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Renal and Male GU
| Question | Answer |
|---|---|
| What are some drugs associated with hematuria? | Warfarin, Heparin, Cyclophosphamide (also risk for TCC) |
| Which type of azotemia would present with BUN/Cr < 15? Why? | Renal azotemia due to damage of tubular epithelium (Prolonged obstruction presents similarly) |
| Describe casts. Where are they formed? | protein matrix that entrap cells, debris, or protein leaking through glomeruli; formed in tubular lumens |
| What determines protein filtration at the GBM? | size and charge; heparan sulfate is (-) thus only permeable to LMW cationic proteins |
| In Nephritic syndrome, what mediates glomerular injury? | IC deposition, Complement activated, C5a recruits neutrophils |
| What are some clinical features of nephritic syndrome? | HTN (Na), Periorbital puffiness, Oligura, Hematuria, |
| In nephrotic syndrome, what mediates glomerular injury? | T cell production of cytokines that cause GBM to lose (-) charge and may cause podocytes to fuse |
| What are some clinical features of nephrotic syndrome? | Proteinuria, Edema, Fatty casts with maltese crosses and oval fat bodies, Hypercoaguable state (loss of ATIII) |
| IgA glomerulopathy | Berger's disease, nephritic mesangial IC deposits w/ granular IF, eposodic bouts of hematuria following URI |
| Post-streptococcal GN | Follows Group A Strep infection; Subepithelial IC depositis with granular "lumpy bumpy" IF; diffuse proliferative pattern with neutrophils;Hematuria, periorbital edema, incr anti-DNase B titers |
| Nephropathy in SLE | (II) increase in mesangial cells and matrix, proteinuria (IV) Diffuse proliferative GN; subendothelial IC deposits w/ granular IF = wire-looping of capilaries; endothelial cell and GBM proliferation |
| RPGN (crescentic) | crescent = proliferation of parietal cells and deposition of fibrin in Bowmans space; Goodpastures, Wegener's (c-ANCA), Microscopic polyarteritis (p-ANCA) |
| Minimal change disease | most common nephrotic syndrome in children; EM shows podocyte fusion; often preceded by URI or immunization; responds well to steroids |
| Focal segmental glomerulosclerosis | similar to MCD but it adults; secondary cause due to HIV |
| Diffuse membranous glomerulopathy | most common nephrotic syndrome in adults; subepithelial IC deposits show "spike and dome" pattern on silver stain; due to drugs, infections, malignancy, SLE |
| Type I MPGN | subendothelial ICs activate complement and cause reduplication of GBM due to mesangial expansion resulting in tram track appearance |
| Type II MPGN | Dense Deposit Disease; C3 nephritic factor is an autoAb to C3 convertase which causes sustained activity and low serum C3 levels |
| What is one of the earliest changes in diabetic nephropathy? | GBM thickening due to deposition of type IV collagen |
| What changes occur to the arterioles in diabetic nephropathy? | Nonenzymatic glycosylation produces hylaine arteriolosclerosis, incr GFR which damages the mesangial cells (proteins); KW nodular masses develop due to incr type IV collagen and trapped proteins |
| Alport's syndrome | X-linked mutation in alpha5 type IV collagen; irregular GBM thickening and splitting of lamina densa; isolated hematuria and nerve deafness |
| Thin Basement Membrane Disease | Benign familial hematuria; mutations in alpha3 and 4 collagen type IV |
| What is the pathogenesis of tubular cell injury in ATN? | depletion of ATP, redistribution of membrane proteins, loss of polarity (Na causes vasoconstriction), cells detach from BM and obstruct lumen |
| What are some drugs commonly associated with ATIN? | penicillin, rifampin, sulfonamides, thiazide diuretics, NSAIDs |
| What are some clinical signs of ATIN? | 2 wks after exposure: fever, oliguria, rash, eosinophlia; kidney: intersitial edema w/ inflamm cell infiltrate |
| What is the most common cause of acute pyelonephritis? | vesicoureteral reflux with ascending infection |
| What are the microscopic findings of chronic pyelonephritis? | U-shaped cortical scar; interstitial fibrosis, some tubules contain hyaline casts that resemble thyroid tissue (thyroidization) |
| Analgesic nephropathy | combination of ASA and acetaminophen; leads to renal papillary necrosis w/ heamaturia, proteinuria, and colicky flank pain |
| Amyloidosis | causes nephrotic syndrome; mesangial expansion w/ GMB irregularly thickened (fringe on a rug) with PAS and silver stains |
| Benign nephrosclerosis | finely granular cortical surface; hyaline arteriolosclerosis, reduplication of int. elastic membrane; interstitial fibrosis, tubular atrophy, glomerular sclerosis |
| Malignant nephrosclerosis | surface has pinpoint flea-bitten hemorrhages; concentrially arranged myofibroblasts w/ collagen = hyperplastic arteriolitis ("onion sknning"); fibrinoid necrosis and thrombosus of arterioles and glomeruli |
| What is a Goldblatt kidney? | blood vessels of ischemic kidney are protected from HTN in renal artery stenosis |
| In what location is Renal Cell Carcinoma most common? Where does it invade? | upper poles, invades renal vein |
| Where is Renal Cell (clear) carcinoma derived from? What is contained in the clear cells? | tubular epithlium; glycogen and lipids |
| What is the most common renal tumor in children? From where is it derived? | Wilm's tumor; mesonephric mesoderm |
| What is the term for bladder muscosa exposed to the anterior body surface? What other abnormality is it associated with? | exstrophy of the bladder; associated with epispadias |
| What is the most common cause of bladder adenocarcinoma? | urachal cyst remnant drainage of urine from umbilicus |
| What is the most common risk factor for TCC? location? | smoking increases risk 5-7 fold; lateral and posterior wall of the bladder |
| What are some risk factors for testicular seminoma? | cryptorhid testicle, testicular feminization, Klinefelter's syndrome |
| What tumor are Schiller-Duval bodies associated with? What do they resemble? | Yolk sac (endodermal sinus) tumor; resemble glomeruli |
| In BPH, where does hyperplasia of glandular and stromal cells develop? | glandular - transitional zone; stromal - periurethral zone |
| Does SHBG have a higher affinity for testosterone or estrogen? | testosterone |
| How do androgens/estrogens affect synthesis of SHBG? | estrogens increase the synthesis while androgens decrease the synthesis |
| What are some causes of leydig cell and seminiferous tubule dysfunction? | chronic alcoholic liver disease (inhibits binding of LH to cells), chronic renal failure (toxins), irradiation, orchitis, trauma |
| What is the most common cause of impotence in men > 50? | vascular insufficiency (Leriche syndrome); aortoiliac atherosclerosis, calf claudication, diminished femoral pulse |
| What is Peyronie's disease? | fibromatosis with painful contractures of the penis causing lateral curvature; may cause infertility |
| What metabolic abnormality is a serious risk in ATN? When does it occur? | In the initial oliguric phase, hyperkalemia can cause a fatal arrhythmia |
| What is Fanconi syndrome? | dysfunction of PT (hereditary or acquired) causing impaired resorption of glucose, AA, phosphate, and bicarbonate |
| What is the most common cause of diffuse cortical necrosis? | obstetric catastrophes (placental abruption or eclampsia); end-organ vasospasm and DIC |
| What are the characteristics of uremia? | azotemia, acidosis (sulfates, phosphates, organic acids), hyperkalemia, abnormal volume control, hypocaclemia, anemia, HTN |
| Define WAGR complex? | Wilm's tumor, Aniridia, GU abnormalities, Mental/Motor retardation; deletions on chromosome 11 |
| In urethritis, what infection should be suspected when bacteria are NOT demonstrated in a purulent urethral discharge? | Chlamydia |
| What diuretic causes a gouty attack? | thiazide diruetics |