DDX Kidney lecture Flashcards

1
Q

Pain - LITRAAA

A

localization, intensity, type, radiation, aggravating – alleviating factors, accompanying signs

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2
Q

Pain - Sudden onset, cramping

A

Obstruction of the urinary tract

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3
Q

Pain - Blunt, unilateral

A

renal cyst infection/bleeding,
tumor,
renal infarct,
renal vein thrombosis,

with fever and UTI:
pyelonephritis,
abscess

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4
Q

Pain - Blunt, bilateral

A

interstitial nephritis,
renal edema,
glomerular diseases are usually not painful

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5
Q

Pain - Dysuria, pollakisuria

A

Lower UTI

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6
Q

Hematuria - Macroscopic

A

suggest urological origin (but may be seen in IgA nephropathy)

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7
Q

Hematuria - Microscopic

A

may be either urological or nephrological in origin

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8
Q

Hematuria - Urology causes

A
Renal/uroepithelial tumor, 
stone, 
UTI (eg. cystitis), 
renal cyst rupture, 
papillary necrosis
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9
Q

Hematuria - Nephrological causes

A

Glomerulonephritis,
Alport-syndrome,
thin basement membrane disease,
acute interstitial nephritis

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10
Q

Hematuria - Healthy person

A

Dipstick negative, sediment < 3-4 RBC/high power field

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11
Q

Hematuria - isomorphic RBCs

A

Urolological

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12
Q

Hematuria - dysmorphic RBCs

A

Nephrological

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13
Q

Proteinuria and albuminuria - „clinically significant” proteinuria:

A

> 500mg/day (>50mg/mmol creatinine)

Dipstick usually positive for proteins

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14
Q

Proteinuria and albuminuria - microalbuminuria

A

> 30mg/day (30 mg/mmol)

May suggest early diabetic nephropathy

Is associated with cardiovascular events

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15
Q

Proteinuria - „nephrotic” proteinuria

A

> 3-3.5g/day (0.3-0.35 g/mmol) that is accompanied with the nephrotic syndrome

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16
Q

Proteinuria - Spurious proteinuria (non renal)

A

inaccurate sampling,
blood in the urine,
colpitis

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17
Q

Proteinuria - Functional

A

temporary:
fever,
intense physical exercise,
venous congestion

Orthostatic proteinuria

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18
Q

Proteinuria - Glomerular: glomerulonephritis, glomerulopathy

A

Damaged glomerular tuft spills albumin and variable amount of globulins in the primary filtrate

(more severe damage more globulin)

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19
Q

Proteinuria - Tubular proteinuria

A

Damage to the proximal tubule leads to failure to reabsorb small molecular weight proteins

(eg. Fanconi syndrome, interstitial nephritis)

20
Q

Proteinuria - „overflow” proteinuria

A

High amount of small molecular weight protein in the serum is being filtered and overflows reabsorption

(kappa/lambda light chains a.k.a. Bence-Jones proteinuria)

21
Q

Urinary electrophoresis - Albumin spike

A

AL amyloidosis

22
Q

Urinary electrophoresis - Gamma spike

A

Multiple myeloma (often w/ albumin spike)

23
Q

Urinary electrophoresis - General increase

A

Nephrotic syndrome

24
Q

Immunological tests - ANA (anti-nuclear antibody)

A

SLE, other systemic autoimmune disease

25
Immunological tests - ANCA (anti-neutrophil cytoplasmic antibody)
Small vessel vasculitis (pauci-immune crescentic GN)
26
Immunological tests - Anti-dsDNS antibody
SLE
27
Immunological tests - SS-A, SS-B antibody
Sjögrens’ syndrome, SLE
28
Immunological tests - Anti-GBM antibody
Goodpasture syndrome
29
Immunological tests - Anti-streptolysin antibody
Poststreptococcal glomerulonephritis
30
„Major” nephrology syndromes
* Nephritis * Rapidly progressive glomerulonephritis (RPGN) * Nephrosis * Acute kidney injury * Asymptomatic proteinuria and/or haematuria * Chronic kidney disease
31
Nephritic syndrome hallmarks
* Hematuria * Proteinuria * Urinary casts (RBC) * Hypertension * Edema * Oliguria * Decreased GFR
32
Differential diagnosis hallmarks: Postinfectiosus glomerulonephritis
subacute endocarditis, abscess
33
Differential diagnosis hallmarks: Membranoproliferative glomerulonephritis
Lupus nephritis, cryoglobulinemia, monoclonal immunoglobulin deposition „dens-deposit” disease, C3 glomerulonephritis
34
Rapidly progressive glomerulonephritis syndrome (RPGN) - general overview
Rapid worsening of kidney function (weeks/months) Nephritic urinary findings • Glomerular hematuria, variable proteinuria • Cellular (RBC) casts ``` Frequent systemic symptoms • vasculitis • Pulmonary (bleeding) • upper airway infection (usually occurs DURING an ongoing mucosal infection) • Arthritis • Fever • Neuropathy ```
35
RPGN Light microscope
Crescents with parietal cell proliferation | Glomerular necrosis
36
Differentiation of crescent glomerulonephritis with RPGN: 1. Linear immunglobulin deposition
* Anti-GBM antibodies * Renal +/- pulmonary symptoms * Goodpasture disease
37
Differentiation of crescent glomerulonephritis with RPGN: 2. Granular immunglobulin deposition
* These are immuncomplexes | * eg. lupus nephritis, IgA nephropathy
38
Differentiation of crescent glomerulonephritis with RPGN: 3. No immunglogulin deposition
``` „pauci-immune” = „hardly any” • These are ANCA vasculitides • Granulomatosis with polyangitis • Microscopic polyangitis • Eosinophil granulomatosis with polyangitis ```
39
Nephrotic syndrome overview
* Proteinuria (usually >3 g/day) * Hypolbuminemia * Edema * Hyperlipoproteinemia * Thromboembolic events * GFR may be normal
40
Differential diagnosis of the nephrotic syndrome: Primary renal disease (no other organ involvement)
– Primary membranous glomerulopathy (usually anti-PLA2 receptor antibody positive) – Minimal change nephropathy – Primary focal segmental glomerulosclerosis
41
Differential diagnosis of the nephrotic syndrome: Renal manifestation of a systemic disease
– Diabetic nephropathy – Amyloidosis – Secondary FSGS (congenital podocytopathy, HIV, extreme obesity, glomerular loss for an unrelated reason) – Secondary membranous glomerulopathy (lupus nephritis, malignancy, drugs, hepatitis B/C, syphilis, NSAIDs, TNF- inhibitors)
42
Indications for renal biopsy
* Nephrotic syndrome * Nephritic syndrome * RPGN * Asymptomatic proteinuria in the 1-3g/day range (particulary if GFR declines or proteinuria increases) * Acute kidney injury (intrinsic) * If there is a suspicion that it is not caused by acute tubular necrosis * Chronic kidney disease of unknown origin * But not if on US small scarred kidneys * Dysfunction of transplanted kidney
43
Contraindications to renal biopsy
* Uncooperative patient * Single kidney * Multiple renal cysts * Renal neoplasm * Acute pyelonephritis * Uncontrolled bleeding diathesis * Uncontrolled blood pressure (BP > 160/95 mmHg)
44
Asymptomatic urinary abnormality - Asymptomatic proteinuria (usually 0,5-2g/day)
Glomerular diseases eg. * Early diabetic nephropathy * secondary FSGS * Hypertensive nephropathy
45
Asymptomatic urinary abnormality - Asymptomatic microhaematuria
Glomerular diseases eg. * IgA nephropathy * Alport syndrome * Thin basement membrane abnormality