Approach to Kidney Disease Flashcards

1
Q

Will a patient with nephritic or nephrotic syndrome outwardly appear to be more unwell?

A

Nephritic syndrome

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2
Q

Dark brown urine can represent increased levels of these three things

A

Bilirubin (liver disease)

Hemoglobin

Myoglobin (rhabdomyolysis)

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3
Q

Method to differentiate if heme in urine is from hemoglobin or myoglobin

A

Microscopic analysis

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4
Q

Three hallmark signs of nephrotic syndrome

A

More than 3.5 grams of protein in the urine per day

Edema

Hypoalbuminemia

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5
Q

A parent with congenital polycystic kidney disease where their progressively growing renal cysts replace normal kidney tissue has this % chance of passing it on to their child

A

50%

ADPKD - autosomal dominant polycystic kidney disease

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6
Q

This condition is associated with a characteristic thickening of basement membranes of the glomerulus

A

Membranous nephropathy

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7
Q

Most common cause of nephrotic syndrome in whites and the elderly

A

Membranous nephropathy

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8
Q

Dysmorphic red blood cells seen on microscopic analysis of urine suggest this condition

A

Damage at the level of the kidney

RBCs misshapen from passing through glomerular basement membrane

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9
Q

Between which ages does anti-GBM disease most commonly occur?

A

Men - 20 to 40
Women - 60 to 80

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10
Q

This IgA nephropathy variant generally occurs in children, and has a clinical tetrad of purpuric rash on thighs, arthralgias, abdominal pain, and gross hematuria (from renal failure)

A

HSP (Henoch-Schonlein Purpura)

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11
Q

This renal condition has a classic “tram tracking” appearance on biopsy, can cause nephrotic OR nephritic syndrome, low complement levels, and a strong relationship with Hep C

A

MPGN (Membranoproliferative Glomerulonephritis)

(tram tracking = double inner and outer membrane)

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12
Q

These two signs/symptoms nearly always co-present with diabetic caused nephrotic syndrome

A

Peripheral nephropathy

Diabetic retinopathy

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13
Q

Leading cause of nephrotic syndrome in adults, especially blacks

A

FSGS (focal segmental glomerular syndrome)

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14
Q

Two causal associations for minimal change disease

A

NSAIDs

Hodgkin’s lymphoma

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15
Q

Most common glomerulonephritis worldwide

A

IgA nephropathy

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16
Q

Your patient has rapidly progressing renal failure with gross hematuria and oliguria, hemoptysis, dyspnea, and pulmonary infiltrates. What do you think they have, and how would you confirm this diagnosis?

A

Anti-glomerular basement membrane disease

Confirm with serology that shows Anti-GBM antibodies

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17
Q

Does a patient who presents with hematuria, flank pain, dysuria, or urinary frequency, but no proteinuria more likely have a renal or non-renal issue?

A

Non-renal source

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18
Q

Area where edema is first seen in cases of significant pediatric proteinuria

A

Periorbital edema (especially in children)

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19
Q

Does a patient who presents with hematuria, increased BUN and creatinine in the blood, and dysmorphic RBC casts in the urine more likely have a renal or non-renal issue?

A

Renal source

20
Q

Gold standard for analysis of proteinuria

A

24 hour urine sample

21
Q

Most common cause of obstructive uropathy in adults

A

BPH

22
Q

Patients with severe and generally acute inflammatory injury to glomerulus where patients are frequently oliguric with tea colored hematuria, and hypertension have this syndrome

A

Nephritic syndrome

23
Q

Podocyte effacement is a hallmark sign of this condition

A

Nephrotic syndrome

24
Q

This condition causes multiple abnormalities including proteinuria which will show on 24 hour urine collection, but not on dipstick

A

Multiple myeloma

25
Q

Patients with a first degree relative who died of a cerebral aneurysm should be screened for this renal condition

A

ADPKD (autosomal dominant polycystic kidney disease)

26
Q

Diagnosis method for orthostatic proteinuria

A

Split day/night urine collection

27
Q

Urine that looks foamy and bubbly suggests this …

A

Proteinuria

28
Q

Four associated conditions with ADPKD (autosomal dominant polycystic kidney disease)

A

Mitral valve prolapse

Cerebral aneurysms

Diverticulitis

Ovarian cysts

29
Q

Orthostatic proteinuria occurs when the patient is upright/active. Which type of patient is this condition most common in?

A

Adolescents

(gets better with time)

30
Q

This condition is associated with massive proteinuria (>10 grams/day), rapid onset of swelling, but kidney structure looks normal on light microscopy

A

Minimal change disease

(need electron microscopy to see squashed podocytes)

31
Q

Number one cause of end stage renal disease in the US

A

Diabetes

32
Q

Three treatments for nephrotic syndrome

A

Statins

ACE/ARBs to decrease protein push through glomerulus

Treat edema with salt restriction and loop diuretic

33
Q

Secondary causes (3) of membranous nephropathy

A

Hepatitis B/C

Lupus

Occult malignancy

34
Q

Microcystic disease, renal scarring, and nephrogenic diabetes insipidus is induced by use of this medication

A

Lithium

(lithium induced renal disease)

35
Q

In nephrotic syndrome, overcompensation as a response to albumin loss can lead to these two conditions

A

Hyperlipidemia

Hypercoagulable state

36
Q

A child develops hypertension, swelling, and has tea-colored/red urine 10-14 days after a strep infection. Diagnose this child.

A

Post-streptococcal GN (glomerulonephritis)

37
Q

Most common secondary cause of FSGS (focal segmental glomerular syndrome)

A

Obesity/OSA

38
Q

Number one cause of proteinuria

A

Type 2 diabetes

39
Q

Your patient has developed blood in their urine within 24 hours of having an upper respiratory infection/sore throat/ear infection. What condition might they have developed and how would you slow its progression?

A

IgA nephropathy “syn-pharyngitic nephritis”

Slow progression with ACE inhibitors

40
Q

Name the classic triad associated with cholesterol emboli

A

Eosinophilia and eosinophiluria

Low complements

Livido reticularis

41
Q

Which of these, minimal change disease or focal segmental glomerular syndrome is the most common cause of nephrotic syndrome in children?

A

Minimal change syndrome

42
Q

Acute interstitial nephritis is usually caused by (blank) and begins (time) after exposure

A

Caused by medications

Occurs 7-10 days after exposure

43
Q

This renal condition is more common after invasive procedures around the heart and can cause acute or chronic renal failure

A

Cholesterol embolitis

44
Q

Which of these, minimal change disease or FSGS (focal segmental glomerular syndrome) is the more treatment resistant?

A

FSGS tends to be treatment resistant

Minimal change disease is very responsive to steroids, especially in children

45
Q

This nephritis is associated with long term NSAID use

A

Chronic interstitial nephritis