Evidence map›Paper›PMID 33796183›Full record

ArticleThe Pan African medical journal2020

[Fibromatosis colli: a rare cervical tumor of the infant].

Nogognan Ignace Lengane, Milckisédek Judicaël Marouruana Some, Mohamed Tall, Alain Saga Ouermi, John Pepin Nikiema, Joséphine Wendemy Ouoba, Moussa Kadyogo, Moustapha Sereme

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in The Pan African medical journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 1 institution in 1 country.

Nogognan Ignace LenganeService ORL et Chirurgie Cervicofaciale, CHU Régional de Ouahigouya, Ouahigouya, Burkina Faso.
Milckisédek Judicaël Marouruana SomeService d´Imagerie Médicale, CHU Régional de Ouahigouya, Ouahigouya, Burkina Faso.
Mohamed TallService d´Imagerie Médicale, CHU Régional de Ouahigouya, Ouahigouya, Burkina Faso.
Alain Saga OuermiService de Pédiatrie, CHU Régional de Ouahigouya, Ouahigouya, Burkina Faso.
John Pepin NikiemaService de Pédiatrie, CHU Régional de Ouahigouya, Ouahigouya, Burkina Faso.
Joséphine Wendemy OuobaService ORL et Chirurgie Cervicofaciale, CHU Pédiatrique Charles De Gaulle, Ouagadougou, Burkina Faso.
Moussa KadyogoService ORL et Chirurgie Cervicofaciale, CHU Bogodogo, Ouagadougou, Burkina Faso.
Moustapha SeremeService ORL et Chirurgie Cervicofaciale, CHU Bogodogo, Ouagadougou, Burkina Faso.
Centre Hospitalier Universitaire Yalgado Ouédraogo · BF

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibratosis colli, or infantile pseudotumor of the sternocleidomastoid muscle, is a rare cause of benign cervical mass in newborns and infants. This study involved all patients admitted with cervical swelling and diagnosed with colli fibromatosis from March 2016 to February 2020. Five patients were retained. In all patients cervical swelling occurred in the first month of life. No patient had had obstetric trauma. The diagnosis of fibromatosis colli was based on ultrasound. All patients received medical treatment. Fibratosis colli is a relatively rare cause of cervical mass in newborns and infants.

Indexed as

FemaleFibromaHead and Neck NeoplasmsHumansInfantMaleMuscle NeoplasmsNeck MusclesUltrasonographyFibromatosis colliinfantsternocleidomastoid muscletorticollis

Identifiers

PMID33796183
PMCPMC7992433
OpenAlexW3116574256

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.