Puthoff Lecture 1 Flashcards

1
Q

What is Berger disease?

Damage is limited to where?

A

Renal IgA nephropathy

Glomerulus

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3
Q

What is an IgG plasma malignancy with Kappa light chains?

What are the light chain deposits called?

A

Multiple myeloma

Bence-Jones

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4
Q

HIV patients with FSGS most likely to develop what?

More common in who?

A

Collapsing variant

Blacks

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7
Q

What disease shows a tri chrome stain (blue) with replacement of virtually all glomeruli?

A

Chronic glomerulonephritis

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8
Q

Membranous Glomerulopathy has involvement with what?

A

MAC

IgG4

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9
Q

Morphology of Membranous Glomerulopathy?

A

Spike and dome appearance on Silver stain

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10
Q

People with CKD have a high prevalence of what?

Associated with what?

Increased risk for what?

A

Hyperhomocysteinemia

Folate deficiency

Stroke

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11
Q

What disease is characterized IgA nephropathy and systemic disease?

What symptoms?

A

Henoch-Schonlein purpura (HSP)

Purpura, abdominal viscera

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14
Q

What is the Pathogenesis of MPGN type II?

Means what?

A

C3NeF nephritic factor

Decreased serum C3
Increased C1q and C4

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15
Q

What is described by uremia, persistent albuminuria, that may be clinically silent?

A

Chronic kidney disease

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18
Q

What is the most common cause of ESRD?

2nd?

A

Diabetes

HTN

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19
Q

What clinical finding characterizes MPGN type I?

Type II?

A

Proteinuria

Hematuria

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20
Q

Name the 3 types of RPGN and give examples

A

1 - anti-GBM antibody (Goodpasture)
2 - immune complex (lupus)
3 - Pauci-immune (ANCA)

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21
Q

What disease has characteristic “tram tracking”?

A

MPGN type I

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22
Q

What disease shows Mesangial cellular proliferation and IgA deposition on IF?

A

IgA nephropathy

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24
Q

What disease is characterized by in situ immune complex formation of PLA2R antigen?

A

Membranous nephropathy

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25
Q

Morphology of RPGN?

3 main things

A

Crescent shape of visceral and parietal epithelial cells
Obliteration of urinary space
Infiltrates of macrophages and leukocytes

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28
Q

DDD occurs how?

What type is it?

A

Primary renal disease in children

MPGN type II

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31
Q

What are the 3 major pathologic responses of the glomerulus to injury?

A

Hypercellularity
BM thickening/deposition
Hyalinosis and sclerosis

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32
Q

What is the most common cause of Nephro sclerosis in U.S. Adults?

Who is there a greater incidence in?

A

primary FSGS

Hispanics, Blacks

35
Q

What defines uremia?

A

Azotemia plus clinical findings

36
Q

What characterizes ESRD?

37
Q

3 major characteristics of nephritic syndrome

A

Hematuria
HTN
Mild-moderate proteinuria

39
Q

What disease is subepithelial humps found in?

A

Acute glomerulonephritis

41
Treatment for anti-glomerular BM disease?
Plasmapheresis
42
what does EM of RPGN show?
GBM disruption | Fibrin
43
What disease occurs mostly in older children and younger adult males with a family history component that has hematuria following a uri? Know associations with gluten enteropathy and liver disease?
IgA nephropathy
44
Diffuse proliferative GN is characterized by what?
Hypercellularity | Leukocyte infiltration
46
What are the 2 most common etiologies of nephrotic syndromes in systemic diseases?
DM | SLE
47
What are the 6 main nephrotic syndromes? Think of groups of 2 like in pathoma
MCD and FSGS Membranous and Membranoproliferative GN DM and systemic amyloidosis
48
Membranous Glomerulopathy changes to the structure of the kidney?
Effaced foot processes thickened GBM Subepithelial deposits (IgG)
49
MPGN type I has what clinical presentation? EM shows what? Light microscopy shows what?
Mixed - hematuria and proteinuria Subendothelial deposits Mesangial cell proliferation
50
Acute proliferative GN occurs in who and because of what?
Children ages 6-10 Due to Group A beta-hemolytic strep infection 1-4 weeks following pharyngitis
51
What are common causes of secondary MPGN type I? Prognosis?
Hep C SLE endocarditis Malignancy Dismal
56
What is characterized by the following morphology? Mesangial cell proliferation BM thickening and splitting Increased lobular architecture Influx of neutrophils?
MPGN type I
57
What are the EM findings of acute proliferative GN? IF findings?
Subepithelial humps Granular deposits of IgG, IgM, and C3
58
Idiopathic FSGS displays what? What kind of progression?
Higher incidence of hematuria, reduced GFR Proteinuria is nonselective CKD (50% w/in 10 years)
59
What disease are Mesangial deposits found in?
IgA nephropathy
60
Where do Bence-Jones deposit?
Tubules
61
Acute proliferative GN may be due to what bacterial infections?
Group A beta-hemolytic Staphylococcal
63
3 major characteristics of nephrotic syndrome?
Proteinuria (>3.5 g/day) Hypoalbuminemia Edema Also lipiduria
68
What disease is epimembranous deposits found in?
Membranous nephropathy | Heymann glomerulonephritis
70
What disease is subendothelial deposits found in?
Lupus nephritis | MPGN
74
What is described by a rapid decline in GFR, oliguria/anuria, and may result from glomerular, interstitial, vascular, or tubular injury?
Acute kidney injury
78
What manifestations are present in RPGN?
Acute nephritis Proteinuria Acute renal failure
79
Hematuria can be caused by what?
SCHITTT Slide 26 if you forget the mneumonic
80
mutation of NPHS1 is on what chromosome? Encodes for what protein? Causes what?
19 Nephrin Congenital nephrotic syndrome of the Finnish type (FSGS)
81
Increased risk to FSGS caused by what mutation on chromosome 22? Common in whom?
APOL1 African American