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126 Cards in this Set
- Front
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Pediatric renal neoplasms
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Wilms tumor (nephroblastoma) and Mesoblastic nephroma
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Adult benign renal neoplasms
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Papillary adenoma, oncocytoma, angiomyolipoma
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Adult malignant renal neoplasms
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Renal cell carcinoma and urothelial carcinoma
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Malignant pediatric tumor of the kidneys comprised of embryonal nephrogenic elements
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Wilms tumor
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Wilms tumor is a triphasic neoplasms: what are the 3 possible tissue constituents?
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Blastema, Epithelium, Stroma
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Wilms tumor 4 Rules of 5
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5% childhood cancers, 5% bilateral, 5% multicentric, 5% anaplastic (worse prognosis)
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Organomegaly, hemihypertrophy; WT2 gene mutation; 5% develop Wilms tumor
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Beckwith-Wiedeman syndrome
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Wilms-aniridia-genital anomaly-retardation; WT1 gene mutation; 33% develop Wilms tumor
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WAGR syndrome
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Glomerulonephritis, male pseudohermaphroditism; WT1 gene mutation; 90% develop Wilms tumor
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Denys-Drash syndrome
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Loss of or mutation in tumor suppressor genes on chromosome 11 (WT1 and WT2 genes)
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Wilms Tumor
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Most common renal tumor of infancy; composed fo spindled cells with varying resemblance to immature tissues from mesoderm
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Mesoblastic Nephroma
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Papillary renal tumor <0.5 cm
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Renal papillary adenoma
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Papillary renal tumor >0.5 cm
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Papillary renal cell carcinoma
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Most common renal tubular epithelial neoplasm
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Renal papillary adenoma
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Central Stellate Scar
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Oncocytoma
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Multiple angiomyolipomas suggests
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Tuberous sclerosis
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Most common malignant renal neoplasm in adults
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Renal cell carcinoma
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Transitional cell carcinoma (TCC) involving the collecting system (calyces and pelvis)
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Urothelial carcinoma
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Classic triad of Renal Cell Carcinoma
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Flank pain, palpable mass, and hematuria
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Most common neoplastic recipient of a metastasis from another malignant neoplasm
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Renal cell carcinoma
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Mutation of VHL gene in >90% of cases
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Clear Cell Renal Cell Carcinoma
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Second most common type of RCC - rarely a germline mutation in c-met; more often multiple than any other type of RCC
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Papillary Renal Cell Carcinoma
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Fibrovascular cores contain numerous "foam cells"
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Characteristic of Papillary RCC
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Worse prognosis of typical RCC subtypes
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Collecting Duct Carcinoma
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Very rare, very aggressive; all have been African-American or Mediterranean; associated with sickle cell trait or disease
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Renal Medullary Carcinoma
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Urolithiasis
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Formation of urinary stones
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4 main types of Urolithiasis
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Calcium, Struvite, Uric acid, Cystine
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"Triple stones": magnesium ammonium phosphate
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Struvite
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Struvite stones indicative of
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Bacterial infections (Proteus); large stones (staghorn calculi)
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Muscularis mucosa
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Incomplete slips of smooth muscle
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Muscularis propria
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Detrusor muscle- thick bundles of smooth muscle
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Exposes bladder muscosa to external environment; anterior bladder wall and abdominal wall are absent
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Exstrophy
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Out-pouchings of visceral organ consisting of all layers of the wall of the organ
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True Diverticula
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Vestigial remnant of the connection of the bladder apex to the allantois
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Urachus
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Michaelis-Gutmann bodies within lysosomes of macrophages
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Malacoplakia
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Not all of this kind of urothelial carcinoma are invasive
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Papillary Urothelial Carcinoma
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Invasive, by definition, is this kind of urothelial carcinoma
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Flat - associated with urothelial carcinoma in situ
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Ta
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noninvasive, papillary
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Tis
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Carcinoma in situ (noninvasive, flat)
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T1
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Lamina propria invasion
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T2
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Muscularis propria invasion
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T3a
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Microscopic extra-vesicle invasion
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T3b
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Grossly apparent extra-vesicle invasion
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T4
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Invades adjacent structures
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Most common in countries where urinary schistosomiasis is endemic
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Squamous cell carcinoma
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Normal PCO2; Normal HCO3-
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PCO2= 40; HCO3-= 24
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For each Gram drop in serum albumin, the anion gap decreases by a factor of
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Around 2.5
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Urine Anion Gap =
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Na + K - Cl
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Normal Urinary Anion Gap =
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-10 - 10
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An increase in ammonium excretion is synonymous with an increase in excretion of this
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Chloride
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As chloride excretion increases, the urinary anion gap becomes more
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Negative (Na + K - Cl)
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If there is a loss of bicarb from the kidneys; what happens to ammonium and the urinary anion gap
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Ammonium excretion is decreased and the urinary gap becomes more positive
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An osmolar gap over 20 indicates
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The presence of other osmolarly active substances in the blood
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Normal Flora of urinary tract in women
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Lactobacillus, Coag negative staph, streptococcus, mycoplasma (low numbers), enteric gram-negatives (low numbers)
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Normal Flora of urinary tract in Men
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Coag negative staph, streptococcus, mycoplasma
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Most causative bacteria in community aquired UTI
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Escherichia coli
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Biochemical characteristics of E. coli
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Indole positive, Voges-Proskauer negative, Lysine decarboxylase positive, Lactose fermentation positive
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Glomerular Filtration Rate
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Normal=180 L/day; Volume/time
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Filtration Fraction
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GFR/RPF - is greater at low plasma flow than at high flow
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Does vasoconstrict, but normally RBF and GFR remain constant
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ADH (AVP)
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Afferent dilation, thus causes increases in both GFR and RBF; also inhibits the secretion of renin
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ANP
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Generally protective against excessive vasoconstriction like you might see with lots of SNS and ANG II
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Prostaglandins
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Na < 135 mmole/L
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hyponatremia
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Na > 144 mmole/L
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Hypernatremia
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Reflects the concentration of all solutes
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Osmolality
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Reflects the concentration of solutes that will cause a water shift
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Tonicity
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Most abundant cation in the body
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Potassium
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Most of the body's potassium is __ with a concentration of around 150 mEq/L
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Intracellular
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Extracellular potassium is around
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3.5 - 5 mEq/L
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Intracellular transport of potassium is mediated by
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Insulin and Beta-2 adrenergic stimulation
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U WAVE
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Hypokalemia EKG change
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Intermittent episodes of muscle weakness associated with transient acute shifts of K+ into cells
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Hypokalemic periodic paralysis
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Autosomal dominant hypertension, impressive cardiovascular sequalae and in many cases hypokalemia
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Liddle Syndrome
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Treat Liddle Syndrome with
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Triamterene combined with dietary salt restriction (normalizes BP and corrects hypokalemia)
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Defect, usually diagnosed in childhood, of impaired NaCl reabsorption in the loop of Henle (similar to loop diuretics)
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Bartter's Syndrome
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Autosomal recessive, usually diagnosed later in life; findings mimic a thiazide diuretic; don't have high urine Ca but do have low serum magnesium levels
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Gitelman's syndrome
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4 ways for Normotensive Renal Potassium Wasting
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Bartter syndrome, Gitelman syndrome, diuretic use, Distal RTA
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Maximum IV Potassium Replacement
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20 mEq/hr under constant cardiac monitoring
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EKG manifestations of hyperkalemia
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Peaked T waves, Prolonged QT intervals, Widened QRS complex, disappearance of P wave, Sine wave
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Short stature, stiff spine, and deformities of hands and feet; suppressed renin activity
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Gordon syondrome
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Treatment for Gordon syndrome
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Responds well to thiazide diuretics
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3 steps to treat Hyperkalemia
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Stabilize the myocardial membrane, Drive extracellular potassium into the cells, Removal of Potassium from the body
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Two things to give to help stabilize the myocardial membrane in hyperkalemia
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Calcium gluconate and calcium chloride
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2 things to drive extracellular potassium intracellularly
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Beta-2 agonists and Insulin
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Give this if hyperkalemia is secondary to ongoing severe metabolic acidosis
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Sodium Bicarbonate
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Exchanges sodium for potassium and binds it in the gut, primarily the large intestine, decreasing total body potassium
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Sodium Polystyrene Sulfonate
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What controls total body water
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ADH (Vasopressin) and Thirst center
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What controls Na in the body
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Aldosterone
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Where is the thirst center located
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In the hypothalamus
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Calculated Sosm
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2 x (Plasma Na) + (BUN)/2.8 + (Glucose)/18
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Clinical manifestations of hyponatremia are largely related to complications of
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Cerebral edema
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Symptoms of acute hyponatremia
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Nausea, vomiting, lethargy, confusion, seizures, coma
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Pt hyperglycemic: Corrected Na =
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1.6[(Pt glucose - 100)/100] + Pt. Na
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Sodium Replacement Calculation
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(.6 x ideal wt kg)(desired Na - pt Na)
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In Hypervolemic Hyponatremia, is the problem increased or decreased effective circulating volume
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Decreased
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Treatment for Hypervolemic hyponatremia
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Fluid restriction, Na restriction, loop diuretics
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Euvolemic hyponatremia: Uosm < 100
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Primary polydipsia, beer potomania, tea and toast diet
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Euvolemic hyponatremia: Uosm > 100
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SIADH, hypothyroidism, glucocorticoid deficiency
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Caused by HPV; presents with papillary lesions on the glans of shaft of the penis
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Condylomata Acuminata
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Inflammation of prepuce associated with the inability to retract the prepuce over the glands penis
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Phimosis
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Angulation of the penis during erection
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Peyronie's disease
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Cause of Syphylitic hard chancre
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Treponema pallidum
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Cause of chancroid (soft chancre)
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Haemophilus ducreyi
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2 things that can cause Urethritis
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Gonococcal or Nongonococcal
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Nongonococcal urethritis caused by:
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Chlamydia trachomatis (most common), Ureaplasma urealyticum, Trichomonas vaginalis
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Most common site in women for a urethral meatal stenosis
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Bulbous urethra
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Most common cause in men for a urethral meatal stenosis
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Posterior Urethral Valve
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With bloody urine with dysuria think
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Hemorrhagic cystitis
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Kind of cancer to associate with Schistosomiasis hematobium
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Squamous cell carcinoma
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Elevate the scrotum and the pain goes away
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Prehn's Sign
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Most common type of Testicular tumor
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Seminoma
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Cobra head configuration on an IVU
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Ureterocele
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Weigert-Meyer law
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The portion of the ureter that comes from the inferior collecting system will have the superior orifice (and vice versa)
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Most common tumor in the kidney
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Renal (clear) cell carcinoma
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Priaprism
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Maintained erection for over 4 hours which is often painful
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Treat over active bladder syndrome with
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Anticholinergics
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Stage 1 CKD
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GFR > or = 90
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Stage 2 CKD
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GFR 60-89
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Stage 3 CKD
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GFR 30-59
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Stage 4 CKD
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GFR 15-29
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Stage 5 CKD
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GFR < 15 (or dialysis)
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Treatments to slow progression of CKD
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Strict glycemic control, ACE-I/ARBs, Strict BP control (perhaps dietary proteins restricted)
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Cockcroft-Gault
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[(140-age)x wt. kg]/Pcr x 72
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Provides a more accurate estimate of GFR than other equations
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MDRD equation
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Serum Cr levels of 1.5 mg/dL have been considered
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Indicative of Chronic Kidney Disease
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Fraction of calcium that is hormonally regulated - is biologically active
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Ionized Calcium
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