Evidence map›Paper›PMID 35223009›Full record

ArticleClinical case reports2022

Peculiar thousand leaves soft-tissue mass: Elastofibroma dorsi.

Faten Limaiem, Seifeddine Baccouch, Mohamed Hajri

Abstract read
In one paragraph

Article in Clinical case reports, 2022. 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
–field-weighted citation impact
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.

  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

3 authors.

Faten LimaiemTunis Faculty of Medicine University of Tunis El Manar Tunis Tunisia.ORCID https://orcid.org/0000-0003-3805-8390
Seifeddine BaccouchTunis Faculty of Medicine University of Tunis El Manar Tunis Tunisia.
Mohamed HajriTunis Faculty of Medicine University of Tunis El Manar Tunis Tunisia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elastofibroma dorsi is an uncommon benign soft-tissue tumor with uncertain pathogenesis (Medicina (Kaunas), 2021; 57, 370). Surgical excision is the therapeutic option for symptomatic patients. A pathological study confirms the diagnosis after surgery. The prognosis is excellent with extremely rare recurrence cases (Anticancer Res, 2021, 41, 2211).

Indexed as

elastofibromasoft‐tissue tumorsubscapular mass

Identifiers

PMID35223009
PMCPMC8842450

What OpenQuestion holds

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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.