Evidence map›Paper›PMID 28004375›Full record

ReviewClinical reviews in allergy & immunology2017

Gorham-Stout Disease: a Clinical Case Report and Immunological Mechanisms in Bone Erosion.

Maria José Franco-Barrera, Maria Guadalupe Zavala-Cerna, Georgina Aguilar-Portillo, Diana Brisa Sánchez-Gomez, Olivia Torres-Bugarin, Miguel Angel Franco-Barrera, Carlos Manuel Roa-Encarnacion

Abstract readCase ReportsReview
PubMed Publisher
In one paragraph

Review in Clinical reviews in allergy & immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Treatment for Gorham-Stout syndrome with a combination of teriparatide and denosumab.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2024
    Article
  5. Article
  6. Article
  7. Review
  8. Difficult Therapeutic Decisions in Gorham-Stout Disease-Case Report and Review of the Literature.International journal of environmental research and public health · 2022
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
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

7 authors at 4 institutions in 1 country.

Maria José Franco-BarreraDivision de Cirugia Maxilofacial, Hospital Universitario de Puebla, Benemerita Universidad de Puebla, Puebla, Puebla, Mexico.
Maria Guadalupe Zavala-CernaPrograma Internacional de Medicina, Universidad Autónoma de Guadalajara, Guadalajara, Jalisco, Mexico. g_zavala_78@hotmail.com.
Georgina Aguilar-PortilloPrograma Internacional de Medicina, Universidad Autónoma de Guadalajara, Guadalajara, Jalisco, Mexico.
Diana Brisa Sánchez-GomezPrograma Internacional de Medicina, Universidad Autónoma de Guadalajara, Guadalajara, Jalisco, Mexico.
Olivia Torres-BugarinPrograma Internacional de Medicina, Universidad Autónoma de Guadalajara, Guadalajara, Jalisco, Mexico.
Miguel Angel Franco-BarreraFacultad de Medicina, Universidad Autonoma de Guadalajara, Guadalajara, Jalisco, Mexico.
Carlos Manuel Roa-EncarnacionDivision de Cirugia Maxilofacial, Unidad de Alta Especialidad de Pediatria, Centro Medico Nacional de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, Mexico.
Universidad Autónoma de Guadalajara · MXBenemérita Universidad Autónoma de Puebla · MXMexican Social Security Institute · MXUniversidad de Puebla · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gorham-Stout disease (GSD) is a rare condition of osteolysis with excessive lymphangiogenesis within bone tissue. The etiology of this condition remains unknown but seems to affect mainly children and young adults of both genders all over the world. Unfortunately, there is no standardized method for diagnosis; however, histopathology remains as the gold standard. This condition is often misdiagnosed due to its varying clinical presentations from case-to-case. Here, we report the case of an 8-year-old girl who presented with chronic mandibular pain during mastication and received multiple antibiotic treatment due to infectious origin suspicion. After integrating information from clinical manifestations, radiographic, laboratory, and histopathology information, she was diagnosed with GSD. Additionally, due to the lack of literature with respect to insights into biological mechanisms and standardized treatment for this condition, we underwent a literature revision to provide information related to activation of cells from the immune system, such as macrophages, T-cells, and dendritic cells, and their contribution to the lymphangiogenesis, angiogenesis, and osteoclastogenic process in GSD. It is important to consider these mechanisms in patients with GSD, especially since new studies performed in earlier stages are required to confirm their use as novel diagnostic tools and find new possibilities for treatment.

Indexed as

ChildFemaleHumansMandibleOsteolysis, EssentialBone immunologyClinical caseGorham-Stout syndromeVanishing bone

Identifiers

PMID28004375
OpenAlexW2562704154

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.