Evidence map›Paper›PMID 39027358›Full record

ArticleClinical case reports2024

Osteopoikilosis-the incidental finding of a rare bone dysplasia: A case report.

Tejera-Pérez Rosa-Juana, Aguilar-López Ana, Marfil-Daza Julia, Castaño-Pérez Sara

Abstract readCase Reports
In one paragraph

Article in Clinical case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

Tejera-Pérez Rosa-JuanaDepartment of Internal Medicine Complejo Hospitalario Universitario Nuestra Señora de Candelaria Santa Cruz de Tenerife Spain.ORCID https://orcid.org/0000-0001-5361-8099
Aguilar-López AnaDepartment of Internal Medicine Complejo Hospitalario Universitario Nuestra Señora de Candelaria Santa Cruz de Tenerife Spain.
Marfil-Daza JuliaDepartment of Internal Medicine Complejo Hospitalario Universitario Nuestra Señora de Candelaria Santa Cruz de Tenerife Spain.
Castaño-Pérez SaraDepartment of Internal Medicine Complejo Hospitalario Universitario Nuestra Señora de Candelaria Santa Cruz de Tenerife Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Key Clinical Message: Osteopoikilosis is an asymptomatic osteosclerotic dysplasia, of autosomal dominant inheritance, which does not cause deformity or alteration in bone development, of incidental diagnosis. The differential diagnosis should be made with osteoblastic metastases, among others, especially if it is asymmetric and in patients over 50 years of age. Abstract: Osteopoikilosis is a rare benign bone disease, characterized by the appearance of bone islands in the osseous tissue, which could be confused with bone metastasis. We present the case of a 69-year-old man, in whom the presence of multiple punctate lesions spread throughout the skeleton was discovered after an accidental fall with a fracture of the T11 vertebral body complicated by acute osteomyelitis. The importance of this clinical case lies in the need to rule out neoplastic cause after the vertebral fracture, since osteopoikilosis is usually an incidental finding and the specific characteristics of the radiological image would avoid unnecessary interventions.

Indexed as

bone sclerosishereditary bone dysplasiaosteopoikilosisTc 99m gammagraphy

Identifiers

PMID39027358
PMCPMC11257685

What OpenQuestion holds

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Registered trials

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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.