Evidence map›Paper›PMID 34865192›Full record

ArticleSkeletal radiology2022

Multicentric infantile myofibromatosis with extensive involvement limited to bone.

María Luque-Cabal, Estíbaliz Obregón-Martínez, María Díez-Blanco, Marta Álvarez-García, Gabriel Fernández-Pérez

Abstract readCase Reports
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In one paragraph

Article in Skeletal radiology, 2022. 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
0.2field-weighted citation impact, top 44% 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, 1 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

5 authors at 2 institutions in 1 country.

María Luque-CabalDepartment of Radiology, Hospital Universitario Río Hortega, Valladolid, Spain. marialc@saludcastillayleon.es.
Estíbaliz Obregón-MartínezDepartment of Clinical Pathology, Hospital Clínico Universitario de Valladolid, Valladolid, Spain.
María Díez-BlancoDepartment of Radiology, Hospital Universitario Río Hortega, Valladolid, Spain.
Marta Álvarez-GarcíaDepartment of Radiology, Hospital Universitario Río Hortega, Valladolid, Spain.
Gabriel Fernández-PérezDepartment of Radiology, Hospital Universitario Río Hortega, Valladolid, Spain.
Hospital Universitario Río Hortega · ESHospital Clínico Universitario de Valladolid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infantile myofibromatosis (IM) is the most common benign fibrous tumor of infancy, characterized by the development of single or multiple nodules in the skin, soft tissues, bone, and/or viscera. Multicentric forms are less frequent and can affect different tissues simultaneously and their prognosis depends on their extension and visceral involvement. Rarely, these forms are limited to the skeleton, in which case the absence of extraosseous lesions makes it difficult to suspect this entity. We present the case of an infant with multiple radiolucent lesions involving the skull, ribs, spine, and long bones, discovered in a radiological study performed after a minor trauma. A broad differential diagnosis was considered based on the osteolytic and polyostotic nature of the lesions on imaging studies. This report details and illustrates the typical radiological findings in bony involvement of IM, which suggest this disorder over other diagnostic options.

Indexed as

MyofibromatosisSoft Tissue NeoplasmsDiagnosis, DifferentialHumansInfantRibsBoneInfantile myofibromatosisMulticentricOsteolytic

Identifiers

PMID34865192
OpenAlexW4200395506

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.