Nephrology Flashcards

1
Q

What is the definition of microscopic hematuria?

A

Greater than five RBCs per HPF

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2
Q

What is the first step of evaluation of microscopic hematuria?

A

Urine calcium and urine creatinine.

  • Calcium:creatinine > 0.25 -> hypercalciuria w/u
  • Calcium:creatinine < 0.25 -> renal ultrasound to look for structural anomalies

OR

Imaging, serum BUN, serum creatinine, coagulation studies, platelet count, ANA, ds-DNA, ESR, complement levels depending on the clinical picture

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3
Q

What is the work up for hypercalciuria?

A

Urine calcium to creatinine ratio.
- > 0.25 = hypercalciuria (idiopathic, Loop diuretics) -> repeat ratio from a 24 hour urine collection -> if greater than 4.0, get a renal ultrasound to look for a stone

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4
Q

What is the evaluation for proteinuria?

A
  • 1+: repeat in 2 weeks
  • 2+: get an AM void
    • No protein: transient due to orthostasis
      - Get a creatinine to check renal fxn
    • +: random protein-to-creatinine ratio
      - >0.2: renal dz -> get renal bx
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5
Q

What is the evaluation of UPJ obstruction?

A
  • suggested on ultrasound by dilated renal calyces, pelvis, or frank hydronephrosis
  • May be born with signs of oligohydramnios
  • Confirm with postnatal ultrasound
  • Get a VCUG to rule out other anomalies, look for reflux, and PUV
  • Once ruled out, get a MAG3 furosemide renal scan to look for slow flow of urine from the renal pelvis into the ureter
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6
Q

What is the most common cause of urinary retention in girls?

A

Ureterocele
Symptoms are similar to those with UTI
Get IV pyelogram to look for a filling defect

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7
Q

What are the clinical features of post streptococcal glomerulonephritis?

A
  • Proteinuria + hematuria +- edema +- HTN
  • Labs: low C3, normal C4 +- renal impairment
  • Follow C3 until back to normal
  • If C3 still abnormal after six weeks, consider a different diagnosis
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8
Q

What are the clinical features of hemolytic uremic syndrome?

A
  • Diarrhea caused by EHEC
  • fever
  • hemolytic anemia (Coombs negative)
  • thrombocytopenia
  • renal failure
  • neurologic changes
  • normal complement levels
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9
Q

What are the findings in glomerulonephritis?

A

Hematuria, elevated BUN, proteinuria, oliguria, hypertension

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10
Q

What are the findings of IGA nephropathy?

A
  • Most common cause of primary glomerulonephritis
  • Recurrent episodes of hematuria
  • May be worse after a URI or G.I. illness
  • Urinalysis shows rbc casts
  • Diagnosed with renal biopsy, which will show IgA and IgG mesangial deposits
  • Complement is normal
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11
Q

What are the findings in membranoproliferative glomerulonephritis?

A
  • Hematuria
  • Proteinuria
  • High blood pressure
  • Low C3 and C4
  • Dx: biopsy showing TRAM TRACK LESIONS
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12
Q

What are the findings in nephrotic syndrome?

A

“They swell up like that big O in nephrotic syndrome.”

  • Classic triad: Edema + Proteinuria + Hypoalbuminemia
  • Albumin lost in urine
  • Low urine sodium
  • Low FeNa
  • Etiologies: minimal change disease, focal segmental glomerular nephritis, membranous nephropathy, congenital nephrotic syndrome, membranoproliferative glomerulonephritis
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13
Q

What are the findings in a minimal change nephrotic syndrome?

A
  • Common in toddlers or elementary school age children
  • Most common etiology of nephrotic syndrome
  • Abdominal pain, diarrhea, decreased urine output, normal creatinine
  • Bx: loss of FOOT PROCESSES
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14
Q

What are the findings in focal segmental glomerulonephrosis?

A

Bx: segments of some glomeruli that have scarring

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15
Q

What are the findings in membranous nephropathy?

A

“Adolescent boys play with their thick loops (balls) and thick membranes until they get nephropathy- thickened capillary loops.”

  • Adolescent with nephrotic syndrome
  • Bx: diffusely thickened capillary loops
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