Evidence map›Paper›PMID 31974818›Full record

ReviewClinical rheumatology2020

The use of tocilizumab in the treatment of refractory eosinophilic fasciitis: a case-based review.

Francisco Vílchez-Oya, Julia María Sánchez-Schmidt, Anna Agustí, Ana Pros

Abstract readCase ReportsReview
PubMed Publisher
In one paragraph

Review in Clinical rheumatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% of its field
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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Eosinophilic fasciitis.Medicina clinica · 2025
    Review
  4. Article
  5. Treatment and Monitoring of Eosinophilic Fasciitis.Current treatment options in rheumatology · 2025
    Article
  6. Juvenile eosinophilic fasciitis: a single center case series.Pediatric rheumatology online journal · 2024
    Article
  7. [Paraneoplastic syndromes in rheumatology].Zeitschrift fur Rheumatologie · 2023
    Review
  8. Review
  9. Eosinophilic Fasciitis: Current and Remaining Challenges.International journal of molecular sciences · 2023
    Review
  10. Article
  11. 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

4 authors at 1 institution in 1 country.

Francisco Vílchez-OyaDepartment of Rheumatology, Parc de Salut Mar/Hospital del Mar, Passeig Marítim 25-29, 08003, Barcelona, Spain. fvilchez@outlook.es.ORCID https://orcid.org/0000-0002-0304-7993
Julia María Sánchez-SchmidtDepartment of Dermatology, Parc de Salut Mar/Hospital del Mar, Barcelona, Spain.
Anna AgustíDepartment of Radiology, Parc de Salut Mar/Hospital del Mar, Barcelona, Spain.ORCID https://orcid.org/0000-0002-8507-8565
Ana ProsDepartment of Rheumatology, Parc de Salut Mar/Hospital del Mar, Passeig Marítim 25-29, 08003, Barcelona, Spain.ORCID https://orcid.org/0000-0003-0266-0531
Parc de Salut · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eosinophilic fasciitis (EF) is a rare disorder involving chronic inflammation of the fascia and connective tissue of unknown aetiology and poorly understood pathogenesis. We present the case of a 60-year-old man diagnosed with eosinophilic fasciitis with extensive cutaneous involvement and severe functional repercussion, which appeared weeks after suffering from pneumonia due to Legionella pneumophila. The patient did not experience any clinical response with high-dose corticosteroids, subcutaneous methotrexate, and intravenous immunoglobulins. Consequently, tocilizumab was initiated at 8 mg/Kg monthly achieving clinical response measured by a control MRI at the fifth dose. Response in terms of cutaneous thickness has been slower however favourable, therefore, more months of follow-up are necessary to assess the complete remission at skin level. EF treatment still constitutes a challenge, and experience with tocilizumab in the management of the disease is very limited. Through a systematic search of medical literature, we retrieved two cases describing EF treated with tocilizumab and several cases using another monoclonal antibody or Janus kinase inhibitor. We report the third case to our knowledge of the efficacy of tocilizumab in a refractory EF to corticosteroids and other immunosuppressive drugs.

Indexed as

Adrenal Cortex HormonesAntibodies, Monoclonal, HumanizedAnti-Inflammatory AgentsEosinophiliaFasciitisHumansImmunosuppressive AgentsMagnetic Resonance ImagingMaleMiddle AgedTreatment OutcomeAdrenal Cortex HormonesAntibodies, Monoclonal, HumanizedAnti-Inflammatory AgentsImmunosuppressive AgentstocilizumabEosinophiliaEosinophilic fasciitisFibrosisMonoclonal antibodiesScleroderma-like disordersTocilizumab

Identifiers

PMID31974818
OpenAlexW3002639459

What OpenQuestion holds

Textmetadata
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.