All Histology Flashcards
Do nephrotic syndromes ever decrease complement?
no
What is a hallmark feature of nephritic syndrome?
dysmorphic RBCs / RBC casts
What 4 nephritic syndromes decrease serum complement?
Cryoglobulinemia
Membranoproliferative GN
Post-infectious GN
SLE
CMPS
What does light microscopy look like for Postinfectious GN?
mesangial proliferation which leads to lack of lumens
What does IF look like for postinfectious GN?
granular
What does electron microscopy look like for postinfectious GN?
hump-like subepithelial deposits
Difference between membranous nephropathy and PIGN if both have subendothelial deposits?
membranous nephropathy is a nephrotic syndrome
PIGN is a nephritic syndrome
which you can tell from question stem
Difference between IgA nephropathy and PIGN?
PIGN occurs weeks later when infection is already gone (immune reaction)
IgA nephropathy occurs at same time as infection
Is IgA nephropathy recurrent?
yes
IgA nephropathy and serum complement
normal levels
What are a defining features of RPGN? (2)
acute renal failure with quick GFR drop
crescents on biopsy
How do you determine the type of RPGN?
look at IF study
Linear IF study and RPGN indicates …
Goodpasture syndrome / anti-GBM syndrome
Goodpasture syndrome
associated with hemoptysis as well as RPGN
antibodies attacking the basement membrane (type IV collagen)
What is a common cause of membranoproliferative GN?
HBV and HCV
also mixed with cryoglubinemia
If someone is an IVDU, what should we be thinking about?
blood borne diseases
Serum complement and MPGN
decreased serum complement
How can you determine if something is a mixed disease? What 2 syndromes can be mixed?
MPGN and DPGN
look for proteinuria or fatty casts
What is the defining feature of membranoproliferative GN?
tram-track GBM on silver stain
What does silver stain show on membranous nephropathy?
membranous nephopathy is supposed to have “spikes”
hard to tell apart from MPGN!
look for clinical clues: membranous nephropathy is a nephrotic disorder
What is the most common type of nephritic lupus disease?
DPGN
How does DPGN appear on IF?
granular
What is the next step in a SLE patient with kidney symptoms?
renal biopsy
What 2 complement proteins are decreases in lupus?
C3 and C4
Which gene is associated with X-linked Alport syndrome?
COL4a5
Which gene is associated with autosomal Alport syndrome?
COL4a4 and COL4a3
can be dominant or recessive
Why is Alport syndrome more common in young men?
due to X-linked pattern of COL4a5
X-linked
What is Alport syndrome?
genetic condition associated with kidney disease, vision and hearing loss
problem with type IV collagen
What can Alport syndrome look like on light microscopy?
FSGS