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ArticleEuropean journal of pediatrics2025

Pediatric eosinophilic fasciitis: similarities and differences with adult forms.

Thibaut César, Diane Giovannini, Alban Deroux, Laurence Bouillet, Frédérique Nugues, Aurélia Carbasse, Isabelle Koné-Paut, Charlotte Borocco, Christine Pietrement, Brigitte Bader-Meunier and 8 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in European journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Recurrent Eosinophilic Fasciitis: The First Case Report.Clinical, cosmetic and investigational dermatology · 2025
    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

18 authors.

Thibaut CésarDepartment of Pediatrics, Grenoble-Alpes University Hospital, Grenoble, France.
Diane GiovanniniPathology Department, Grenoble-Alpes University Hospital, Grenoble, France.
Alban DerouxInternal Medicine Department, Grenoble-Alpes University Hospital, Grenoble, France.
Laurence BouilletInternal Medicine Department, Grenoble-Alpes University Hospital, Grenoble, France.
Frédérique NuguesPediatric Radiology, Grenoble-Alpes University Hospital, Grenoble, France.
Aurélia CarbasseDepartment of Pediatrics, Montpellier University Hospital, Montpellier, France.
Isabelle Koné-PautParis Saclay University and Department of Pediatric Rheumatology, Bicêtre Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.
Charlotte BoroccoParis Saclay University and Department of Pediatric Rheumatology, Bicêtre Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.
Christine PietrementDepartment of Pediatrics, Reims University Hospital, Reims, France.
Brigitte Bader-MeunierParis-Cité University and Pediatric Hematology-Immunology and Rheumatology Department, Assistance Publique Hôpitaux de Paris (APHP), Necker University Hospital, Paris, France.
Pierre QuartierParis-Cité University and Pediatric Hematology-Immunology and Rheumatology Department, Assistance Publique Hôpitaux de Paris (APHP), Necker University Hospital, Paris, France.
Audrey LaurentDepartment of Pediatric Rheumatology, Hospices Civils de Lyon, Lyon, France.
Teresa GianiDepartment of Rheumatology, Anna Meyer Children Hospital, Florence, Italy.
Normi BrückDepartment of Pediatric Rheumatology, Carl Gustav Carus University Hospital, Dresden, Germany.
Joan Calzada-HernàndezDepartment of Pediatric Rheumatology, Hospital San Joan de Déu, Barcelona, Spain.
Anne PagnierDepartment of Pediatrics, Grenoble-Alpes University Hospital, Grenoble, France.
Charlotte Kevorkian-VerguetDepartment of Pediatrics, Grenoble-Alpes University Hospital, Grenoble, France. ckevorkianverguet@chu-grenoble.fr.
GKJR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of this study was to identify pediatric eosinophilic fasciitis, which is an extremely rare condition, in order to describe their clinical, paraclinical, and therapeutic characteristics. We made a call for observations via societies for pediatric rheumatology in France and surrounding countries and collected clinical and paraclinical data of the cases fulfilling the diagnostic criteria. Eight patients under 18 years of age with confirmed eosinophilic fasciitis followed between April 2004 and July 2022 in France, Germany, Italy, and Spain were included. The median age of onset of symptoms was 8.7 years (range 3 to 12.6). All patients had skin and joint involvement at diagnosis. Eosinophilia was present at diagnosis in 5/8 patients and 5/7 patients presented hypergammaglobulinemia. All the patients had an MRI, and in 6, we observed thickened fascia with a T2 hypersignal. Five patients had undergone a full-thickness biopsy showing a polymorphic lymphoplasmacytic infiltrate of the fascia in all and the presence of eosinophils in 4 of them. All the patients were treated with corticosteroids with variable regimens and all received at least an immunosuppressant. Conclusion: To our knowledge, this is the largest pediatric series of eosinophilic fasciitis. The clinical and paraclinical presentation seems similar to that of adults except for a form that appears to be distinguished with isolated joint contractures, and hypergammaglobulinemia which appears to be more frequent in children. Dermatological and pathological expertise and MRI are key elements of the diagnosis. The most consensual treatment includes physiotherapy, prolonged corticosteroid therapy, and methotrexate as first-line therapy. What is Known • Eosinophilic fasciitis is a rare condition, especially in children with approximately 60 reported pediatric cases. • Some pediatric specificities tend to emerge from some reports. What is New • Possible isolated joints contractures and more frequent hypergammaglobulinemia seem to characterize pediatric eosinophilic fasciitis in comparison with adult forms. • The most frequently used first-line therapy combines physiotherapy, corticosteroids and methrotrexate.

Indexed as

EosinophiliaFasciitisAdolescentAdrenal Cortex HormonesAdultChildChild, PreschoolFemaleHumansImmunosuppressive AgentsMagnetic Resonance ImagingMaleAdrenal Cortex HormonesImmunosuppressive AgentsHypergammaglobulinemiaMRIPediatric eosinophilic fasciitis

Identifiers

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.