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Go back to clinical information and images Diagnosis: Membranoproliferative Glomerulonephritis with Monoclonal Deposits of IgG/kappa Proliferative Glomerulonephritis with monoclonal IgG deposits (PGNMID) is a entity characterized by monoclonal IgG deposits in the kidney. The incidence of PGNMID in the native kidneys is about 0.17%. It can mimic other monoclonal diseases such as light and heavy chain deposition disease, light and heavy chain amyloid, immunotactoid and fibrillary glomerulonephritides and type I cryoglobulinemic glomerulonephritis. In PGNMID, monoclonal deposits are strictly glomerular consisting of single light chain isotype and single heavy chain subtype, most commonly IgG3 k. Membranoproliferative or endocapillary patterns of glomerulonephritis are seen on light microscopy with glomerular electron dense deposits on electron microscopy (Hussain SM, Sureshkumar KK. Proliferative glomerulonephritis with monoclonal IgG deposits; an unusual cause of de novo disease in kidney allograft. J Nephropathol. 2017;6:220-224. [PubMed link]). In our patient, bone marrow studies domonstrated plasm cell neoplasm, and a diagnosis of multiple myeloma was made. See the chapter: Membranoproliferative Glomerulonephritis of our Tutorial. Go back to clinical information and images References
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