Membranoproliferative Glomerulonephritis with Isolated C3 Deposits: Case Report and Literature Review

Abstract

Membranoproliferative glomerulonephritis with isolated C3 deposits (MPGNC3) is an uncommon condition characterized by overt glomerular C3 deposits in the absence of immunoglobulins and intramembranous dense deposits. Here the authors describe the clinical and morphological features of primary MPGNC3 in a 13-year-old boy and critically review the previously published cases. The patient presented with nephrotic syndrome and microscopic hematuria. Blood tests revealed very low circulating C3 levels. The renal biopsy exhibited subendothelial, subepithelial, and mesangial deposits, with C3 but not immunoglobulins seen on immunofluorescence. This case and the review of the literature indicate that the serum complement profile with decreased levels of C3 and normal levels of classical pathway components together with glomerular deposits containing exclusively complement C3 is highly suggestive of alternative pathway activation. The diagnosis of acquired and/or genetic complement abnormalities in some cases supports that complement dysregulation is implicated in the pathogenesis of MPGNC3. Such data show great promise to provide new therapy strategies based on modulation of the complement system activity.

Keywords::

• Complement C3
• Electron microscopy
• Hypocomplementemia
• Immunofluorescence
• Light microscopy
• Membranoproliferative glomerulonephritis
• Renal biopsy

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Corrigendum

ACKNOWLEDGMENT

The authors thank Aouatef Ben Ammar and Ismahène Aouadi as well as all members of the Laboratory of Kidney Pathology 02 for their expert technical assistance.

Declaration of interest: The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.