Evidence map›Paper›PMID 30248728›Full record

ArticleLymphology2018

Primary versus trauma-induced Gorham-Stout disease.

N Tanoue, L Moedano, M Witte, M Montague, A Lukefahr, M Bernas

Open access · greenAbstract readCase Reports
In one paragraph

Article in Lymphology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Difficult Therapeutic Decisions in Gorham-Stout Disease-Case Report and Review of the Literature.International journal of environmental research and public health · 2022
    Review
  7. Osteopathy in Complex Lymphatic Anomalies.International journal of molecular sciences · 2022
    Review
  8. Article
  9. Review
  10. 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

6 authors at 1 institution in 1 country.

N TanoueDepartment of Surgery, University of Arizona College of Medicine, Tucson, Arizona USA.
L MoedanoDepartment of Surgery, University of Arizona College of Medicine, Tucson, Arizona USA.
M WitteDepartment of Surgery, University of Arizona College of Medicine, Tucson, Arizona USA.
M MontagueDepartment of Surgery, University of Arizona College of Medicine, Tucson, Arizona USA.
A LukefahrDepartment of Pahtology, University of Arizona College of Medicine, Tucson, Arizona USA.
M BernasDepartment of Surgery, University of Arizona College of Medicine, Tucson, Arizona USA.
University of Arizona · US

Funding

Short-Term Training to Increase the Diversity Pipeline in Heart/Lung/Blood ResearchR25HL108837 · NHLBI · UNIVERSITY OF ARIZONA · PI WITTE, MARLYS HEARST · 2011 to 2021
$2.4M
NHLBI NIH HHS R25 HL108837
6 · The paper itself

Abstract

Gorham-Stout disease - also known as "disappearing bone disease" is currently considered a single entity with varying clinical manifestations. We reviewed the existent literature from the earliest historic description(Jackson in 1838) and Gorham and Stout's original series of patients, multiple case reports and series since. After analyzing 212 reported cases, we identified 76 cases with details that recorded either a history of multifocal disease or an identifiable history of preceding trauma. From this review, we have defined two distinct Gorham-Stout entities - those characteristically associated with lymphangiomatosis [a form of GLA (generalized lymphangiomatosis) questionably distinguishable by bone biopsy and radiologic appearance] with multifocal distributed bone lesions, and those others, usually self-limited, first appearing after a traumatic event and always confined to a single bone or closely adjacent one. Multifocal disease is more likely to have chylothorax as a complication. These two Gorham-Stout entities differ in their demographic distribution, clinical history and manifestations, and they follow divergent clinical courses. The prognosis differs, and so should approaches to monitoring as well as acute and long-term treatment. Further research should seek to identify and define the differences in pathology and molecular mechanisms.

Indexed as

AdolescentAdultAgedBone and BonesChildChild, PreschoolChylothoraxContusionsDisease ManagementFemaleFractures, BoneHumansInfantLymphangiomaMaleMiddle Ageddisappearing bone diseasegeneralized lymphangiomatosis (GLA)Gorham-Stout disease (GSD)lymphangiogenesisosteolysistrauma

Identifiers

PMID30248728
PMCPMC7852030
OpenAlexW2884586726

What OpenQuestion holds

Textmetadata
LicenceTDM
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.