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44 Cards in this Set

  • Front
  • Back

Azotemia

elevation of BUN and Creatinine, due to decreased GFR

Prerenal Azotemia

occurs during hypoperfusion of the kidney



(CHF, shock, hemorrhage)

Postrental Azotemia

Occurs when urinary outflow is compromised

Uremia

signs of azotemia, include: metabolic, hemtologic, cardiovascular, and endocrine effects

Nephrotic Syndrome

>3.5g/day proteinurea, hypoalbuminemia, hyperlipidemia, and edema

Nephritic Syndrome

hematuria, mild to moderate proteinuria, hypertension, due to glomerular injury

Rapidly Progressive Glomerulonephritis

nephritic syndrome with rapid decline in GFR

Phases of Renal Failure

1. Diminished Renal Reserve- 50% GFR


2. Renal Insufficiency- 20-50% GFR


3. Chronic Renal Failure- <20% GFR


4. End Stage renal Disease- <5% GFR

Horseshoe Kidney

Most common congenital anomaly



Kidney is abnormally located in lower abdomen due to Inferior Mesenteric artery

Renal Agenisis

may be unilateral or bilateral (Potters sequence)



Unilateral- asymptomatic until later in life when hyperfiltration injury may occur



Bilateral- incompatible with life, causes oligohyrdaminos (no amniotic fluid) leads to facial deformation hypoplasia of the lungs, and extremity deformity

Dysplastic Kidney

noninheritied- characterized by cysts and abnormal cartilage.



Typically only affects a single kidney.

Polycystic Kidney Disease

Inherited- bilateral enlarged kidneys



leads to enlarged kidneys with cysts in both cortex and medulla.



AR- infantile, associated with hepatic fibrosis


AD- adult form, due to AKPD1/2 cysts develop overtime.

Medullary Cystic Kidney Disease

leads to small kidneys and fibrosis of the medulla over time.

ARF

Acute Renal Failure



hallmark Azotemia, with oliguria

Acute Tubular Necrosis

(Intrarenal Azotemia)- injury and necrosis of tubular epithelium



Can be ischemic: decreased blood supply often prerenal azotemia



nephrotoxic: drugs, chemicals damage proximal tubule

Acute Interstitial Nephritis

drug induced hypesensitivity



NSAIDs, Penicillin, diuretics

Renal Papillary Necrosis

necrosis of renal papillae



presents with gross hematuria and flank pain



Analgesic Abuse


Diabetes


Sickle Cell


Pyelonephritis

Nephrotic Syndrome

Hypoalbuminemia- pitting edema (decreased osmotic pressure)


Hypogammaglobulinemia- increased infection


Hypercoaguable state- loss of AT III


Hyperlipidemia- beefs up blood

MCD

Minimal Change Disease- common in children



No immunofluorescence, it is an effacement of foot process (podocytes)



Treat with Steroids

FSGS

Focal Segment Glomerulosclerosis



Commonly seen in AfroAmericans/Hispanics


Assoc- w/ AIDs/Heroin/SickleCellDisease



Some glomeruli/some parts of it



No IF, w/ effacement of podocytes



Poor response to steroids

Membranous Nephropathy

commonly seen in White adults



HepB/C, tumors, SLE, or drugs



Thick glomerular membranes w/ granular IF



Subepithelial deposit with "spike and dome"


Poor response to steroids

Membarnoproliferative Glomerulonephritis

Thick "tram-track glomerular membranes w/ granular IF



Type I- subendothelial (HBV/HCV)


Type II- intramembranous assoc. w/ C3 nephritic factor which stabilizes C3 convertase

Diabetes Mellitus

high serum glucose leads to glycosylation of membrane and hyaline arteriolosclerosis



Efferent artierole is most affected leading to high GFR



ACE Inhibitors can slow progression

Systemic Amyloidosis

most commonly involved organ in amyloidosis



deposits in mesangium and results in nephrotic



Apple green birefringence and Congo Red Stain

Nephritic Syndrome

Characterized by inflammation and bleeding



<3.5g/day = limited protienuria


RBC Casts in urine= hematuria

PSGN

Postreptoccal Glomerulonephritis



arises after infectino with Group A Beta Hemolytic strep of skin or phaynx



M protien for kidney... present 2-3 weeks after with hematuria, HTN, and periorbital edema.



Granular IF, subepithelial humps

Rapidly Progressive Glomerulonephritis

nephritis that progresses quickly to renal failure



Crescents in the bowman space (fibrin and macs)



clinical picture and IF determine etiology

Linear IF Pattern

Goodpasture Syndrome: antibody against collagen in glomerular and basement membranes



seen in young adults

Granular

Immune Complex Deposition



PSGN or diffuse proliferative glomerulonephritis



common type of renal disease in SLE

Negative IF

Pauci Immune (immune limited)



wegener granulomatosis, microscopic polyangitis, Churg-Strauss Syndrome



c-ANCA and p-ANCA

IgA Nephropathy

Berger Disease



IgA deposits in the mesangium, most common



Follows mucusal infections

Alport Syndrome

familial defect in type IV Collagen (x-linked)



thins and splits glomerular basement membrane

UTI

Urinary Tract Infection



bladder, ureter, kidney, urethra



Arises due to ascending infection, increased risk in Females



Sex, urinary stasis, and catheters increase risk

Cystitis

Infection of the Bladder



Dysuria, polyuria, suprapubic pain



Urinalysis: cloudy w/ >10 WBC


Dipstick: + pyuria


Culture: greater than 100000



E. Coli, Staph Sapro, K. Pneumonae, Proteus Mirabillis

Pyelonephritis

infection of the kidney- systemic symptoms



fever, flank pain, WBC Casts, leukocytosis



E. Coli, Entero Faecalis, Klebsiella

Chronic Pyelonephritis

interstital fibrosis and atrophy of tubules due to multiple infections



vesicoureteral reflux or obstruction (BPH)

Nephrolithiasis

precipitation of urinary solute as a stone



risk factors= high concentration of solute, low urine volume



Colicky pain with hematuria and flank pain

Calcium Oxalate

most common type in adults



hypercalcemia and Crohns disease



Hydrocholothiazide

AMP

Ammonium Maganesium phosphate



Second most common, alkaline urine leads to stone



staghorn caliculi in the calyces. Need surgery to remove

Uric Acid

third most common, does not show up on X-Ray



Often seen in patients with Gout



Treat: Hydration, and alkalinization of urine

Cysteine

seen in children, genetic defect in tubules that decreases reabsoprtion of cysteine



May form staghorns

Angiomyolipoma

Hamartoma of bloodvessels, muscle, and fat

Renal Cell Carcinoma

malignant epithelial tumor of the tubules



Hematurie, Palpable mass, and Flank pain



Can present with left sided varicocele due to left renal vein block.

Wilms Tumor

malignant kidney involving the blastema (immature mesenchyme)