Evidence map›Paper›PMID 35386172›Full record

ArticleCureus2022

Phosphaturic Mesenchymal Tumor: A Case Report of a Rare Entity.

Rawan E Hudairy, Abdelrazak Meliti, Ghadeer Mokhtar, Maram Alanazi

Open access · diamondAbstract readCase Reports
In one paragraph

Article in Cureus, 2022. 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
0.9field-weighted citation impact, top 30% 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, 6 citations in OpenAlex.

  1. Sinonasal Phosphaturic Mesenchymal Tumor: A Case Report.Turkish archives of otorhinolaryngology · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Phosphaturic mesenchymal tumor in right thigh: 2 cases report and literature review.Clinical pathology (Thousand Oaks, Ventura County, Calif.)
    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

4 authors at 1 institution in 1 country.

Rawan E HudairyAnatomic Pathology, King Faisal Specialist Hospital and Research Centre, Jeddah, SAU.
Abdelrazak MelitiAnatomic Pathology, King Faisal Specialist Hospital and Research Centre, Jeddah, SAU.
Ghadeer MokhtarAnatomic Pathology, King Faisal Specialist Hospital and Research Centre, Jeddah, SAU.
Maram AlanaziAnatomic Pathology, King Faisal Specialist Hospital and Research Centre, Jeddah, SAU.
King Faisal Specialist Hospital & Research Centre · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phosphaturic mesenchymal tumor (PMT) is a rare entity that presents as a paraneoplastic syndrome that causes tumor-induced osteomalacia (TIO). Most of these cases were located in the extremities. We report a case of a phosphaturic mesenchymal tumor arising in the left upper thigh. The tumor was discovered during the clinical workup of a patient complaining of osteomalacia symptoms with multiple fractures.

Indexed as

grungy basophilic matrixhypophosphatemiaparaneoplastic syndromephosphaturic mesenchymal tumortumor-induced osteomalacia

Identifiers

PMID35386172
PMCPMC8967444
OpenAlexW4214560763

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.