Concurrent Giant Cell Arteritis and Anti-PLA2R-Positive Membranous Nephropathy: A Case Report

Background: Giant cell arteritis (GCA) is a vasculitis mostly affecting older people. Primary membranous nephropathy (MN) is an immune-mediated glomerulopathy recently shown to be caused by autoantibodies. We report a case of both illnesses in an older gentleman. Case Presentation: A 63-year-old man developed systemic inflammatory signs and symptoms and near simultaneous nephrotic-range proteinuria. Investigations demonstrated both giant cell arteritis (GCA) and membranous nephropathy, with the presence of the M-type phospholipase A2 receptor (PLA2R) within subepithelial immune deposits. Renal function remained normal throughout the course. The patient achieved complete clinical and biochemical remission of both illnesses coincident with corticosteroid therapy. Conclusions: Although rare cases of concurrent GCA and MN have been reported, GCA occurring with PLA2R-positive MN has not been documented. This case raises the possibility of overlapping immunological pathways and may offer clues to the pathogenesis of GCA.

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Journal
Rheumato
Published
2026-09-09
DOI
https://doi.org/10.3390/rheumato6030021
Primary Topic
Vasculitis and related conditions
Type
article
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article

Concurrent Giant Cell Arteritis and Anti-PLA2R-Positive Membranous Nephropathy: A Case Report

Gerald J. Berry, Philip L. Cohen, Kudret Arslan, John Mulligan et al.
Rheumato
Vasculitis and related conditions
article

Concurrent Giant Cell Arteritis and Anti-PLA2R-Positive Membranous Nephropathy: A Case Report

Gerald J. Berry, Philip L. Cohen, Kudret Arslan, John Mulligan, Jared Hassler
article en

Abstract

Background: Giant cell arteritis (GCA) is a vasculitis mostly affecting older people. Primary membranous nephropathy (MN) is an immune-mediated glomerulopathy recently shown to be caused by autoantibodies. We report a case of both illnesses in an older gentleman. Case Presentation: A 63-year-old man developed systemic inflammatory signs and symptoms and near simultaneous nephrotic-range proteinuria. Investigations demonstrated both giant cell arteritis (GCA) and membranous nephropathy, with the presence of the M-type phospholipase A2 receptor (PLA2R) within subepithelial immune deposits. Renal function remained normal throughout the course. The patient achieved complete clinical and biochemical remission of both illnesses coincident with corticosteroid therapy. Conclusions: Although rare cases of concurrent GCA and MN have been reported, GCA occurring with PLA2R-positive MN has not been documented. This case raises the possibility of overlapping immunological pathways and may offer clues to the pathogenesis of GCA.

RheumatoVol. 6(3)
Temple University (US), Stanford University (US)
Good health and well-being
Openalex Percentile: Top 11%
Vasculitis and related conditions
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Concurrent Giant Cell Arteritis and Anti-PLA2R-Positive Membranous Nephropathy: A Case Report — Gerald J. Berry, Philip L. Cohen, et al. · Rheumato (2026) | TGRS Research Map | TGRS