Evidence map›Paper›PMID 34974549›Full record

ReviewPathologica2021

Recurrent primary endobronchial fetal rhabdomyoma: a case report and literature review.

Stefano Marletta, Anna Caliò, Adele Fioravanzo, Enrico Cavallo, Evelin Torresani, Federica Zampieri, Eliana Gilioli

Open access · diamondAbstract readCase ReportsReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Pathologica, 2021. 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
0.6field-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, 4 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

7 authors at 1 institution in 1 country.

Stefano MarlettaDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Anna CaliòDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Adele FioravanzoDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Enrico CavalloDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Evelin TorresaniDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Federica ZampieriDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Eliana GilioliDepartment of Pathology and Diagnostics, University and Hospital Trust of Verona, Verona, Italy.
University of Verona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fetal rhabdomyoma is an extremely rare benign rhabdomyoblastic tumor with myotube-like differentiation, mainly arising on mucosal surfaces of the head and neck region of both children and young patients, almost invariably definitively treated with surgical excision. Herein the case of a male adult suffering from a recurrent fetal rhabdomyoma primary involving the bronchial structures is reported, along with a detailed literature review. This is the first fetal rhabdomyoma described to originate in such a localization; furthermore, an 11-year interval period between the first lesion and the recurrent one has never been reported.

Indexed as

RhabdomyomaAdultChildHeadHumansMaleNeckbenign mesenchymal neoplasmendobronchialfetal rhabdomyomarecurrenceskeletal muscle differentiation

Identifiers

PMID34974549
PMCPMC8720399
OpenAlexW4200446263

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.