Current day classification.
First, immunofluorescence microscopy. You know what that means.
Immunofluorescence is literally looking for immunoglobulins.
Let’s first take a look at the arm on your left, shaded light gray,
where we find immunofluorescence shows immunoglobulin Ig
plus C3 deposits in the capillary wall plus the mesangium.
Now, you’re anatomically or you’re thinking and seeing all this at this juncture.
Next, this is immune-complex mediated MPGN.
Membranoproliferative glomerulonephritis, stop there.
Immune-complex mediated. What does that mean to you?
It will be a type III type of hypersensitivy.
This would be the most common type MPGN etiology that we’ll take a look at in general.
Next, well, we'll take a look at to determine the source
of the circulating immunoglobulin or immune complexes.
By that I mean, that immune complex that's being deposit
now as a whole, as I said, this will be the most common etiology.
And you’ll see the differentials upcoming.
To determine the source, maybe it was an infection.
The big infection that you wanna keep in mind here is Hepatitis C.
What others? Well, the other ones, we have autoimmune diseases
including rheumatologic diseases and this...
that will include things like Sjogren rheumatoid arthritis, Scleroderma, SLE, and so forth.
What else may have immune-complex deposition?
Monoclonal gammopathies or dysproteinemias.
Big example here
will be monoclonal gammopathy of undetermined significance and multi-myeloma.
Or something like Waldenstrom macroglobulinemia.
This is our first category of MPGN, it’s immune-complex mediated.
Next, what if the immunofluorescence
shows dominant C3 staining with little or no C1q?
That then brings us to our branch on the right.
This will be complement-mediated MPGN.
Complement-mediated. Stop there.
Take a look at the two major classifications.
We have immune-complex and we have complement-mediated.
If it is complement-mediated then your next step of management
or at least your next step at diagnosis would be in fact your electron microscopy.
Now, what's this electron microscopy?
If you find that your entire basement membrane is black and thick,
thick and black, a rare, but you still need to know it big time, then it’s DDD.
That triple D stands for dense deposit disease.
Once again, dense deposit disease.
Where? On the basement membrane, it's black and thick.
This is your electron microscopy.
Whereas, well, you can have issues with what's known as C3 glomerulonephritis, as well.
A separate issue. We’re not gonna spend a lot of time there.
But we will spend time with type II MPGN.
Listen, type II MPGN, is only associated with dense deposit disease.
Is that clear?
Let me ask you something else.
Well, let me finish this up then I’ll ask you,
of the two, immune-complex or complement-mediated,
which one of these would be more common in terms of occurrence?
And you’ll see what I'm getting to.
Dysregulation of alternative complement pathway, the alternative complement pathway.
So what do you end up having?
Is the fact that you have antibodies to complement regulators.
These are the important points that you wanna take away from this flow chart
to give yourself a bird’s eye view how to approach your patient with MPGN
and then as we go further through here we’re gonna plug-in the details.
Let us now continue.