Evidence map›Paper›PMID 42311693›Full record

ArticleFrontiers in immunology2026

SAPHO syndrome with membranous nephropathy and analgesic-induced nephropathy: a case report.

Yuxin Qiao, Zuo Wang, Guohua Li, Duo Zhang

Abstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Yuxin QiaoClinical College of Traditional Chinese Medicine, Inner Mongolia Medical University, Hohhot, China.
Zuo WangClinical College of Traditional Chinese Medicine, Inner Mongolia Medical University, Hohhot, China.
Guohua LiClinical College of Traditional Chinese Medicine, Inner Mongolia Medical University, Hohhot, China.
Duo ZhangDepartment of Nephrology, Inner Mongolia Autonomous Region Hospital of Traditional Chinese Medicine, Hohhot, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SAPHO syndrome is a rare autoimmune disorder, and the occurrence of renal involvement in this condition is even more uncommon. We report the case of a 43-year-old male patient with SAPHO syndrome, who initially presented with palmoplantar pustulosis and pain in the chest wall and sternoclavicular joints, accompanied by proteinuria and microscopic hematuria. He was admitted to the hospital due to headache, lower limb edema, and elevated serum creatinine. Renal biopsy revealed stage II membranous nephropathy combined with analgesic nephropathy. Following treatment, his symptoms resolved, and at one-year follow-up, proteinuria had nearly achieved clinical complete remission, with stable renal function.

Indexed as

Acquired Hyperostosis SyndromeAnalgesicsGlomerulonephritis, MembranousAdultHumansMaleAnalgesicsanalgesic nephropathycase reportheadachemembranous nephropathySAPHO syndrome

Identifiers

PMID42311693
PMCPMC13269111

What OpenQuestion holds

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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.