Evidence map›Paper›PMID 24214028›Full record

ReviewPediatric blood & cancer2014

Novel molecular pathways in Gorham disease: implications for treatment.

Jeroen Hagendoorn, Torunn I Yock, Inne H M Borel Rinkes, Timothy P Padera, David H Ebb

Open access · greenAbstract readReview
In one paragraph

Review in Pediatric blood & cancer, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Complex lymphatic anomalies.Pediatric radiology · 2025
    Review
  2. Review
  3. Review
  4. Article
  5. Difficult Therapeutic Decisions in Gorham-Stout Disease-Case Report and Review of the Literature.International journal of environmental research and public health · 2022
    Review
  6. Article
  7. Review
  8. A Rare Case of Vanishing Bone Disease of Metacarpals.Journal of orthopaedic case reports · 2021
    Article
  9. Article
  10. Observational
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. 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

5 authors at 2 institutions in 2 countries.

Jeroen HagendoornDepartment of Surgical Oncology, University Medical Center Utrecht, Utrecht, The Netherlands.
Torunn I Yock
Inne H M Borel Rinkes
Timothy P Padera
David H Ebb
Harvard University · USUniversity Medical Center Utrecht · NL

Funding

Characterizing lymphatic micrometastases: prognostic and therapeutic implicationsDP2OD008780 · OD · MASSACHUSETTS GENERAL HOSPITAL · PI PADERA, TIMOTHY P · 2011 to 2011
$2.6M
Lymphatic RadiobiologyR00CA137167 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI PADERA, TIMOTHY P · 2011 to 2013
$699k
NCI NIH HHS R00 CA137167NCI NIH HHS R00CA137167NIH HHS DP2 OD008780NIH HHS DP2OD008780
6 · The paper itself

Abstract

Rapid advances in evidence-based treatment schedules are a hallmark of modern oncology. In rare neoplastic diseases, however, clinical expertise is hard to build and evidence based on randomized trials almost impossible to collect. Gorham disease is a rare form of lymphatic proliferation accompanied by osteolysis, which usually occurs in young adults. Despite the fact that the clinical course of Gorham disease is often devastating and occasionally fatal, insights into its biological background are sparse and standardized treatment unavailable. Interestingly, recent knowledge on the mechanisms of lymphangiogenesis may help elucidate the pathophysiology of Gorham disease and lead to novel treatment targets. Here, we discuss our current understanding of Gorham disease, discuss established and emerging therapeutic strategies, and attempt to frame a treatment rationale.

Indexed as

BiomarkersBone ResorptionHumansImmunohistochemistryOsteolysis, EssentialBiomarkersGorham diseaselymphangiogenesismolecular biologyrare tumorstumor biologyvascular malformations

Identifiers

PMID24214028
PMCPMC4123459
OpenAlexW1954748471

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.