Monoclonal gammopathy is increasingly recognized as a common cause of
membranoproliferative glomerulonephritis (MPGN); however, establishing this diagnosis can be challenging. We report the case of a 58-year-old asymptomatic woman who presented with
proteinuria with
protein excretion of 5,000mg/d, microscopic
hematuria, and normal kidney function. Kidney biopsy was consistent with MPGN pattern of injury. Immunofluorescence studies were positive for nonspecific segmental
immunoglobulin M (
IgM) and C3 staining. Electron microscopy showed subendothelial, subepithelial, and mesangial electron-dense deposits. The workup excluded an infectious or
autoimmune disease, but
IgG κ monoclonal
protein was detected in serum at a concentration of 0.4mg/dL. Because there was a mismatch between the serum monoclonal
protein (
IgG κ) and immunofluorescence staining pattern (nonspecific
IgM, no light chain restriction),
laser microdissection and mass spectrometry were performed on the kidney biopsy tissue. This identified the deposits as monoclonal
IgG κ, thereby leading to the diagnosis of
monoclonal gammopathy-associated MPGN. Our case emphasizes the importance of searching for an underlying cause of MPGN, reviews the technique of
laser microdissection-mass spectrometry, and highlights its application as a pathology tool for the evaluation of
monoclonal gammopathy-related
glomerulonephritis.