Evidence map›Paper›PMID 20676642›Full record

ArticleRheumatology international2011

Overlapping juvenile idiopathic arthritis and systemic lupus erythematosus: a case report.

Anna Bazsó, Krisztina Sevcic, Ilonka Orbán, Gyula Poór, Zsolt Balogh, Emese Kiss

Open access · goldAbstract readCase Reports
PubMed Publisher
In one paragraph

Article in Rheumatology international, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Anna BazsóNational Institute of Rheumatology and Physiotherapy, Budapest, Hungary. bazsoanna@yahoo.com
Krisztina Sevcic
Ilonka Orbán
Gyula Poór
Zsolt Balogh
Emese Kiss
Institute of Rheumatology · CZNational Institute of Oncology · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereby, we report the case of a 12-year-old girl developing oligoarthritis and progressing into a polyarticular form. Rheumatoid factor was positive, and juvenile idiopathic arthritis (JIA) was diagnosed. After a poor response to DMARDs, an anti-TNF agent (infliximab) was initiated, but to be discontinued due to an allergic reaction. The same complication was observed with the fully human derivative, adalimumab. At the age of 22, the patient presented septicemia with severe anemia and subsequent development of leukopenia, myocarditis with heart failure, and ANA, aSm, aSS-A, aCL positives, and nephrotic syndrome. These new clinical manifestations fulfilled the classification criteria for the diagnosis of systemic lupus erythematosus. Due to the poor therapeutic responses for both diseases, alternative medical options have to be considered, such as targeted therapy with anti-CD20 or interleukin-6 receptor antagonist monoclonal antibodies. This patient may also be a candidate for autologous hemopoietic stem cell transplantation.

Indexed as

Antirheumatic AgentsArthritis, JuvenileBiological ProductsChildDrug HypersensitivityFemaleHumansImmunosuppressive AgentsLupus Erythematosus, SystemicRecurrenceTreatment OutcomeTumor Necrosis Factor-alphaYoung AdultAntirheumatic AgentsBiological ProductsImmunosuppressive AgentsTumor Necrosis Factor-alpha

Identifiers

PMID20676642
OpenAlexW2109367134

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.