Evidence map›Paper›PMID 40281557›Full record

ReviewPediatric rheumatology online journal2025

Imaging assessment of calcinosis in juvenile dermatomyositis: a narrative review.

Belina Y Yi, Jessica Perfetto, Evin Rothschild, Kelly Rouster-Stevens, Amanda Robinson, Kathryn Cook, Delaney D Ding, Andrea Eagle Child, Ovgu Kul Cinar, Barbara Limbach and 8 more

Abstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Pediatric rheumatology online journal, 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. Review
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

18 authors.

Belina Y YiJohns Hopkins University School of Medicine, Baltimore, MD, USA. byi4@jh.edu.
Jessica PerfettoHassenfeld Children's Hospital at NYU Langone, New York, NY, USA.
Evin RothschildJohns Hopkins University School of Medicine, Baltimore, MD, USA.
Kelly Rouster-StevensEmory University, Children's Healthcare of Atlanta, Atlanta, GA, USA.
Amanda RobinsonUniversity of Utah, Salt Lake City, UT, USA.
Kathryn CookAkron Children's Hospital, Akron, OH, USA.
Delaney D DingUniversity of Florida College of Medicine, Gainesville, FL, USA.
Andrea Eagle ChildChildhood Arthritis and Rheumatology Research Alliance (CARRA), Calgary, AB, Canada.
Ovgu Kul CinarGreat Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Barbara LimbachCure JM, Childhood Arthritis and Rheumatology Research Alliance (CARRA), Wolcottville, IN, USA.
Charalampia PapadopoulouGreat Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Lesley Ann SaketkooNew Orleans Scleroderma and Sarcoidosis Patient Care and Research Center, Louisiana State University and Tulane University Medical Schools, New Orleans, LA, USA.
Adam SchiffenbauerNational Institute of Environmental Health Sciences (NIEHS), National Institutes of Health (NIH), Bethesda, MD, USA.
Heinrike SchmelingSection of Rheumatology, Department of Pediatrics, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Antonia ValenzuelaDepartment of Clinical Immunology and Rheumatology, Pontificia Universidad Católica de Chile, Santiago, Chile.
Susan ShenoiSeattle Children's Hospital and Research Center, University of Washington, Seattle, USA.
Dawn M WaheziChildren's Hospital at Montefiore, Bronx, NY, USA.
CARRA JDM Calcinosis workgroup

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Calcinosis is a severe manifestation of juvenile and adult idiopathic inflammatory myopathies, which can lead to pain, limited range of motion, disfigurement, and infection. It is more common in juvenile idiopathic inflammatory myopathies, especially in juvenile dermatomyositis (JDM). Calcinosis can be visible on cutaneous surfaces, although can also present in muscles and internal organs, making a thorough assessment difficult without imaging modalities. In this narrative review, we discuss different imaging modalities used in evaluating JDM-associated calcinosis including X-ray, computed tomography (CT), magnetic resonance imaging (MRI), and ultrasound (US).

Indexed as

CalcinosisDermatomyositisChildHumansMagnetic Resonance ImagingTomography, X-Ray ComputedUltrasonographyCalcinosisComputed tomographyIdiopathic inflammatory myopathyJuvenile dermatomyositisMagnetic resonance imagingUltrasoundx-ray

Identifiers

PMID40281557
PMCPMC12032750

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.