I'm currently about 20 weeks pregnant and I was just diagnosed with secondary membranous nephropathy after reviewing my renal biopsy with my nephrologist and University of Washington pathologists.
A little bit of background:
They found 4500 mg of protein in my urine at 10 weeks pregnant. Two months later, I receive renal biopsy reports I am diagnosed with secondary membranous nephropathy and was told something underlying is causing my kidney issue.
My biopsy states they found 3+ kappa light chain, 0 lambda light chain. IgG and c3 3+ and trace C1q (am I even speaking English anymore ...) Rare possible tubuloreticular inclusion in endothelial cells, not sure what that means.
My nephrologist was a little brief with me, and I probably wasn't asking the right questions, but basically my plasma cells should be making both kappa and lambda light chains but that's not what they are seeing in the biopsy. Sound okay so far?
I now have an appointment with the hematologist to see why this is and my doctor mentioned I will probably have a bone marrow biopsy done to rule out myeloma? I'm still not even sure if I heard her right, I was by myself trying to take this all in.
Is this a routine next step? Should I be concerned?
I'm a little lost right now. I've had labs taken for lambda kappa ratio and all of that. Still waiting on results. Thank you in advance
