Evidence map›Paper›PMID 40951084›Full record

ArticleCureus2025

Anti-TIF1-Gamma Autoantibodies-Positive Juvenile Dermatomyositis Associated With Interstitial Lung Disease: A Case Report.

Ricardo Cid-Puente, Isaac A Carreon-Meza, David A Herrera-VanOostdam

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. 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.

Ricardo Cid-PuenteDepartment of Immunology, Biological Sciences School, Universidad Autónoma de Zacatecas, Zacatecas, MEX.
Isaac A Carreon-MezaDepartment of Pediatrics, Hospital del Niño y la Mujer "Dr. Alberto López Hermosa", San Luis Potosi, MEX.
David A Herrera-VanOostdamDepartment of Rheumatology, Hospital Central "Dr. Ignacio Morones Prieto", San Luis Potosi, MEX.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Juvenile dermatomyositis (JDM) is a rare autoimmune disease in children, characterized by muscle inflammation and skin manifestations. This case report describes a nine-year-old boy with JDM associated with anti-TIF1-γ antibodies and interstitial lung disease (ILD). The patient presented with progressive muscle weakness and characteristic skin lesions. Imaging confirmed ILD, and treatment with methylprednisolone pulses and rituximab resulted in significant improvement. This case emphasizes the need for pulmonary monitoring in JDM patients, regardless of antibody profile, and highlights the importance of personalized treatment approaches.

Indexed as

anti-tif-1γinflammatory myositisinterstitial lung diseasejuvenile dermatomyositisjuvenile idiopathic inflammatory myositis

Identifiers

PMID40951084
PMCPMC12425170

What OpenQuestion holds

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Registered trials

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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.