Dual MPO-ANCA and PLA2R positivity in crescentic glomerulonephritis with MPO-associated membranous nephropathy: a

Chikayuki Morimoto1, Yoshihide Fujigaki2,3, Hitoshi Anzai1

  • 1Department of Internal Medicine, Teikyo University School of Medicine, Itabashi-ku, Tokyo, Japan.

CEN Case Reports
|January 19, 2026
PubMed

Insights

Myeloperoxidase (MPO)-antineutrophil cytoplasmic antibody (ANCA)-associated glomerulonephritis (GN) and membranous nephropathy (MN) can occur together. Treatment led to remission of both conditions, suggesting MPO-ANCA

Area of Science:

  • Nephrology
  • Immunology
  • Pathology

Background:

  • Myeloperoxidase (MPO)-associated membranous nephropathy (MN) is increasingly recognized.
  • Concurrent MPO-antineutrophil cytoplasmic antibody (ANCA)-associated crescentic glomerulonephritis (GN) with MN is rare.
  • The role of MPO-ANCA in dual glomerular pathology requires further investigation.

Purpose of the Study:

  • To report a case of MPO-ANCA-positive rapidly progressive glomerulonephritis (RPGN) with concurrent MPO-associated MN and phospholipase A2 receptor (PLA2R)-positive disease.
  • To investigate the clinical course and treatment response in this complex presentation.
  • To explore potential pathogenic mechanisms linking MPO-ANCA, crescentic GN, and MN.

Main Methods:

  • Case report of a 41-year-old male with MPO-ANCA-positive RPGN and nephrotic syndrome.
  • Renal biopsy analysis showing crescentic GN and MPO-associated MN with PLA2R staining.
  • Treatment with immunosuppressive therapy and monitoring of clinical parameters and MPO-ANCA titers.

Main Results:

  • The patient presented with RPGN and developed nephrotic syndrome.
  • Kidney biopsy confirmed crescentic GN and MPO-associated MN (Churg stage II-III) with PLA2R positivity.
  • Immunosuppressive therapy resulted in concurrent remission of RPGN and nephrotic syndrome, with decreased MPO-ANCA titers.

Conclusions:

  • MPO-ANCA may play a role in the pathogenesis of both crescentic GN and MN in select patients.
  • Two potential mechanisms are proposed: MPO-IgG complex formation preceding PLA2R deposition, or MPO deposition in pre-existing PLA2R-positive MN.
  • Further research is needed to clarify the pathogenic role of MPO in these overlapping glomerular diseases.

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