 proliferative glomerulonephritis with monoclonal IgG deposits, in mid, is a recently identified condition that can occur in both native and transplanted kidneys. It is characterized by mesangial proliferation and hypercellularity on light microscopy, mesangial staining for IgG3, capillite chains, C1Q and C3 on immunofluorescence, and electron-dense deposits without substructures on electron microscopy. The condition is often misdiagnosed as transplant glomerulopathy due to its similarities to other forms of glomerulopathies. In this case report, we describe a patient who developed a novocon mid in their kidney allograft after a successful spk transplantation. The patient's proton area improved and serum creatinine stabilized with conservative treatment. Further research is needed to better understand the pathophysiology of this condition and to develop effective treatments. This article was authored by Sabiha M. Hussein and Califil K. Suresh Kumar. We are article.tv, links in the description below.