Glomerular Disease and such... Flashcards

(41 cards)

1
Q

Causes of heme-negative red urine

A

Meds – Doxorubicin, Chloroquine, Ibuprofen
Dyes – Beets, Blackberries, Food Coloring
Metabolites – Bile, Melanin, Porphyrin

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2
Q

Main risk factors for urologic malignancy?

A

Age, Gross hematuria, Smoking, Env. Exposure

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3
Q

Urine dipstick for hematuria is positive…now what?

A

Microscopic exam. If over 3 RBCs/hpf with no obvious cause, refer to urologic evaluation

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4
Q

Extraglomerular source of hematuria. Color? Clots? Proteinuria? RBC Details?

A

Red/Pink
Maybe
Less than 500 mg/day
Normal RBC morphology w/out Casts

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5
Q

Glomerular source of hematuria. Color? Clots? Proteinuria? RBC Details?

A

Red, Smoky brown, or Coca-Cola
No clots
Can be over 500 mg/day
Dysmorpic possibly with Casts

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6
Q

Best way to rule out renal mass as a cause for hemato.?

A

Multiphasic CT Urography

If any indicator, move forward with cystoscopy

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7
Q

Most common renal biopsy discoveries

A

IgA nephropathy, thin BA disease, NORMAL

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8
Q

Pathogenesis of IgA Nephropathy (Bergers disease)

A

Two hit hypothesis –> abberantly glycosylated IgA1

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9
Q

Pathology of Bergers Disease

A

Mesangial Proliferative GN with IgA deposits on IF

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10
Q

Three types of proteinuria?

A

Glomerular, Tubular, Overflow

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11
Q

What is glomerular proteinuria?

A

Increased filtration of macromolecules across glomerular capillary wall

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12
Q

What is tubular proteinuria?

A

Excretion of low-molecular weight proteins (like beta2-microglobulin, Ig Light Chains, and albumin break down products).

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13
Q

What is overflow proteinuria?

A

Increased excretion of low-mol weight proteins due to Ig light chains of multiple myeloma, lysozyme of AML, or myoglobin in rhabdo

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14
Q

Nephrotic Levels of Urine Protein?

A

Over 3.5 g

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15
Q

Elevated urinary albumin excretion is defined as

A

Over 30 microgram/mg

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16
Q

Difference between microalbuminuria and macroalbuminuria?

A

Micro – 30-300mg

Macro – Over 300mg

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17
Q

Preferred method of measuring urine albumin

A

Urine Albumin/Creatinine

Helps overcome the limits of variations in urine volume

18
Q

Relationship of albuminuria and DM

A

Type 1 – Often earliest sign of diabetic nephropathy

TII – Usually present at diagnosis, can reflect CV disease or nephropahy

19
Q

Shortcoming of the urine dipstick

A

Can’t detect microalbuminuria or globin (in myeloma)

20
Q

Three symptoms common in nephrotic syndrome

A

Proteinuria over 3g per 24 hours
Edema due to hypoalbuminemia
Hyperlipidemia (increased albumin, increased LDL chol)

21
Q

Four examples of primary nephrotic syndrome

A

Membranous GN
Lipoid Nephrosis
Focal Segmental Glomerular Sclerosis
Membranoproliferative GN

22
Q

Four main examples of secondary nephrotic syndrome

A

DM
Amyloidosis
Myeloma
SLE

23
Q

Six Complications of Nephrotic syndrome (from protein loss)

A

Hypercoagulation (Loss of Anti-thrombin, proteinC,S)
Infections, esp. G+ (Loss of IgG, Complement)
Anemia (EPO)
Malnutrition (Albumin)
Hypothyroidism (Thyroid Binding Globulin)
Vit D Deficiency (VitD Binding Protein)

24
Q

Two main contraindications for renal biopsy

A

Solitary kidney, Marked coagulopathy

25
Pathogenesis of Membranous GN
In situ formation about antigen-antibody complex Usually Phospholipase A2 target antigen Membrane width increase, sub-epithelial deposits on EM
26
Clinical Presentation/Treatment of Membranous GN
Proteinuria or nephrotic syndrome Increased incidence of renal vein thrombosis Tx - ACEi to reduce proteinuria. If persistent, severe neph. syndrome, Steroids + Cyclophosphamides
27
Pathogenesis of lipoid nephrosis
Primarily related to abnormalities in cellular immunity | Effacement of foot processes
28
Clinical presentation/Treatment of Lipoid Nephrosis
Usually presents w/ nephrotic (most common in children) | Tx - Usually steroids, can relapse, Cyclophosphamide if dependent
29
Pathogenesis of Focal Segmental Glomerular Sclerosis
1. Primary - like Lipoid Nephrosis 2. Genetic Abnormalities in structural proteins 3. Adaptive sclerotic response to primary glomerular injury
30
Clinical presentation of Focal Segmental Glomerular Sclerosis?
Proteinuria+Nephrotic Syndome Much higher incidence in African Americans Less response to steroids than Lipoid Nephrosis
31
What tends to be seen with Nephritic syndrome
Hematuria, Oliguria, Azotemia, HTN, Edema
32
Three primary types of nephritic syndrome?
MPGN Type I and II | C3 Glomerulopathy
33
Three important infectious correlations with nephritic syndrome
Post streptococcal GN Staphylococcal Infection HIV assocaited nephropathy
34
Important features in rapidly progressive glomerulonephritis
Acute kidney injury w/ hematuria, proteinuria, and HTN | Crecenteric glomerulonephritis on biopsy
35
Three types of RPGN
Linear glomerular BM Deposits (Goodpastures) Granular Immune Complexes (SLE, cryoglob) No Immune Complexes (If only renal, Renal - pauci immune)
36
RPGN associated with cANCA (PR3)?
Wegener's granulomatosis
37
RPGN associated with pANCA (MPA)
Micro-PAN
38
Mutations associated with primary Thrombotic Microangiopathy
TTP -- ADAM TS13 HUS -- Shiga toxin Can also be drug induced, from complement overactivity
39
Primary treatment for TTP
Plasmaphoreses
40
Three labs/scans that suggest chronic, rather than acute, kidney damage
Anemia Very high PTH Small kidneys
41
Urine tests suggestive of a glomerular process? Suggestive of non-glomerular?
Glom -- RBC Casts | Non -- Clots in the urine