Nephritic Syndrome Flashcards

1
Q

Disorders

A

Acute proliferative / post streptococcal glomerulonephritis

Cresentric glomerulonephritis

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2
Q

APG/Post straptococcal target Age

A

1-6yrs

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3
Q

APG causes

A

Exogenous: HIV, malaria, straptococcal

Endogenous: SLE

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4
Q

APG Microscopy

A

LM: hypercellularity due to leukocyte infiltration and proliferation of endothelial and mesangial cells

IF: granular membranous/mesangial IgA IgM
IgG C3 post infection

EM: subendothelial deposits called HUMPS

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5
Q

Pathogenesis of APG

A

Immune complex mediated

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6
Q

Types of RPGN

A

Type 1- Anti GBM
Type 2- immune complex mediated
Type 3- pauci immune

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7
Q

Features of RPGN

A

Progressive loss of renal function
Oligouria
Nephritic Syndrome

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8
Q

Features of RPGN

A

Progressive loss of renal function
Oligouria
Nephritic Syndrome

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9
Q

Good pastures syndrome

A

Anti GBM disease with Hemoptysis

Due to antigen against noncollagenous portion of alpha 3 chain or Collagen type 4

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10
Q

Type 1 RPGN features

A

IF: Linear membranous IgG and C3

EM: rupture of GBM

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11
Q

Type 2 RPGN features

A

IF: Granular

EM: ELECTRON dense deposits and rupture of GBM

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12
Q

Wegners Granulomatosis

A

Upper and lower respiratory tracts + kidney disease

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13
Q

Type 3 RPGN features

A

IF negative

Rupture of GBM

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14
Q

Bergers disease/ IgA nephropathy

A

Effects YA

IgA deposits and recurrent hematuria

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15
Q

Pathogenesis of IgA nephropathy

A

Immune complex mediated

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16
Q

1 week after mucosal infection

A

IgA nephropathy

17
Q

4 weeks after infection

A

Post straph/Apg

18
Q

Most common glomerulonephritis worldwide

A

IgA nephropathy

19
Q

IgA nephropathy features

A

LM: mesangio or focal polferative or cresentric

IF: granular, mesangial and IgA positive

EM: DENSE DEPOSITS in the mesangium