Evidence map›Paper›PMID 20422214›Full record

ArticleVirchows Archiv : an international journal of pathology2010

High-resolution genome-wide analysis of chromosomal alterations in elastofibroma.

Juan Luis García Hernández, Javier Ortiz Rodríguez-Parets, José María Valero, María Asunción Gomez Muñoz, M Rocío Benito, Jesus M Hernandez, Agustín Bullón

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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Retrospective analysis of 73 cases of elastofibroma.Annals of the Royal College of Surgeons of England · 2020
    Article
  7. Review
  8. Article
  9. Article
  10. Elastofibroma dorsi: a histochemical and immunohistochemical study.European journal of histochemistry : EJH · 2015
    Article
  11. Article
  12. Review
  13. 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

7 authors at 4 institutions in 1 country.

Juan Luis García HernándezResearch Unit, IECSCYL-Hospital Universitario de Salamanca, Paseo San Vicente, 58, E-37007, Salamanca, Spain. jlgarcia@usal.es
Javier Ortiz Rodríguez-Parets
José María Valero
María Asunción Gomez Muñoz
M Rocío Benito
Jesus M Hernandez
Agustín Bullón
Complejo Hospitalario de Salamanca · ESUniversidad de Salamanca · ESInstituto de Estudios de Ciencias de la Salud de Castilla y León · ESInstituto de Investigación Biomédica de Salamanca · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elastofibroma is a rare, benign fibrous proliferation that most commonly occur in periscapular soft tissues and is characterized by accumulated elastic fibers. Although the lesion is generally regarded as a reactive process, an unusual fibroblastic pseudotumor or as a fibroelastic tumor-like lesion, its etiology remains unknown. Cytogenetic studies in these lesions detected chromosomal instability and some recurrent clonal chromosomal changes, which raised the possibility that the lesion represents a neoplastic process. Here, we report the genomic alterations detected by array-based comparative genomic hybridization (aCGH) and by multiplex ligation-dependent probe amplification (MLPA) in two cases of elastofibroma. Both cases showed losses on 1p, 13q, 19p, and 22q by aCGH. In addition, deletion of CASR (3q21), GSTP1 (11q13), BRCA2 (13q12) and gains on APC (5q21) and PAH (12q23) were observed by MLPA in both samples. Genomic screening studies of this fibrous proliferation may lead to identify chromosomal regions containing genes involved in the development of elastofibromas.

Indexed as

Chromosome AberrationsComparative Genomic HybridizationNucleic Acid Amplification TechniquesFemaleFibromaHumansMaleMiddle AgedSoft Tissue Neoplasms

Identifiers

PMID20422214
OpenAlexW2071811722

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.