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59 Cards in this Set
- Front
- Back
Potter's syndrome
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bilateral renal agenesis-->oligohydramnios-->limb deformities, facial deformities, pulm hypoplasia
caused by malformation of utereric bud |
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Horseshoe kidney
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inf poles of kidneys fuse; get trapped under IMA and remain low in abdomen
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RBC casts
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glomerular inflammation (nephrotic syndromes), ischemia, malignant hypertension
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WBC casts
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pyelonephritis, AIN
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bacterial casts
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pyelonephritis
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epithelial cell cast
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renal tubular damage
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waxy cast
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stasis of urine flow
advanced renal disease, CRF |
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fatty cast
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nephrotic syndrome
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granular cast
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N/S, ATN
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nephritic syndrome
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hematuria, hypertension, oliguria, azotemia, mild proteinuria
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PSGN
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LM: glomeruli enlarged and hypercellular, neutrophils, lumpy bumpy
EM: subepi humps IF: granular pattern most often in children; peripheral and periorbital edema |
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RPGN (cresentic)
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LM and IF: crescent moon shape
rapid course to renal failure number of crescents indicates prognosis |
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Goodpastures (type II HS)
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IF: linear pattern, anti-GBM AB
hemoptysis and hematuria |
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MPGN
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EM: subendo humps, tram track
slow progress to renal failure |
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IgA nephropathy (Bergers)
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IF and EM: mesangial deposits of IgA
mild disease, often post infectious |
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Alports
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split basement membrane
collagen IV mutation nerve deafness and ocular disorders |
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Nephrotic syndrome
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massive proteinuria, hypoalbuminemia, peripheral and periorbital edema, hyperlipidemia (fatty casts)
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membranous GN
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LM: diffuse capillary and BM thickening
IF: granular pattern EM: spike and dome most common cause of adult nephrotic syndrome |
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MCD (lipoid nephrosis)
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LM: normal glomeruli
EM: foot process effacement most common cause of childhood nephrotic syndrome, responds well to steroids |
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FSGS
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LM: segmental sclerossi and hyalinosis, more severe in HIV pts
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Diabetic nephropathy
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LM: Kimmelstiel Wilson wire loop lesions, BM thickening
expansion of mesangial matrix |
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SLE
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LM: in membranous glomerulonephritis pattern, wire loop lesion with subendo deposits
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Amyloidosis
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IF: congo red stain, apple green birefringence
assoc with multiple myeloma, chronic conditions, TB, RA |
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Ca kidney stone
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most common; CaOx or CaP
conditions that cause hyperCa radioopaque |
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Struvite kidney stone
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Ammonium magnesium phosphate
caused by infection with urease positive bugs (Proteus, Staph, Kleb) staghorn calculi radioopaque, worsened by alkaluria |
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Uric acid kidney stones
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assoc with hyperuricemia or result of disease with increased cell turnover
radiolucent worsened by aciduria |
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cysteine kidney stones
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radioopaque
tx with bicarb |
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RCC
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men 50-70; increased incidenced with smoking and obesity
assoc with VHL hematuria, palpable mass, polycythemia, flank pain, fever, weight loss; heme spread by IVC |
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RCC paraneoplastic syndromes
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ectopic EPO, ACTH, PTHrP and prolactin
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Wilms tumor
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ages 2-4; presents with huge palpable flank mass, hemihypertrophy; deletion of TSG WT1 on chromo 11; can be part of WAGR complex- Wilms tumor, aniridia, genitourinary malformation, MR
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transitional cell carc
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most common tumor of urinary tract system; painless hematuria
assoc: phenacetin, smoking, aniline dyes, cyclophosphamide, schistosomiasis |
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Pyelonephritis- acute
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affects cortex with sparing of glomeruli/vessels
white cell casts in urine fever, CVA tenderness |
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Pyelonephritis- chronic
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coarse, assym corticomedullary scarring, blunted calyx; tubules contain eosinophilic casts (thyroidization of kidney)
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DCN
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acute generalized infarction of cortices of both kidneys; likely due to a combination of vasospasm and DIC
assoc with obstetic catastrophes and septic shock |
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drug induced interstitial nephritis (AIN)
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acute interstitial renal inflammation
fever, rash, eosinophilia, hematuria 2 weeks after admin; drugs act as haptens inducing HS |
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drugs causing AIN
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sulfa, cephalo, cipro, cimetidine, allopurinol, PPI, indinavir, salicylates
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ATN
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most common cause of ARF; reversible but fatal if untreated; assoc with renal ischemia (shock), crush injury (myoglobulinuria), toxins (AG, cephalo, polymixins, contrast dye)
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ATN pathogenesis
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loss of cell polaritiy, epithelial cell detachment, necrosis, granular casts
stages: inciting event, maintenance, recovery death in oliguric phase |
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renal papillary necrosis associated with
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diabetes, acute pyelonephritis, chronic phenacetin due, sickle ccell anemia
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fanconi's syndrome
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defect in proximal tubule transport of AA, glucose, phosphate, uric acid, protein and electrolytes
assoc with Rickets, osteomalacia, hypokalemia, met acid |
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APKD
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multiple, large bilateral cysts that ultimately destroy parenchyma; presents with flank pain, hematuia, HTN, urinary infection, progressive renal failure
AD assoc with polycystic liver dz, berry aneurysms, mitral valve prolapse |
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Infantile PKD
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infantile presentation in parenchyma; AR
assoc with hepatic cysts and fibrosis |
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dialysis cysts
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cortical and medulalry cysts resulting from long standing dialysis
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simple cysts
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benign, incidental finding
cortex only |
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medullary cystic disease
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medullary cysts
U/S: small kidney poor prognosis |
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medullary sponge disease
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collecting duct cysts; good prognosis
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low Na
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disorientation, stupor, coma
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high Na
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neuro: irritability, delirum, coma
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if you correct Na too quickly
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central pontine myelinosis
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low Cl
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secondary to met alka
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high Cl
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secondary to non anion gap acidosis
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low K
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U waves on ECG; flattened T waves, arrythmias, paralysis
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high K
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peaked T waves, arrythmias
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low Ca
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tetany, NM irritability
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high Ca
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delirium, renal stones, ab pain
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low Mg
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NM irritability, arrythmias
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high Mg
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delirium, decr DTRs, cardiopulm arrest
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low PO4
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low mineal ion product causes bone loss
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high PO4
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high mineral ion product causes met calc, renal stones
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