Evidence map›Paper›PMID 41948588›Full record

ArticleFrontiers in medicine2026

Evolution of idiopathic membranous nephropathy to class v lupus nephritis: a case report and literature review.

Bo Shen, Cheng Peng, Weicheng Xiao

Abstract readCase Reports
In one paragraph

Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Bo ShenDepartment of Blood Purification Center, Shaoxing Second Hospital, Shaoxing, Zhejiang, China.
Cheng PengDepartment of Nephrology, Shaoxing Second Hospital, Shaoxing, Zhejiang, China.
Weicheng XiaoDepartment of Blood Purification Center, Shaoxing Second Hospital, Shaoxing, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The M-type phospholipase A2 receptor (PLA2R) antibody positivity is considered a specific serological marker for idiopathic membranous nephropathy (IMN), and its presence in class V lupus nephritis (LN) is rare. There is limited reporting on the longitudinal progression from IMN to systemic lupus erythematosus (SLE) with class V LN, particularly in cases with persistently positive anti-PLA2R antibodies. Case presentation: A 54-year-old woman presented with nephrotic syndrome in 2016, with initial renal biopsy showing podocyte disease. In 2020, disease recurrence with positive serum anti-PLA2R antibodies led to a second biopsy diagnosing IMN stage II. In 2024, she presented with edema and facial erythema. Serology revealed new-onset positive ANA and anti-dsDNA antibodies alongside persistent anti-PLA2R positivity, meeting SLE criteria. A third renal biopsy confirmed class V LN. After treatment with methylprednisolone and hydroxychloroquine, and following a rituximab infusion reaction, she achieved clinical remission with obinutuzumab. Conclusion: This case highlights that positive anti-PLA2R antibodies do not definitively exclude secondary MN such as class V LN. Long-term serological monitoring and repeat renal biopsy should be considered in IMN patients with atypical clinical evolution to identify potential transformation to LN.

Indexed as

anti-PLA2R antibodiescase reportclass V lupus nephritisidiopathic membranous nephropathyobinutuzumab

Identifiers

PMID41948588
PMCPMC13050730

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.