Nephrotic vs Nephritic Flashcards

1
Q

Nephrotic Syndrome

A

Proteinuria (>3.5g/d)

Hypoalbuminemia (

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2
Q

Nephritic Syndrome

A
Decreased renal function
Hypertension
RBC and RBC casts
Edema
Proteinuria (
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3
Q

nephrotic

general management

A
low salt diet
diuretics
BP control
Other:
-cholesterol lowering drugs
-ACE inhibitors
-vitamin D
-normal/low protein diet
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4
Q

glomerular diseases
primarily renal
nephritic

A
post strep GN
IgA nephropathy
RPGN
-anti-GMB
-idiopathic
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5
Q

glomerular diseases
primarily renal
nephrotic

A
hereditary nephrotic syndromes
minimal change disease (MCD)
focal segmental glomerulosclerosis
membranous nephropathy (MN)
membranoproliferative GN (MPGN)
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6
Q

glomerular diseases
systemic
nephrotic

A

diabetes
amyloid and light chain disease
SLE (membranous)

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7
Q

glomerular diseases
systemic
nephritic

A

vasculitis
immune complex
-SLE
-HSP

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8
Q

Minimal Change Disease

Presentation

A

Peak incidence: 2-6 y/o
more common in males
Edema, ascites,
Hypertension (20%)

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9
Q

minimal change disease

labs

A

renal function is normal or slightly depressed

urinalysis: 4+ proteinuria, hyaline casts, rare microscopic hematuria

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10
Q

minimal change disease

associations

A

history of allergy/atopy
Hodgkin’s lymphoma
nonsteroidal drugs (idiosyncratic rxn)

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11
Q

minimal change disease

pathophysiology

A

T cell disorder??
loss of charge barrier
effacement of podocytes

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12
Q

Focal Segmental Glomerulosclerosis

presentation

A

proteinuria, hypertension

urinary sediment often w/ RBCs

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13
Q

FSGS treatment

A

Steroids (6 mo); relapse is high

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14
Q

most common cause of nephrotic syndrome in young adults and African Americans

A

focal segmental glomerulosclerosis (FSGS)

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15
Q

FSGS etiology

A

Idiopathic or related to previous minimal change disease
IV heroin
HIV
Other (sickle cell, obesity)

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16
Q

HIV Nephropathy

A

Collapsing focal and segmental glomerulosclerosis, reticuloendothelial inclusions
5-10% of all AIDS patients
80% black, 50% IVDA

17
Q

HIV Nephropathy treatment

A

Anti-retrovirals

18
Q

FSGS pathogenesis

A

circulating factor: soluble UPAR

pathology factor: APO lipoprotein L1

19
Q

Membranous nephropathy (MN) etiology

A

Primary (idiopathic): due to antibodies to phospholipase A2 on the podocyte
Secondary:
Hepatitis B; Drugs (gold, mercury); SLE; Cancer

20
Q

Membranous nephropathy

types of cancer

A

carcinoma

lung, breast, GI tract, renal

21
Q

Membranoproliferative glomerular nephropathy (MPGN)

associations

A

Hepatitis C
Nephrotic or nonnephrotic proteinuria, hypertension, elevated creatinine
low C3 and C4 (complement disorder)
treat with interferons

22
Q

nephritic syndrome

A

Reduction in GFR (elevated serum creatinine)
Active urine sediment (RBC, WBC, RBC casts)
Proteinuria (usually sub-nephrotic)
Edema
Hypertension

23
Q

glomerulonephritis workup

A
CBC
electrolytes
24 hr urine
liver function tests
serologies (?)