Evidence map›Paper›PMID 31798921›Full record

ArticleOxford medical case reports2019

Alveolar rhabdomyosarcoma with unusual cytogenetic findings: one more case and review of the literature.

Maria Ioannou, Konstantinos Perivoliotis, Nikolaos-Marios Zaharos, Athanasios Tsanakas, Konstantinos Tepetes, George Koukoulis

Open access · goldAbstract readCase Reports
In one paragraph

Article in Oxford medical case reports, 2019. 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
0.3field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 1 institution in 1 country.

Maria IoannouDepartment of Pathology, University Hospital of Larissa, Mezourlo, 41110 Larissa, Greece.
Konstantinos PerivoliotisDepartment of Surgery, University Hospital of Larissa, Mezourlo, 41110 Larissa, Greece.ORCID 0000-0002-6622-5734
Nikolaos-Marios ZaharosDepartment of Pathology, University Hospital of Larissa, Mezourlo, 41110 Larissa, Greece.
Athanasios TsanakasDepartment of Pathology, University Hospital of Larissa, Mezourlo, 41110 Larissa, Greece.
Konstantinos TepetesDepartment of Surgery, University Hospital of Larissa, Mezourlo, 41110 Larissa, Greece.
George KoukoulisDepartment of Pathology, University Hospital of Larissa, Mezourlo, 41110 Larissa, Greece.
University Hospital of Larissa · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alveolar rhabdomyosarcoma (ARMS), a histological subtype of rhabdomyosarcoma (RMS), is characterized by an unfavorable clinical outcome. In most ARMS cases, an indicative chromosomal alteration is identified. The recurrent translocation of FKHR with either PAX3 or PAX7 genes results in the encoding of chimeric transcription factors that boost tumorigenesis. Besides structural mutations, the copy number of these genes also contributes to the oncogenic activity. In our case, a 12-year-old female patient was diagnosed with a 4 cm pelvic mass. Histopathological examination indicated an alveolar type of RMS. Subsequent FISH analysis with a dual color break-apart probe identified positive signals of FKHR3 gene break, as well as the rare event of a synchronous aneuploidy and gene deletion of FKHR. Our findings lead to the conclusion that a systematic break-apart probe FKHR FISH analysis in ARMS, confirms the diagnosis and elucidates the full spectrum of genomic alterations of this malignancy.

Identifiers

PMID31798921
PMCPMC6874863
OpenAlexW2991169395

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.