disease?
|
(Borrelia burgdorferi via Ixodes tick)
- Transient arthralgias - Bell's palsy - Atrioventricular nodal block - 2ndary annular rashes - Carditis |
|
|
What characterizes the 3rd phase of Lyme disease?
|
Migratory joint pain
Chronic arthritis Encephalopathy Acrodermatitis |
|
|
What infection is characterized by relapsing fevers (~5 days of fever with ~ 1 week between episodes)?
|
Borrelia burgdorferi (spirochete): fever pattern is due to its ability to undergo antigenic variation
|
|
|
How can lymphoblasts be distinguished from mature lymphocytes?
|
lymphoblasts have fine, homogenous chromatin, irregular nuclear boarders, & scant cytoplasm
- Found in ALL (Dx: peripheral blood smear) |
|
|
What heart murmur indicates a VSD?
|
II-III/VI holosystolic murmur
- Best heard @ the left sternal boarder |
|
|
What 3 defects can result in a VSD?
|
1) Septum of the atrioventricular canal
2) Muscular septum 3) Distal conal septum |
|
|
What are the GRAIN lab results that indicated sarcoidosis?
|
gamma-Globulinemia
Rheumatoid arthritis elevated ACEnzyme levels Interstitial fibrosis Noncaseating granulomas |
|
|
Where are Mallory-Weiss tears found?
|
gastroesophageal junction: a nonpenetrating mucosal tear
|
|
|
What is Boerhaave's perforation?
|
- Transmural perforation of the esophagus
- Presents with Mackler triad: vomiting, lower thoracic pain, subcutaneous emphysema - Dx: endoscopy & Rx: surgery |
|
|
What is the major distinguishing factor of hepatitis E?
|
- Severe, often-fatal disease course in pregnant women: fulminate (20% mortality)
- Hep E = RNA herpesvirus (nonenveloped, ssRNA) |
|
|
What type of virus is Hep C?
|
RNA flavivirus (Enveloped RNA)
- Blood borne |
|
|
What type of virus is Hep B?
|
DNA hepadnavirus (enveloped, circular DNA)
|
|
|
What type of virus is Hep D?
|
Defective RNA deltavirus (requires Hep B to serve as an envelope)
|
|
|
How does FSH induce the conversion of testosterone to 17-beta-estradiol in the ovaries?
|
Stimulates the enzyme aromatase within the graulosa cells to convert testosterone to 17-beta-estradiol in the overian follicle.
- Testosterone gets to the granulosa cells via diffusion from the theca cells where it is produced |
|
|
What are the 4 causes of Parkinsonism?
|
1) Neurodegeneration of the substantia nigra (idiopathic)
2) MPTP exposure 3) Adverse effects of neuroleptic meds 4) Ischemic damage to the basal ganglia |
|
|
What causes hemiballism of the limbs?
|
lesion of the contralateral subthalamic nucleus cause uncontrollable flailing
|
|
|
Describe the (INHIBITORY) indirect pathway in the brain.
|
1) Substantia nigra pars compacta sense INHIBITORY neurons to the striatum.
2) Striatum sense INHIBITORY output to the external segment of the globus pallidus; this inhibits the subthalamic nucleus 3) Subthalamic nucleus sends EXCITATORY neurons to the internal segment of the globus pallidus: this increases firing of GABA neurons that run from the GPi to the thalamus 4) Movement on the contralateral side of the body is inhibited |
|
|
What brain lesion would cause a spastic paralysis of the arm & leg on one side of the body?
|
On the CONTRALATERAL side of the brain either:
1) primary motor cortex 2) medullary pyramid 3) lateral white matter tract of the spinal cord above C5 |
|
|
What does paralysis in general indicate?
|
A problem in the motor neurons themselves (i.e. not a ganglion)
|
|