Evidence map›Paper›PMID 29804209›Full record

ArticleSkeletal radiology2019

Mutational analysis of high-grade spindle cell sarcoma of the femur in Mazabraud's syndrome.

Michele Calleja, Fernanda Amary, Paul O'Donnell

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In one paragraph

Article in Skeletal radiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

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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 at 2 institutions in 1 country.

Michele CallejaDepartment of Radiology, The Royal National Orthopaedic Hospital, Stanmore, HA7 4LP, UK. michc@doctors.org.uk.
Fernanda AmaryDepartment of Histopathology, The Royal National Orthopaedic Hospital, Stanmore, UK.
Paul O'DonnellDepartment of Radiology, The Royal National Orthopaedic Hospital, Stanmore, HA7 4LP, UK.
University College London · GBRoyal National Orthopaedic Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mazabraud's syndrome is a rare disorder characterised by the association of fibrous dysplasia with intramuscular myxomas. We present a 36-year-old woman with right anterior knee pain and a buttock mass. Imaging showed aggressive bone destruction within an area of fibrous dysplasia in the right femur and a mass with myxoid signal characteristics in the right adductor region. Biopsy of the femur revealed both fibrous dysplasia and a high-grade spindle cell sarcoma. Biopsy of the adductor mass confirmed a soft-tissue myxoma. Molecular genetic analysis revealed an identical R201H substitution in the GNAS1 gene in the sarcoma, the myxoma, and also the conventional fibrous dysplasia.

Indexed as

AdultBiopsyButtocksChromograninsDiagnosis, DifferentialFemaleFemoral NeoplasmsFemurGTP-Binding Protein alpha Subunits, GsHumansMagnetic Resonance ImagingMyxomaNeoplasm GradingPoint MutationSarcomaSoft Tissue NeoplasmsChromograninsGNAS protein, humanGTP-Binding Protein alpha Subunits, GsFibrous dysplasiaGNAS1 geneHigh-grade spindle cell sarcomaMazabraud’s syndromeMyxoma

Identifiers

PMID29804209
OpenAlexW2803317728

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.