N17 - Differential diagnostics of renal diseases Flashcards

(22 cards)

1
Q

Differential diagnosis of lumbal pain

A

sudden onset, cramping
- obstruction of urinary tract (ie. stone, blood clot, papilla necrosis)
- usually unilateral, radiating downwards toward bladder, genitalia

blunt pain
- unilateral: renal cyst infection/bleeding, tumor, renal infarct, renal vein thrombosis
- with fever and UTI: pyelonephritis, abscess
- bilateral: interstitial nephritis, renal edema, glomerular diseases are usually not painful

dysuria, pollakisuria
- lower UTI

lumbal pain of extrarenal origin
- lumbar spine, muscles, neurological
- atypical: acute cholecystitis, pancreatic tumor, pancreatitis, colon neoplasm, spleen

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2
Q

What do hematuria labarotory findings look like in a healthy person?

A
  • dipstick negative
  • sediment <3-4 RBC/high power field (x400)
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3
Q

What does macroscopic hematuria suggest?

A

urological origin (exception: IgA nephropathy)

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4
Q

What does microscopic hematuria suggest?

A

urological or nephrological origin

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5
Q

What are the urological causes of hematuria?

A
  • renal/uroepithelial tumor
  • stone
  • UTI (ie. cystitis)
  • renal cyst rupture
  • papillary necrosis
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6
Q

What are nephrological causes of hematuria?

A
  • glomerulonephritis
  • Alport-syndrome
  • thin basement membrane disease
  • acute interstitial nephritis
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7
Q

What does microscopic urinary sediment help differentiate?

A
  • urological: similar RBCs (isomorphic)
  • nephrological: variable appearance of RBCs (dysmorphic) (ie. acanthocytes - glomerular origin)
  • RBC casts suggest glomerular origin
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8
Q

What are the laboratory findings for proteinuria and albuminuria?

A

urine dipstick
- positive = urine albumin conc. >500mg/L
- detects mainly albumin so can be false negative if the protein is not albumin (ie. light-chains)

“clinically significant” proteinuria
- >500mg/day (creatinine >50mg/mmol)
- Heralds poor renal prognosis
- treatment target is less than 500mg/day

albuminuria
- >30mg/day (3mg/mmol)
- may suggest early diabetic nephropathy
- >300mg/day corresponds to about 500mg/day proteinuria

“nephrotic” range proteinuria
- >3-3.5g/day (0.3-0.35g/mmol) accompanied with nephrotic syndrome

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9
Q

What can the urinary sediment indicate?

A
  • RBC:
    - isomorphic: urological bleeding (cystitis, stone, tumor)
    - dysmorphic: glomerular, interstitial disease
  • WBC: UTI, acute interstitial nephritis, glomerulonephritis
  • tubular cells: acute tubular necrosis, glomerulonephritis, allograft rejection
  • transitional (urothel): normal, UTI, malignancy
  • squamous epithelial cell: normal
  • RBC cast: glomerulonephritis
  • WBC cast: pyelonephritis, glomerulonephritis, AIN
  • brown granular cast: ATN
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10
Q

What are the major nephrology syndromes?

A
  • nephrotic syndrome
  • nephritic syndrome (RPGN)
  • acute kidney injury
  • asymptomatic proteinuria/hematuria
  • chronic kidney disease
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11
Q

What are the clinical features of nephrotic syndrome?

A
  • proteinuria (>3.5g/day)
  • hyperalbuminemia
  • edema
  • hyperlipoproteinemia
  • thromboembolic events
  • GFR may be normal

immunoserology and kidney biopsy for further differentiation

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12
Q

What is the differential diagnosis for nephrotic syndrome?

A

primary renal disease
- primary membranous glomerulonephropathy (usually anti-PLA2 receptor antibody positive)
- minimal change nephropathy
- focal segmental glomerulosclerosis

renal manifestation of a systemic disease
- diabetic nephropathy
- amyloidosis
- secondary FSGS
- secondary membranous glomerulopathy

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13
Q

What is the differential diagnosis of nephritic syndrome?

A
  • poststreptococcalis glomerulonephritis
  • postinfectious glomerulonephritis (ie. subacute endocarditis, abscess)
  • membranoproliferative glomerulonephritis
  • membranoproliferative glomerulonephritis

renal biopsy, immune serology and electrophoresis for further morphologic/etiologic diagnosis

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14
Q

Diagnosis of RPGN

A
  • RPGN = rapid progressive glomerulonephritis
  • renal biopsy w/ immunofluorescein staining and serology for further differentiation
  • light microscopy shows crescents with parietal cell proliferation
  • further differentiation is based on immunofluorescence and immunoserology
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15
Q

How is crescent glomerulonephritis differentiated from RPGN?

A

1. linear immunoglobulin deposition
- anti-GBM antibodies
- renal +/- pulmonary symptoms
- good pasture disease

2. granular immunoglobulin deposition
- these are immunocomplexes
- ie. lupus nephritis IgA nephropathy

3. no immunoglobulin deposition
- these are ANCA vasculitides
- granulomatosis w/ polyangitis
- microscopic polyangitis
- eosinophil granulomatosis w/ polyangitis

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16
Q

What are the indications for renal biopsy?

A
  • nephrotic syndrome
  • nephritic syndrome
  • RPGN
  • asymptomatic proteinuria (1-3g/day range)
  • acute kidney injury (intrinsic): if it is not caused by ATN
  • chronic kidney disease of unknown origin: not on small, scarred kidneys
  • dysfunction of transplanted kidney
17
Q

What are the contraindications of renal biopsy?

A
  • uncooperative patient
  • single kidney
  • multiple renal cysts
  • acute pyelonephritis
  • uncontrolled bleeding diathesis
  • uncontrolled blood pressure (BP> 160/95mmHg)
18
Q

How is renal biopsy conducted?

A
  • under local anesthesia, ultrasound guided
  • evaluated by light, immunofluorescent or electron microscopy
19
Q

What glomerular diseases cause asymptomatic proteinuria?

A
  • proteinuria = 0.5-2g/day
  • early diabetic nephropathy
  • secondary FSGS
  • hypertensive nephropathy
20
Q

What glomerular diseases cause asymptomatic microhematuria?

A
  • IgA nephropathy
  • alport syndrom
  • thin basement membrane abnormality
21
Q

What are the signs and symptoms of chronic kidney disease?

A
  • decreased GFR, variable progression
  • usually small kidneys with echogenic parenchyma
  • variable urinary abnormalities
  • complications according to the stages of CKD
22
Q

Differential diagnosis and therapy for CKD

A
  • usually no diagnostic problem
  • original kidney disease may not be identified
  • slow progression so prepare for renal replacement therapy
  • prevent further complications